Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.38071054A=CA1245626097CYP1B1c.1300T= (p.Trp434=)
n.678T=
c.187T= (p.Trp63=)
2g.38071054A>CCA346327442CYP1B1c.1300T>G (p.Trp434Gly)
n.678T>G
c.187T>G (p.Trp63Gly)
2g.38071054A>GCA346327443CYP1B1c.1300T>C (p.Trp434Arg)
n.678T>C
c.187T>C (p.Trp63Arg)
dbSNP gnomAD v2 gnomAD v4
2g.38071054A>TCA346327444CYP1B1c.1300T>A (p.Trp434Arg)
n.678T>A
c.187T>A (p.Trp63Arg)
2g.38071055C>ACA346327445CYP1B1c.1299G>T (p.Lys433Asn)
n.677G>T
c.186G>T (p.Lys62Asn)
2g.38071055C=CA1245626098CYP1B1c.1299G= (p.Lys433=)
n.677G=
c.186G= (p.Lys62=)
2g.38071055C>GCA346327446CYP1B1c.1299G>C (p.Lys433Asn)
n.677G>C
c.186G>C (p.Lys62Asn)
2g.38071055C>TCA1619822CYP1B1c.1299G>A (p.Lys433=)
n.677G>A
c.186G>A (p.Lys62=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
2g.38071056T>ACA1619823CYP1B1c.1298A>T (p.Lys433Met)
n.676A>T
c.185A>T (p.Lys62Met)
dbSNP ExAC gnomAD v2 gnomAD v4
2g.38071056T>CCA346327447CYP1B1c.1298A>G (p.Lys433Arg)
n.676A>G
c.185A>G (p.Lys62Arg)
2g.38071056T>GCA346327448CYP1B1c.1298A>C (p.Lys433Thr)
n.676A>C
c.185A>C (p.Lys62Thr)
2g.38071056T=CA1245626099CYP1B1c.1298A= (p.Lys433=)
n.676A=
c.185A= (p.Lys62=)
2g.38071057T>ACA346327451CYP1B1c.1297A>T (p.Lys433Ter)
n.675A>T
c.184A>T (p.Lys62Ter)
2g.38071057T>CCA346327449CYP1B1c.1297A>G (p.Lys433Glu)
n.675A>G
c.184A>G (p.Lys62Glu)
2g.38071057T>GCA346327450CYP1B1c.1297A>C (p.Lys433Gln)
n.675A>C
c.184A>C (p.Lys62Gln)
2g.38071058C>ACA425864492CYP1B1c.1296G>T (p.Leu432=)
n.674G>T
c.183G>T (p.Leu61=)
2g.38071058C>GCA425864493CYP1B1c.1296G>C (p.Leu432=)
n.674G>C
c.183G>C (p.Leu61=)
2g.38071058C>TCA425864494CYP1B1c.1296G>A (p.Leu432=)
n.674G>A
c.183G>A (p.Leu61=)
gnomAD v4
2g.38071059A=CA1245626100CYP1B1c.1295T= (p.Leu432=)
n.673T=
c.182T= (p.Leu61=)
2g.38071059A>CCA346327452CYP1B1c.1295T>G (p.Leu432Arg)
n.673T>G
c.182T>G (p.Leu61Arg)
2g.38071059A>GCA346327453CYP1B1c.1295T>C (p.Leu432Pro)
n.673T>C
c.182T>C (p.Leu61Pro)
dbSNP gnomAD v3 gnomAD v4
2g.38071059A>TCA346327454CYP1B1c.1295T>A (p.Leu432Gln)
n.673T>A
c.182T>A (p.Leu61Gln)
dbSNP gnomAD v2 gnomAD v4
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)

Number of alleles fetched