Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.38071166A>CCA425864608CYP1B1c.1188T>G (p.Pro396=)
n.566T>G
c.75T>G (p.Pro25=)
2g.38071166A>GCA425864609CYP1B1c.1188T>C (p.Pro396=)
n.566T>C
c.75T>C (p.Pro25=)
2g.38071166A>TCA425864610CYP1B1c.1188T>A (p.Pro396=)
n.566T>A
c.75T>A (p.Pro25=)
2g.38071166_38071167delCA2658667731CYP1B1c.1187_1188del (p.Pro396ArgfsTer?)
n.565_566del
c.74_75del (p.Pro25ArgfsTer?)
gnomAD v4
2g.38071167G>ACA346327675CYP1B1c.1187C>T (p.Pro396Leu)
n.565C>T
c.74C>T (p.Pro25Leu)
2g.38071167G>CCA346327674CYP1B1c.1187C>G (p.Pro396Arg)
n.565C>G
c.74C>G (p.Pro25Arg)
2g.38071167G>TCA346327673CYP1B1c.1187C>A (p.Pro396His)
n.565C>A
c.74C>A (p.Pro25His)
gnomAD v4
2g.38071168G>ACA346327676CYP1B1c.1186C>T (p.Pro396Ser)
n.564C>T
c.73C>T (p.Pro25Ser)
gnomAD v4
2g.38071168G>CCA346327677CYP1B1c.1186C>G (p.Pro396Ala)
n.564C>G
c.73C>G (p.Pro25Ala)
2g.38071168G>TCA346327678CYP1B1c.1186C>A (p.Pro396Thr)
n.564C>A
c.73C>A (p.Pro25Thr)
gnomAD v4
2g.38071169C>ACA425864613CYP1B1c.1185G>T (p.Val395=)
n.563G>T
c.72G>T (p.Val24=)
ClinVar dbSNP
2g.38071169C=CA1245626158CYP1B1c.1185G= (p.Val395=)
n.563G=
c.72G= (p.Val24=)
2g.38071169C>GCA425864615CYP1B1c.1185G>C (p.Val395=)
n.563G>C
c.72G>C (p.Val24=)
2g.38071169C>TCA425864616CYP1B1c.1185G>A (p.Val395=)
n.563G>A
c.72G>A (p.Val24=)
2g.38071170A=CA1245626159CYP1B1c.1184T= (p.Val395=)
n.562T=
c.71T= (p.Val24=)
2g.38071170A>CCA346327679CYP1B1c.1184T>G (p.Val395Gly)
n.562T>G
c.71T>G (p.Val24Gly)
2g.38071170A>GCA1619841CYP1B1c.1184T>C (p.Val395Ala)
n.562T>C
c.71T>C (p.Val24Ala)
dbSNP ExAC gnomAD v2 gnomAD v4
2g.38071170A>TCA346327680CYP1B1c.1184T>A (p.Val395Glu)
n.562T>A
c.71T>A (p.Val24Glu)
2g.38071171C>ACA346327681CYP1B1c.1183G>T (p.Val395Leu)
n.561G>T
c.70G>T (p.Val24Leu)
gnomAD v4
2g.38071171C=CA1245626160CYP1B1c.1183G= (p.Val395=)
n.561G=
c.70G= (p.Val24=)
2g.38071171C>GCA1619842CYP1B1c.1183G>C (p.Val395Leu)
n.561G>C
c.70G>C (p.Val24Leu)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.38071171C>TCA346327682CYP1B1c.1183G>A (p.Val395Met)
n.561G>A
c.70G>A (p.Val24Met)
2g.38071172A=CA1245626161CYP1B1c.1182T= (p.Phe394=)
n.560T=
c.69T= (p.Phe23=)
2g.38071172A>CCA346327683CYP1B1c.1182T>G (p.Phe394Leu)
n.560T>G
c.69T>G (p.Phe23Leu)
2g.38071172A>GCA1619843CYP1B1c.1182T>C (p.Phe394=)
n.560T>C
c.69T>C (p.Phe23=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
2g.38071172A>TCA346327684CYP1B1c.1182T>A (p.Phe394Leu)
n.560T>A
c.69T>A (p.Phe23Leu)
2g.38071173A>CCA346327687CYP1B1c.1181T>G (p.Phe394Cys)
n.559T>G
c.68T>G (p.Phe23Cys)
2g.38071173A>GCA346327686CYP1B1c.1181T>C (p.Phe394Ser)
n.559T>C
c.68T>C (p.Phe23Ser)
2g.38071173A>TCA346327685CYP1B1c.1181T>A (p.Phe394Tyr)
n.559T>A
c.68T>A (p.Phe23Tyr)
2g.38071174A>CCA346327688CYP1B1c.1180T>G (p.Phe394Val)
n.558T>G
c.67T>G (p.Phe23Val)
2g.38071174A>GCA346327689CYP1B1c.1180T>C (p.Phe394Leu)
n.558T>C
c.67T>C (p.Phe23Leu)
2g.38071174A>TCA346327690CYP1B1c.1180T>A (p.Phe394Ile)
n.558T>A
c.67T>A (p.Phe23Ile)
2g.38071175G>ACA425690743CYP1B1c.1179C>T (p.Ser393=)
n.557C>T
c.66C>T (p.Ser22=)
2g.38071175G>CCA346327691CYP1B1c.1179C>G (p.Ser393Arg)
n.557C>G
c.66C>G (p.Ser22Arg)
gnomAD v4
2g.38071175G>TCA346327692CYP1B1c.1179C>A (p.Ser393Arg)
n.557C>A
c.66C>A (p.Ser22Arg)
2g.38071176C>ACA346327693CYP1B1c.1178G>T (p.Ser393Ile)
n.556G>T
c.65G>T (p.Ser22Ile)
n.573G>T
2g.38071176C>GCA346327694CYP1B1c.1178G>C (p.Ser393Thr)
n.556G>C
c.65G>C (p.Ser22Thr)
n.573G>C
2g.38071176C>TCA346327695CYP1B1c.1178G>A (p.Ser393Asn)
n.556G>A
c.65G>A (p.Ser22Asn)
n.573G>A
2g.38071177T>ACA346327696CYP1B1c.1177A>T (p.Ser393Cys)
n.555A>T
c.64A>T (p.Ser22Cys)
n.572A>T
2g.38071177T>CCA346327698CYP1B1c.1177A>G (p.Ser393Gly)
n.555A>G
c.64A>G (p.Ser22Gly)
n.572A>G
2g.38071177T>GCA346327697CYP1B1c.1177A>C (p.Ser393Arg)
n.555A>C
c.64A>C (p.Ser22Arg)
n.572A>C
2g.38071178G>ACA1619844CYP1B1c.1176C>T (p.Ser392=)
n.554C>T
c.63C>T (p.Ser21=)
n.571C>T
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.38071178G>CCA425690744CYP1B1c.1176C>G (p.Ser392=)
n.554C>G
c.63C>G (p.Ser21=)
n.571C>G
2g.38071178G=CA1245626162CYP1B1c.1176C= (p.Ser392=)
n.554C=
c.63C= (p.Ser21=)
n.571C=
2g.38071178G>TCA425690745CYP1B1c.1176C>A (p.Ser392=)
n.554C>A
c.63C>A (p.Ser21=)
n.571C>A
2g.38071179G>ACA346327699CYP1B1c.1175C>T (p.Ser392Phe)
n.553C>T
c.62C>T (p.Ser21Phe)
n.570C>T
gnomAD v4
2g.38071179G>CCA346327700CYP1B1c.1175C>G (p.Ser392Cys)
n.553C>G
c.62C>G (p.Ser21Cys)
n.570C>G
2g.38071179G>TCA346327701CYP1B1c.1175C>A (p.Ser392Tyr)
n.553C>A
c.62C>A (p.Ser21Tyr)
n.570C>A
2g.38071180A>CCA346327702CYP1B1c.1174T>G (p.Ser392Ala)
n.552T>G
c.61T>G (p.Ser21Ala)
n.569T>G
2g.38071180A>GCA346327704CYP1B1c.1174T>C (p.Ser392Pro)
n.552T>C
c.61T>C (p.Ser21Pro)
n.569T>C

Number of alleles fetched