Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
9	g.132327630C>A	CA375327791	SETX	c.3968G>T (p.Arg1323Leu) n.4152G>T	gnomAD v4
9	g.132327630C=	CA1882147433	SETX	c.3968G= (p.Arg1323=) n.4152G=
9	g.132327630C>G	CA375327792	SETX	c.3968G>C (p.Arg1323Pro) n.4152G>C
9	g.132327630C>T	CA233096	SETX	c.3968G>A (p.Arg1323Gln) n.4152G>A	ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9	g.132327631G>A	CA200807604	SETX	c.3967C>T (p.Arg1323Ter) n.4151C>T	dbSNP gnomAD v4
9	g.132327631G>C	CA375327793	SETX	c.3967C>G (p.Arg1323Gly) n.4151C>G
9	g.132327631G=	CA1882147434	SETX	c.3967C= (p.Arg1323=) n.4151C=
9	g.132327631G>T	CA467807487	SETX	c.3967C>A (p.Arg1323=) n.4151C>A
9	g.132327632G>A	CA5297294	SETX	c.3966C>T (p.Thr1322=) n.4150C>T	ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9	g.132327632G>C	CA467807492	SETX	c.3966C>G (p.Thr1322=) n.4150C>G
9	g.132327632G=	CA1882147435	SETX	c.3966C= (p.Thr1322=) n.4150C=
9	g.132327632G>T	CA5297295	SETX	c.3966C>A (p.Thr1322=) n.4150C>A	ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9	g.132327633G>A	CA375327794	SETX	c.3965C>T (p.Thr1322Ile) n.4149C>T
9	g.132327633G>C	CA375327795	SETX	c.3965C>G (p.Thr1322Ser) n.4149C>G	gnomAD v4
9	g.132327633G=	CA1882147436	SETX	c.3965C= (p.Thr1322=) n.4149C=
9	g.132327633G>T	CA5297296	SETX	c.3965C>A (p.Thr1322Asn) n.4149C>A	ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9	g.132327634T>A	CA375327796	SETX	c.3964A>T (p.Thr1322Ser) n.4148A>T
9	g.132327634T>C	CA375327797	SETX	c.3964A>G (p.Thr1322Ala) n.4148A>G	dbSNP gnomAD v2 gnomAD v4
9	g.132327634T>G	CA375327798	SETX	c.3964A>C (p.Thr1322Pro) n.4148A>C
9	g.132327634T=	CA1882147437	SETX	c.3964A= (p.Thr1322=) n.4148A=
9	g.132327635A>C	CA375327799	SETX	c.3963T>G (p.Asp1321Glu) n.4147T>G
9	g.132327635A>G	CA467807502	SETX	c.3963T>C (p.Asp1321=) n.4147T>C
9	g.132327635A>T	CA375327800	SETX	c.3963T>A (p.Asp1321Glu) n.4147T>A
9	g.132327636T>A	CA375327801	SETX	c.3962A>T (p.Asp1321Val) n.4146A>T
9	g.132327636T>C	CA375327802	SETX	c.3962A>G (p.Asp1321Gly) n.4146A>G	gnomAD v4
9	g.132327636T>G	CA375327805	SETX	c.3962A>C (p.Asp1321Ala) n.4146A>C
9	g.132327637C>A	CA375327809	SETX	c.3961G>T (p.Asp1321Tyr) n.4145G>T
9	g.132327637C>G	CA375327811	SETX	c.3961G>C (p.Asp1321His) n.4145G>C
9	g.132327637C>T	CA375327812	SETX	c.3961G>A (p.Asp1321Asn) n.4145G>A	COSMIC COSMIC
9	g.132327638A=	CA1882147438	SETX	c.3960T= (p.Val1320=) n.4144T=
9	g.132327638A>C	CA467807514	SETX	c.3960T>G (p.Val1320=) n.4144T>G
9	g.132327638A>G	CA467807516	SETX	c.3960T>C (p.Val1320=) n.4144T>C
9	g.132327638A>T	CA467807512	SETX	c.3960T>A (p.Val1320=) n.4144T>A	dbSNP gnomAD v2 gnomAD v3 gnomAD v4
9	g.132327639A>C	CA375327815	SETX	c.3959T>G (p.Val1320Gly) n.4143T>G	gnomAD v4
9	g.132327639A>G	CA375327817	SETX	c.3959T>C (p.Val1320Ala) n.4143T>C
9	g.132327639A>T	CA375327819	SETX	c.3959T>A (p.Val1320Asp) n.4143T>A
9	g.132327640C>A	CA375327821	SETX	c.3958G>T (p.Val1320Phe) n.4142G>T
9	g.132327640C=	CA1882147439	SETX	c.3958G= (p.Val1320=) n.4142G=
9	g.132327640C>G	CA375327823	SETX	c.3958G>C (p.Val1320Leu) n.4142G>C
9	g.132327640C>T	CA375327825	SETX	c.3958G>A (p.Val1320Ile) n.4142G>A	dbSNP gnomAD v3 gnomAD v4
9	g.132327641T>A	CA467807528	SETX	c.3957A>T (p.Val1319=) n.4141A>T
9	g.132327641T>C	CA467807525	SETX	c.3957A>G (p.Val1319=) n.4141A>G	gnomAD v4
9	g.132327641T>G	CA467807526	SETX	c.3957A>C (p.Val1319=) n.4141A>C
9	g.132327642A=	CA1882147440	SETX	c.3956T= (p.Val1319=) n.4140T=
9	g.132327642A>C	CA375327831	SETX	c.3956T>G (p.Val1319Gly) n.4140T>G	dbSNP gnomAD v2 gnomAD v3 gnomAD v4
9	g.132327642A>G	CA375327829	SETX	c.3956T>C (p.Val1319Ala) n.4140T>C
9	g.132327642A>T	CA375327827	SETX	c.3956T>A (p.Val1319Glu) n.4140T>A
9	g.132327643C>A	CA375327834	SETX	c.3955G>T (p.Val1319Leu) n.4139G>T
9	g.132327643C=	CA1882147441	SETX	c.3955G= (p.Val1319=) n.4139G=
9	g.132327643C>G	CA375327835	SETX	c.3955G>C (p.Val1319Leu) n.4139G>C

Number of alleles fetched