Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.38071060G>ACA1245626101CYP1B1c.1294C>T (p.Leu432=)
n.672C>T
c.181C>T (p.Leu61=)
dbSNP
2g.38071060G>CCA45506319CYP1B1c.1294C>G (p.Leu432Val)
n.672C>G
c.181C>G (p.Leu61Val)
ClinVar dbSNP gnomAD v3 gnomAD v4
2g.38071060G=CA179949CYP1B1c.1294C= (p.Leu432=)
n.672C=
c.181C= (p.Leu61=)
2g.38071060G>TCA658682730CYP1B1c.1294C>A (p.Leu432Met)
n.672C>A
c.181C>A (p.Leu61Met)
2g.38071061T>ACA425864495CYP1B1c.1293A>T (p.Pro431=)
n.671A>T
c.180A>T (p.Pro60=)
2g.38071061T>CCA425864496CYP1B1c.1293A>G (p.Pro431=)
n.671A>G
c.180A>G (p.Pro60=)
2g.38071061T>GCA425864497CYP1B1c.1293A>C (p.Pro431=)
n.671A>C
c.180A>C (p.Pro60=)
2g.38071062G>ACA346327455CYP1B1c.1292C>T (p.Pro431Leu)
n.670C>T
c.179C>T (p.Pro60Leu)
dbSNP gnomAD v2 gnomAD v4
2g.38071062G>CCA346327456CYP1B1c.1292C>G (p.Pro431Arg)
n.670C>G
c.179C>G (p.Pro60Arg)
2g.38071062G=CA1245626102CYP1B1c.1292C= (p.Pro431=)
n.670C=
c.179C= (p.Pro60=)
2g.38071062G>TCA346327457CYP1B1c.1292C>A (p.Pro431Gln)
n.670C>A
c.179C>A (p.Pro60Gln)
2g.38071063G>ACA346327458CYP1B1c.1291C>T (p.Pro431Ser)
n.669C>T
c.178C>T (p.Pro60Ser)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.38071063G>CCA346327459CYP1B1c.1291C>G (p.Pro431Ala)
n.669C>G
c.178C>G (p.Pro60Ala)
2g.38071063G=CA1245626103CYP1B1c.1291C= (p.Pro431=)
n.669C=
c.178C= (p.Pro60=)
2g.38071063G>TCA346327460CYP1B1c.1291C>A (p.Pro431Thr)
n.669C>A
c.178C>A (p.Pro60Thr)
2g.38071064G>ACA425864499CYP1B1c.1290C>T (p.Asp430=)
n.668C>T
c.177C>T (p.Asp59=)
dbSNP gnomAD v4
2g.38071064G>CCA243092CYP1B1c.1290C>G (p.Asp430Glu)
n.668C>G
c.177C>G (p.Asp59Glu)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
2g.38071064G=CA1245626104CYP1B1c.1290C= (p.Asp430=)
n.668C=
c.177C= (p.Asp59=)
2g.38071064G>TCA346327461CYP1B1c.1290C>A (p.Asp430Glu)
n.668C>A
c.177C>A (p.Asp59Glu)
2g.38071065T>ACA346327463CYP1B1c.1289A>T (p.Asp430Val)
n.667A>T
c.176A>T (p.Asp59Val)
dbSNP
2g.38071065T>CCA346327464CYP1B1c.1289A>G (p.Asp430Gly)
n.667A>G
c.176A>G (p.Asp59Gly)
2g.38071065T>GCA346327462CYP1B1c.1289A>C (p.Asp430Ala)
n.667A>C
c.176A>C (p.Asp59Ala)
2g.38071066C>ACA346327467CYP1B1c.1288G>T (p.Asp430Tyr)
n.666G>T
c.175G>T (p.Asp59Tyr)
2g.38071066C>GCA346327465CYP1B1c.1288G>C (p.Asp430His)
n.666G>C
c.175G>C (p.Asp59His)
2g.38071066C>TCA346327466CYP1B1c.1288G>A (p.Asp430Asn)
n.666G>A
c.175G>A (p.Asp59Asn)
2g.38071067A>CCA346327468CYP1B1c.1287T>G (p.His429Gln)
n.665T>G
c.174T>G (p.His58Gln)
2g.38071067A>GCA425864500CYP1B1c.1287T>C (p.His429=)
n.665T>C
c.174T>C (p.His58=)
gnomAD v4
2g.38071067A>TCA346327469CYP1B1c.1287T>A (p.His429Gln)
n.665T>A
c.174T>A (p.His58Gln)
2g.38071068T>ACA346327470CYP1B1c.1286A>T (p.His429Leu)
n.664A>T
c.173A>T (p.His58Leu)
2g.38071068T>CCA346327471CYP1B1c.1286A>G (p.His429Arg)
n.664A>G
c.173A>G (p.His58Arg)
gnomAD v4
2g.38071068T>GCA346327472CYP1B1c.1286A>C (p.His429Pro)
n.664A>C
c.173A>C (p.His58Pro)
dbSNP
2g.38071068T=CA1245626105CYP1B1c.1286A= (p.His429=)
n.664A=
c.173A= (p.His58=)
2g.38071069G>ACA1619824CYP1B1c.1285C>T (p.His429Tyr)
n.663C>T
c.172C>T (p.His58Tyr)
dbSNP ExAC gnomAD v2 gnomAD v4
2g.38071069G>CCA346327473CYP1B1c.1285C>G (p.His429Asp)
n.663C>G
c.172C>G (p.His58Asp)
dbSNP gnomAD v3 gnomAD v4
2g.38071069G=CA1245626106CYP1B1c.1285C= (p.His429=)
n.663C=
c.172C= (p.His58=)
2g.38071069G>TCA346327474CYP1B1c.1285C>A (p.His429Asn)
n.663C>A
c.172C>A (p.His58Asn)
2g.38071070A>CCA346327475CYP1B1c.1284T>G (p.Asn428Lys)
n.662T>G
c.171T>G (p.Asn57Lys)
2g.38071070A>GCA425864504CYP1B1c.1284T>C (p.Asn428=)
n.662T>C
c.171T>C (p.Asn57=)
2g.38071070A>TCA346327476CYP1B1c.1284T>A (p.Asn428Lys)
n.662T>A
c.171T>A (p.Asn57Lys)
2g.38071071T>ACA346327479CYP1B1c.1283A>T (p.Asn428Ile)
n.661A>T
c.170A>T (p.Asn57Ile)
2g.38071071T>CCA346327478CYP1B1c.1283A>G (p.Asn428Ser)
n.661A>G
c.170A>G (p.Asn57Ser)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.38071071T>GCA346327477CYP1B1c.1283A>C (p.Asn428Thr)
n.661A>C
c.170A>C (p.Asn57Thr)
2g.38071071T=CA1245626107CYP1B1c.1283A= (p.Asn428=)
n.661A=
c.170A= (p.Asn57=)
2g.38071072T>ACA346327480CYP1B1c.1282A>T (p.Asn428Tyr)
n.660A>T
c.169A>T (p.Asn57Tyr)
2g.38071072T>CCA346327481CYP1B1c.1282A>G (p.Asn428Asp)
n.660A>G
c.169A>G (p.Asn57Asp)
gnomAD v4
2g.38071072T>GCA346327482CYP1B1c.1282A>C (p.Asn428His)
n.660A>C
c.169A>C (p.Asn57His)
2g.38071073C>ACA425864509CYP1B1c.1281G>T (p.Val427=)
n.659G>T
c.168G>T (p.Val56=)
2g.38071073C>GCA425864505CYP1B1c.1281G>C (p.Val427=)
n.659G>C
c.168G>C (p.Val56=)
2g.38071073C>TCA425864507CYP1B1c.1281G>A (p.Val427=)
n.659G>A
c.168G>A (p.Val56=)
2g.38071074A>CCA346327483CYP1B1c.1280T>G (p.Val427Gly)
n.658T>G
c.167T>G (p.Val56Gly)

Number of alleles fetched