Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.102832611G>TCA377938856CYP17A1,WBP1Lc.1039C>A (p.Arg347Ser)
c.736C>A (p.Arg246Ser)
c.583C>A (p.Arg195Ser)
c.952C>A (p.Arg318Ser)
n.801C>A
c.*1642G>T (n.*1642G>T)
dbSNP gnomAD v2 gnomAD v4 COSMIC
10g.102832611G>ACA115191CYP17A1,WBP1Lc.1039C>T (p.Arg347Cys)
c.736C>T (p.Arg246Cys)
c.583C>T (p.Arg195Cys)
c.952C>T (p.Arg318Cys)
n.801C>T
c.*1642G>A (n.*1642G>A)
ClinVar dbSNP gnomAD v2 gnomAD v4
10g.102832611G>CCA377938855CYP17A1,WBP1Lc.1039C>G (p.Arg347Gly)
c.736C>G (p.Arg246Gly)
c.583C>G (p.Arg195Gly)
c.952C>G (p.Arg318Gly)
n.801C>G
c.*1642G>C (n.*1642G>C)
ClinVar dbSNP
10g.102832611G=CA1932870666CYP17A1,WBP1Lc.1039C= (p.Arg347=)
c.736C= (p.Arg246=)
c.583C= (p.Arg195=)
c.952C= (p.Arg318=)
n.801C=
c.*1642G= (n.*1642G=)
dbSNP

Number of alleles fetched