Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
2	g.135804812G>A	CA1887864	LCT	c.4419C>T (p.Tyr1473=) c.2715C>T (p.Tyr905=)	ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
2	g.135804812G>C	CA144315	LCT	c.4419C>G (p.Tyr1473Ter) c.2715C>G (p.Tyr905Ter)	ClinVar dbSNP
2	g.135804812G=	CA1290829335	LCT	c.4419C= (p.Tyr1473=) c.2715C= (p.Tyr905=)
2	g.135804812G>T	CA348595759	LCT	c.4419C>A (p.Tyr1473Ter) c.2715C>A (p.Tyr905Ter)
2	g.135804813T>A	CA348595764	LCT	c.4418A>T (p.Tyr1473Phe) c.2714A>T (p.Tyr905Phe)
2	g.135804813T>C	CA348595768	LCT	c.4418A>G (p.Tyr1473Cys) c.2714A>G (p.Tyr905Cys)
2	g.135804813T>G	CA348595765	LCT	c.4418A>C (p.Tyr1473Ser) c.2714A>C (p.Tyr905Ser)	gnomAD v4
2	g.135804814A>C	CA348595770	LCT	c.4417T>G (p.Tyr1473Asp) c.2713T>G (p.Tyr905Asp)
2	g.135804814A>G	CA348595773	LCT	c.4417T>C (p.Tyr1473His) c.2713T>C (p.Tyr905His)	gnomAD v4
2	g.135804814A>T	CA348595772	LCT	c.4417T>A (p.Tyr1473Asn) c.2713T>A (p.Tyr905Asn)
2	g.135804815G>A	CA429202990	LCT	c.4416C>T (p.Tyr1472=) c.2712C>T (p.Tyr904=)	dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2	g.135804815G>C	CA348595777	LCT	c.4416C>G (p.Tyr1472Ter) c.2712C>G (p.Tyr904Ter)
2	g.135804815G=	CA1290829336	LCT	c.4416C= (p.Tyr1472=) c.2712C= (p.Tyr904=)
2	g.135804815G>T	CA348595779	LCT	c.4416C>A (p.Tyr1472Ter) c.2712C>A (p.Tyr904Ter)	gnomAD v4
2	g.135804816T>A	CA348595782	LCT	c.4415A>T (p.Tyr1472Phe) c.2711A>T (p.Tyr904Phe)
2	g.135804816T>C	CA348595784	LCT	c.4415A>G (p.Tyr1472Cys) c.2711A>G (p.Tyr904Cys)	gnomAD v4
2	g.135804816T>G	CA348595786	LCT	c.4415A>C (p.Tyr1472Ser) c.2711A>C (p.Tyr904Ser)
2	g.135804817A>C	CA348595790	LCT	c.4414T>G (p.Tyr1472Asp) c.2710T>G (p.Tyr904Asp)
2	g.135804817A>G	CA348595793	LCT	c.4414T>C (p.Tyr1472His) c.2710T>C (p.Tyr904His)	gnomAD v4
2	g.135804817A>T	CA348595795	LCT	c.4414T>A (p.Tyr1472Asn) c.2710T>A (p.Tyr904Asn)
2	g.135804818G>A	CA429202997	LCT	c.4413C>T (p.Asn1471=) c.2709C>T (p.Asn903=)
2	g.135804818G>C	CA348595797	LCT	c.4413C>G (p.Asn1471Lys) c.2709C>G (p.Asn903Lys)
2	g.135804818G>T	CA348595799	LCT	c.4413C>A (p.Asn1471Lys) c.2709C>A (p.Asn903Lys)
2	g.135804819T>A	CA348595802	LCT	c.4412A>T (p.Asn1471Ile) c.2708A>T (p.Asn903Ile)
2	g.135804819T>C	CA348595804	LCT	c.4412A>G (p.Asn1471Ser) c.2708A>G (p.Asn903Ser)	gnomAD v4
2	g.135804819T>G	CA348595807	LCT	c.4412A>C (p.Asn1471Thr) c.2708A>C (p.Asn903Thr)
2	g.135804820T>A	CA348595815	LCT	c.4411A>T (p.Asn1471Tyr) c.2707A>T (p.Asn903Tyr)
2	g.135804820T>C	CA348595812	LCT	c.4411A>G (p.Asn1471Asp) c.2707A>G (p.Asn903Asp)
2	g.135804820T>G	CA348595809	LCT	c.4411A>C (p.Asn1471His) c.2707A>C (p.Asn903His)
2	g.135804821C>A	CA429202999	LCT	c.4410G>T (p.Leu1470=) c.2706G>T (p.Leu902=)
2	g.135804821C=	CA1290829337	LCT	c.4410G= (p.Leu1470=) c.2706G= (p.Leu902=)
2	g.135804821C>G	CA429203000	LCT	c.4410G>C (p.Leu1470=) c.2706G>C (p.Leu902=)	dbSNP COSMIC
2	g.135804821C>T	CA429203001	LCT	c.4410G>A (p.Leu1470=) c.2706G>A (p.Leu902=)	dbSNP gnomAD v2
2	g.135804822A>C	CA348595819	LCT	c.4409T>G (p.Leu1470Arg) c.2705T>G (p.Leu902Arg)
2	g.135804822A>G	CA348595821	LCT	c.4409T>C (p.Leu1470Pro) c.2705T>C (p.Leu902Pro)
2	g.135804822A>T	CA348595824	LCT	c.4409T>A (p.Leu1470Gln) c.2705T>A (p.Leu902Gln)
2	g.135804823G>A	CA429203002	LCT	c.4408C>T (p.Leu1470=) c.2704C>T (p.Leu902=)
2	g.135804823G>C	CA348595828	LCT	c.4408C>G (p.Leu1470Val) c.2704C>G (p.Leu902Val)
2	g.135804823G>T	CA348595830	LCT	c.4408C>A (p.Leu1470Met) c.2704C>A (p.Leu902Met)
2	g.135804824G>A	CA429203004	LCT	c.4407C>T (p.Gly1469=) c.2703C>T (p.Gly901=)	ClinVar dbSNP
2	g.135804824G>C	CA429203006	LCT	c.4407C>G (p.Gly1469=) c.2703C>G (p.Gly901=)
2	g.135804824G=	CA1290829338	LCT	c.4407C= (p.Gly1469=) c.2703C= (p.Gly901=)
2	g.135804824G>T	CA429203007	LCT	c.4407C>A (p.Gly1469=) c.2703C>A (p.Gly901=)
2	g.135804825C>A	CA348595832	LCT	c.4406G>T (p.Gly1469Val) c.2702G>T (p.Gly901Val)
2	g.135804825C>G	CA348595835	LCT	c.4406G>C (p.Gly1469Ala) c.2702G>C (p.Gly901Ala)
2	g.135804825C>T	CA348595837	LCT	c.4406G>A (p.Gly1469Asp) c.2702G>A (p.Gly901Asp)
2	g.135804826C>A	CA348595841	LCT	c.4405G>T (p.Gly1469Cys) c.2701G>T (p.Gly901Cys)
2	g.135804826C>G	CA348595843	LCT	c.4405G>C (p.Gly1469Arg) c.2701G>C (p.Gly901Arg)
2	g.135804826C>T	CA348595845	LCT	c.4405G>A (p.Gly1469Ser) c.2701G>A (p.Gly901Ser)
2	g.135804827C>A	CA429203009	LCT	c.4404G>T (p.Ala1468=) c.2700G>T (p.Ala900=)

Number of alleles fetched