Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.102832630G>ACA471288708CYP17A1,WBP1Lc.1020C>T (p.Arg340=)
c.717C>T (p.Arg239=)
c.564C>T (p.Arg188=)
c.933C>T (p.Arg311=)
n.782C>T
c.*1661G>A (n.*1661G>A)
10g.102832630G>CCA471288712CYP17A1,WBP1Lc.1020C>G (p.Arg340=)
c.717C>G (p.Arg239=)
c.564C>G (p.Arg188=)
c.933C>G (p.Arg311=)
n.782C>G
c.*1661G>C (n.*1661G>C)
10g.102832630G>TCA471288710CYP17A1,WBP1Lc.1020C>A (p.Arg340=)
c.717C>A (p.Arg239=)
c.564C>A (p.Arg188=)
c.933C>A (p.Arg311=)
n.782C>A
c.*1661G>T (n.*1661G>T)
gnomAD v4
10g.102832631C>ACA377938897CYP17A1,WBP1Lc.1019G>T (p.Arg340Leu)
c.716G>T (p.Arg239Leu)
c.563G>T (p.Arg188Leu)
c.932G>T (p.Arg311Leu)
n.781G>T
c.*1662C>A (n.*1662C>A)
10g.102832631C=CA1932870727CYP17A1,WBP1Lc.1019G= (p.Arg340=)
c.716G= (p.Arg239=)
c.563G= (p.Arg188=)
c.932G= (p.Arg311=)
n.781G=
c.*1662C= (n.*1662C=)
10g.102832631C>GCA377938898CYP17A1,WBP1Lc.1019G>C (p.Arg340Pro)
c.716G>C (p.Arg239Pro)
c.563G>C (p.Arg188Pro)
c.932G>C (p.Arg311Pro)
n.781G>C
c.*1662C>G (n.*1662C>G)
10g.102832631C>TCA5669414CYP17A1,WBP1Lc.1019G>A (p.Arg340His)
c.716G>A (p.Arg239His)
c.563G>A (p.Arg188His)
c.932G>A (p.Arg311His)
n.781G>A
c.*1662C>T (n.*1662C>T)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.102832632G>ACA377938899CYP17A1,WBP1Lc.1018C>T (p.Arg340Cys)
c.715C>T (p.Arg239Cys)
c.562C>T (p.Arg188Cys)
c.931C>T (p.Arg311Cys)
n.780C>T
c.*1663G>A (n.*1663G>A)
dbSNP gnomAD v4
10g.102832632G>CCA377938900CYP17A1,WBP1Lc.1018C>G (p.Arg340Gly)
c.715C>G (p.Arg239Gly)
c.562C>G (p.Arg188Gly)
c.931C>G (p.Arg311Gly)
n.780C>G
c.*1663G>C (n.*1663G>C)
10g.102832632G=CA1932870738CYP17A1,WBP1Lc.1018C= (p.Arg340=)
c.715C= (p.Arg239=)
c.562C= (p.Arg188=)
c.931C= (p.Arg311=)
n.780C=
c.*1663G= (n.*1663G=)
10g.102832632G>TCA377938901CYP17A1,WBP1Lc.1018C>A (p.Arg340Ser)
c.715C>A (p.Arg239Ser)
c.562C>A (p.Arg188Ser)
c.931C>A (p.Arg311Ser)
n.780C>A
c.*1663G>T (n.*1663G>T)
gnomAD v4
10g.102832632_102832635delinsGGCTCA1932870741CYP17A1,WBP1Lc.1015_1018delinsAGCC (p.Ser339=)
c.712_715delinsAGCC (p.Ser238=)
c.559_562delinsAGCC (p.Ser187=)
c.928_931delinsAGCC (p.Ser310=)
n.777_780delinsAGCC
c.*1663_*1666delinsGGCT (n.*1663_*1666delinsGGCT)
10g.102832633G>ACA471288719CYP17A1,WBP1Lc.1017C>T (p.Ser339=)
c.714C>T (p.Ser238=)
c.561C>T (p.Ser187=)
c.930C>T (p.Ser310=)
n.779C>T
c.*1664G>A (n.*1664G>A)
gnomAD v4
10g.102832633G>CCA377938902CYP17A1,WBP1Lc.1017C>G (p.Ser339Arg)
c.714C>G (p.Ser238Arg)
c.561C>G (p.Ser187Arg)
c.930C>G (p.Ser310Arg)
n.779C>G
c.*1664G>C (n.*1664G>C)
dbSNP
10g.102832633G=CA1932870767CYP17A1,WBP1Lc.1017C= (p.Ser339=)
c.714C= (p.Ser238=)
c.561C= (p.Ser187=)
c.930C= (p.Ser310=)
n.779C=
c.*1664G= (n.*1664G=)
10g.102832633G>TCA377938903CYP17A1,WBP1Lc.1017C>A (p.Ser339Arg)
c.714C>A (p.Ser238Arg)
c.561C>A (p.Ser187Arg)
c.930C>A (p.Ser310Arg)
n.779C>A
c.*1664G>T (n.*1664G>T)
gnomAD v4
10g.102832634_102832636delCA595636697CYP17A1,WBP1Lc.1015_1017del (p.Ser339del)
c.712_714del (p.Ser238del)
c.559_561del (p.Ser187del)
c.928_930del (p.Ser310del)
n.777_779del
c.*1665_*1667del (n.*1665_*1667del)
dbSNP gnomAD v2 gnomAD v4
10g.102832634C>ACA377938904CYP17A1,WBP1Lc.1016G>T (p.Ser339Ile)
c.713G>T (p.Ser238Ile)
c.560G>T (p.Ser187Ile)
c.929G>T (p.Ser310Ile)
n.778G>T
c.*1665C>A (n.*1665C>A)
10g.102832634C>GCA377938905CYP17A1,WBP1Lc.1016G>C (p.Ser339Thr)
c.713G>C (p.Ser238Thr)
c.560G>C (p.Ser187Thr)
c.929G>C (p.Ser310Thr)
n.778G>C
c.*1665C>G (n.*1665C>G)
COSMIC
10g.102832634C>TCA377938906CYP17A1,WBP1Lc.1016G>A (p.Ser339Asn)
c.713G>A (p.Ser238Asn)
c.560G>A (p.Ser187Asn)
c.929G>A (p.Ser310Asn)
n.778G>A
c.*1665C>T (n.*1665C>T)
10g.102832635T>ACA377938907CYP17A1,WBP1Lc.1015A>T (p.Ser339Cys)
c.712A>T (p.Ser238Cys)
c.559A>T (p.Ser187Cys)
c.928A>T (p.Ser310Cys)
n.777A>T
c.*1666T>A (n.*1666T>A)
10g.102832635T>CCA377938908CYP17A1,WBP1Lc.1015A>G (p.Ser339Gly)
c.712A>G (p.Ser238Gly)
c.559A>G (p.Ser187Gly)
c.928A>G (p.Ser310Gly)
n.777A>G
c.*1666T>C (n.*1666T>C)
gnomAD v4
10g.102832635T>GCA377938909CYP17A1,WBP1Lc.1015A>C (p.Ser339Arg)
c.712A>C (p.Ser238Arg)
c.559A>C (p.Ser187Arg)
c.928A>C (p.Ser310Arg)
n.777A>C
c.*1666T>G (n.*1666T>G)
10g.102832636G>ACA5669415CYP17A1,WBP1Lc.1014C>T (p.Phe338=)
c.711C>T (p.Phe237=)
c.558C>T (p.Phe186=)
c.927C>T (p.Phe309=)
n.776C>T
c.*1667G>A (n.*1667G>A)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
10g.102832636G>CCA377938910CYP17A1,WBP1Lc.1014C>G (p.Phe338Leu)
c.711C>G (p.Phe237Leu)
c.558C>G (p.Phe186Leu)
c.927C>G (p.Phe309Leu)
n.776C>G
c.*1667G>C (n.*1667G>C)
10g.102832636G=CA1932870772CYP17A1,WBP1Lc.1014C= (p.Phe338=)
c.711C= (p.Phe237=)
c.558C= (p.Phe186=)
c.927C= (p.Phe309=)
n.776C=
c.*1667G= (n.*1667G=)
10g.102832636G>TCA377938911CYP17A1,WBP1Lc.1014C>A (p.Phe338Leu)
c.711C>A (p.Phe237Leu)
c.558C>A (p.Phe186Leu)
c.927C>A (p.Phe309Leu)
n.776C>A
c.*1667G>T (n.*1667G>T)
gnomAD v4
10g.102832637A=CA1932870775CYP17A1,WBP1Lc.1013T= (p.Phe338=)
c.710T= (p.Phe237=)
c.557T= (p.Phe186=)
c.926T= (p.Phe309=)
n.775T=
c.*1668A= (n.*1668A=)
10g.102832637A>CCA377938912CYP17A1,WBP1Lc.1013T>G (p.Phe338Cys)
c.710T>G (p.Phe237Cys)
c.557T>G (p.Phe186Cys)
c.926T>G (p.Phe309Cys)
n.775T>G
c.*1668A>C (n.*1668A>C)
10g.102832637A>GCA377938913CYP17A1,WBP1Lc.1013T>C (p.Phe338Ser)
c.710T>C (p.Phe237Ser)
c.557T>C (p.Phe186Ser)
c.926T>C (p.Phe309Ser)
n.775T>C
c.*1668A>G (n.*1668A>G)
dbSNP gnomAD v4
10g.102832637A>TCA377938914CYP17A1,WBP1Lc.1013T>A (p.Phe338Tyr)
c.710T>A (p.Phe237Tyr)
c.557T>A (p.Phe186Tyr)
c.926T>A (p.Phe309Tyr)
n.775T>A
c.*1668A>T (n.*1668A>T)
10g.102832638A>CCA377938915CYP17A1,WBP1Lc.1012T>G (p.Phe338Val)
c.709T>G (p.Phe237Val)
c.556T>G (p.Phe186Val)
c.925T>G (p.Phe309Val)
n.774T>G
c.*1669A>C (n.*1669A>C)
10g.102832638A>GCA377938916CYP17A1,WBP1Lc.1012T>C (p.Phe338Leu)
c.709T>C (p.Phe237Leu)
c.556T>C (p.Phe186Leu)
c.925T>C (p.Phe309Leu)
n.774T>C
c.*1669A>G (n.*1669A>G)
gnomAD v4
10g.102832638A>TCA377938917CYP17A1,WBP1Lc.1012T>A (p.Phe338Ile)
c.709T>A (p.Phe237Ile)
c.556T>A (p.Phe186Ile)
c.925T>A (p.Phe309Ile)
n.774T>A
c.*1669A>T (n.*1669A>T)
10g.102832639A>CCA471288733CYP17A1,WBP1Lc.1011T>G (p.Gly337=)
c.708T>G (p.Gly236=)
c.555T>G (p.Gly185=)
c.924T>G (p.Gly308=)
n.773T>G
c.*1670A>C (n.*1670A>C)
10g.102832639A>GCA471288734CYP17A1,WBP1Lc.1011T>C (p.Gly337=)
c.708T>C (p.Gly236=)
c.555T>C (p.Gly185=)
c.924T>C (p.Gly308=)
n.773T>C
c.*1670A>G (n.*1670A>G)
10g.102832639A>TCA471288735CYP17A1,WBP1Lc.1011T>A (p.Gly337=)
c.708T>A (p.Gly236=)
c.555T>A (p.Gly185=)
c.924T>A (p.Gly308=)
n.773T>A
c.*1670A>T (n.*1670A>T)
10g.102832640C>ACA377938920CYP17A1,WBP1Lc.1010G>T (p.Gly337Val)
c.707G>T (p.Gly236Val)
c.554G>T (p.Gly185Val)
c.923G>T (p.Gly308Val)
n.772G>T
c.*1671C>A (n.*1671C>A)
10g.102832640C>GCA377938919CYP17A1,WBP1Lc.1010G>C (p.Gly337Ala)
c.707G>C (p.Gly236Ala)
c.554G>C (p.Gly185Ala)
c.923G>C (p.Gly308Ala)
n.772G>C
c.*1671C>G (n.*1671C>G)
10g.102832640C>TCA377938918CYP17A1,WBP1Lc.1010G>A (p.Gly337Asp)
c.707G>A (p.Gly236Asp)
c.554G>A (p.Gly185Asp)
c.923G>A (p.Gly308Asp)
n.772G>A
c.*1671C>T (n.*1671C>T)
10g.102832642delCA2610723247CYP17A1,WBP1Lc.1010del (p.Gly337ValfsTer?)
c.707del (p.Gly236ValfsTer?)
c.554del (p.Gly185ValfsTer?)
c.923del (p.Gly308ValfsTer?)
n.772del
c.*1673del (n.*1673del)
gnomAD v4
10g.102832641C>ACA377938921CYP17A1,WBP1Lc.1009G>T (p.Gly337Cys)
c.706G>T (p.Gly236Cys)
c.553G>T (p.Gly185Cys)
c.922G>T (p.Gly308Cys)
n.771G>T
c.*1672C>A (n.*1672C>A)
10g.102832641C>GCA377938922CYP17A1,WBP1Lc.1009G>C (p.Gly337Arg)
c.706G>C (p.Gly236Arg)
c.553G>C (p.Gly185Arg)
c.922G>C (p.Gly308Arg)
n.771G>C
c.*1672C>G (n.*1672C>G)
10g.102832641C>TCA377938923CYP17A1,WBP1Lc.1009G>A (p.Gly337Ser)
c.706G>A (p.Gly236Ser)
c.553G>A (p.Gly185Ser)
c.922G>A (p.Gly308Ser)
n.771G>A
c.*1672C>T (n.*1672C>T)
gnomAD v4
10g.102832642C>ACA471288741CYP17A1,WBP1Lc.1008G>T (p.Val336=)
c.705G>T (p.Val235=)
c.552G>T (p.Val184=)
c.921G>T (p.Val307=)
n.770G>T
c.*1673C>A (n.*1673C>A)
10g.102832642C>GCA471288743CYP17A1,WBP1Lc.1008G>C (p.Val336=)
c.705G>C (p.Val235=)
c.552G>C (p.Val184=)
c.921G>C (p.Val307=)
n.770G>C
c.*1673C>G (n.*1673C>G)
10g.102832642C>TCA471288744CYP17A1,WBP1Lc.1008G>A (p.Val336=)
c.705G>A (p.Val235=)
c.552G>A (p.Val184=)
c.921G>A (p.Val307=)
n.770G>A
c.*1673C>T (n.*1673C>T)
ClinVar
10g.102832643A>CCA377938924CYP17A1,WBP1Lc.1007T>G (p.Val336Gly)
c.704T>G (p.Val235Gly)
c.551T>G (p.Val184Gly)
c.920T>G (p.Val307Gly)
n.769T>G
c.*1674A>C (n.*1674A>C)
10g.102832643A>GCA377938925CYP17A1,WBP1Lc.1007T>C (p.Val336Ala)
c.704T>C (p.Val235Ala)
c.551T>C (p.Val184Ala)
c.920T>C (p.Val307Ala)
n.769T>C
c.*1674A>G (n.*1674A>G)
10g.102832643A>TCA377938926CYP17A1,WBP1Lc.1007T>A (p.Val336Glu)
c.704T>A (p.Val235Glu)
c.551T>A (p.Val184Glu)
c.920T>A (p.Val307Glu)
n.769T>A
c.*1674A>T (n.*1674A>T)

Number of alleles fetched