Chr Mutation (hg38) CAid Gene Transcript Linkouts
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.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)
ClinVar 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
10g.102832538A=CA1932870541CYP17A1,WBP1Lc.1112T= (p.Ile371=)
c.809T= (p.Ile270=)
c.656T= (p.Ile219=)
c.1025T= (p.Ile342=)
n.874T=
c.*1569A= (n.*1569A=)
10g.102832538A>CCA377938711CYP17A1,WBP1Lc.1112T>G (p.Ile371Ser)
c.809T>G (p.Ile270Ser)
c.656T>G (p.Ile219Ser)
c.1025T>G (p.Ile342Ser)
n.874T>G
c.*1569A>C (n.*1569A>C)
10g.102832538A>GCA5669403CYP17A1,WBP1Lc.1112T>C (p.Ile371Thr)
c.809T>C (p.Ile270Thr)
c.656T>C (p.Ile219Thr)
c.1025T>C (p.Ile342Thr)
n.874T>C
c.*1569A>G (n.*1569A>G)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.102832538A>TCA377938712CYP17A1,WBP1Lc.1112T>A (p.Ile371Asn)
c.809T>A (p.Ile270Asn)
c.656T>A (p.Ile219Asn)
c.1025T>A (p.Ile342Asn)
n.874T>A
c.*1569A>T (n.*1569A>T)
10g.102832539T>ACA377938713CYP17A1,WBP1Lc.1111A>T (p.Ile371Phe)
c.808A>T (p.Ile270Phe)
c.655A>T (p.Ile219Phe)
c.1024A>T (p.Ile342Phe)
n.873A>T
c.*1570T>A (n.*1570T>A)
10g.102832539T>CCA377938714CYP17A1,WBP1Lc.1111A>G (p.Ile371Val)
c.808A>G (p.Ile270Val)
c.655A>G (p.Ile219Val)
c.1024A>G (p.Ile342Val)
n.873A>G
c.*1570T>C (n.*1570T>C)
10g.102832539T>GCA377938715CYP17A1,WBP1Lc.1111A>C (p.Ile371Leu)
c.808A>C (p.Ile270Leu)
c.655A>C (p.Ile219Leu)
c.1024A>C (p.Ile342Leu)
n.873A>C
c.*1570T>G (n.*1570T>G)
10g.102832540G>ACA471288391CYP17A1,WBP1Lc.1110C>T (p.Leu370=)
c.807C>T (p.Leu269=)
c.654C>T (p.Leu218=)
c.1023C>T (p.Leu341=)
n.872C>T
c.*1571G>A (n.*1571G>A)
10g.102832540G>CCA471288392CYP17A1,WBP1Lc.1110C>G (p.Leu370=)
c.807C>G (p.Leu269=)
c.654C>G (p.Leu218=)
c.1023C>G (p.Leu341=)
n.872C>G
c.*1571G>C (n.*1571G>C)
10g.102832540G>TCA471288394CYP17A1,WBP1Lc.1110C>A (p.Leu370=)
c.807C>A (p.Leu269=)
c.654C>A (p.Leu218=)
c.1023C>A (p.Leu341=)
n.872C>A
c.*1571G>T (n.*1571G>T)
10g.102832541A>CCA377938716CYP17A1,WBP1Lc.1109T>G (p.Leu370Arg)
c.806T>G (p.Leu269Arg)
c.653T>G (p.Leu218Arg)
c.1022T>G (p.Leu341Arg)
n.871T>G
c.*1572A>C (n.*1572A>C)
10g.102832541A>GCA377938717CYP17A1,WBP1Lc.1109T>C (p.Leu370Pro)
c.806T>C (p.Leu269Pro)
c.653T>C (p.Leu218Pro)
c.1022T>C (p.Leu341Pro)
n.871T>C
c.*1572A>G (n.*1572A>G)
10g.102832541A>TCA377938718CYP17A1,WBP1Lc.1109T>A (p.Leu370His)
c.806T>A (p.Leu269His)
c.653T>A (p.Leu218His)
c.1022T>A (p.Leu341His)
n.871T>A
c.*1572A>T (n.*1572A>T)
10g.102832542G>ACA377938719CYP17A1,WBP1Lc.1108C>T (p.Leu370Phe)
c.805C>T (p.Leu269Phe)
c.652C>T (p.Leu218Phe)
c.1021C>T (p.Leu341Phe)
n.870C>T
c.*1573G>A (n.*1573G>A)
10g.102832542G>CCA377938720CYP17A1,WBP1Lc.1108C>G (p.Leu370Val)
c.805C>G (p.Leu269Val)
c.652C>G (p.Leu218Val)
c.1021C>G (p.Leu341Val)
n.870C>G
c.*1573G>C (n.*1573G>C)
10g.102832542G>TCA377938721CYP17A1,WBP1Lc.1108C>A (p.Leu370Ile)
c.805C>A (p.Leu269Ile)
c.652C>A (p.Leu218Ile)
c.1021C>A (p.Leu341Ile)
n.870C>A
c.*1573G>T (n.*1573G>T)
10g.102832543C>ACA377938724CYP17A1,WBP1Lc.1107G>T (p.Met369Ile)
c.804G>T (p.Met268Ile)
c.651G>T (p.Met217Ile)
c.1020G>T (p.Met340Ile)
n.869G>T
c.*1574C>A (n.*1574C>A)
10g.102832543C>GCA377938723CYP17A1,WBP1Lc.1107G>C (p.Met369Ile)
c.804G>C (p.Met268Ile)
c.651G>C (p.Met217Ile)
c.1020G>C (p.Met340Ile)
n.869G>C
c.*1574C>G (n.*1574C>G)
10g.102832543C>TCA377938722CYP17A1,WBP1Lc.1107G>A (p.Met369Ile)
c.804G>A (p.Met268Ile)
c.651G>A (p.Met217Ile)
c.1020G>A (p.Met340Ile)
n.869G>A
c.*1574C>T (n.*1574C>T)
10g.102832544A=CA1932870546CYP17A1,WBP1Lc.1106T= (p.Met369=)
c.803T= (p.Met268=)
c.650T= (p.Met217=)
c.1019T= (p.Met340=)
n.868T=
c.*1575A= (n.*1575A=)
10g.102832544A>CCA377938725CYP17A1,WBP1Lc.1106T>G (p.Met369Arg)
c.803T>G (p.Met268Arg)
c.650T>G (p.Met217Arg)
c.1019T>G (p.Met340Arg)
n.868T>G
c.*1575A>C (n.*1575A>C)
10g.102832544A>GCA377938726CYP17A1,WBP1Lc.1106T>C (p.Met369Thr)
c.803T>C (p.Met268Thr)
c.650T>C (p.Met217Thr)
c.1019T>C (p.Met340Thr)
n.868T>C
c.*1575A>G (n.*1575A>G)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.102832544A>TCA377938727CYP17A1,WBP1Lc.1106T>A (p.Met369Lys)
c.803T>A (p.Met268Lys)
c.650T>A (p.Met217Lys)
c.1019T>A (p.Met340Lys)
n.868T>A
c.*1575A>T (n.*1575A>T)
10g.102832545T>ACA377938728CYP17A1,WBP1Lc.1105A>T (p.Met369Leu)
c.802A>T (p.Met268Leu)
c.649A>T (p.Met217Leu)
c.1018A>T (p.Met340Leu)
n.867A>T
c.*1576T>A (n.*1576T>A)
10g.102832545T>CCA377938729CYP17A1,WBP1Lc.1105A>G (p.Met369Val)
c.802A>G (p.Met268Val)
c.649A>G (p.Met217Val)
c.1018A>G (p.Met340Val)
n.867A>G
c.*1576T>C (n.*1576T>C)
dbSNP gnomAD v3 gnomAD v4
10g.102832545T>GCA377938730CYP17A1,WBP1Lc.1105A>C (p.Met369Leu)
c.802A>C (p.Met268Leu)
c.649A>C (p.Met217Leu)
c.1018A>C (p.Met340Leu)
n.867A>C
c.*1576T>G (n.*1576T>G)
10g.102832545T=CA1932870550CYP17A1,WBP1Lc.1105A= (p.Met369=)
c.802A= (p.Met268=)
c.649A= (p.Met217=)
c.1018A= (p.Met340=)
n.867A=
c.*1576T= (n.*1576T=)
10g.102832546delCA2610723245CYP17A1,WBP1Lc.1104del (p.Met369CysfsTer?)
c.801del (p.Met268CysfsTer?)
c.648del (p.Met217CysfsTer?)
c.1017del (p.Met340CysfsTer?)
n.866del
c.*1577del (n.*1577del)
gnomAD v4
10g.102832546A>CCA471288415CYP17A1,WBP1Lc.1104T>G (p.Pro368=)
c.801T>G (p.Pro267=)
c.648T>G (p.Pro216=)
c.1017T>G (p.Pro339=)
n.866T>G
c.*1577A>C (n.*1577A>C)
10g.102832546A>GCA471288413CYP17A1,WBP1Lc.1104T>C (p.Pro368=)
c.801T>C (p.Pro267=)
c.648T>C (p.Pro216=)
c.1017T>C (p.Pro339=)
n.866T>C
c.*1577A>G (n.*1577A>G)
10g.102832546A>TCA471288411CYP17A1,WBP1Lc.1104T>A (p.Pro368=)
c.801T>A (p.Pro267=)
c.648T>A (p.Pro216=)
c.1017T>A (p.Pro339=)
n.866T>A
c.*1577A>T (n.*1577A>T)
10g.102832547G>ACA377938731CYP17A1,WBP1Lc.1103C>T (p.Pro368Leu)
c.800C>T (p.Pro267Leu)
c.647C>T (p.Pro216Leu)
c.1016C>T (p.Pro339Leu)
n.865C>T
c.*1578G>A (n.*1578G>A)
10g.102832547G>CCA377938732CYP17A1,WBP1Lc.1103C>G (p.Pro368Arg)
c.800C>G (p.Pro267Arg)
c.647C>G (p.Pro216Arg)
c.1016C>G (p.Pro339Arg)
n.865C>G
c.*1578G>C (n.*1578G>C)
10g.102832547G>TCA377938733CYP17A1,WBP1Lc.1103C>A (p.Pro368His)
c.800C>A (p.Pro267His)
c.647C>A (p.Pro216His)
c.1016C>A (p.Pro339His)
n.865C>A
c.*1578G>T (n.*1578G>T)
10g.102832548G>ACA377938734CYP17A1,WBP1Lc.1102C>T (p.Pro368Ser)
c.799C>T (p.Pro267Ser)
c.646C>T (p.Pro216Ser)
c.1015C>T (p.Pro339Ser)
n.864C>T
c.*1579G>A (n.*1579G>A)
10g.102832548G>CCA377938735CYP17A1,WBP1Lc.1102C>G (p.Pro368Ala)
c.799C>G (p.Pro267Ala)
c.646C>G (p.Pro216Ala)
c.1015C>G (p.Pro339Ala)
n.864C>G
c.*1579G>C (n.*1579G>C)
10g.102832548G>TCA377938736CYP17A1,WBP1Lc.1102C>A (p.Pro368Thr)
c.799C>A (p.Pro267Thr)
c.646C>A (p.Pro216Thr)
c.1015C>A (p.Pro339Thr)
n.864C>A
c.*1579G>T (n.*1579G>T)
10g.102832549G>ACA471288427CYP17A1,WBP1Lc.1101C>T (p.Ala367=)
c.798C>T (p.Ala266=)
c.645C>T (p.Ala215=)
c.1014C>T (p.Ala338=)
n.863C>T
c.*1580G>A (n.*1580G>A)
10g.102832549G>CCA471288429CYP17A1,WBP1Lc.1101C>G (p.Ala367=)
c.798C>G (p.Ala266=)
c.645C>G (p.Ala215=)
c.1014C>G (p.Ala338=)
n.863C>G
c.*1580G>C (n.*1580G>C)
10g.102832549G>TCA471288431CYP17A1,WBP1Lc.1101C>A (p.Ala367=)
c.798C>A (p.Ala266=)
c.645C>A (p.Ala215=)
c.1014C>A (p.Ala338=)
n.863C>A
c.*1580G>T (n.*1580G>T)
10g.102832550G>ACA5669404CYP17A1,WBP1Lc.1100C>T (p.Ala367Val)
c.797C>T (p.Ala266Val)
c.644C>T (p.Ala215Val)
c.1013C>T (p.Ala338Val)
n.862C>T
c.*1581G>A (n.*1581G>A)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
10g.102832550G>CCA377938738CYP17A1,WBP1Lc.1100C>G (p.Ala367Gly)
c.797C>G (p.Ala266Gly)
c.644C>G (p.Ala215Gly)
c.1013C>G (p.Ala338Gly)
n.862C>G
c.*1581G>C (n.*1581G>C)

Number of alleles fetched