Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.102830888C>ACA471287288CYP17A1,WBP1Lc.1341G>T (p.Leu447=)
c.1038G>T (p.Leu346=)
c.885G>T (p.Leu295=)
c.1254G>T (p.Leu418=)
c.1344G>T (p.Leu448=)
n.1103G>T
c.*570C>A (n.*570C>A)
gnomAD v4
10g.102830888C=CA1932867082CYP17A1,WBP1Lc.1341G= (p.Leu447=)
c.1038G= (p.Leu346=)
c.885G= (p.Leu295=)
c.1254G= (p.Leu418=)
c.1344G= (p.Leu448=)
n.1103G=
c.*570C= (n.*570C=)
10g.102830888C>GCA471287290CYP17A1,WBP1Lc.1341G>C (p.Leu447=)
c.1038G>C (p.Leu346=)
c.885G>C (p.Leu295=)
c.1254G>C (p.Leu418=)
c.1344G>C (p.Leu448=)
n.1103G>C
c.*570C>G (n.*570C>G)
10g.102830888C>TCA471287291CYP17A1,WBP1Lc.1341G>A (p.Leu447=)
c.1038G>A (p.Leu346=)
c.885G>A (p.Leu295=)
c.1254G>A (p.Leu418=)
c.1344G>A (p.Leu448=)
n.1103G>A
c.*570C>T (n.*570C>T)
dbSNP gnomAD v2
10g.102830889A>CCA377938183CYP17A1,WBP1Lc.1340T>G (p.Leu447Arg)
c.1037T>G (p.Leu346Arg)
c.884T>G (p.Leu295Arg)
c.1253T>G (p.Leu418Arg)
c.1343T>G (p.Leu448Arg)
n.1102T>G
c.*571A>C (n.*571A>C)
10g.102830889A>GCA377938184CYP17A1,WBP1Lc.1340T>C (p.Leu447Pro)
c.1037T>C (p.Leu346Pro)
c.884T>C (p.Leu295Pro)
c.1253T>C (p.Leu418Pro)
c.1343T>C (p.Leu448Pro)
n.1102T>C
c.*571A>G (n.*571A>G)
gnomAD v4
10g.102830889A>TCA377938185CYP17A1,WBP1Lc.1340T>A (p.Leu447Gln)
c.1037T>A (p.Leu346Gln)
c.884T>A (p.Leu295Gln)
c.1253T>A (p.Leu418Gln)
c.1343T>A (p.Leu448Gln)
n.1102T>A
c.*571A>T (n.*571A>T)
10g.102830890G>ACA471287293CYP17A1,WBP1Lc.1339C>T (p.Leu447=)
c.1036C>T (p.Leu346=)
c.883C>T (p.Leu295=)
c.1252C>T (p.Leu418=)
c.1342C>T (p.Leu448=)
n.1101C>T
c.*572G>A (n.*572G>A)
dbSNP gnomAD v2 gnomAD v4
10g.102830890G>CCA377938186CYP17A1,WBP1Lc.1339C>G (p.Leu447Val)
c.1036C>G (p.Leu346Val)
c.883C>G (p.Leu295Val)
c.1252C>G (p.Leu418Val)
c.1342C>G (p.Leu448Val)
n.1101C>G
c.*572G>C (n.*572G>C)
gnomAD v4
10g.102830890G=CA1932867107CYP17A1,WBP1Lc.1339C= (p.Leu447=)
c.1036C= (p.Leu346=)
c.883C= (p.Leu295=)
c.1252C= (p.Leu418=)
c.1342C= (p.Leu448=)
n.1101C=
c.*572G= (n.*572G=)
10g.102830890G>TCA377938187CYP17A1,WBP1Lc.1339C>A (p.Leu447Met)
c.1036C>A (p.Leu346Met)
c.883C>A (p.Leu295Met)
c.1252C>A (p.Leu418Met)
c.1342C>A (p.Leu448Met)
n.1101C>A
c.*572G>T (n.*572G>T)
gnomAD v4
10g.102830891G>ACA471287296CYP17A1,WBP1Lc.1338C>T (p.Ile446=)
c.1035C>T (p.Ile345=)
c.882C>T (p.Ile294=)
c.1251C>T (p.Ile417=)
c.1341C>T (p.Ile447=)
n.1100C>T
c.*573G>A (n.*573G>A)
10g.102830891G>CCA377938188CYP17A1,WBP1Lc.1338C>G (p.Ile446Met)
c.1035C>G (p.Ile345Met)
c.882C>G (p.Ile294Met)
c.1251C>G (p.Ile417Met)
c.1341C>G (p.Ile447Met)
n.1100C>G
c.*573G>C (n.*573G>C)
10g.102830891G>TCA471287298CYP17A1,WBP1Lc.1338C>A (p.Ile446=)
c.1035C>A (p.Ile345=)
c.882C>A (p.Ile294=)
c.1251C>A (p.Ile417=)
c.1341C>A (p.Ile447=)
n.1100C>A
c.*573G>T (n.*573G>T)
gnomAD v4
10g.102830892A>CCA377938189CYP17A1,WBP1Lc.1337T>G (p.Ile446Ser)
c.1034T>G (p.Ile345Ser)
c.881T>G (p.Ile294Ser)
c.1250T>G (p.Ile417Ser)
c.1340T>G (p.Ile447Ser)
n.1099T>G
c.*574A>C (n.*574A>C)
10g.102830892A>GCA377938191CYP17A1,WBP1Lc.1337T>C (p.Ile446Thr)
c.1034T>C (p.Ile345Thr)
c.881T>C (p.Ile294Thr)
c.1250T>C (p.Ile417Thr)
c.1340T>C (p.Ile447Thr)
n.1099T>C
c.*574A>G (n.*574A>G)
10g.102830892A>TCA377938190CYP17A1,WBP1Lc.1337T>A (p.Ile446Asn)
c.1034T>A (p.Ile345Asn)
c.881T>A (p.Ile294Asn)
c.1250T>A (p.Ile417Asn)
c.1340T>A (p.Ile447Asn)
n.1099T>A
c.*574A>T (n.*574A>T)
gnomAD v4
10g.102830893T>ACA377938192CYP17A1,WBP1Lc.1336A>T (p.Ile446Phe)
c.1033A>T (p.Ile345Phe)
c.880A>T (p.Ile294Phe)
c.1249A>T (p.Ile417Phe)
c.1339A>T (p.Ile447Phe)
n.1098A>T
c.*575T>A (n.*575T>A)
gnomAD v4
10g.102830893T>CCA377938194CYP17A1,WBP1Lc.1336A>G (p.Ile446Val)
c.1033A>G (p.Ile345Val)
c.880A>G (p.Ile294Val)
c.1249A>G (p.Ile417Val)
c.1339A>G (p.Ile447Val)
n.1098A>G
c.*575T>C (n.*575T>C)
10g.102830893T>GCA377938193CYP17A1,WBP1Lc.1336A>C (p.Ile446Leu)
c.1033A>C (p.Ile345Leu)
c.880A>C (p.Ile294Leu)
c.1249A>C (p.Ile417Leu)
c.1339A>C (p.Ile447Leu)
n.1098A>C
c.*575T>G (n.*575T>G)
gnomAD v4
10g.102830894C>ACA377938195CYP17A1,WBP1Lc.1335G>T (p.Glu445Asp)
c.1032G>T (p.Glu344Asp)
c.879G>T (p.Glu293Asp)
c.1248G>T (p.Glu416Asp)
c.1338G>T (p.Glu446Asp)
n.1097G>T
c.*576C>A (n.*576C>A)
10g.102830894C>GCA377938196CYP17A1,WBP1Lc.1335G>C (p.Glu445Asp)
c.1032G>C (p.Glu344Asp)
c.879G>C (p.Glu293Asp)
c.1248G>C (p.Glu416Asp)
c.1338G>C (p.Glu446Asp)
n.1097G>C
c.*576C>G (n.*576C>G)
10g.102830894C>TCA471287300CYP17A1,WBP1Lc.1335G>A (p.Glu445=)
c.1032G>A (p.Glu344=)
c.879G>A (p.Glu293=)
c.1248G>A (p.Glu416=)
c.1338G>A (p.Glu446=)
n.1097G>A
c.*576C>T (n.*576C>T)
gnomAD v4
10g.102830895T>ACA377938197CYP17A1,WBP1Lc.1334A>T (p.Glu445Val)
c.1031A>T (p.Glu344Val)
c.878A>T (p.Glu293Val)
c.1247A>T (p.Glu416Val)
c.1337A>T (p.Glu446Val)
n.1096A>T
c.*577T>A (n.*577T>A)
10g.102830895T>CCA377938198CYP17A1,WBP1Lc.1334A>G (p.Glu445Gly)
c.1031A>G (p.Glu344Gly)
c.878A>G (p.Glu293Gly)
c.1247A>G (p.Glu416Gly)
c.1337A>G (p.Glu446Gly)
n.1096A>G
c.*577T>C (n.*577T>C)
10g.102830895T>GCA377938199CYP17A1,WBP1Lc.1334A>C (p.Glu445Ala)
c.1031A>C (p.Glu344Ala)
c.878A>C (p.Glu293Ala)
c.1247A>C (p.Glu416Ala)
c.1337A>C (p.Glu446Ala)
n.1096A>C
c.*577T>G (n.*577T>G)
10g.102830896C>ACA377938200CYP17A1,WBP1Lc.1333G>T (p.Glu445Ter)
c.1030G>T (p.Glu344Ter)
c.877G>T (p.Glu293Ter)
c.1246G>T (p.Glu416Ter)
c.1336G>T (p.Glu446Ter)
n.1095G>T
c.*578C>A (n.*578C>A)
gnomAD v4
10g.102830896C=CA1932867112CYP17A1,WBP1Lc.1333G= (p.Glu445=)
c.1030G= (p.Glu344=)
c.877G= (p.Glu293=)
c.1246G= (p.Glu416=)
c.1336G= (p.Glu446=)
n.1095G=
c.*578C= (n.*578C=)
10g.102830896C>GCA377938201CYP17A1,WBP1Lc.1333G>C (p.Glu445Gln)
c.1030G>C (p.Glu344Gln)
c.877G>C (p.Glu293Gln)
c.1246G>C (p.Glu416Gln)
c.1336G>C (p.Glu446Gln)
n.1095G>C
c.*578C>G (n.*578C>G)
dbSNP
10g.102830896C>TCA377938202CYP17A1,WBP1Lc.1333G>A (p.Glu445Lys)
c.1030G>A (p.Glu344Lys)
c.877G>A (p.Glu293Lys)
c.1246G>A (p.Glu416Lys)
c.1336G>A (p.Glu446Lys)
n.1095G>A
c.*578C>T (n.*578C>T)
gnomAD v4
10g.102830897A>CCA471287305CYP17A1,WBP1Lc.1332T>G (p.Gly444=)
c.1029T>G (p.Gly343=)
c.876T>G (p.Gly292=)
c.1245T>G (p.Gly415=)
c.1335T>G (p.Gly445=)
n.1094T>G
c.*579A>C (n.*579A>C)
10g.102830897A>GCA471287307CYP17A1,WBP1Lc.1332T>C (p.Gly444=)
c.1029T>C (p.Gly343=)
c.876T>C (p.Gly292=)
c.1245T>C (p.Gly415=)
c.1335T>C (p.Gly445=)
n.1094T>C
c.*579A>G (n.*579A>G)
10g.102830897A>TCA471287308CYP17A1,WBP1Lc.1332T>A (p.Gly444=)
c.1029T>A (p.Gly343=)
c.876T>A (p.Gly292=)
c.1245T>A (p.Gly415=)
c.1335T>A (p.Gly445=)
n.1094T>A
c.*579A>T (n.*579A>T)
10g.102830897_102830898delinsACCA1932867113CYP17A1,WBP1Lc.1331_1332delinsGT (p.Gly444=)
c.1028_1029delinsGT (p.Gly343=)
c.875_876delinsGT (p.Gly292=)
c.1244_1245delinsGT (p.Gly415=)
c.1334_1335delinsGT (p.Gly445=)
n.1093_1094delinsGT
c.*579_*580delinsAC (n.*579_*580delinsAC)
10g.102830898C>ACA377938203CYP17A1,WBP1Lc.1331G>T (p.Gly444Val)
c.1028G>T (p.Gly343Val)
c.875G>T (p.Gly292Val)
c.1244G>T (p.Gly415Val)
c.1334G>T (p.Gly445Val)
n.1093G>T
c.*580C>A (n.*580C>A)
10g.102830898C=CA1932867118CYP17A1,WBP1Lc.1331G= (p.Gly444=)
c.1028G= (p.Gly343=)
c.875G= (p.Gly292=)
c.1244G= (p.Gly415=)
c.1334G= (p.Gly445=)
n.1093G=
c.*580C= (n.*580C=)
10g.102830898C>GCA377938204CYP17A1,WBP1Lc.1331G>C (p.Gly444Ala)
c.1028G>C (p.Gly343Ala)
c.875G>C (p.Gly292Ala)
c.1244G>C (p.Gly415Ala)
c.1334G>C (p.Gly445Ala)
n.1093G>C
c.*580C>G (n.*580C>G)
10g.102830898C>TCA377938205CYP17A1,WBP1Lc.1331G>A (p.Gly444Asp)
c.1028G>A (p.Gly343Asp)
c.875G>A (p.Gly292Asp)
c.1244G>A (p.Gly415Asp)
c.1334G>A (p.Gly445Asp)
n.1093G>A
c.*580C>T (n.*580C>T)
dbSNP gnomAD v2 gnomAD v4
10g.102830899delCA595226116CYP17A1,WBP1Lc.1331del (p.Gly444ValfsTer?)
c.1028del (p.Gly343ValfsTer?)
c.875del (p.Gly292ValfsTer?)
c.1244del (p.Gly415ValfsTer?)
c.1334del (p.Gly445ValfsTer?)
n.1093del
c.*581del (n.*581del)
dbSNP gnomAD v2
10g.102830899C>ACA377938208CYP17A1,WBP1Lc.1330G>T (p.Gly444Cys)
c.1027G>T (p.Gly343Cys)
c.874G>T (p.Gly292Cys)
c.1243G>T (p.Gly415Cys)
c.1333G>T (p.Gly445Cys)
n.1092G>T
c.*581C>A (n.*581C>A)
gnomAD v4
10g.102830899C>GCA377938207CYP17A1,WBP1Lc.1330G>C (p.Gly444Arg)
c.1027G>C (p.Gly343Arg)
c.874G>C (p.Gly292Arg)
c.1243G>C (p.Gly415Arg)
c.1333G>C (p.Gly445Arg)
n.1092G>C
c.*581C>G (n.*581C>G)
10g.102830899C>TCA377938206CYP17A1,WBP1Lc.1330G>A (p.Gly444Ser)
c.1027G>A (p.Gly343Ser)
c.874G>A (p.Gly292Ser)
c.1243G>A (p.Gly415Ser)
c.1333G>A (p.Gly445Ser)
n.1092G>A
c.*581C>T (n.*581C>T)
10g.102830900T>ACA471287312CYP17A1,WBP1Lc.1329A>T (p.Ile443=)
c.1026A>T (p.Ile342=)
c.873A>T (p.Ile291=)
c.1242A>T (p.Ile414=)
c.1332A>T (p.Ile444=)
n.1091A>T
c.*582T>A (n.*582T>A)
10g.102830900T>CCA377938209CYP17A1,WBP1Lc.1329A>G (p.Ile443Met)
c.1026A>G (p.Ile342Met)
c.873A>G (p.Ile291Met)
c.1242A>G (p.Ile414Met)
c.1332A>G (p.Ile444Met)
n.1091A>G
c.*582T>C (n.*582T>C)
10g.102830900T>GCA471287315CYP17A1,WBP1Lc.1329A>C (p.Ile443=)
c.1026A>C (p.Ile342=)
c.873A>C (p.Ile291=)
c.1242A>C (p.Ile414=)
c.1332A>C (p.Ile444=)
n.1091A>C
c.*582T>G (n.*582T>G)
10g.102830901A=CA1932867123CYP17A1,WBP1Lc.1328T= (p.Ile443=)
c.1025T= (p.Ile342=)
c.872T= (p.Ile291=)
c.1241T= (p.Ile414=)
c.1331T= (p.Ile444=)
n.1090T=
c.*583A= (n.*583A=)
10g.102830901A>CCA377938210CYP17A1,WBP1Lc.1328T>G (p.Ile443Arg)
c.1025T>G (p.Ile342Arg)
c.872T>G (p.Ile291Arg)
c.1241T>G (p.Ile414Arg)
c.1331T>G (p.Ile444Arg)
n.1090T>G
c.*583A>C (n.*583A>C)
10g.102830901A>GCA377938211CYP17A1,WBP1Lc.1328T>C (p.Ile443Thr)
c.1025T>C (p.Ile342Thr)
c.872T>C (p.Ile291Thr)
c.1241T>C (p.Ile414Thr)
c.1331T>C (p.Ile444Thr)
n.1090T>C
c.*583A>G (n.*583A>G)
dbSNP gnomAD v3 gnomAD v4
10g.102830901A>TCA377938212CYP17A1,WBP1Lc.1328T>A (p.Ile443Lys)
c.1025T>A (p.Ile342Lys)
c.872T>A (p.Ile291Lys)
c.1241T>A (p.Ile414Lys)
c.1331T>A (p.Ile444Lys)
n.1090T>A
c.*583A>T (n.*583A>T)
10g.102830902T>ACA377938213CYP17A1,WBP1Lc.1327A>T (p.Ile443Leu)
c.1024A>T (p.Ile342Leu)
c.871A>T (p.Ile291Leu)
c.1240A>T (p.Ile414Leu)
c.1330A>T (p.Ile444Leu)
n.1089A>T
c.*584T>A (n.*584T>A)
gnomAD v4

Number of alleles fetched