Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
2	g.38070995G>A	CA425864356	CYP1B1	c.1359C>T (p.Asn453=) n.737C>T c.246C>T (p.Asn82=)	dbSNP gnomAD v3 gnomAD v4
2	g.38070995G>C	CA346327327	CYP1B1	c.1359C>G (p.Asn453Lys) n.737C>G c.246C>G (p.Asn82Lys)	dbSNP gnomAD v4 COSMIC
2	g.38070995G=	CA1245626060	CYP1B1	c.1359C= (p.Asn453=) n.737C= c.246C= (p.Asn82=)
2	g.38070995G>T	CA346327328	CYP1B1	c.1359C>A (p.Asn453Lys) n.737C>A c.246C>A (p.Asn82Lys)
2	g.38070996T>A	CA346327329	CYP1B1	c.1358A>T (p.Asn453Ile) n.736A>T c.245A>T (p.Asn82Ile)
2	g.38070996T>C	CA179945	CYP1B1	c.1358A>G (p.Asn453Ser) n.736A>G c.245A>G (p.Asn82Ser)	ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2	g.38070996T>G	CA1619802	CYP1B1	c.1358A>C (p.Asn453Thr) n.736A>C c.245A>C (p.Asn82Thr)	dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2	g.38070996T=	CA1245626061	CYP1B1	c.1358A= (p.Asn453=) n.736A= c.245A= (p.Asn82=)
2	g.38070997T>A	CA346327330	CYP1B1	c.1357A>T (p.Asn453Tyr) n.735A>T c.244A>T (p.Asn82Tyr)
2	g.38070997T>C	CA346327331	CYP1B1	c.1357A>G (p.Asn453Asp) n.735A>G c.244A>G (p.Asn82Asp)	dbSNP gnomAD v4
2	g.38070997T>G	CA346327332	CYP1B1	c.1357A>C (p.Asn453His) n.735A>C c.244A>C (p.Asn82His)	gnomAD v4
2	g.38070997T=	CA1245626062	CYP1B1	c.1357A= (p.Asn453=) n.735A= c.244A= (p.Asn82=)
2	g.38070998G>A	CA425864358	CYP1B1	c.1356C>T (p.Ile452=) n.734C>T c.243C>T (p.Ile81=)
2	g.38070998G>C	CA346327333	CYP1B1	c.1356C>G (p.Ile452Met) n.734C>G c.243C>G (p.Ile81Met)	gnomAD v4
2	g.38070998G=	CA1245626063	CYP1B1	c.1356C= (p.Ile452=) n.734C= c.243C= (p.Ile81=)
2	g.38070998G>T	CA425864360	CYP1B1	c.1356C>A (p.Ile452=) n.734C>A c.243C>A (p.Ile81=)	dbSNP
2	g.38070999A>C	CA346327334	CYP1B1	c.1355T>G (p.Ile452Ser) n.733T>G c.242T>G (p.Ile81Ser)
2	g.38070999A>G	CA346327335	CYP1B1	c.1355T>C (p.Ile452Thr) n.733T>C c.242T>C (p.Ile81Thr)
2	g.38070999A>T	CA346327336	CYP1B1	c.1355T>A (p.Ile452Asn) n.733T>A c.242T>A (p.Ile81Asn)
2	g.38071000T>A	CA346327337	CYP1B1	c.1354A>T (p.Ile452Phe) n.732A>T c.241A>T (p.Ile81Phe)
2	g.38071000T>C	CA346327338	CYP1B1	c.1354A>G (p.Ile452Val) n.732A>G c.241A>G (p.Ile81Val)
2	g.38071000T>G	CA346327339	CYP1B1	c.1354A>C (p.Ile452Leu) n.732A>C c.241A>C (p.Ile81Leu)
2	g.38071001G>A	CA425864363	CYP1B1	c.1353C>T (p.Leu451=) n.731C>T c.240C>T (p.Leu80=)	ClinVar gnomAD v4
2	g.38071001G>C	CA425864362	CYP1B1	c.1353C>G (p.Leu451=) n.731C>G c.240C>G (p.Leu80=)
2	g.38071001G>T	CA425864361	CYP1B1	c.1353C>A (p.Leu451=) n.731C>A c.240C>A (p.Leu80=)
2	g.38071002A>C	CA346327342	CYP1B1	c.1352T>G (p.Leu451Arg) n.730T>G c.239T>G (p.Leu80Arg)
2	g.38071002A>G	CA346327340	CYP1B1	c.1352T>C (p.Leu451Pro) n.730T>C c.239T>C (p.Leu80Pro)
2	g.38071002A>T	CA346327341	CYP1B1	c.1352T>A (p.Leu451His) n.730T>A c.239T>A (p.Leu80His)
2	g.38071003G>A	CA346327343	CYP1B1	c.1351C>T (p.Leu451Phe) n.729C>T c.238C>T (p.Leu80Phe)	dbSNP
2	g.38071003G>C	CA346327344	CYP1B1	c.1351C>G (p.Leu451Val) n.729C>G c.238C>G (p.Leu80Val)
2	g.38071003G>T	CA346327345	CYP1B1	c.1351C>A (p.Leu451Ile) n.729C>A c.238C>A (p.Leu80Ile)
2	g.38071004G>A	CA425864367	CYP1B1	c.1350C>T (p.Gly450=) n.728C>T c.237C>T (p.Gly79=)
2	g.38071004G>C	CA425864368	CYP1B1	c.1350C>G (p.Gly450=) n.728C>G c.237C>G (p.Gly79=)
2	g.38071004G>T	CA425864369	CYP1B1	c.1350C>A (p.Gly450=) n.728C>A c.237C>A (p.Gly79=)
2	g.38071005C>A	CA346327346	CYP1B1	c.1349G>T (p.Gly450Val) n.727G>T c.236G>T (p.Gly79Val)
2	g.38071005C>G	CA346327347	CYP1B1	c.1349G>C (p.Gly450Ala) n.727G>C c.236G>C (p.Gly79Ala)
2	g.38071005C>T	CA346327348	CYP1B1	c.1349G>A (p.Gly450Asp) n.727G>A c.236G>A (p.Gly79Asp)	gnomAD v4
2	g.38071006C>A	CA346327350	CYP1B1	c.1348G>T (p.Gly450Cys) n.726G>T c.235G>T (p.Gly79Cys)
2	g.38071006C=	CA1245626064	CYP1B1	c.1348G= (p.Gly450=) n.726G= c.235G= (p.Gly79=)
2	g.38071006C>G	CA346327349	CYP1B1	c.1348G>C (p.Gly450Arg) n.726G>C c.235G>C (p.Gly79Arg)
2	g.38071006C>T	CA1619803	CYP1B1	c.1348G>A (p.Gly450Ser) n.726G>A c.235G>A (p.Gly79Ser)	dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2	g.38071007A=	CA1245626065	CYP1B1	c.1347T= (p.Asp449=) n.725T= c.234T= (p.Asp78=)
2	g.38071007A>C	CA346327351	CYP1B1	c.1347T>G (p.Asp449Glu) n.725T>G c.234T>G (p.Asp78Glu)
2	g.38071007A>G	CA179947	CYP1B1	c.1347T>C (p.Asp449=) n.725T>C c.234T>C (p.Asp78=)	ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2	g.38071007A>T	CA45506106	CYP1B1	c.1347T>A (p.Asp449Glu) n.725T>A c.234T>A (p.Asp78Glu)	dbSNP
2	g.38071007_38071009delinsGT	CA2586969061	CYP1B1	c.1345_1347delinsAC (p.Asp449ThrfsTer8) n.723_725delinsAC c.232_234delinsAC (p.Asp78ThrfsTer8)
2	g.38071008T>A	CA346327352	CYP1B1	c.1346A>T (p.Asp449Val) n.724A>T c.233A>T (p.Asp78Val)
2	g.38071008T>C	CA346327353	CYP1B1	c.1346A>G (p.Asp449Gly) n.724A>G c.233A>G (p.Asp78Gly)
2	g.38071008T>G	CA346327354	CYP1B1	c.1346A>C (p.Asp449Ala) n.724A>C c.233A>C (p.Asp78Ala)
2	g.38071008_38071009delinsTC	CA1245626066	CYP1B1	c.1345_1346delinsGA (p.Asp449=) n.723_724delinsGA c.232_233delinsGA (p.Asp78=)

Number of alleles fetched