Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
12 | g.6019309C>A | CA383504528 | VWF | c.4109G>T (p.Ser1370Ile) n.421-25375G>T | |
12 | g.6019309C>G | CA383504530 | VWF | c.4109G>C (p.Ser1370Thr) n.421-25375G>C | |
12 | g.6019309C>T | CA383504532 | VWF | c.4109G>A (p.Ser1370Asn) n.421-25375G>A | |
12 | g.6019310T>A | CA383504535 | VWF | c.4108A>T (p.Ser1370Cys) n.421-25376A>T | |
12 | g.6019310T>C | CA383504537 | VWF | c.4108A>G (p.Ser1370Gly) n.421-25376A>G | |
12 | g.6019310T>G | CA383504538 | VWF | c.4108A>C (p.Ser1370Arg) n.421-25376A>C | |
12 | g.6019311G>A | CA6402600 | VWF | c.4107C>T (p.Phe1369=) n.421-25377C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
12 | g.6019311G>C | CA383504541 | VWF | c.4107C>G (p.Phe1369Leu) n.421-25377C>G | gnomAD v4 |
12 | g.6019311G= | CA2013872910 | VWF | c.4107C= (p.Phe1369=) n.421-25377C= | |
12 | g.6019311G>T | CA383504542 | VWF | c.4107C>A (p.Phe1369Leu) n.421-25377C>A | |
12 | g.6019312A>C | CA383505285 | VWF | c.4106T>G (p.Phe1369Cys) n.421-25378T>G | |
12 | g.6019312A>G | CA383505286 | VWF | c.4106T>C (p.Phe1369Ser) n.421-25378T>C | |
12 | g.6019312A>T | CA383505287 | VWF | c.4106T>A (p.Phe1369Tyr) n.421-25378T>A | |
12 | g.6019313A= | CA2013872911 | VWF | c.4105T= (p.Phe1369=) n.421-25379T= | |
12 | g.6019313A>C | CA383505290 | VWF | c.4105T>G (p.Phe1369Val) n.421-25379T>G | |
12 | g.6019313A>G | CA383505291 | VWF | c.4105T>C (p.Phe1369Leu) n.421-25379T>C | ClinVar dbSNP |
12 | g.6019313A>T | CA228533 | VWF | c.4105T>A (p.Phe1369Ile) n.421-25379T>A | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.6019314G>A | CA478502327 | VWF | c.4104C>T (p.Ile1368=) n.421-25380C>T | |
12 | g.6019314G>C | CA383505292 | VWF | c.4104C>G (p.Ile1368Met) n.421-25380C>G | |
12 | g.6019314G= | CA2013872912 | VWF | c.4104C= (p.Ile1368=) n.421-25380C= | |
12 | g.6019314G>T | CA478502328 | VWF | c.4104C>A (p.Ile1368=) n.421-25380C>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.6019315A= | CA2013872913 | VWF | c.4103T= (p.Ile1368=) n.421-25381T= | |
12 | g.6019315A>C | CA383505293 | VWF | c.4103T>G (p.Ile1368Ser) n.421-25381T>G | |
12 | g.6019315A>G | CA6402601 | VWF | c.4103T>C (p.Ile1368Thr) n.421-25381T>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.6019315A>T | CA383505295 | VWF | c.4103T>A (p.Ile1368Asn) n.421-25381T>A | |
12 | g.6019316T>A | CA383505297 | VWF | c.4102A>T (p.Ile1368Phe) n.421-25382A>T | |
12 | g.6019316T>C | CA232297772 | VWF | c.4102A>G (p.Ile1368Val) n.421-25382A>G | dbSNP gnomAD v4 |
12 | g.6019316T>G | CA383505299 | VWF | c.4102A>C (p.Ile1368Leu) n.421-25382A>C | |
12 | g.6019316T= | CA2013872914 | VWF | c.4102A= (p.Ile1368=) n.421-25382A= | |
12 | g.6019317T>A | CA383505302 | VWF | c.4101A>T (p.Gln1367His) n.421-25383A>T | dbSNP gnomAD v3 gnomAD v4 |
12 | g.6019317T>C | CA478502329 | VWF | c.4101A>G (p.Gln1367=) n.421-25383A>G | |
12 | g.6019317T>G | CA383505306 | VWF | c.4101A>C (p.Gln1367His) n.421-25383A>C | |
12 | g.6019318T>A | CA383505309 | VWF | c.4100A>T (p.Gln1367Leu) n.421-25384A>T | |
12 | g.6019318T>C | CA383505311 | VWF | c.4100A>G (p.Gln1367Arg) n.421-25384A>G | |
12 | g.6019318T>G | CA383505308 | VWF | c.4100A>C (p.Gln1367Pro) n.421-25384A>C | |
12 | g.6019319G>A | CA383505314 | VWF | c.4099C>T (p.Gln1367Ter) n.421-25385C>T | |
12 | g.6019319G>C | CA383505315 | VWF | c.4099C>G (p.Gln1367Glu) n.421-25385C>G | |
12 | g.6019319G>T | CA383505317 | VWF | c.4099C>A (p.Gln1367Lys) n.421-25385C>A | |
12 | g.6019320G>A | CA478502330 | VWF | c.4098C>T (p.Phe1366=) n.421-25386C>T | dbSNP gnomAD v3 gnomAD v4 |
12 | g.6019320G>C | CA6402602 | VWF | c.4098C>G (p.Phe1366Leu) n.421-25386C>G | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.6019320G= | CA2013872915 | VWF | c.4098C= (p.Phe1366=) n.421-25386C= | |
12 | g.6019320G>T | CA383505320 | VWF | c.4098C>A (p.Phe1366Leu) n.421-25386C>A | dbSNP gnomAD v4 |
12 | g.6019321A= | CA2013872916 | VWF | c.4097T= (p.Phe1366=) n.421-25387T= | |
12 | g.6019321A>C | CA383505326 | VWF | c.4097T>G (p.Phe1366Cys) n.421-25387T>G | gnomAD v4 |
12 | g.6019321A>G | CA383505322 | VWF | c.4097T>C (p.Phe1366Ser) n.421-25387T>C | dbSNP |
12 | g.6019321A>T | CA383505324 | VWF | c.4097T>A (p.Phe1366Tyr) n.421-25387T>A | |
12 | g.6019322A>C | CA383505327 | VWF | c.4096T>G (p.Phe1366Val) n.421-25388T>G | |
12 | g.6019322A>G | CA383505328 | VWF | c.4096T>C (p.Phe1366Leu) n.421-25388T>C | |
12 | g.6019322A>T | CA383505329 | VWF | c.4096T>A (p.Phe1366Ile) n.421-25388T>A | |
12 | g.6019323C>A | CA6402604 | VWF | c.4095G>T (p.Leu1365=) n.421-25389G>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
12 | g.6019323C= | CA2013872917 | VWF | c.4095G= (p.Leu1365=) n.421-25389G= | |
12 | g.6019323C>G | CA478502331 | VWF | c.4095G>C (p.Leu1365=) n.421-25389G>C | |
12 | g.6019323C>T | CA6402603 | VWF | c.4095G>A (p.Leu1365=) n.421-25389G>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
12 | g.6019324A= | CA2013872919 | VWF | c.4094T= (p.Leu1365=) n.421-25390T= | |
12 | g.6019324A>C | CA383505335 | VWF | c.4094T>G (p.Leu1365Arg) n.421-25390T>G | gnomAD v4 |
12 | g.6019324A>G | CA383505339 | VWF | c.4094T>C (p.Leu1365Pro) n.421-25390T>C | ClinVar dbSNP |
12 | g.6019324A>T | CA6402605 | VWF | c.4094T>A (p.Leu1365Gln) n.421-25390T>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
12 | g.6019324_6019325del | CA2617230629 | VWF | c.4093_4094del (p.Leu1365ValfsTer11) n.421-25391_421-25390del | gnomAD v4 |
12 | g.6019324_6019326delinsAGT | CA2013872918 | VWF | c.4092_4094delinsACT (p.Thr1364=) n.421-25392_421-25390delinsACT | |
12 | g.6019325G>A | CA478502332 | VWF | c.4093C>T (p.Leu1365=) n.421-25391C>T | |
12 | g.6019325G>C | CA383505341 | VWF | c.4093C>G (p.Leu1365Val) n.421-25391C>G | |
12 | g.6019325G>T | CA383505343 | VWF | c.4093C>A (p.Leu1365Met) n.421-25391C>A | |
12 | g.6019329_6019330del | CA228532 | VWF | c.4092_4093del (p.Leu1365ValfsTer11) n.421-25392_421-25391del | ClinVar dbSNP |
12 | g.6019326T>A | CA478502333 | VWF | c.4092A>T (p.Thr1364=) n.421-25392A>T | |
12 | g.6019326T>C | CA6402606 | VWF | c.4092A>G (p.Thr1364=) n.421-25392A>G | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.6019326T>G | CA478502334 | VWF | c.4092A>C (p.Thr1364=) n.421-25392A>C | |
12 | g.6019326T= | CA2013872920 | VWF | c.4092A= (p.Thr1364=) n.421-25392A= | |
12 | g.6019327G>A | CA383505347 | VWF | c.4091C>T (p.Thr1364Ile) n.421-25393C>T | dbSNP |
12 | g.6019327G>C | CA383505349 | VWF | c.4091C>G (p.Thr1364Arg) n.421-25393C>G | |
12 | g.6019327G= | CA2013872921 | VWF | c.4091C= (p.Thr1364=) n.421-25393C= | |
12 | g.6019327G>T | CA383505351 | VWF | c.4091C>A (p.Thr1364Lys) n.421-25393C>A | |
12 | g.6019328T>A | CA6402607 | VWF | c.4090A>T (p.Thr1364Ser) n.421-25394A>T | dbSNP ExAC |
12 | g.6019328T>C | CA383505353 | VWF | c.4090A>G (p.Thr1364Ala) n.421-25394A>G | dbSNP gnomAD v3 gnomAD v4 |
12 | g.6019328T>G | CA383505354 | VWF | c.4090A>C (p.Thr1364Pro) n.421-25394A>C | |
12 | g.6019328T= | CA2013872922 | VWF | c.4090A= (p.Thr1364=) n.421-25394A= | |
12 | g.6019328_6019329delinsTG | CA2013872923 | VWF | c.4089_4090delinsCA (p.Tyr1363=) n.421-25395_421-25394delinsCA | |
12 | g.6019329del | CA2013872924 | VWF | c.4089del (p.Tyr1363Ter) n.421-25395del | dbSNP |
12 | g.6019329G>A | CA478502335 | VWF | c.4089C>T (p.Tyr1363=) n.421-25395C>T | gnomAD v4 |
12 | g.6019329G>C | CA383505356 | VWF | c.4089C>G (p.Tyr1363Ter) n.421-25395C>G | |
12 | g.6019329G>T | CA383505358 | VWF | c.4089C>A (p.Tyr1363Ter) n.421-25395C>A | |
12 | g.6019330T>A | CA383505362 | VWF | c.4088A>T (p.Tyr1363Phe) n.421-25396A>T | |
12 | g.6019330T>C | CA383505363 | VWF | c.4088A>G (p.Tyr1363Cys) n.421-25396A>G | gnomAD v4 |
12 | g.6019330T>G | CA383505360 | VWF | c.4088A>C (p.Tyr1363Ser) n.421-25396A>C | |
12 | g.6019331A>C | CA383505368 | VWF | c.4087T>G (p.Tyr1363Asp) n.421-25397T>G | |
12 | g.6019331A>G | CA383505366 | VWF | c.4087T>C (p.Tyr1363His) n.421-25397T>C | |
12 | g.6019331A>T | CA383505372 | VWF | c.4087T>A (p.Tyr1363Asn) n.421-25397T>A | |
12 | g.6019332T>A | CA383505373 | VWF | c.4086A>T (p.Lys1362Asn) n.421-25398A>T | |
12 | g.6019332T>C | CA478502336 | VWF | c.4086A>G (p.Lys1362=) n.421-25398A>G | dbSNP gnomAD v2 gnomAD v4 |
12 | g.6019332T>G | CA383505374 | VWF | c.4086A>C (p.Lys1362Asn) n.421-25398A>C | |
12 | g.6019332T= | CA2013872925 | VWF | c.4086A= (p.Lys1362=) n.421-25398A= | |
12 | g.6019333T>A | CA383505376 | VWF | c.4085A>T (p.Lys1362Ile) n.421-25399A>T | |
12 | g.6019333T>C | CA383505378 | VWF | c.4085A>G (p.Lys1362Arg) n.421-25399A>G | |
12 | g.6019333T>G | CA228530 | VWF | c.4085A>C (p.Lys1362Thr) n.421-25399A>C | ClinVar dbSNP |
12 | g.6019333T= | CA2013872926 | VWF | c.4085A= (p.Lys1362=) n.421-25399A= | |
12 | g.6019334T>A | CA383505380 | VWF | c.4084A>T (p.Lys1362Ter) n.421-25400A>T | |
12 | g.6019334T>C | CA383505382 | VWF | c.4084A>G (p.Lys1362Glu) n.421-25400A>G | |
12 | g.6019334T>G | CA383505384 | VWF | c.4084A>C (p.Lys1362Gln) n.421-25400A>C | |
12 | g.6019335C>A | CA383505387 | VWF | c.4083G>T (p.Leu1361Phe) n.421-25401G>T | |
12 | g.6019335C= | CA2013872927 | VWF | c.4083G= (p.Leu1361=) n.421-25401G= | |
12 | g.6019335C>G | CA383505389 | VWF | c.4083G>C (p.Leu1361Phe) n.421-25401G>C | |
12 | g.6019335C>T | CA6402608 | VWF | c.4083G>A (p.Leu1361=) n.421-25401G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.6019336A= | CA2013872928 | VWF | c.4082T= (p.Leu1361=) n.421-25402T= | |
12 | g.6019336A>C | CA383505395 | VWF | c.4082T>G (p.Leu1361Trp) n.421-25402T>G | |
12 | g.6019336A>G | CA228528 | VWF | c.4082T>C (p.Leu1361Ser) n.421-25402T>C | ClinVar dbSNP gnomAD v4 |
12 | g.6019336A>T | CA383505393 | VWF | c.4082T>A (p.Leu1361Ter) n.421-25402T>A | |
12 | g.6019337A>C | CA383505397 | VWF | c.4081T>G (p.Leu1361Val) n.421-25403T>G | |
12 | g.6019337A>G | CA478502337 | VWF | c.4081T>C (p.Leu1361=) n.421-25403T>C | gnomAD v4 |
12 | g.6019337A>T | CA383505399 | VWF | c.4081T>A (p.Leu1361Met) n.421-25403T>A | |
12 | g.6019338G>A | CA6402609 | VWF | c.4080C>T (p.Val1360=) n.421-25404C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.6019338G>C | CA478502338 | VWF | c.4080C>G (p.Val1360=) n.421-25404C>G | |
12 | g.6019338G= | CA2013872929 | VWF | c.4080C= (p.Val1360=) n.421-25404C= | |
12 | g.6019338G>T | CA478502339 | VWF | c.4080C>A (p.Val1360=) n.421-25404C>A | |
12 | g.6019339A= | CA2013872930 | VWF | c.4079T= (p.Val1360=) n.421-25405T= | |
12 | g.6019339A>C | CA383505402 | VWF | c.4079T>G (p.Val1360Gly) n.421-25405T>G | |
12 | g.6019339A>G | CA228526 | VWF | c.4079T>C (p.Val1360Ala) n.421-25405T>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.6019339A>T | CA383505405 | VWF | c.4079T>A (p.Val1360Asp) n.421-25405T>A | |
12 | g.6019340C>A | CA383505406 | VWF | c.4078G>T (p.Val1360Phe) n.421-25406G>T | ClinVar |
12 | g.6019340C>G | CA383505407 | VWF | c.4078G>C (p.Val1360Leu) n.421-25406G>C | |
12 | g.6019340C>T | CA383505408 | VWF | c.4078G>A (p.Val1360Ile) n.421-25406G>A | |
12 | g.6019341C>A | CA383505411 | VWF | c.4077G>T (p.Glu1359Asp) n.421-25407G>T | |
12 | g.6019341C>G | CA383505413 | VWF | c.4077G>C (p.Glu1359Asp) n.421-25407G>C | |
12 | g.6019341C>T | CA478502340 | VWF | c.4077G>A (p.Glu1359=) n.421-25407G>A | |
12 | g.6019342T>A | CA383505420 | VWF | c.4076A>T (p.Glu1359Val) n.421-25408A>T | |
12 | g.6019342T>C | CA383505422 | VWF | c.4076A>G (p.Glu1359Gly) n.421-25408A>G | |
12 | g.6019342T>G | CA383505417 | VWF | c.4076A>C (p.Glu1359Ala) n.421-25408A>C | |
12 | g.6019343C>A | CA383505426 | VWF | c.4075G>T (p.Glu1359Ter) n.421-25409G>T | |
12 | g.6019343C= | CA2013872931 | VWF | c.4075G= (p.Glu1359=) n.421-25409G= | |
12 | g.6019343C>G | CA383505430 | VWF | c.4075G>C (p.Glu1359Gln) n.421-25409G>C | gnomAD v4 |
12 | g.6019343C>T | CA228524 | VWF | c.4075G>A (p.Glu1359Lys) n.421-25409G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.6019344G>A | CA6402610 | VWF | c.4074C>T (p.Ser1358=) n.421-25410C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.6019344G>C | CA383505434 | VWF | c.4074C>G (p.Ser1358Arg) n.421-25410C>G | |
12 | g.6019344G= | CA2013872932 | VWF | c.4074C= (p.Ser1358=) n.421-25410C= | |
12 | g.6019344G>T | CA383505435 | VWF | c.4074C>A (p.Ser1358Arg) n.421-25410C>A | |
12 | g.6019345C>A | CA383505439 | VWF | c.4073G>T (p.Ser1358Ile) n.421-25411G>T | |
12 | g.6019345C>G | CA383505441 | VWF | c.4073G>C (p.Ser1358Thr) n.421-25411G>C | |
12 | g.6019345C>T | CA383505443 | VWF | c.4073G>A (p.Ser1358Asn) n.421-25411G>A | |
12 | g.6019346T>A | CA383505449 | VWF | c.4072A>T (p.Ser1358Cys) n.421-25412A>T | |
12 | g.6019346T>C | CA383505451 | VWF | c.4072A>G (p.Ser1358Gly) n.421-25412A>G | |
12 | g.6019346T>G | CA383505452 | VWF | c.4072A>C (p.Ser1358Arg) n.421-25412A>C | gnomAD v4 |
12 | g.6019347G>A | CA478502341 | VWF | c.4071C>T (p.Thr1357=) n.421-25413C>T | gnomAD v4 |
12 | g.6019347G>C | CA478502342 | VWF | c.4071C>G (p.Thr1357=) n.421-25413C>G | gnomAD v4 |
12 | g.6019347G>T | CA478502343 | VWF | c.4071C>A (p.Thr1357=) n.421-25413C>A | |
12 | g.6019348G>A | CA383505459 | VWF | c.4070C>T (p.Thr1357Ile) n.421-25414C>T | gnomAD v4 |
12 | g.6019348G>C | CA6402611 | VWF | c.4070C>G (p.Thr1357Ser) n.421-25414C>G | dbSNP ExAC gnomAD v2 gnomAD v4 |
12 | g.6019348G= | CA2013872933 | VWF | c.4070C= (p.Thr1357=) n.421-25414C= | |
12 | g.6019348G>T | CA383505455 | VWF | c.4070C>A (p.Thr1357Asn) n.421-25414C>A | |
12 | g.6019349T>A | CA383505464 | VWF | c.4069A>T (p.Thr1357Ser) n.421-25415A>T | |
12 | g.6019349T>C | CA383505468 | VWF | c.4069A>G (p.Thr1357Ala) n.421-25415A>G | |
12 | g.6019349T>G | CA383505475 | VWF | c.4069A>C (p.Thr1357Pro) n.421-25415A>C | gnomAD v4 |
12 | g.6019350G>A | CA478502344 | VWF | c.4068C>T (p.Ser1356=) n.421-25416C>T | gnomAD v4 |
12 | g.6019350G>C | CA478502346 | VWF | c.4068C>G (p.Ser1356=) n.421-25416C>G | |
12 | g.6019350G>T | CA478502345 | VWF | c.4068C>A (p.Ser1356=) n.421-25416C>A | |
12 | g.6019351del | CA2575053891 | VWF | c.4068del (p.Thr1357ProfsTer5) n.421-25416del | |
12 | g.6019351G>A | CA383505478 | VWF | c.4067C>T (p.Ser1356Phe) n.421-25417C>T | ClinVar |
12 | g.6019351G>C | CA383505481 | VWF | c.4067C>G (p.Ser1356Cys) n.421-25417C>G | |
12 | g.6019351G>T | CA383505483 | VWF | c.4067C>A (p.Ser1356Tyr) n.421-25417C>A | |
12 | g.6019352A>C | CA383505487 | VWF | c.4066T>G (p.Ser1356Ala) n.421-25418T>G | |
12 | g.6019352A>G | CA383505488 | VWF | c.4066T>C (p.Ser1356Pro) n.421-25418T>C | |
12 | g.6019352A>T | CA383505502 | VWF | c.4066T>A (p.Ser1356Thr) n.421-25418T>A | |
12 | g.6019353G>A | CA478502347 | VWF | c.4065C>T (p.Ala1355=) n.421-25419C>T | |
12 | g.6019353G>C | CA6402612 | VWF | c.4065C>G (p.Ala1355=) n.421-25419C>G | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.6019353G= | CA2013872934 | VWF | c.4065C= (p.Ala1355=) n.421-25419C= | |
12 | g.6019353G>T | CA478502348 | VWF | c.4065C>A (p.Ala1355=) n.421-25419C>A | |
12 | g.6019354G>A | CA383505508 | VWF | c.4064C>T (p.Ala1355Val) n.421-25420C>T | dbSNP gnomAD v3 gnomAD v4 |
12 | g.6019354G>C | CA383505509 | VWF | c.4064C>G (p.Ala1355Gly) n.421-25420C>G | |
12 | g.6019354G= | CA2013872935 | VWF | c.4064C= (p.Ala1355=) n.421-25420C= | |
12 | g.6019354G>T | CA383505511 | VWF | c.4064C>A (p.Ala1355Asp) n.421-25420C>A | |
12 | g.6019355C>A | CA383505518 | VWF | c.4063G>T (p.Ala1355Ser) n.421-25421G>T | |
12 | g.6019355C>G | CA383505523 | VWF | c.4063G>C (p.Ala1355Pro) n.421-25421G>C | |
12 | g.6019355C>T | CA383505516 | VWF | c.4063G>A (p.Ala1355Thr) n.421-25421G>A | |
12 | g.6019356dup | CA2532169638 | VWF | c.4063dup (p.Ala1355GlyfsTer22) n.421-25421dup | |
12 | g.6019356C>A | CA478502349 | VWF | c.4062G>T (p.Val1354=) n.421-25422G>T | |
12 | g.6019356C= | CA2013872936 | VWF | c.4062G= (p.Val1354=) n.421-25422G= | |
12 | g.6019356C>G | CA478502350 | VWF | c.4062G>C (p.Val1354=) n.421-25422G>C | |
12 | g.6019356C>T | CA6402613 | VWF | c.4062G>A (p.Val1354=) n.421-25422G>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
12 | g.6019357A>C | CA383505528 | VWF | c.4061T>G (p.Val1354Gly) n.421-25423T>G | |
12 | g.6019357A>G | CA383505533 | VWF | c.4061T>C (p.Val1354Ala) n.421-25423T>C | |
12 | g.6019357A>T | CA383505537 | VWF | c.4061T>A (p.Val1354Glu) n.421-25423T>A | |
12 | g.6019358C>A | CA383505542 | VWF | c.4060G>T (p.Val1354Leu) n.421-25424G>T | |
12 | g.6019358C>G | CA383505544 | VWF | c.4060G>C (p.Val1354Leu) n.421-25424G>C | |
12 | g.6019358C>T | CA383505547 | VWF | c.4060G>A (p.Val1354Met) n.421-25424G>A | |
12 | g.6019359C>A | CA6402614 | VWF | c.4059G>T (p.Gln1353His) n.421-25425G>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
12 | g.6019359C= | CA2013872937 | VWF | c.4059G= (p.Gln1353=) n.421-25425G= | |
12 | g.6019359C>G | CA383505551 | VWF | c.4059G>C (p.Gln1353His) n.421-25425G>C | |
12 | g.6019359C>T | CA478502351 | VWF | c.4059G>A (p.Gln1353=) n.421-25425G>A | |
12 | g.6019360T>A | CA383505555 | VWF | c.4058A>T (p.Gln1353Leu) n.421-25426A>T | gnomAD v3 gnomAD v4 |
12 | g.6019360T>C | CA383505558 | VWF | c.4058A>G (p.Gln1353Arg) n.421-25426A>G | |
12 | g.6019360T>G | CA383505561 | VWF | c.4058A>C (p.Gln1353Pro) n.421-25426A>C | |
12 | g.6019361G>A | CA383505565 | VWF | c.4057C>T (p.Gln1353Ter) n.421-25427C>T | dbSNP gnomAD v2 gnomAD v4 |
12 | g.6019361G>C | CA383505568 | VWF | c.4057C>G (p.Gln1353Glu) n.421-25427C>G | |
12 | g.6019361G= | CA2013872938 | VWF | c.4057C= (p.Gln1353=) n.421-25427C= | |
12 | g.6019361G>T | CA383505570 | VWF | c.4057C>A (p.Gln1353Lys) n.421-25427C>A | |
12 | g.6019362G>A | CA478502352 | VWF | c.4056C>T (p.Ser1352=) n.421-25428C>T | gnomAD v4 |
12 | g.6019362G>C | CA383505575 | VWF | c.4056C>G (p.Ser1352Arg) n.421-25428C>G | |
12 | g.6019362G>T | CA383505577 | VWF | c.4056C>A (p.Ser1352Arg) n.421-25428C>A | |
12 | g.6019363C>A | CA383505582 | VWF | c.4055G>T (p.Ser1352Ile) n.421-25429G>T | gnomAD v4 |
12 | g.6019363C>G | CA383505592 | VWF | c.4055G>C (p.Ser1352Thr) n.421-25429G>C | |
12 | g.6019363C>T | CA383505596 | VWF | c.4055G>A (p.Ser1352Asn) n.421-25429G>A | gnomAD v4 |
12 | g.6019364T>A | CA383505600 | VWF | c.4054A>T (p.Ser1352Cys) n.421-25430A>T | |
12 | g.6019364T>C | CA383505602 | VWF | c.4054A>G (p.Ser1352Gly) n.421-25430A>G | COSMIC |
12 | g.6019364T>G | CA383505608 | VWF | c.4054A>C (p.Ser1352Arg) n.421-25430A>C | |
12 | g.6019365G>A | CA478502353 | VWF | c.4053C>T (p.Gly1351=) n.421-25431C>T | |
12 | g.6019365G>C | CA478502354 | VWF | c.4053C>G (p.Gly1351=) n.421-25431C>G | |
12 | g.6019365G>T | CA478502355 | VWF | c.4053C>A (p.Gly1351=) n.421-25431C>A | |
12 | g.6019366C>A | CA383505611 | VWF | c.4052G>T (p.Gly1351Val) n.421-25432G>T | |
12 | g.6019366C>G | CA383505612 | VWF | c.4052G>C (p.Gly1351Ala) n.421-25432G>C | gnomAD v4 |
12 | g.6019366C>T | CA383505619 | VWF | c.4052G>A (p.Gly1351Asp) n.421-25432G>A | |
12 | g.6019367C>A | CA383505621 | VWF | c.4051G>T (p.Gly1351Cys) n.421-25433G>T | |
12 | g.6019367C= | CA2013872939 | VWF | c.4051G= (p.Gly1351=) n.421-25433G= | |
12 | g.6019367C>G | CA383505625 | VWF | c.4051G>C (p.Gly1351Arg) n.421-25433G>C | |
12 | g.6019367C>T | CA383505629 | VWF | c.4051G>A (p.Gly1351Ser) n.421-25433G>A | dbSNP gnomAD v2 gnomAD v4 |
12 | g.6019368C>A | CA478502356 | VWF | c.4050G>T (p.Ala1350=) n.421-25434G>T | |
12 | g.6019368C= | CA2013872940 | VWF | c.4050G= (p.Ala1350=) n.421-25434G= | |
12 | g.6019368C>G | CA478502357 | VWF | c.4050G>C (p.Ala1350=) n.421-25434G>C | |
12 | g.6019368C>T | CA6402615 | VWF | c.4050G>A (p.Ala1350=) n.421-25434G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.6019369G>A | CA6402616 | VWF | c.4049C>T (p.Ala1350Val) n.421-25435C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
12 | g.6019369G>C | CA383505634 | VWF | c.4049C>G (p.Ala1350Gly) n.421-25435C>G | |
12 | g.6019369G= | CA2013872941 | VWF | c.4049C= (p.Ala1350=) n.421-25435C= | |
12 | g.6019369G>T | CA383505632 | VWF | c.4049C>A (p.Ala1350Glu) n.421-25435C>A | |
12 | g.6019370C>A | CA383505638 | VWF | c.4048G>T (p.Ala1350Ser) n.421-25436G>T | |
12 | g.6019370C>G | CA383505640 | VWF | c.4048G>C (p.Ala1350Pro) n.421-25436G>C | |
12 | g.6019370C>T | CA383505643 | VWF | c.4048G>A (p.Ala1350Thr) n.421-25436G>A | |
12 | g.6019371A= | CA2013872942 | VWF | c.4047T= (p.Tyr1349=) n.421-25437T= | |
12 | g.6019371A>C | CA383505646 | VWF | c.4047T>G (p.Tyr1349Ter) n.421-25437T>G | |
12 | g.6019371A>G | CA478502359 | VWF | c.4047T>C (p.Tyr1349=) n.421-25437T>C | dbSNP gnomAD v2 gnomAD v4 |
12 | g.6019371A>T | CA383505647 | VWF | c.4047T>A (p.Tyr1349Ter) n.421-25437T>A | |
12 | g.6019372T>A | CA383505653 | VWF | c.4046A>T (p.Tyr1349Phe) n.421-25438A>T | dbSNP gnomAD v4 |
12 | g.6019372T>C | CA383505652 | VWF | c.4046A>G (p.Tyr1349Cys) n.421-25438A>G | |
12 | g.6019372T>G | CA383505651 | VWF | c.4046A>C (p.Tyr1349Ser) n.421-25438A>C | |
12 | g.6019373A>C | CA383505656 | VWF | c.4045T>G (p.Tyr1349Asp) n.421-25439T>G | |
12 | g.6019373A>G | CA383505658 | VWF | c.4045T>C (p.Tyr1349His) n.421-25439T>C | |
12 | g.6019373A>T | CA383505660 | VWF | c.4045T>A (p.Tyr1349Asn) n.421-25439T>A | |
12 | g.6019374C>A | CA383505663 | VWF | c.4044G>T (p.Lys1348Asn) n.421-25440G>T | dbSNP gnomAD v3 gnomAD v4 |
12 | g.6019374C= | CA2013872943 | VWF | c.4044G= (p.Lys1348=) n.421-25440G= | |
12 | g.6019374C>G | CA383505664 | VWF | c.4044G>C (p.Lys1348Asn) n.421-25440G>C | |
12 | g.6019374C>T | CA6402617 | VWF | c.4044G>A (p.Lys1348=) n.421-25440G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.6019375T>A | CA383505668 | VWF | c.4043A>T (p.Lys1348Met) n.421-25441A>T | |
12 | g.6019375T>C | CA383505672 | VWF | c.4043A>G (p.Lys1348Arg) n.421-25441A>G | |
12 | g.6019375T>G | CA383505670 | VWF | c.4043A>C (p.Lys1348Thr) n.421-25441A>C | |
12 | g.6019376T>A | CA383505673 | VWF | c.4042A>T (p.Lys1348Ter) n.421-25442A>T | |
12 | g.6019376T>C | CA6402618 | VWF | c.4042A>G (p.Lys1348Glu) n.421-25442A>G | dbSNP ExAC gnomAD v2 gnomAD v4 |
12 | g.6019376T>G | CA383505675 | VWF | c.4042A>C (p.Lys1348Gln) n.421-25442A>C | |
12 | g.6019376T= | CA2013872944 | VWF | c.4042A= (p.Lys1348=) n.421-25442A= | |
12 | g.6019377C>A | CA478502360 | VWF | c.4041G>T (p.Val1347=) n.421-25443G>T | |
12 | g.6019377C= | CA2013872945 | VWF | c.4041G= (p.Val1347=) n.421-25443G= | |
12 | g.6019377C>G | CA478502361 | VWF | c.4041G>C (p.Val1347=) n.421-25443G>C | |
12 | g.6019377C>T | CA478502362 | VWF | c.4041G>A (p.Val1347=) n.421-25443G>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.6019378A>C | CA383505677 | VWF | c.4040T>G (p.Val1347Gly) n.421-25444T>G | |
12 | g.6019378A>G | CA383505679 | VWF | c.4040T>C (p.Val1347Ala) n.421-25444T>C | |
12 | g.6019378A>T | CA383505681 | VWF | c.4040T>A (p.Val1347Glu) n.421-25444T>A | |
12 | g.6019379C>A | CA383505684 | VWF | c.4039G>T (p.Val1347Leu) n.421-25445G>T | |
12 | g.6019379C>G | CA383505686 | VWF | c.4039G>C (p.Val1347Leu) n.421-25445G>C | |
12 | g.6019379C>T | CA383505687 | VWF | c.4039G>A (p.Val1347Met) n.421-25445G>A | |
12 | g.6019380C>A | CA383505690 | VWF | c.4038G>T (p.Gln1346His) n.421-25446G>T | |
12 | g.6019380C>G | CA383505692 | VWF | c.4038G>C (p.Gln1346His) n.421-25446G>C | |
12 | g.6019380C>T | CA478502363 | VWF | c.4038G>A (p.Gln1346=) n.421-25446G>A | gnomAD v4 |
12 | g.6019381T>A | CA383505697 | VWF | c.4037A>T (p.Gln1346Leu) n.421-25447A>T | |
12 | g.6019381T>C | CA6402619 | VWF | c.4037A>G (p.Gln1346Arg) n.421-25447A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
12 | g.6019381T>G | CA383505695 | VWF | c.4037A>C (p.Gln1346Pro) n.421-25447A>C | |
12 | g.6019381T= | CA2013872946 | VWF | c.4037A= (p.Gln1346=) n.421-25447A= | |
12 | g.6019382G>A | CA228522 | VWF | c.4036C>T (p.Gln1346Ter) n.421-25448C>T | ClinVar dbSNP |
12 | g.6019382G>C | CA383505701 | VWF | c.4036C>G (p.Gln1346Glu) n.421-25448C>G | |
12 | g.6019382G= | CA2013872947 | VWF | c.4036C= (p.Gln1346=) n.421-25448C= | |
12 | g.6019382G>T | CA383505703 | VWF | c.4036C>A (p.Gln1346Lys) n.421-25448C>A | |
12 | g.6019383G>A | CA6402620 | VWF | c.4035C>T (p.Ser1345=) n.421-25449C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.6019383G>C | CA383505705 | VWF | c.4035C>G (p.Ser1345Arg) n.421-25449C>G | |
12 | g.6019383G= | CA2013872948 | VWF | c.4035C= (p.Ser1345=) n.421-25449C= | |
12 | g.6019383G>T | CA383505704 | VWF | c.4035C>A (p.Ser1345Arg) n.421-25449C>A | |
12 | g.6019384C>A | CA383505706 | VWF | c.4034G>T (p.Ser1345Ile) n.421-25450G>T | |
12 | g.6019384C>G | CA383505707 | VWF | c.4034G>C (p.Ser1345Thr) n.421-25450G>C | |
12 | g.6019384C>T | CA383505708 | VWF | c.4034G>A (p.Ser1345Asn) n.421-25450G>A | |
12 | g.6019385T>A | CA383505709 | VWF | c.4033A>T (p.Ser1345Cys) n.421-25451A>T | |
12 | g.6019385T>C | CA383505710 | VWF | c.4033A>G (p.Ser1345Gly) n.421-25451A>G | |
12 | g.6019385T>G | CA383505711 | VWF | c.4033A>C (p.Ser1345Arg) n.421-25451A>C | |
12 | g.6019386G>A | CA478502364 | VWF | c.4032C>T (p.Ala1344=) n.421-25452C>T | COSMIC |
12 | g.6019386G>C | CA478502365 | VWF | c.4032C>G (p.Ala1344=) n.421-25452C>G | |
12 | g.6019386G>T | CA478502366 | VWF | c.4032C>A (p.Ala1344=) n.421-25452C>A | |
12 | g.6019387G>A | CA383505712 | VWF | c.4031C>T (p.Ala1344Val) n.421-25453C>T | |
12 | g.6019387G>C | CA383505713 | VWF | c.4031C>G (p.Ala1344Gly) n.421-25453C>G | |
12 | g.6019387G>T | CA383505714 | VWF | c.4031C>A (p.Ala1344Asp) n.421-25453C>A | |
12 | g.6019388C>A | CA383505715 | VWF | c.4030G>T (p.Ala1344Ser) n.421-25454G>T | |
12 | g.6019388C>G | CA383505716 | VWF | c.4030G>C (p.Ala1344Pro) n.421-25454G>C | |
12 | g.6019388C>T | CA383505717 | VWF | c.4030G>A (p.Ala1344Thr) n.421-25454G>A | |
12 | g.6019389A= | CA2013872949 | VWF | c.4029T= (p.Ile1343=) n.421-25455T= | |
12 | g.6019389A>C | CA383505718 | VWF | c.4029T>G (p.Ile1343Met) n.421-25455T>G | |
12 | g.6019389A>G | CA478502367 | VWF | c.4029T>C (p.Ile1343=) n.421-25455T>C | |
12 | g.6019389A>T | CA6402621 | VWF | c.4029T>A (p.Ile1343=) n.421-25455T>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.6019390dup | CA2575053892 | VWF | c.4029dup (p.Ala1344CysfsTer?) n.421-25455dup | |
12 | g.6019390A>C | CA383505719 | VWF | c.4028T>G (p.Ile1343Ser) n.421-25456T>G | |
12 | g.6019390A>G | CA383505720 | VWF | c.4028T>C (p.Ile1343Thr) n.421-25456T>C | gnomAD v4 |
12 | g.6019390A>T | CA383505721 | VWF | c.4028T>A (p.Ile1343Asn) n.421-25456T>A | |
12 | g.6019391T>A | CA383505722 | VWF | c.4027A>T (p.Ile1343Phe) n.421-25457A>T | |
12 | g.6019391T>C | CA228520 | VWF | c.4027A>G (p.Ile1343Val) n.421-25457A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.6019391T>G | CA383505723 | VWF | c.4027A>C (p.Ile1343Leu) n.421-25457A>C | |
12 | g.6019391T= | CA2013872950 | VWF | c.4027A= (p.Ile1343=) n.421-25457A= | |
12 | g.6019392G>A | CA478502368 | VWF | c.4026C>T (p.Arg1342=) n.421-25458C>T | |
12 | g.6019392G>C | CA6402622 | VWF | c.4026C>G (p.Arg1342=) n.421-25458C>G | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.6019392G= | CA2013872951 | VWF | c.4026C= (p.Arg1342=) n.421-25458C= | |
12 | g.6019392G>T | CA478502369 | VWF | c.4026C>A (p.Arg1342=) n.421-25458C>A | |
12 | g.6019393C>A | CA383505724 | VWF | c.4025G>T (p.Arg1342Leu) n.421-25459G>T | |
12 | g.6019393C= | CA2013872952 | VWF | c.4025G= (p.Arg1342=) n.421-25459G= | |
12 | g.6019393C>G | CA383505726 | VWF | c.4025G>C (p.Arg1342Pro) n.421-25459G>C | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.6019393C>T | CA6402623 | VWF | c.4025G>A (p.Arg1342His) n.421-25459G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
12 | g.6019393_6019394delinsCG | CA2013872953 | VWF | c.4024_4025delinsCG (p.Arg1342=) n.421-25460_421-25459delinsCG | |
12 | g.6019394del | CA2013872954 | VWF | c.4024del (p.Arg1342AlafsTer6) n.421-25460del | |
12 | g.6019394G>A | CA228959 | VWF | c.4024C>T (p.Arg1342Cys) n.421-25460C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.6019394G>C | CA383505733 | VWF | c.4024C>G (p.Arg1342Gly) n.421-25460C>G | |
12 | g.6019394G= | CA2013872955 | VWF | c.4024C= (p.Arg1342=) n.421-25460C= | |
12 | g.6019394G>T | CA383505729 | VWF | c.4024C>A (p.Arg1342Ser) n.421-25460C>A | |
12 | g.6019395C>A | CA478502370 | VWF | c.4023G>T (p.Arg1341=) n.421-25461G>T | |
12 | g.6019395C>G | CA478502371 | VWF | c.4023G>C (p.Arg1341=) n.421-25461G>C | |
12 | g.6019395C>T | CA478502372 | VWF | c.4023G>A (p.Arg1341=) n.421-25461G>A | |
12 | g.6019396C>A | CA228518 | VWF | c.4022G>T (p.Arg1341Leu) n.421-25462G>T | ClinVar dbSNP |
12 | g.6019396C= | CA2013872956 | VWF | c.4022G= (p.Arg1341=) n.421-25462G= | |
12 | g.6019396C>G | CA228516 | VWF | c.4022G>C (p.Arg1341Pro) n.421-25462G>C | ClinVar dbSNP |
12 | g.6019396C>T | CA114129 | VWF | c.4022G>A (p.Arg1341Gln) n.421-25462G>A | ClinVar dbSNP gnomAD v2 gnomAD v4 |
12 | g.6019397G>A | CA228514 | VWF | c.4021C>T (p.Arg1341Trp) n.421-25463C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.6019397G>C | CA383505741 | VWF | c.4021C>G (p.Arg1341Gly) n.421-25463C>G | |
12 | g.6019397G= | CA2013872957 | VWF | c.4021C= (p.Arg1341=) n.421-25463C= | |
12 | g.6019397G>T | CA478502373 | VWF | c.4021C>A (p.Arg1341=) n.421-25463C>A | |
12 | g.6019398C>A | CA478502374 | VWF | c.4020G>T (p.Leu1340=) n.421-25464G>T | |
12 | g.6019398C>G | CA478502375 | VWF | c.4020G>C (p.Leu1340=) n.421-25464G>C | |
12 | g.6019398C>T | CA478502376 | VWF | c.4020G>A (p.Leu1340=) n.421-25464G>A | |
12 | g.6019399A>C | CA383505742 | VWF | c.4019T>G (p.Leu1340Arg) n.421-25465T>G | |
12 | g.6019399A>G | CA383505745 | VWF | c.4019T>C (p.Leu1340Pro) n.421-25465T>C | ClinVar |
12 | g.6019399A>T | CA383505747 | VWF | c.4019T>A (p.Leu1340Gln) n.421-25465T>A | |
12 | g.6019400G>A | CA478502377 | VWF | c.4018C>T (p.Leu1340=) n.421-25466C>T | |
12 | g.6019400G>C | CA383505750 | VWF | c.4018C>G (p.Leu1340Val) n.421-25466C>G | |
12 | g.6019400G>T | CA383505752 | VWF | c.4018C>A (p.Leu1340Met) n.421-25466C>A | |
12 | g.6019401C>A | CA383505754 | VWF | c.4017G>T (p.Glu1339Asp) n.421-25467G>T | |
12 | g.6019401C= | CA2013872958 | VWF | c.4017G= (p.Glu1339=) n.421-25467G= | |
12 | g.6019401C>G | CA383505756 | VWF | c.4017G>C (p.Glu1339Asp) n.421-25467G>C | ClinVar |
12 | g.6019401C>T | CA232297773 | VWF | c.4017G>A (p.Glu1339=) n.421-25467G>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.6019402T>A | CA383505760 | VWF | c.4016A>T (p.Glu1339Val) n.421-25468A>T | dbSNP gnomAD v2 gnomAD v4 |
12 | g.6019402T>C | CA383505758 | VWF | c.4016A>G (p.Glu1339Gly) n.421-25468A>G | |
12 | g.6019402T>G | CA383505759 | VWF | c.4016A>C (p.Glu1339Ala) n.421-25468A>C | |
12 | g.6019402T= | CA2013872959 | VWF | c.4016A= (p.Glu1339=) n.421-25468A= | |
12 | g.6019403C>A | CA383505763 | VWF | c.4015G>T (p.Glu1339Ter) n.421-25469G>T | |
12 | g.6019403C>G | CA383505765 | VWF | c.4015G>C (p.Glu1339Gln) n.421-25469G>C | |
12 | g.6019403C>T | CA383505766 | VWF | c.4015G>A (p.Glu1339Lys) n.421-25469G>A | |
12 | g.6019404T>A | CA478502381 | VWF | c.4014A>T (p.Ser1338=) n.421-25470A>T | |
12 | g.6019404T>C | CA478502380 | VWF | c.4014A>G (p.Ser1338=) n.421-25470A>G | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.6019404T>G | CA478502379 | VWF | c.4014A>C (p.Ser1338=) n.421-25470A>C | |
12 | g.6019404T= | CA2013872960 | VWF | c.4014A= (p.Ser1338=) n.421-25470A= | |
12 | g.6019405G>A | CA383505768 | VWF | c.4013C>T (p.Ser1338Leu) n.421-25471C>T | COSMIC |
12 | g.6019405G>C | CA228512 | VWF | c.4013C>G (p.Ser1338Ter) n.421-25471C>G | ClinVar dbSNP |
12 | g.6019405G= | CA2013872961 | VWF | c.4013C= (p.Ser1338=) n.421-25471C= | |
12 | g.6019405G>T | CA383505770 | VWF | c.4013C>A (p.Ser1338Ter) n.421-25471C>A | |
12 | g.6019406A= | CA2013872962 | VWF | c.4012T= (p.Ser1338=) n.421-25472T= | |
12 | g.6019406A>C | CA6402624 | VWF | c.4012T>G (p.Ser1338Ala) n.421-25472T>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.6019406A>G | CA383505773 | VWF | c.4012T>C (p.Ser1338Pro) n.421-25472T>C | |
12 | g.6019406A>T | CA383505776 | VWF | c.4012T>A (p.Ser1338Thr) n.421-25472T>A | dbSNP |
12 | g.6019407C>A | CA478502382 | VWF | c.4011G>T (p.Pro1337=) n.421-25473G>T | |
12 | g.6019407C= | CA2013872963 | VWF | c.4011G= (p.Pro1337=) n.421-25473G= | |
12 | g.6019407C>G | CA478502383 | VWF | c.4011G>C (p.Pro1337=) n.421-25473G>C | |
12 | g.6019407C>T | CA6402625 | VWF | c.4011G>A (p.Pro1337=) n.421-25473G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
12 | g.6019408G>A | CA228510 | VWF | c.4010C>T (p.Pro1337Leu) n.421-25474C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
12 | g.6019408G>C | CA383505781 | VWF | c.4010C>G (p.Pro1337Arg) n.421-25474C>G | |
12 | g.6019408G= | CA2013872964 | VWF | c.4010C= (p.Pro1337=) n.421-25474C= | |
12 | g.6019408G>T | CA383505783 | VWF | c.4010C>A (p.Pro1337Gln) n.421-25474C>A | ClinVar dbSNP gnomAD v2 gnomAD v4 |
12 | g.6019409G>A | CA383505788 | VWF | c.4009C>T (p.Pro1337Ser) n.421-25475C>T | gnomAD v4 |
12 | g.6019409G>C | CA383505790 | VWF | c.4009C>G (p.Pro1337Ala) n.421-25475C>G | |
12 | g.6019409G= | CA2013872965 | VWF | c.4009C= (p.Pro1337=) n.421-25475C= | |
12 | g.6019409G>T | CA383505786 | VWF | c.4009C>A (p.Pro1337Thr) n.421-25475C>A | dbSNP gnomAD v2 gnomAD v4 |