Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
12	g.52676326A=	CA2036619576	KRT1	c.1424T= (p.Leu475=) n.498T=
12	g.52676326A>C	CA384962333	KRT1	c.1424T>G (p.Leu475Arg) n.498T>G
12	g.52676326A>G	CA126050	KRT1	c.1424T>C (p.Leu475Pro) n.498T>C	ClinVar dbSNP
12	g.52676326A>T	CA384962336	KRT1	c.1424T>A (p.Leu475Gln) n.498T>A
12	g.52676327G>A	CA6586172	KRT1	c.1423C>T (p.Leu475=) n.497C>T	dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12	g.52676327G>C	CA384962339	KRT1	c.1423C>G (p.Leu475Val) n.497C>G
12	g.52676327G=	CA2036619577	KRT1	c.1423C= (p.Leu475=) n.497C=
12	g.52676327G>T	CA384962341	KRT1	c.1423C>A (p.Leu475Met) n.497C>A
12	g.52676328G>A	CA479872116	KRT1	c.1422C>T (p.Ala474=) n.496C>T	dbSNP gnomAD v3 gnomAD v4
12	g.52676328G>C	CA479872117	KRT1	c.1422C>G (p.Ala474=) n.496C>G
12	g.52676328G=	CA2036619578	KRT1	c.1422C= (p.Ala474=) n.496C=
12	g.52676328G>T	CA479872120	KRT1	c.1422C>A (p.Ala474=) n.496C>A
12	g.52676329G>A	CA384962343	KRT1	c.1421C>T (p.Ala474Val) n.495C>T
12	g.52676329G>C	CA384962346	KRT1	c.1421C>G (p.Ala474Gly) n.495C>G
12	g.52676329G>T	CA384962345	KRT1	c.1421C>A (p.Ala474Asp) n.495C>A
12	g.52676330C>A	CA384962349	KRT1	c.1420G>T (p.Ala474Ser) n.494G>T
12	g.52676330C=	CA2036619579	KRT1	c.1420G= (p.Ala474=) n.494G=
12	g.52676330C>G	CA384962351	KRT1	c.1420G>C (p.Ala474Pro) n.494G>C
12	g.52676330C>T	CA384962352	KRT1	c.1420G>A (p.Ala474Thr) n.494G>A	dbSNP gnomAD v2 gnomAD v4
12	g.52676331C>A	CA479872140	KRT1	c.1419G>T (p.Leu473=) n.493G>T
12	g.52676331C>G	CA479872145	KRT1	c.1419G>C (p.Leu473=) n.493G>C
12	g.52676331C>T	CA479872143	KRT1	c.1419G>A (p.Leu473=) n.493G>A
12	g.52676332A>C	CA384962355	KRT1	c.1418T>G (p.Leu473Arg) n.492T>G
12	g.52676332A>G	CA384962357	KRT1	c.1418T>C (p.Leu473Pro) n.492T>C
12	g.52676332A>T	CA384962359	KRT1	c.1418T>A (p.Leu473Gln) n.492T>A
12	g.52676333G>A	CA479872155	KRT1	c.1417C>T (p.Leu473=) n.491C>T
12	g.52676333G>C	CA384962361	KRT1	c.1417C>G (p.Leu473Val) n.491C>G	dbSNP
12	g.52676333G=	CA2036619580	KRT1	c.1417C= (p.Leu473=) n.491C=
12	g.52676333G>T	CA384962363	KRT1	c.1417C>A (p.Leu473Met) n.491C>A	dbSNP gnomAD v2 gnomAD v4
12	g.52676334C>A	CA6586173	KRT1	c.1416G>T (p.Lys472Asn) n.490G>T	dbSNP ExAC gnomAD v2
12	g.52676334C=	CA2036619581	KRT1	c.1416G= (p.Lys472=) n.490G=
12	g.52676334C>G	CA384962366	KRT1	c.1416G>C (p.Lys472Asn) n.490G>C	dbSNP gnomAD v2 gnomAD v3 gnomAD v4
12	g.52676334C>T	CA479872170	KRT1	c.1416G>A (p.Lys472=) n.490G>A	dbSNP gnomAD v2 gnomAD v4
12	g.52676335T>A	CA384962369	KRT1	c.1415A>T (p.Lys472Met) n.489A>T
12	g.52676335T>C	CA384962372	KRT1	c.1415A>G (p.Lys472Arg) n.489A>G	gnomAD v4
12	g.52676335T>G	CA384962370	KRT1	c.1415A>C (p.Lys472Thr) n.489A>C
12	g.52676336T>A	CA384962374	KRT1	c.1414A>T (p.Lys472Ter) n.488A>T
12	g.52676336T>C	CA384962376	KRT1	c.1414A>G (p.Lys472Glu) n.488A>G
12	g.52676336T>G	CA384962377	KRT1	c.1414A>C (p.Lys472Gln) n.488A>C
12	g.52676337T>A	CA479873082	KRT1	c.1413A>T (p.Thr471=) n.487A>T	dbSNP
12	g.52676337T>C	CA479873084	KRT1	c.1413A>G (p.Thr471=) n.487A>G	dbSNP gnomAD v2 gnomAD v3 gnomAD v4
12	g.52676337T>G	CA6586174	KRT1	c.1413A>C (p.Thr471=) n.487A>C	ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12	g.52676337T=	CA217417	KRT1	c.1413A= (p.Thr471=) n.487A=
12	g.52676338G>A	CA384962383	KRT1	c.1412C>T (p.Thr471Ile) n.486C>T
12	g.52676338G>C	CA384962385	KRT1	c.1412C>G (p.Thr471Arg) n.486C>G c.1412C>G (p.Thr471Ser)
12	g.52676338G>T	CA384962386	KRT1	c.1412C>A (p.Thr471Lys) n.486C>A c.1412C>A (p.Thr471Asn)
12	g.52676339T>A	CA384962389	KRT1	c.1411A>T (p.Thr471Ser) n.485A>T
12	g.52676339T>C	CA384962391	KRT1	c.1411A>G (p.Thr471Ala) n.485A>G
12	g.52676339T>G	CA384962393	KRT1	c.1411A>C (p.Thr471Pro) n.485A>C
12	g.52676340G>A	CA479873111	KRT1	c.1410C>T (p.Asn470=) n.484C>T	dbSNP gnomAD v4

Number of alleles fetched