Chr Mutation (hg38) CAid Gene Transcript Linkouts
12g.6023703T>ACA383512169VWFc.3307A>T (p.Thr1103Ser)
n.421-29769A>T
gnomAD v4
12g.6023703T>CCA383512170VWFc.3307A>G (p.Thr1103Ala)
n.421-29769A>G
dbSNP gnomAD v2 gnomAD v4
12g.6023703T>GCA232298114VWFc.3307A>C (p.Thr1103Pro)
n.421-29769A>C
dbSNP
12g.6023703T=CA2013874889VWFc.3307A= (p.Thr1103=)
n.421-29769A=
12g.6023703_6023725delinsGGACA2499221805VWFc.3285_3307delinsTCC (p.Asp1096ProfsTer?)
n.421-29791_421-29769delinsTCC
ClinVar dbSNP
12g.6023704G>ACA478101602VWFc.3306C>T (p.Asp1102=)
n.421-29770C>T
12g.6023704G>CCA383512171VWFc.3306C>G (p.Asp1102Glu)
n.421-29770C>G
12g.6023704G>TCA383512172VWFc.3306C>A (p.Asp1102Glu)
n.421-29770C>A
12g.6023705T>ACA383512173VWFc.3305A>T (p.Asp1102Val)
n.421-29771A>T
12g.6023705T>CCA383512174VWFc.3305A>G (p.Asp1102Gly)
n.421-29771A>G
12g.6023705T>GCA383512175VWFc.3305A>C (p.Asp1102Ala)
n.421-29771A>C
12g.6023706C>ACA383512176VWFc.3304G>T (p.Asp1102Tyr)
n.421-29772G>T
12g.6023706C=CA2013874890VWFc.3304G= (p.Asp1102=)
n.421-29772G=
12g.6023706C>GCA383512177VWFc.3304G>C (p.Asp1102His)
n.421-29772G>C
12g.6023706C>TCA6402779VWFc.3304G>A (p.Asp1102Asn)
n.421-29772G>A
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.6023707G>ACA6402780VWFc.3303C>T (p.Cys1101=)
n.421-29773C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.6023707G>CCA228390VWFc.3303C>G (p.Cys1101Trp)
n.421-29773C>G
ClinVar dbSNP
12g.6023707G=CA2013874891VWFc.3303C= (p.Cys1101=)
n.421-29773C=
12g.6023707G>TCA383512178VWFc.3303C>A (p.Cys1101Ter)
n.421-29773C>A
gnomAD v4
12g.6023708C>ACA383512179VWFc.3302G>T (p.Cys1101Phe)
n.421-29774G>T
COSMIC
12g.6023708C>GCA383512180VWFc.3302G>C (p.Cys1101Ser)
n.421-29774G>C
12g.6023708C>TCA383512181VWFc.3302G>A (p.Cys1101Tyr)
n.421-29774G>A
12g.6023709A=CA2013874892VWFc.3301T= (p.Cys1101=)
n.421-29775T=
12g.6023709A>CCA232298115VWFc.3301T>G (p.Cys1101Gly)
n.421-29775T>G
dbSNP gnomAD v4
12g.6023709A>GCA228388VWFc.3301T>C (p.Cys1101Arg)
n.421-29775T>C
ClinVar dbSNP
12g.6023709A>TCA383512182VWFc.3301T>A (p.Cys1101Ser)
n.421-29775T>A
12g.6023710G>ACA478101611VWFc.3300C>T (p.Phe1100=)
n.421-29776C>T
gnomAD v4 COSMIC
12g.6023710G>CCA383512183VWFc.3300C>G (p.Phe1100Leu)
n.421-29776C>G
12g.6023710G>TCA383512184VWFc.3300C>A (p.Phe1100Leu)
n.421-29776C>A
12g.6023711A>CCA383512185VWFc.3299T>G (p.Phe1100Cys)
n.421-29777T>G
12g.6023711A>GCA383512186VWFc.3299T>C (p.Phe1100Ser)
n.421-29777T>C
gnomAD v4
12g.6023711A>TCA383512187VWFc.3299T>A (p.Phe1100Tyr)
n.421-29777T>A
12g.6023712A>CCA383512189VWFc.3298T>G (p.Phe1100Val)
n.421-29778T>G
12g.6023712A>GCA383512190VWFc.3298T>C (p.Phe1100Leu)
n.421-29778T>C
12g.6023712A>TCA383512188VWFc.3298T>A (p.Phe1100Ile)
n.421-29778T>A
12g.6023718_6023747delCA2695216052VWFc.3269_3298del (p.Ser1090_Cys1099del)
n.421-29807_421-29778del
12g.6023713G>ACA478101613VWFc.3297C>T (p.Cys1099=)
n.421-29779C>T
12g.6023713G>CCA383512191VWFc.3297C>G (p.Cys1099Trp)
n.421-29779C>G
12g.6023713G>TCA383512192VWFc.3297C>A (p.Cys1099Ter)
n.421-29779C>A
12g.6023714C>ACA383512193VWFc.3296G>T (p.Cys1099Phe)
n.421-29780G>T
12g.6023714C=CA2013874893VWFc.3296G= (p.Cys1099=)
n.421-29780G=
12g.6023714C>GCA383512194VWFc.3296G>C (p.Cys1099Ser)
n.421-29780G>C
12g.6023714C>TCA383512195VWFc.3296G>A (p.Cys1099Tyr)
n.421-29780G>A
dbSNP
12g.6023714_6023715delinsGGCA2695216053VWFc.3295_3296delinsCC (p.Cys1099Pro)
n.421-29781_421-29780delinsCC
12g.6023715A>CCA383512198VWFc.3295T>G (p.Cys1099Gly)
n.421-29781T>G
12g.6023715A>GCA383512197VWFc.3295T>C (p.Cys1099Arg)
n.421-29781T>C
12g.6023715A>TCA383512196VWFc.3295T>A (p.Cys1099Ser)
n.421-29781T>A
12g.6023716G>ACA478101614VWFc.3294C>T (p.Ala1098=)
n.421-29782C>T
12g.6023716G>CCA478101615VWFc.3294C>G (p.Ala1098=)
n.421-29782C>G
gnomAD v4
12g.6023716G>TCA478101617VWFc.3294C>A (p.Ala1098=)
n.421-29782C>A
12g.6023717G>ACA383512199VWFc.3293C>T (p.Ala1098Val)
n.421-29783C>T
12g.6023717G>CCA383512200VWFc.3293C>G (p.Ala1098Gly)
n.421-29783C>G
12g.6023717G>TCA383512201VWFc.3293C>A (p.Ala1098Asp)
n.421-29783C>A
12g.6023718C>ACA383512202VWFc.3292G>T (p.Ala1098Ser)
n.421-29784G>T
gnomAD v4
12g.6023718C=CA2013874894VWFc.3292G= (p.Ala1098=)
n.421-29784G=
12g.6023718C>GCA383512203VWFc.3292G>C (p.Ala1098Pro)
n.421-29784G>C
12g.6023718C>TCA6402781VWFc.3292G>A (p.Ala1098Thr)
n.421-29784G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
12g.6023719G>ACA6402782VWFc.3291C>T (p.Cys1097=)
n.421-29785C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.6023719G>CCA383512205VWFc.3291C>G (p.Cys1097Trp)
n.421-29785C>G
dbSNP gnomAD v2 gnomAD v4
12g.6023719G=CA2013874895VWFc.3291C= (p.Cys1097=)
n.421-29785C=
12g.6023719G>TCA383512204VWFc.3291C>A (p.Cys1097Ter)
n.421-29785C>A
12g.6023720C>ACA383512206VWFc.3290G>T (p.Cys1097Phe)
n.421-29786G>T
12g.6023720C=CA2013874897VWFc.3290G= (p.Cys1097=)
n.421-29786G=
12g.6023720C>GCA383512207VWFc.3290G>C (p.Cys1097Ser)
n.421-29786G>C
12g.6023720C>TCA232298116VWFc.3290G>A (p.Cys1097Tyr)
n.421-29786G>A
dbSNP
12g.6023721A>CCA383512208VWFc.3289T>G (p.Cys1097Gly)
n.421-29787T>G
12g.6023721A>GCA383512209VWFc.3289T>C (p.Cys1097Arg)
n.421-29787T>C
gnomAD v4
12g.6023721A>TCA383512210VWFc.3289T>A (p.Cys1097Ser)
n.421-29787T>A
12g.6023722G>ACA478101623VWFc.3288C>T (p.Asp1096=)
n.421-29788C>T
12g.6023722G>CCA383512211VWFc.3288C>G (p.Asp1096Glu)
n.421-29788C>G
12g.6023722G>TCA383512212VWFc.3288C>A (p.Asp1096Glu)
n.421-29788C>A
12g.6023723T>ACA383512213VWFc.3287A>T (p.Asp1096Val)
n.421-29789A>T
12g.6023723T>CCA383512214VWFc.3287A>G (p.Asp1096Gly)
n.421-29789A>G
12g.6023723T>GCA383512215VWFc.3287A>C (p.Asp1096Ala)
n.421-29789A>C
12g.6023724C>ACA383512217VWFc.3286G>T (p.Asp1096Tyr)
n.421-29790G>T
gnomAD v4
12g.6023724C=CA2013874900VWFc.3286G= (p.Asp1096=)
n.421-29790G=
12g.6023724C>GCA383512216VWFc.3286G>C (p.Asp1096His)
n.421-29790G>C
ClinVar dbSNP gnomAD v4
12g.6023724C>TCA6402783VWFc.3286G>A (p.Asp1096Asn)
n.421-29790G>A
dbSNP ExAC gnomAD v2 gnomAD v4
12g.6023725C>ACA478101626VWFc.3285G>T (p.Gly1095=)
n.421-29791G>T
12g.6023725C=CA2013874902VWFc.3285G= (p.Gly1095=)
n.421-29791G=
12g.6023725C>GCA478101627VWFc.3285G>C (p.Gly1095=)
n.421-29791G>C
12g.6023725C>TCA478101628VWFc.3285G>A (p.Gly1095=)
n.421-29791G>A
dbSNP gnomAD v2 gnomAD v4
12g.6023726C>ACA383512218VWFc.3284G>T (p.Gly1095Val)
n.421-29792G>T
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
12g.6023726C=CA2013874903VWFc.3284G= (p.Gly1095=)
n.421-29792G=
12g.6023726C>GCA383512220VWFc.3284G>C (p.Gly1095Ala)
n.421-29792G>C
12g.6023726C>TCA383512219VWFc.3284G>A (p.Gly1095Glu)
n.421-29792G>A
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
12g.6023727C>ACA383512221VWFc.3283G>T (p.Gly1095Trp)
n.421-29793G>T
gnomAD v4
12g.6023727C>GCA383512223VWFc.3283G>C (p.Gly1095Arg)
n.421-29793G>C
12g.6023727C>TCA383512222VWFc.3283G>A (p.Gly1095Arg)
n.421-29793G>A
12g.6023728A>CCA383512224VWFc.3282T>G (p.Ile1094Met)
n.421-29794T>G
gnomAD v4
12g.6023728A>GCA478101630VWFc.3282T>C (p.Ile1094=)
n.421-29794T>C
12g.6023728A>TCA478101631VWFc.3282T>A (p.Ile1094=)
n.421-29794T>A
gnomAD v4
12g.6023729A=CA2013874906VWFc.3281T= (p.Ile1094=)
n.421-29795T=
12g.6023729A>CCA383512226VWFc.3281T>G (p.Ile1094Ser)
n.421-29795T>G
COSMIC
12g.6023729A>GCA228386VWFc.3281T>C (p.Ile1094Thr)
n.421-29795T>C
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.6023729A>TCA383512225VWFc.3281T>A (p.Ile1094Asn)
n.421-29795T>A
12g.6023730T>ACA383512227VWFc.3280A>T (p.Ile1094Phe)
n.421-29796A>T
12g.6023730T>CCA383512228VWFc.3280A>G (p.Ile1094Val)
n.421-29796A>G
12g.6023730T>GCA383512229VWFc.3280A>C (p.Ile1094Leu)
n.421-29796A>C
12g.6023731G>ACA478101635VWFc.3279C>T (p.Ser1093=)
n.421-29797C>T
gnomAD v4
12g.6023731G>CCA478101636VWFc.3279C>G (p.Ser1093=)
n.421-29797C>G
12g.6023731G>TCA478101637VWFc.3279C>A (p.Ser1093=)
n.421-29797C>A
12g.6023732G>ACA383512230VWFc.3278C>T (p.Ser1093Phe)
n.421-29798C>T
12g.6023732G>CCA383512231VWFc.3278C>G (p.Ser1093Cys)
n.421-29798C>G
12g.6023732G>TCA383512232VWFc.3278C>A (p.Ser1093Tyr)
n.421-29798C>A
12g.6023733A>CCA383512233VWFc.3277T>G (p.Ser1093Ala)
n.421-29799T>G
12g.6023733A>GCA383512234VWFc.3277T>C (p.Ser1093Pro)
n.421-29799T>C
12g.6023733A>TCA383512235VWFc.3277T>A (p.Ser1093Thr)
n.421-29799T>A
12g.6023734C>ACA383512237VWFc.3276G>T (p.Glu1092Asp)
n.421-29800G>T
12g.6023734C>GCA383512236VWFc.3276G>C (p.Glu1092Asp)
n.421-29800G>C
gnomAD v4
12g.6023734C>TCA478101641VWFc.3276G>A (p.Glu1092=)
n.421-29800G>A
12g.6023735T>ACA383512238VWFc.3275A>T (p.Glu1092Val)
n.421-29801A>T
12g.6023735T>CCA383512239VWFc.3275A>G (p.Glu1092Gly)
n.421-29801A>G
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
12g.6023735T>GCA383512240VWFc.3275A>C (p.Glu1092Ala)
n.421-29801A>C
12g.6023735T=CA2013874907VWFc.3275A= (p.Glu1092=)
n.421-29801A=
12g.6023736C>ACA383512241VWFc.3274G>T (p.Glu1092Ter)
n.421-29802G>T
12g.6023736C>GCA383512242VWFc.3274G>C (p.Glu1092Gln)
n.421-29802G>C
12g.6023736C>TCA383512243VWFc.3274G>A (p.Glu1092Lys)
n.421-29802G>A
12g.6023737A>CCA383512244VWFc.3273T>G (p.Cys1091Trp)
n.421-29803T>G
12g.6023737A>GCA478101645VWFc.3273T>C (p.Cys1091=)
n.421-29803T>C
12g.6023737A>TCA383512245VWFc.3273T>A (p.Cys1091Ter)
n.421-29803T>A
12g.6023738C>ACA383512246VWFc.3272G>T (p.Cys1091Phe)
n.421-29804G>T
12g.6023738C>GCA383512247VWFc.3272G>C (p.Cys1091Ser)
n.421-29804G>C
12g.6023738C>TCA383512248VWFc.3272G>A (p.Cys1091Tyr)
n.421-29804G>A
12g.6023739A>CCA383512250VWFc.3271T>G (p.Cys1091Gly)
n.421-29805T>G
12g.6023739A>GCA383512251VWFc.3271T>C (p.Cys1091Arg)
n.421-29805T>C
gnomAD v4
12g.6023739A>TCA383512249VWFc.3271T>A (p.Cys1091Ser)
n.421-29805T>A
12g.6023739_6023740delinsAGCA2013874909VWFc.3270_3271delinsCT (p.Ser1090=)
n.421-29806_421-29805delinsCT
12g.6023740G>ACA478101651VWFc.3270C>T (p.Ser1090=)
n.421-29806C>T
dbSNP gnomAD v3 gnomAD v4
12g.6023740G>CCA478101650VWFc.3270C>G (p.Ser1090=)
n.421-29806C>G
12g.6023740G=CA2013874911VWFc.3270C= (p.Ser1090=)
n.421-29806C=
12g.6023740G>TCA478101653VWFc.3270C>A (p.Ser1090=)
n.421-29806C>A
COSMIC
12g.6023741delCA6402784VWFc.3270del (p.Cys1091ValfsTer28)
n.421-29806del
dbSNP ExAC gnomAD v2 gnomAD v4
12g.6023741G>ACA6402785VWFc.3269C>T (p.Ser1090Phe)
n.421-29807C>T
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.6023741G>CCA383512252VWFc.3269C>G (p.Ser1090Cys)
n.421-29807C>G
12g.6023741G=CA2013874913VWFc.3269C= (p.Ser1090=)
n.421-29807C=
12g.6023741G>TCA383512253VWFc.3269C>A (p.Ser1090Tyr)
n.421-29807C>A
dbSNP gnomAD v3 gnomAD v4
12g.6023742A>CCA383512254VWFc.3268T>G (p.Ser1090Ala)
n.421-29808T>G
12g.6023742A>GCA383512255VWFc.3268T>C (p.Ser1090Pro)
n.421-29808T>C
12g.6023742A>TCA383512256VWFc.3268T>A (p.Ser1090Thr)
n.421-29808T>A
12g.6023744_6023746delCA2794406197VWFc.3266_3268del (p.Cys1089del)
n.421-29810_421-29808del
12g.6023743G>ACA478101655VWFc.3267C>T (p.Cys1089=)
n.421-29809C>T
gnomAD v4
12g.6023743G>CCA383512257VWFc.3267C>G (p.Cys1089Trp)
n.421-29809C>G
12g.6023743G>TCA383512258VWFc.3267C>A (p.Cys1089Ter)
n.421-29809C>A
12g.6023744C>ACA383512259VWFc.3266G>T (p.Cys1089Phe)
n.421-29810G>T
12g.6023744C>GCA383512260VWFc.3266G>C (p.Cys1089Ser)
n.421-29810G>C
12g.6023744C>TCA383512261VWFc.3266G>A (p.Cys1089Tyr)
n.421-29810G>A
gnomAD v4
12g.6023745A>CCA383512264VWFc.3265T>G (p.Cys1089Gly)
n.421-29811T>G
12g.6023745A>GCA383512262VWFc.3265T>C (p.Cys1089Arg)
n.421-29811T>C
12g.6023745A>TCA383512263VWFc.3265T>A (p.Cys1089Ser)
n.421-29811T>A
12g.6023746G>ACA6402786VWFc.3264C>T (p.Thr1088=)
n.421-29812C>T
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.6023746G>CCA478101663VWFc.3264C>G (p.Thr1088=)
n.421-29812C>G
gnomAD v4
12g.6023746G=CA2013874915VWFc.3264C= (p.Thr1088=)
n.421-29812C=
12g.6023746G>TCA478101665VWFc.3264C>A (p.Thr1088=)
n.421-29812C>A
12g.6023747G>ACA383512265VWFc.3263C>T (p.Thr1088Ile)
n.421-29813C>T
gnomAD v4
12g.6023747G>CCA383512266VWFc.3263C>G (p.Thr1088Ser)
n.421-29813C>G
12g.6023747G>TCA383512267VWFc.3263C>A (p.Thr1088Asn)
n.421-29813C>A
12g.6023748T>ACA383512268VWFc.3262A>T (p.Thr1088Ser)
n.421-29814A>T
12g.6023748T>CCA383512269VWFc.3262A>G (p.Thr1088Ala)
n.421-29814A>G
12g.6023748T>GCA383512270VWFc.3262A>C (p.Thr1088Pro)
n.421-29814A>C
dbSNP
12g.6023748T=CA2013874918VWFc.3262A= (p.Thr1088=)
n.421-29814A=
12g.6023748_6023751delinsTGTCCA2013874917VWFc.3259_3262delinsGACA (p.Asp1087=)
n.421-29817_421-29814delinsGACA
12g.6023749G>ACA478101669VWFc.3261C>T (p.Asp1087=)
n.421-29815C>T
gnomAD v4
12g.6023749G>CCA383512271VWFc.3261C>G (p.Asp1087Glu)
n.421-29815C>G
12g.6023749G>TCA383512272VWFc.3261C>A (p.Asp1087Glu)
n.421-29815C>A
12g.6023751_6023753delCA603483077VWFc.3259_3261del (p.Asp1087del)
n.421-29817_421-29815del
dbSNP gnomAD v2 gnomAD v4
12g.6023750T>ACA383512273VWFc.3260A>T (p.Asp1087Val)
n.421-29816A>T
12g.6023750T>CCA383512274VWFc.3260A>G (p.Asp1087Gly)
n.421-29816A>G
12g.6023750T>GCA383512275VWFc.3260A>C (p.Asp1087Ala)
n.421-29816A>C
12g.6023751C>ACA383512276VWFc.3259G>T (p.Asp1087Tyr)
n.421-29817G>T
12g.6023751C=CA2013874921VWFc.3259G= (p.Asp1087=)
n.421-29817G=
12g.6023751C>GCA383512277VWFc.3259G>C (p.Asp1087His)
n.421-29817G>C
gnomAD v4
12g.6023751C>TCA6402787VWFc.3259G>A (p.Asp1087Asn)
n.421-29817G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
12g.6023751_6023752insACA2695216054VWFc.3258_3259insT (p.Asp1087Ter)
n.421-29818_421-29817insT
12g.6023752G>ACA6402788VWFc.3258C>T (p.Tyr1086=)
n.421-29818C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.6023752G>CCA383512278VWFc.3258C>G (p.Tyr1086Ter)
n.421-29818C>G
12g.6023752G=CA2013874923VWFc.3258C= (p.Tyr1086=)
n.421-29818C=
12g.6023752G>TCA383512279VWFc.3258C>A (p.Tyr1086Ter)
n.421-29818C>A
12g.6023753T>ACA383512280VWFc.3257A>T (p.Tyr1086Phe)
n.421-29819A>T
12g.6023753T>CCA383512281VWFc.3257A>G (p.Tyr1086Cys)
n.421-29819A>G
gnomAD v4
12g.6023753T>GCA383512282VWFc.3257A>C (p.Tyr1086Ser)
n.421-29819A>C
12g.6023753_6023754delinsTACA2013874925VWFc.3256_3257delinsTA (p.Tyr1086=)
n.421-29820_421-29819delinsTA
12g.6023754A>CCA383512283VWFc.3256T>G (p.Tyr1086Asp)
n.421-29820T>G
12g.6023754A>GCA383512284VWFc.3256T>C (p.Tyr1086His)
n.421-29820T>C
12g.6023754A>TCA383512285VWFc.3256T>A (p.Tyr1086Asn)
n.421-29820T>A
12g.6023756delCA690482698VWFc.3256del (p.Tyr1086ThrfsTer?)
n.421-29820del
dbSNP gnomAD v3 gnomAD v4
12g.6023755A>CCA383512286VWFc.3255T>G (p.Ile1085Met)
n.421-29821T>G
12g.6023755A>GCA478101676VWFc.3255T>C (p.Ile1085=)
n.421-29821T>C
12g.6023755A>TCA478101675VWFc.3255T>A (p.Ile1085=)
n.421-29821T>A
12g.6023756A>CCA383512287VWFc.3254T>G (p.Ile1085Ser)
n.421-29822T>G
12g.6023756A>GCA383512288VWFc.3254T>C (p.Ile1085Thr)
n.421-29822T>C
12g.6023756A>TCA383512289VWFc.3254T>A (p.Ile1085Asn)
n.421-29822T>A
12g.6023757T>ACA383512292VWFc.3253A>T (p.Ile1085Phe)
n.421-29823A>T
12g.6023757T>CCA383512291VWFc.3253A>G (p.Ile1085Val)
n.421-29823A>G
12g.6023757T>GCA383512290VWFc.3253A>C (p.Ile1085Leu)
n.421-29823A>C
12g.6023757_6023758delinsTGCA2013874927VWFc.3252_3253delinsCA (p.Cys1084=)
n.421-29824_421-29823delinsCA
12g.6023758delCA6402789VWFc.3252del (p.Cys1084Ter)
n.421-29824del
dbSNP ExAC gnomAD v2
12g.6023758G>ACA478101679VWFc.3252C>T (p.Cys1084=)
n.421-29824C>T
dbSNP gnomAD v2 gnomAD v4
12g.6023758G>CCA383512293VWFc.3252C>G (p.Cys1084Trp)
n.421-29824C>G
12g.6023758G=CA2013874929VWFc.3252C= (p.Cys1084=)
n.421-29824C=
12g.6023758G>TCA383512294VWFc.3252C>A (p.Cys1084Ter)
n.421-29824C>A
12g.6023759C>ACA383512295VWFc.3251G>T (p.Cys1084Phe)
n.421-29825G>T
12g.6023759C=CA2013874931VWFc.3251G= (p.Cys1084=)
n.421-29825G=
12g.6023759C>GCA383512296VWFc.3251G>C (p.Cys1084Ser)
n.421-29825G>C
12g.6023759C>TCA6402790VWFc.3251G>A (p.Cys1084Tyr)
n.421-29825G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
12g.6023760A>CCA383512297VWFc.3250T>G (p.Cys1084Gly)
n.421-29826T>G
12g.6023760A>GCA383512298VWFc.3250T>C (p.Cys1084Arg)
n.421-29826T>C
12g.6023760A>TCA383512299VWFc.3250T>A (p.Cys1084Ser)
n.421-29826T>A
12g.6023761G>ACA478101684VWFc.3249C>T (p.Val1083=)
n.421-29827C>T
dbSNP
12g.6023761G>CCA478101688VWFc.3249C>G (p.Val1083=)
n.421-29827C>G
12g.6023761G=CA2013874934VWFc.3249C= (p.Val1083=)
n.421-29827C=
12g.6023761G>TCA478101685VWFc.3249C>A (p.Val1083=)
n.421-29827C>A
12g.6023762A=CA2013874936VWFc.3248T= (p.Val1083=)
n.421-29828T=
12g.6023762A>CCA383512300VWFc.3248T>G (p.Val1083Gly)
n.421-29828T>G
12g.6023762A>GCA383512301VWFc.3248T>C (p.Val1083Ala)
n.421-29828T>C
dbSNP gnomAD v3 gnomAD v4
12g.6023762A>TCA383512302VWFc.3248T>A (p.Val1083Asp)
n.421-29828T>A
12g.6023763C>ACA383512305VWFc.3247G>T (p.Val1083Phe)
n.421-29829G>T
12g.6023763C>GCA383512304VWFc.3247G>C (p.Val1083Leu)
n.421-29829G>C
12g.6023763C>TCA383512303VWFc.3247G>A (p.Val1083Ile)
n.421-29829G>A
ClinVar gnomAD v4
12g.6023764A>CCA383512306VWFc.3246T>G (p.Asp1082Glu)
n.421-29830T>G
12g.6023764A>GCA478101691VWFc.3246T>C (p.Asp1082=)
n.421-29830T>C
12g.6023764A>TCA383512307VWFc.3246T>A (p.Asp1082Glu)
n.421-29830T>A
12g.6023765T>ACA383512308VWFc.3245A>T (p.Asp1082Val)
n.421-29831A>T
12g.6023765T>CCA6402791VWFc.3245A>G (p.Asp1082Gly)
n.421-29831A>G
dbSNP ExAC gnomAD v2 gnomAD v4
12g.6023765T>GCA383512309VWFc.3245A>C (p.Asp1082Ala)
n.421-29831A>C
12g.6023765T=CA2013874937VWFc.3245A= (p.Asp1082=)
n.421-29831A=
12g.6023766C>ACA383512310VWFc.3244G>T (p.Asp1082Tyr)
n.421-29832G>T
12g.6023766C>GCA383512311VWFc.3244G>C (p.Asp1082His)
n.421-29832G>C
12g.6023766C>TCA383512312VWFc.3244G>A (p.Asp1082Asn)
n.421-29832G>A
12g.6023767C>ACA478101694VWFc.3243G>T (p.Leu1081=)
n.421-29833G>T
12g.6023767C>GCA478101696VWFc.3243G>C (p.Leu1081=)
n.421-29833G>C
12g.6023767C>TCA478101695VWFc.3243G>A (p.Leu1081=)
n.421-29833G>A
12g.6023768A>CCA383512313VWFc.3242T>G (p.Leu1081Arg)
n.421-29834T>G
12g.6023768A>GCA383512314VWFc.3242T>C (p.Leu1081Pro)
n.421-29834T>C
12g.6023768A>TCA383512315VWFc.3242T>A (p.Leu1081Gln)
n.421-29834T>A
12g.6023769G>ACA478101698VWFc.3241C>T (p.Leu1081=)
n.421-29835C>T
12g.6023769G>CCA383512316VWFc.3241C>G (p.Leu1081Val)
n.421-29835C>G
dbSNP
12g.6023769G=CA2013874939VWFc.3241C= (p.Leu1081=)
n.421-29835C=
12g.6023769G>TCA383512317VWFc.3241C>A (p.Leu1081Met)
n.421-29835C>A
12g.6023770A=CA2013874941VWFc.3240T= (p.Tyr1080=)
n.421-29836T=
12g.6023770A>CCA383512319VWFc.3240T>G (p.Tyr1080Ter)
n.421-29836T>G
12g.6023770A>GCA6402792VWFc.3240T>C (p.Tyr1080=)
n.421-29836T>C
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.6023770A>TCA383512318VWFc.3240T>A (p.Tyr1080Ter)
n.421-29836T>A
gnomAD v4
12g.6023771T>ACA383512320VWFc.3239A>T (p.Tyr1080Phe)
n.421-29837A>T
12g.6023771T>CCA383512321VWFc.3239A>G (p.Tyr1080Cys)
n.421-29837A>G
12g.6023771T>GCA383512322VWFc.3239A>C (p.Tyr1080Ser)
n.421-29837A>C
12g.6023772A>CCA383512323VWFc.3238T>G (p.Tyr1080Asp)
n.421-29838T>G
12g.6023772A>GCA383512324VWFc.3238T>C (p.Tyr1080His)
n.421-29838T>C
gnomAD v4
12g.6023772A>TCA383512325VWFc.3238T>A (p.Tyr1080Asn)
n.421-29838T>A
12g.6023773delCA2695216055VWFc.3237del (p.Tyr1080IlefsTer?)
n.421-29839del
12g.6023773T>ACA478101707VWFc.3237A>T (p.Pro1079=)
n.421-29839A>T
12g.6023773T>CCA6402793VWFc.3237A>G (p.Pro1079=)
n.421-29839A>G
dbSNP ExAC gnomAD v2 gnomAD v4
12g.6023773T>GCA478101709VWFc.3237A>C (p.Pro1079=)
n.421-29839A>C
12g.6023773T=CA2013874944VWFc.3237A= (p.Pro1079=)
n.421-29839A=
12g.6023774G>ACA383512326VWFc.3236C>T (p.Pro1079Leu)
n.421-29840C>T
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
12g.6023774G>CCA383512327VWFc.3236C>G (p.Pro1079Arg)
n.421-29840C>G
12g.6023774G=CA2013874946VWFc.3236C= (p.Pro1079=)
n.421-29840C=
12g.6023774G>TCA383512328VWFc.3236C>A (p.Pro1079Gln)
n.421-29840C>A
12g.6023777_6023797dupCA1139532066VWFc.3223-7_3236dup
n.421-29860_421-29840dup
12g.6023775G>ACA383512329VWFc.3235C>T (p.Pro1079Ser)
n.421-29841C>T
12g.6023775G>CCA383512330VWFc.3235C>G (p.Pro1079Ala)
n.421-29841C>G
12g.6023775G>TCA383512331VWFc.3235C>A (p.Pro1079Thr)
n.421-29841C>A
12g.6023776C>ACA383512333VWFc.3234G>T (p.Glu1078Asp)
n.421-29842G>T
12g.6023776C=CA2013874948VWFc.3234G= (p.Glu1078=)
n.421-29842G=
12g.6023776C>GCA383512332VWFc.3234G>C (p.Glu1078Asp)
n.421-29842G>C
12g.6023776C>TCA478101714VWFc.3234G>A (p.Glu1078=)
n.421-29842G>A
dbSNP gnomAD v2 gnomAD v4
12g.6023777T>ACA383512334VWFc.3233A>T (p.Glu1078Val)
n.421-29843A>T
12g.6023777T>CCA383512336VWFc.3233A>G (p.Glu1078Gly)
n.421-29843A>G
12g.6023777T>GCA383512335VWFc.3233A>C (p.Glu1078Ala)
n.421-29843A>C
12g.6023777T=CA2013874949VWFc.3233A= (p.Glu1078=)
n.421-29843A=
12g.6023778C>ACA383512337VWFc.3232G>T (p.Glu1078Ter)
n.421-29844G>T
12g.6023778C=CA2013874951VWFc.3232G= (p.Glu1078=)
n.421-29844G=
12g.6023778C>GCA232298117VWFc.3232G>C (p.Glu1078Gln)
n.421-29844G>C
dbSNP gnomAD v3 gnomAD v4
12g.6023778C>TCA228384VWFc.3232G>A (p.Glu1078Lys)
n.421-29844G>A
ClinVar dbSNP gnomAD v4
12g.6023778_6023779insCCCA2741226869VWFc.3232_3233insGG (p.Glu1078GlyfsTer?)
n.421-29844_421-29843insGG
12g.6023778dupCA6402794VWFc.3232dup (p.Glu1078GlyfsTer15)
n.421-29844dup
dbSNP ExAC gnomAD v2 gnomAD v4
12g.6023779G>ACA6402796VWFc.3231C>T (p.Pro1077=)
n.421-29845C>T
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.6023779G>CCA6402795VWFc.3231C>G (p.Pro1077=)
n.421-29845C>G
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.6023779G=CA2013874955VWFc.3231C= (p.Pro1077=)
n.421-29845C=
12g.6023779G>TCA478101719VWFc.3231C>A (p.Pro1077=)
n.421-29845C>A
12g.6023782dupCA2580086230VWFc.3231dup (p.Glu1078ArgfsTer15)
n.421-29845dup
ClinVar gnomAD v4
12g.6023782delCA2739271830VWFc.3231del (p.Glu1078SerfsTer?)
n.421-29845del
ClinVar
12g.6023780G>ACA383512339VWFc.3230C>T (p.Pro1077Leu)
n.421-29846C>T
12g.6023780G>CCA6402797VWFc.3230C>G (p.Pro1077Arg)
n.421-29846C>G
dbSNP ExAC gnomAD v2 gnomAD v4
12g.6023780G=CA2013874958VWFc.3230C= (p.Pro1077=)
n.421-29846C=
12g.6023780G>TCA383512338VWFc.3230C>A (p.Pro1077His)
n.421-29846C>A
12g.6023781G>ACA383512340VWFc.3229C>T (p.Pro1077Ser)
n.421-29847C>T
dbSNP gnomAD v4
12g.6023781G>CCA383512341VWFc.3229C>G (p.Pro1077Ala)
n.421-29847C>G
12g.6023781G=CA2013874960VWFc.3229C= (p.Pro1077=)
n.421-29847C=
12g.6023781G>TCA383512342VWFc.3229C>A (p.Pro1077Thr)
n.421-29847C>A
ClinVar
12g.6023782G>ACA478101725VWFc.3228C>T (p.Asp1076=)
n.421-29848C>T
12g.6023782G>CCA383512343VWFc.3228C>G (p.Asp1076Glu)
n.421-29848C>G
12g.6023782G>TCA383512344VWFc.3228C>A (p.Asp1076Glu)
n.421-29848C>A
12g.6023783T>ACA383512346VWFc.3227A>T (p.Asp1076Val)
n.421-29849A>T
12g.6023783T>CCA383512345VWFc.3227A>G (p.Asp1076Gly)
n.421-29849A>G
gnomAD v4
12g.6023783T>GCA6402798VWFc.3227A>C (p.Asp1076Ala)
n.421-29849A>C
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.6023783T=CA2013874963VWFc.3227A= (p.Asp1076=)
n.421-29849A=
12g.6023784C>ACA383512347VWFc.3226G>T (p.Asp1076Tyr)
n.421-29850G>T
12g.6023784C>GCA383512348VWFc.3226G>C (p.Asp1076His)
n.421-29850G>C
12g.6023784C>TCA383512349VWFc.3226G>A (p.Asp1076Asn)
n.421-29850G>A
12g.6023785C>ACA478101733VWFc.3225G>T (p.Val1075=)
n.421-29851G>T
12g.6023785C>GCA478101735VWFc.3225G>C (p.Val1075=)
n.421-29851G>C
12g.6023785C>TCA478101736VWFc.3225G>A (p.Val1075=)
n.421-29851G>A
12g.6023786A=CA2013874966VWFc.3224T= (p.Val1075=)
n.421-29852T=
12g.6023786A>CCA383512350VWFc.3224T>G (p.Val1075Gly)
n.421-29852T>G
dbSNP gnomAD v4
12g.6023786A>GCA383512351VWFc.3224T>C (p.Val1075Ala)
n.421-29852T>C
12g.6023786A>TCA383512352VWFc.3224T>A (p.Val1075Glu)
n.421-29852T>A
12g.6023787C>ACA383512353VWFc.3223G>T (p.Val1075Leu)
n.421-29853G>T
12g.6023787C>GCA383512354VWFc.3223G>C (p.Val1075Leu)
n.421-29853G>C
12g.6023787C>TCA383512355VWFc.3223G>A (p.Val1075Met)
n.421-29853G>A
12g.6023788C>ACA383512356VWFc.3223-1G>T (n.3223-1G>T)
n.421-29854G>T
12g.6023788C>GCA383512357VWFc.3223-1G>C (n.3223-1G>C)
n.421-29854G>C
12g.6023788C>TCA383512358VWFc.3223-1G>A (n.3223-1G>A)
n.421-29854G>A
gnomAD v4
12g.6023789T>ACA383512359VWFc.3223-2A>T (n.3223-2A>T)
n.421-29855A>T
12g.6023789T>CCA383512361VWFc.3223-2A>G (n.3223-2A>G)
n.421-29855A>G
12g.6023789T>GCA383512360VWFc.3223-2A>C (n.3223-2A>C)
n.421-29855A>C
12g.6023790G=CA2013874967VWFc.3223-3C= (n.3223-3C=)
n.421-29856C=
12g.6023790G>TCA6402799VWFc.3223-3C>A (n.3223-3C>A)
n.421-29856C>A
dbSNP ExAC
12g.6023793A>CCA2617230400VWFc.3223-6T>G (n.3223-6T>G)
n.421-29859T>G
gnomAD v4
12g.6023794A>TCA2617230401VWFc.3223-7T>A (n.3223-7T>A)
n.421-29860T>A
gnomAD v4
12g.6023795G>CCA603483078VWFc.3223-8C>G (n.3223-8C>G)
n.421-29861C>G
dbSNP gnomAD v2 gnomAD v4
12g.6023795G=CA2013874969VWFc.3223-8C= (n.3223-8C=)
n.421-29861C=
12g.6023796G>ACA2617230402VWFc.3223-9C>T (n.3223-9C>T)
n.421-29862C>T
gnomAD v4
12g.6023797C>ACA2617230403VWFc.3223-10G>T (n.3223-10G>T)
n.421-29863G>T
gnomAD v4
12g.6023797C>TCA2575053936VWFc.3223-10G>A (n.3223-10G>A)
n.421-29863G>A
gnomAD v4
12g.6023800C>ACA2013874972VWFc.3223-13G>T (n.3223-13G>T)
n.421-29866G>T
dbSNP
12g.6023800C=CA2013874971VWFc.3223-13G= (n.3223-13G=)
n.421-29866G=
12g.6023800C>TCA603483079VWFc.3223-13G>A (n.3223-13G>A)
n.421-29866G>A
dbSNP gnomAD v2
12g.6023801C>TCA2617230404VWFc.3223-14G>A (n.3223-14G>A)
n.421-29867G>A
gnomAD v4
12g.6023802T>ACA603483080VWFc.3223-15A>T (n.3223-15A>T)
n.421-29868A>T
dbSNP gnomAD v2 gnomAD v4
12g.6023802T=CA2013874974VWFc.3223-15A= (n.3223-15A=)
n.421-29868A=

Number of alleles fetched