Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
12	g.6018397_6018423del	CA2617229996	VWF	c.5003_5029del (p.Arg1668_Gln1676del) n.421-24481_421-24455del	gnomAD v4
12	g.6018392G>A	CA383498473	VWF	c.5026C>T (p.Gln1676Ter) n.421-24458C>T	dbSNP gnomAD v4
12	g.6018392G>C	CA383498475	VWF	c.5026C>G (p.Gln1676Glu) n.421-24458C>G
12	g.6018392G=	CA2013872493	VWF	c.5026C= (p.Gln1676=) n.421-24458C=
12	g.6018392G>T	CA383498474	VWF	c.5026C>A (p.Gln1676Lys) n.421-24458C>A	gnomAD v4
12	g.6018393C>A	CA478493952	VWF	c.5025G>T (p.Leu1675=) n.421-24459G>T
12	g.6018393C>G	CA478493953	VWF	c.5025G>C (p.Leu1675=) n.421-24459G>C
12	g.6018393C>T	CA478493954	VWF	c.5025G>A (p.Leu1675=) n.421-24459G>A	dbSNP gnomAD v4
12	g.6018394A>C	CA383498476	VWF	c.5024T>G (p.Leu1675Arg) n.421-24460T>G
12	g.6018394A>G	CA383498477	VWF	c.5024T>C (p.Leu1675Pro) n.421-24460T>C
12	g.6018394A>T	CA383498478	VWF	c.5024T>A (p.Leu1675Gln) n.421-24460T>A
12	g.6018394_6018395delinsAG	CA2013872494	VWF	c.5023_5024delinsCT (p.Leu1675=) n.421-24461_421-24460delinsCT
12	g.6018394_6018395delinsTA	CA228698	VWF	c.5023_5024delinsTA (p.Leu1675Ter) n.421-24461_421-24460delinsTA	ClinVar dbSNP
12	g.6018395G>A	CA6402422	VWF	c.5023C>T (p.Leu1675=) n.421-24461C>T	dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12	g.6018395G>C	CA383498480	VWF	c.5023C>G (p.Leu1675Val) n.421-24461C>G
12	g.6018395G=	CA2013872495	VWF	c.5023C= (p.Leu1675=) n.421-24461C=
12	g.6018395G>T	CA383498479	VWF	c.5023C>A (p.Leu1675Met) n.421-24461C>A
12	g.6018396C>A	CA478493955	VWF	c.5022G>T (p.Gly1674=) n.421-24462G>T
12	g.6018396C=	CA2013872496	VWF	c.5022G= (p.Gly1674=) n.421-24462G=
12	g.6018396C>G	CA478493956	VWF	c.5022G>C (p.Gly1674=) n.421-24462G>C	dbSNP gnomAD v2 gnomAD v4
12	g.6018396C>T	CA478493957	VWF	c.5022G>A (p.Gly1674=) n.421-24462G>A
12	g.6018397C>A	CA383498481	VWF	c.5021G>T (p.Gly1674Val) n.421-24463G>T
12	g.6018397C>G	CA383498482	VWF	c.5021G>C (p.Gly1674Ala) n.421-24463G>C
12	g.6018397C>T	CA383498483	VWF	c.5021G>A (p.Gly1674Glu) n.421-24463G>A	COSMIC
12	g.6018398C>A	CA383498484	VWF	c.5020G>T (p.Gly1674Trp) n.421-24464G>T
12	g.6018398C>G	CA383498485	VWF	c.5020G>C (p.Gly1674Arg) n.421-24464G>C
12	g.6018398C>T	CA383498486	VWF	c.5020G>A (p.Gly1674Arg) n.421-24464G>A	gnomAD v4
12	g.6018399C>A	CA383498487	VWF	c.5019G>T (p.Glu1673Asp) n.421-24465G>T	gnomAD v4
12	g.6018399C=	CA2013872497	VWF	c.5019G= (p.Glu1673=) n.421-24465G=
12	g.6018399C>G	CA383498488	VWF	c.5019G>C (p.Glu1673Asp) n.421-24465G>C
12	g.6018399C>T	CA478493958	VWF	c.5019G>A (p.Glu1673=) n.421-24465G>A	dbSNP
12	g.6018400T>A	CA383498489	VWF	c.5018A>T (p.Glu1673Val) n.421-24466A>T
12	g.6018400T>C	CA383498490	VWF	c.5018A>G (p.Glu1673Gly) n.421-24466A>G
12	g.6018400T>G	CA383498491	VWF	c.5018A>C (p.Glu1673Ala) n.421-24466A>C
12	g.6018401C>A	CA383498492	VWF	c.5017G>T (p.Glu1673Ter) n.421-24467G>T
12	g.6018401C=	CA2013872498	VWF	c.5017G= (p.Glu1673=) n.421-24467G=
12	g.6018401C>G	CA383498493	VWF	c.5017G>C (p.Glu1673Gln) n.421-24467G>C
12	g.6018401C>T	CA6402423	VWF	c.5017G>A (p.Glu1673Lys) n.421-24467G>A	dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12	g.6018402T>A	CA478493961	VWF	c.5016A>T (p.Gly1672=) n.421-24468A>T
12	g.6018402T>C	CA478493960	VWF	c.5016A>G (p.Gly1672=) n.421-24468A>G	gnomAD v4
12	g.6018402T>G	CA478493959	VWF	c.5016A>C (p.Gly1672=) n.421-24468A>C
12	g.6018403C>A	CA383498494	VWF	c.5015G>T (p.Gly1672Val) n.421-24469G>T
12	g.6018403C>G	CA383498495	VWF	c.5015G>C (p.Gly1672Ala) n.421-24469G>C	gnomAD v4
12	g.6018403C>T	CA383498496	VWF	c.5015G>A (p.Gly1672Glu) n.421-24469G>A	gnomAD v4
12	g.6018404C>A	CA383498497	VWF	c.5014G>T (p.Gly1672Ter) n.421-24470G>T	gnomAD v4
12	g.6018404C=	CA2013872499	VWF	c.5014G= (p.Gly1672=) n.421-24470G=
12	g.6018404C>G	CA383498498	VWF	c.5014G>C (p.Gly1672Arg) n.421-24470G>C
12	g.6018404C>T	CA228696	VWF	c.5014G>A (p.Gly1672Arg) n.421-24470G>A	ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12	g.6018405G>A	CA6402424	VWF	c.5013C>T (p.Ser1671=) n.421-24471C>T	dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12	g.6018405G>C	CA478493962	VWF	c.5013C>G (p.Ser1671=) n.421-24471C>G

Number of alleles fetched