Chr Mutation (hg38) CAid Gene Transcript Linkouts
12g.6019307T>ACA383504519VWFc.4111A>T (p.Lys1371Ter)
n.421-25373A>T
12g.6019307T>CCA383504522VWFc.4111A>G (p.Lys1371Glu)
n.421-25373A>G
12g.6019307T>GCA383504521VWFc.4111A>C (p.Lys1371Gln)
n.421-25373A>C
12g.6019308G>ACA478503001VWFc.4110C>T (p.Ser1370=)
n.421-25374C>T
12g.6019308G>CCA383504525VWFc.4110C>G (p.Ser1370Arg)
n.421-25374C>G
12g.6019308G>TCA383504526VWFc.4110C>A (p.Ser1370Arg)
n.421-25374C>A
12g.6019309C>ACA383504528VWFc.4109G>T (p.Ser1370Ile)
n.421-25375G>T
12g.6019309C>GCA383504530VWFc.4109G>C (p.Ser1370Thr)
n.421-25375G>C
12g.6019309C>TCA383504532VWFc.4109G>A (p.Ser1370Asn)
n.421-25375G>A
12g.6019310T>ACA383504535VWFc.4108A>T (p.Ser1370Cys)
n.421-25376A>T
12g.6019310T>CCA383504537VWFc.4108A>G (p.Ser1370Gly)
n.421-25376A>G
12g.6019310T>GCA383504538VWFc.4108A>C (p.Ser1370Arg)
n.421-25376A>C
12g.6019311G>ACA6402600VWFc.4107C>T (p.Phe1369=)
n.421-25377C>T
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
12g.6019311G>CCA383504541VWFc.4107C>G (p.Phe1369Leu)
n.421-25377C>G
gnomAD v4
12g.6019311G=CA2013872910VWFc.4107C= (p.Phe1369=)
n.421-25377C=
12g.6019311G>TCA383504542VWFc.4107C>A (p.Phe1369Leu)
n.421-25377C>A
12g.6019312A>CCA383505285VWFc.4106T>G (p.Phe1369Cys)
n.421-25378T>G
12g.6019312A>GCA383505286VWFc.4106T>C (p.Phe1369Ser)
n.421-25378T>C
12g.6019312A>TCA383505287VWFc.4106T>A (p.Phe1369Tyr)
n.421-25378T>A
12g.6019313A=CA2013872911VWFc.4105T= (p.Phe1369=)
n.421-25379T=
12g.6019313A>CCA383505290VWFc.4105T>G (p.Phe1369Val)
n.421-25379T>G
12g.6019313A>GCA383505291VWFc.4105T>C (p.Phe1369Leu)
n.421-25379T>C
ClinVar dbSNP
12g.6019313A>TCA228533VWFc.4105T>A (p.Phe1369Ile)
n.421-25379T>A
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
12g.6019314G>ACA478502327VWFc.4104C>T (p.Ile1368=)
n.421-25380C>T
12g.6019314G>CCA383505292VWFc.4104C>G (p.Ile1368Met)
n.421-25380C>G
12g.6019314G=CA2013872912VWFc.4104C= (p.Ile1368=)
n.421-25380C=
12g.6019314G>TCA478502328VWFc.4104C>A (p.Ile1368=)
n.421-25380C>A
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
12g.6019315A=CA2013872913VWFc.4103T= (p.Ile1368=)
n.421-25381T=
12g.6019315A>CCA383505293VWFc.4103T>G (p.Ile1368Ser)
n.421-25381T>G
12g.6019315A>GCA6402601VWFc.4103T>C (p.Ile1368Thr)
n.421-25381T>C
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.6019315A>TCA383505295VWFc.4103T>A (p.Ile1368Asn)
n.421-25381T>A
12g.6019316T>ACA383505297VWFc.4102A>T (p.Ile1368Phe)
n.421-25382A>T
12g.6019316T>CCA232297772VWFc.4102A>G (p.Ile1368Val)
n.421-25382A>G
dbSNP gnomAD v4
12g.6019316T>GCA383505299VWFc.4102A>C (p.Ile1368Leu)
n.421-25382A>C
12g.6019316T=CA2013872914VWFc.4102A= (p.Ile1368=)
n.421-25382A=
12g.6019317T>ACA383505302VWFc.4101A>T (p.Gln1367His)
n.421-25383A>T
dbSNP gnomAD v3 gnomAD v4
12g.6019317T>CCA478502329VWFc.4101A>G (p.Gln1367=)
n.421-25383A>G
12g.6019317T>GCA383505306VWFc.4101A>C (p.Gln1367His)
n.421-25383A>C
12g.6019318T>ACA383505309VWFc.4100A>T (p.Gln1367Leu)
n.421-25384A>T
12g.6019318T>CCA383505311VWFc.4100A>G (p.Gln1367Arg)
n.421-25384A>G
12g.6019318T>GCA383505308VWFc.4100A>C (p.Gln1367Pro)
n.421-25384A>C
12g.6019319G>ACA383505314VWFc.4099C>T (p.Gln1367Ter)
n.421-25385C>T
12g.6019319G>CCA383505315VWFc.4099C>G (p.Gln1367Glu)
n.421-25385C>G
12g.6019319G>TCA383505317VWFc.4099C>A (p.Gln1367Lys)
n.421-25385C>A
12g.6019320G>ACA478502330VWFc.4098C>T (p.Phe1366=)
n.421-25386C>T
dbSNP gnomAD v3 gnomAD v4
12g.6019320G>CCA6402602VWFc.4098C>G (p.Phe1366Leu)
n.421-25386C>G
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.6019320G=CA2013872915VWFc.4098C= (p.Phe1366=)
n.421-25386C=
12g.6019320G>TCA383505320VWFc.4098C>A (p.Phe1366Leu)
n.421-25386C>A
dbSNP gnomAD v4
12g.6019321A=CA2013872916VWFc.4097T= (p.Phe1366=)
n.421-25387T=
12g.6019321A>CCA383505326VWFc.4097T>G (p.Phe1366Cys)
n.421-25387T>G
gnomAD v4
12g.6019321A>GCA383505322VWFc.4097T>C (p.Phe1366Ser)
n.421-25387T>C
dbSNP
12g.6019321A>TCA383505324VWFc.4097T>A (p.Phe1366Tyr)
n.421-25387T>A
12g.6019322A>CCA383505327VWFc.4096T>G (p.Phe1366Val)
n.421-25388T>G
12g.6019322A>GCA383505328VWFc.4096T>C (p.Phe1366Leu)
n.421-25388T>C
12g.6019322A>TCA383505329VWFc.4096T>A (p.Phe1366Ile)
n.421-25388T>A
12g.6019323C>ACA6402604VWFc.4095G>T (p.Leu1365=)
n.421-25389G>T
dbSNP ExAC gnomAD v2 gnomAD v4
12g.6019323C=CA2013872917VWFc.4095G= (p.Leu1365=)
n.421-25389G=
12g.6019323C>GCA478502331VWFc.4095G>C (p.Leu1365=)
n.421-25389G>C
12g.6019323C>TCA6402603VWFc.4095G>A (p.Leu1365=)
n.421-25389G>A
dbSNP ExAC gnomAD v2 gnomAD v4
12g.6019324A=CA2013872919VWFc.4094T= (p.Leu1365=)
n.421-25390T=
12g.6019324A>CCA383505335VWFc.4094T>G (p.Leu1365Arg)
n.421-25390T>G
gnomAD v4
12g.6019324A>GCA383505339VWFc.4094T>C (p.Leu1365Pro)
n.421-25390T>C
ClinVar dbSNP
12g.6019324A>TCA6402605VWFc.4094T>A (p.Leu1365Gln)
n.421-25390T>A
dbSNP ExAC gnomAD v2 gnomAD v4
12g.6019324_6019325delCA2617230629VWFc.4093_4094del (p.Leu1365ValfsTer11)
n.421-25391_421-25390del
gnomAD v4
12g.6019324_6019326delinsAGTCA2013872918VWFc.4092_4094delinsACT (p.Thr1364=)
n.421-25392_421-25390delinsACT
12g.6019325G>ACA478502332VWFc.4093C>T (p.Leu1365=)
n.421-25391C>T
12g.6019325G>CCA383505341VWFc.4093C>G (p.Leu1365Val)
n.421-25391C>G
12g.6019325G>TCA383505343VWFc.4093C>A (p.Leu1365Met)
n.421-25391C>A
12g.6019329_6019330delCA228532VWFc.4092_4093del (p.Leu1365ValfsTer11)
n.421-25392_421-25391del
ClinVar dbSNP
12g.6019326T>ACA478502333VWFc.4092A>T (p.Thr1364=)
n.421-25392A>T
12g.6019326T>CCA6402606VWFc.4092A>G (p.Thr1364=)
n.421-25392A>G
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.6019326T>GCA478502334VWFc.4092A>C (p.Thr1364=)
n.421-25392A>C
12g.6019326T=CA2013872920VWFc.4092A= (p.Thr1364=)
n.421-25392A=
12g.6019327G>ACA383505347VWFc.4091C>T (p.Thr1364Ile)
n.421-25393C>T
dbSNP
12g.6019327G>CCA383505349VWFc.4091C>G (p.Thr1364Arg)
n.421-25393C>G
12g.6019327G=CA2013872921VWFc.4091C= (p.Thr1364=)
n.421-25393C=
12g.6019327G>TCA383505351VWFc.4091C>A (p.Thr1364Lys)
n.421-25393C>A
12g.6019328T>ACA6402607VWFc.4090A>T (p.Thr1364Ser)
n.421-25394A>T
dbSNP ExAC
12g.6019328T>CCA383505353VWFc.4090A>G (p.Thr1364Ala)
n.421-25394A>G
dbSNP gnomAD v3 gnomAD v4
12g.6019328T>GCA383505354VWFc.4090A>C (p.Thr1364Pro)
n.421-25394A>C
12g.6019328T=CA2013872922VWFc.4090A= (p.Thr1364=)
n.421-25394A=
12g.6019328_6019329delinsTGCA2013872923VWFc.4089_4090delinsCA (p.Tyr1363=)
n.421-25395_421-25394delinsCA
12g.6019329delCA2013872924VWFc.4089del (p.Tyr1363Ter)
n.421-25395del
dbSNP
12g.6019329G>ACA478502335VWFc.4089C>T (p.Tyr1363=)
n.421-25395C>T
gnomAD v4
12g.6019329G>CCA383505356VWFc.4089C>G (p.Tyr1363Ter)
n.421-25395C>G
12g.6019329G>TCA383505358VWFc.4089C>A (p.Tyr1363Ter)
n.421-25395C>A
12g.6019330T>ACA383505362VWFc.4088A>T (p.Tyr1363Phe)
n.421-25396A>T
12g.6019330T>CCA383505363VWFc.4088A>G (p.Tyr1363Cys)
n.421-25396A>G
gnomAD v4
12g.6019330T>GCA383505360VWFc.4088A>C (p.Tyr1363Ser)
n.421-25396A>C
12g.6019331A>CCA383505368VWFc.4087T>G (p.Tyr1363Asp)
n.421-25397T>G
12g.6019331A>GCA383505366VWFc.4087T>C (p.Tyr1363His)
n.421-25397T>C
12g.6019331A>TCA383505372VWFc.4087T>A (p.Tyr1363Asn)
n.421-25397T>A
12g.6019332T>ACA383505373VWFc.4086A>T (p.Lys1362Asn)
n.421-25398A>T
12g.6019332T>CCA478502336VWFc.4086A>G (p.Lys1362=)
n.421-25398A>G
dbSNP gnomAD v2 gnomAD v4
12g.6019332T>GCA383505374VWFc.4086A>C (p.Lys1362Asn)
n.421-25398A>C
12g.6019332T=CA2013872925VWFc.4086A= (p.Lys1362=)
n.421-25398A=
12g.6019333T>ACA383505376VWFc.4085A>T (p.Lys1362Ile)
n.421-25399A>T
12g.6019333T>CCA383505378VWFc.4085A>G (p.Lys1362Arg)
n.421-25399A>G
12g.6019333T>GCA228530VWFc.4085A>C (p.Lys1362Thr)
n.421-25399A>C
ClinVar dbSNP
12g.6019333T=CA2013872926VWFc.4085A= (p.Lys1362=)
n.421-25399A=
12g.6019334T>ACA383505380VWFc.4084A>T (p.Lys1362Ter)
n.421-25400A>T
12g.6019334T>CCA383505382VWFc.4084A>G (p.Lys1362Glu)
n.421-25400A>G
12g.6019334T>GCA383505384VWFc.4084A>C (p.Lys1362Gln)
n.421-25400A>C
12g.6019335C>ACA383505387VWFc.4083G>T (p.Leu1361Phe)
n.421-25401G>T
12g.6019335C=CA2013872927VWFc.4083G= (p.Leu1361=)
n.421-25401G=
12g.6019335C>GCA383505389VWFc.4083G>C (p.Leu1361Phe)
n.421-25401G>C
12g.6019335C>TCA6402608VWFc.4083G>A (p.Leu1361=)
n.421-25401G>A
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.6019336A=CA2013872928VWFc.4082T= (p.Leu1361=)
n.421-25402T=
12g.6019336A>CCA383505395VWFc.4082T>G (p.Leu1361Trp)
n.421-25402T>G
12g.6019336A>GCA228528VWFc.4082T>C (p.Leu1361Ser)
n.421-25402T>C
ClinVar dbSNP gnomAD v4
12g.6019336A>TCA383505393VWFc.4082T>A (p.Leu1361Ter)
n.421-25402T>A
12g.6019337A>CCA383505397VWFc.4081T>G (p.Leu1361Val)
n.421-25403T>G
12g.6019337A>GCA478502337VWFc.4081T>C (p.Leu1361=)
n.421-25403T>C
gnomAD v4
12g.6019337A>TCA383505399VWFc.4081T>A (p.Leu1361Met)
n.421-25403T>A
12g.6019338G>ACA6402609VWFc.4080C>T (p.Val1360=)
n.421-25404C>T
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.6019338G>CCA478502338VWFc.4080C>G (p.Val1360=)
n.421-25404C>G
12g.6019338G=CA2013872929VWFc.4080C= (p.Val1360=)
n.421-25404C=
12g.6019338G>TCA478502339VWFc.4080C>A (p.Val1360=)
n.421-25404C>A
12g.6019339A=CA2013872930VWFc.4079T= (p.Val1360=)
n.421-25405T=
12g.6019339A>CCA383505402VWFc.4079T>G (p.Val1360Gly)
n.421-25405T>G
12g.6019339A>GCA228526VWFc.4079T>C (p.Val1360Ala)
n.421-25405T>C
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.6019339A>TCA383505405VWFc.4079T>A (p.Val1360Asp)
n.421-25405T>A
12g.6019340C>ACA383505406VWFc.4078G>T (p.Val1360Phe)
n.421-25406G>T
ClinVar
12g.6019340C>GCA383505407VWFc.4078G>C (p.Val1360Leu)
n.421-25406G>C
12g.6019340C>TCA383505408VWFc.4078G>A (p.Val1360Ile)
n.421-25406G>A
12g.6019341C>ACA383505411VWFc.4077G>T (p.Glu1359Asp)
n.421-25407G>T
12g.6019341C>GCA383505413VWFc.4077G>C (p.Glu1359Asp)
n.421-25407G>C
12g.6019341C>TCA478502340VWFc.4077G>A (p.Glu1359=)
n.421-25407G>A
12g.6019342T>ACA383505420VWFc.4076A>T (p.Glu1359Val)
n.421-25408A>T
12g.6019342T>CCA383505422VWFc.4076A>G (p.Glu1359Gly)
n.421-25408A>G
12g.6019342T>GCA383505417VWFc.4076A>C (p.Glu1359Ala)
n.421-25408A>C
12g.6019343C>ACA383505426VWFc.4075G>T (p.Glu1359Ter)
n.421-25409G>T
12g.6019343C=CA2013872931VWFc.4075G= (p.Glu1359=)
n.421-25409G=
12g.6019343C>GCA383505430VWFc.4075G>C (p.Glu1359Gln)
n.421-25409G>C
gnomAD v4
12g.6019343C>TCA228524VWFc.4075G>A (p.Glu1359Lys)
n.421-25409G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.6019344G>ACA6402610VWFc.4074C>T (p.Ser1358=)
n.421-25410C>T
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.6019344G>CCA383505434VWFc.4074C>G (p.Ser1358Arg)
n.421-25410C>G
12g.6019344G=CA2013872932VWFc.4074C= (p.Ser1358=)
n.421-25410C=
12g.6019344G>TCA383505435VWFc.4074C>A (p.Ser1358Arg)
n.421-25410C>A
12g.6019345C>ACA383505439VWFc.4073G>T (p.Ser1358Ile)
n.421-25411G>T
12g.6019345C>GCA383505441VWFc.4073G>C (p.Ser1358Thr)
n.421-25411G>C
12g.6019345C>TCA383505443VWFc.4073G>A (p.Ser1358Asn)
n.421-25411G>A
12g.6019346T>ACA383505449VWFc.4072A>T (p.Ser1358Cys)
n.421-25412A>T
12g.6019346T>CCA383505451VWFc.4072A>G (p.Ser1358Gly)
n.421-25412A>G
12g.6019346T>GCA383505452VWFc.4072A>C (p.Ser1358Arg)
n.421-25412A>C
gnomAD v4
12g.6019347G>ACA478502341VWFc.4071C>T (p.Thr1357=)
n.421-25413C>T
gnomAD v4
12g.6019347G>CCA478502342VWFc.4071C>G (p.Thr1357=)
n.421-25413C>G
gnomAD v4
12g.6019347G>TCA478502343VWFc.4071C>A (p.Thr1357=)
n.421-25413C>A
12g.6019348G>ACA383505459VWFc.4070C>T (p.Thr1357Ile)
n.421-25414C>T
gnomAD v4
12g.6019348G>CCA6402611VWFc.4070C>G (p.Thr1357Ser)
n.421-25414C>G
dbSNP ExAC gnomAD v2 gnomAD v4
12g.6019348G=CA2013872933VWFc.4070C= (p.Thr1357=)
n.421-25414C=
12g.6019348G>TCA383505455VWFc.4070C>A (p.Thr1357Asn)
n.421-25414C>A
12g.6019349T>ACA383505464VWFc.4069A>T (p.Thr1357Ser)
n.421-25415A>T
12g.6019349T>CCA383505468VWFc.4069A>G (p.Thr1357Ala)
n.421-25415A>G
12g.6019349T>GCA383505475VWFc.4069A>C (p.Thr1357Pro)
n.421-25415A>C
gnomAD v4
12g.6019350G>ACA478502344VWFc.4068C>T (p.Ser1356=)
n.421-25416C>T
gnomAD v4
12g.6019350G>CCA478502346VWFc.4068C>G (p.Ser1356=)
n.421-25416C>G
12g.6019350G>TCA478502345VWFc.4068C>A (p.Ser1356=)
n.421-25416C>A
12g.6019351delCA2575053891VWFc.4068del (p.Thr1357ProfsTer5)
n.421-25416del
12g.6019351G>ACA383505478VWFc.4067C>T (p.Ser1356Phe)
n.421-25417C>T
ClinVar
12g.6019351G>CCA383505481VWFc.4067C>G (p.Ser1356Cys)
n.421-25417C>G
12g.6019351G>TCA383505483VWFc.4067C>A (p.Ser1356Tyr)
n.421-25417C>A
12g.6019352A>CCA383505487VWFc.4066T>G (p.Ser1356Ala)
n.421-25418T>G
12g.6019352A>GCA383505488VWFc.4066T>C (p.Ser1356Pro)
n.421-25418T>C
12g.6019352A>TCA383505502VWFc.4066T>A (p.Ser1356Thr)
n.421-25418T>A
12g.6019353G>ACA478502347VWFc.4065C>T (p.Ala1355=)
n.421-25419C>T
12g.6019353G>CCA6402612VWFc.4065C>G (p.Ala1355=)
n.421-25419C>G
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.6019353G=CA2013872934VWFc.4065C= (p.Ala1355=)
n.421-25419C=
12g.6019353G>TCA478502348VWFc.4065C>A (p.Ala1355=)
n.421-25419C>A
12g.6019354G>ACA383505508VWFc.4064C>T (p.Ala1355Val)
n.421-25420C>T
dbSNP gnomAD v3 gnomAD v4
12g.6019354G>CCA383505509VWFc.4064C>G (p.Ala1355Gly)
n.421-25420C>G
12g.6019354G=CA2013872935VWFc.4064C= (p.Ala1355=)
n.421-25420C=
12g.6019354G>TCA383505511VWFc.4064C>A (p.Ala1355Asp)
n.421-25420C>A
12g.6019355C>ACA383505518VWFc.4063G>T (p.Ala1355Ser)
n.421-25421G>T
12g.6019355C>GCA383505523VWFc.4063G>C (p.Ala1355Pro)
n.421-25421G>C
12g.6019355C>TCA383505516VWFc.4063G>A (p.Ala1355Thr)
n.421-25421G>A
12g.6019356dupCA2532169638VWFc.4063dup (p.Ala1355GlyfsTer22)
n.421-25421dup
12g.6019356C>ACA478502349VWFc.4062G>T (p.Val1354=)
n.421-25422G>T
12g.6019356C=CA2013872936VWFc.4062G= (p.Val1354=)
n.421-25422G=
12g.6019356C>GCA478502350VWFc.4062G>C (p.Val1354=)
n.421-25422G>C
12g.6019356C>TCA6402613VWFc.4062G>A (p.Val1354=)
n.421-25422G>A
dbSNP ExAC gnomAD v2 gnomAD v4
12g.6019357A>CCA383505528VWFc.4061T>G (p.Val1354Gly)
n.421-25423T>G
12g.6019357A>GCA383505533VWFc.4061T>C (p.Val1354Ala)
n.421-25423T>C
12g.6019357A>TCA383505537VWFc.4061T>A (p.Val1354Glu)
n.421-25423T>A
12g.6019358C>ACA383505542VWFc.4060G>T (p.Val1354Leu)
n.421-25424G>T
12g.6019358C>GCA383505544VWFc.4060G>C (p.Val1354Leu)
n.421-25424G>C
12g.6019358C>TCA383505547VWFc.4060G>A (p.Val1354Met)
n.421-25424G>A
12g.6019359C>ACA6402614VWFc.4059G>T (p.Gln1353His)
n.421-25425G>T
dbSNP ExAC gnomAD v2 gnomAD v4
12g.6019359C=CA2013872937VWFc.4059G= (p.Gln1353=)
n.421-25425G=
12g.6019359C>GCA383505551VWFc.4059G>C (p.Gln1353His)
n.421-25425G>C
12g.6019359C>TCA478502351VWFc.4059G>A (p.Gln1353=)
n.421-25425G>A
12g.6019360T>ACA383505555VWFc.4058A>T (p.Gln1353Leu)
n.421-25426A>T
gnomAD v3 gnomAD v4
12g.6019360T>CCA383505558VWFc.4058A>G (p.Gln1353Arg)
n.421-25426A>G
12g.6019360T>GCA383505561VWFc.4058A>C (p.Gln1353Pro)
n.421-25426A>C
12g.6019361G>ACA383505565VWFc.4057C>T (p.Gln1353Ter)
n.421-25427C>T
dbSNP gnomAD v2 gnomAD v4
12g.6019361G>CCA383505568VWFc.4057C>G (p.Gln1353Glu)
n.421-25427C>G
12g.6019361G=CA2013872938VWFc.4057C= (p.Gln1353=)
n.421-25427C=
12g.6019361G>TCA383505570VWFc.4057C>A (p.Gln1353Lys)
n.421-25427C>A
12g.6019362G>ACA478502352VWFc.4056C>T (p.Ser1352=)
n.421-25428C>T
gnomAD v4
12g.6019362G>CCA383505575VWFc.4056C>G (p.Ser1352Arg)
n.421-25428C>G
12g.6019362G>TCA383505577VWFc.4056C>A (p.Ser1352Arg)
n.421-25428C>A
12g.6019363C>ACA383505582VWFc.4055G>T (p.Ser1352Ile)
n.421-25429G>T
gnomAD v4
12g.6019363C>GCA383505592VWFc.4055G>C (p.Ser1352Thr)
n.421-25429G>C
12g.6019363C>TCA383505596VWFc.4055G>A (p.Ser1352Asn)
n.421-25429G>A
gnomAD v4
12g.6019364T>ACA383505600VWFc.4054A>T (p.Ser1352Cys)
n.421-25430A>T
12g.6019364T>CCA383505602VWFc.4054A>G (p.Ser1352Gly)
n.421-25430A>G
COSMIC
12g.6019364T>GCA383505608VWFc.4054A>C (p.Ser1352Arg)
n.421-25430A>C
12g.6019365G>ACA478502353VWFc.4053C>T (p.Gly1351=)
n.421-25431C>T
12g.6019365G>CCA478502354VWFc.4053C>G (p.Gly1351=)
n.421-25431C>G
12g.6019365G>TCA478502355VWFc.4053C>A (p.Gly1351=)
n.421-25431C>A
12g.6019366C>ACA383505611VWFc.4052G>T (p.Gly1351Val)
n.421-25432G>T
12g.6019366C>GCA383505612VWFc.4052G>C (p.Gly1351Ala)
n.421-25432G>C
gnomAD v4
12g.6019366C>TCA383505619VWFc.4052G>A (p.Gly1351Asp)
n.421-25432G>A
12g.6019367C>ACA383505621VWFc.4051G>T (p.Gly1351Cys)
n.421-25433G>T
12g.6019367C=CA2013872939VWFc.4051G= (p.Gly1351=)
n.421-25433G=
12g.6019367C>GCA383505625VWFc.4051G>C (p.Gly1351Arg)
n.421-25433G>C
12g.6019367C>TCA383505629VWFc.4051G>A (p.Gly1351Ser)
n.421-25433G>A
dbSNP gnomAD v2 gnomAD v4
12g.6019368C>ACA478502356VWFc.4050G>T (p.Ala1350=)
n.421-25434G>T
12g.6019368C=CA2013872940VWFc.4050G= (p.Ala1350=)
n.421-25434G=
12g.6019368C>GCA478502357VWFc.4050G>C (p.Ala1350=)
n.421-25434G>C
12g.6019368C>TCA6402615VWFc.4050G>A (p.Ala1350=)
n.421-25434G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.6019369G>ACA6402616VWFc.4049C>T (p.Ala1350Val)
n.421-25435C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
12g.6019369G>CCA383505634VWFc.4049C>G (p.Ala1350Gly)
n.421-25435C>G
12g.6019369G=CA2013872941VWFc.4049C= (p.Ala1350=)
n.421-25435C=
12g.6019369G>TCA383505632VWFc.4049C>A (p.Ala1350Glu)
n.421-25435C>A
12g.6019370C>ACA383505638VWFc.4048G>T (p.Ala1350Ser)
n.421-25436G>T
12g.6019370C>GCA383505640VWFc.4048G>C (p.Ala1350Pro)
n.421-25436G>C
12g.6019370C>TCA383505643VWFc.4048G>A (p.Ala1350Thr)
n.421-25436G>A
12g.6019371A=CA2013872942VWFc.4047T= (p.Tyr1349=)
n.421-25437T=
12g.6019371A>CCA383505646VWFc.4047T>G (p.Tyr1349Ter)
n.421-25437T>G
12g.6019371A>GCA478502359VWFc.4047T>C (p.Tyr1349=)
n.421-25437T>C
dbSNP gnomAD v2 gnomAD v4
12g.6019371A>TCA383505647VWFc.4047T>A (p.Tyr1349Ter)
n.421-25437T>A
12g.6019372T>ACA383505653VWFc.4046A>T (p.Tyr1349Phe)
n.421-25438A>T
dbSNP gnomAD v4
12g.6019372T>CCA383505652VWFc.4046A>G (p.Tyr1349Cys)
n.421-25438A>G
12g.6019372T>GCA383505651VWFc.4046A>C (p.Tyr1349Ser)
n.421-25438A>C
12g.6019373A>CCA383505656VWFc.4045T>G (p.Tyr1349Asp)
n.421-25439T>G
12g.6019373A>GCA383505658VWFc.4045T>C (p.Tyr1349His)
n.421-25439T>C
12g.6019373A>TCA383505660VWFc.4045T>A (p.Tyr1349Asn)
n.421-25439T>A
12g.6019374C>ACA383505663VWFc.4044G>T (p.Lys1348Asn)
n.421-25440G>T
dbSNP gnomAD v3 gnomAD v4
12g.6019374C=CA2013872943VWFc.4044G= (p.Lys1348=)
n.421-25440G=
12g.6019374C>GCA383505664VWFc.4044G>C (p.Lys1348Asn)
n.421-25440G>C
12g.6019374C>TCA6402617VWFc.4044G>A (p.Lys1348=)
n.421-25440G>A
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.6019375T>ACA383505668VWFc.4043A>T (p.Lys1348Met)
n.421-25441A>T
12g.6019375T>CCA383505672VWFc.4043A>G (p.Lys1348Arg)
n.421-25441A>G
12g.6019375T>GCA383505670VWFc.4043A>C (p.Lys1348Thr)
n.421-25441A>C
12g.6019376T>ACA383505673VWFc.4042A>T (p.Lys1348Ter)
n.421-25442A>T
12g.6019376T>CCA6402618VWFc.4042A>G (p.Lys1348Glu)
n.421-25442A>G
dbSNP ExAC gnomAD v2 gnomAD v4
12g.6019376T>GCA383505675VWFc.4042A>C (p.Lys1348Gln)
n.421-25442A>C
12g.6019376T=CA2013872944VWFc.4042A= (p.Lys1348=)
n.421-25442A=
12g.6019377C>ACA478502360VWFc.4041G>T (p.Val1347=)
n.421-25443G>T
12g.6019377C=CA2013872945VWFc.4041G= (p.Val1347=)
n.421-25443G=
12g.6019377C>GCA478502361VWFc.4041G>C (p.Val1347=)
n.421-25443G>C
12g.6019377C>TCA478502362VWFc.4041G>A (p.Val1347=)
n.421-25443G>A
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
12g.6019378A>CCA383505677VWFc.4040T>G (p.Val1347Gly)
n.421-25444T>G
12g.6019378A>GCA383505679VWFc.4040T>C (p.Val1347Ala)
n.421-25444T>C
12g.6019378A>TCA383505681VWFc.4040T>A (p.Val1347Glu)
n.421-25444T>A
12g.6019379C>ACA383505684VWFc.4039G>T (p.Val1347Leu)
n.421-25445G>T
12g.6019379C>GCA383505686VWFc.4039G>C (p.Val1347Leu)
n.421-25445G>C
12g.6019379C>TCA383505687VWFc.4039G>A (p.Val1347Met)
n.421-25445G>A
12g.6019380C>ACA383505690VWFc.4038G>T (p.Gln1346His)
n.421-25446G>T
12g.6019380C>GCA383505692VWFc.4038G>C (p.Gln1346His)
n.421-25446G>C
12g.6019380C>TCA478502363VWFc.4038G>A (p.Gln1346=)
n.421-25446G>A
gnomAD v4
12g.6019381T>ACA383505697VWFc.4037A>T (p.Gln1346Leu)
n.421-25447A>T
12g.6019381T>CCA6402619VWFc.4037A>G (p.Gln1346Arg)
n.421-25447A>G
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
12g.6019381T>GCA383505695VWFc.4037A>C (p.Gln1346Pro)
n.421-25447A>C
12g.6019381T=CA2013872946VWFc.4037A= (p.Gln1346=)
n.421-25447A=
12g.6019382G>ACA228522VWFc.4036C>T (p.Gln1346Ter)
n.421-25448C>T
ClinVar dbSNP
12g.6019382G>CCA383505701VWFc.4036C>G (p.Gln1346Glu)
n.421-25448C>G
12g.6019382G=CA2013872947VWFc.4036C= (p.Gln1346=)
n.421-25448C=
12g.6019382G>TCA383505703VWFc.4036C>A (p.Gln1346Lys)
n.421-25448C>A
12g.6019383G>ACA6402620VWFc.4035C>T (p.Ser1345=)
n.421-25449C>T
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.6019383G>CCA383505705VWFc.4035C>G (p.Ser1345Arg)
n.421-25449C>G
12g.6019383G=CA2013872948VWFc.4035C= (p.Ser1345=)
n.421-25449C=
12g.6019383G>TCA383505704VWFc.4035C>A (p.Ser1345Arg)
n.421-25449C>A
12g.6019384C>ACA383505706VWFc.4034G>T (p.Ser1345Ile)
n.421-25450G>T
12g.6019384C>GCA383505707VWFc.4034G>C (p.Ser1345Thr)
n.421-25450G>C
12g.6019384C>TCA383505708VWFc.4034G>A (p.Ser1345Asn)
n.421-25450G>A
12g.6019385T>ACA383505709VWFc.4033A>T (p.Ser1345Cys)
n.421-25451A>T
12g.6019385T>CCA383505710VWFc.4033A>G (p.Ser1345Gly)
n.421-25451A>G
12g.6019385T>GCA383505711VWFc.4033A>C (p.Ser1345Arg)
n.421-25451A>C
12g.6019386G>ACA478502364VWFc.4032C>T (p.Ala1344=)
n.421-25452C>T
COSMIC
12g.6019386G>CCA478502365VWFc.4032C>G (p.Ala1344=)
n.421-25452C>G
12g.6019386G>TCA478502366VWFc.4032C>A (p.Ala1344=)
n.421-25452C>A
12g.6019387G>ACA383505712VWFc.4031C>T (p.Ala1344Val)
n.421-25453C>T
12g.6019387G>CCA383505713VWFc.4031C>G (p.Ala1344Gly)
n.421-25453C>G
12g.6019387G>TCA383505714VWFc.4031C>A (p.Ala1344Asp)
n.421-25453C>A
12g.6019388C>ACA383505715VWFc.4030G>T (p.Ala1344Ser)
n.421-25454G>T
12g.6019388C>GCA383505716VWFc.4030G>C (p.Ala1344Pro)
n.421-25454G>C
12g.6019388C>TCA383505717VWFc.4030G>A (p.Ala1344Thr)
n.421-25454G>A
12g.6019389A=CA2013872949VWFc.4029T= (p.Ile1343=)
n.421-25455T=
12g.6019389A>CCA383505718VWFc.4029T>G (p.Ile1343Met)
n.421-25455T>G
12g.6019389A>GCA478502367VWFc.4029T>C (p.Ile1343=)
n.421-25455T>C
12g.6019389A>TCA6402621VWFc.4029T>A (p.Ile1343=)
n.421-25455T>A
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.6019390dupCA2575053892VWFc.4029dup (p.Ala1344CysfsTer?)
n.421-25455dup
12g.6019390A>CCA383505719VWFc.4028T>G (p.Ile1343Ser)
n.421-25456T>G
12g.6019390A>GCA383505720VWFc.4028T>C (p.Ile1343Thr)
n.421-25456T>C
gnomAD v4
12g.6019390A>TCA383505721VWFc.4028T>A (p.Ile1343Asn)
n.421-25456T>A
12g.6019391T>ACA383505722VWFc.4027A>T (p.Ile1343Phe)
n.421-25457A>T
12g.6019391T>CCA228520VWFc.4027A>G (p.Ile1343Val)
n.421-25457A>G
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.6019391T>GCA383505723VWFc.4027A>C (p.Ile1343Leu)
n.421-25457A>C
12g.6019391T=CA2013872950VWFc.4027A= (p.Ile1343=)
n.421-25457A=
12g.6019392G>ACA478502368VWFc.4026C>T (p.Arg1342=)
n.421-25458C>T
12g.6019392G>CCA6402622VWFc.4026C>G (p.Arg1342=)
n.421-25458C>G
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.6019392G=CA2013872951VWFc.4026C= (p.Arg1342=)
n.421-25458C=
12g.6019392G>TCA478502369VWFc.4026C>A (p.Arg1342=)
n.421-25458C>A
12g.6019393C>ACA383505724VWFc.4025G>T (p.Arg1342Leu)
n.421-25459G>T
12g.6019393C=CA2013872952VWFc.4025G= (p.Arg1342=)
n.421-25459G=
12g.6019393C>GCA383505726VWFc.4025G>C (p.Arg1342Pro)
n.421-25459G>C
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
12g.6019393C>TCA6402623VWFc.4025G>A (p.Arg1342His)
n.421-25459G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
12g.6019393_6019394delinsCGCA2013872953VWFc.4024_4025delinsCG (p.Arg1342=)
n.421-25460_421-25459delinsCG
12g.6019394delCA2013872954VWFc.4024del (p.Arg1342AlafsTer6)
n.421-25460del
12g.6019394G>ACA228959VWFc.4024C>T (p.Arg1342Cys)
n.421-25460C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.6019394G>CCA383505733VWFc.4024C>G (p.Arg1342Gly)
n.421-25460C>G
12g.6019394G=CA2013872955VWFc.4024C= (p.Arg1342=)
n.421-25460C=
12g.6019394G>TCA383505729VWFc.4024C>A (p.Arg1342Ser)
n.421-25460C>A
12g.6019395C>ACA478502370VWFc.4023G>T (p.Arg1341=)
n.421-25461G>T
12g.6019395C>GCA478502371VWFc.4023G>C (p.Arg1341=)
n.421-25461G>C
12g.6019395C>TCA478502372VWFc.4023G>A (p.Arg1341=)
n.421-25461G>A
12g.6019396C>ACA228518VWFc.4022G>T (p.Arg1341Leu)
n.421-25462G>T
ClinVar dbSNP
12g.6019396C=CA2013872956VWFc.4022G= (p.Arg1341=)
n.421-25462G=
12g.6019396C>GCA228516VWFc.4022G>C (p.Arg1341Pro)
n.421-25462G>C
ClinVar dbSNP
12g.6019396C>TCA114129VWFc.4022G>A (p.Arg1341Gln)
n.421-25462G>A
ClinVar dbSNP gnomAD v2 gnomAD v4
12g.6019397G>ACA228514VWFc.4021C>T (p.Arg1341Trp)
n.421-25463C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.6019397G>CCA383505741VWFc.4021C>G (p.Arg1341Gly)
n.421-25463C>G
12g.6019397G=CA2013872957VWFc.4021C= (p.Arg1341=)
n.421-25463C=
12g.6019397G>TCA478502373VWFc.4021C>A (p.Arg1341=)
n.421-25463C>A
12g.6019398C>ACA478502374VWFc.4020G>T (p.Leu1340=)
n.421-25464G>T
12g.6019398C>GCA478502375VWFc.4020G>C (p.Leu1340=)
n.421-25464G>C
12g.6019398C>TCA478502376VWFc.4020G>A (p.Leu1340=)
n.421-25464G>A
12g.6019399A>CCA383505742VWFc.4019T>G (p.Leu1340Arg)
n.421-25465T>G
12g.6019399A>GCA383505745VWFc.4019T>C (p.Leu1340Pro)
n.421-25465T>C
ClinVar
12g.6019399A>TCA383505747VWFc.4019T>A (p.Leu1340Gln)
n.421-25465T>A
12g.6019400G>ACA478502377VWFc.4018C>T (p.Leu1340=)
n.421-25466C>T
12g.6019400G>CCA383505750VWFc.4018C>G (p.Leu1340Val)
n.421-25466C>G
12g.6019400G>TCA383505752VWFc.4018C>A (p.Leu1340Met)
n.421-25466C>A
12g.6019401C>ACA383505754VWFc.4017G>T (p.Glu1339Asp)
n.421-25467G>T
12g.6019401C=CA2013872958VWFc.4017G= (p.Glu1339=)
n.421-25467G=
12g.6019401C>GCA383505756VWFc.4017G>C (p.Glu1339Asp)
n.421-25467G>C
ClinVar
12g.6019401C>TCA232297773VWFc.4017G>A (p.Glu1339=)
n.421-25467G>A
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
12g.6019402T>ACA383505760VWFc.4016A>T (p.Glu1339Val)
n.421-25468A>T
dbSNP gnomAD v2 gnomAD v4
12g.6019402T>CCA383505758VWFc.4016A>G (p.Glu1339Gly)
n.421-25468A>G
12g.6019402T>GCA383505759VWFc.4016A>C (p.Glu1339Ala)
n.421-25468A>C
12g.6019402T=CA2013872959VWFc.4016A= (p.Glu1339=)
n.421-25468A=
12g.6019403C>ACA383505763VWFc.4015G>T (p.Glu1339Ter)
n.421-25469G>T
12g.6019403C>GCA383505765VWFc.4015G>C (p.Glu1339Gln)
n.421-25469G>C
12g.6019403C>TCA383505766VWFc.4015G>A (p.Glu1339Lys)
n.421-25469G>A
12g.6019404T>ACA478502381VWFc.4014A>T (p.Ser1338=)
n.421-25470A>T
12g.6019404T>CCA478502380VWFc.4014A>G (p.Ser1338=)
n.421-25470A>G
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
12g.6019404T>GCA478502379VWFc.4014A>C (p.Ser1338=)
n.421-25470A>C
12g.6019404T=CA2013872960VWFc.4014A= (p.Ser1338=)
n.421-25470A=
12g.6019405G>ACA383505768VWFc.4013C>T (p.Ser1338Leu)
n.421-25471C>T
COSMIC
12g.6019405G>CCA228512VWFc.4013C>G (p.Ser1338Ter)
n.421-25471C>G
ClinVar dbSNP
12g.6019405G=CA2013872961VWFc.4013C= (p.Ser1338=)
n.421-25471C=
12g.6019405G>TCA383505770VWFc.4013C>A (p.Ser1338Ter)
n.421-25471C>A
12g.6019406A=CA2013872962VWFc.4012T= (p.Ser1338=)
n.421-25472T=
12g.6019406A>CCA6402624VWFc.4012T>G (p.Ser1338Ala)
n.421-25472T>G
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.6019406A>GCA383505773VWFc.4012T>C (p.Ser1338Pro)
n.421-25472T>C
12g.6019406A>TCA383505776VWFc.4012T>A (p.Ser1338Thr)
n.421-25472T>A
dbSNP
12g.6019407C>ACA478502382VWFc.4011G>T (p.Pro1337=)
n.421-25473G>T
12g.6019407C=CA2013872963VWFc.4011G= (p.Pro1337=)
n.421-25473G=
12g.6019407C>GCA478502383VWFc.4011G>C (p.Pro1337=)
n.421-25473G>C
12g.6019407C>TCA6402625VWFc.4011G>A (p.Pro1337=)
n.421-25473G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC

Number of alleles fetched