| 5 | g.154477451A>T | CA2578462604 | HAND1 | c.543+15T>A (n.543+15T>A)
| |
| 5 | g.154477452G>A | CA3526542 | HAND1 | c.543+14C>T (n.543+14C>T)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 5 | g.154477452G= | CA1592792900 | HAND1 | c.543+14C= (n.543+14C=)
| |
| 5 | g.154477452G>T | CA2676143353 | HAND1 | c.543+14C>A (n.543+14C>A)
| gnomAD v4 |
| 5 | g.154477453C= | CA1592792903 | HAND1 | c.543+13G= (n.543+13G=)
| |
| 5 | g.154477453C>T | CA130059670 | HAND1 | c.543+13G>A (n.543+13G>A)
| dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 5 | g.154477456del | CA2578462605 | HAND1 | c.543+13del (n.543+13del)
| gnomAD v3 gnomAD v4 |
| 5 | g.154477454C= | CA1592792908 | HAND1 | c.543+12G= (n.543+12G=)
| |
| 5 | g.154477454C>T | CA130059675 | HAND1 | c.543+12G>A (n.543+12G>A)
| dbSNP gnomAD v4 |
| 5 | g.154477455C= | CA1592792910 | HAND1 | c.543+11G= (n.543+11G=)
| |
| 5 | g.154477455C>G | CA563652037 | HAND1 | c.543+11G>C (n.543+11G>C)
| dbSNP gnomAD v2 gnomAD v4 |
| 5 | g.154477457A= | CA1592792912 | HAND1 | c.543+9T= (n.543+9T=)
| |
| 5 | g.154477457A>G | CA563652038 | HAND1 | c.543+9T>C (n.543+9T>C)
| dbSNP gnomAD v2 gnomAD v4 |
| 5 | g.154477458G>A | CA1592792917 | HAND1 | c.543+8C>T (n.543+8C>T)
| dbSNP gnomAD v4 |
| 5 | g.154477458G= | CA1592792915 | HAND1 | c.543+8C= (n.543+8C=)
| |
| 5 | g.154477458G>T | CA2676143367 | HAND1 | c.543+8C>A (n.543+8C>A)
| gnomAD v4 |
| 5 | g.154477459G>A | CA563652039 | HAND1 | c.543+7C>T (n.543+7C>T)
| dbSNP gnomAD v2 gnomAD v4 |
| 5 | g.154477459G= | CA1592792919 | HAND1 | c.543+7C= (n.543+7C=)
| |
| 5 | g.154477459G>T | CA2578462606 | HAND1 | c.543+7C>A (n.543+7C>A)
| gnomAD v4 |
| 5 | g.154477460A>T | CA645549418 | HAND1 | c.543+6T>A (n.543+6T>A)
| COSMIC |
| 5 | g.154477462T>C | CA805958460 | HAND1 | c.543+4A>G (n.543+4A>G)
| dbSNP |
| 5 | g.154477462T= | CA1592792922 | HAND1 | c.543+4A= (n.543+4A=)
| |
| 5 | g.154477463C= | CA1592792926 | HAND1 | c.543+3G= (n.543+3G=)
| |
| 5 | g.154477463C>T | CA563652040 | HAND1 | c.543+3G>A (n.543+3G>A)
| dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 5 | g.154477464A>C | CA361921375 | HAND1 | c.543+2T>G (n.543+2T>G)
| |
| 5 | g.154477464A>G | CA361921373 | HAND1 | c.543+2T>C (n.543+2T>C)
| |
| 5 | g.154477464A>T | CA361921370 | HAND1 | c.543+2T>A (n.543+2T>A)
| |
| 5 | g.154477465C>A | CA361921377 | HAND1 | c.543+1G>T (n.543+1G>T)
| gnomAD v4 |
| 5 | g.154477465C>G | CA361921378 | HAND1 | c.543+1G>C (n.543+1G>C)
| |
| 5 | g.154477465C>T | CA361921380 | HAND1 | c.543+1G>A (n.543+1G>A)
| |
| 5 | g.154477466C>A | CA447235221 | HAND1 | c.543G>T (p.Leu181=)
| |
| 5 | g.154477466C>G | CA447235225 | HAND1 | c.543G>C (p.Leu181=)
| |
| 5 | g.154477466C>T | CA447235223 | HAND1 | c.543G>A (p.Leu181=)
| |
| 5 | g.154477467A>C | CA361921383 | HAND1 | c.542T>G (p.Leu181Arg)
| |
| 5 | g.154477467A>G | CA361921384 | HAND1 | c.542T>C (p.Leu181Pro)
| gnomAD v4 |
| 5 | g.154477467A>T | CA361921385 | HAND1 | c.542T>A (p.Leu181Gln)
| |
| 5 | g.154477468G>A | CA447235230 | HAND1 | c.541C>T (p.Leu181=)
| gnomAD v4 |
| 5 | g.154477468G>C | CA361921386 | HAND1 | c.541C>G (p.Leu181Val)
| gnomAD v4 |
| 5 | g.154477468G>T | CA361921387 | HAND1 | c.541C>A (p.Leu181Met)
| |
| 5 | g.154477469C>A | CA361921389 | HAND1 | c.540G>T (p.Glu180Asp)
| |
| 5 | g.154477469C>G | CA361921391 | HAND1 | c.540G>C (p.Glu180Asp)
| |
| 5 | g.154477469C>T | CA447235236 | HAND1 | c.540G>A (p.Glu180=)
| |
| 5 | g.154477470T>A | CA361921394 | HAND1 | c.539A>T (p.Glu180Val)
| |
| 5 | g.154477470T>C | CA361921399 | HAND1 | c.539A>G (p.Glu180Gly)
| |
| 5 | g.154477470T>G | CA361921397 | HAND1 | c.539A>C (p.Glu180Ala)
| |
| 5 | g.154477471C>A | CA361921403 | HAND1 | c.538G>T (p.Glu180Ter)
| |
| 5 | g.154477471C>G | CA361921406 | HAND1 | c.538G>C (p.Glu180Gln)
| |
| 5 | g.154477471C>T | CA361921414 | HAND1 | c.538G>A (p.Glu180Lys)
| |
| 5 | g.154477472C>A | CA361921415 | HAND1 | c.537G>T (p.Arg179Ser)
| gnomAD v4 |
| 5 | g.154477472C>G | CA361921421 | HAND1 | c.537G>C (p.Arg179Ser)
| |
| 5 | g.154477472C>T | CA447235241 | HAND1 | c.537G>A (p.Arg179=)
| COSMIC |
| 5 | g.154477473C>A | CA361921424 | HAND1 | c.536G>T (p.Arg179Met)
| |
| 5 | g.154477473C>G | CA361921427 | HAND1 | c.536G>C (p.Arg179Thr)
| |
| 5 | g.154477473C>T | CA361921430 | HAND1 | c.536G>A (p.Arg179Lys)
| gnomAD v4 |
| 5 | g.154477474T>A | CA361921434 | HAND1 | c.535A>T (p.Arg179Trp)
| ClinVar |
| 5 | g.154477474T>C | CA361921433 | HAND1 | c.535A>G (p.Arg179Gly)
| |
| 5 | g.154477474T>G | CA447235245 | HAND1 | c.535A>C (p.Arg179=)
| |
| 5 | g.154477477del | CA2676143384 | HAND1 | c.535del (p.Arg179GlyfsTer?)
| gnomAD v4 |
| 5 | g.154477475T>A | CA361921435 | HAND1 | c.534A>T (p.Lys178Asn)
| |
| 5 | g.154477475T>C | CA447235247 | HAND1 | c.534A>G (p.Lys178=)
| |
| 5 | g.154477475T>G | CA361921436 | HAND1 | c.534A>C (p.Lys178Asn)
| |
| 5 | g.154477476T>A | CA361921438 | HAND1 | c.533A>T (p.Lys178Ile)
| |
| 5 | g.154477476T>C | CA361921439 | HAND1 | c.533A>G (p.Lys178Arg)
| dbSNP |
| 5 | g.154477476T>G | CA361921441 | HAND1 | c.533A>C (p.Lys178Thr)
| |
| 5 | g.154477476T= | CA1592792929 | HAND1 | c.533A= (p.Lys178=)
| |
| 5 | g.154477477T>A | CA361921443 | HAND1 | c.532A>T (p.Lys178Ter)
| |
| 5 | g.154477477T>C | CA361921444 | HAND1 | c.532A>G (p.Lys178Glu)
| |
| 5 | g.154477477T>G | CA361921445 | HAND1 | c.532A>C (p.Lys178Gln)
| |
| 5 | g.154477478C>A | CA447235252 | HAND1 | c.531G>T (p.Arg177=)
| |
| 5 | g.154477478C= | CA1592792935 | HAND1 | c.531G= (p.Arg177=)
| |
| 5 | g.154477478C>G | CA3526543 | HAND1 | c.531G>C (p.Arg177=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 5 | g.154477478C>T | CA447235253 | HAND1 | c.531G>A (p.Arg177=)
| gnomAD v4 |
| 5 | g.154477479C>A | CA130059683 | HAND1 | c.530G>T (p.Arg177Leu)
| dbSNP |
| 5 | g.154477479C= | CA1592792940 | HAND1 | c.530G= (p.Arg177=)
| |
| 5 | g.154477479C>G | CA361921449 | HAND1 | c.530G>C (p.Arg177Pro)
| |
| 5 | g.154477479C>T | CA3526544 | HAND1 | c.530G>A (p.Arg177Gln)
| dbSNP ExAC |
| 5 | g.154477480G>A | CA361921456 | HAND1 | c.529C>T (p.Arg177Trp)
| dbSNP gnomAD v2 |
| 5 | g.154477480G>C | CA361921465 | HAND1 | c.529C>G (p.Arg177Gly)
| |
| 5 | g.154477480G= | CA1592792945 | HAND1 | c.529C= (p.Arg177=)
| |
| 5 | g.154477480G>T | CA3526545 | HAND1 | c.529C>A (p.Arg177=)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
| 5 | g.154477481C>A | CA361921467 | HAND1 | c.528G>T (p.Lys176Asn)
| |
| 5 | g.154477481C>G | CA361921474 | HAND1 | c.528G>C (p.Lys176Asn)
| |
| 5 | g.154477481C>T | CA447235259 | HAND1 | c.528G>A (p.Lys176=)
| |
| 5 | g.154477482T>A | CA361921477 | HAND1 | c.527A>T (p.Lys176Met)
| |
| 5 | g.154477482T>C | CA361921478 | HAND1 | c.527A>G (p.Lys176Arg)
| |
| 5 | g.154477482T>G | CA361921482 | HAND1 | c.527A>C (p.Lys176Thr)
| |
| 5 | g.154477483T>A | CA361921483 | HAND1 | c.526A>T (p.Lys176Ter)
| |
| 5 | g.154477483T>C | CA361921484 | HAND1 | c.526A>G (p.Lys176Glu)
| COSMIC |
| 5 | g.154477483T>G | CA361921485 | HAND1 | c.526A>C (p.Lys176Gln)
| |
| 5 | g.154477484G>A | CA447235261 | HAND1 | c.525C>T (p.Ser175=)
| |
| 5 | g.154477484G>C | CA361921493 | HAND1 | c.525C>G (p.Ser175Arg)
| |
| 5 | g.154477484G>T | CA361921490 | HAND1 | c.525C>A (p.Ser175Arg)
| |
| 5 | g.154477485C>A | CA361921497 | HAND1 | c.524G>T (p.Ser175Ile)
| |
| 5 | g.154477485C= | CA1592792947 | HAND1 | c.524G= (p.Ser175=)
| |
| 5 | g.154477485C>G | CA361921507 | HAND1 | c.524G>C (p.Ser175Thr)
| |
| 5 | g.154477485C>T | CA361921513 | HAND1 | c.524G>A (p.Ser175Asn)
| dbSNP COSMIC |
| 5 | g.154477486T>A | CA361921515 | HAND1 | c.523A>T (p.Ser175Cys)
| |
| 5 | g.154477486T>C | CA361921516 | HAND1 | c.523A>G (p.Ser175Gly)
| gnomAD v4 |
| 5 | g.154477486T>G | CA361921517 | HAND1 | c.523A>C (p.Ser175Arg)
| |
| 5 | g.154477487C>A | CA361921518 | HAND1 | c.522G>T (p.Glu174Asp)
| |
| 5 | g.154477487C>G | CA361921519 | HAND1 | c.522G>C (p.Glu174Asp)
| |
| 5 | g.154477487C>T | CA447235263 | HAND1 | c.522G>A (p.Glu174=)
| |
| 5 | g.154477488T>A | CA361921520 | HAND1 | c.521A>T (p.Glu174Val)
| |
| 5 | g.154477488T>C | CA3526546 | HAND1 | c.521A>G (p.Glu174Gly)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
| 5 | g.154477488T>G | CA361921522 | HAND1 | c.521A>C (p.Glu174Ala)
| |
| 5 | g.154477488T= | CA1592792950 | HAND1 | c.521A= (p.Glu174=)
| |
| 5 | g.154477489C>A | CA361921524 | HAND1 | c.520G>T (p.Glu174Ter)
| |
| 5 | g.154477489C>G | CA361921526 | HAND1 | c.520G>C (p.Glu174Gln)
| |
| 5 | g.154477489C>T | CA361921525 | HAND1 | c.520G>A (p.Glu174Lys)
| |
| 5 | g.154477490A= | CA1592792954 | HAND1 | c.519T= (p.Arg173=)
| |
| 5 | g.154477490A>C | CA447421469 | HAND1 | c.519T>G (p.Arg173=)
| dbSNP |
| 5 | g.154477490A>G | CA447421471 | HAND1 | c.519T>C (p.Arg173=)
| |
| 5 | g.154477490A>T | CA447421474 | HAND1 | c.519T>A (p.Arg173=)
| |
| 5 | g.154477491C>A | CA3526547 | HAND1 | c.518G>T (p.Arg173Leu)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 5 | g.154477491C= | CA1592792957 | HAND1 | c.518G= (p.Arg173=)
| |
| 5 | g.154477491C>G | CA361921527 | HAND1 | c.518G>C (p.Arg173Pro)
| |
| 5 | g.154477491C>T | CA130059698 | HAND1 | c.518G>A (p.Arg173His)
| dbSNP |
| 5 | g.154477492G>A | CA361921530 | HAND1 | c.517C>T (p.Arg173Cys)
| dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 5 | g.154477492G>C | CA361921533 | HAND1 | c.517C>G (p.Arg173Gly)
| gnomAD v4 |
| 5 | g.154477492G= | CA1592792961 | HAND1 | c.517C= (p.Arg173=)
| |
| 5 | g.154477492G>T | CA361921534 | HAND1 | c.517C>A (p.Arg173Ser)
| dbSNP gnomAD v2 gnomAD v4 |
| 5 | g.154477493G>A | CA447421483 | HAND1 | c.516C>T (p.Gly172=)
| |
| 5 | g.154477493G>C | CA447421485 | HAND1 | c.516C>G (p.Gly172=)
| |
| 5 | g.154477493G>T | CA447421486 | HAND1 | c.516C>A (p.Gly172=)
| ClinVar gnomAD v4 |
| 5 | g.154477494C>A | CA361921535 | HAND1 | c.515G>T (p.Gly172Val)
| |
| 5 | g.154477494C>G | CA361921536 | HAND1 | c.515G>C (p.Gly172Ala)
| |
| 5 | g.154477494C>T | CA361921537 | HAND1 | c.515G>A (p.Gly172Asp)
| |
| 5 | g.154477495C>A | CA361921540 | HAND1 | c.514G>T (p.Gly172Cys)
| dbSNP gnomAD v3 gnomAD v4 |
| 5 | g.154477495C= | CA1592792966 | HAND1 | c.514G= (p.Gly172=)
| |
| 5 | g.154477495C>G | CA361921541 | HAND1 | c.514G>C (p.Gly172Arg)
| |
| 5 | g.154477495C>T | CA361921538 | HAND1 | c.514G>A (p.Gly172Ser)
| |
| 5 | g.154477496G>A | CA447421496 | HAND1 | c.513C>T (p.Gly171=)
| |
| 5 | g.154477496G>C | CA447421497 | HAND1 | c.513C>G (p.Gly171=)
| |
| 5 | g.154477496G= | CA1592792969 | HAND1 | c.513C= (p.Gly171=)
| |
| 5 | g.154477496G>T | CA447421498 | HAND1 | c.513C>A (p.Gly171=)
| dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 5 | g.154477497C>A | CA361921544 | HAND1 | c.512G>T (p.Gly171Val)
| |
| 5 | g.154477497C= | CA1592792972 | HAND1 | c.512G= (p.Gly171=)
| |
| 5 | g.154477497C>G | CA361921542 | HAND1 | c.512G>C (p.Gly171Ala)
| |
| 5 | g.154477497C>T | CA3526548 | HAND1 | c.512G>A (p.Gly171Asp)
| ClinVar dbSNP ExAC gnomAD v3 gnomAD v4 |
| 5 | g.154477498C>A | CA361921568 | HAND1 | c.511G>T (p.Gly171Cys)
| |
| 5 | g.154477498C>G | CA361921570 | HAND1 | c.511G>C (p.Gly171Arg)
| |
| 5 | g.154477498C>T | CA361921574 | HAND1 | c.511G>A (p.Gly171Ser)
| gnomAD v4 |
| 5 | g.154477499A= | CA1592792974 | HAND1 | c.510T= (p.Asp170=)
| |
| 5 | g.154477499A>C | CA361921577 | HAND1 | c.510T>G (p.Asp170Glu)
| |
| 5 | g.154477499A>G | CA447421504 | HAND1 | c.510T>C (p.Asp170=)
| dbSNP gnomAD v2 gnomAD v4 |
| 5 | g.154477499A>T | CA361921579 | HAND1 | c.510T>A (p.Asp170Glu)
| |
| 5 | g.154477500T>A | CA361921587 | HAND1 | c.509A>T (p.Asp170Val)
| |
| 5 | g.154477500T>C | CA361921590 | HAND1 | c.509A>G (p.Asp170Gly)
| gnomAD v4 |
| 5 | g.154477500T>G | CA361921591 | HAND1 | c.509A>C (p.Asp170Ala)
| |
| 5 | g.154477501C>A | CA361921602 | HAND1 | c.508G>T (p.Asp170Tyr)
| |
| 5 | g.154477501C>G | CA361921597 | HAND1 | c.508G>C (p.Asp170His)
| |
| 5 | g.154477501C>T | CA361921594 | HAND1 | c.508G>A (p.Asp170Asn)
| gnomAD v4 |
| 5 | g.154477502C>A | CA447421512 | HAND1 | c.507G>T (p.Ala169=)
| gnomAD v4 |
| 5 | g.154477502C= | CA1592792978 | HAND1 | c.507G= (p.Ala169=)
| |
| 5 | g.154477502C>G | CA447421515 | HAND1 | c.507G>C (p.Ala169=)
| |
| 5 | g.154477502C>T | CA3526549 | HAND1 | c.507G>A (p.Ala169=)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
| 5 | g.154477503G>A | CA361921605 | HAND1 | c.506C>T (p.Ala169Val)
| dbSNP gnomAD v4 |
| 5 | g.154477503G>C | CA361921608 | HAND1 | c.506C>G (p.Ala169Gly)
| |
| 5 | g.154477503G>T | CA361921610 | HAND1 | c.506C>A (p.Ala169Glu)
| |
| 5 | g.154477504C>A | CA361921613 | HAND1 | c.505G>T (p.Ala169Ser)
| |
| 5 | g.154477504C>G | CA361921614 | HAND1 | c.505G>C (p.Ala169Pro)
| |
| 5 | g.154477504C>T | CA361921615 | HAND1 | c.505G>A (p.Ala169Thr)
| |
| 5 | g.154477505C>A | CA361921616 | HAND1 | c.504G>T (p.Lys168Asn)
| |
| 5 | g.154477505C>G | CA361921617 | HAND1 | c.504G>C (p.Lys168Asn)
| |
| 5 | g.154477505C>T | CA447421522 | HAND1 | c.504G>A (p.Lys168=)
| ClinVar dbSNP |
| 5 | g.154477506T>A | CA361921622 | HAND1 | c.503A>T (p.Lys168Met)
| |
| 5 | g.154477506T>C | CA361921625 | HAND1 | c.503A>G (p.Lys168Arg)
| |
| 5 | g.154477506T>G | CA361921618 | HAND1 | c.503A>C (p.Lys168Thr)
| |
| 5 | g.154477507T>A | CA361921628 | HAND1 | c.502A>T (p.Lys168Ter)
| dbSNP gnomAD v2 |
| 5 | g.154477507T>C | CA361921630 | HAND1 | c.502A>G (p.Lys168Glu)
| |
| 5 | g.154477507T>G | CA361921634 | HAND1 | c.502A>C (p.Lys168Gln)
| |
| 5 | g.154477507T= | CA1592792982 | HAND1 | c.502A= (p.Lys168=)
| |
| 5 | g.154477508C>A | CA361921637 | HAND1 | c.501G>T (p.Lys167Asn)
| |
| 5 | g.154477508C= | CA1592792985 | HAND1 | c.501G= (p.Lys167=)
| |
| 5 | g.154477508C>G | CA361921642 | HAND1 | c.501G>C (p.Lys167Asn)
| |
| 5 | g.154477508C>T | CA3526550 | HAND1 | c.501G>A (p.Lys167=)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
| 5 | g.154477509T>A | CA3526552 | HAND1 | c.500A>T (p.Lys167Met)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
| 5 | g.154477509T>C | CA3526551 | HAND1 | c.500A>G (p.Lys167Arg)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 5 | g.154477509T>G | CA361921649 | HAND1 | c.500A>C (p.Lys167Thr)
| |
| 5 | g.154477509T= | CA1592792988 | HAND1 | c.500A= (p.Lys167=)
| |
| 5 | g.154477510T>A | CA361921658 | HAND1 | c.499A>T (p.Lys167Ter)
| |
| 5 | g.154477510T>C | CA361921656 | HAND1 | c.499A>G (p.Lys167Glu)
| dbSNP |
| 5 | g.154477510T>G | CA361921651 | HAND1 | c.499A>C (p.Lys167Gln)
| dbSNP gnomAD v2 gnomAD v4 |
| 5 | g.154477510T= | CA1592792992 | HAND1 | c.499A= (p.Lys167=)
| |
| 5 | g.154477511G>A | CA447421532 | HAND1 | c.498C>T (p.Leu166=)
| |
| 5 | g.154477511G>C | CA447421534 | HAND1 | c.498C>G (p.Leu166=)
| |
| 5 | g.154477511G>T | CA447421533 | HAND1 | c.498C>A (p.Leu166=)
| |
| 5 | g.154477512A>C | CA361921661 | HAND1 | c.497T>G (p.Leu166Arg)
| |
| 5 | g.154477512A>G | CA361921663 | HAND1 | c.497T>C (p.Leu166Pro)
| |
| 5 | g.154477512A>T | CA361921664 | HAND1 | c.497T>A (p.Leu166His)
| |
| 5 | g.154477513G>A | CA361921668 | HAND1 | c.496C>T (p.Leu166Phe)
| ClinVar dbSNP gnomAD v4 |
| 5 | g.154477513G>C | CA361921670 | HAND1 | c.496C>G (p.Leu166Val)
| |
| 5 | g.154477513G>T | CA361921673 | HAND1 | c.496C>A (p.Leu166Ile)
| |
| 5 | g.154477514T>A | CA361921674 | HAND1 | c.495A>T (p.Glu165Asp)
| |
| 5 | g.154477514T>C | CA447421541 | HAND1 | c.495A>G (p.Glu165=)
| |
| 5 | g.154477514T>G | CA361921675 | HAND1 | c.495A>C (p.Glu165Asp)
| |
| 5 | g.154477515T>A | CA361921676 | HAND1 | c.494A>T (p.Glu165Val)
| |
| 5 | g.154477515T>C | CA361921678 | HAND1 | c.494A>G (p.Glu165Gly)
| |
| 5 | g.154477515T>G | CA361921680 | HAND1 | c.494A>C (p.Glu165Ala)
| |
| 5 | g.154477516C>A | CA361921688 | HAND1 | c.493G>T (p.Glu165Ter)
| |
| 5 | g.154477516C>G | CA361921685 | HAND1 | c.493G>C (p.Glu165Gln)
| gnomAD v4 |
| 5 | g.154477516C>T | CA361921682 | HAND1 | c.493G>A (p.Glu165Lys)
| gnomAD v4 |
| 5 | g.154477517A= | CA1592792996 | HAND1 | c.492T= (p.Ala164=)
| |
| 5 | g.154477517A>C | CA3526553 | HAND1 | c.492T>G (p.Ala164=)
| dbSNP ExAC gnomAD v2 |
| 5 | g.154477517A>G | CA447421546 | HAND1 | c.492T>C (p.Ala164=)
| |
| 5 | g.154477517A>T | CA447421547 | HAND1 | c.492T>A (p.Ala164=)
| |
| 5 | g.154477518G>A | CA361921704 | HAND1 | c.491C>T (p.Ala164Val)
| gnomAD v4 |
| 5 | g.154477518G>C | CA361921698 | HAND1 | c.491C>G (p.Ala164Gly)
| |
| 5 | g.154477518G>T | CA361921701 | HAND1 | c.491C>A (p.Ala164Asp)
| |
| 5 | g.154477519C>A | CA361921706 | HAND1 | c.490G>T (p.Ala164Ser)
| |
| 5 | g.154477519C>G | CA361921709 | HAND1 | c.490G>C (p.Ala164Pro)
| |
| 5 | g.154477519C>T | CA361921711 | HAND1 | c.490G>A (p.Ala164Thr)
| COSMIC |
| 5 | g.154477520C>A | CA361921715 | HAND1 | c.489G>T (p.Lys163Asn)
| |
| 5 | g.154477520C>G | CA361921717 | HAND1 | c.489G>C (p.Lys163Asn)
| |
| 5 | g.154477520C>T | CA447421561 | HAND1 | c.489G>A (p.Lys163=)
| |
| 5 | g.154477521T>A | CA361921718 | HAND1 | c.488A>T (p.Lys163Met)
| |
| 5 | g.154477521T>C | CA361921719 | HAND1 | c.488A>G (p.Lys163Arg)
| |
| 5 | g.154477521T>G | CA361921720 | HAND1 | c.488A>C (p.Lys163Thr)
| |
| 5 | g.154477522T>A | CA361921725 | HAND1 | c.487A>T (p.Lys163Ter)
| |
| 5 | g.154477522T>C | CA361921723 | HAND1 | c.487A>G (p.Lys163Glu)
| gnomAD v4 |
| 5 | g.154477522T>G | CA361921724 | HAND1 | c.487A>C (p.Lys163Gln)
| dbSNP gnomAD v3 gnomAD v4 |
| 5 | g.154477522T= | CA1592792999 | HAND1 | c.487A= (p.Lys163=)
| |
| 5 | g.154477523G>A | CA447421566 | HAND1 | c.486C>T (p.Phe162=)
| |
| 5 | g.154477523G>C | CA361921726 | HAND1 | c.486C>G (p.Phe162Leu)
| |
| 5 | g.154477523G>T | CA361921727 | HAND1 | c.486C>A (p.Phe162Leu)
| |
| 5 | g.154477524A>C | CA361921729 | HAND1 | c.485T>G (p.Phe162Cys)
| |
| 5 | g.154477524A>G | CA361921731 | HAND1 | c.485T>C (p.Phe162Ser)
| |
| 5 | g.154477524A>T | CA361921733 | HAND1 | c.485T>A (p.Phe162Tyr)
| |
| 5 | g.154477525A= | CA1592793002 | HAND1 | c.484T= (p.Phe162=)
| |
| 5 | g.154477525A>C | CA361921735 | HAND1 | c.484T>G (p.Phe162Val)
| |
| 5 | g.154477525A>G | CA361921738 | HAND1 | c.484T>C (p.Phe162Leu)
| dbSNP gnomAD v2 gnomAD v4 |
| 5 | g.154477525A>T | CA361921741 | HAND1 | c.484T>A (p.Phe162Ile)
| |
| 5 | g.154477526G>A | CA447421570 | HAND1 | c.483C>T (p.Ala161=)
| gnomAD v4 COSMIC |
| 5 | g.154477526G>C | CA447421573 | HAND1 | c.483C>G (p.Ala161=)
| |
| 5 | g.154477526G>T | CA447421571 | HAND1 | c.483C>A (p.Ala161=)
| |
| 5 | g.154477527G>A | CA361921751 | HAND1 | c.482C>T (p.Ala161Val)
| dbSNP gnomAD v2 COSMIC |
| 5 | g.154477527G>C | CA361921748 | HAND1 | c.482C>G (p.Ala161Gly)
| |
| 5 | g.154477527G= | CA1592793005 | HAND1 | c.482C= (p.Ala161=)
| |
| 5 | g.154477527G>T | CA361921746 | HAND1 | c.482C>A (p.Ala161Asp)
| |
| 5 | g.154477528C>A | CA361921754 | HAND1 | c.481G>T (p.Ala161Ser)
| dbSNP gnomAD v3 gnomAD v4 |
| 5 | g.154477528C= | CA1592793010 | HAND1 | c.481G= (p.Ala161=)
| |
| 5 | g.154477528C>G | CA361921757 | HAND1 | c.481G>C (p.Ala161Pro)
| |
| 5 | g.154477528C>T | CA361921760 | HAND1 | c.481G>A (p.Ala161Thr)
| dbSNP gnomAD v3 gnomAD v4 |
| 5 | g.154477529C>A | CA361921765 | HAND1 | c.480G>T (p.Glu160Asp)
| gnomAD v4 |
| 5 | g.154477529C= | CA1592793012 | HAND1 | c.480G= (p.Glu160=)
| |
| 5 | g.154477529C>G | CA361921766 | HAND1 | c.480G>C (p.Glu160Asp)
| |
| 5 | g.154477529C>T | CA447421577 | HAND1 | c.480G>A (p.Glu160=)
| ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 5 | g.154477530T>A | CA361921768 | HAND1 | c.479A>T (p.Glu160Val)
| |
| 5 | g.154477530T>C | CA130059728 | HAND1 | c.479A>G (p.Glu160Gly)
| ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 5 | g.154477530T>G | CA361921772 | HAND1 | c.479A>C (p.Glu160Ala)
| |
| 5 | g.154477530T= | CA1592793014 | HAND1 | c.479A= (p.Glu160=)
| |
| 5 | g.154477531C>A | CA361921775 | HAND1 | c.478G>T (p.Glu160Ter)
| |
| 5 | g.154477531C>G | CA361921778 | HAND1 | c.478G>C (p.Glu160Gln)
| |
| 5 | g.154477531C>T | CA361921779 | HAND1 | c.478G>A (p.Glu160Lys)
| COSMIC |
| 5 | g.154477532G>A | CA447421580 | HAND1 | c.477C>T (p.Pro159=)
| |
| 5 | g.154477532G>C | CA447421581 | HAND1 | c.477C>G (p.Pro159=)
| |
| 5 | g.154477532G= | CA1592793017 | HAND1 | c.477C= (p.Pro159=)
| |
| 5 | g.154477532G>T | CA447421582 | HAND1 | c.477C>A (p.Pro159=)
| dbSNP |
| 5 | g.154477533G>A | CA361921780 | HAND1 | c.476C>T (p.Pro159Leu)
| dbSNP gnomAD v2 gnomAD v4 |
| 5 | g.154477533G>C | CA361921782 | HAND1 | c.476C>G (p.Pro159Arg)
| |
| 5 | g.154477533G= | CA1592793021 | HAND1 | c.476C= (p.Pro159=)
| |
| 5 | g.154477533G>T | CA361921781 | HAND1 | c.476C>A (p.Pro159His)
| |
| 5 | g.154477534G>A | CA361921785 | HAND1 | c.475C>T (p.Pro159Ser)
| |
| 5 | g.154477534G>C | CA361921786 | HAND1 | c.475C>G (p.Pro159Ala)
| |
| 5 | g.154477534G= | CA1592793025 | HAND1 | c.475C= (p.Pro159=)
| |
| 5 | g.154477534G>T | CA361921790 | HAND1 | c.475C>A (p.Pro159Thr)
| dbSNP COSMIC |
| 5 | g.154477535A>C | CA361921794 | HAND1 | c.474T>G (p.Asp158Glu)
| |
| 5 | g.154477535A>G | CA447421590 | HAND1 | c.474T>C (p.Asp158=)
| |
| 5 | g.154477535A>T | CA361921796 | HAND1 | c.474T>A (p.Asp158Glu)
| |
| 5 | g.154477536T>A | CA361921799 | HAND1 | c.473A>T (p.Asp158Val)
| ClinVar |
| 5 | g.154477536T>C | CA361921800 | HAND1 | c.473A>G (p.Asp158Gly)
| |
| 5 | g.154477536T>G | CA361921805 | HAND1 | c.473A>C (p.Asp158Ala)
| |
| 5 | g.154477537C>A | CA361921816 | HAND1 | c.472G>T (p.Asp158Tyr)
| |
| 5 | g.154477537C>G | CA361921814 | HAND1 | c.472G>C (p.Asp158His)
| |
| 5 | g.154477537C>T | CA361921811 | HAND1 | c.472G>A (p.Asp158Asn)
| |
| 5 | g.154477538G>A | CA447421600 | HAND1 | c.471C>T (p.Gly157=)
| gnomAD v4 |
| 5 | g.154477538G>C | CA447421601 | HAND1 | c.471C>G (p.Gly157=)
| dbSNP |
| 5 | g.154477538G= | CA1592793027 | HAND1 | c.471C= (p.Gly157=)
| |
| 5 | g.154477538G>T | CA3526554 | HAND1 | c.471C>A (p.Gly157=)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
| 5 | g.154477539C>A | CA361921824 | HAND1 | c.470G>T (p.Gly157Val)
| |
| 5 | g.154477539C>G | CA361921821 | HAND1 | c.470G>C (p.Gly157Ala)
| |
| 5 | g.154477539C>T | CA361921829 | HAND1 | c.470G>A (p.Gly157Asp)
| |
| 5 | g.154477540C>A | CA361921833 | HAND1 | c.469G>T (p.Gly157Cys)
| |
| 5 | g.154477540C>G | CA361921840 | HAND1 | c.469G>C (p.Gly157Arg)
| |
| 5 | g.154477540C>T | CA361921838 | HAND1 | c.469G>A (p.Gly157Ser)
| |
| 5 | g.154477541A= | CA1592793034 | HAND1 | c.468T= (p.Ser156=)
| |
| 5 | g.154477541A>C | CA3526555 | HAND1 | c.468T>G (p.Ser156=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 5 | g.154477541A>G | CA130059742 | HAND1 | c.468T>C (p.Ser156=)
| ClinVar dbSNP |
| 5 | g.154477541A>T | CA447421605 | HAND1 | c.468T>A (p.Ser156=)
| |
| 5 | g.154477542G>A | CA361921864 | HAND1 | c.467C>T (p.Ser156Phe)
| dbSNP |
| 5 | g.154477542G>C | CA361921859 | HAND1 | c.467C>G (p.Ser156Cys)
| |
| 5 | g.154477542G= | CA1592793039 | HAND1 | c.467C= (p.Ser156=)
| |
| 5 | g.154477542G>T | CA361921862 | HAND1 | c.467C>A (p.Ser156Tyr)
| gnomAD v4 |
| 5 | g.154477543A= | CA1592793042 | HAND1 | c.466T= (p.Ser156=)
| |
| 5 | g.154477543A>C | CA361921867 | HAND1 | c.466T>G (p.Ser156Ala)
| |
| 5 | g.154477543A>G | CA361921870 | HAND1 | c.466T>C (p.Ser156Pro)
| dbSNP gnomAD v4 |
| 5 | g.154477543A>T | CA361921872 | HAND1 | c.466T>A (p.Ser156Thr)
| |
| 5 | g.154477544C>A | CA361921880 | HAND1 | c.465G>T (p.Gln155His)
| |
| 5 | g.154477544C>G | CA361921881 | HAND1 | c.465G>C (p.Gln155His)
| |
| 5 | g.154477544C>T | CA447421610 | HAND1 | c.465G>A (p.Gln155=)
| |
| 5 | g.154477545T>A | CA361921885 | HAND1 | c.464A>T (p.Gln155Leu)
| gnomAD v4 |
| 5 | g.154477545T>C | CA361921886 | HAND1 | c.464A>G (p.Gln155Arg)
| |
| 5 | g.154477545T>G | CA361921897 | HAND1 | c.464A>C (p.Gln155Pro)
| |
| 5 | g.154477546G>A | CA361921907 | HAND1 | c.463C>T (p.Gln155Ter)
| |
| 5 | g.154477546G>C | CA361921901 | HAND1 | c.463C>G (p.Gln155Glu)
| |
| 5 | g.154477546G>T | CA361921904 | HAND1 | c.463C>A (p.Gln155Lys)
| |
| 5 | g.154477547T>A | CA447421616 | HAND1 | c.462A>T (p.Ala154=)
| |
| 5 | g.154477547T>C | CA447421618 | HAND1 | c.462A>G (p.Ala154=)
| gnomAD v4 |
| 5 | g.154477547T>G | CA447421615 | HAND1 | c.462A>C (p.Ala154=)
| gnomAD v4 |
| 5 | g.154477548G>A | CA361921911 | HAND1 | c.461C>T (p.Ala154Val)
| gnomAD v4 |
| 5 | g.154477548G>C | CA361921913 | HAND1 | c.461C>G (p.Ala154Gly)
| |
| 5 | g.154477548G>T | CA361921917 | HAND1 | c.461C>A (p.Ala154Glu)
| |
| 5 | g.154477549C>A | CA361921921 | HAND1 | c.460G>T (p.Ala154Ser)
| |
| 5 | g.154477549C>G | CA361921925 | HAND1 | c.460G>C (p.Ala154Pro)
| |
| 5 | g.154477549C>T | CA361921926 | HAND1 | c.460G>A (p.Ala154Thr)
| |
| 5 | g.154477550A>C | CA361921927 | HAND1 | c.459T>G (p.Asp153Glu)
| |
| 5 | g.154477550A>G | CA447421621 | HAND1 | c.459T>C (p.Asp153=)
| |
| 5 | g.154477550A>T | CA361921928 | HAND1 | c.459T>A (p.Asp153Glu)
| |
| 5 | g.154477551T>A | CA361921933 | HAND1 | c.458A>T (p.Asp153Val)
| |
| 5 | g.154477551T>C | CA361921931 | HAND1 | c.458A>G (p.Asp153Gly)
| |
| 5 | g.154477551T>G | CA361921929 | HAND1 | c.458A>C (p.Asp153Ala)
| |
