Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
12	g.6018493A=	CA2013872543	VWF	c.4925T= (p.Ile1642=) n.421-24559T=
12	g.6018493A>C	CA383498681	VWF	c.4925T>G (p.Ile1642Ser) n.421-24559T>G
12	g.6018493A>G	CA6402438	VWF	c.4925T>C (p.Ile1642Thr) n.421-24559T>C	dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
12	g.6018493A>T	CA383498682	VWF	c.4925T>A (p.Ile1642Asn) n.421-24559T>A
12	g.6018494T>A	CA383498685	VWF	c.4924A>T (p.Ile1642Phe) n.421-24560A>T
12	g.6018494T>C	CA383498683	VWF	c.4924A>G (p.Ile1642Val) n.421-24560A>G
12	g.6018494T>G	CA383498684	VWF	c.4924A>C (p.Ile1642Leu) n.421-24560A>C
12	g.6018495C>A	CA383498686	VWF	c.4923G>T (p.Arg1641Ser) n.421-24561G>T
12	g.6018495C=	CA2013872544	VWF	c.4923G= (p.Arg1641=) n.421-24561G=
12	g.6018495C>G	CA383498687	VWF	c.4923G>C (p.Arg1641Ser) n.421-24561G>C
12	g.6018495C>T	CA6402439	VWF	c.4923G>A (p.Arg1641=) n.421-24561G>A	dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12	g.6018496C>A	CA383498688	VWF	c.4922G>T (p.Arg1641Met) n.421-24562G>T	COSMIC
12	g.6018496C=	CA2013872545	VWF	c.4922G= (p.Arg1641=) n.421-24562G=
12	g.6018496C>G	CA383498689	VWF	c.4922G>C (p.Arg1641Thr) n.421-24562G>C
12	g.6018496C>T	CA383498690	VWF	c.4922G>A (p.Arg1641Lys) n.421-24562G>A	ClinVar dbSNP gnomAD v4 COSMIC
12	g.6018497T>A	CA383498691	VWF	c.4921A>T (p.Arg1641Trp) n.421-24563A>T
12	g.6018497T>C	CA383498692	VWF	c.4921A>G (p.Arg1641Gly) n.421-24563A>G
12	g.6018497T>G	CA478494021	VWF	c.4921A>C (p.Arg1641=) n.421-24563A>C
12	g.6018498C>A	CA383498693	VWF	c.4920G>T (p.Glu1640Asp) n.421-24564G>T
12	g.6018498C>G	CA383498694	VWF	c.4920G>C (p.Glu1640Asp) n.421-24564G>C
12	g.6018498C>T	CA478494022	VWF	c.4920G>A (p.Glu1640=) n.421-24564G>A
12	g.6018499T>A	CA383498695	VWF	c.4919A>T (p.Glu1640Val) n.421-24565A>T
12	g.6018499T>C	CA383498696	VWF	c.4919A>G (p.Glu1640Gly) n.421-24565A>G
12	g.6018499T>G	CA383498697	VWF	c.4919A>C (p.Glu1640Ala) n.421-24565A>C
12	g.6018500C>A	CA383498698	VWF	c.4918G>T (p.Glu1640Ter) n.421-24566G>T
12	g.6018500C>G	CA383498699	VWF	c.4918G>C (p.Glu1640Gln) n.421-24566G>C
12	g.6018500C>T	CA383498700	VWF	c.4918G>A (p.Glu1640Lys) n.421-24566G>A
12	g.6018501C>A	CA478494023	VWF	c.4917G>T (p.Leu1639=) n.421-24567G>T
12	g.6018501C=	CA2013872546	VWF	c.4917G= (p.Leu1639=) n.421-24567G=
12	g.6018501C>G	CA478494024	VWF	c.4917G>C (p.Leu1639=) n.421-24567G>C
12	g.6018501C>T	CA6402440	VWF	c.4917G>A (p.Leu1639=) n.421-24567G>A	ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12	g.6018502A=	CA2013872547	VWF	c.4916T= (p.Leu1639=) n.421-24568T=
12	g.6018502A>C	CA383498701	VWF	c.4916T>G (p.Leu1639Arg) n.421-24568T>G
12	g.6018502A>G	CA228678	VWF	c.4916T>C (p.Leu1639Pro) n.421-24568T>C	ClinVar dbSNP
12	g.6018502A>T	CA383498702	VWF	c.4916T>A (p.Leu1639Gln) n.421-24568T>A
12	g.6018503G>A	CA478494025	VWF	c.4915C>T (p.Leu1639=) n.421-24569C>T	dbSNP gnomAD v3 gnomAD v4
12	g.6018503G>C	CA383498703	VWF	c.4915C>G (p.Leu1639Val) n.421-24569C>G
12	g.6018503G=	CA2013872548	VWF	c.4915C= (p.Leu1639=) n.421-24569C=
12	g.6018503G>T	CA383498704	VWF	c.4915C>A (p.Leu1639Met) n.421-24569C>A
12	g.6018504C>A	CA383498706	VWF	c.4914G>T (p.Glu1638Asp) n.421-24570G>T	gnomAD v4
12	g.6018504C>G	CA383498705	VWF	c.4914G>C (p.Glu1638Asp) n.421-24570G>C	gnomAD v4
12	g.6018504C>T	CA478494026	VWF	c.4914G>A (p.Glu1638=) n.421-24570G>A
12	g.6018505T>A	CA383498707	VWF	c.4913A>T (p.Glu1638Val) n.421-24571A>T
12	g.6018505T>C	CA383498708	VWF	c.4913A>G (p.Glu1638Gly) n.421-24571A>G
12	g.6018505T>G	CA383498709	VWF	c.4913A>C (p.Glu1638Ala) n.421-24571A>C
12	g.6018505_6018526delinsCAAT	CA2695196767	VWF	c.4892_4913delinsATTG (p.Gly1631_Glu1638delinsAspTrp) n.421-24592_421-24571delinsATTG
12	g.6018506C>A	CA383498710	VWF	c.4912G>T (p.Glu1638Ter) n.421-24572G>T
12	g.6018506C=	CA2013872549	VWF	c.4912G= (p.Glu1638=) n.421-24572G=
12	g.6018506C>G	CA232297755	VWF	c.4912G>C (p.Glu1638Gln) n.421-24572G>C	ClinVar dbSNP gnomAD v3 gnomAD v4
12	g.6018506C>T	CA228676	VWF	c.4912G>A (p.Glu1638Lys) n.421-24572G>A	ClinVar dbSNP gnomAD v4

Number of alleles fetched