Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.38070863T>ACA425864421CYP1B1c.1491A>T (p.Pro497=)
c.378A>T (p.Pro126=)
2g.38070863T>CCA425864422CYP1B1c.1491A>G (p.Pro497=)
c.378A>G (p.Pro126=)
 gnomAD v4
2g.38070863T>GCA425864423CYP1B1c.1491A>C (p.Pro497=)
c.378A>C (p.Pro126=)
2g.38070864G>ACA346327043CYP1B1c.1490C>T (p.Pro497Leu)
c.377C>T (p.Pro126Leu)
2g.38070864G>CCA346327044CYP1B1c.1490C>G (p.Pro497Arg)
c.377C>G (p.Pro126Arg)
2g.38070864G>TCA346327045CYP1B1c.1490C>A (p.Pro497Gln)
c.377C>A (p.Pro126Gln)
2g.38070865G>ACA346327046CYP1B1c.1489C>T (p.Pro497Ser)
c.376C>T (p.Pro126Ser)
 dbSNP gnomAD v3 gnomAD v4
2g.38070865G>CCA346327047CYP1B1c.1489C>G (p.Pro497Ala)
c.376C>G (p.Pro126Ala)
 COSMIC
2g.38070865G=CA1245625989CYP1B1c.1489C= (p.Pro497=)
c.376C= (p.Pro126=)
2g.38070865G>TCA346327048CYP1B1c.1489C>A (p.Pro497Thr)
c.376C>A (p.Pro126Thr)
2g.38070866G>ACA425864424CYP1B1c.1488C>T (p.Asn496=)
c.375C>T (p.Asn125=)
 gnomAD v4
2g.38070866G>CCA346327049CYP1B1c.1488C>G (p.Asn496Lys)
c.375C>G (p.Asn125Lys)
2g.38070866G>TCA346327050CYP1B1c.1488C>A (p.Asn496Lys)
c.375C>A (p.Asn125Lys)
2g.38070867T>ACA346327053CYP1B1c.1487A>T (p.Asn496Ile)
c.374A>T (p.Asn125Ile)
2g.38070867T>CCA346327051CYP1B1c.1487A>G (p.Asn496Ser)
c.374A>G (p.Asn125Ser)
2g.38070867T>GCA346327052CYP1B1c.1487A>C (p.Asn496Thr)
c.374A>C (p.Asn125Thr)
2g.38070868T>ACA346327054CYP1B1c.1486A>T (p.Asn496Tyr)
c.373A>T (p.Asn125Tyr)
2g.38070868T>CCA1619770CYP1B1c.1486A>G (p.Asn496Asp)
c.373A>G (p.Asn125Asp)
 dbSNP ExAC gnomAD v2
2g.38070868T>GCA346327055CYP1B1c.1486A>C (p.Asn496His)
c.373A>C (p.Asn125His)
2g.38070868T=CA1245625990CYP1B1c.1486A= (p.Asn496=)
c.373A= (p.Asn125=)
2g.38070869G>ACA425864426CYP1B1c.1485C>T (p.Ala495=)
c.372C>T (p.Ala124=)
2g.38070869G>CCA425864428CYP1B1c.1485C>G (p.Ala495=)
c.372C>G (p.Ala124=)
2g.38070869G>TCA425864427CYP1B1c.1485C>A (p.Ala495=)
c.372C>A (p.Ala124=)
2g.38070870G>ACA346327056CYP1B1c.1484C>T (p.Ala495Val)
c.371C>T (p.Ala124Val)
 dbSNP
2g.38070870G>CCA346327057CYP1B1c.1484C>G (p.Ala495Gly)
c.371C>G (p.Ala124Gly)
 dbSNP gnomAD v3 gnomAD v4
2g.38070870G=CA1245625991CYP1B1c.1484C= (p.Ala495=)
c.371C= (p.Ala124=)
2g.38070870G>TCA346327058CYP1B1c.1484C>A (p.Ala495Asp)
c.371C>A (p.Ala124Asp)
2g.38070871C>ACA346327059CYP1B1c.1483G>T (p.Ala495Ser)
c.370G>T (p.Ala124Ser)
2g.38070871C=CA1245625992CYP1B1c.1483G= (p.Ala495=)
c.370G= (p.Ala124=)
2g.38070871C>GCA346327060CYP1B1c.1483G>C (p.Ala495Pro)
c.370G>C (p.Ala124Pro)
2g.38070871C>TCA1619771CYP1B1c.1483G>A (p.Ala495Thr)
c.370G>A (p.Ala124Thr)
 dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
2g.38070872C>ACA346327061CYP1B1c.1482G>T (p.Arg494Ser)
c.369G>T (p.Arg123Ser)
2g.38070872C>GCA346327062CYP1B1c.1482G>C (p.Arg494Ser)
c.369G>C (p.Arg123Ser)
2g.38070872C>TCA425864433CYP1B1c.1482G>A (p.Arg494=)
c.369G>A (p.Arg123=)
 gnomAD v4
2g.38070873C>ACA346327064CYP1B1c.1481G>T (p.Arg494Met)
c.368G>T (p.Arg123Met)
2g.38070873C>GCA346327065CYP1B1c.1481G>C (p.Arg494Thr)
c.368G>C (p.Arg123Thr)
 gnomAD v4
2g.38070873C>TCA346327063CYP1B1c.1481G>A (p.Arg494Lys)
c.368G>A (p.Arg123Lys)
 COSMIC
2g.38070874T>ACA346327066CYP1B1c.1480A>T (p.Arg494Trp)
c.367A>T (p.Arg123Trp)
2g.38070874T>CCA346327067CYP1B1c.1480A>G (p.Arg494Gly)
c.367A>G (p.Arg123Gly)
 gnomAD v4
2g.38070874T>GCA425864434CYP1B1c.1480A>C (p.Arg494=)
c.367A>C (p.Arg123=)
 gnomAD v4
2g.38070875G>ACA425864436CYP1B1c.1479C>T (p.Phe493=)
c.366C>T (p.Phe122=)
2g.38070875G>CCA346327068CYP1B1c.1479C>G (p.Phe493Leu)
c.366C>G (p.Phe122Leu)
2g.38070875G>TCA346327069CYP1B1c.1479C>A (p.Phe493Leu)
c.366C>A (p.Phe122Leu)
2g.38070876A>CCA346327070CYP1B1c.1478T>G (p.Phe493Cys)
c.365T>G (p.Phe122Cys)
2g.38070876A>GCA346327071CYP1B1c.1478T>C (p.Phe493Ser)
c.365T>C (p.Phe122Ser)
 gnomAD v3 gnomAD v4
2g.38070876A>TCA346327072CYP1B1c.1478T>A (p.Phe493Tyr)
c.365T>A (p.Phe122Tyr)
2g.38070877A>CCA346327073CYP1B1c.1477T>G (p.Phe493Val)
c.364T>G (p.Phe122Val)
2g.38070877A>GCA346327074CYP1B1c.1477T>C (p.Phe493Leu)
c.364T>C (p.Phe122Leu)
2g.38070877A>TCA346327075CYP1B1c.1477T>A (p.Phe493Ile)
c.364T>A (p.Phe122Ile)
2g.38070878A=CA1245625993CYP1B1c.1476T= (p.Asp492=)
c.363T= (p.Asp121=)

Number of alleles fetched