Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.102832526G>ACA377938683CYP17A1,WBP1Lc.1124C>T (p.Ala375Val)
c.821C>T (p.Ala274Val)
c.668C>T (p.Ala223Val)
c.1037C>T (p.Ala346Val)
n.886C>T
c.*1557G>A (n.*1557G>A)
10g.102832526G>CCA377938685CYP17A1,WBP1Lc.1124C>G (p.Ala375Gly)
c.821C>G (p.Ala274Gly)
c.668C>G (p.Ala223Gly)
c.1037C>G (p.Ala346Gly)
n.886C>G
c.*1557G>C (n.*1557G>C)
10g.102832526G>TCA377938684CYP17A1,WBP1Lc.1124C>A (p.Ala375Asp)
c.821C>A (p.Ala274Asp)
c.668C>A (p.Ala223Asp)
c.1037C>A (p.Ala346Asp)
n.886C>A
c.*1557G>T (n.*1557G>T)
gnomAD v4
10g.102832527C>ACA377938686CYP17A1,WBP1Lc.1123G>T (p.Ala375Ser)
c.820G>T (p.Ala274Ser)
c.667G>T (p.Ala223Ser)
c.1036G>T (p.Ala346Ser)
n.885G>T
c.*1558C>A (n.*1558C>A)
10g.102832527C=CA1932870478CYP17A1,WBP1Lc.1123G= (p.Ala375=)
c.820G= (p.Ala274=)
c.667G= (p.Ala223=)
c.1036G= (p.Ala346=)
n.885G=
c.*1558C= (n.*1558C=)
10g.102832527C>GCA377938687CYP17A1,WBP1Lc.1123G>C (p.Ala375Pro)
c.820G>C (p.Ala274Pro)
c.667G>C (p.Ala223Pro)
c.1036G>C (p.Ala346Pro)
n.885G>C
c.*1558C>G (n.*1558C>G)
10g.102832527C>TCA377938688CYP17A1,WBP1Lc.1123G>A (p.Ala375Thr)
c.820G>A (p.Ala274Thr)
c.667G>A (p.Ala223Thr)
c.1036G>A (p.Ala346Thr)
n.885G>A
c.*1558C>T (n.*1558C>T)
dbSNP gnomAD v3 gnomAD v4
10g.102832528delCA2610723240CYP17A1,WBP1Lc.1123del (p.Ala375ProfsTer?)
c.820del (p.Ala274ProfsTer?)
c.667del (p.Ala223ProfsTer?)
c.1036del (p.Ala346ProfsTer?)
n.885del
c.*1559del (n.*1559del)
gnomAD v4
10g.102832528C>ACA377938689CYP17A1,WBP1Lc.1122G>T (p.Lys374Asn)
c.819G>T (p.Lys273Asn)
c.666G>T (p.Lys222Asn)
c.1035G>T (p.Lys345Asn)
n.884G>T
c.*1559C>A (n.*1559C>A)
gnomAD v4
10g.102832528C=CA1932870497CYP17A1,WBP1Lc.1122G= (p.Lys374=)
c.819G= (p.Lys273=)
c.666G= (p.Lys222=)
c.1035G= (p.Lys345=)
n.884G=
c.*1559C= (n.*1559C=)
10g.102832528C>GCA377938690CYP17A1,WBP1Lc.1122G>C (p.Lys374Asn)
c.819G>C (p.Lys273Asn)
c.666G>C (p.Lys222Asn)
c.1035G>C (p.Lys345Asn)
n.884G>C
c.*1559C>G (n.*1559C>G)
10g.102832528C>TCA471288342CYP17A1,WBP1Lc.1122G>A (p.Lys374=)
c.819G>A (p.Lys273=)
c.666G>A (p.Lys222=)
c.1035G>A (p.Lys345=)
n.884G>A
c.*1559C>T (n.*1559C>T)
dbSNP gnomAD v3 gnomAD v4
10g.102832529T>ACA377938691CYP17A1,WBP1Lc.1121A>T (p.Lys374Met)
c.818A>T (p.Lys273Met)
c.665A>T (p.Lys222Met)
c.1034A>T (p.Lys345Met)
n.883A>T
c.*1560T>A (n.*1560T>A)
gnomAD v4
10g.102832529T>CCA377938692CYP17A1,WBP1Lc.1121A>G (p.Lys374Arg)
c.818A>G (p.Lys273Arg)
c.665A>G (p.Lys222Arg)
c.1034A>G (p.Lys345Arg)
n.883A>G
c.*1560T>C (n.*1560T>C)
10g.102832529T>GCA377938693CYP17A1,WBP1Lc.1121A>C (p.Lys374Thr)
c.818A>C (p.Lys273Thr)
c.665A>C (p.Lys222Thr)
c.1034A>C (p.Lys345Thr)
n.883A>C
c.*1560T>G (n.*1560T>G)
10g.102832530T>ACA377938694CYP17A1,WBP1Lc.1120A>T (p.Lys374Ter)
c.817A>T (p.Lys273Ter)
c.664A>T (p.Lys222Ter)
c.1033A>T (p.Lys345Ter)
n.882A>T
c.*1561T>A (n.*1561T>A)
10g.102832530T>CCA377938695CYP17A1,WBP1Lc.1120A>G (p.Lys374Glu)
c.817A>G (p.Lys273Glu)
c.664A>G (p.Lys222Glu)
c.1033A>G (p.Lys345Glu)
n.882A>G
c.*1561T>C (n.*1561T>C)
10g.102832530T>GCA377938696CYP17A1,WBP1Lc.1120A>C (p.Lys374Gln)
c.817A>C (p.Lys273Gln)
c.664A>C (p.Lys222Gln)
c.1033A>C (p.Lys345Gln)
n.882A>C
c.*1561T>G (n.*1561T>G)
gnomAD v4
10g.102832532_102832533delCA2610723241CYP17A1,WBP1Lc.1119_1120del (p.His373GlnfsTer5)
c.816_817del (p.His272GlnfsTer5)
c.663_664del (p.His221GlnfsTer5)
c.1032_1033del (p.His344GlnfsTer5)
n.881_882del
c.*1563_*1564del (n.*1563_*1564del)
gnomAD v4
10g.102832531G>ACA5669400CYP17A1,WBP1Lc.1119C>T (p.His373=)
c.816C>T (p.His272=)
c.663C>T (p.His221=)
c.1032C>T (p.His344=)
n.881C>T
c.*1562G>A (n.*1562G>A)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.102832531G>CCA377938697CYP17A1,WBP1Lc.1119C>G (p.His373Gln)
c.816C>G (p.His272Gln)
c.663C>G (p.His221Gln)
c.1032C>G (p.His344Gln)
n.881C>G
c.*1562G>C (n.*1562G>C)
10g.102832531G=CA1932870499CYP17A1,WBP1Lc.1119C= (p.His373=)
c.816C= (p.His272=)
c.663C= (p.His221=)
c.1032C= (p.His344=)
n.881C=
c.*1562G= (n.*1562G=)
10g.102832531G>TCA377938698CYP17A1,WBP1Lc.1119C>A (p.His373Gln)
c.816C>A (p.His272Gln)
c.663C>A (p.His221Gln)
c.1032C>A (p.His344Gln)
n.881C>A
c.*1562G>T (n.*1562G>T)
gnomAD v4
10g.102832532T>ACA5669401CYP17A1,WBP1Lc.1118A>T (p.His373Leu)
c.815A>T (p.His272Leu)
c.662A>T (p.His221Leu)
c.1031A>T (p.His344Leu)
n.880A>T
c.*1563T>A (n.*1563T>A)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
10g.102832532T>CCA377938699CYP17A1,WBP1Lc.1118A>G (p.His373Arg)
c.815A>G (p.His272Arg)
c.662A>G (p.His221Arg)
c.1031A>G (p.His344Arg)
n.880A>G
c.*1563T>C (n.*1563T>C)
10g.102832532T>GCA377938700CYP17A1,WBP1Lc.1118A>C (p.His373Pro)
c.815A>C (p.His272Pro)
c.662A>C (p.His221Pro)
c.1031A>C (p.His344Pro)
n.880A>C
c.*1563T>G (n.*1563T>G)
10g.102832532T=CA1932870504CYP17A1,WBP1Lc.1118A= (p.His373=)
c.815A= (p.His272=)
c.662A= (p.His221=)
c.1031A= (p.His344=)
n.880A=
c.*1563T= (n.*1563T=)
10g.102832533G>ACA377938701CYP17A1,WBP1Lc.1117C>T (p.His373Tyr)
c.814C>T (p.His272Tyr)
c.661C>T (p.His221Tyr)
c.1030C>T (p.His344Tyr)
n.879C>T
c.*1564G>A (n.*1564G>A)
ClinVar dbSNP gnomAD v4
10g.102832533G>CCA377938702CYP17A1,WBP1Lc.1117C>G (p.His373Asp)
c.814C>G (p.His272Asp)
c.661C>G (p.His221Asp)
c.1030C>G (p.His344Asp)
n.879C>G
c.*1564G>C (n.*1564G>C)
ClinVar dbSNP gnomAD v4
10g.102832533G=CA1932870514CYP17A1,WBP1Lc.1117C= (p.His373=)
c.814C= (p.His272=)
c.661C= (p.His221=)
c.1030C= (p.His344=)
n.879C=
c.*1564G= (n.*1564G=)
10g.102832533G>TCA377938703CYP17A1,WBP1Lc.1117C>A (p.His373Asn)
c.814C>A (p.His272Asn)
c.661C>A (p.His221Asn)
c.1030C>A (p.His344Asn)
n.879C>A
c.*1564G>T (n.*1564G>T)
ClinVar dbSNP gnomAD v4
10g.102832537dupCA5669402CYP17A1,WBP1Lc.1117dup (p.His373ProfsTer6)
c.814dup (p.His272ProfsTer6)
c.661dup (p.His221ProfsTer6)
c.1030dup (p.His344ProfsTer6)
n.879dup
c.*1568dup (n.*1568dup)
dbSNP ExAC gnomAD v2 gnomAD v4
10g.102832537delCA2610723242CYP17A1,WBP1Lc.1117del (p.His373ThrfsTer?)
c.814del (p.His272ThrfsTer?)
c.661del (p.His221ThrfsTer?)
c.1030del (p.His344ThrfsTer?)
n.879del
c.*1568del (n.*1568del)
gnomAD v4
10g.102832536_102832537delCA2610723243CYP17A1,WBP1Lc.1116_1117del (p.His373GlnfsTer5)
c.813_814del (p.His272GlnfsTer5)
c.660_661del (p.His221GlnfsTer5)
c.1029_1030del (p.His344GlnfsTer5)
n.878_879del
c.*1567_*1568del (n.*1567_*1568del)
gnomAD v4
10g.102832534G>ACA471288363CYP17A1,WBP1Lc.1116C>T (p.Pro372=)
c.813C>T (p.Pro271=)
c.660C>T (p.Pro220=)
c.1029C>T (p.Pro343=)
n.878C>T
c.*1565G>A (n.*1565G>A)
ClinVar dbSNP gnomAD v4
10g.102832534G>CCA471288367CYP17A1,WBP1Lc.1116C>G (p.Pro372=)
c.813C>G (p.Pro271=)
c.660C>G (p.Pro220=)
c.1029C>G (p.Pro343=)
n.878C>G
c.*1565G>C (n.*1565G>C)
10g.102832534G>TCA471288370CYP17A1,WBP1Lc.1116C>A (p.Pro372=)
c.813C>A (p.Pro271=)
c.660C>A (p.Pro220=)
c.1029C>A (p.Pro343=)
n.878C>A
c.*1565G>T (n.*1565G>T)
10g.102832535G>ACA377938704CYP17A1,WBP1Lc.1115C>T (p.Pro372Leu)
c.812C>T (p.Pro271Leu)
c.659C>T (p.Pro220Leu)
c.1028C>T (p.Pro343Leu)
n.877C>T
c.*1566G>A (n.*1566G>A)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.102832535G>CCA377938705CYP17A1,WBP1Lc.1115C>G (p.Pro372Arg)
c.812C>G (p.Pro271Arg)
c.659C>G (p.Pro220Arg)
c.1028C>G (p.Pro343Arg)
n.877C>G
c.*1566G>C (n.*1566G>C)
10g.102832535G=CA1932870518CYP17A1,WBP1Lc.1115C= (p.Pro372=)
c.812C= (p.Pro271=)
c.659C= (p.Pro220=)
c.1028C= (p.Pro343=)
n.877C=
c.*1566G= (n.*1566G=)
10g.102832535G>TCA377938706CYP17A1,WBP1Lc.1115C>A (p.Pro372His)
c.812C>A (p.Pro271His)
c.659C>A (p.Pro220His)
c.1028C>A (p.Pro343His)
n.877C>A
c.*1566G>T (n.*1566G>T)
gnomAD v4
10g.102832536G>ACA377938708CYP17A1,WBP1Lc.1114C>T (p.Pro372Ser)
c.811C>T (p.Pro271Ser)
c.658C>T (p.Pro220Ser)
c.1027C>T (p.Pro343Ser)
n.876C>T
c.*1567G>A (n.*1567G>A)
COSMIC
10g.102832536G>CCA377938709CYP17A1,WBP1Lc.1114C>G (p.Pro372Ala)
c.811C>G (p.Pro271Ala)
c.658C>G (p.Pro220Ala)
c.1027C>G (p.Pro343Ala)
n.876C>G
c.*1567G>C (n.*1567G>C)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.102832536G=CA1932870523CYP17A1,WBP1Lc.1114C= (p.Pro372=)
c.811C= (p.Pro271=)
c.658C= (p.Pro220=)
c.1027C= (p.Pro343=)
n.876C=
c.*1567G= (n.*1567G=)
10g.102832536G>TCA377938707CYP17A1,WBP1Lc.1114C>A (p.Pro372Thr)
c.811C>A (p.Pro271Thr)
c.658C>A (p.Pro220Thr)
c.1027C>A (p.Pro343Thr)
n.876C>A
c.*1567G>T (n.*1567G>T)
gnomAD v4
10g.102832537G>ACA471288379CYP17A1,WBP1Lc.1113C>T (p.Ile371=)
c.810C>T (p.Ile270=)
c.657C>T (p.Ile219=)
c.1026C>T (p.Ile342=)
n.875C>T
c.*1568G>A (n.*1568G>A)
ClinVar dbSNP gnomAD v4
10g.102832537G>CCA377938710CYP17A1,WBP1Lc.1113C>G (p.Ile371Met)
c.810C>G (p.Ile270Met)
c.657C>G (p.Ile219Met)
c.1026C>G (p.Ile342Met)
n.875C>G
c.*1568G>C (n.*1568G>C)
10g.102832537G=CA1932870537CYP17A1,WBP1Lc.1113C= (p.Ile371=)
c.810C= (p.Ile270=)
c.657C= (p.Ile219=)
c.1026C= (p.Ile342=)
n.875C=
c.*1568G= (n.*1568G=)
10g.102832537G>TCA471288382CYP17A1,WBP1Lc.1113C>A (p.Ile371=)
c.810C>A (p.Ile270=)
c.657C>A (p.Ile219=)
c.1026C>A (p.Ile342=)
n.875C>A
c.*1568G>T (n.*1568G>T)
dbSNP gnomAD v2 gnomAD v4
10g.102832538delCA2610723244CYP17A1,WBP1Lc.1112del (p.Ile371ThrfsTer?)
c.809del (p.Ile270ThrfsTer?)
c.656del (p.Ile219ThrfsTer?)
c.1025del (p.Ile342ThrfsTer?)
n.874del
c.*1569del (n.*1569del)
gnomAD v4

Number of alleles fetched