Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.47284484_47284486dup | CA2594684431 | ITGB3 | c.403_405dup (p.Asp135_Tyr136insAsp) c.368_370dup | gnomAD v3 gnomAD v4 |
17 | g.47284486T>A | CA400021796 | ITGB3 | c.405T>A (p.Asp135Glu) c.370T>A | |
17 | g.47284486T>C | CA500430453 | ITGB3 | c.405T>C (p.Asp135=) c.370T>C | |
17 | g.47284486T>G | CA400021797 | ITGB3 | c.405T>G (p.Asp135Glu) c.370T>G | |
17 | g.47284487T>A | CA400021800 | ITGB3 | c.406T>A (p.Tyr136Asn) c.371T>A | |
17 | g.47284487T>C | CA400021801 | ITGB3 | c.406T>C (p.Tyr136His) c.371T>C | |
17 | g.47284487T>G | CA400021803 | ITGB3 | c.406T>G (p.Tyr136Asp) c.371T>G | |
17 | g.47284488A>C | CA400021806 | ITGB3 | c.407A>C (p.Tyr136Ser) c.372A>C | |
17 | g.47284488A>G | CA400021807 | ITGB3 | c.407A>G (p.Tyr136Cys) c.372A>G | |
17 | g.47284488A>T | CA400021809 | ITGB3 | c.407A>T (p.Tyr136Phe) c.372A>T | |
17 | g.47284489C>A | CA400021813 | ITGB3 | c.408C>A (p.Tyr136Ter) c.373C>A | |
17 | g.47284489C>G | CA400021812 | ITGB3 | c.408C>G (p.Tyr136Ter) c.373C>G | |
17 | g.47284489C>T | CA500430468 | ITGB3 | c.408C>T (p.Tyr136=) c.373C>T | |
17 | g.47284490C>A | CA400021815 | ITGB3 | c.409C>A (p.Pro137Thr) c.374C>A | |
17 | g.47284490C>G | CA400021816 | ITGB3 | c.409C>G (p.Pro137Ala) c.374C>G | |
17 | g.47284490C>T | CA400021818 | ITGB3 | c.409C>T (p.Pro137Ser) c.374C>T | |
17 | g.47284491C>A | CA400021820 | ITGB3 | c.410C>A (p.Pro137His) c.375C>A | |
17 | g.47284491C= | CA2262605294 | ITGB3 | c.410C= (p.Pro137=) c.375C= | |
17 | g.47284491C>G | CA400021822 | ITGB3 | c.410C>G (p.Pro137Arg) c.375C>G | dbSNP gnomAD v3 gnomAD v4 |
17 | g.47284491C>T | CA400021823 | ITGB3 | c.410C>T (p.Pro137Leu) c.375C>T | |
17 | g.47284492T>A | CA500430487 | ITGB3 | c.411T>A (p.Pro137=) c.376T>A | |
17 | g.47284492T>C | CA8622958 | ITGB3 | c.411T>C (p.Pro137=) c.376T>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.47284492T>G | CA500430483 | ITGB3 | c.411T>G (p.Pro137=) c.376T>G | |
17 | g.47284492T= | CA2262605295 | ITGB3 | c.411T= (p.Pro137=) c.376T= | |
17 | g.47284493G>A | CA400021826 | ITGB3 | c.412G>A (p.Val138Met) c.377G>A | ClinVar dbSNP gnomAD v4 |
17 | g.47284493G>C | CA400021829 | ITGB3 | c.412G>C (p.Val138Leu) c.377G>C | gnomAD v4 |
17 | g.47284493G= | CA2262605296 | ITGB3 | c.412G= (p.Val138=) c.377G= | |
17 | g.47284493G>T | CA400021828 | ITGB3 | c.412G>T (p.Val138Leu) c.377G>T | |
17 | g.47284494T>A | CA400021830 | ITGB3 | c.413T>A (p.Val138Glu) c.378T>A | |
17 | g.47284494T>C | CA400021832 | ITGB3 | c.413T>C (p.Val138Ala) c.378T>C | gnomAD v4 |
17 | g.47284494T>G | CA400021834 | ITGB3 | c.413T>G (p.Val138Gly) c.378T>G | |
17 | g.47284495G>A | CA500430499 | ITGB3 | c.414G>A (p.Val138=) c.379G>A | |
17 | g.47284495G>C | CA8622959 | ITGB3 | c.414G>C (p.Val138=) c.379G>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.47284495G= | CA2262605297 | ITGB3 | c.414G= (p.Val138=) c.379G= | |
17 | g.47284495G>T | CA500430504 | ITGB3 | c.414G>T (p.Val138=) c.379G>T | |
17 | g.47284496G>A | CA400021839 | ITGB3 | c.415G>A (p.Asp139Asn) c.380G>A | gnomAD v4 |
17 | g.47284496G>C | CA400021843 | ITGB3 | c.415G>C (p.Asp139His) c.380G>C | ClinVar dbSNP |
17 | g.47284496G>T | CA400021841 | ITGB3 | c.415G>T (p.Asp139Tyr) c.380G>T | |
17 | g.47284497A>C | CA400021846 | ITGB3 | c.416A>C (p.Asp139Ala) c.381A>C | |
17 | g.47284497A>G | CA400021848 | ITGB3 | c.416A>G (p.Asp139Gly) c.381A>G | |
17 | g.47284497A>T | CA400021849 | ITGB3 | c.416A>T (p.Asp139Val) c.381A>T | |
17 | g.47284498C>A | CA400021852 | ITGB3 | c.417C>A (p.Asp139Glu) c.382C>A | |
17 | g.47284498C>G | CA400021854 | ITGB3 | c.417C>G (p.Asp139Glu) c.382C>G | |
17 | g.47284498C>T | CA500430519 | ITGB3 | c.417C>T (p.Asp139=) c.382C>T | |
17 | g.47284499A= | CA2262605298 | ITGB3 | c.418A= (p.Ile140=) c.383A= | |
17 | g.47284499A>C | CA400021857 | ITGB3 | c.418A>C (p.Ile140Leu) c.383A>C | dbSNP gnomAD v2 gnomAD v4 |
17 | g.47284499A>G | CA400021859 | ITGB3 | c.418A>G (p.Ile140Val) c.383A>G | |
17 | g.47284499A>T | CA400021860 | ITGB3 | c.418A>T (p.Ile140Phe) c.383A>T | |
17 | g.47284500T>A | CA400021863 | ITGB3 | c.419T>A (p.Ile140Asn) c.384T>A | |
17 | g.47284500T>C | CA400021865 | ITGB3 | c.419T>C (p.Ile140Thr) c.384T>C | |
17 | g.47284500T>G | CA400021867 | ITGB3 | c.419T>G (p.Ile140Ser) c.384T>G | |
17 | g.47284501C>A | CA291224643 | ITGB3 | c.420C>A (p.Ile140=) c.385C>A | dbSNP |
17 | g.47284501C= | CA2262605299 | ITGB3 | c.420C= (p.Ile140=) c.385C= | |
17 | g.47284501C>G | CA400021870 | ITGB3 | c.420C>G (p.Ile140Met) c.385C>G | |
17 | g.47284501C>T | CA500430533 | ITGB3 | c.420C>T (p.Ile140=) c.385C>T | |
17 | g.47284502T>A | CA400021874 | ITGB3 | c.421T>A (p.Tyr141Asn) c.386T>A | |
17 | g.47284502T>C | CA400021876 | ITGB3 | c.421T>C (p.Tyr141His) c.386T>C | |
17 | g.47284502T>G | CA400021875 | ITGB3 | c.421T>G (p.Tyr141Asp) c.386T>G | |
17 | g.47284503A= | CA2262605300 | ITGB3 | c.422A= (p.Tyr141=) c.387A= | |
17 | g.47284503A>C | CA400021879 | ITGB3 | c.422A>C (p.Tyr141Ser) c.387A>C | |
17 | g.47284503A>G | CA400021881 | ITGB3 | c.422A>G (p.Tyr141Cys) c.387A>G | ClinVar dbSNP gnomAD v3 gnomAD v4 |
17 | g.47284503A>T | CA400021883 | ITGB3 | c.422A>T (p.Tyr141Phe) c.387A>T | |
17 | g.47284504C>A | CA400021886 | ITGB3 | c.423C>A (p.Tyr141Ter) c.388C>A | |
17 | g.47284504C>G | CA400021887 | ITGB3 | c.423C>G (p.Tyr141Ter) c.388C>G | |
17 | g.47284504C>T | CA500430543 | ITGB3 | c.423C>T (p.Tyr141=) c.388C>T | |
17 | g.47284505T>A | CA400021890 | ITGB3 | c.424T>A (p.Tyr142Asn) c.389T>A | |
17 | g.47284505T>C | CA400021891 | ITGB3 | c.424T>C (p.Tyr142His) c.389T>C | gnomAD v4 |
17 | g.47284505T>G | CA400021894 | ITGB3 | c.424T>G (p.Tyr142Asp) c.389T>G | |
17 | g.47284506A>C | CA400021896 | ITGB3 | c.425A>C (p.Tyr142Ser) c.390A>C | |
17 | g.47284506A>G | CA400021898 | ITGB3 | c.425A>G (p.Tyr142Cys) c.390A>G | |
17 | g.47284506A>T | CA400021901 | ITGB3 | c.425A>T (p.Tyr142Phe) c.390A>T | |
17 | g.47284507C>A | CA400021905 | ITGB3 | c.426C>A (p.Tyr142Ter) c.391C>A | |
17 | g.47284507C>G | CA400021903 | ITGB3 | c.426C>G (p.Tyr142Ter) c.391C>G | |
17 | g.47284507C>T | CA500430562 | ITGB3 | c.426C>T (p.Tyr142=) c.391C>T | gnomAD v4 |
17 | g.47284508T>A | CA400021907 | ITGB3 | c.427T>A (p.Leu143Met) c.392T>A | |
17 | g.47284508T>C | CA500430566 | ITGB3 | c.427T>C (p.Leu143=) c.392T>C | ClinVar |
17 | g.47284508T>G | CA400021909 | ITGB3 | c.427T>G (p.Leu143Val) c.392T>G | |
17 | g.47284509T>A | CA400021910 | ITGB3 | c.428T>A (p.Leu143Ter) c.393T>A | |
17 | g.47284509T>C | CA400021913 | ITGB3 | c.428T>C (p.Leu143Ser) c.393T>C | |
17 | g.47284509T>G | CA123252 | ITGB3 | c.428T>G (p.Leu143Trp) c.393T>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.47284509T= | CA2262605301 | ITGB3 | c.428T= (p.Leu143=) c.393T= | |
17 | g.47284510G>A | CA500430572 | ITGB3 | c.429G>A (p.Leu143=) c.394G>A | |
17 | g.47284510G>C | CA400021917 | ITGB3 | c.429G>C (p.Leu143Phe) c.394G>C | |
17 | g.47284510G>T | CA400021918 | ITGB3 | c.429G>T (p.Leu143Phe) c.394G>T | |
17 | g.47284511A>C | CA400021922 | ITGB3 | c.430A>C (p.Met144Leu) c.395A>C | |
17 | g.47284511A>G | CA400021923 | ITGB3 | c.430A>G (p.Met144Val) c.395A>G | |
17 | g.47284511A>T | CA400021925 | ITGB3 | c.430A>T (p.Met144Leu) c.395A>T | |
17 | g.47284512T>A | CA400021927 | ITGB3 | c.431T>A (p.Met144Lys) c.396T>A | gnomAD v4 |
17 | g.47284512T>C | CA400021929 | ITGB3 | c.431T>C (p.Met144Thr) c.396T>C | |
17 | g.47284512T>G | CA291224645 | ITGB3 | c.431T>G (p.Met144Arg) c.396T>G | ClinVar dbSNP gnomAD v3 gnomAD v4 |
17 | g.47284512T= | CA2262605302 | ITGB3 | c.431T= (p.Met144=) c.396T= | |
17 | g.47284513G>A | CA400021937 | ITGB3 | c.432G>A (p.Met144Ile) c.397G>A | COSMIC COSMIC |
17 | g.47284513G>C | CA400021935 | ITGB3 | c.432G>C (p.Met144Ile) c.397G>C | COSMIC COSMIC COSMIC |
17 | g.47284513G>T | CA400021933 | ITGB3 | c.432G>T (p.Met144Ile) c.397G>T | |
17 | g.47284514G>A | CA400021939 | ITGB3 | c.433G>A (p.Asp145Asn) c.398G>A | ClinVar dbSNP |
17 | g.47284514G>C | CA400021940 | ITGB3 | c.433G>C (p.Asp145His) c.398G>C | |
17 | g.47284514G= | CA2262605303 | ITGB3 | c.433G= (p.Asp145=) c.398G= | |
17 | g.47284514G>T | CA123226 | ITGB3 | c.433G>T (p.Asp145Tyr) c.398G>T | ClinVar dbSNP |
17 | g.47284515A>C | CA400021943 | ITGB3 | c.434A>C (p.Asp145Ala) c.399A>C | |
17 | g.47284515A>G | CA400021945 | ITGB3 | c.434A>G (p.Asp145Gly) c.399A>G | |
17 | g.47284515A>T | CA400021947 | ITGB3 | c.434A>T (p.Asp145Val) c.399A>T | |
17 | g.47284516C>A | CA400021950 | ITGB3 | c.435C>A (p.Asp145Glu) c.400C>A | |
17 | g.47284516C>G | CA400021951 | ITGB3 | c.435C>G (p.Asp145Glu) c.400C>G | |
17 | g.47284516C>T | CA500430603 | ITGB3 | c.435C>T (p.Asp145=) c.400C>T | |
17 | g.47284517C>A | CA400021954 | ITGB3 | c.436C>A (p.Leu146Met) c.401C>A | |
17 | g.47284517C>G | CA400021956 | ITGB3 | c.436C>G (p.Leu146Val) c.401C>G | |
17 | g.47284517C>T | CA500430609 | ITGB3 | c.436C>T (p.Leu146=) c.401C>T | gnomAD v4 |
17 | g.47284518T>A | CA400021959 | ITGB3 | c.437T>A (p.Leu146Gln) c.402T>A | |
17 | g.47284518T>C | CA400021960 | ITGB3 | c.437T>C (p.Leu146Pro) c.402T>C | ClinVar dbSNP gnomAD v4 |
17 | g.47284518T>G | CA400021962 | ITGB3 | c.437T>G (p.Leu146Arg) c.402T>G | gnomAD v4 |
17 | g.47284518T= | CA2262605304 | ITGB3 | c.437T= (p.Leu146=) c.402T= | |
17 | g.47284519G>A | CA8622960 | ITGB3 | c.438G>A (p.Leu146=) c.403G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.47284519G>C | CA500430618 | ITGB3 | c.438G>C (p.Leu146=) c.403G>C | |
17 | g.47284519G= | CA2262605305 | ITGB3 | c.438G= (p.Leu146=) c.403G= | |
17 | g.47284519G>T | CA500430620 | ITGB3 | c.438G>T (p.Leu146=) c.403G>T | |
17 | g.47284520T>A | CA400021970 | ITGB3 | c.439T>A (p.Ser147Thr) c.404T>A | |
17 | g.47284520T>C | CA400021968 | ITGB3 | c.439T>C (p.Ser147Pro) c.404T>C | dbSNP |
17 | g.47284520T>G | CA400021966 | ITGB3 | c.439T>G (p.Ser147Ala) c.404T>G | |
17 | g.47284520T= | CA2262605306 | ITGB3 | c.439T= (p.Ser147=) c.404T= | |
17 | g.47284521C>A | CA400021972 | ITGB3 | c.440C>A (p.Ser147Tyr) c.405C>A | |
17 | g.47284521C= | CA2262605307 | ITGB3 | c.440C= (p.Ser147=) c.405C= | |
17 | g.47284521C>G | CA400021974 | ITGB3 | c.440C>G (p.Ser147Cys) c.405C>G | |
17 | g.47284521C>T | CA400021976 | ITGB3 | c.440C>T (p.Ser147Phe) c.405C>T | dbSNP |
17 | g.47284522T>A | CA500430635 | ITGB3 | c.441T>A (p.Ser147=) c.406T>A | |
17 | g.47284522T>C | CA500430638 | ITGB3 | c.441T>C (p.Ser147=) c.406T>C | |
17 | g.47284522T>G | CA500430637 | ITGB3 | c.441T>G (p.Ser147=) c.406T>G | |
17 | g.47284523T>A | CA400021977 | ITGB3 | c.442T>A (p.Tyr148Asn) c.407T>A | |
17 | g.47284523T>C | CA400021979 | ITGB3 | c.442T>C (p.Tyr148His) c.407T>C | |
17 | g.47284523T>G | CA400021981 | ITGB3 | c.442T>G (p.Tyr148Asp) c.407T>G | |
17 | g.47284524A>C | CA400021988 | ITGB3 | c.443A>C (p.Tyr148Ser) c.408A>C | |
17 | g.47284524A>G | CA400021984 | ITGB3 | c.443A>G (p.Tyr148Cys) c.408A>G | |
17 | g.47284524A>T | CA400021986 | ITGB3 | c.443A>T (p.Tyr148Phe) c.408A>T | |
17 | g.47284525del | CA2638435393 | ITGB3 | c.444del (p.Ser149ProfsTer2) c.409del | gnomAD v4 |
17 | g.47284525C>A | CA400021991 | ITGB3 | c.444C>A (p.Tyr148Ter) c.409C>A | |
17 | g.47284525C= | CA2262605308 | ITGB3 | c.444C= (p.Tyr148=) c.409C= | |
17 | g.47284525C>G | CA400021992 | ITGB3 | c.444C>G (p.Tyr148Ter) c.409C>G | ClinVar dbSNP gnomAD v4 |
17 | g.47284525C>T | CA291224647 | ITGB3 | c.444C>T (p.Tyr148=) c.409C>T | ClinVar dbSNP gnomAD v3 gnomAD v4 |
17 | g.47284526T>A | CA400021995 | ITGB3 | c.445T>A (p.Ser149Thr) c.410T>A | |
17 | g.47284526T>C | CA400021997 | ITGB3 | c.445T>C (p.Ser149Pro) c.410T>C | ClinVar |
17 | g.47284526T>G | CA400021999 | ITGB3 | c.445T>G (p.Ser149Ala) c.410T>G | |
17 | g.47284527C>A | CA400022006 | ITGB3 | c.446C>A (p.Ser149Tyr) c.411C>A | |
17 | g.47284527C>G | CA400022002 | ITGB3 | c.446C>G (p.Ser149Cys) c.411C>G | |
17 | g.47284527C>T | CA400022005 | ITGB3 | c.446C>T (p.Ser149Phe) c.411C>T | |
17 | g.47284528C>A | CA500430661 | ITGB3 | c.447C>A (p.Ser149=) c.412C>A | |
17 | g.47284528C>G | CA500430663 | ITGB3 | c.447C>G (p.Ser149=) c.412C>G | |
17 | g.47284528C>T | CA500430660 | ITGB3 | c.447C>T (p.Ser149=) c.412C>T | COSMIC COSMIC COSMIC |
17 | g.47284529A= | CA2262605309 | ITGB3 | c.448A= (p.Met150=) c.413A= | |
17 | g.47284529A>C | CA400022009 | ITGB3 | c.448A>C (p.Met150Leu) c.413A>C | dbSNP gnomAD v2 gnomAD v4 |
17 | g.47284529A>G | CA8622961 | ITGB3 | c.448A>G (p.Met150Val) c.413A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.47284529A>T | CA400022012 | ITGB3 | c.448A>T (p.Met150Leu) c.413A>T | |
17 | g.47284530T>A | CA400022015 | ITGB3 | c.449T>A (p.Met150Lys) c.414T>A | |
17 | g.47284530T>C | CA400022017 | ITGB3 | c.449T>C (p.Met150Thr) c.414T>C | ClinVar |
17 | g.47284530T>G | CA400022019 | ITGB3 | c.449T>G (p.Met150Arg) c.414T>G | |
17 | g.47284531G>A | CA400022022 | ITGB3 | c.450G>A (p.Met150Ile) c.415G>A | gnomAD v4 |
17 | g.47284531G>C | CA400022024 | ITGB3 | c.450G>C (p.Met150Ile) c.415G>C | |
17 | g.47284531G>T | CA400022025 | ITGB3 | c.450G>T (p.Met150Ile) c.415G>T | |
17 | g.47284532A>C | CA400022028 | ITGB3 | c.451A>C (p.Lys151Gln) c.416A>C | |
17 | g.47284532A>G | CA400022030 | ITGB3 | c.451A>G (p.Lys151Glu) c.416A>G | |
17 | g.47284532A>T | CA400022032 | ITGB3 | c.451A>T (p.Lys151Ter) c.416A>T | |
17 | g.47284533A>C | CA400022034 | ITGB3 | c.452A>C (p.Lys151Thr) c.417A>C | |
17 | g.47284533A>G | CA400022038 | ITGB3 | c.452A>G (p.Lys151Arg) c.417A>G | |
17 | g.47284533A>T | CA400022036 | ITGB3 | c.452A>T (p.Lys151Met) c.417A>T | |
17 | g.47284534G>A | CA500430689 | ITGB3 | c.453G>A (p.Lys151=) c.418G>A | |
17 | g.47284534G>C | CA400022040 | ITGB3 | c.453G>C (p.Lys151Asn) c.418G>C | |
17 | g.47284534G>T | CA400022042 | ITGB3 | c.453G>T (p.Lys151Asn) c.418G>T | |
17 | g.47284535G>A | CA400022045 | ITGB3 | c.454G>A (p.Asp152Asn) c.419G>A | |
17 | g.47284535G>C | CA400022047 | ITGB3 | c.454G>C (p.Asp152His) c.419G>C | |
17 | g.47284535G>T | CA400022049 | ITGB3 | c.454G>T (p.Asp152Tyr) c.419G>T | COSMIC COSMIC COSMIC |
17 | g.47284536A= | CA2262605310 | ITGB3 | c.455A= (p.Asp152=) c.420A= | |
17 | g.47284536A>C | CA8622962 | ITGB3 | c.455A>C (p.Asp152Ala) c.420A>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.47284536A>G | CA400022053 | ITGB3 | c.455A>G (p.Asp152Gly) c.420A>G | |
17 | g.47284536A>T | CA400022054 | ITGB3 | c.455A>T (p.Asp152Val) c.420A>T | |
17 | g.47284537T>A | CA400022057 | ITGB3 | c.456T>A (p.Asp152Glu) c.421T>A | |
17 | g.47284537T>C | CA291224651 | ITGB3 | c.456T>C (p.Asp152=) c.421T>C | dbSNP gnomAD v4 |
17 | g.47284537T>G | CA400022059 | ITGB3 | c.456T>G (p.Asp152Glu) c.421T>G | |
17 | g.47284537T= | CA2262605311 | ITGB3 | c.456T= (p.Asp152=) c.421T= | |
17 | g.47284538G>A | CA400022061 | ITGB3 | c.457G>A (p.Asp153Asn) c.422G>A | |
17 | g.47284538G>C | CA400022063 | ITGB3 | c.457G>C (p.Asp153His) c.422G>C | |
17 | g.47284538G>T | CA400022065 | ITGB3 | c.457G>T (p.Asp153Tyr) c.422G>T | gnomAD v4 |
17 | g.47284539A= | CA2262605312 | ITGB3 | c.458A= (p.Asp153=) c.423A= | |
17 | g.47284539A>C | CA400022069 | ITGB3 | c.458A>C (p.Asp153Ala) c.423A>C | |
17 | g.47284539A>G | CA400022067 | ITGB3 | c.458A>G (p.Asp153Gly) c.423A>G | dbSNP |
17 | g.47284539A>T | CA400022066 | ITGB3 | c.458A>T (p.Asp153Val) c.423A>T | |
17 | g.47284540T>A | CA400022071 | ITGB3 | c.459T>A (p.Asp153Glu) c.424T>A | |
17 | g.47284540T>C | CA500430719 | ITGB3 | c.459T>C (p.Asp153=) c.424T>C | |
17 | g.47284540T>G | CA400022073 | ITGB3 | c.459T>G (p.Asp153Glu) c.424T>G | |
17 | g.47284541C>A | CA400022075 | ITGB3 | c.460C>A (p.Leu154Met) c.425C>A | |
17 | g.47284541C>G | CA400022077 | ITGB3 | c.460C>G (p.Leu154Val) c.425C>G | |
17 | g.47284541C>T | CA500430724 | ITGB3 | c.460C>T (p.Leu154=) c.425C>T | |
17 | g.47284542T>A | CA400022079 | ITGB3 | c.461T>A (p.Leu154Gln) c.426T>A | |
17 | g.47284542T>C | CA400022081 | ITGB3 | c.461T>C (p.Leu154Pro) c.426T>C | |
17 | g.47284542T>G | CA400022084 | ITGB3 | c.461T>G (p.Leu154Arg) c.426T>G | |
17 | g.47284543G>A | CA500430732 | ITGB3 | c.462G>A (p.Leu154=) c.427G>A | |
17 | g.47284543G>C | CA500430734 | ITGB3 | c.462G>C (p.Leu154=) c.427G>C | |
17 | g.47284543G>T | CA500430740 | ITGB3 | c.462G>T (p.Leu154=) c.427G>T | |
17 | g.47284544T>A | CA400022085 | ITGB3 | c.463T>A (p.Trp155Arg) c.428T>A | |
17 | g.47284544T>C | CA8622963 | ITGB3 | c.463T>C (p.Trp155Arg) c.428T>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.47284544T>G | CA400022086 | ITGB3 | c.463T>G (p.Trp155Gly) c.428T>G | |
17 | g.47284544T= | CA2262605313 | ITGB3 | c.463T= (p.Trp155=) c.428T= | |
17 | g.47284545G>A | CA400022087 | ITGB3 | c.464G>A (p.Trp155Ter) c.429G>A | |
17 | g.47284545G>C | CA400022088 | ITGB3 | c.464G>C (p.Trp155Ser) c.429G>C | |
17 | g.47284545G>T | CA400022089 | ITGB3 | c.464G>T (p.Trp155Leu) c.429G>T | |
17 | g.47284546G>A | CA400022091 | ITGB3 | c.465G>A (p.Trp155Ter) c.430G>A | |
17 | g.47284546G>C | CA400022092 | ITGB3 | c.465G>C (p.Trp155Cys) c.430G>C | |
17 | g.47284546G>T | CA400022090 | ITGB3 | c.465G>T (p.Trp155Cys) c.430G>T | |
17 | g.47284547A= | CA2262605314 | ITGB3 | c.466A= (p.Ser156=) c.431A= | |
17 | g.47284547A>C | CA400022093 | ITGB3 | c.466A>C (p.Ser156Arg) c.431A>C | |
17 | g.47284547A>G | CA8622964 | ITGB3 | c.466A>G (p.Ser156Gly) c.431A>G | dbSNP ExAC gnomAD v4 |
17 | g.47284547A>T | CA400022094 | ITGB3 | c.466A>T (p.Ser156Cys) c.431A>T | |
17 | g.47284548G>A | CA400022095 | ITGB3 | c.467G>A (p.Ser156Asn) c.432G>A | |
17 | g.47284548G>C | CA400022096 | ITGB3 | c.467G>C (p.Ser156Thr) c.432G>C | |
17 | g.47284548G>T | CA400022097 | ITGB3 | c.467G>T (p.Ser156Ile) c.432G>T | COSMIC |
17 | g.47284549C>A | CA400022098 | ITGB3 | c.468C>A (p.Ser156Arg) c.433C>A | gnomAD v3 gnomAD v4 |
17 | g.47284549C>G | CA400022099 | ITGB3 | c.468C>G (p.Ser156Arg) c.433C>G | |
17 | g.47284549C>T | CA500430775 | ITGB3 | c.468C>T (p.Ser156=) c.433C>T | |
17 | g.47284550A>C | CA400022100 | ITGB3 | c.469A>C (p.Ile157Leu) c.434A>C | |
17 | g.47284550A>G | CA400022101 | ITGB3 | c.469A>G (p.Ile157Val) c.434A>G | |
17 | g.47284550A>T | CA400022102 | ITGB3 | c.469A>T (p.Ile157Phe) c.434A>T | |
17 | g.47284551T>A | CA400022105 | ITGB3 | c.470T>A (p.Ile157Asn) c.435T>A | |
17 | g.47284551T>C | CA400022104 | ITGB3 | c.470T>C (p.Ile157Thr) c.435T>C | |
17 | g.47284551T>G | CA400022103 | ITGB3 | c.470T>G (p.Ile157Ser) c.435T>G | |
17 | g.47284552C>A | CA500430793 | ITGB3 | c.471C>A (p.Ile157=) c.436C>A | gnomAD v4 |
17 | g.47284552C>G | CA400022106 | ITGB3 | c.471C>G (p.Ile157Met) c.436C>G | |
17 | g.47284552C>T | CA500430789 | ITGB3 | c.471C>T (p.Ile157=) c.436C>T | |
17 | g.47284553C>A | CA400022107 | ITGB3 | c.472C>A (p.Gln158Lys) c.437C>A | |
17 | g.47284553C>G | CA400022108 | ITGB3 | c.472C>G (p.Gln158Glu) c.437C>G | |
17 | g.47284553C>T | CA400022109 | ITGB3 | c.472C>T (p.Gln158Ter) c.437C>T | |
17 | g.47284554A= | CA2262605315 | ITGB3 | c.473A= (p.Gln158=) c.438A= | |
17 | g.47284554A>C | CA400022110 | ITGB3 | c.473A>C (p.Gln158Pro) c.438A>C | |
17 | g.47284554A>G | CA8622965 | ITGB3 | c.473A>G (p.Gln158Arg) c.438A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.47284554A>T | CA400022111 | ITGB3 | c.473A>T (p.Gln158Leu) c.438A>T | ClinVar |
17 | g.47284555G>A | CA500430807 | ITGB3 | c.474G>A (p.Gln158=) c.439G>A | COSMIC |
17 | g.47284555G>C | CA400022112 | ITGB3 | c.474G>C (p.Gln158His) c.439G>C | |
17 | g.47284555G>T | CA400022113 | ITGB3 | c.474G>T (p.Gln158His) c.439G>T | |
17 | g.47284556A>C | CA400022114 | ITGB3 | c.475A>C (p.Asn159His) c.440A>C | |
17 | g.47284556A>G | CA400022115 | ITGB3 | c.475A>G (p.Asn159Asp) c.440A>G | gnomAD v4 |
17 | g.47284556A>T | CA400022116 | ITGB3 | c.475A>T (p.Asn159Tyr) c.440A>T | gnomAD v4 |
17 | g.47284557A>C | CA400022119 | ITGB3 | c.476A>C (p.Asn159Thr) c.441A>C | |
17 | g.47284557A>G | CA400022118 | ITGB3 | c.476A>G (p.Asn159Ser) c.441A>G | gnomAD v4 |
17 | g.47284557A>T | CA400022117 | ITGB3 | c.476A>T (p.Asn159Ile) c.441A>T | |
17 | g.47284558C>A | CA400022120 | ITGB3 | c.477C>A (p.Asn159Lys) c.442C>A | |
17 | g.47284558C>G | CA400022121 | ITGB3 | c.477C>G (p.Asn159Lys) c.442C>G | |
17 | g.47284558C>T | CA500430826 | ITGB3 | c.477C>T (p.Asn159=) c.442C>T | |
17 | g.47284559C>A | CA400022122 | ITGB3 | c.478C>A (p.Leu160Met) c.443C>A | |
17 | g.47284559C= | CA2262605316 | ITGB3 | c.478C= (p.Leu160=) c.443C= | |
17 | g.47284559C>G | CA400022123 | ITGB3 | c.478C>G (p.Leu160Val) c.443C>G | |
17 | g.47284559C>T | CA500430835 | ITGB3 | c.478C>T (p.Leu160=) c.443C>T | dbSNP gnomAD v2 gnomAD v4 |
17 | g.47284560T>A | CA400022124 | ITGB3 | c.479T>A (p.Leu160Gln) c.444T>A | |
17 | g.47284560T>C | CA400022126 | ITGB3 | c.479T>C (p.Leu160Pro) c.444T>C | gnomAD v4 COSMIC COSMIC COSMIC |
17 | g.47284560T>G | CA400022125 | ITGB3 | c.479T>G (p.Leu160Arg) c.444T>G | |
17 | g.47284561G>A | CA500430845 | ITGB3 | c.480G>A (p.Leu160=) c.445G>A | |
17 | g.47284561G>C | CA500430849 | ITGB3 | c.480G>C (p.Leu160=) c.445G>C | |
17 | g.47284561G>T | CA500430847 | ITGB3 | c.480G>T (p.Leu160=) c.445G>T | COSMIC COSMIC COSMIC |
17 | g.47284562G>A | CA400022127 | ITGB3 | c.481G>A (p.Gly161Ser) c.446G>A | |
17 | g.47284562G>C | CA400022128 | ITGB3 | c.481G>C (p.Gly161Arg) c.446G>C | |
17 | g.47284562G>T | CA400022129 | ITGB3 | c.481G>T (p.Gly161Cys) c.446G>T | |
17 | g.47284562_47284571del | CA2638435394 | ITGB3 | c.481_490del (p.Gly161TrpfsTer?) c.446_455del | gnomAD v4 |
17 | g.47284563G>A | CA291224653 | ITGB3 | c.482G>A (p.Gly161Asp) c.447G>A | dbSNP |
17 | g.47284563G>C | CA400022130 | ITGB3 | c.482G>C (p.Gly161Ala) c.447G>C | |
17 | g.47284563G= | CA2262605317 | ITGB3 | c.482G= (p.Gly161=) c.447G= | |
17 | g.47284563G>T | CA400022131 | ITGB3 | c.482G>T (p.Gly161Val) c.447G>T | |
17 | g.47284564T>A | CA500430871 | ITGB3 | c.483T>A (p.Gly161=) c.448T>A | |
17 | g.47284564T>C | CA500430866 | ITGB3 | c.483T>C (p.Gly161=) c.448T>C | |
17 | g.47284564T>G | CA500430868 | ITGB3 | c.483T>G (p.Gly161=) c.448T>G | |
17 | g.47284565A= | CA2262605318 | ITGB3 | c.484A= (p.Thr162=) c.449A= | |
17 | g.47284565A>C | CA400022132 | ITGB3 | c.484A>C (p.Thr162Pro) c.449A>C | |
17 | g.47284565A>G | CA400022133 | ITGB3 | c.484A>G (p.Thr162Ala) c.449A>G | |
17 | g.47284565A>T | CA400022134 | ITGB3 | c.484A>T (p.Thr162Ser) c.449A>T | |
17 | g.47284566C>A | CA400022135 | ITGB3 | c.485C>A (p.Thr162Asn) c.450C>A | |
17 | g.47284566C>G | CA400022136 | ITGB3 | c.485C>G (p.Thr162Ser) c.450C>G | |
17 | g.47284566C>T | CA400022137 | ITGB3 | c.485C>T (p.Thr162Ile) c.450C>T | |
17 | g.47284566_47284567insACC | CA772536150 | ITGB3 | c.485_486insACC (p.Thr162_Lys163insPro) c.450_451insACC | dbSNP gnomAD v4 |
17 | g.47284567C>A | CA8622966 | ITGB3 | c.486C>A (p.Thr162=) c.451C>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.47284567C= | CA2262605319 | ITGB3 | c.486C= (p.Thr162=) c.451C= | |
17 | g.47284567C>G | CA500430887 | ITGB3 | c.486C>G (p.Thr162=) c.451C>G | |
17 | g.47284567C>T | CA500430891 | ITGB3 | c.486C>T (p.Thr162=) c.451C>T | |
17 | g.47284568A= | CA2262605320 | ITGB3 | c.487A= (p.Lys163=) c.452A= | |
17 | g.47284568A>C | CA291224655 | ITGB3 | c.487A>C (p.Lys163Gln) c.452A>C | ClinVar dbSNP gnomAD v4 |
17 | g.47284568A>G | CA400022138 | ITGB3 | c.487A>G (p.Lys163Glu) c.452A>G | gnomAD v4 |
17 | g.47284568A>T | CA400022139 | ITGB3 | c.487A>T (p.Lys163Ter) c.452A>T | |
17 | g.47284569dup | CA626378340 | ITGB3 | c.488dup (p.Leu164AlafsTer11) c.453dup | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.47284569A>C | CA400022140 | ITGB3 | c.488A>C (p.Lys163Thr) c.453A>C | |
17 | g.47284569A>G | CA400022141 | ITGB3 | c.488A>G (p.Lys163Arg) c.453A>G | |
17 | g.47284569A>T | CA400022142 | ITGB3 | c.488A>T (p.Lys163Met) c.453A>T | |
17 | g.47284570G>A | CA500430903 | ITGB3 | c.489G>A (p.Lys163=) c.454G>A | |
17 | g.47284570G>C | CA400022143 | ITGB3 | c.489G>C (p.Lys163Asn) c.454G>C | |
17 | g.47284570G>T | CA400022144 | ITGB3 | c.489G>T (p.Lys163Asn) c.454G>T | |
17 | g.47284571C>A | CA400022145 | ITGB3 | c.490C>A (p.Leu164Met) c.455C>A | |
17 | g.47284571C>G | CA400022146 | ITGB3 | c.490C>G (p.Leu164Val) c.455C>G | |
17 | g.47284571C>T | CA500430911 | ITGB3 | c.490C>T (p.Leu164=) c.455C>T | |
17 | g.47284572T>A | CA400022875 | ITGB3 | c.491T>A (p.Leu164Gln) c.456T>A | |
17 | g.47284572T>C | CA400022877 | ITGB3 | c.491T>C (p.Leu164Pro) c.456T>C | |
17 | g.47284572T>G | CA400022880 | ITGB3 | c.491T>G (p.Leu164Arg) c.456T>G | |
17 | g.47284573G>A | CA500431590 | ITGB3 | c.492G>A (p.Leu164=) c.457G>A | gnomAD v4 |
17 | g.47284573G>C | CA500431594 | ITGB3 | c.492G>C (p.Leu164=) c.457G>C | |
17 | g.47284573G>T | CA500431592 | ITGB3 | c.492G>T (p.Leu164=) c.457G>T | |
17 | g.47284574G>A | CA400022887 | ITGB3 | c.493G>A (p.Ala165Thr) c.458G>A | |
17 | g.47284574G>C | CA400022883 | ITGB3 | c.493G>C (p.Ala165Pro) c.458G>C | |
17 | g.47284574G>T | CA400022885 | ITGB3 | c.493G>T (p.Ala165Ser) c.458G>T | |
17 | g.47284575C>A | CA400022890 | ITGB3 | c.494C>A (p.Ala165Asp) c.459C>A | |
17 | g.47284575C>G | CA400022892 | ITGB3 | c.494C>G (p.Ala165Gly) c.459C>G | gnomAD v4 |
17 | g.47284575C>T | CA400022894 | ITGB3 | c.494C>T (p.Ala165Val) c.459C>T | gnomAD v4 |
17 | g.47284576C>A | CA500431610 | ITGB3 | c.495C>A (p.Ala165=) c.460C>A | |
17 | g.47284576C>G | CA500431613 | ITGB3 | c.495C>G (p.Ala165=) c.460C>G | |
17 | g.47284576C>T | CA500431608 | ITGB3 | c.495C>T (p.Ala165=) c.460C>T | |
17 | g.47284577A>C | CA400022896 | ITGB3 | c.496A>C (p.Thr166Pro) c.461A>C | |
17 | g.47284577A>G | CA400022898 | ITGB3 | c.496A>G (p.Thr166Ala) c.461A>G | gnomAD v4 |
17 | g.47284577A>T | CA400022900 | ITGB3 | c.496A>T (p.Thr166Ser) c.461A>T | gnomAD v4 |
17 | g.47284578C>A | CA400022903 | ITGB3 | c.497C>A (p.Thr166Asn) c.462C>A | |
17 | g.47284578C= | CA2262605321 | ITGB3 | c.497C= (p.Thr166=) c.462C= | |
17 | g.47284578C>G | CA400022905 | ITGB3 | c.497C>G (p.Thr166Ser) c.462C>G | |
17 | g.47284578C>T | CA291224656 | ITGB3 | c.497C>T (p.Thr166Ile) c.462C>T | dbSNP |
17 | g.47284579C>A | CA500431632 | ITGB3 | c.498C>A (p.Thr166=) c.463C>A | |
17 | g.47284579C>G | CA500431627 | ITGB3 | c.498C>G (p.Thr166=) c.463C>G | gnomAD v4 |
17 | g.47284579C>T | CA500431629 | ITGB3 | c.498C>T (p.Thr166=) c.463C>T | |
17 | g.47284580C>A | CA400022910 | ITGB3 | c.499C>A (p.Gln167Lys) c.464C>A | |
17 | g.47284580C= | CA2262605322 | ITGB3 | c.499C= (p.Gln167=) c.464C= | |
17 | g.47284580C>G | CA8622967 | ITGB3 | c.499C>G (p.Gln167Glu) c.464C>G | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.47284580C>T | CA400022913 | ITGB3 | c.499C>T (p.Gln167Ter) c.464C>T | dbSNP |
17 | g.47284581A>C | CA400022920 | ITGB3 | c.500A>C (p.Gln167Pro) c.465A>C | |
17 | g.47284581A>G | CA400022918 | ITGB3 | c.500A>G (p.Gln167Arg) c.465A>G | gnomAD v4 |
17 | g.47284581A>T | CA400022915 | ITGB3 | c.500A>T (p.Gln167Leu) c.465A>T | |
17 | g.47284582G>A | CA500431649 | ITGB3 | c.501G>A (p.Gln167=) c.466G>A | |
17 | g.47284582G>C | CA400022921 | ITGB3 | c.501G>C (p.Gln167His) c.466G>C | |
17 | g.47284582G>T | CA400022923 | ITGB3 | c.501G>T (p.Gln167His) c.466G>T | gnomAD v4 |
17 | g.47284583A>C | CA400022926 | ITGB3 | c.502A>C (p.Met168Leu) c.467A>C | |
17 | g.47284583A>G | CA400022927 | ITGB3 | c.502A>G (p.Met168Val) c.467A>G | |
17 | g.47284583A>T | CA400022930 | ITGB3 | c.502A>T (p.Met168Leu) c.467A>T | |
17 | g.47284584T>A | CA400022932 | ITGB3 | c.503T>A (p.Met168Lys) c.468T>A | |
17 | g.47284584T>C | CA400022934 | ITGB3 | c.503T>C (p.Met168Thr) c.468T>C | |
17 | g.47284584T>G | CA400022936 | ITGB3 | c.503T>G (p.Met168Arg) c.468T>G | |
17 | g.47284585G>A | CA400022939 | ITGB3 | c.504G>A (p.Met168Ile) c.469G>A | |
17 | g.47284585G>C | CA400022940 | ITGB3 | c.504G>C (p.Met168Ile) c.469G>C | |
17 | g.47284585G>T | CA400022943 | ITGB3 | c.504G>T (p.Met168Ile) c.469G>T | |
17 | g.47284586C>A | CA500431662 | ITGB3 | c.505C>A (p.Arg169=) c.470C>A | COSMIC COSMIC COSMIC |
17 | g.47284586C= | CA2262605323 | ITGB3 | c.505C= (p.Arg169=) c.470C= | |
17 | g.47284586C>G | CA400022946 | ITGB3 | c.505C>G (p.Arg169Gly) c.470C>G | |
17 | g.47284586C>T | CA291224658 | ITGB3 | c.505C>T (p.Arg169Ter) c.470C>T | ClinVar dbSNP gnomAD v4 |