Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
6	g.49451593G>A	CA364398892	MMUT	c.1205C>T (p.Ala402Val)	dbSNP gnomAD v2 gnomAD v4
6	g.49451593G>C	CA3846944	MMUT	c.1205C>G (p.Ala402Gly)	dbSNP ExAC gnomAD v2 gnomAD v4
6	g.49451593G=	CA1627389335	MMUT	c.1205C= (p.Ala402=)
6	g.49451593G>T	CA364398891	MMUT	c.1205C>A (p.Ala402Asp)
6	g.49451594C>A	CA364398893	MMUT	c.1204G>T (p.Ala402Ser)
6	g.49451594C>G	CA364398894	MMUT	c.1204G>C (p.Ala402Pro)
6	g.49451594C>T	CA364398895	MMUT	c.1204G>A (p.Ala402Thr)	gnomAD v4
6	g.49451595A>C	CA364398896	MMUT	c.1203T>G (p.Ser401Arg)
6	g.49451595A>G	CA450606489	MMUT	c.1203T>C (p.Ser401=)
6	g.49451595A>T	CA364398897	MMUT	c.1203T>A (p.Ser401Arg)
6	g.49451596C>A	CA364398898	MMUT	c.1202G>T (p.Ser401Ile)
6	g.49451596C>G	CA364398899	MMUT	c.1202G>C (p.Ser401Thr)
6	g.49451596C>T	CA364398900	MMUT	c.1202G>A (p.Ser401Asn)	gnomAD v4
6	g.49451596_49451597delinsCT	CA1627389336	MMUT	c.1201_1202delinsAG (p.Ser401=)
6	g.49451597T>A	CA364398901	MMUT	c.1201A>T (p.Ser401Cys)
6	g.49451597T>C	CA364398902	MMUT	c.1201A>G (p.Ser401Gly)
6	g.49451597T>G	CA364398903	MMUT	c.1201A>C (p.Ser401Arg)
6	g.49451600del	CA825477395	MMUT	c.1201del (p.Ser401ValfsTer30)	dbSNP
6	g.49451598T>A	CA364398904	MMUT	c.1200A>T (p.Lys400Asn)
6	g.49451598T>C	CA450606500	MMUT	c.1200A>G (p.Lys400=)
6	g.49451598T>G	CA364398905	MMUT	c.1200A>C (p.Lys400Asn)
6	g.49451599T>A	CA364398908	MMUT	c.1199A>T (p.Lys400Ile)
6	g.49451599T>C	CA364398907	MMUT	c.1199A>G (p.Lys400Arg)
6	g.49451599T>G	CA364398906	MMUT	c.1199A>C (p.Lys400Thr)
6	g.49451600T>A	CA364398909	MMUT	c.1198A>T (p.Lys400Ter)	ClinVar dbSNP
6	g.49451600T>C	CA364398910	MMUT	c.1198A>G (p.Lys400Glu)
6	g.49451600T>G	CA364398911	MMUT	c.1198A>C (p.Lys400Gln)
6	g.49451600T=	CA1627389337	MMUT	c.1198A= (p.Lys400=)
6	g.49451600_49451602delinsTCA	CA1627389338	MMUT	c.1196_1198delinsTGA (p.Val399=)
6	g.49451601C>A	CA450606509	MMUT	c.1197G>T (p.Val399=)	ClinVar
6	g.49451601C>G	CA450606511	MMUT	c.1197G>C (p.Val399=)
6	g.49451601C>T	CA450606513	MMUT	c.1197G>A (p.Val399=)
6	g.49451603_49451604del	CA567155985	MMUT	c.1196_1197del (p.Val399GlufsTer24)	ClinVar dbSNP gnomAD v2 gnomAD v4
6	g.49451602A>C	CA364398912	MMUT	c.1196T>G (p.Val399Gly)
6	g.49451602A>G	CA364398913	MMUT	c.1196T>C (p.Val399Ala)	gnomAD v4
6	g.49451602A>T	CA364398914	MMUT	c.1196T>A (p.Val399Glu)
6	g.49451603C>A	CA364398915	MMUT	c.1195G>T (p.Val399Leu)
6	g.49451603C>G	CA364398916	MMUT	c.1195G>C (p.Val399Leu)
6	g.49451603C>T	CA364398917	MMUT	c.1195G>A (p.Val399Met)	gnomAD v4
6	g.49451604A>C	CA450606520	MMUT	c.1194T>G (p.Thr398=)
6	g.49451604A>G	CA450606521	MMUT	c.1194T>C (p.Thr398=)
6	g.49451604A>T	CA450606522	MMUT	c.1194T>A (p.Thr398=)
6	g.49451605G>A	CA364398918	MMUT	c.1193C>T (p.Thr398Ile)	gnomAD v4
6	g.49451605G>C	CA364398919	MMUT	c.1193C>G (p.Thr398Ser)
6	g.49451605G>T	CA364398920	MMUT	c.1193C>A (p.Thr398Asn)
6	g.49451606T>A	CA364398921	MMUT	c.1192A>T (p.Thr398Ser)
6	g.49451606T>C	CA364398922	MMUT	c.1192A>G (p.Thr398Ala)	gnomAD v4 COSMIC
6	g.49451606T>G	CA364398923	MMUT	c.1192A>C (p.Thr398Pro)	gnomAD v4
6	g.49451607T>A	CA450606531	MMUT	c.1191A>T (p.Pro397=)
6	g.49451607T>C	CA450606532	MMUT	c.1191A>G (p.Pro397=)

Number of alleles fetched