Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.38071188A=CA1245626168CYP1B1c.1166T= (p.Met389=)
n.544T=
c.53T= (p.Met18=)
n.561T=
2g.38071188A>CCA346327718CYP1B1c.1166T>G (p.Met389Arg)
n.544T>G
c.53T>G (p.Met18Arg)
n.561T>G
2g.38071188A>GCA346327719CYP1B1c.1166T>C (p.Met389Thr)
n.544T>C
c.53T>C (p.Met18Thr)
n.561T>C
2g.38071188A>TCA346327720CYP1B1c.1166T>A (p.Met389Lys)
n.544T>A
c.53T>A (p.Met18Lys)
n.561T>A
dbSNP gnomAD v3 gnomAD v4
2g.38071189T>ACA346327721CYP1B1c.1165A>T (p.Met389Leu)
n.543A>T
c.52A>T (p.Met18Leu)
n.560A>T
2g.38071189T>CCA346327722CYP1B1c.1165A>G (p.Met389Val)
n.543A>G
c.52A>G (p.Met18Val)
n.560A>G
gnomAD v4
2g.38071189T>GCA346327723CYP1B1c.1165A>C (p.Met389Leu)
n.543A>C
c.52A>C (p.Met18Leu)
n.560A>C
2g.38071190G>ACA425690749CYP1B1c.1164C>T (p.Ala388=)
n.542C>T
c.51C>T (p.Ala17=)
n.559C>T
2g.38071190G>CCA425690750CYP1B1c.1164C>G (p.Ala388=)
n.542C>G
c.51C>G (p.Ala17=)
n.559C>G
2g.38071190G>TCA425690751CYP1B1c.1164C>A (p.Ala388=)
n.542C>A
c.51C>A (p.Ala17=)
n.559C>A
2g.38071191G>ACA346327724CYP1B1c.1163C>T (p.Ala388Val)
n.541C>T
c.50C>T (p.Ala17Val)
n.558C>T
2g.38071191G>CCA346327725CYP1B1c.1163C>G (p.Ala388Gly)
n.541C>G
c.50C>G (p.Ala17Gly)
n.558C>G
2g.38071191G>TCA346327726CYP1B1c.1163C>A (p.Ala388Asp)
n.541C>A
c.50C>A (p.Ala17Asp)
n.558C>A
2g.38071192C>ACA346327729CYP1B1c.1162G>T (p.Ala388Ser)
n.540G>T
c.49G>T (p.Ala17Ser)
n.557G>T
2g.38071192C>GCA346327728CYP1B1c.1162G>C (p.Ala388Pro)
n.540G>C
c.49G>C (p.Ala17Pro)
n.557G>C
2g.38071192C>TCA346327727CYP1B1c.1162G>A (p.Ala388Thr)
n.540G>A
c.49G>A (p.Ala17Thr)
n.557G>A
2g.38071193T>ACA346327730CYP1B1c.1161A>T (p.Glu387Asp)
n.539A>T
c.48A>T (p.Glu16Asp)
n.556A>T
2g.38071193T>CCA425690752CYP1B1c.1161A>G (p.Glu387=)
n.539A>G
c.48A>G (p.Glu16=)
n.556A>G
2g.38071193T>GCA346327731CYP1B1c.1161A>C (p.Glu387Asp)
n.539A>C
c.48A>C (p.Glu16Asp)
n.556A>C
2g.38071194T>ACA346327732CYP1B1c.1160A>T (p.Glu387Val)
n.538A>T
c.47A>T (p.Glu16Val)
n.555A>T
2g.38071194T>CCA346327733CYP1B1c.1160A>G (p.Glu387Gly)
n.538A>G
c.47A>G (p.Glu16Gly)
n.555A>G
gnomAD v4
2g.38071194T>GCA346327734CYP1B1c.1160A>C (p.Glu387Ala)
n.538A>C
c.47A>C (p.Glu16Ala)
n.555A>C
2g.38071195C>ACA346327735CYP1B1c.1159G>T (p.Glu387Ter)
n.537G>T
c.46G>T (p.Glu16Ter)
n.554G>T
2g.38071195C=CA1245626169CYP1B1c.1159G= (p.Glu387=)
n.537G=
c.46G= (p.Glu16=)
n.554G=
2g.38071195C>GCA45506580CYP1B1c.1159G>C (p.Glu387Gln)
n.537G>C
c.46G>C (p.Glu16Gln)
n.554G>C
dbSNP
2g.38071195C>TCA254241CYP1B1c.1159G>A (p.Glu387Lys)
n.537G>A
c.46G>A (p.Glu16Lys)
n.554G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.38071196A>CCA346327736CYP1B1c.1158T>G (p.Tyr386Ter)
n.536T>G
c.45T>G (p.Tyr15Ter)
n.553T>G
2g.38071196A>GCA425690753CYP1B1c.1158T>C (p.Tyr386=)
n.536T>C
c.45T>C (p.Tyr15=)
n.553T>C
2g.38071196A>TCA346327737CYP1B1c.1158T>A (p.Tyr386Ter)
n.536T>A
c.45T>A (p.Tyr15Ter)
n.553T>A
2g.38071197T>ACA346327738CYP1B1c.1157A>T (p.Tyr386Phe)
n.535A>T
c.44A>T (p.Tyr15Phe)
n.552A>T
2g.38071197T>CCA346327739CYP1B1c.1157A>G (p.Tyr386Cys)
n.535A>G
c.44A>G (p.Tyr15Cys)
n.552A>G
gnomAD v4
2g.38071197T>GCA346327740CYP1B1c.1157A>C (p.Tyr386Ser)
n.535A>C
c.44A>C (p.Tyr15Ser)
n.552A>C
2g.38071198A>CCA346327742CYP1B1c.1156T>G (p.Tyr386Asp)
n.534T>G
c.43T>G (p.Tyr15Asp)
n.551T>G
2g.38071198A>GCA346327743CYP1B1c.1156T>C (p.Tyr386His)
n.534T>C
c.43T>C (p.Tyr15His)
n.551T>C
2g.38071198A>TCA346327741CYP1B1c.1156T>A (p.Tyr386Asn)
n.534T>A
c.43T>A (p.Tyr15Asn)
n.551T>A
2g.38071199A>CCA425690756CYP1B1c.1155T>G (p.Leu385=)
n.533T>G
c.42T>G (p.Leu14=)
n.550T>G
2g.38071199A>GCA425690754CYP1B1c.1155T>C (p.Leu385=)
n.533T>C
c.42T>C (p.Leu14=)
n.550T>C
gnomAD v4
2g.38071199A>TCA425690755CYP1B1c.1155T>A (p.Leu385=)
n.533T>A
c.42T>A (p.Leu14=)
n.550T>A
2g.38071200A>CCA346327746CYP1B1c.1154T>G (p.Leu385Arg)
n.532T>G
c.41T>G (p.Leu14Arg)
n.549T>G
2g.38071200A>GCA346327744CYP1B1c.1154T>C (p.Leu385Pro)
n.532T>C
c.41T>C (p.Leu14Pro)
n.549T>C
2g.38071200A>TCA346327745CYP1B1c.1154T>A (p.Leu385His)
n.532T>A
c.41T>A (p.Leu14His)
n.549T>A
2g.38071201G>ACA45506612CYP1B1c.1153C>T (p.Leu385Phe)
n.531C>T
c.40C>T (p.Leu14Phe)
n.548C>T
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.38071201G>CCA346327747CYP1B1c.1153C>G (p.Leu385Val)
n.531C>G
c.40C>G (p.Leu14Val)
n.548C>G
2g.38071201G=CA1245626170CYP1B1c.1153C= (p.Leu385=)
n.531C=
c.40C= (p.Leu14=)
n.548C=
2g.38071201G>TCA346327748CYP1B1c.1153C>A (p.Leu385Ile)
n.531C>A
c.40C>A (p.Leu14Ile)
n.548C>A
2g.38071202G>ACA425690757CYP1B1c.1152C>T (p.Phe384=)
n.530C>T
c.39C>T (p.Phe13=)
n.547C>T
2g.38071202G>CCA346327749CYP1B1c.1152C>G (p.Phe384Leu)
n.530C>G
c.39C>G (p.Phe13Leu)
n.547C>G
2g.38071202G>TCA346327750CYP1B1c.1152C>A (p.Phe384Leu)
n.530C>A
c.39C>A (p.Phe13Leu)
n.547C>A
2g.38071203A>CCA346327751CYP1B1c.1151T>G (p.Phe384Cys)
n.529T>G
c.38T>G (p.Phe13Cys)
n.546T>G
2g.38071203A>GCA346327752CYP1B1c.1151T>C (p.Phe384Ser)
n.529T>C
c.38T>C (p.Phe13Ser)
n.546T>C

Number of alleles fetched