Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
2	g.135817362G>A	CA429204480	LCT	c.1686C>T (p.Asp562=)
2	g.135817362G>C	CA348605612	LCT	c.1686C>G (p.Asp562Glu)
2	g.135817362G>T	CA348605613	LCT	c.1686C>A (p.Asp562Glu)
2	g.135817363T>A	CA348605616	LCT	c.1685A>T (p.Asp562Val)
2	g.135817363T>C	CA348605615	LCT	c.1685A>G (p.Asp562Gly)
2	g.135817363T>G	CA348605614	LCT	c.1685A>C (p.Asp562Ala)
2	g.135817364C>A	CA348605617	LCT	c.1684G>T (p.Asp562Tyr)
2	g.135817364C>G	CA348605618	LCT	c.1684G>C (p.Asp562His)
2	g.135817364C>T	CA348605619	LCT	c.1684G>A (p.Asp562Asn)
2	g.135817365A=	CA1290834750	LCT	c.1683T= (p.Ser561=)
2	g.135817365A>C	CA429204481	LCT	c.1683T>G (p.Ser561=)	ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2	g.135817365A>G	CA429204482	LCT	c.1683T>C (p.Ser561=)
2	g.135817365A>T	CA429204483	LCT	c.1683T>A (p.Ser561=)
2	g.135817366G>A	CA348605620	LCT	c.1682C>T (p.Ser561Phe)
2	g.135817366G>C	CA348605621	LCT	c.1682C>G (p.Ser561Cys)	dbSNP gnomAD v4 COSMIC
2	g.135817366G=	CA1290834751	LCT	c.1682C= (p.Ser561=)
2	g.135817366G>T	CA348605622	LCT	c.1682C>A (p.Ser561Tyr)
2	g.135817367A>C	CA348605623	LCT	c.1681T>G (p.Ser561Ala)
2	g.135817367A>G	CA348605625	LCT	c.1681T>C (p.Ser561Pro)
2	g.135817367A>T	CA348605624	LCT	c.1681T>A (p.Ser561Thr)
2	g.135817368G>A	CA429204484	LCT	c.1680C>T (p.Ile560=)
2	g.135817368G>C	CA56623340	LCT	c.1680C>G (p.Ile560Met)	dbSNP gnomAD v4
2	g.135817368G=	CA1290834752	LCT	c.1680C= (p.Ile560=)
2	g.135817368G>T	CA429204485	LCT	c.1680C>A (p.Ile560=)
2	g.135817369A>C	CA348605626	LCT	c.1679T>G (p.Ile560Ser)
2	g.135817369A>G	CA348605627	LCT	c.1679T>C (p.Ile560Thr)
2	g.135817369A>T	CA348605628	LCT	c.1679T>A (p.Ile560Asn)
2	g.135817370T>A	CA348605629	LCT	c.1678A>T (p.Ile560Phe)
2	g.135817370T>C	CA348605630	LCT	c.1678A>G (p.Ile560Val)	dbSNP gnomAD v2 gnomAD v4
2	g.135817370T>G	CA348605631	LCT	c.1678A>C (p.Ile560Leu)
2	g.135817370T=	CA1290834753	LCT	c.1678A= (p.Ile560=)
2	g.135817371G>A	CA429204486	LCT	c.1677C>T (p.Gly559=)
2	g.135817371G>C	CA429204487	LCT	c.1677C>G (p.Gly559=)	gnomAD v4
2	g.135817371G>T	CA429204488	LCT	c.1677C>A (p.Gly559=)
2	g.135817372C>A	CA348605632	LCT	c.1676G>T (p.Gly559Val)	dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2	g.135817372C=	CA1290834754	LCT	c.1676G= (p.Gly559=)
2	g.135817372C>G	CA348605633	LCT	c.1676G>C (p.Gly559Ala)
2	g.135817372C>T	CA348605634	LCT	c.1676G>A (p.Gly559Asp)	gnomAD v4
2	g.135817373C>A	CA348605636	LCT	c.1675G>T (p.Gly559Cys)
2	g.135817373C=	CA1290834755	LCT	c.1675G= (p.Gly559=)
2	g.135817373C>G	CA348605635	LCT	c.1675G>C (p.Gly559Arg)	COSMIC
2	g.135817373C>T	CA1888362	LCT	c.1675G>A (p.Gly559Ser)	dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2	g.135817374G>A	CA1888363	LCT	c.1674C>T (p.Pro558=)	ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2	g.135817374G>C	CA429204489	LCT	c.1674C>G (p.Pro558=)
2	g.135817374G=	CA1290834756	LCT	c.1674C= (p.Pro558=)
2	g.135817374G>T	CA429204490	LCT	c.1674C>A (p.Pro558=)	dbSNP
2	g.135817375G>A	CA348605637	LCT	c.1673C>T (p.Pro558Leu)
2	g.135817375G>C	CA348605638	LCT	c.1673C>G (p.Pro558Arg)
2	g.135817375G>T	CA348605639	LCT	c.1673C>A (p.Pro558His)	gnomAD v4
2	g.135817376G>A	CA348605640	LCT	c.1672C>T (p.Pro558Ser)	dbSNP

Number of alleles fetched