Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
2	g.240878783_240878794del	CA2664012447	AGXT	c.1141_1152del (p.Arg381_Leu384del) n.919_930del	gnomAD v4
2	g.240878782_240878783delinsGA	CA1339336161	AGXT	c.1140_1141delinsGA (p.Leu380=) n.918_919delinsGA
2	g.240878783del	CA540538906	AGXT	c.1141del (p.Arg381GlyfsTer?) n.919del	dbSNP gnomAD v2
2	g.240878783A>C	CA432027162	AGXT	c.1141A>C (p.Arg381=) n.919A>C
2	g.240878783A>G	CA351319849	AGXT	c.1141A>G (p.Arg381Gly) n.919A>G	gnomAD v4
2	g.240878783A>T	CA351319848	AGXT	c.1141A>T (p.Arg381Trp) n.919A>T
2	g.240878784G>A	CA275605	AGXT	c.1142G>A (p.Arg381Lys) n.920G>A	ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2	g.240878784G>C	CA351319850	AGXT	c.1142G>C (p.Arg381Thr) n.920G>C
2	g.240878784G=	CA1339336162	AGXT	c.1142G= (p.Arg381=) n.920G=
2	g.240878784G>T	CA351319851	AGXT	c.1142G>T (p.Arg381Met) n.920G>T	gnomAD v4
2	g.240878785G>A	CA2209431	AGXT	c.1143G>A (p.Arg381=) n.921G>A	ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
2	g.240878785G>C	CA351319852	AGXT	c.1143G>C (p.Arg381Ser) n.921G>C
2	g.240878785G=	CA1339336163	AGXT	c.1143G= (p.Arg381=) n.921G=
2	g.240878785G>T	CA351319853	AGXT	c.1143G>T (p.Arg381Ser) n.921G>T	gnomAD v4
2	g.240878786G>A	CA2209432	AGXT	c.1144G>A (p.Ala382Thr) n.922G>A	dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2	g.240878786G>C	CA351319854	AGXT	c.1144G>C (p.Ala382Pro) n.922G>C
2	g.240878786G=	CA1339336164	AGXT	c.1144G= (p.Ala382=) n.922G=
2	g.240878786G>T	CA351319855	AGXT	c.1144G>T (p.Ala382Ser) n.922G>T	gnomAD v4
2	g.240878787C>A	CA2209433	AGXT	c.1145C>A (p.Ala382Glu) n.923C>A	dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2	g.240878787C=	CA1339336165	AGXT	c.1145C= (p.Ala382=) n.923C=
2	g.240878787C>G	CA351319856	AGXT	c.1145C>G (p.Ala382Gly) n.923C>G
2	g.240878787C>T	CA2209434	AGXT	c.1145C>T (p.Ala382Val) n.923C>T	ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2	g.240878788G>A	CA432027176	AGXT	c.1146G>A (p.Ala382=) n.924G>A	ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2	g.240878788G>C	CA432027179	AGXT	c.1146G>C (p.Ala382=) n.924G>C
2	g.240878788G=	CA1339336166	AGXT	c.1146G= (p.Ala382=) n.924G=
2	g.240878788G>T	CA432027181	AGXT	c.1146G>T (p.Ala382=) n.924G>T	gnomAD v4
2	g.240878789G>A	CA351319857	AGXT	c.1147G>A (p.Ala383Thr) n.925G>A	gnomAD v4
2	g.240878789G>C	CA351319859	AGXT	c.1147G>C (p.Ala383Pro) n.925G>C
2	g.240878789G>T	CA351319858	AGXT	c.1147G>T (p.Ala383Ser) n.925G>T	gnomAD v4
2	g.240878790C>A	CA275787	AGXT	c.1148C>A (p.Ala383Asp) n.926C>A	ClinVar dbSNP gnomAD v4
2	g.240878790C=	CA1339336167	AGXT	c.1148C= (p.Ala383=) n.926C=
2	g.240878790C>G	CA351319861	AGXT	c.1148C>G (p.Ala383Gly) n.926C>G
2	g.240878790C>T	CA351319860	AGXT	c.1148C>T (p.Ala383Val) n.926C>T	gnomAD v4 COSMIC
2	g.240878791C>A	CA432027188	AGXT	c.1149C>A (p.Ala383=) n.927C>A
2	g.240878791C>G	CA432027191	AGXT	c.1149C>G (p.Ala383=) n.927C>G
2	g.240878791C>T	CA432027193	AGXT	c.1149C>T (p.Ala383=) n.927C>T	gnomAD v4
2	g.240878792C>A	CA351319862	AGXT	c.1150C>A (p.Leu384Met) n.928C>A	gnomAD v4
2	g.240878792C>G	CA351319863	AGXT	c.1150C>G (p.Leu384Val) n.928C>G
2	g.240878792C>T	CA432027197	AGXT	c.1150C>T (p.Leu384=) n.928C>T	gnomAD v4
2	g.240878793T>A	CA351319864	AGXT	c.1151T>A (p.Leu384Gln) n.929T>A	gnomAD v4
2	g.240878793T>C	CA275789	AGXT	c.1151T>C (p.Leu384Pro) n.929T>C	ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2	g.240878793T>G	CA351319865	AGXT	c.1151T>G (p.Leu384Arg) n.929T>G
2	g.240878793T=	CA1339336168	AGXT	c.1151T= (p.Leu384=) n.929T=
2	g.240878794G>A	CA432027202	AGXT	c.1152G>A (p.Leu384=) n.930G>A	ClinVar dbSNP gnomAD v2 gnomAD v4
2	g.240878794G>C	CA432027204	AGXT	c.1152G>C (p.Leu384=) n.930G>C
2	g.240878794G=	CA1339336169	AGXT	c.1152G= (p.Leu384=) n.930G=
2	g.240878794G>T	CA432027206	AGXT	c.1152G>T (p.Leu384=) n.930G>T	gnomAD v4
2	g.240878795C>A	CA68181110	AGXT	c.1153C>A (p.Gln385Lys) n.931C>A	ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2	g.240878795C=	CA1339336170	AGXT	c.1153C= (p.Gln385=) n.931C=
2	g.240878795C>G	CA351319866	AGXT	c.1153C>G (p.Gln385Glu) n.931C>G

Number of alleles fetched