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Genes:
ABCA1, ABCA2, ABL1, ACO1, ACTL7B, ADAMTS13, ADAMTSL1, ADAMTSL2, AGPAT2, AIF1L, AK1, AKAP2, AKNA, ALAD, ALDH1B1, AMBP, ANAPC2, ANGPTL2, ANKRD18A, ANKRD18B, ANKS6, APBA1, AQP3, AQP7, ARHGEF39, ARID3C, ASB6, ASPN, ASS1, ASTN2, BAAT, BAG1, BARX1, BRD3, BRINP1, BSPRY, C5, C8G, C9orf114, C9orf117, C9orf129, C9orf131, C9orf139, C9orf141, C9orf147, C9orf152, C9orf156, C9orf163, C9orf171, C9orf172, C9orf173, C9orf24, C9orf3, C9orf38, C9orf40, C9orf41, C9orf43, C9orf47, C9orf57, C9orf62, C9orf66, C9orf69, C9orf84, C9orf89, C9orf9, C9orf96, CACFD1, CACNA1B, CAMSAP1, CARD9, CBWD1, CCDC107, CCDC171, CCDC183, CDK20, CDK5RAP2, CERCAM, CIZ1, CLIC3, CNTLN, CNTNAP3, CNTNAP3B, CNTRL, COL15A1, COL27A1, COL5A1, COQ4, CRAT, CRB2, CTNNAL1, CTSL, DAPK1, DBH, DDX31, DDX58, DEC1, DENND1A, DENND4C, DFNB31, DMRT1, DMRT2, DMRT3, DNAJA1, DNM1, DOCK8, DOLPP1, DPM2, DPP7, ECM2, EGFL7, ENG, ENTPD8, EPB41L4B, EQTN, ERCC6L2, ERMP1, EXD3, EXOSC3, FAM102A, FAM129B, FAM154A, FAM166A, FAM166B, FAM189A2, FAM205A, FAM214B, FAM219A, FAM221B, FAM69B, FAM78A, FBP1, FBP2, FBXO10, FBXW5, FCN1, FCN2, FGD3, FKBP15, FNBP1, FOCAD, FOXE1, FREM1, FRMD3, FRMPD1, FRRS1L, FSD1L, FUT7, FXN, GABBR2, GAPVD1, GDA, GLDC, GLE1, GLIS3, GLT6D1, GNA14, GOLGA1, GPR107, GPR144, GPSM1, GRHPR, GRIN1, GRIN3A, GTF3C4, HABP4, HAUS6, HDHD3, HMCN2, HRCT1, IDNK, IFNA1, IFNA16, IFNA5, IFNA6, IFNB1, IFNK, IKBKAP, IL33, INPP5E, INVS, IZUMO3, KANK1, KCNT1, KCNV2, KDM4C, KIAA0020, KIAA1161, KIAA1432, KIAA2026, KIF24, KIF27, KLHL9, LAMC3, LCN12, LCN15, LCN9, LHX2, LHX3, LMX1B, LRRC26, LRRC8A, LRSAM1, LURAP1L, MAMDC2, MAMDC4, MAN1B1, MAPKAP1, MEGF9, MELK, MLLT3, MOB3B, MORN5, MPDZ, MSANTD3, MTAP, MUSK, MVB12B, NACC2, NAIF1, NANS, NDOR1, NEK6, NELFB, NFIL3, NINJ1, NIPSNAP3A, NMRK1, NOL6, NOL8, NOTCH1, NOXA1, NPDC1, NPR2, NR4A3, NTMT1, NTNG2, NUP188, NUP214, NUTM2F, OBP2A, OBP2B, ODF2, OLFM1, OLFML2A, OR13C3, OR13C5, OR13C9, OR13D1, OR13F1, OR13J1, OR1B1, OR1J1, OR1L1, OR1L4, OR1L6, OR1L8, OR1N1, OR1N2, OR1Q1, ORM1, ORM2, OSTF1, PALM2-AKAP2, PAPPA, PAPPA-AS1, PAX5, PCSK5, PDCD1LG2, PHF19, PHYHD1, PIP5K1B, PIP5KL1, PMPCA, PNPLA7, POLR1E, POMT1, PPAPDC3, PPP1R26, PPP6C, PRDM12, PRRC2B, PRSS3, PRUNE2, PSAT1, PSMD5, PTCH1, PTGDS, PTGES2, PTGS1, PTPLAD2, PTPRD, QSOX2, RABEPK, RABL6, RAD23B, RALGDS, RAPGEF1, RASEF, RC3H2, REXO4, RFK, RGP1, RGS3, RLN1, RMI1, RNF224, ROR2, RORB, RP11-145E5.5, RUSC2, SARDH, SCAI, SDCCAG3, SEC16A, SECISBP2, SEMA4D, SETX, SH2D3C, SH3GLB2, SHB, SLC1A1, SLC24A2, SLC25A25, SLC2A6, SLC31A2, SLC34A3, SLC35D2, SLC46A2, SMARCA2, SMC5, SNAPC4, SNX30, SOHLH1, SPATA31D1, SPATA31E1, SPTAN1, STRBP, SURF2, SVEP1, SYK, TAF1L, TBC1D13, TBC1D2, TDRD7, TEK, TJP2, TLE1, TLE4, TLN1, TLR4, TMC1, TMEFF1, TMEM2, TMEM215, TMEM245, TMEM246, TMEM8C, TNC, TNFSF15, TNFSF8, TOR1B, TOR2A, TPD52L3, TPRN, TRAF1, TRBV23OR9-2, TRPM3, TRPM6, TSTD2, TTC16, TTC39B, TTF1, TTLL11, TUSC1, TYRP1, UAP1L1, UBAC1, UBAP2, UCK1, UGCG, UHRF2, USP20, VAV2, WDR34, WDR38, WDR5, WNK2, ZBTB43, ZBTB5, ZCCHC6, ZDHHC12, ZDHHC21, ZFAND5, ZFP37, ZNF462, ZNF618, ZNF658, ZNF79,

Genes at Omim

ABCA1, ABL1, ADAMTS13, ADAMTSL2, AGPAT2, AK1, ALAD, ANKS6, AQP3, AQP7, ASPN, ASS1, BAAT, C5, CACNA1B, CARD9, CDK5RAP2, COL27A1, COL5A1, COQ4, CRAT, CRB2, DBH, DDX58, DEC1, DNM1, DOCK8, DPM2, ENG, ERCC6L2, EXOSC3, FBP1, FOXE1, FREM1, FRRS1L, FXN, GLDC, GLE1, GLIS3, GRHPR, GRIN1, IFNA1, IKBKAP, INPP5E, INVS, KANK1, KCNT1, KCNV2, LAMC3, LHX3, LMX1B, LRRC8A, LRSAM1, MAN1B1, MPDZ, MTAP, MUSK, NANS, NOTCH1, NPR2, NUP214, PAX5, PMPCA, POMT1, PRDM12, PSAT1, PTCH1, ROR2, SARDH, SECISBP2, SETX, SLC1A1, SLC34A3, SMARCA2, SPTAN1, TDRD7, TEK, TJP2, TMC1, TNC, TPRN, TRPM6, TYRP1, WDR34,
ABCA1 HDL deficiency, type 2, 604091 (3)
Tangier disease, 205400 (3)
{Coronary artery disease in familial hypercholesterolemia, protection against}, 143890 (3)
ABL1 Leukemia, Philadelphia chromosome-positive, resistant to imatinib (3)
ADAMTS13 Thrombotic thrombocytopenic purpura, familial, 274150 (3)
ADAMTSL2 Geleophysic dysplasia 1, 231050 (3)
AGPAT2 Lipodystrophy, congenital generalized, type 1, 608594 (3)
AK1 Hemolytic anemia due to adenylate kinase deficiency, 612631 (3)
ALAD Porphyria, acute hepatic, 612740 (3)
{Lead poisoning, susceptibility to}, 612740 (3)
ANKS6 Nephronophthisis 16, 615382 (3)
AQP3 [Blood group GIL], 607457 (3)
AQP7 [Glycerol quantitative trait locus], 614411 (3)
ASPN {Lumbar disc degeneration}, 603932 (3)
{Osteoarthritis susceptibility 3}, 607850 (3)
ASS1 Citrullinemia, 215700 (3)
BAAT Hypercholanemia, familial, 607748 (3)
C5 C5 deficiency, 609536 (3)
[Eculizumab, poor response to], 615749 (3)
CACNA1B ?Dystonia 23, 614860 (3)
CARD9 Candidiasis, familial, 2, autosomal recessive, 212050 (3)
CDK5RAP2 Microcephaly 3, primary, autosomal recessive, 604804 (3)
COL27A1 ?Steel syndrome, 615155 (3)
COL5A1 Ehlers-Danlos syndrome, classic type, 130000 (3)
COQ4 Coenzyme Q10 deficiency, primary, 7, 616276 (3)
CRAT ?Carnitine acetyltransferase deficiency (1)
CRB2 Focal segmental glomerulosclerosis 9, 616220 (3)
Ventriculomegaly with cystic kidney disease, 219730 (3)
DBH Dopamine beta-hydroxylase deficiency, 223360 (3)
[Dopamine-beta-hydroxylase activity levels, plasma] (3)
DDX58 Singleton-Merten syndrome 2, 616298 (3)
DEC1 Esophageal squamous cell carcinoma, 133239 (1)
DNM1 Epileptic encephalopathy, early infantile, 31, 616346 (3)
DOCK8 Hyper-IgE recurrent infection syndrome, autosomal recessive, 243700 (3)
DPM2 Congenital disorder of glycosylation, type Iu, 615042 (3)
ENG Telangiectasia, hereditary hemorrhagic, type 1, 187300 (3)
ERCC6L2 Bone marrow failure syndrome 2, 615715 (3)
EXOSC3 Pontocerebellar hypoplasia, type 1B, 614678 (3)
FBP1 Fructose-1,6-bisphosphatase deficiency, 229700 (3)
FOXE1 Bamforth-Lazarus syndrome, 241850 (3)
{Thyroid cancer, nonmedullary, 4}, 616534 (3)
FREM1 Bifid nose with or without anorectal and renal anomalies, 608980 (3)
Manitoba oculotrichoanal syndrome, 248450 (3)
Trigonocephaly 2, 614485 (3)
FRRS1L Epileptic encephalopathy, early infantile, 37, 616981 (3)
FXN Friedreich ataxia with retained reflexes, 229300 (3)
Friedreich ataxia, 229300 (3)
GLDC Glycine encephalopathy, 605899 (3)
GLE1 Arthrogryposis, lethal, with anterior horn cell disease, 611890 (3)
Lethal congenital contracture syndrome 1, 253310 (3)
GLIS3 Diabetes mellitus, neonatal, with congenital hypothyroidism, 610199 (3)
GRHPR Hyperoxaluria, primary, type II, 260000 (3)
GRIN1 Mental retardation, autosomal dominant 8, 614254 (3)
IFNA1 Interferon, alpha, deficiency (1)
IKBKAP Dysautonomia, familial, 223900 (3)
INPP5E Joubert syndrome 1, 213300 (3)
Mental retardation, truncal obesity, retinal dystrophy, and micropenis, 610156 (3)
INVS Nephronophthisis 2, infantile, 602088 (3)
KANK1 Cerebral palsy, spastic quadriplegic, 2, 612900 (3)
KCNT1 Epilepsy, nocturnal frontal lobe, 5, 615005 (3)
Epileptic encephalopathy, early infantile, 14, 614959 (3)
KCNV2 Retinal cone dystrophy 3B, 610356 (3)
LAMC3 Cortical malformations, occipital, 614115 (3)
LHX3 Pituitary hormone deficiency, combined, 3, 221750 (3)
LMX1B Nail-patella syndrome, 161200 (3)
LRRC8A ?Agammaglobulinemia 5, 613506 (3)
LRSAM1 Charcot-Marie-Toothe disease, axonal, type 2P, 614436 (3)
MAN1B1 Mental retardation, autosomal recessive 15, 614202 (3)
MPDZ Hydrocephalus, nonsyndromic, autosomal recessive 2, 615219 (3)
MTAP Diaphyseal medullary stenosis with malignant fibrous histiocytoma, 112250 (3)
MUSK Fetal akinesia deformation sequence, 208150 (3)
Myasthenic syndrome, congenital, 9, associated with acetylcholine receptor deficiency, 616325 (3)
NANS Spondyloepimetaphyseal dysplasia, Camera-Genevieve type, 610442 (3)
NOTCH1 Adams-Oliver syndrome 5, 616028 (3)
Aortic valve disease 1, 109730 (3)
NPR2 Acromesomelic dysplasia, Maroteaux type, 602875 (3)
Epiphyseal chondrodysplasia, Miura type, 615923 (3)
Short stature with nonspecific skeletal abnormalities, 616255 (3)
NUP214 Leukemia, T-cell acute lymphoblastic, somatic, 613065 (3)
Leukemia, acute myeloid, somatic, 601626 (3)
PAX5 {Leukemia, acute lymphoblastic, susceptibility to, 3}, 615545 (3)
PMPCA Spinocerebellar ataxia, autosomal recessive 2, 213200 (3)
POMT1 Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1, 236670 (3)
Muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type B, 1, 613155 (3)
Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 1, 609308 (3)
PRDM12 Neuropathy, hereditary sensory and autonomic, type VIII, 616488 (3)
PSAT1 ?Phosphoserine aminotransferase deficiency, 610992 (3)
Neu-Laxova syndrome 2, 616038 (3)
PTCH1 Basal cell carcinoma, somatic, 605462 (3)
Basal cell nevus syndrome, 109400 (3)
Holoprosencephaly 7, 610828 (3)
ROR2 Brachydactyly, type B1, 113000 (3)
Robinow syndrome, autosomal recessive, 268310 (3)
SARDH [Sarcosinemia], 268900 (3)
SECISBP2 Thyroid hormone metabolism, abnormal, 609698 (3)
SETX Amyotrophic lateral sclerosis 4, juvenile, 602433 (3)
Spinocerebellar ataxia, autosomal recessive 1, 606002 (3)
SLC1A1 Dicarboxylic aminoaciduria, 222730 (3)
{?Schizophrenia susceptibility 18}, 615232 (3)
SLC34A3 Hypophosphatemic rickets with hypercalciuria, 241530 (3)
SMARCA2 Nicolaides-Baraitser syndrome, 601358 (3)
SPTAN1 Epileptic encephalopathy, early infantile, 5, 613477 (3)
TDRD7 Cataract 36, 613887 (3)
TEK Venous malformations, multiple cutaneous and mucosal, 600195 (3)
TJP2 Cholestasis, progressive familial intrahepatic 4, 615878 (3)
Hypercholanemia, familial, 607748 (3)
TMC1 Deafness, autosomal dominant 36, 606705 (3)
Deafness, autosomal recessive 7, 600974 (3)
TNC Deafness, autosomal dominant 56, 615629 (3)
TPRN Deafness, autosomal recessive 79, 613307 (3)
TRPM6 Hypomagnesemia 1, intestinal, 602014 (3)
TYRP1 Albinism, oculocutaneous, type III, 203290 (3)
[Skin/hair/eye pigmentation, variation in, 11 (Melanesian blond hair)], 612271 (3)
WDR34 Short-rib thoracic dysplasia 11 with or without polydactyly, 615633 (3)

Genes at Clinical Genomics Database

ABCA1, ADAMTS13, ADAMTSL2, AGPAT2, AK1, ALAD, ANKS6, AQP3, ASS1, BAAT, C5, CACNA1B, CARD9, CDK5RAP2, CIZ1, COL27A1, COL5A1, COQ4, CRB2, DBH, DDX58, DNM1, DOCK8, DPM2, ENG, ERCC6L2, EXOSC3, FBP1, FOXE1, FREM1, FXN, GLDC, GLE1, GLIS3, GRHPR, GRIN1, IKBKAP, INPP5E, INVS, KANK1, KCNT1, KCNV2, LAMC3, LHX3, LMX1B, LRRC8A, LRSAM1, MAN1B1, MPDZ, MTAP, MUSK, NOTCH1, NPR2, PAX5, PMPCA, POMT1, PRDM12, PSAT1, PTCH1, ROR2, SECISBP2, SETX, SLC1A1, SLC34A3, SMARCA2, SPTAN1, TDRD7, TEK, TJP2, TMC1, TNC, TPRN, TRPM6, TYRP1, WDR34,
ABCA1 HDL deficiency, type 2
Tangier disease
ABCA1 deficiency
ADAMTS13 Schulman-Upshaw syndrome
Thrombotic thrombocytopenic purpura, familial
ADAMTSL2 Geleophysic dysplasia 1
AGPAT2 Lipodystrophy, congenital generalized, type 1
AK1 Adenylate kinase deficiency, hemolytic anemia due to
ALAD Porphyria, acute hepatic
ANKS6 Nephronophthisis 16
AQP3 Blood group, GIL
ASS1 Citrullinemia
BAAT Hypercholanemia, familial
C5 Complement component 5 deficiency
Eculizumab, poor response to
CACNA1B Dystonia 23
CARD9 Candidiasis, familial, 2
CDK5RAP2 Microcephaly, primary autosomal recessive, 3
CIZ1 Primary cervical dystonia, adult-onset
COL27A1 Steel syndrome
COL5A1 Ehlers-Danlos syndrome, type II
Ehlers-Danlos syndrome, type I
COQ4 Coenzyme Q10 deficiency 7
CRB2 Ventriculomegaly with cystic kidney disease
Focal segmental glomerulosclerosis 9
DBH Dopamine beta-hydroxylase deficiency
DDX58 Singleton-Merten syndrome 2
DNM1 Epileptic encephalopathy, early infantile 31
DOCK8 Hyper-IgE recurrent infection syndrome, autosomal recessive
DPM2 Congenital disorder of glycosylation, type Iu
ENG Juvenile polyposis syndrome
Hereditary hemorrhagic telangiectasia, type 1
ERCC6L2 Bone marrow failure syndrome 2
EXOSC3 Pontocerebellar hypoplasia type 1B
FBP1 Fructose-1,6-bisphosphatase deficiency
FOXE1 Congenital hypothyroidism
Hypothyroidism, thyroidal, with spiky hair and cleft palate (Bamforth-Lazarus syndrome)
Thyroid cancer, nonmedullary 4
FREM1 Congenital diaphragmatic hernia, autosomal recessive
Manitoba oculotrichoanal syndrome
Trigonocephaly 2
Bifid nose with or without anorectal and renal anomalies
FXN Friedreich ataxia
GLDC Glycine encephalopathy
GLE1 Lethal congenital contracture syndrome 1
Arthrogryposis, lethal, with anterior horn cell disease
GLIS3 Diabetes mellitus, neonatal, with congenital hypothyroidism
GRHPR Hyperoxaluria, primary, type II
GRIN1 Mental retardation, autosomal dominant 8
IKBKAP Dysautonomia, familial
INPP5E Mental retardation, truncal obesity, retinal dystrophy, and micropenis (MORM syndrome)
Joubert syndrome 1
INVS Nephronophthisis 2
KANK1 Cerebral palsy, spastic quadriplegic, 2
KCNT1 Early infantile epileptic encephalopathy 14
Epilepsy, nocturnal frontal lobe, 5
KCNV2 Retinal cone dystrophy 3B
LAMC3 Cortical malformations, occipital
LHX3 Pituitary hormone deficiency, combined, 3
LMX1B Nail-patella syndrome
LRRC8A Agammaglobulinemia 5
LRSAM1 Charcot-Marie-Tooth disease, axonal, type 2P
MAN1B1 Mental retardation, autosomal recessive 15
MPDZ Hydrocephalus, nonsyndromic, autosomal recessive 2
MTAP Diaphyseal medullary stenosis with malignant fibrous histiocytoma
MUSK Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency
NOTCH1 Aortic valve disease
NPR2 Acromesomelic dysplasia, Maroteaux type
Short stature with nonspecific skeletal abnormalities
Epiphyseal chondrodysplasia, Miura type
PAX5 Pre-B cell acute lymphoblastic leukemia
PMPCA Spinocerebellar ataxia, autosomal recessive 2
POMT1 Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 1
Muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type B, 1
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1
PRDM12 Neuropathy, hereditary sensory and autonomic, type VIII
PSAT1 Phosphoserine aminotransferase deficiency
PTCH1 Basal cell nevus syndrome
ROR2 Brachydactyly, type B1
Robinow syndrome, autosomal recessive
SECISBP2 Selenoprotein deficiency
SETX Ataxia with oculomotor apraxia, type 2
Amyotrophic lateral sclerosis 4, juvenile
Spinocerebellar ataxia, autosomal recessive 1
SLC1A1 Dicarboxylic aminoaciduria
SLC34A3 Hypophosphatemic rickets with hypercalciuria, hereditary
SMARCA2 Nicolaides-Baraitser syndrome
SPTAN1 Epileptic encephalopathy, early infantile, 5
TDRD7 Cataract, autosomal recessive congenital 4
TEK Venous malformations, multiple cutaneous and mucosal
TJP2 Cholestasis, progressive familial intrahepatic 4
Hypercholanemia, familial
TMC1 Deafness, autosomal recessive 7
TNC Deafness, autosomal dominant 56
TPRN Deafness, autosomal recessive 79
TRPM6 Hypomagnesemia 1, intestinal
TYRP1 Albinism, oculocutaneous, type III
WDR34 Short -rib thoracic dysplasia 11 with or without polydactyly

Genes at HGMD

Summary

Number of Variants: 5391
Number of Genes: 398

Export to: CSV

ABCA1

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 rs2853579
dbSNP
107591272 424.77 G T . 0/1 43 SYNONYMOUS_CODING LOW SILENT 0.33906 0.33910 0.22413 None None None None None None None
View mm170241ct 9 rs2230806
dbSNP
107620867 1046.77 C T . 0/1 80 NON_SYNONYMOUS_CODING MODERATE MISSENSE 0.43970 0.43970 0.39151 0.66 0.00 None None None None None None None
View mm170241ct 9 rs33918808
dbSNP
107579632 394.77 C G . 0/1 26 NON_SYNONYMOUS_CODING MODERATE MISSENSE 0.05671 0.05671 0.07558 0.53 0.02 None None None None None None None
View mm170241ct 9 rs34788556
dbSNP
107578529 465.77 T C . 0/1 32 SYNONYMOUS_CODING LOW SILENT 0.03554 0.03554 0.04121 None None None None None None None
View mm170241ct 9 rs34879708
dbSNP
107546653 1686.77 G T . 0/1 141 NON_SYNONYMOUS_CODING MODERATE MISSENSE 0.00439 0.00439 0.00661 0.22 0.01 None None None None None None None
View mm170241ct 9 rs9282537
dbSNP
107550222 1556.77 G A . 0/1 90 SYNONYMOUS_CODING LOW SILENT 0.07648 0.07648 0.08581 None None None None None None None
View mm170241ct 9 rs2066714
dbSNP
107586753 540.77 T C . 0/1 40 NON_SYNONYMOUS_CODING MODERATE MISSENSE 0.35683 0.35680 0.24596 0.28 0.00 None None None None None None None
View mm170241ct 9 rs2230808
dbSNP
107562804 2042.77 T C . 0/1 143 NON_SYNONYMOUS_CODING MODERATE MISSENSE 0.53834 0.53830 0.41496 0.61 0.09 None None None None None None None

ABCA2

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 rs7048567
dbSNP
139904037 1252.77 A G . 1/1 40 SYNONYMOUS_CODING LOW SILENT 0.72005 0.72000 0.29152 None None None None None None None
View mm170241ct 9 rs35590326
dbSNP
139916833 266.77 T G . 0/1 24 SYNONYMOUS_CODING LOW SILENT 0.09185 0.09185 0.11928 None None None None None None None
View mm170241ct 9 rs908828
dbSNP
139913239 710.77 T G . 1/1 24 NON_SYNONYMOUS_CODING MODERATE MISSENSE 1.00000 1.00000 0.00008 1.00 0.00 None None None None None None None
View mm170241ct 9 rs4880189
dbSNP
139923265 832.77 A G . 1/1 24 None None None 0.76657 0.76660 0.22882 None None None None None None None
View mm170241ct 9 rs908832
dbSNP
139912484 867.77 A G . 1/1 28 SYNONYMOUS_CODING LOW SILENT 0.96386 0.96390 0.03809 None None None None None None None
View mm170241ct 9 rs2271862
dbSNP
139906359 1440.77 G A . 1/1 48 SYNONYMOUS_CODING LOW SILENT 0.68730 0.68730 0.32231 None None None None None None None
View mm170241ct 9 rs12348881
dbSNP
139911983 222.77 T G . 0/1 26 SYNONYMOUS_CODING LOW SILENT 0.10443 0.10440 0.12916 None None None None None None None
View mm170241ct 9 rs34039859
dbSNP
139916879 393.77 C T . 0/1 32 NON_SYNONYMOUS_CODING MODERATE MISSENSE 0.03195 0.03195 0.05812 0.23 0.01 None None None None None None None

ABL1

Omim - GeneCards - NCBI
Options Individual Chr
RsId
Pos
Qual
Ref
Alt
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Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 9 rs1056171
dbSNP
133761001 622.77 A G . 0/1 60 SYNONYMOUS_CODING LOW SILENT 0.65415 0.65420 0.41512 None None None None None None None

ACO1

Omim - GeneCards - NCBI
Options Individual Chr
RsId
Pos
Qual
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Alt
Filter Gen
Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 9 rs3780473
dbSNP
32425910 3014.77 A G . 0/1 259 SYNONYMOUS_CODING LOW SILENT 0.35383 0.35380 0.32693 None None None None None None None

ACTL7B

Omim - GeneCards - NCBI
Options Individual Chr
RsId
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Qual
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Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 9 rs3750468
dbSNP
111618163 656.77 G A . 1/1 19 SYNONYMOUS_CODING LOW SILENT 0.22644 0.22640 0.21036 None None None None None None None
View mm170241ct 9 rs11543179
dbSNP
111617650 1680.77 G A . 1/1 56 SYNONYMOUS_CODING LOW SILENT 0.22764 0.22760 0.21492 None None None None None None None

ADAMTS13

Omim - GeneCards - NCBI
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Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 9 rs3118667
dbSNP
136291063 1092.77 C T . 1/1 33 SYNONYMOUS_CODING LOW SILENT 0.58187 0.58190 0.48355 None None None None None None None
View mm170241ct 9 rs3124767
dbSNP
136308542 366.77 C T . 1/1 12 SYNONYMOUS_CODING LOW SILENT 0.49681 0.49680 0.38725 None None None None None None None
View mm170241ct 9 rs3124768
dbSNP
136304497 1726.77 A G . 1/1 57 SYNONYMOUS_CODING LOW SILENT 0.51597 0.51600 0.41542 None None None None None None None

ADAMTSL1

Omim - GeneCards - NCBI
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Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 9 rs41304755
dbSNP
18829952 577.77 A G . 0/1 54 NON_SYNONYMOUS_CODING MODERATE MISSENSE 0.10943 0.10940 0.17681 0.25 0.17 None None None None None None None
View mm170241ct 9 rs13293151
dbSNP
18681821 554.77 A G . 0/1 65 SYNONYMOUS_CODING LOW SILENT 0.27716 0.27720 0.32608 None None None None None None D
View mm170241ct 9 rs934472
dbSNP
18775810 2354.77 C A . 1/1 69 NON_SYNONYMOUS_CODING MODERATE MISSENSE 0.43570 0.43570 0.44970 0.36 0.00 None None None None None None None
View mm170241ct 9 rs35525189,rs796576662
dbSNP
18826261 1692.73 GT G . 1/1 66 None None None None None None None None None None
View mm170241ct 9 rs149221350
dbSNP
18684731 1608.77 G T . 0/1 148 NON_SYNONYMOUS_CODING MODERATE MISSENSE 0.00120 0.00120 0.00146 0.00 1.00 None None None None None None None
View mm170241ct 9 rs1549986
dbSNP
18776840 862.77 A C . 1/1 23 SYNONYMOUS_CODING LOW SILENT 0.97205 0.97200 0.06223 None None None None None None T
View mm170241ct 9 rs7033684
dbSNP
18777368 2612.77 T C . 1/1 78 SYNONYMOUS_CODING LOW SILENT 0.68930 0.68930 0.28568 None None None None None None T

ADAMTSL2

Omim - GeneCards - NCBI
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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
View mm170241ct 9 rs534165083
dbSNP
136433542 470.77 C T . 0/1 42 SYNONYMOUS_CODING LOW SILENT None None None None None None None
View mm170241ct 9 rs2073877
dbSNP
136412296 397.77 C T . 0/1 37 SYNONYMOUS_CODING LOW SILENT 0.09585 0.09585 0.09803 None None None None None None None
View mm170241ct 9 rs2073876
dbSNP
136412255 1863.77 A C . 1/1 61 SYNONYMOUS_CODING LOW SILENT 0.72464 0.72460 0.12440 None None None None None None None
View mm170241ct 9 rs1064975
dbSNP
136434598 1336.77 A G . 1/1 40 SYNONYMOUS_CODING LOW SILENT None None None None None None None
View mm170241ct 9 rs62637566
dbSNP
136438985 455.77 G A . 0/1 31 SYNONYMOUS_CODING LOW SILENT None None None None None None None
View mm170241ct 9 rs2073875
dbSNP
136412236 2318.77 A T . 1/1 68 SYNONYMOUS_CODING LOW SILENT 0.72464 0.72460 0.12448 None None None None None None None
View mm170241ct 9 rs2073874
dbSNP
136412170 1947.77 C T . 1/1 59 SYNONYMOUS_CODING LOW SILENT 0.72404 0.72400 0.12464 None None None None None None None

AGPAT2

Omim - GeneCards - NCBI
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Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 9 rs201504151,rs768646064,rs77891680
dbSNP
139581758 1553.73 C CCAG . 0/1 83 CODON_INSERTION MODERATE 0.04892 0.04892 None None None None None None None

AIF1L

Omim - GeneCards - NCBI
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Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 9 rs353510
dbSNP
133996503 1432.77 T A . 1/1 42 None None None 0.64537 0.64540 None None None None None None None

AK1

Omim - GeneCards - NCBI
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Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 9 rs913986
dbSNP
130630639 458.77 A G . 1/1 15 SYNONYMOUS_CODING LOW SILENT 0.99820 0.99820 0.00185 None None None None None None T

AKAP2

Omim - GeneCards - NCBI
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Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 9 rs78923754
dbSNP
112811038 71.77 C T . 0/1 10 None None None 0.07568 0.07568 0.08051 0.11 0.86 None None None None None None None

AKNA

Omim - GeneCards - NCBI
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Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 9 rs3748177
dbSNP
117122202 1994.77 C T . 1/1 56 SYNONYMOUS_CODING LOW SILENT 0.38998 0.39000 0.41865 None None None None None None None
View mm170241ct 9 rs2250242
dbSNP
117103973 58.77 A G . 0/1 11 NON_SYNONYMOUS_CODING MODERATE MISSENSE 0.61022 0.61020 0.40720 1.00 0.00 None None None None None None None
View mm170241ct 9 rs3748176
dbSNP
117124731 930.77 G A . 1/1 30 NON_SYNONYMOUS_CODING MODERATE MISSENSE 0.38419 0.38420 0.41504 0.01 0.03 None None None None None None None

ALAD

Omim - GeneCards - NCBI
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Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 9 rs1139488
dbSNP
116153900 677.77 A G . 0/1 50 SYNONYMOUS_CODING LOW SILENT 0.35224 0.35220 0.35422 None None None None None None None

ALDH1B1

Omim - GeneCards - NCBI
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Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 9 rs2073477
dbSNP
38395928 673.77 C T . 0/1 51 SYNONYMOUS_CODING LOW SILENT 0.26777 0.26780 0.16523 None None None None None None None
View mm170241ct 9 rs2073478
dbSNP
38396065 920.77 G T . 0/1 66 NON_SYNONYMOUS_CODING MODERATE MISSENSE 0.39497 0.39500 0.49669 0.00 0.13 None None None None None None None
View mm170241ct 9 rs2228093
dbSNP
38396002 613.77 C T . 0/1 52 NON_SYNONYMOUS_CODING MODERATE MISSENSE 0.23043 0.23040 0.12417 0.00 0.99 None None None None None None None
View mm170241ct 9 rs4878199
dbSNP
38396502 1269.77 G A . 1/1 36 NON_SYNONYMOUS_CODING MODERATE MISSENSE 0.93850 0.93850 0.07812 1.00 0.00 None None None None None None None
View mm170241ct 9 rs2228094
dbSNP
38395940 1577.77 T C . 1/1 53 SYNONYMOUS_CODING LOW SILENT 0.93670 0.93670 0.07919 None None None None None None None

AMBP

Omim - GeneCards - NCBI
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Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 9 rs150403120
dbSNP
116837295 632.77 C T . 0/1 43 SYNONYMOUS_CODING LOW SILENT 0.00023 None None None None None None None

ANAPC2

Omim - GeneCards - NCBI
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Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 9 rs11549106
dbSNP
140079522 646.77 G A . 0/1 46 SYNONYMOUS_CODING LOW SILENT 0.18510 0.18510 0.21032 None None None None None None None
View mm170241ct 9 rs11549105
dbSNP
140077639 550.77 G A . 0/1 44 SYNONYMOUS_CODING LOW SILENT 0.10204 0.10200 0.18807 None None None None None None None

ANGPTL2

Omim - GeneCards - NCBI
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Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 9 rs2297866
dbSNP
129854199 1260.77 G A . 1/1 39 SYNONYMOUS_CODING LOW SILENT 0.29054 0.29050 0.36191 None None None None None None None

ANKRD18A

Omim - GeneCards - NCBI
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Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 9 rs192086168
dbSNP
38596059 6185.77 C T . 0/1 386 SYNONYMOUS_CODING LOW SILENT 0.01378 0.01378 0.00767 None None None None None None None
View mm170241ct 9 rs1832313
dbSNP
38615698 264.77 C T . 0/1 29 NON_SYNONYMOUS_CODING MODERATE MISSENSE 0.42173 0.42170 0.41984 1.00 0.00 None None None None None None D
View mm170241ct 9 rs150196189
dbSNP
38586247 6932.77 C T . 0/1 540 NON_SYNONYMOUS_CODING MODERATE MISSENSE 0.03215 0.03215 0.02240 0.24 0.48 None None None None None None .|T
View mm170241ct 9 rs12349568
dbSNP
38571130 226.77 C A . 0/1 24 NON_SYNONYMOUS_CODING MODERATE MISSENSE 0.10024 0.10020 0.02 0.12 None None None None None None None

ANKRD18B

Omim - GeneCards - NCBI
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Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 9 rs10971566
dbSNP
33568789 5887.77 T G . 1/1 165 SYNONYMOUS_CODING LOW SILENT 0.19968 0.19970 None None None None None None None
View mm170241ct 9 rs3843933
dbSNP
33524684 420.77 G A . 1/1 12 NON_SYNONYMOUS_CODING MODERATE MISSENSE 0.75320 0.75320 1.00 0.92 None None None None None None None

ANKS6

Omim - GeneCards - NCBI
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Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 9 rs138948716
dbSNP
101558609 38.77 G A . 0/1 4 SYNONYMOUS_CODING LOW SILENT 0.26597 0.26600 None None None None None None None
View mm170241ct 9 rs6415847
dbSNP
101533220 1058.77 C T . 1/1 29 NON_SYNONYMOUS_CODING MODERATE MISSENSE 0.87520 0.87520 0.03696 0.99 0.00 None None None None None None None

APBA1

Omim - GeneCards - NCBI
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Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 9 rs34788368
dbSNP
72131577 351.77 A C . 0/1 38 NON_SYNONYMOUS_CODING MODERATE MISSENSE 0.20328 0.20330 0.15325 1.00 0.00 None None None None None None None

AQP3

Omim - GeneCards - NCBI
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Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 9 rs591810
dbSNP
33447424 425.77 C G . 0/1 46 SYNONYMOUS_CODING LOW SILENT 0.74121 0.74120 0.25759 None None None None None None None

AQP7

Omim - GeneCards - NCBI
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Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 9 rs74668961
dbSNP
33386465 231.77 A G . 0/1 39 NON_SYNONYMOUS_CODING MODERATE MISSENSE 0.02 0.41 None None None None None None None
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 rs78695486
dbSNP
33386469 202.77 C T . 0/1 41 SYNONYMOUS_CODING LOW SILENT 0.00040 0.00040 None None None None None None None
View mm170241ct 9 rs77962308
dbSNP
33386510 274.77 C T . 0/1 42 NON_SYNONYMOUS_CODING MODERATE MISSENSE 1.00 0.01 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
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 rs72707424
dbSNP
33386511 298.77 A G . 0/1 43 SYNONYMOUS_CODING LOW SILENT None None None None None None None
View mm170241ct 9 rs79202054
dbSNP
33386526 275.77 G A . 0/1 47 SYNONYMOUS_CODING LOW SILENT 0.00020 0.00020 None None None None None None D|D|D|D|D|.|.
View mm170241ct 9 rs642636
dbSNP
33395196 1576.77 A G . 1/1 51 None None None 0.99082 0.99080 0.00692 None None None None None None None
View mm170241ct 9 rs2381003
dbSNP
33395108 41.77 G A . 0/1 62 SYNONYMOUS_CODING LOW SILENT None None None None None None None
View mm170241ct 9 rs74589499
dbSNP
33386430 62.77 C T . 0/1 24 SYNONYMOUS_CODING LOW SILENT None None None None None None None
View mm170241ct 9 rs79172651
dbSNP
33386167 80.77 G C . 0/1 29 NON_SYNONYMOUS_CODING MODERATE MISSENSE 0.00020 1.00 0.00 None None None None None None None

ARHGEF39

Omim - GeneCards - NCBI
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Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 9 rs2297879
dbSNP
35662251 1244.77 T C . 0/1 75 NON_SYNONYMOUS_CODING MODERATE MISSENSE 0.30571 0.30570 0.25065 0.33 0.00 None None None None None None D

ARID3C

Omim - GeneCards - NCBI
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Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 9 rs13283357
dbSNP
34627940 952.77 C T . 1/1 30 SYNONYMOUS_CODING LOW SILENT 0.18690 0.18690 0.27163 None None None None None None None

ASB6

Omim - GeneCards - NCBI
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Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 9 rs2241247
dbSNP
132402908 522.77 C G . 1/1 18 SYNONYMOUS_CODING LOW SILENT 0.93490 0.93490 0.04060 None None None None None None None
View mm170241ct 9 rs3739851
dbSNP
132400480 2789.77 G A . 1/1 81 SYNONYMOUS_CODING LOW SILENT 0.46146 0.46150 0.47178 None None None None None None None

ASPN

Omim - GeneCards - NCBI
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Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 9 rs4744132
dbSNP
95219597 3654.77 G A . 1/1 104 SYNONYMOUS_CODING LOW SILENT 0.99101 0.99100 0.01261 None None None None None None None
View mm170241ct 9 rs3078372,rs764248772,rs113747060
dbSNP
95237024 2979.73 C CTCA . 1/1 131 CODON_CHANGE_PLUS_CODON_INSERTION MODERATE None None None None None None None

ASS1

Omim - GeneCards - NCBI
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Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 9 rs555717331
dbSNP
133327633 372.77 C T . 0/1 21 SYNONYMOUS_CODING LOW SILENT None None None None None None None

ASTN2

Omim - GeneCards - NCBI
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Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 9 rs7848630
dbSNP
120053776 581.77 T C . 1/1 17 SYNONYMOUS_CODING LOW SILENT 0.96466 0.96470 0.03360 None None None None None None None
View mm170241ct 9 . 120177082 11.12 C T LowQual 0/1 3 SYNONYMOUS_CODING LOW SILENT None None None None None None None
View mm170241ct 9 rs3761845
dbSNP
119770480 2121.77 C T . 1/1 68 SYNONYMOUS_CODING LOW SILENT 0.48982 0.48980 0.43357 None None None None None None None
View mm170241ct 9 rs7018569
dbSNP
119199820 1018.77 C G . 1/1 31 None None None 0.92213 0.92210 0.58 0.00 None None None None None None None
View mm170241ct 9 rs7863560
dbSNP
119495697 393.77 T C . 1/1 12 SYNONYMOUS_CODING LOW SILENT 0.99241 0.99240 0.00484 None None None None None None None

BAAT

Omim - GeneCards - NCBI
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Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 9 rs1572983
dbSNP
104133628 1761.77 C T . 1/1 50 NON_SYNONYMOUS_CODING MODERATE MISSENSE 0.56290 0.56290 0.36860 0.44 0.02 None None None None None None None

BAG1

Omim - GeneCards - NCBI
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Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 9 rs77199588
dbSNP
33262141 2063.77 G C . 0/1 186 None None None 0.02496 0.02496 None None None None None None None
View mm170241ct 9 rs1071545
dbSNP
33264540 590.77 C G . 1/1 17 NON_SYNONYMOUS_CODING MODERATE MISSENSE 0.97943 0.97940 0.01767 0.02 0.00 None None None None None None None

BARX1

Omim - GeneCards - NCBI
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Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 9 rs11793856
dbSNP
96714491 416.77 C G . 0/1 35 SYNONYMOUS_CODING LOW SILENT 0.20387 0.20390 0.25150 None None None None None None None

BRD3

Omim - GeneCards - NCBI
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Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 9 rs464826
dbSNP
136913355 899.77 T C . 1/1 25 SYNONYMOUS_CODING LOW SILENT 0.72504 0.72500 0.29230 None None None None None None None

BRINP1

Omim - GeneCards - NCBI
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Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 9 rs28453
dbSNP
121929575 688.77 T C . 0/1 53 SYNONYMOUS_CODING LOW SILENT 0.18630 0.18630 0.20183 None None None None None None None

BSPRY

Omim - GeneCards - NCBI
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Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 9 rs370456129
dbSNP
116132395 511.77 C T . 0/1 37 SYNONYMOUS_CODING LOW SILENT 0.00008 None None None None None None None

C5

Omim - GeneCards - NCBI
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Read Depth Effect Impact Func Class 1kgenomes dbSNP ESP6500 Sift PP2 CADD M-CAP CLINVAR HI Score
View mm170241ct 9 rs10985126
dbSNP
123783934 2602.77 T C . 0/1 222 SYNONYMOUS_CODING LOW SILENT 0.24121 0.24120 0.24796 None None None None None None None
View mm170241ct 9 rs17216529
dbSNP
123800218 1458.77 C T . 0/1 115 NON_SYNONYMOUS_CODING MODERATE MISSENSE 0.14657 0.14660 0.12396 0.10 0.40 None None None None None None None
View mm170241ct 9 rs25681
dbSNP
123780005 2789.77 G A . 0/1 208 SYNONYMOUS_CODING LOW SILENT 0.40575 0.40580 0.32454 None None None None None None None
View mm170241ct 9 rs17611
dbSNP
123769200 1407.77 C T . 0/1 91 NON_SYNONYMOUS_CODING MODERATE MISSENSE 0.40475 0.40480 0.32485 0.20 0.12 None None None None None None None