Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
12	g.13866007C>A	CA384054514	GRIN2B	c.202G>T (p.Val68Leu)
12	g.13866007C=	CA2017578227	GRIN2B	c.202G= (p.Val68=)
12	g.13866007C>G	CA384054512	GRIN2B	c.202G>C (p.Val68Leu)
12	g.13866007C>T	CA384054510	GRIN2B	c.202G>A (p.Val68Met)	dbSNP gnomAD v3 gnomAD v4
12	g.13866008C>A	CA478853879	GRIN2B	c.201G>T (p.Arg67=)	COSMIC
12	g.13866008C>G	CA478853877	GRIN2B	c.201G>C (p.Arg67=)
12	g.13866008C>T	CA478853878	GRIN2B	c.201G>A (p.Arg67=)
12	g.13866009C>A	CA384054515	GRIN2B	c.200G>T (p.Arg67Leu)
12	g.13866009C=	CA2017578228	GRIN2B	c.200G= (p.Arg67=)
12	g.13866009C>G	CA384054516	GRIN2B	c.200G>C (p.Arg67Pro)
12	g.13866009C>T	CA233148009	GRIN2B	c.200G>A (p.Arg67Gln)	ClinVar dbSNP gnomAD v4
12	g.13866010G>A	CA233148010	GRIN2B	c.199C>T (p.Arg67Trp)	ClinVar dbSNP gnomAD v2 gnomAD v4
12	g.13866010G>C	CA384054519	GRIN2B	c.199C>G (p.Arg67Gly)
12	g.13866010G=	CA2017578229	GRIN2B	c.199C= (p.Arg67=)
12	g.13866010G>T	CA478853880	GRIN2B	c.199C>A (p.Arg67=)	ClinVar dbSNP gnomAD v3 gnomAD v4
12	g.13866011G>A	CA478853881	GRIN2B	c.198C>T (p.Pro66=)
12	g.13866011G>C	CA478853882	GRIN2B	c.198C>G (p.Pro66=)
12	g.13866011G>T	CA478853883	GRIN2B	c.198C>A (p.Pro66=)	COSMIC
12	g.13866012G>A	CA384054524	GRIN2B	c.197C>T (p.Pro66Leu)	COSMIC
12	g.13866012G>C	CA384054522	GRIN2B	c.197C>G (p.Pro66Arg)
12	g.13866012G>T	CA384054520	GRIN2B	c.197C>A (p.Pro66His)	gnomAD v4
12	g.13866013G>A	CA384054526	GRIN2B	c.196C>T (p.Pro66Ser)	ClinVar dbSNP gnomAD v4
12	g.13866013G>C	CA384054528	GRIN2B	c.196C>G (p.Pro66Ala)
12	g.13866013G=	CA2017578230	GRIN2B	c.196C= (p.Pro66=)
12	g.13866013G>T	CA384054530	GRIN2B	c.196C>A (p.Pro66Thr)
12	g.13866014T>A	CA478853884	GRIN2B	c.195A>T (p.Val65=)
12	g.13866014T>C	CA478853885	GRIN2B	c.195A>G (p.Val65=)
12	g.13866014T>G	CA478853886	GRIN2B	c.195A>C (p.Val65=)	dbSNP
12	g.13866014T=	CA2017578231	GRIN2B	c.195A= (p.Val65=)
12	g.13866015A>C	CA384054533	GRIN2B	c.194T>G (p.Val65Gly)
12	g.13866015A>G	CA384054534	GRIN2B	c.194T>C (p.Val65Ala)
12	g.13866015A>T	CA384054535	GRIN2B	c.194T>A (p.Val65Glu)
12	g.13866016C>A	CA233148011	GRIN2B	c.193G>T (p.Val65Leu)	dbSNP
12	g.13866016C=	CA2017578232	GRIN2B	c.193G= (p.Val65=)
12	g.13866016C>G	CA384054539	GRIN2B	c.193G>C (p.Val65Leu)
12	g.13866016C>T	CA6461444	GRIN2B	c.193G>A (p.Val65Ile)	dbSNP ExAC gnomAD v2 gnomAD v4
12	g.13866017C>A	CA478853887	GRIN2B	c.192G>T (p.Val64=)
12	g.13866017C>G	CA478853889	GRIN2B	c.192G>C (p.Val64=)
12	g.13866017C>T	CA478853888	GRIN2B	c.192G>A (p.Val64=)
12	g.13866018A>C	CA384054541	GRIN2B	c.191T>G (p.Val64Gly)
12	g.13866018A>G	CA384054542	GRIN2B	c.191T>C (p.Val64Ala)
12	g.13866018A>T	CA384054544	GRIN2B	c.191T>A (p.Val64Glu)
12	g.13866019C>A	CA6461445	GRIN2B	c.190G>T (p.Val64Leu)	dbSNP ExAC gnomAD v2 gnomAD v4
12	g.13866019C=	CA2017578233	GRIN2B	c.190G= (p.Val64=)
12	g.13866019C>G	CA384054548	GRIN2B	c.190G>C (p.Val64Leu)	dbSNP
12	g.13866019C>T	CA315042	GRIN2B	c.190G>A (p.Val64Met)	ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12	g.13866020G>A	CA6461447	GRIN2B	c.189C>T (p.Ser63=)	ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
12	g.13866020G>C	CA478853890	GRIN2B	c.189C>G (p.Ser63=)
12	g.13866020G=	CA2017578234	GRIN2B	c.189C= (p.Ser63=)
12	g.13866020G>T	CA6461446	GRIN2B	c.189C>A (p.Ser63=)	ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4

Number of alleles fetched