Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
2	g.240878054_240878055delinsTG	CA1339335765	AGXT	c.975_976delinsTG (p.Ala325=) n.753_754delinsTG
2	g.240878055del	CA274440	AGXT	c.976del (p.Val326TyrfsTer15) n.754del	ClinVar dbSNP gnomAD v2 gnomAD v4
2	g.240878055G>A	CA275602	AGXT	c.976G>A (p.Val326Ile) n.754G>A	ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2	g.240878055G>C	CA351319515	AGXT	c.976G>C (p.Val326Leu) n.754G>C
2	g.240878055G=	CA1339335766	AGXT	c.976G= (p.Val326=) n.754G=
2	g.240878055G>T	CA351319516	AGXT	c.976G>T (p.Val326Leu) n.754G>T	gnomAD v4
2	g.240878056del	CA351319520	AGXT	c.977del (p.Val326AspfsTer15) n.755del
2	g.240878056T>A	CA351319517	AGXT	c.977T>A (p.Val326Glu) n.755T>A
2	g.240878056T>C	CA351319518	AGXT	c.977T>C (p.Val326Ala) n.755T>C	dbSNP gnomAD v3 gnomAD v4
2	g.240878056T>G	CA351319519	AGXT	c.977T>G (p.Val326Gly) n.755T>G
2	g.240878056T=	CA1339335767	AGXT	c.977T= (p.Val326=) n.755T=
2	g.240878057A>C	CA432026213	AGXT	c.978A>C (p.Val326=) n.756A>C
2	g.240878057A>G	CA432026215	AGXT	c.978A>G (p.Val326=) n.756A>G
2	g.240878057A>T	CA432026216	AGXT	c.978A>T (p.Val326=) n.756A>T	ClinVar dbSNP
2	g.240878058C>A	CA351319521	AGXT	c.979C>A (p.Pro327Thr) n.757C>A
2	g.240878058C=	CA1339335768	AGXT	c.979C= (p.Pro327=) n.757C=
2	g.240878058C>G	CA351319522	AGXT	c.979C>G (p.Pro327Ala) n.757C>G
2	g.240878058C>T	CA351319523	AGXT	c.979C>T (p.Pro327Ser) n.757C>T	dbSNP
2	g.240878059C>A	CA351319524	AGXT	c.980C>A (p.Pro327His) n.758C>A
2	g.240878059C>G	CA351319525	AGXT	c.980C>G (p.Pro327Arg) n.758C>G
2	g.240878059C>T	CA351319526	AGXT	c.980C>T (p.Pro327Leu) n.758C>T
2	g.240878060C>A	CA432026222	AGXT	c.981C>A (p.Pro327=) n.759C>A	gnomAD v4
2	g.240878060C=	CA1339335769	AGXT	c.981C= (p.Pro327=) n.759C=
2	g.240878060C>G	CA432026224	AGXT	c.981C>G (p.Pro327=) n.759C>G
2	g.240878060C>T	CA2209366	AGXT	c.981C>T (p.Pro327=) n.759C>T	ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2	g.240878061G>A	CA2209367	AGXT	c.982G>A (p.Ala328Thr) n.760G>A	dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2	g.240878061G>C	CA351319528	AGXT	c.982G>C (p.Ala328Pro) n.760G>C	dbSNP
2	g.240878061G=	CA1339335771	AGXT	c.982G= (p.Ala328=) n.760G=
2	g.240878061G>T	CA351319527	AGXT	c.982G>T (p.Ala328Ser) n.760G>T	dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2	g.240878061_240878067delinsGCTGGCT	CA1339335770	AGXT	c.982_988delinsGCTGGCT (p.Ala328=) n.760_766delinsGCTGGCT
2	g.240878062C>A	CA351319529	AGXT	c.983C>A (p.Ala328Asp) n.761C>A
2	g.240878062C>G	CA351319530	AGXT	c.983C>G (p.Ala328Gly) n.761C>G
2	g.240878062C>T	CA351319531	AGXT	c.983C>T (p.Ala328Val) n.761C>T
2	g.240878062dup	CA2580068044	AGXT	c.983dup (p.Gly329TrpfsTer3) n.761dup	ClinVar
2	g.240878062_240878067del	CA275863	AGXT	c.983_988del (p.Ala328_Tyr330delinsAsp) n.761_766del	ClinVar dbSNP
2	g.240878063T>A	CA432026227	AGXT	c.984T>A (p.Ala328=) n.762T>A
2	g.240878063T>C	CA432026229	AGXT	c.984T>C (p.Ala328=) n.762T>C	ClinVar
2	g.240878063T>G	CA432026231	AGXT	c.984T>G (p.Ala328=) n.762T>G	ClinVar dbSNP gnomAD v4
2	g.240878063T=	CA1339335772	AGXT	c.984T= (p.Ala328=) n.762T=
2	g.240878064G>A	CA2209368	AGXT	c.985G>A (p.Gly329Ser) n.763G>A	dbSNP ExAC gnomAD v2 gnomAD v4
2	g.240878064G>C	CA351319532	AGXT	c.985G>C (p.Gly329Arg) n.763G>C
2	g.240878064G=	CA1339335773	AGXT	c.985G= (p.Gly329=) n.763G=
2	g.240878064G>T	CA351319533	AGXT	c.985G>T (p.Gly329Cys) n.763G>T
2	g.240878065G>A	CA351319534	AGXT	c.986G>A (p.Gly329Asp) n.764G>A
2	g.240878065G>C	CA351319535	AGXT	c.986G>C (p.Gly329Ala) n.764G>C
2	g.240878065G>T	CA351319536	AGXT	c.986G>T (p.Gly329Val) n.764G>T
2	g.240878066C>A	CA432026240	AGXT	c.987C>A (p.Gly329=) n.765C>A
2	g.240878066C=	CA1339335774	AGXT	c.987C= (p.Gly329=) n.765C=
2	g.240878066C>G	CA68180834	AGXT	c.987C>G (p.Gly329=) n.765C>G	dbSNP
2	g.240878066C>T	CA2209369	AGXT	c.987C>T (p.Gly329=) n.765C>T	ClinVar dbSNP ExAC gnomAD v2 gnomAD v4

Number of alleles fetched