Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.102830871A>GCA115205CYP17A1,WBP1Lc.1358T>C (p.Phe453Ser)
c.1055T>C (p.Phe352Ser)
c.902T>C (p.Phe301Ser)
c.1271T>C (p.Phe424Ser)
c.1361T>C (p.Phe454Ser)
n.1120T>C
c.*553A>G (n.*553A>G)
ClinVar dbSNP
10g.102830871A=CA1932866979CYP17A1,WBP1Lc.1358T= (p.Phe453=)
c.1055T= (p.Phe352=)
c.902T= (p.Phe301=)
c.1271T= (p.Phe424=)
c.1361T= (p.Phe454=)
n.1120T=
c.*553A= (n.*553A=)
dbSNP

Number of alleles fetched