Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
2	g.240878092A=	CA1339335787	AGXT	c.1013A= (p.Tyr338=) n.791A=
2	g.240878092A>C	CA351319593	AGXT	c.1013A>C (p.Tyr338Ser) n.791A>C
2	g.240878092A>G	CA351319594	AGXT	c.1013A>G (p.Tyr338Cys) n.791A>G
2	g.240878092A>T	CA2209374	AGXT	c.1013A>T (p.Tyr338Phe) n.791A>T	dbSNP ExAC gnomAD v2 gnomAD v4
2	g.240878093C>A	CA351319595	AGXT	c.1014C>A (p.Tyr338Ter) n.792C>A	ClinVar
2	g.240878093C=	CA1339335788	AGXT	c.1014C= (p.Tyr338=) n.792C=
2	g.240878093C>G	CA275776	AGXT	c.1014C>G (p.Tyr338Ter) n.792C>G	ClinVar dbSNP
2	g.240878093C>T	CA2209375	AGXT	c.1014C>T (p.Tyr338=) n.792C>T	ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2	g.240878094del	CA2586971646	AGXT	c.1015del (p.Val339SerfsTer2) n.793del
2	g.240878094G>A	CA2209376	AGXT	c.1015G>A (p.Val339Ile) n.793G>A	dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2	g.240878094G>C	CA351319596	AGXT	c.1015G>C (p.Val339Leu) n.793G>C
2	g.240878094G=	CA1339335789	AGXT	c.1015G= (p.Val339=) n.793G=
2	g.240878094G>T	CA351319597	AGXT	c.1015G>T (p.Val339Phe) n.793G>T
2	g.240878095T>A	CA351319598	AGXT	c.1016T>A (p.Val339Asp) n.794T>A
2	g.240878095T>C	CA351319599	AGXT	c.1016T>C (p.Val339Ala) n.794T>C	gnomAD v4
2	g.240878095T>G	CA351319600	AGXT	c.1016T>G (p.Val339Gly) n.794T>G
2	g.240878096C>A	CA432026326	AGXT	c.1017C>A (p.Val339=) n.795C>A
2	g.240878096C>G	CA432026328	AGXT	c.1017C>G (p.Val339=) n.795C>G
2	g.240878096C>T	CA432026329	AGXT	c.1017C>T (p.Val339=) n.795C>T	gnomAD v4
2	g.240878097A>C	CA351319601	AGXT	c.1018A>C (p.Ile340Leu) n.796A>C
2	g.240878097A>G	CA351319602	AGXT	c.1018A>G (p.Ile340Val) n.796A>G
2	g.240878097A>T	CA351319603	AGXT	c.1018A>T (p.Ile340Leu) n.796A>T
2	g.240878098T>A	CA351319604	AGXT	c.1019T>A (p.Ile340Lys) n.797T>A
2	g.240878098T>C	CA2209377	AGXT	c.1019T>C (p.Ile340Thr) n.797T>C	ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2	g.240878098T>G	CA351319605	AGXT	c.1019T>G (p.Ile340Arg) n.797T>G
2	g.240878098T=	CA1339335790	AGXT	c.1019T= (p.Ile340=) n.797T=
2	g.240878099A=	CA1339335791	AGXT	c.1020A= (p.Ile340=) n.798A=
2	g.240878099A>C	CA432026339	AGXT	c.1020A>C (p.Ile340=) n.798A>C
2	g.240878099A>G	CA343786	AGXT	c.1020A>G (p.Ile340Met) n.798A>G	ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2	g.240878099A>T	CA432026341	AGXT	c.1020A>T (p.Ile340=) n.798A>T
2	g.240878100G>A	CA351319608	AGXT	c.1021G>A (p.Asp341Asn) n.799G>A
2	g.240878100G>C	CA351319606	AGXT	c.1021G>C (p.Asp341His) n.799G>C
2	g.240878100G>T	CA351319607	AGXT	c.1021G>T (p.Asp341Tyr) n.799G>T
2	g.240878101A>C	CA351319609	AGXT	c.1022A>C (p.Asp341Ala) n.800A>C
2	g.240878101A>G	CA351319610	AGXT	c.1022A>G (p.Asp341Gly) n.800A>G
2	g.240878101A>T	CA351319611	AGXT	c.1022A>T (p.Asp341Val) n.800A>T	gnomAD v4
2	g.240878102C>A	CA2209378	AGXT	c.1023C>A (p.Asp341Glu) n.801C>A	ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
2	g.240878102C=	CA1339335792	AGXT	c.1023C= (p.Asp341=) n.801C=
2	g.240878102C>G	CA351319612	AGXT	c.1023C>G (p.Asp341Glu) n.801C>G	gnomAD v4
2	g.240878102C>T	CA432026351	AGXT	c.1023C>T (p.Asp341=) n.801C>T	gnomAD v4
2	g.240878103C>A	CA351319613	AGXT	c.1024C>A (p.His342Asn) n.802C>A
2	g.240878103C>G	CA351319614	AGXT	c.1024C>G (p.His342Asp) n.802C>G
2	g.240878103C>T	CA351319615	AGXT	c.1024C>T (p.His342Tyr) n.802C>T
2	g.240878104A>C	CA351319616	AGXT	c.1025A>C (p.His342Pro) n.803A>C
2	g.240878104A>G	CA351319617	AGXT	c.1025A>G (p.His342Arg) n.803A>G
2	g.240878104A>T	CA351319618	AGXT	c.1025A>T (p.His342Leu) n.803A>T
2	g.240878105C>A	CA351319620	AGXT	c.1026C>A (p.His342Gln) n.804C>A
2	g.240878105C>G	CA351319619	AGXT	c.1026C>G (p.His342Gln) n.804C>G
2	g.240878105C>T	CA432026362	AGXT	c.1026C>T (p.His342=) n.804C>T	ClinVar dbSNP
2	g.240878106T>A	CA351319621	AGXT	c.1027T>A (p.Phe343Ile) n.805T>A	gnomAD v4

Number of alleles fetched