SELECT VARIANTS FROM EXCLUDE VARIANTS FROM
INDIVIDUALS:

SNP LIST:
GROUPS:

SAVED GENE LIST:

GENE LIST:
INDIVIDUALS:

EXCLUDE SNP LIST:
EXCLUDE GROUPS:

EXCLUDE SAVED GENE LIST:

EXCLUDE GENE LIST:
SELECT YOUR DISEASES:
OMIM:
CLINICAL GENOMICS DATABASE:
HGMD:
MUTATION TYPE:
CHR:

POS:
VARIANT EFFECT FUNCTIONAL CLASS IMPACT
DBSNP BUILD:


EXCLUDE VARIANTS AT VARISNP
READ DEPTH:

QUAL:
VARIANTS PER GENE:
SHOW ONLY VARIANTS PRESENT IN COMMON GENES BETWEEN ALL THE INDIVIDUALS SELECTED
SHOW ONLY VARIANTS AT EXACTLY SAME POSITION BETWEEN ALL THE INDIVIDUALS SELECTED
EXCLUDE ALL VARIANTS PRESENT IN LATEST DBSNP BUILD
SHOW ONLY VARIANTS PRESENT AT HGMD

FREQUENCIES

1000 GENOMES FREQUENCY

EXCLUDE ALL VARIANTS PRESENT IN 1000GENOMES
DBSNP FREQUENCY

EXCLUDE ALL VARIANTS PRESENT IN DBSNP
ESP6500 FREQUENCY

EXCLUDE ALL VARIANTS PRESENT IN EXOME SEQUENCING PROJECT

SCORES

SIFT SCORE

EXCLUDE VARIANTS WITHOUT SIFT SCORE
POLYPHEN2 SCORE

EXCLUDE VARIANTS WITHOUT POLYPHEN SCORE
CADD

EXCLUDE VARIANTS WITHOUT CADD SCORE
MCAP

EXCLUDE VARIANTS WITHOUT M-CAP SCORE
OPEN RESULT IN A NEW WINDOW
RESET FILTER | Save Config | Save Analysis

Genes:
ABTB1, AC004824.2, AC008394.1, ACIN1, ADAMTSL2, ADCY5, AGRN, AL450307.1, ALOX15, AMDHD1, ANKLE1, ANKRD36, AP003062.1, APOBEC3A, APOE, AQP7, ARAP1, ARHGAP22, ARHGEF37, ARMCX4, ASB10, ASTN2, ATP9B, ATPAF1, C16orf3, C1orf86, C22orf23, C22orf34, CABP1, CACNA1A, CAMTA2, CCDC57, CCDC61, CCDC63, CDC27, CDC34, CERS1, CES1, CHRND, CIT, CLIC3, CMTM4, COX4I1, CRIPAK, CYP11B1, CYP2A13, CYP2D7P, DFNB31, DTX2, DUSP8, EP400, EPPK1, FAM131C, FAM186A, FAM207A, FAM231D, FAM71E2, FCGBP, FLG, FMN2, FRG1, FRG2B, FSCB, FUT5, GARS, GATA5, GFM1, GGT1, GIPC1, GLRX3, GLT8D2, GOLGA6L2, GOLGA8B, GRIN2D, GRIN3B, HCN2, HECA, HERC2, HES6, HKR1, HLA-C, HLA-DRB5, HOXB1, IDNK, IFNL2, IGHD3-10, IGHG1, IGHV4-28, IGHV4-4, IGLJ2, IGSF3, IL32, KANK3, KCNJ12, KCNK18, KLRG2, KRT14, KRT6A, KRT6C, KRT86, KRTAP10-6, KRTAP10-7, KRTAP17-1, KRTAP4-3, KRTAP5-1, KRTAP5-2, KSR1, LAD1, LGALS9B, LHCGR, LILRA1, MAGEC1, MAPK3, MBOAT4, MED26, MEP1A, MLLT3, MROH6, MST1, MUC16, MUC3A, MUC4, MUC6, MYB, MYPOP, NAF1, NBPF3, NCCRP1, NCF1, NCOR2, NCR2, NHS, NIPSNAP3A, NKD2, NOB1, NOMO2, NOTCH2, NTN1, NUDT18, NUMBL, OBSCN, OPN1MW2, OR2T27, OR2T29, OR2T7, OR9G1, OTUD7A, PABPC3, PAM16, PARP4, PCDHB16, PCMTD1, PCSK5, PHLDB3, PPP1R15A, PRB4, PRG4, PRNP, PRSS1, PTPRE, RAP1GAP, RBM15B, RP11-830F9.6, RP11-998D10.1, RPTN, RSPH10B2, RUNX2, SAMD11, SBK3, SDHA, SETD8, SHANK1, SIRPB1, SLC39A4, SLC4A2, SOX18, SYT15, TCF3, TCN2, TCP10, TCP10L2, THEMIS, TMEM238, TNRC18, TPRXL, TPSAB1, TPSB2, TPSD1, TRBV6-5, TRBV7-1, TRBV7-8, TRIM66, TTC40, TUBB8P7, UQCRFS1, USH1C, USP6, UTF1, VARS2, VN1R2, WDR86, ZFR2, ZNF208, ZNF717, ZNF787, ZYX, hsa-mir-150,

Genes at Omim

ADAMTSL2, ADCY5, AGRN, APOE, AQP7, ASB10, CACNA1A, CERS1, CES1, CHRND, CIT, CYP11B1, FLG, FMN2, GARS, GFM1, GGT1, HERC2, HLA-C, HOXB1, IGSF3, KCNK18, KRT14, KRT6A, KRT6C, KRT86, LHCGR, MYB, NCF1, NHS, NOTCH2, PAM16, PRG4, PRNP, PRSS1, RUNX2, SDHA, SLC39A4, SOX18, TCF3, TCN2, USH1C, VARS2,
ADAMTSL2 Geleophysic dysplasia 1, 231050 (3)
ADCY5 Dyskinesia, familial, with facial myokymia, 606703 (3)
AGRN Myasthenic syndrome, congenital, 8, with pre- and postsynaptic defects, 615120 (3)
APOE Alzheimer disease-2, 104310 (3)
Hyperlipoproteinemia, type III (3)
Lipoprotein glomerulopathy, 611771 (3)
Sea-blue histiocyte disease, 269600 (3)
{?Macular degeneration, age-related}, 603075 (3)
{Myocardial infarction susceptibility} (3)
AQP7 [Glycerol quantitative trait locus], 614411 (3)
ASB10 Glaucoma 1, open angle, F, 603383 (3)
CACNA1A Epileptic encephalopathy, early infantile, 42, 617106 (3)
Episodic ataxia, type 2, 108500 (3)
Migraine, familial hemiplegic, 1, 141500 (3)
Migraine, familial hemiplegic, 1, with progressive cerebellar ataxia, 141500 (3)
Spinocerebellar ataxia 6, 183086 (3)
CERS1 ?Epilepsy, progressive myoclonic, 8, 616230 (3)
CES1 Carboxylesterase 1 deficiency (3)
CHRND ?Myasthenic syndrome, congenital, 3A, slow-channel, 616321 (3)
?Myasthenic syndrome, congenital, 3C, associated with acetylcholine receptor deficiency, 616323 (3)
Multiple pterygium syndrome, lethal type, 253290 (3)
Myasthenic syndrome, congenital, 3B, fast-channel, 616322 (3)
CIT Microcephaly 17, primary, autosomal recessive, 617090 (3)
CYP11B1 Adrenal hyperplasia, congenital, due to 11-beta-hydroxylase deficiency, 202010 (3)
Aldosteronism, glucocorticoid-remediable, 103900 (3)
FLG Ichthyosis vulgaris, 146700 (3)
{Dermatitis, atopic, susceptibility to, 2}, 605803 (3)
FMN2 Mental retardation, autosomal recessive 47, 616193 (3)
GARS Charcot-Marie-Tooth disease, type 2D, 601472 (3)
Neuropathy, distal hereditary motor, type VA, 600794 (3)
GFM1 Combined oxidative phosphorylation deficiency 1, 609060 (3)
GGT1 Glutathioninuria (1)
HERC2 Mental retardation, autosomal recessive 38, 615516 (3)
[Skin/hair/eye pigmentation 1, blond/brown hair], 227220 (3)
[Skin/hair/eye pigmentation 1, blue/nonblue eyes], 227220 (3)
HLA-C {HIV-1 viremia, susceptibility to}, 609423 (3)
{Psoriasis susceptibility 1}, 177900 (3)
HOXB1 Facial paresis, hereditary congenital, 3, 614744 (3)
IGSF3 ?Lacrimal duct defect, 149700 (3)
KCNK18 {Migraine, with or without aura, susceptibility to, 13}, 613656 (3)
KRT14 Dermatopathia pigmentosa reticularis, 125595 (3)
Epidermolysis bullosa simplex, Dowling-Meara type, 131760 (3)
Epidermolysis bullosa simplex, Koebner type, 131900 (3)
Epidermolysis bullosa simplex, Weber-Cockayne type, 131800 (3)
Epidermolysis bullosa simplex, recessive 1, 601001 (3)
Naegeli-Franceschetti-Jadassohn syndrome, 161000 (3)
KRT6A Pachyonychia congenita 3, 615726 (3)
KRT6C Palmoplantar keratoderma, nonepidermolytic, focal or diffuse, 615735 (3)
KRT86 Monilethrix, 158000 (3)
LHCGR Leydig cell adenoma, somatic, with precocious puberty, 176410 (3)
Leydig cell hypoplasia with hypergonadotropic hypogonadism, 238320 (3)
Leydig cell hypoplasia with pseudohermaphroditism, 238320 (3)
Luteinizing hormone resistance, female, 238320 (3)
Precocious puberty, male, 176410 (3)
MYB {T-cell acute lymphoblastic leukemia} (3)
NCF1 Chronic granulomatous disease due to deficiency of NCF-1, 233700 (3)
NHS Cataract 40, X-linked, 302200 (3)
Nance-Horan syndrome, 302350 (3)
NOTCH2 Alagille syndrome 2, 610205 (3)
Hajdu-Cheney syndrome, 102500 (3)
PAM16 Spondylometaphyseal dysplasia, Megarbane-Dagher-Melike type, 613320 (3)
PRG4 Camptodactyly-arthropathy-coxa vara-pericarditis syndrome, 208250 (3)
PRNP Cerebral amyloid angiopathy, PRNP-related, 137440 (3)
Creutzfeldt-Jakob disease, 123400 (3)
Gerstmann-Straussler disease, 137440 (3)
Huntington disease-like 1, 603218 (3)
Insomnia, fatal familial, 600072 (3)
Prion disease with protracted course, 606688 (3)
{Kuru, susceptibility to}, 245300 (3)
PRSS1 Pancreatitis, hereditary, 167800 (3)
Trypsinogen deficiency, 614044 (1)
RUNX2 Cleidocranial dysplasia, 119600 (3)
Cleidocranial dysplasia, forme fruste, dental anomalies only, 119600 (3)
Cleidocranial dysplasia, forme fruste, with brachydactyly, 119600 (3)
Metaphyseal dysplasia with maxillary hypoplasia with or without brachydactyly, 156510 (3)
SDHA Cardiomyopathy, dilated, 1GG, 613642 (3)
Leigh syndrome, 256000 (3)
Mitochondrial respiratory chain complex II deficiency, 252011 (3)
Paragangliomas 5, 614165 (3)
SLC39A4 Acrodermatitis enteropathica, 201100 (3)
SOX18 Hypotrichosis-lymphedema-telangiectasia syndrome, 607823 (3)
Hypotrichosis-lymphedema-telangiectasia-renal defect syndrome, 137940 (3)
TCF3 Agammaglobulinemia 8, autosomal dominant, 616941 (3)
TCN2 Transcobalamin II deficiency, 275350 (3)
USH1C Deafness, autosomal recessive 18A, 602092 (3)
Usher syndrome, type 1C, 276904 (3)
VARS2 Combined oxidative phosphorylation deficiency 20, 615917 (3)

Genes at Clinical Genomics Database

ADAMTSL2, ADCY5, AGRN, APOE, CACNA1A, CERS1, CES1, CHRND, CYP11B1, FLG, FMN2, GARS, GFM1, HERC2, HOXB1, IGSF3, KCNK18, KRT14, KRT6A, KRT6C, KRT86, LHCGR, NCF1, NHS, NOTCH2, PAM16, PRG4, PRNP, PRSS1, RUNX2, SDHA, SLC39A4, SOX18, TCF3, TCN2, USH1C, VARS2,
ADAMTSL2 Geleophysic dysplasia 1
ADCY5 Dyskinesia, familial, with facial myokymia
AGRN Myasthenic syndrome, congenital 8
APOE Sea-blue histiocyte disease
Lipoprotein glomerulopathy
Dysbetalipoproteinemia, familial (Hyperlipoproteinemia, type III)
CACNA1A Migraine, familial hemiplegic 1
Episodic ataxia, type 2
CERS1 Epilepsy, progressive myoclonic 8
CES1 Carboxylesterase 1 deficiency
CHRND Myasthenic syndrome, congenital, 3C
Myasthenic syndrome,congenital, slow-channel
Myasthenic syndrome, congenital, fast channel
CYP11B1 Glucocorticoid-remediable aldosteronism
Adrenal hyperplasia, congenital, due to 11-beta-hydroxylase deficiency
FLG Icthyosis vulgaris
FMN2 Mental retardation, autosomal recessive, 47
GARS Neuropathy, distal hereditary motor, type V
Charcot-Marie-Tooth disease, type 2D
GFM1 Combined oxidative phosphorylation deficiency 1
HERC2 Mental retardation, autosomal recessive 38
Skin/hair/eye pigmentation 1
HOXB1 Facial paresis, hereditary congenital, 3
IGSF3 Lacrimal duct defect
KCNK18 Migraine, with or without aura, susceptibility to, 13
KRT14 Epidermolysis bullosa simplex, Dowling-Meara type
Epidermolysis bullosa simplex, Weber-Cockayne type
Epidermolysis bullosa simplex, Koebner type
Dermatopathia pigmentosa reticularis
Naegeli-Franceschetti-Jadassohn syndrome
Epidermolysis bullosa simplex, autosomal recessive
KRT6A Pachyonychia congenita 3
KRT6C Palmoplantar keratoderma, nonepidermolytic, focal or diffuse
KRT86 Monilethrix
LHCGR Precocious puberty, male
Luteinizing hormone resistance, female
Leydig cell hypoplasia type II
Leydig cell hypoplasia type I
NCF1 Chronic granulomatous disease, autosomal recessive, cytochrome b-positive, type I
NHS Cataract 40
Nance-Horan syndrome
NOTCH2 Alagille syndrome 2
PAM16 Spondylometaphyseal dysplasia, Megarbane-Dagher-Melki type
PRG4 Camptodactyly-arthropathy-coxa vara-pericarditis syndrome
PRNP Dementia, Lewy body
Insomnia, fatal familial
Creutzfeldt-Jakob disease
Gerstmann-Straussler disease
Huntington disease-like 1
Spongiform encephalopathy with neuropsychiatric features
PRSS1 Pancreatitis, hereditary
RUNX2 Metaphyseal dysplasia with maxillary hypoplasia with or without brachydactyly
Cleidocranial dysplasia
SDHA Leigh syndrome/Mitochondrial respiratory chain complex II deficiency
Cardiomyopathy, dilated, 1GG
Gastrointestinal stromal tumors
Paragangliomas 5
SLC39A4 Acrodermatitis enteropathica
SOX18 Hypotrichosis-lymphedema-telangiectasia-renal defect syndrome
Hypotrichosis-lymphedema-telangiectasia syndrome
TCF3 Agammaglobulinemia 8, autosomal dominant
TCN2 Transcobalamin II deficiency
USH1C Deafness, autosomal recessive 18A
Usher syndrome, type IC
VARS2 Combined oxidative phosphorylation deficiency 20

Genes at HGMD

Summary

Number of Variants: 5767
Number of Genes: 207

Export to: CSV

ABTB1

Omim - GeneCards - NCBI
Options Individual Chr
RsId
Pos
Qual
Ref
Alt
Filter Gen
Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 3 rs35703629
dbSNP
127394820 29.77 C T LowQual 0/1 8 SYNONYMOUS_CODING LOW SILENT 0.11522 0.11520 0.16818 None None None None None None None

AC004824.2

Omim - GeneCards - NCBI
Options Individual Chr
RsId
Pos
Qual
Ref
Alt
Filter Gen
Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 1 rs1635587
dbSNP
17664280 12.77 T C LowQual 1/1 1 SYNONYMOUS_CODING LOW SILENT 0.60164 0.60160 None None None None None None None
View mm170241ct 1 rs1748026
dbSNP
17664235 11.83 T C LowQual 1/1 1 SYNONYMOUS_CODING LOW SILENT 0.60184 0.60180 None None None None None None None

AC008394.1

Omim - GeneCards - NCBI
Options Individual Chr
RsId
Pos
Qual
Ref
Alt
Filter Gen
Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 5 rs254643
dbSNP
86513974 29.77 A G LowQual 0/1 5 NON_SYNONYMOUS_CODING MODERATE MISSENSE 0.87800 0.87800 0.00 None None None None None None None

ACIN1

Omim - GeneCards - NCBI
Options Individual Chr
RsId
Pos
Qual
Ref
Alt
Filter Gen
Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 14 rs80007670
dbSNP
23548793 15.88 C T LowQual 0/1 111 NON_SYNONYMOUS_CODING MODERATE MISSENSE 0.00231 0.01 None None None None None None None

ADAMTSL2

Omim - GeneCards - NCBI
Options Individual Chr
RsId
Pos
Qual
Ref
Alt
Filter Gen
Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 9 rs7868941
dbSNP
136421044 26.78 C T LowQual 0/1 7 SYNONYMOUS_CODING LOW SILENT None None None None None None None

ADCY5

Omim - GeneCards - NCBI
Options Individual Chr
RsId
Pos
Qual
Ref
Alt
Filter Gen
Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 3 . 123023016 20.8 T G LowQual 0/1 23 SYNONYMOUS_CODING LOW SILENT None None None None None None None

AGRN

Omim - GeneCards - NCBI
Options Individual Chr
RsId
Pos
Qual
Ref
Alt
Filter Gen
Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 1 . 983577 12.05 A C LowQual 0/1 11 NON_SYNONYMOUS_CODING MODERATE MISSENSE 0.07 0.03 None None None None None None None

AL450307.1

Omim - GeneCards - NCBI
Options Individual Chr
RsId
Pos
Qual
Ref
Alt
Filter Gen
Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 10 rs4897781
dbSNP
133607904 12.77 G A LowQual 1/1 1 NON_SYNONYMOUS_CODING MODERATE MISSENSE 0.58367 0.58370 0.00 None None None None None None None

ALOX15

Omim - GeneCards - NCBI
Options Individual Chr
RsId
Pos
Qual
Ref
Alt
Filter Gen
Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 17 rs3887815
dbSNP
4541560 12.77 G A LowQual 1/1 9 SYNONYMOUS_CODING LOW SILENT None None None None None None None

AMDHD1

Omim - GeneCards - NCBI
Options Individual Chr
RsId
Pos
Qual
Ref
Alt
Filter Gen
Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 12 rs7955450
dbSNP
96337183 26.78 A G LowQual 0/1 8 NON_SYNONYMOUS_CODING MODERATE MISSENSE 0.71845 0.71850 0.56 0.00 None None None None None None None

ANKLE1

Omim - GeneCards - NCBI
Options Individual Chr
RsId
Pos
Qual
Ref
Alt
Filter Gen
Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 19 rs1465581
dbSNP
17397481 24.78 G T LowQual 0/1 10 None None None 1.00 0.00 None None None None None None None

ANKRD36

Omim - GeneCards - NCBI
Options Individual Chr
RsId
Pos
Qual
Ref
Alt
Filter Gen
Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 2 . 97911776 12.05 T C LowQual 0/1 461 NON_SYNONYMOUS_CODING MODERATE MISSENSE 0.35 0.07 None None None None None None None
View mm170241ct 2 rs370246796
dbSNP
97911762 12.99 C T LowQual 0/1 460 NON_SYNONYMOUS_CODING MODERATE MISSENSE 1.00 0.20 None None None None None None None

AP003062.1

Omim - GeneCards - NCBI
Options Individual Chr
RsId
Pos
Qual
Ref
Alt
Filter Gen
Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 11 rs11822068
dbSNP
134856358 29.77 C A LowQual 0/1 4 SYNONYMOUS_CODING LOW SILENT None None None None None None None

APOBEC3A

Omim - GeneCards - NCBI
Options Individual Chr
RsId
Pos
Qual
Ref
Alt
Filter Gen
Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 22 rs2294363
dbSNP
39357634 10.2 A G LowQual 0/1 32 SYNONYMOUS_CODING LOW SILENT None None None None None None None

APOE

Omim - GeneCards - NCBI
Options Individual Chr
RsId
Pos
Qual
Ref
Alt
Filter Gen
Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 19 rs440446
dbSNP
45409167 23.79 C G LowQual 0/1 8 None None None 0.62620 0.62620 0.00 None None None None None None None

AQP7

Omim - GeneCards - NCBI
Options Individual Chr
RsId
Pos
Qual
Ref
Alt
Filter Gen
Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 9 rs145516206
dbSNP
33385698 17.84 A G LowQual 0/1 12 NON_SYNONYMOUS_CODING MODERATE MISSENSE 0.02 0.06 None None None None None None None
View mm170241ct 9 rs79779983
dbSNP
33385667 29.77 A G LowQual 0/1 7 SYNONYMOUS_CODING LOW SILENT None None None None None None None
View mm170241ct 9 rs139024279
dbSNP
33385690 17.84 G T LowQual 0/1 11 NON_SYNONYMOUS_CODING MODERATE MISSENSE 0.00020 0.03 0.46 None None None None None None None

ARAP1

Omim - GeneCards - NCBI
Options Individual Chr
RsId
Pos
Qual
Ref
Alt
Filter Gen
Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 11 . 72418366 15.88 C T LowQual 0/1 18 NON_SYNONYMOUS_CODING MODERATE MISSENSE 0.60 0.00 None None None None None None None

ARHGAP22

Omim - GeneCards - NCBI
Options Individual Chr
RsId
Pos
Qual
Ref
Alt
Filter Gen
Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 10 rs7089439
dbSNP
49732141 17.84 C T LowQual 0/1 16 None None None 0.23063 0.23060 None None None None None None None

ARHGEF37

Omim - GeneCards - NCBI
Options Individual Chr
RsId
Pos
Qual
Ref
Alt
Filter Gen
Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 5 rs3733661
dbSNP
149008484 29.77 G A LowQual 0/1 8 SYNONYMOUS_CODING LOW SILENT 0.05691 0.05691 0.00418 None None None None None None None

ARMCX4

Omim - GeneCards - NCBI
Options Individual Chr
RsId
Pos
Qual
Ref
Alt
Filter Gen
Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct X rs34379067
dbSNP
100749038 11.83 C T LowQual 1/1 1 NON_SYNONYMOUS_CODING MODERATE MISSENSE 0.69 None None None None None None None
View mm170241ct X rs782433301
dbSNP
100749041 11.83 A G LowQual 1/1 1 NON_SYNONYMOUS_CODING MODERATE MISSENSE 0.62 None None None None None None None

ASB10

Omim - GeneCards - NCBI
Options Individual Chr
RsId
Pos
Qual
Ref
Alt
Filter Gen
Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 7 rs104886485
dbSNP
150878034 11.83 G A LowQual 1/1 1 NON_SYNONYMOUS_CODING MODERATE MISSENSE 0.22 0.34 None None None None None None None

ASTN2

Omim - GeneCards - NCBI
Options Individual Chr
RsId
Pos
Qual
Ref
Alt
Filter Gen
Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 9 . 120177082 11.12 C T LowQual 0/1 3 SYNONYMOUS_CODING LOW SILENT None None None None None None None

ATP9B

Omim - GeneCards - NCBI
Options Individual Chr
RsId
Pos
Qual
Ref
Alt
Filter Gen
Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 18 rs4078115
dbSNP
76829525 26.78 A G LowQual 0/1 10 NON_SYNONYMOUS_CODING MODERATE MISSENSE 0.31430 0.31430 0.17122 0.23 0.00 None None None None None None None

ATPAF1

Omim - GeneCards - NCBI
Options Individual Chr
RsId
Pos
Qual
Ref
Alt
Filter Gen
Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 1 . 47134063 11.83 T G LowQual 1/1 1 NON_SYNONYMOUS_START LOW MISSENSE 0.00 0.00 None None None None None None None

C16orf3

Omim - GeneCards - NCBI
Options Individual Chr
RsId
Pos
Qual
Ref
Alt
Filter Gen
Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 16 rs61118444
dbSNP
90095597 16.86 T C LowQual 0/1 11 NON_SYNONYMOUS_CODING MODERATE MISSENSE 0.46266 0.46270 0.49 0.00 None None None None None None None
View mm170241ct 16 rs62640380
dbSNP
90095582 13.95 T C LowQual 0/1 15 NON_SYNONYMOUS_CODING MODERATE MISSENSE 0.38 0.00 None None None None None None None

C1orf86

Omim - GeneCards - NCBI
Options Individual Chr
RsId
Pos
Qual
Ref
Alt
Filter Gen
Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 1 rs6662296
dbSNP
2126139 10.9 C G LowQual 1/1 1 None None None 1.00 0.00 None None None None None None None

C22orf23

Omim - GeneCards - NCBI
Options Individual Chr
RsId
Pos
Qual
Ref
Alt
Filter Gen
Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 22 . 38340464 11.12 C T LowQual 0/1 18 NON_SYNONYMOUS_CODING MODERATE MISSENSE 0.06 0.35 None None None None None None None

C22orf34

Omim - GeneCards - NCBI
Options Individual Chr
RsId
Pos
Qual
Ref
Alt
Filter Gen
Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 22 . 50017984 23.82 T G LowQual 0/1 6 SYNONYMOUS_CODING LOW SILENT None None None None None None None

CABP1

Omim - GeneCards - NCBI
Options Individual Chr
RsId
Pos
Qual
Ref
Alt
Filter Gen
Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 12 . 121078820 12.77 C T LowQual 1/1 1 NON_SYNONYMOUS_CODING MODERATE MISSENSE 0.17 0.32 None None None None None None None

CACNA1A

Omim - GeneCards - NCBI
Options Individual Chr
RsId
Pos
Qual
Ref
Alt
Filter Gen
Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 19 rs147221323
dbSNP
13318811 20.8 C T LowQual 0/1 9 SYNONYMOUS_CODING LOW SILENT 0.02137 0.02137 0.02552 None None None None None None None

CAMTA2

Omim - GeneCards - NCBI
Options Individual Chr
RsId
Pos
Qual
Ref
Alt
Filter Gen
Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 17 . 4883207 21.8 T G LowQual 0/1 23 SYNONYMOUS_CODING LOW SILENT None None None None None None None

CCDC57

Omim - GeneCards - NCBI
Options Individual Chr
RsId
Pos
Qual
Ref
Alt
Filter Gen
Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 17 rs7406163
dbSNP
80086389 28.77 C T LowQual 0/1 6 NON_SYNONYMOUS_CODING MODERATE MISSENSE 0.41294 0.41290 0.44123 0.70 0.73 None None None None None None None

CCDC61

Omim - GeneCards - NCBI
Options Individual Chr
RsId
Pos
Qual
Ref
Alt
Filter Gen
Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 19 rs7271
dbSNP
46518682 29.77 G A LowQual 0/1 13 NON_SYNONYMOUS_CODING MODERATE MISSENSE 0.11522 0.11520 0.32 0.00 None None None None None None None

CCDC63

Omim - GeneCards - NCBI
Options Individual Chr
RsId
Pos
Qual
Ref
Alt
Filter Gen
Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 12 rs114266945
dbSNP
111336918 25.78 C T LowQual 0/1 9 NON_SYNONYMOUS_CODING MODERATE MISSENSE 0.00200 0.00200 0.00162 0.40 0.01 None None None None None None None

CDC27

Omim - GeneCards - NCBI
Options Individual Chr
RsId
Pos
Qual
Ref
Alt
Filter Gen
Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 17 rs200940073
dbSNP
45219247 21.8 G A LowQual 0/1 34 NON_SYNONYMOUS_CODING MODERATE MISSENSE 0.00 0.99 None None None None None None None
View mm170241ct 17 rs78108688
dbSNP
45234657 12.99 T C LowQual 0/1 39 NON_SYNONYMOUS_CODING MODERATE MISSENSE 0.49 0.00 None None None None None None None

CDC34

Omim - GeneCards - NCBI
Options Individual Chr
RsId
Pos
Qual
Ref
Alt
Filter Gen
Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 19 rs16990638
dbSNP
541242 21.8 T C LowQual 0/1 5 None None None 0.06150 0.06150 None None None None None None None

CERS1

Omim - GeneCards - NCBI
Options Individual Chr
RsId
Pos
Qual
Ref
Alt
Filter Gen
Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 19 rs113536478
dbSNP
19006648 11.12 A G LowQual 0/1 3 SYNONYMOUS_CODING LOW SILENT 0.24561 0.24560 None None None None None None None

CES1

Omim - GeneCards - NCBI
Options Individual Chr
RsId
Pos
Qual
Ref
Alt
Filter Gen
Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 16 rs3826194
dbSNP
55862762 12.05 C G LowQual 0/1 64 SYNONYMOUS_CODING LOW SILENT None None None None None None None

CHRND

Omim - GeneCards - NCBI
Options Individual Chr
RsId
Pos
Qual
Ref
Alt
Filter Gen
Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 2 rs2245601
dbSNP
233390937 27.77 A G LowQual 0/1 7 SYNONYMOUS_CODING LOW SILENT 0.48343 0.48340 0.44871 None None None None None None None

CIT

Omim - GeneCards - NCBI
Options Individual Chr
RsId
Pos
Qual
Ref
Alt
Filter Gen
Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 12 rs904654
dbSNP
120189888 18.82 T C LowQual 0/1 14 SYNONYMOUS_CODING LOW SILENT 0.53854 0.53850 0.48778 None None None None None None None

CLIC3

Omim - GeneCards - NCBI
Options Individual Chr
RsId
Pos
Qual
Ref
Alt
Filter Gen
Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 9 rs149417490
dbSNP
139889162 29.77 C A LowQual 0/1 9 NON_SYNONYMOUS_CODING MODERATE MISSENSE 0.00799 0.00799 0.01520 0.02 0.96 None None None None None None None

CMTM4

Omim - GeneCards - NCBI
Options Individual Chr
RsId
Pos
Qual
Ref
Alt
Filter Gen
Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 16 rs192164111
dbSNP
66730270 11.12 C T LowQual 0/1 3 SYNONYMOUS_CODING LOW SILENT 0.03514 0.03514 None None None None None None None

COX4I1

Omim - GeneCards - NCBI
Options Individual Chr
RsId
Pos
Qual
Ref
Alt
Filter Gen
Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 16 rs2733964
dbSNP
85838195 12.77 A C LowQual 1/1 2 None None None 0.97684 0.97680 None None None None None None None
View mm170241ct 16 rs2599089
dbSNP
85838166 11.83 G A LowQual 1/1 1 None None None 0.97704 0.97700 0.51 0.00 None None None None None None None

CRIPAK

Omim - GeneCards - NCBI
Options Individual Chr
RsId
Pos
Qual
Ref
Alt
Filter Gen
Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 4 rs527798572
dbSNP
1389034 12.99 C G LowQual 0/1 22 SYNONYMOUS_CODING LOW SILENT 0.02656 0.02656 None None None None None None None
View mm170241ct 4 rs76728908
dbSNP
1388724 12.99 C G LowQual 0/1 19 NON_SYNONYMOUS_CODING MODERATE MISSENSE 0.11102 0.11100 0.30 0.00 None None None None None None None

CYP11B1

Omim - GeneCards - NCBI
Options Individual Chr
RsId
Pos
Qual
Ref
Alt
Filter Gen
Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 8 rs61752794
dbSNP
143956748 24.78 T C LowQual 0/1 16 None None None 0.02097 0.02097 0.01508 0.23 0.00 None None None None None None None

CYP2A13

Omim - GeneCards - NCBI
Options Individual Chr
RsId
Pos
Qual
Ref
Alt
Filter Gen
Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 19 rs75703079
dbSNP
41595958 29.77 C T LowQual 0/1 15 NON_SYNONYMOUS_CODING MODERATE MISSENSE 1.00 0.02 None None None None None None None

CYP2D7P

Omim - GeneCards - NCBI
Options Individual Chr
RsId
Pos
Qual
Ref
Alt
Filter Gen
Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 22 rs2267448
dbSNP
42538618 12.05 A G LowQual 0/1 12 NON_SYNONYMOUS_CODING MODERATE MISSENSE 0.40136 0.40140 0.15 0.00 None None None None None None None

DFNB31

Omim - GeneCards - NCBI
Options Individual Chr
RsId
Pos
Qual
Ref
Alt
Filter Gen
Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 9 rs2274158
dbSNP
117166206 19.81 G T LowQual 0/1 11 NON_SYNONYMOUS_CODING MODERATE MISSENSE 0.22244 0.22240 0.17992 0.46 0.00 None None None None None None None

DTX2

Omim - GeneCards - NCBI
Options Individual Chr
RsId
Pos
Qual
Ref
Alt
Filter Gen
Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 7 rs147644708
dbSNP
76129758 11.12 G A LowQual 0/1 47 NON_SYNONYMOUS_CODING+SPLICE_SITE_REGION MODERATE MISSENSE 0.32 0.00 None None None None None None None

DUSP8

Omim - GeneCards - NCBI
Options Individual Chr
RsId
Pos
Qual
Ref
Alt
Filter Gen
Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 11 rs7129499
dbSNP
1578090 12.77 G A LowQual 1/1 1 SYNONYMOUS_CODING LOW SILENT 0.48622 0.48620 None None None None None None None

EP400

Omim - GeneCards - NCBI
Options Individual Chr
RsId
Pos
Qual
Ref
Alt
Filter Gen
Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 12 rs74479394
dbSNP
132547096 11.12 G A LowQual 0/1 12 SYNONYMOUS_CODING LOW SILENT 0.14657 0.14660 0.00008 None None None None None None None

EPPK1

Omim - GeneCards - NCBI
Options Individual Chr
RsId
Pos
Qual
Ref
Alt
Filter Gen
Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 8 rs112377501
dbSNP
144940706 16.86 C T LowQual 0/1 154 NON_SYNONYMOUS_CODING MODERATE MISSENSE 0.83 None None None None None None None

FAM131C

Omim - GeneCards - NCBI
Options Individual Chr
RsId
Pos
Qual
Ref
Alt
Filter Gen
Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 1 rs75273615
dbSNP
16385184 18.82 G A LowQual 0/1 8 SYNONYMOUS_CODING LOW SILENT None None None None None None None

FAM186A

Omim - GeneCards - NCBI
Options Individual Chr
RsId
Pos
Qual
Ref
Alt
Filter Gen
Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 12 rs201307392
dbSNP
50745703 15.88 T G LowQual 0/1 49 NON_SYNONYMOUS_CODING MODERATE MISSENSE 0.25 0.00 None None None None None None None

FAM207A

Omim - GeneCards - NCBI
Options Individual Chr
RsId
Pos
Qual
Ref
Alt
Filter Gen
Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 21 rs3737075
dbSNP
46396659 19.81 G C LowQual 0/1 5 NON_SYNONYMOUS_CODING MODERATE MISSENSE 0.15216 0.15220 0.17443 1.00 0.00 None None None None None None None

FAM231D

Omim - GeneCards - NCBI
Options Individual Chr
RsId
Pos
Qual
Ref
Alt
Filter Gen
Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 1 rs149550720
dbSNP
149676574 24.78 G C LowQual 0/1 25 NON_SYNONYMOUS_CODING MODERATE MISSENSE 0.96 None None None None None None None
View mm170241ct 1 rs523903
dbSNP
149676075 12.77 G A LowQual 1/1 1 SYNONYMOUS_CODING LOW SILENT 0.91114 0.91110 None None None None None None None

FAM71E2

Omim - GeneCards - NCBI
Options Individual Chr
RsId
Pos
Qual
Ref
Alt
Filter Gen
Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 19 rs113307911
dbSNP
55870835 20.8 A C LowQual 0/1 8 SYNONYMOUS_CODING LOW SILENT 0.03375 0.03375 None None None None None None None

FCGBP

Omim - GeneCards - NCBI
Options Individual Chr
RsId
Pos
Qual
Ref
Alt
Filter Gen
Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 19 rs62108883,rs75294622
dbSNP
40392482 26.75 A G LowQual 1/1 7 SYNONYMOUS_CODING LOW SILENT None None None None None None None
View mm170241ct 19 rs11669847
dbSNP
40384605 12.77 A G LowQual 1/1 26 SYNONYMOUS_CODING LOW SILENT None None None None None None None

FLG

Omim - GeneCards - NCBI
Options Individual Chr
RsId
Pos
Qual
Ref
Alt
Filter Gen
Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 1 rs71625191
dbSNP
152284814 18.82 T C LowQual 0/1 49 NON_SYNONYMOUS_CODING MODERATE MISSENSE 0.01 None None None None None None None
View mm170241ct 1 rs2065958
dbSNP
152278049 20.83 A C LowQual 0/1 3 NON_SYNONYMOUS_CODING MODERATE MISSENSE 0.17292 0.17290 0.00 None None None None None None None

FMN2

Omim - GeneCards - NCBI
Options Individual Chr
RsId
Pos
Qual
Ref
Alt
Filter Gen
Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 1 rs12732924
dbSNP
240371554 12.77 A G LowQual 1/1 1 NON_SYNONYMOUS_CODING MODERATE MISSENSE 0.95887 0.95890 0.00 None None None None None None None
View mm170241ct 1 rs111896385
dbSNP
240370985 23.79 C T LowQual 0/1 5 NON_SYNONYMOUS_CODING MODERATE MISSENSE 0.00 None None None None None None None

FRG1

Omim - GeneCards - NCBI
Options Individual Chr
RsId
Pos
Qual
Ref
Alt
Filter Gen
Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 4 . 190876305 28.77 A T LowQual 0/1 494 NON_SYNONYMOUS_CODING+SPLICE_SITE_REGION MODERATE MISSENSE 0.00 0.02 None None None None None None None

FRG2B

Omim - GeneCards - NCBI
Options Individual Chr
RsId
Pos
Qual
Ref
Alt
Filter Gen
Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 10 rs200347477
dbSNP
135439049 10.2 G C LowQual 0/1 157 NON_SYNONYMOUS_CODING MODERATE MISSENSE 0.00020 0.00020 0.85 0.00 None None None None None None None

FSCB

Omim - GeneCards - NCBI
Options Individual Chr
RsId
Pos
Qual
Ref
Alt
Filter Gen
Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 14 . 44974214 12.77 C A LowQual 1/1 3 NON_SYNONYMOUS_CODING MODERATE MISSENSE 0.13 0.00 None None None None None None None

FUT5

Omim - GeneCards - NCBI
Options Individual Chr
RsId
Pos
Qual
Ref
Alt
Filter Gen
Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 19 rs4807054
dbSNP
5866724 21.8 G A LowQual 0/1 7 NON_SYNONYMOUS_CODING MODERATE MISSENSE 0.40016 0.40020 0.32631 0.22 0.20 None None None None None None None

GARS

Omim - GeneCards - NCBI
Options Individual Chr
RsId
Pos
Qual
Ref
Alt
Filter Gen
Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 7 rs1049402
dbSNP
30634661 10.2 C G LowQual 0/1 17 NON_SYNONYMOUS_CODING MODERATE MISSENSE 0.64936 0.64940 0.26012 0.87 0.00 None None None None None None None

GATA5

Omim - GeneCards - NCBI
Options Individual Chr
RsId
Pos
Qual
Ref
Alt
Filter Gen
Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 20 rs6061550
dbSNP
61039958 23.79 T C LowQual 0/1 8 SYNONYMOUS_CODING LOW SILENT 0.62919 0.62920 0.39940 None None None None None None None

GFM1

Omim - GeneCards - NCBI
Options Individual Chr
RsId
Pos
Qual
Ref
Alt
Filter Gen
Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 3 rs1864507
dbSNP
158362441 23.79 T C LowQual 0/1 13 SYNONYMOUS_CODING LOW SILENT 0.58307 0.58310 0.40100 None None None None None None None

GGT1

Omim - GeneCards - NCBI
Options Individual Chr
RsId
Pos
Qual
Ref
Alt
Filter Gen
Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 22 rs2330843
dbSNP
25010872 20.8 A T LowQual 0/1 21 SPLICE_SITE_REGION+SYNONYMOUS_CODING LOW SILENT None None None None None None None
View mm170241ct 22 rs142987478
dbSNP
25011031 12.05 C T LowQual 0/1 16 PROTEIN_INTERACTION_LOCUS HIGH 0.00 1.00 None None None None None None None
View mm170241ct 22 rs201519055
dbSNP
25011062 20.8 C G LowQual 0/1 10 NON_SYNONYMOUS_CODING MODERATE MISSENSE 0.34 0.00 None None None None None None None
View mm170241ct 22 . 25011033 10.2 C A LowQual 0/1 15 SYNONYMOUS_CODING LOW SILENT None None None None None None None

GIPC1

Omim - GeneCards - NCBI
Options Individual Chr
RsId
Pos
Qual
Ref
Alt
Filter Gen
Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 19 rs3815715
dbSNP
14590236 29.77 C T LowQual 0/1 6 SYNONYMOUS_CODING LOW SILENT 0.30731 0.30730 0.22656 None None None None None None None

GLRX3

Omim - GeneCards - NCBI
Options Individual Chr
RsId
Pos
Qual
Ref
Alt
Filter Gen
Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 10 rs13991
dbSNP
131934747 12.77 G C LowQual 1/1 1 NON_SYNONYMOUS_CODING MODERATE MISSENSE 0.16254 0.16250 0.13805 0.20 0.00 None None None None None None None

GLT8D2

Omim - GeneCards - NCBI
Options Individual Chr
RsId
Pos
Qual
Ref
Alt
Filter Gen
Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 12 rs3817602
dbSNP
104390525 27.77 G A LowQual 0/1 15 SYNONYMOUS_CODING LOW SILENT 0.11462 0.11460 0.08488 None None None None None None None

GOLGA6L2

Omim - GeneCards - NCBI
Options Individual Chr
RsId
Pos
Qual
Ref
Alt
Filter Gen
Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 15 rs759748627
dbSNP
23686019 28.77 G C LowQual 0/1 37 NON_SYNONYMOUS_CODING MODERATE MISSENSE 0.00 None None None None None None None
View mm170241ct 15 rs75983100
dbSNP
23686031 17.84 T C LowQual 0/1 39 NON_SYNONYMOUS_CODING MODERATE MISSENSE 0.00 None None None None None None None
View mm170241ct 15 rs370576161
dbSNP
23685185 23.79 C A LowQual 0/1 14 NON_SYNONYMOUS_CODING MODERATE MISSENSE 0.00 None None None None None None None
View mm170241ct 15 rs71401069
dbSNP
23685126 22.79 T C LowQual 0/1 9 SYNONYMOUS_CODING LOW SILENT 0.72224 0.72220 None None None None None None None
View mm170241ct 15 rs796298120
dbSNP
23685178 24.78 C G LowQual 0/1 12 NON_SYNONYMOUS_CODING MODERATE MISSENSE 0.00 None None None None None None None

GOLGA8B

Omim - GeneCards - NCBI
Options Individual Chr
RsId
Pos
Qual
Ref
Alt
Filter Gen
Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 15 rs564951643
dbSNP
34820227 25.8 C T LowQual 0/1 3 NON_SYNONYMOUS_CODING MODERATE MISSENSE 0.45567 0.45570 1.00 0.00 None None None None None None None

GRIN2D

Omim - GeneCards - NCBI
Options Individual Chr
RsId
Pos
Qual
Ref
Alt
Filter Gen
Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 19 rs62130268
dbSNP
48945880 29.77 T C LowQual 0/1 4 SYNONYMOUS_CODING LOW SILENT 0.74720 0.74720 0.10580 None None None None None None None

GRIN3B

Omim - GeneCards - NCBI
Options Individual Chr
RsId
Pos
Qual
Ref
Alt
Filter Gen
Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 19 rs2301813
dbSNP
1000799 12.77 G C LowQual 1/1 2 SYNONYMOUS_CODING LOW SILENT 0.67352 0.67350 None None None None None None None
View mm170241ct 19 rs112236900
dbSNP
1000568 11.83 C A LowQual 1/1 1 SYNONYMOUS_CODING LOW SILENT 0.32488 0.32490 None None None None None None D

HCN2

Omim - GeneCards - NCBI
Options Individual Chr
RsId
Pos
Qual
Ref
Alt
Filter Gen
Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 19 rs55691080,rs201222040
dbSNP
616057 25.78 G C LowQual 0/1 9 SYNONYMOUS_CODING LOW SILENT 0.20667 0.20670 None None None None None None None
View mm170241ct 19 rs2301778
dbSNP
613307 29.77 C T LowQual 0/1 10 SYNONYMOUS_CODING LOW SILENT 0.28514 0.28510 0.28707 None None None None None None None

HECA

Omim - GeneCards - NCBI
Options Individual Chr
RsId
Pos
Qual
Ref
Alt
Filter Gen
Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 6 rs185694700
dbSNP
139456761 18.59 T C LowQual 1/1 2 SYNONYMOUS_CODING LOW SILENT 0.63518 0.63520 None None None None None None None

HERC2

Omim - GeneCards - NCBI
Options Individual Chr
RsId
Pos
Qual
Ref
Alt
Filter Gen
Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 15 rs150363648
dbSNP
28518046 29.77 G A LowQual 0/1 10 NON_SYNONYMOUS_CODING MODERATE MISSENSE 0.81 None None None None None None None