Chr Mutation (hg38) CAid Gene Transcript Linkouts
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
12g.6019408G>ACA228510VWFc.4010C>T (p.Pro1337Leu)
n.421-25474C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
12g.6019408G>CCA383505781VWFc.4010C>G (p.Pro1337Arg)
n.421-25474C>G
12g.6019408G=CA2013872964VWFc.4010C= (p.Pro1337=)
n.421-25474C=
12g.6019408G>TCA383505783VWFc.4010C>A (p.Pro1337Gln)
n.421-25474C>A
ClinVar dbSNP gnomAD v2 gnomAD v4
12g.6019409G>ACA383505788VWFc.4009C>T (p.Pro1337Ser)
n.421-25475C>T
gnomAD v4
12g.6019409G>CCA383505790VWFc.4009C>G (p.Pro1337Ala)
n.421-25475C>G
12g.6019409G=CA2013872965VWFc.4009C= (p.Pro1337=)
n.421-25475C=
12g.6019409G>TCA383505786VWFc.4009C>A (p.Pro1337Thr)
n.421-25475C>A
dbSNP gnomAD v2 gnomAD v4
12g.6019410T>ACA6402626VWFc.4008A>T (p.Arg1336=)
n.421-25476A>T
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.6019410T>CCA478502384VWFc.4008A>G (p.Arg1336=)
n.421-25476A>G
dbSNP gnomAD v3 gnomAD v4
12g.6019410T>GCA478502385VWFc.4008A>C (p.Arg1336=)
n.421-25476A>C
12g.6019410T=CA2013872966VWFc.4008A= (p.Arg1336=)
n.421-25476A=
12g.6019411C>ACA383505794VWFc.4007G>T (p.Arg1336Leu)
n.421-25477G>T
12g.6019411C=CA2013872967VWFc.4007G= (p.Arg1336=)
n.421-25477G=
12g.6019411C>GCA383505796VWFc.4007G>C (p.Arg1336Pro)
n.421-25477G>C
COSMIC
12g.6019411C>TCA10638269VWFc.4007G>A (p.Arg1336Gln)
n.421-25477G>A
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
12g.6019412G>ACA383505798VWFc.4006C>T (p.Arg1336Ter)
n.421-25478C>T
ClinVar dbSNP gnomAD v4
12g.6019412G>CCA383505800VWFc.4006C>G (p.Arg1336Gly)
n.421-25478C>G
12g.6019412G=CA2013872968VWFc.4006C= (p.Arg1336=)
n.421-25478C=
12g.6019412G>TCA478502386VWFc.4006C>A (p.Arg1336=)
n.421-25478C>A
12g.6019413C>ACA383505805VWFc.4005G>T (p.Lys1335Asn)
n.421-25479G>T
12g.6019413C>GCA383505803VWFc.4005G>C (p.Lys1335Asn)
n.421-25479G>C
12g.6019413C>TCA478502387VWFc.4005G>A (p.Lys1335=)
n.421-25479G>A
gnomAD v4
12g.6019414T>ACA383505808VWFc.4004A>T (p.Lys1335Met)
n.421-25480A>T
12g.6019414T>CCA383505810VWFc.4004A>G (p.Lys1335Arg)
n.421-25480A>G
12g.6019414T>GCA383505812VWFc.4004A>C (p.Lys1335Thr)
n.421-25480A>C
12g.6019415T>ACA383505816VWFc.4003A>T (p.Lys1335Ter)
n.421-25481A>T
12g.6019415T>CCA383505818VWFc.4003A>G (p.Lys1335Glu)
n.421-25481A>G
dbSNP gnomAD v2 gnomAD v4
12g.6019415T>GCA383505820VWFc.4003A>C (p.Lys1335Gln)
n.421-25481A>C
12g.6019415T=CA2013872969VWFc.4003A= (p.Lys1335=)
n.421-25481A=
12g.6019416C>ACA478502388VWFc.4002G>T (p.Arg1334=)
n.421-25482G>T
12g.6019416C>GCA478502389VWFc.4002G>C (p.Arg1334=)
n.421-25482G>C
12g.6019416C>TCA478502390VWFc.4002G>A (p.Arg1334=)
n.421-25482G>A
12g.6019417C>ACA383505827VWFc.4001G>T (p.Arg1334Leu)
n.421-25483G>T
12g.6019417C=CA2013872970VWFc.4001G= (p.Arg1334=)
n.421-25483G=
12g.6019417C>GCA383505823VWFc.4001G>C (p.Arg1334Pro)
n.421-25483G>C
dbSNP gnomAD v2
12g.6019417C>TCA6402627VWFc.4001G>A (p.Arg1334Gln)
n.421-25483G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.6019418G>ACA6402628VWFc.4000C>T (p.Arg1334Trp)
n.421-25484C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
12g.6019418G>CCA383505829VWFc.4000C>G (p.Arg1334Gly)
n.421-25484C>G
12g.6019418G=CA2013872971VWFc.4000C= (p.Arg1334=)
n.421-25484C=
12g.6019418G>TCA478502391VWFc.4000C>A (p.Arg1334=)
n.421-25484C>A
gnomAD v4
12g.6019419G>ACA478502392VWFc.3999C>T (p.Asp1333=)
n.421-25485C>T
12g.6019419G>CCA383505831VWFc.3999C>G (p.Asp1333Glu)
n.421-25485C>G
12g.6019419G>TCA383505832VWFc.3999C>A (p.Asp1333Glu)
n.421-25485C>A
12g.6019420T>ACA383505835VWFc.3998A>T (p.Asp1333Val)
n.421-25486A>T
12g.6019420T>CCA383505836VWFc.3998A>G (p.Asp1333Gly)
n.421-25486A>G
12g.6019420T>GCA383505838VWFc.3998A>C (p.Asp1333Ala)
n.421-25486A>C
12g.6019421C>ACA383505841VWFc.3997G>T (p.Asp1333Tyr)
n.421-25487G>T
12g.6019421C=CA2013872972VWFc.3997G= (p.Asp1333=)
n.421-25487G=
12g.6019421C>GCA383505842VWFc.3997G>C (p.Asp1333His)
n.421-25487G>C
12g.6019421C>TCA6402629VWFc.3997G>A (p.Asp1333Asn)
n.421-25487G>A
dbSNP ExAC gnomAD v2
12g.6019422C>ACA383505846VWFc.3996G>T (p.Lys1332Asn)
n.421-25488G>T
gnomAD v4
12g.6019422C=CA2013872973VWFc.3996G= (p.Lys1332=)
n.421-25488G=
12g.6019422C>GCA383505847VWFc.3996G>C (p.Lys1332Asn)
n.421-25488G>C
12g.6019422C>TCA6402630VWFc.3996G>A (p.Lys1332=)
n.421-25488G>A
dbSNP ExAC gnomAD v2 gnomAD v4
12g.6019423T>ACA383505850VWFc.3995A>T (p.Lys1332Met)
n.421-25489A>T
12g.6019423T>CCA383505852VWFc.3995A>G (p.Lys1332Arg)
n.421-25489A>G
12g.6019423T>GCA383505851VWFc.3995A>C (p.Lys1332Thr)
n.421-25489A>C
12g.6019424T>ACA383505855VWFc.3994A>T (p.Lys1332Ter)
n.421-25490A>T
12g.6019424T>CCA383505856VWFc.3994A>G (p.Lys1332Glu)
n.421-25490A>G
12g.6019424T>GCA383505857VWFc.3994A>C (p.Lys1332Gln)
n.421-25490A>C
12g.6019425G>ACA478502395VWFc.3993C>T (p.Leu1331=)
n.421-25491C>T
dbSNP
12g.6019425G>CCA478502394VWFc.3993C>G (p.Leu1331=)
n.421-25491C>G
dbSNP gnomAD v4
12g.6019425G=CA2013872974VWFc.3993C= (p.Leu1331=)
n.421-25491C=
12g.6019425G>TCA478502393VWFc.3993C>A (p.Leu1331=)
n.421-25491C>A
12g.6019426A>CCA383505859VWFc.3992T>G (p.Leu1331Arg)
n.421-25492T>G
12g.6019426A>GCA383505861VWFc.3992T>C (p.Leu1331Pro)
n.421-25492T>C
12g.6019426A>TCA383505863VWFc.3992T>A (p.Leu1331His)
n.421-25492T>A
12g.6019427G>ACA383505866VWFc.3991C>T (p.Leu1331Phe)
n.421-25493C>T
dbSNP gnomAD v4
12g.6019427G>CCA383505868VWFc.3991C>G (p.Leu1331Val)
n.421-25493C>G
12g.6019427G=CA2013872975VWFc.3991C= (p.Leu1331=)
n.421-25493C=
12g.6019427G>TCA383505870VWFc.3991C>A (p.Leu1331Ile)
n.421-25493C>A
12g.6019428C>ACA478502402VWFc.3990G>T (p.Gly1330=)
n.421-25494G>T
12g.6019428C>GCA478502400VWFc.3990G>C (p.Gly1330=)
n.421-25494G>C
12g.6019428C>TCA478502399VWFc.3990G>A (p.Gly1330=)
n.421-25494G>A
12g.6019429C>ACA383505871VWFc.3989G>T (p.Gly1330Val)
n.421-25495G>T
12g.6019429C>GCA383505874VWFc.3989G>C (p.Gly1330Ala)
n.421-25495G>C
12g.6019429C>TCA383505876VWFc.3989G>A (p.Gly1330Glu)
n.421-25495G>A
12g.6019430C>ACA383505880VWFc.3988G>T (p.Gly1330Trp)
n.421-25496G>T
12g.6019430C=CA2013872976VWFc.3988G= (p.Gly1330=)
n.421-25496G=
12g.6019430C>GCA383505881VWFc.3988G>C (p.Gly1330Arg)
n.421-25496G>C
12g.6019430C>TCA6402631VWFc.3988G>A (p.Gly1330Arg)
n.421-25496G>A
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
12g.6019431G>ACA6402632VWFc.3987C>T (p.Ile1329=)
n.421-25497C>T
dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
12g.6019431G>CCA6402633VWFc.3987C>G (p.Ile1329Met)
n.421-25497C>G
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.6019431G=CA2013872977VWFc.3987C= (p.Ile1329=)
n.421-25497C=
12g.6019431G>TCA478502406VWFc.3987C>A (p.Ile1329=)
n.421-25497C>A
12g.6019432A>CCA383505887VWFc.3986T>G (p.Ile1329Ser)
n.421-25498T>G
12g.6019432A>GCA383505889VWFc.3986T>C (p.Ile1329Thr)
n.421-25498T>C
12g.6019432A>TCA383505891VWFc.3986T>A (p.Ile1329Asn)
n.421-25498T>A
12g.6019433T>ACA383505898VWFc.3985A>T (p.Ile1329Phe)
n.421-25499A>T
12g.6019433T>CCA6402634VWFc.3985A>G (p.Ile1329Val)
n.421-25499A>G
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.6019433T>GCA383505896VWFc.3985A>C (p.Ile1329Leu)
n.421-25499A>C
gnomAD v4
12g.6019433T=CA2013872978VWFc.3985A= (p.Ile1329=)
n.421-25499A=
12g.6019434G>ACA478502411VWFc.3984C>T (p.Tyr1328=)
n.421-25500C>T
gnomAD v4
12g.6019434G>CCA383505901VWFc.3984C>G (p.Tyr1328Ter)
n.421-25500C>G
12g.6019434G>TCA383505903VWFc.3984C>A (p.Tyr1328Ter)
n.421-25500C>A
12g.6019435T>ACA383505906VWFc.3983A>T (p.Tyr1328Phe)
n.421-25501A>T
12g.6019435T>CCA383505907VWFc.3983A>G (p.Tyr1328Cys)
n.421-25501A>G
12g.6019435T>GCA383505909VWFc.3983A>C (p.Tyr1328Ser)
n.421-25501A>C
12g.6019436A>CCA383505916VWFc.3982T>G (p.Tyr1328Asp)
n.421-25502T>G
12g.6019436A>GCA383505914VWFc.3982T>C (p.Tyr1328His)
n.421-25502T>C
12g.6019436A>TCA383505912VWFc.3982T>A (p.Tyr1328Asn)
n.421-25502T>A
12g.6019437G>ACA478502416VWFc.3981C>T (p.Ala1327=)
n.421-25503C>T
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
12g.6019437G>CCA478502418VWFc.3981C>G (p.Ala1327=)
n.421-25503C>G
12g.6019437G=CA2013872979VWFc.3981C= (p.Ala1327=)
n.421-25503C=
12g.6019437G>TCA478502420VWFc.3981C>A (p.Ala1327=)
n.421-25503C>A
COSMIC
12g.6019438G>ACA6402635VWFc.3980C>T (p.Ala1327Val)
n.421-25504C>T
dbSNP ExAC gnomAD v2 gnomAD v4
12g.6019438G>CCA383505922VWFc.3980C>G (p.Ala1327Gly)
n.421-25504C>G
12g.6019438G=CA2013872980VWFc.3980C= (p.Ala1327=)
n.421-25504C=
12g.6019438G>TCA383505919VWFc.3980C>A (p.Ala1327Asp)
n.421-25504C>A
12g.6019439C>ACA383505924VWFc.3979G>T (p.Ala1327Ser)
n.421-25505G>T
dbSNP gnomAD v2 gnomAD v4
12g.6019439C=CA2013872981VWFc.3979G= (p.Ala1327=)
n.421-25505G=
12g.6019439C>GCA383505927VWFc.3979G>C (p.Ala1327Pro)
n.421-25505G>C
12g.6019439C>TCA6402636VWFc.3979G>A (p.Ala1327Thr)
n.421-25505G>A
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.6019440G>ACA6402637VWFc.3978C>T (p.His1326=)
n.421-25506C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.6019440G>CCA383505930VWFc.3978C>G (p.His1326Gln)
n.421-25506C>G
COSMIC
12g.6019440G=CA2013872982VWFc.3978C= (p.His1326=)
n.421-25506C=
12g.6019440G>TCA383505932VWFc.3978C>A (p.His1326Gln)
n.421-25506C>A
12g.6019441T>ACA383505934VWFc.3977A>T (p.His1326Leu)
n.421-25507A>T
12g.6019441T>CCA383505937VWFc.3977A>G (p.His1326Arg)
n.421-25507A>G
12g.6019441T>GCA383505939VWFc.3977A>C (p.His1326Pro)
n.421-25507A>C
12g.6019442G>ACA383505941VWFc.3976C>T (p.His1326Tyr)
n.421-25508C>T
12g.6019442G>CCA383505942VWFc.3976C>G (p.His1326Asp)
n.421-25508C>G
12g.6019442G>TCA383505945VWFc.3976C>A (p.His1326Asn)
n.421-25508C>A
12g.6019444delCA645595301VWFc.3976del (p.His1326ThrfsTer22)
n.421-25508del
COSMIC
12g.6019443G>ACA478502710VWFc.3975C>T (p.Ser1325=)
n.421-25509C>T
12g.6019443G>CCA478502712VWFc.3975C>G (p.Ser1325=)
n.421-25509C>G
gnomAD v4
12g.6019443G>TCA478502714VWFc.3975C>A (p.Ser1325=)
n.421-25509C>A
12g.6019444G>ACA6402638VWFc.3974C>T (p.Ser1325Phe)
n.421-25510C>T
ClinVar dbSNP ExAC gnomAD v3 gnomAD v4
12g.6019444G>CCA383505949VWFc.3974C>G (p.Ser1325Cys)
n.421-25510C>G
12g.6019444G=CA2013872983VWFc.3974C= (p.Ser1325=)
n.421-25510C=
12g.6019444G>TCA383505951VWFc.3974C>A (p.Ser1325Tyr)
n.421-25510C>A
12g.6019445A>CCA383505954VWFc.3973T>G (p.Ser1325Ala)
n.421-25511T>G
12g.6019445A>GCA383505958VWFc.3973T>C (p.Ser1325Pro)
n.421-25511T>C
12g.6019445A>TCA383505955VWFc.3973T>A (p.Ser1325Thr)
n.421-25511T>A
12g.6019446G>ACA478502729VWFc.3972C>T (p.Gly1324=)
n.421-25512C>T
12g.6019446G>CCA478502728VWFc.3972C>G (p.Gly1324=)
n.421-25512C>G
12g.6019446G>TCA478502726VWFc.3972C>A (p.Gly1324=)
n.421-25512C>A
12g.6019447C>ACA383505961VWFc.3971G>T (p.Gly1324Val)
n.421-25513G>T
12g.6019447C=CA2013872984VWFc.3971G= (p.Gly1324=)
n.421-25513G=
12g.6019447C>GCA228508VWFc.3971G>C (p.Gly1324Ala)
n.421-25513G>C
ClinVar dbSNP
12g.6019447C>TCA383505964VWFc.3971G>A (p.Gly1324Asp)
n.421-25513G>A
12g.6019448C>ACA383505967VWFc.3970G>T (p.Gly1324Cys)
n.421-25514G>T
12g.6019448C=CA2013872985VWFc.3970G= (p.Gly1324=)
n.421-25514G=
12g.6019448C>GCA383505969VWFc.3970G>C (p.Gly1324Arg)
n.421-25514G>C
12g.6019448C>TCA114147VWFc.3970G>A (p.Gly1324Ser)
n.421-25514G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.6019449G>ACA6402640VWFc.3969C>T (p.Asp1323=)
n.421-25515C>T
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.6019449G>CCA383505974VWFc.3969C>G (p.Asp1323Glu)
n.421-25515C>G
12g.6019449G=CA2013872986VWFc.3969C= (p.Asp1323=)
n.421-25515C=
12g.6019449G>TCA6402639VWFc.3969C>A (p.Asp1323Glu)
n.421-25515C>A
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.6019450T>ACA383505981VWFc.3968A>T (p.Asp1323Val)
n.421-25516A>T
12g.6019450T>CCA383505983VWFc.3968A>G (p.Asp1323Gly)
n.421-25516A>G
gnomAD v4
12g.6019450T>GCA383505979VWFc.3968A>C (p.Asp1323Ala)
n.421-25516A>C
12g.6019451C>ACA383505985VWFc.3967G>T (p.Asp1323Tyr)
n.421-25517G>T
12g.6019451C=CA2013872987VWFc.3967G= (p.Asp1323=)
n.421-25517G=
12g.6019451C>GCA383505987VWFc.3967G>C (p.Asp1323His)
n.421-25517G>C
dbSNP
12g.6019451C>TCA6402641VWFc.3967G>A (p.Asp1323Asn)
n.421-25517G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.6019452G>ACA6402642VWFc.3966C>T (p.His1322=)
n.421-25518C>T
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.6019452G>CCA383505993VWFc.3966C>G (p.His1322Gln)
n.421-25518C>G
12g.6019452G=CA2013872988VWFc.3966C= (p.His1322=)
n.421-25518C=
12g.6019452G>TCA383505995VWFc.3966C>A (p.His1322Gln)
n.421-25518C>A
12g.6019454_6019456delCA2695216045VWFc.3964_3966del (p.His1322del)
n.421-25520_421-25518del
12g.6019453T>ACA383506001VWFc.3965A>T (p.His1322Leu)
n.421-25519A>T
12g.6019453T>CCA383505997VWFc.3965A>G (p.His1322Arg)
n.421-25519A>G
12g.6019453T>GCA383505999VWFc.3965A>C (p.His1322Pro)
n.421-25519A>C
ClinVar dbSNP
12g.6019453T=CA2013872989VWFc.3965A= (p.His1322=)
n.421-25519A=
12g.6019454G>ACA6402643VWFc.3964C>T (p.His1322Tyr)
n.421-25520C>T
dbSNP ExAC gnomAD v2 gnomAD v4
12g.6019454G>CCA383506005VWFc.3964C>G (p.His1322Asp)
n.421-25520C>G
gnomAD v4
12g.6019454G=CA2013872990VWFc.3964C= (p.His1322=)
n.421-25520C=
12g.6019454G>TCA383506007VWFc.3964C>A (p.His1322Asn)
n.421-25520C>A
gnomAD v4
12g.6019455G>ACA478502770VWFc.3963C>T (p.Tyr1321=)
n.421-25521C>T
dbSNP
12g.6019455G>CCA383506010VWFc.3963C>G (p.Tyr1321Ter)
n.421-25521C>G
12g.6019455G=CA2013872991VWFc.3963C= (p.Tyr1321=)
n.421-25521C=
12g.6019455G>TCA383506011VWFc.3963C>A (p.Tyr1321Ter)
n.421-25521C>A
12g.6019456T>ACA383506015VWFc.3962A>T (p.Tyr1321Phe)
n.421-25522A>T
12g.6019456T>CCA383506019VWFc.3962A>G (p.Tyr1321Cys)
n.421-25522A>G
ClinVar dbSNP
12g.6019456T>GCA383506017VWFc.3962A>C (p.Tyr1321Ser)
n.421-25522A>C
12g.6019456T=CA2013872992VWFc.3962A= (p.Tyr1321=)
n.421-25522A=
12g.6019457A>CCA383506021VWFc.3961T>G (p.Tyr1321Asp)
n.421-25523T>G
12g.6019457A>GCA383506024VWFc.3961T>C (p.Tyr1321His)
n.421-25523T>C
12g.6019457A>TCA383506026VWFc.3961T>A (p.Tyr1321Asn)
n.421-25523T>A
12g.6019458C>ACA383506028VWFc.3960G>T (p.Glu1320Asp)
n.421-25524G>T
12g.6019458C=CA2013872993VWFc.3960G= (p.Glu1320=)
n.421-25524G=
12g.6019458C>GCA383506030VWFc.3960G>C (p.Glu1320Asp)
n.421-25524G>C
12g.6019458C>TCA478502778VWFc.3960G>A (p.Glu1320=)
n.421-25524G>A
dbSNP gnomAD v2 gnomAD v4
12g.6019459T>ACA383506033VWFc.3959A>T (p.Glu1320Val)
n.421-25525A>T
12g.6019459T>CCA383506035VWFc.3959A>G (p.Glu1320Gly)
n.421-25525A>G
dbSNP
12g.6019459T>GCA383506036VWFc.3959A>C (p.Glu1320Ala)
n.421-25525A>C
12g.6019459T=CA2013872994VWFc.3959A= (p.Glu1320=)
n.421-25525A=
12g.6019460C>ACA383506038VWFc.3958G>T (p.Glu1320Ter)
n.421-25526G>T
12g.6019460C>GCA383506039VWFc.3958G>C (p.Glu1320Gln)
n.421-25526G>C
12g.6019460C>TCA383506041VWFc.3958G>A (p.Glu1320Lys)
n.421-25526G>A
12g.6019461C>ACA478502780VWFc.3957G>T (p.Val1319=)
n.421-25527G>T
12g.6019461C=CA2013872995VWFc.3957G= (p.Val1319=)
n.421-25527G=
12g.6019461C>GCA478502782VWFc.3957G>C (p.Val1319=)
n.421-25527G>C
12g.6019461C>TCA478502784VWFc.3957G>A (p.Val1319=)
n.421-25527G>A
dbSNP gnomAD v2 gnomAD v4
12g.6019462A>CCA383506046VWFc.3956T>G (p.Val1319Gly)
n.421-25528T>G
12g.6019462A>GCA383506044VWFc.3956T>C (p.Val1319Ala)
n.421-25528T>C
12g.6019462A>TCA383506042VWFc.3956T>A (p.Val1319Glu)
n.421-25528T>A
12g.6019463C>ACA383506049VWFc.3955G>T (p.Val1319Leu)
n.421-25529G>T
12g.6019463C>GCA383506053VWFc.3955G>C (p.Val1319Leu)
n.421-25529G>C
12g.6019463C>TCA383506051VWFc.3955G>A (p.Val1319Met)
n.421-25529G>A
12g.6019464C>ACA478502787VWFc.3954G>T (p.Val1318=)
n.421-25530G>T
12g.6019464C>GCA478502788VWFc.3954G>C (p.Val1318=)
n.421-25530G>C
12g.6019464C>TCA478502789VWFc.3954G>A (p.Val1318=)
n.421-25530G>A
12g.6019465A>CCA383506056VWFc.3953T>G (p.Val1318Gly)
n.421-25531T>G
12g.6019465A>GCA383506057VWFc.3953T>C (p.Val1318Ala)
n.421-25531T>C
12g.6019465A>TCA383506059VWFc.3953T>A (p.Val1318Glu)
n.421-25531T>A
12g.6019466C>ACA383506062VWFc.3952G>T (p.Val1318Leu)
n.421-25532G>T
dbSNP gnomAD v2 gnomAD v4
12g.6019466C=CA2013872996VWFc.3952G= (p.Val1318=)
n.421-25532G=
12g.6019466C>GCA383506064VWFc.3952G>C (p.Val1318Leu)
n.421-25532G>C
12g.6019466C>TCA6402644VWFc.3952G>A (p.Val1318Met)
n.421-25532G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.6019467G>ACA6402645VWFc.3951C>T (p.Ala1317=)
n.421-25533C>T
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
12g.6019467G>CCA478502802VWFc.3951C>G (p.Ala1317=)
n.421-25533C>G
12g.6019467G=CA2013872997VWFc.3951C= (p.Ala1317=)
n.421-25533C=
12g.6019467G>TCA478502804VWFc.3951C>A (p.Ala1317=)
n.421-25533C>A
12g.6019468G>ACA383506069VWFc.3950C>T (p.Ala1317Val)
n.421-25534C>T
12g.6019468G>CCA383506071VWFc.3950C>G (p.Ala1317Gly)
n.421-25534C>G
12g.6019468G>TCA383506072VWFc.3950C>A (p.Ala1317Asp)
n.421-25534C>A
12g.6019469C>ACA383506075VWFc.3949G>T (p.Ala1317Ser)
n.421-25535G>T
12g.6019469C>GCA383506077VWFc.3949G>C (p.Ala1317Pro)
n.421-25535G>C
12g.6019469C>TCA383506079VWFc.3949G>A (p.Ala1317Thr)
n.421-25535G>A
12g.6019470C>ACA478502814VWFc.3948G>T (p.Val1316=)
n.421-25536G>T
12g.6019470C>GCA478502818VWFc.3948G>C (p.Val1316=)
n.421-25536G>C
12g.6019470C>TCA478502820VWFc.3948G>A (p.Val1316=)
n.421-25536G>A
12g.6019471A>CCA383506082VWFc.3947T>G (p.Val1316Gly)
n.421-25537T>G
12g.6019471A>GCA383506086VWFc.3947T>C (p.Val1316Ala)
n.421-25537T>C
12g.6019471A>TCA383506084VWFc.3947T>A (p.Val1316Glu)
n.421-25537T>A
12g.6019472C>ACA383506089VWFc.3946G>T (p.Val1316Leu)
n.421-25538G>T
ClinVar dbSNP
12g.6019472C=CA2013872998VWFc.3946G= (p.Val1316=)
n.421-25538G=
12g.6019472C>GCA6402646VWFc.3946G>C (p.Val1316Leu)
n.421-25538G>C
dbSNP ExAC gnomAD v2 gnomAD v4
12g.6019472C>TCA114127VWFc.3946G>A (p.Val1316Met)
n.421-25538G>A
ClinVar dbSNP
12g.6019473G>ACA6402647VWFc.3945C>T (p.Arg1315=)
n.421-25539C>T
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
12g.6019473G>CCA478502834VWFc.3945C>G (p.Arg1315=)
n.421-25539C>G
12g.6019473G=CA2013872999VWFc.3945C= (p.Arg1315=)
n.421-25539C=
12g.6019473G>TCA478502837VWFc.3945C>A (p.Arg1315=)
n.421-25539C>A
12g.6019474C>ACA228506VWFc.3944G>T (p.Arg1315Leu)
n.421-25540G>T
ClinVar dbSNP
12g.6019474C=CA2013873000VWFc.3944G= (p.Arg1315=)
n.421-25540G=
12g.6019474C>GCA383506096VWFc.3944G>C (p.Arg1315Pro)
n.421-25540G>C
12g.6019474C>TCA228504VWFc.3944G>A (p.Arg1315His)
n.421-25540G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.6019475G>ACA228502VWFc.3943C>T (p.Arg1315Cys)
n.421-25541C>T
ClinVar dbSNP gnomAD v4 COSMIC
12g.6019475G>CCA383506100VWFc.3943C>G (p.Arg1315Gly)
n.421-25541C>G
12g.6019475G=CA2013873001VWFc.3943C= (p.Arg1315=)
n.421-25541C=
12g.6019475G>TCA383506103VWFc.3943C>A (p.Arg1315Ser)
n.421-25541C>A
gnomAD v4
12g.6019476G>ACA478502847VWFc.3942C>T (p.Val1314=)
n.421-25542C>T
12g.6019476G>CCA478502848VWFc.3942C>G (p.Val1314=)
n.421-25542C>G
12g.6019476G>TCA478502849VWFc.3942C>A (p.Val1314=)
n.421-25542C>A
12g.6019477A=CA2013873002VWFc.3941T= (p.Val1314=)
n.421-25543T=
12g.6019477A>CCA383506108VWFc.3941T>G (p.Val1314Gly)
n.421-25543T>G
12g.6019477A>GCA383506106VWFc.3941T>C (p.Val1314Ala)
n.421-25543T>C
12g.6019477A>TCA228500VWFc.3941T>A (p.Val1314Asp)
n.421-25543T>A
ClinVar dbSNP
12g.6019478C>ACA228498VWFc.3940G>T (p.Val1314Phe)
n.421-25544G>T
ClinVar dbSNP
12g.6019478C=CA2013873003VWFc.3940G= (p.Val1314=)
n.421-25544G=
12g.6019478C>GCA114151VWFc.3940G>C (p.Val1314Leu)
n.421-25544G>C
ClinVar dbSNP
12g.6019478C>TCA383506114VWFc.3940G>A (p.Val1314Ile)
n.421-25544G>A
gnomAD v4
12g.6019480delCA2499221796VWFc.3940del (p.Val1314SerfsTer?)
n.421-25544del
ClinVar dbSNP
12g.6019479C>ACA383506117VWFc.3939G>T (p.Trp1313Cys)
n.421-25545G>T
12g.6019479C=CA2013873004VWFc.3939G= (p.Trp1313=)
n.421-25545G=
12g.6019479C>GCA114121VWFc.3939G>C (p.Trp1313Cys)
n.421-25545G>C
ClinVar dbSNP
12g.6019479C>TCA383506120VWFc.3939G>A (p.Trp1313Ter)
n.421-25545G>A
12g.6019480C>ACA383506126VWFc.3938G>T (p.Trp1313Leu)
n.421-25546G>T
12g.6019480C>GCA383506122VWFc.3938G>C (p.Trp1313Ser)
n.421-25546G>C
12g.6019480C>TCA383506124VWFc.3938G>A (p.Trp1313Ter)
n.421-25546G>A
COSMIC
12g.6019481A>CCA383506129VWFc.3937T>G (p.Trp1313Gly)
n.421-25547T>G
12g.6019481A>GCA383506131VWFc.3937T>C (p.Trp1313Arg)
n.421-25547T>C
12g.6019481A>TCA383506133VWFc.3937T>A (p.Trp1313Arg)
n.421-25547T>A
12g.6019482C>ACA383506136VWFc.3936G>T (p.Lys1312Asn)
n.421-25548G>T
ClinVar dbSNP gnomAD v4
12g.6019482C=CA2013873005VWFc.3936G= (p.Lys1312=)
n.421-25548G=
12g.6019482C>GCA383506138VWFc.3936G>C (p.Lys1312Asn)
n.421-25548G>C
12g.6019482C>TCA478502876VWFc.3936G>A (p.Lys1312=)
n.421-25548G>A
gnomAD v4
12g.6019483T>ACA383506140VWFc.3935A>T (p.Lys1312Met)
n.421-25549A>T
12g.6019483T>CCA383506143VWFc.3935A>G (p.Lys1312Arg)
n.421-25549A>G
12g.6019483T>GCA383506141VWFc.3935A>C (p.Lys1312Thr)
n.421-25549A>C
12g.6019484T>ACA383506146VWFc.3934A>T (p.Lys1312Ter)
n.421-25550A>T
12g.6019484T>CCA383506148VWFc.3934A>G (p.Lys1312Glu)
n.421-25550A>G
gnomAD v4
12g.6019484T>GCA383506150VWFc.3934A>C (p.Lys1312Gln)
n.421-25550A>C
gnomAD v4
12g.6019485C>ACA383506152VWFc.3933G>T (p.Gln1311His)
n.421-25551G>T
12g.6019485C>GCA383506154VWFc.3933G>C (p.Gln1311His)
n.421-25551G>C
12g.6019485C>TCA478502884VWFc.3933G>A (p.Gln1311=)
n.421-25551G>A
12g.6019486T>ACA383506157VWFc.3932A>T (p.Gln1311Leu)
n.421-25552A>T
12g.6019486T>CCA383506159VWFc.3932A>G (p.Gln1311Arg)
n.421-25552A>G
12g.6019486T>GCA383506161VWFc.3932A>C (p.Gln1311Pro)
n.421-25552A>C
12g.6019487G>ACA228496VWFc.3931C>T (p.Gln1311Ter)
n.421-25553C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.6019487G>CCA383506165VWFc.3931C>G (p.Gln1311Glu)
n.421-25553C>G
gnomAD v4
12g.6019487G=CA2013873006VWFc.3931C= (p.Gln1311=)
n.421-25553C=
12g.6019487G>TCA6402648VWFc.3931C>A (p.Gln1311Lys)
n.421-25553C>A
dbSNP ExAC gnomAD v2 gnomAD v4
12g.6019488G>ACA478502893VWFc.3930C>T (p.Ser1310=)
n.421-25554C>T
gnomAD v4
12g.6019488G>CCA478502895VWFc.3930C>G (p.Ser1310=)
n.421-25554C>G
12g.6019488G>TCA478502898VWFc.3930C>A (p.Ser1310=)
n.421-25554C>A
12g.6019489G>ACA228494VWFc.3929C>T (p.Ser1310Phe)
n.421-25555C>T
ClinVar dbSNP
12g.6019489G>CCA383506170VWFc.3929C>G (p.Ser1310Cys)
n.421-25555C>G
12g.6019489G=CA2013873007VWFc.3929C= (p.Ser1310=)
n.421-25555C=
12g.6019489G>TCA383506168VWFc.3929C>A (p.Ser1310Tyr)
n.421-25555C>A
12g.6019490A>CCA383506174VWFc.3928T>G (p.Ser1310Ala)
n.421-25556T>G
12g.6019490A>GCA383506177VWFc.3928T>C (p.Ser1310Pro)
n.421-25556T>C
ClinVar dbSNP
12g.6019490A>TCA383506176VWFc.3928T>A (p.Ser1310Thr)
n.421-25556T>A
12g.6019491G>ACA478502910VWFc.3927C>T (p.Ile1309=)
n.421-25557C>T
dbSNP
12g.6019491G>CCA383506180VWFc.3927C>G (p.Ile1309Met)
n.421-25557C>G
12g.6019491G=CA2013873008VWFc.3927C= (p.Ile1309=)
n.421-25557C=
12g.6019491G>TCA478502912VWFc.3927C>A (p.Ile1309=)
n.421-25557C>A
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
12g.6019492A>CCA383506183VWFc.3926T>G (p.Ile1309Ser)
n.421-25558T>G
12g.6019492A>GCA383506181VWFc.3926T>C (p.Ile1309Thr)
n.421-25558T>C
12g.6019492A>TCA383506185VWFc.3926T>A (p.Ile1309Asn)
n.421-25558T>A
ClinVar dbSNP
12g.6019493T>ACA383506188VWFc.3925A>T (p.Ile1309Phe)
n.421-25559A>T
12g.6019493T>CCA228492VWFc.3925A>G (p.Ile1309Val)
n.421-25559A>G
ClinVar dbSNP
12g.6019493T>GCA383506190VWFc.3925A>C (p.Ile1309Leu)
n.421-25559A>C
12g.6019493T=CA2013873009VWFc.3925A= (p.Ile1309=)
n.421-25559A=
12g.6019494G>ACA6402649VWFc.3924C>T (p.Arg1308=)
n.421-25560C>T
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.6019494G>CCA478502922VWFc.3924C>G (p.Arg1308=)
n.421-25560C>G
12g.6019494G=CA2013873010VWFc.3924C= (p.Arg1308=)
n.421-25560C=
12g.6019494G>TCA478502924VWFc.3924C>A (p.Arg1308=)
n.421-25560C>A
12g.6019495C>ACA6402650VWFc.3923G>T (p.Arg1308Leu)
n.421-25561G>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
12g.6019495C=CA2013873011VWFc.3923G= (p.Arg1308=)
n.421-25561G=
12g.6019495C>GCA228490VWFc.3923G>C (p.Arg1308Pro)
n.421-25561G>C
ClinVar dbSNP
12g.6019495C>TCA228488VWFc.3923G>A (p.Arg1308His)
n.421-25561G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
12g.6019496G>ACA114125VWFc.3922C>T (p.Arg1308Cys)
n.421-25562C>T
ClinVar dbSNP
12g.6019496G>CCA383506201VWFc.3922C>G (p.Arg1308Gly)
n.421-25562C>G
12g.6019496G=CA2013873012VWFc.3922C= (p.Arg1308=)
n.421-25562C=
12g.6019496G>TCA383506203VWFc.3922C>A (p.Arg1308Ser)
n.421-25562C>A
12g.6019497C>ACA478502927VWFc.3921G>T (p.Leu1307=)
n.421-25563G>T
12g.6019497C>GCA478502928VWFc.3921G>C (p.Leu1307=)
n.421-25563G>C
12g.6019497C>TCA478502930VWFc.3921G>A (p.Leu1307=)
n.421-25563G>A
12g.6019498A=CA2013873013VWFc.3920T= (p.Leu1307=)
n.421-25564T=
12g.6019498A>CCA383506205VWFc.3920T>G (p.Leu1307Arg)
n.421-25564T>G
12g.6019498A>GCA228486VWFc.3920T>C (p.Leu1307Pro)
n.421-25564T>C
ClinVar dbSNP
12g.6019498A>TCA383506207VWFc.3920T>A (p.Leu1307Gln)
n.421-25564T>A
12g.6019499G>ACA478502933VWFc.3919C>T (p.Leu1307=)
n.421-25565C>T
dbSNP
12g.6019499G>CCA383506209VWFc.3919C>G (p.Leu1307Val)
n.421-25565C>G
12g.6019499G=CA2013873014VWFc.3919C= (p.Leu1307=)
n.421-25565C=
12g.6019499G>TCA383506211VWFc.3919C>A (p.Leu1307Met)
n.421-25565C>A
12g.6019500C>ACA478502936VWFc.3918G>T (p.Arg1306=)
n.421-25566G>T
gnomAD v4
12g.6019500C>GCA478502937VWFc.3918G>C (p.Arg1306=)
n.421-25566G>C
12g.6019500C>TCA478502935VWFc.3918G>A (p.Arg1306=)
n.421-25566G>A
gnomAD v4
12g.6019501C>ACA228484VWFc.3917G>T (p.Arg1306Leu)
n.421-25567G>T
ClinVar dbSNP gnomAD v4
12g.6019501C=CA2013873015VWFc.3917G= (p.Arg1306=)
n.421-25567G=
12g.6019501C>GCA383506213VWFc.3917G>C (p.Arg1306Pro)
n.421-25567G>C
ClinVar dbSNP
12g.6019501C>TCA228482VWFc.3917G>A (p.Arg1306Gln)
n.421-25567G>A
ClinVar dbSNP gnomAD v3 gnomAD v4
12g.6019502G>ACA114123VWFc.3916C>T (p.Arg1306Trp)
n.421-25568C>T
ClinVar dbSNP
12g.6019502G>CCA383506218VWFc.3916C>G (p.Arg1306Gly)
n.421-25568C>G
12g.6019502G=CA2013873016VWFc.3916C= (p.Arg1306=)
n.421-25568C=
12g.6019502G>TCA478502941VWFc.3916C>A (p.Arg1306=)
n.421-25568C>A
dbSNP gnomAD v4
12g.6019503C>ACA383506221VWFc.3915G>T (p.Glu1305Asp)
n.421-25569G>T
12g.6019503C>GCA383506223VWFc.3915G>C (p.Glu1305Asp)
n.421-25569G>C
12g.6019503C>TCA478502942VWFc.3915G>A (p.Glu1305=)
n.421-25569G>A
gnomAD v4 COSMIC

Number of alleles fetched