Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
12	g.13866105dup	CA645595293	GRIN2B	c.105dup (p.Gly36TrpfsTer23) c.105dup	COSMIC
12	g.13866105A=	CA2017578264	GRIN2B	c.104T= (p.Ile35=)
12	g.13866105A>C	CA384054990	GRIN2B	c.104T>G (p.Ile35Ser)
12	g.13866105A>G	CA233148017	GRIN2B	c.104T>C (p.Ile35Thr)	ClinVar dbSNP gnomAD v2 gnomAD v4
12	g.13866105A>T	CA384054989	GRIN2B	c.104T>A (p.Ile35Asn)	ClinVar
12	g.13866106T>A	CA384054991	GRIN2B	c.103A>T (p.Ile35Phe)
12	g.13866106T>C	CA6461458	GRIN2B	c.103A>G (p.Ile35Val)	dbSNP ExAC gnomAD v2 gnomAD v4
12	g.13866106T>G	CA384054992	GRIN2B	c.103A>C (p.Ile35Leu)
12	g.13866106T=	CA2017578265	GRIN2B	c.103A= (p.Ile35=)
12	g.13866107G>A	CA478853939	GRIN2B	c.102C>T (p.Ser34=)
12	g.13866107G>C	CA384054993	GRIN2B	c.102C>G (p.Ser34Arg)
12	g.13866107G>T	CA384054994	GRIN2B	c.102C>A (p.Ser34Arg)
12	g.13866107_13866108del	CA645595294	GRIN2B	c.101_102del (p.Ser34AsnfsTer24) c.101_102del (p.Ser34AsnfsTer?)	COSMIC
12	g.13866108C>A	CA6461459	GRIN2B	c.101G>T (p.Ser34Ile)	dbSNP ExAC gnomAD v2 gnomAD v4
12	g.13866108C=	CA2017578266	GRIN2B	c.101G= (p.Ser34=)
12	g.13866108C>G	CA384054995	GRIN2B	c.101G>C (p.Ser34Thr)	ClinVar
12	g.13866108C>T	CA384054996	GRIN2B	c.101G>A (p.Ser34Asn)	dbSNP gnomAD v4 COSMIC
12	g.13866109T>A	CA384054999	GRIN2B	c.100A>T (p.Ser34Cys)
12	g.13866109T>C	CA384054998	GRIN2B	c.100A>G (p.Ser34Gly)
12	g.13866109T>G	CA384054997	GRIN2B	c.100A>C (p.Ser34Arg)
12	g.13866109T=	CA2017578267	GRIN2B	c.100A= (p.Ser34=)
12	g.13866109dup	CA2560228041	GRIN2B	c.100dup (p.Ser34LysfsTer25) c.100dup (p.Ser34LysfsTer?)
12	g.13866109_13866126del	CA2617757589	GRIN2B	c.83_100del (p.Ser28_Ser34delinsCys)	gnomAD v4
12	g.13866110G>A	CA478853940	GRIN2B	c.99C>T (p.Pro33=)	dbSNP gnomAD v2 gnomAD v4
12	g.13866110G>C	CA478853942	GRIN2B	c.99C>G (p.Pro33=)	gnomAD v4
12	g.13866110G=	CA2017578268	GRIN2B	c.99C= (p.Pro33=)
12	g.13866110G>T	CA6461460	GRIN2B	c.99C>A (p.Pro33=)	ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12	g.13866116dup	CA130434	GRIN2B	c.99dup (p.Ser34GlnfsTer25) c.99dup (p.Ser34GlnfsTer?)	ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
12	g.13866116del	CA478853941	GRIN2B	c.99del (p.Ser34AlafsTer?)	ClinVar gnomAD v4 COSMIC
12	g.13866110_13866111insC	CA478853943	GRIN2B	c.98_99insG (p.Ser34GlnfsTer25) c.98_99insG (p.Ser34GlnfsTer?)
12	g.13866111G>A	CA384055000	GRIN2B	c.98C>T (p.Pro33Leu)	COSMIC
12	g.13866111G>C	CA384055001	GRIN2B	c.98C>G (p.Pro33Arg)	dbSNP gnomAD v2 gnomAD v3 gnomAD v4
12	g.13866111G=	CA2017578269	GRIN2B	c.98C= (p.Pro33=)
12	g.13866111G>T	CA384055002	GRIN2B	c.98C>A (p.Pro33His)
12	g.13866112G>A	CA384055003	GRIN2B	c.97C>T (p.Pro33Ser)	gnomAD v4
12	g.13866112G>C	CA384055004	GRIN2B	c.97C>G (p.Pro33Ala)
12	g.13866112G>T	CA384055005	GRIN2B	c.97C>A (p.Pro33Thr)
12	g.13866113G>A	CA478853944	GRIN2B	c.96C>T (p.Pro32=)	ClinVar dbSNP
12	g.13866113G>C	CA478853945	GRIN2B	c.96C>G (p.Pro32=)
12	g.13866113G=	CA2017578270	GRIN2B	c.96C= (p.Pro32=)
12	g.13866113G>T	CA6461461	GRIN2B	c.96C>A (p.Pro32=)	ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12	g.13866114G>A	CA384055006	GRIN2B	c.95C>T (p.Pro32Leu)
12	g.13866114G>C	CA384055007	GRIN2B	c.95C>G (p.Pro32Arg)
12	g.13866114G>T	CA384055008	GRIN2B	c.95C>A (p.Pro32His)	ClinVar gnomAD v4
12	g.13866115G>A	CA384055010	GRIN2B	c.94C>T (p.Pro32Ser)	ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC
12	g.13866115G>C	CA384055011	GRIN2B	c.94C>G (p.Pro32Ala)	dbSNP gnomAD v3 gnomAD v4 COSMIC
12	g.13866115G=	CA2017578271	GRIN2B	c.94C= (p.Pro32=)
12	g.13866115G>T	CA384055009	GRIN2B	c.94C>A (p.Pro32Thr)	ClinVar dbSNP gnomAD v2 gnomAD v4
12	g.13866116G>A	CA6461462	GRIN2B	c.93C>T (p.Ser31=)	ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
12	g.13866116G>C	CA384055012	GRIN2B	c.93C>G (p.Ser31Arg)

Number of alleles fetched