Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
2	g.240868886G>A	CA432234716	AGXT	c.21G>A (p.Leu7=) n.41G>A n.405+1347C>T	dbSNP
2	g.240868886G>C	CA432234717	AGXT	c.21G>C (p.Leu7=) n.41G>C n.405+1347C>G	ClinVar dbSNP gnomAD v2 gnomAD v4
2	g.240868886G=	CA1339330742	AGXT	c.21G= (p.Leu7=) n.41G= n.405+1347C=
2	g.240868886G>T	CA432234719	AGXT	c.21G>T (p.Leu7=) n.41G>T n.405+1347C>A	ClinVar dbSNP
2	g.240868887G>A	CA351312679	AGXT	c.22G>A (p.Val8Met) n.42G>A n.405+1346C>T	dbSNP gnomAD v3 gnomAD v4
2	g.240868887G>C	CA275617	AGXT	c.22G>C (p.Val8Leu) n.42G>C n.405+1346C>G	ClinVar dbSNP gnomAD v2 gnomAD v4
2	g.240868887G=	CA1339330743	AGXT	c.22G= (p.Val8=) n.42G= n.405+1346C=
2	g.240868887G>T	CA351312678	AGXT	c.22G>T (p.Val8Leu) n.42G>T n.405+1346C>A	dbSNP
2	g.240868888T>A	CA351312680	AGXT	c.23T>A (p.Val8Glu) n.43T>A n.405+1345A>T
2	g.240868888T>C	CA351312684	AGXT	c.23T>C (p.Val8Ala) n.43T>C n.405+1345A>G
2	g.240868888T>G	CA351312687	AGXT	c.23T>G (p.Val8Gly) n.43T>G n.405+1345A>C
2	g.240868888_240868889delinsAT	CA2586971624	AGXT	c.23_24delinsAT (p.Val8Asp) n.43_44delinsAT n.405+1344_405+1345delinsAT
2	g.240868889G>A	CA432234723	AGXT	c.24G>A (p.Val8=) n.44G>A n.405+1344C>T	gnomAD v4
2	g.240868889G>C	CA432234725	AGXT	c.24G>C (p.Val8=) n.44G>C n.405+1344C>G
2	g.240868889G>T	CA432234726	AGXT	c.24G>T (p.Val8=) n.44G>T n.405+1344C>A
2	g.240868889_240868890insC	CA2586971626	AGXT	c.24_25insC (p.Thr9HisfsTer?) n.44_45insC n.405+1343_405+1344insG
2	g.240868890A=	CA1339330745	AGXT	c.25A= (p.Thr9=) n.45A= n.405+1343T=
2	g.240868890A>C	CA351312688	AGXT	c.25A>C (p.Thr9Pro) n.45A>C n.405+1343T>G	dbSNP gnomAD v3 gnomAD v4
2	g.240868890A>G	CA351312689	AGXT	c.25A>G (p.Thr9Ala) n.45A>G n.405+1343T>C	dbSNP
2	g.240868890A>T	CA351312690	AGXT	c.25A>T (p.Thr9Ser) n.45A>T n.405+1343T>A	gnomAD v4
2	g.240868890_240868892delinsACC	CA1339330744	AGXT	c.25_27delinsACC (p.Thr9=) n.45_47delinsACC n.405+1341_405+1343delinsGGT
2	g.240868891C>A	CA275540	AGXT	c.26C>A (p.Thr9Asn) n.46C>A n.405+1342G>T	ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2	g.240868891C=	CA1339330746	AGXT	c.26C= (p.Thr9=) n.46C= n.405+1342G=
2	g.240868891C>G	CA351312710	AGXT	c.26C>G (p.Thr9Ser) n.46C>G n.405+1342G>C	dbSNP
2	g.240868891C>T	CA351312704	AGXT	c.26C>T (p.Thr9Ile) n.46C>T n.405+1342G>A	dbSNP gnomAD v4
2	g.240868898dup	CA345700	AGXT	c.33dup (p.Lys12GlnfsTer?) n.53dup n.405+1342dup	ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC
2	g.240868897_240868898dup	CA2664004508	AGXT	c.32_33dup (p.Lys12ProfsTer?) n.52_53dup n.405+1341_405+1342dup	gnomAD v4
2	g.240868898del	CA273942	AGXT	c.33del (p.Lys12ArgfsTer?) n.53del n.405+1342del	ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
2	g.240868897_240868898del	CA275814	AGXT	c.32_33del (p.Pro11GlnfsTer?) n.52_53del n.405+1341_405+1342del	ClinVar dbSNP
2	g.240868891_240868892insA	CA2573135689	AGXT	c.26_27insA (p.Lys12GlnfsTer?) n.46_47insA n.405+1341_405+1342insT	ClinVar dbSNP
2	g.240868892C>A	CA275541	AGXT	c.27C>A (p.Thr9=) n.47C>A n.405+1341G>T	ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2	g.240868892C=	CA1339330747	AGXT	c.27C= (p.Thr9=) n.47C= n.405+1341G=
2	g.240868892C>G	CA2208962	AGXT	c.27C>G (p.Thr9=) n.47C>G n.405+1341G>C	ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2	g.240868892C>T	CA432234736	AGXT	c.27C>T (p.Thr9=) n.47C>T n.405+1341G>A	ClinVar dbSNP COSMIC
2	g.240868893C>A	CA2208963	AGXT	c.28C>A (p.Pro10Thr) n.48C>A n.405+1340G>T	dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2	g.240868893C=	CA1339330748	AGXT	c.28C= (p.Pro10=) n.48C= n.405+1340G=
2	g.240868893C>G	CA2208964	AGXT	c.28C>G (p.Pro10Ala) n.48C>G n.405+1340G>C	ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2	g.240868893C>T	CA275619	AGXT	c.28C>T (p.Pro10Ser) n.48C>T n.405+1340G>A	ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2	g.240868893_240868894delinsA	CA2586971627	AGXT	c.28_29delinsA (p.Pro10ThrfsTer?) n.48_49delinsA n.405+1339_405+1340delinsT
2	g.240868894C>A	CA2208965	AGXT	c.29C>A (p.Pro10His) n.49C>A n.405+1339G>T	dbSNP ExAC gnomAD v2
2	g.240868894C=	CA1339330749	AGXT	c.29C= (p.Pro10=) n.49C= n.405+1339G=
2	g.240868894C>G	CA351312723	AGXT	c.29C>G (p.Pro10Arg) n.49C>G n.405+1339G>C
2	g.240868894C>T	CA351312726	AGXT	c.29C>T (p.Pro10Leu) n.49C>T n.405+1339G>A	dbSNP gnomAD v2 gnomAD v4
2	g.240868895C>A	CA432234740	AGXT	c.30C>A (p.Pro10=) n.50C>A n.405+1338G>T
2	g.240868895C>G	CA432234741	AGXT	c.30C>G (p.Pro10=) n.50C>G n.405+1338G>C
2	g.240868895C>T	CA432234742	AGXT	c.30C>T (p.Pro10=) n.50C>T n.405+1338G>A
2	g.240868896C>A	CA2208967	AGXT	c.31C>A (p.Pro11Thr) n.51C>A n.405+1337G>T	dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2	g.240868896C=	CA1339330750	AGXT	c.31C= (p.Pro11=) n.51C= n.405+1337G=
2	g.240868896C>G	CA2208966	AGXT	c.31C>G (p.Pro11Ala) n.51C>G n.405+1337G>C	ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
2	g.240868896C>T	CA2208968	AGXT	c.31C>T (p.Pro11Ser) n.51C>T n.405+1337G>A	ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4

Number of alleles fetched