Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
4 | g.154569596G>A | CA358514888 | FGB | c.1041G>A (p.Trp347Ter) n.939+289G>A c.384G>A (p.Trp128Ter) c.864G>A (p.Trp288Ter) c.909G>A (p.Trp303Ter) c.746-5G>A (n.746-5G>A) c.1032G>A (p.Trp344Ter) | |
4 | g.154569596G>C | CA358514889 | FGB | c.1041G>C (p.Trp347Cys) n.939+289G>C c.384G>C (p.Trp128Cys) c.864G>C (p.Trp288Cys) c.909G>C (p.Trp303Cys) c.746-5G>C (n.746-5G>C) c.1032G>C (p.Trp344Cys) | |
4 | g.154569596G>T | CA358514890 | FGB | c.1041G>T (p.Trp347Cys) n.939+289G>T c.384G>T (p.Trp128Cys) c.864G>T (p.Trp288Cys) c.909G>T (p.Trp303Cys) c.746-5G>T (n.746-5G>T) c.1032G>T (p.Trp344Cys) | |
4 | g.154569597A>C | CA358514892 | FGB | c.1042A>C (p.Lys348Gln) n.939+290A>C c.385A>C (p.Lys129Gln) c.865A>C (p.Lys289Gln) c.910A>C (p.Lys304Gln) c.746-4A>C (n.746-4A>C) c.1033A>C (p.Lys345Gln) | |
4 | g.154569597A>G | CA358514894 | FGB | c.1042A>G (p.Lys348Glu) n.939+290A>G c.385A>G (p.Lys129Glu) c.865A>G (p.Lys289Glu) c.910A>G (p.Lys304Glu) c.746-4A>G (n.746-4A>G) c.1033A>G (p.Lys345Glu) | |
4 | g.154569597A>T | CA358514895 | FGB | c.1042A>T (p.Lys348Ter) n.939+290A>T c.385A>T (p.Lys129Ter) c.865A>T (p.Lys289Ter) c.910A>T (p.Lys304Ter) c.746-4A>T (n.746-4A>T) c.1033A>T (p.Lys345Ter) | |
4 | g.154569598A>C | CA358514897 | FGB | c.1043A>C (p.Lys348Thr) n.939+291A>C c.386A>C (p.Lys129Thr) c.866A>C (p.Lys289Thr) c.911A>C (p.Lys304Thr) c.746-3A>C (n.746-3A>C) c.1034A>C (p.Lys345Thr) | |
4 | g.154569598A>G | CA358514899 | FGB | c.1043A>G (p.Lys348Arg) n.939+291A>G c.386A>G (p.Lys129Arg) c.866A>G (p.Lys289Arg) c.911A>G (p.Lys304Arg) c.746-3A>G (n.746-3A>G) c.1034A>G (p.Lys345Arg) | |
4 | g.154569598A>T | CA358514900 | FGB | c.1043A>T (p.Lys348Ile) n.939+291A>T c.386A>T (p.Lys129Ile) c.866A>T (p.Lys289Ile) c.911A>T (p.Lys304Ile) c.746-3A>T (n.746-3A>T) c.1034A>T (p.Lys345Ile) | |
4 | g.154569599A>C | CA358514902 | FGB | c.1044A>C (p.Lys348Asn) n.939+292A>C c.387A>C (p.Lys129Asn) c.867A>C (p.Lys289Asn) c.912A>C (p.Lys304Asn) c.746-2A>C (n.746-2A>C) c.1035A>C (p.Lys345Asn) | |
4 | g.154569599A>G | CA442013252 | FGB | c.1044A>G (p.Lys348=) n.939+292A>G c.387A>G (p.Lys129=) c.867A>G (p.Lys289=) c.912A>G (p.Lys304=) c.746-2A>G (n.746-2A>G) c.1035A>G (p.Lys345=) | |
4 | g.154569599A>T | CA358514904 | FGB | c.1044A>T (p.Lys348Asn) n.939+292A>T c.387A>T (p.Lys129Asn) c.867A>T (p.Lys289Asn) c.912A>T (p.Lys304Asn) c.746-2A>T (n.746-2A>T) c.1035A>T (p.Lys345Asn) | |
4 | g.154569600G>A | CA3114706 | FGB | c.1045G>A (p.Gly349Arg) n.939+293G>A c.388G>A (p.Gly130Arg) c.868G>A (p.Gly290Arg) c.913G>A (p.Gly305Arg) c.746-1G>A (n.746-1G>A) c.1036G>A (p.Gly346Arg) | dbSNP ExAC gnomAD v2 gnomAD v4 |
4 | g.154569600G>C | CA358514907 | FGB | c.1045G>C (p.Gly349Arg) n.939+293G>C c.388G>C (p.Gly130Arg) c.868G>C (p.Gly290Arg) c.913G>C (p.Gly305Arg) c.746-1G>C (n.746-1G>C) c.1036G>C (p.Gly346Arg) | |
4 | g.154569600G= | CA1504935317 | FGB | c.1045G= (p.Gly349=) n.939+293G= c.388G= (p.Gly130=) c.868G= (p.Gly290=) c.913G= (p.Gly305=) c.746-1G= (n.746-1G=) c.1036G= (p.Gly346=) | |
4 | g.154569600G>T | CA358514905 | FGB | c.1045G>T (p.Gly349Ter) n.939+293G>T c.388G>T (p.Gly130Ter) c.868G>T (p.Gly290Ter) c.913G>T (p.Gly305Ter) c.746-1G>T (n.746-1G>T) c.1036G>T (p.Gly346Ter) | |
4 | g.154569601G>A | CA358514908 | FGB | c.1046G>A (p.Gly349Glu) n.939+294G>A c.389G>A (p.Gly130Glu) c.869G>A (p.Gly290Glu) c.914G>A (p.Gly305Glu) c.746G>A (p.Gly249Glu) c.1037G>A (p.Gly346Glu) | COSMIC |
4 | g.154569601G>C | CA3114707 | FGB | c.1046G>C (p.Gly349Ala) n.939+294G>C c.389G>C (p.Gly130Ala) c.869G>C (p.Gly290Ala) c.914G>C (p.Gly305Ala) c.746G>C (p.Gly249Ala) c.1037G>C (p.Gly346Ala) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.154569601G= | CA1504935319 | FGB | c.1046G= (p.Gly349=) n.939+294G= c.389G= (p.Gly130=) c.869G= (p.Gly290=) c.914G= (p.Gly305=) c.746G= (p.Gly249=) c.1037G= (p.Gly346=) | |
4 | g.154569601G>T | CA358514909 | FGB | c.1046G>T (p.Gly349Val) n.939+294G>T c.389G>T (p.Gly130Val) c.869G>T (p.Gly290Val) c.914G>T (p.Gly305Val) c.746G>T (p.Gly249Val) c.1037G>T (p.Gly346Val) | |
4 | g.154569602A>C | CA442013259 | FGB | c.1047A>C (p.Gly349=) n.939+295A>C c.390A>C (p.Gly130=) c.870A>C (p.Gly290=) c.915A>C (p.Gly305=) c.747A>C (p.Gly249=) c.1038A>C (p.Gly346=) | |
4 | g.154569602A>G | CA442013260 | FGB | c.1047A>G (p.Gly349=) n.939+295A>G c.390A>G (p.Gly130=) c.870A>G (p.Gly290=) c.915A>G (p.Gly305=) c.747A>G (p.Gly249=) c.1038A>G (p.Gly346=) | |
4 | g.154569602A>T | CA442013261 | FGB | c.1047A>T (p.Gly349=) n.939+295A>T c.390A>T (p.Gly130=) c.870A>T (p.Gly290=) c.915A>T (p.Gly305=) c.747A>T (p.Gly249=) c.1038A>T (p.Gly346=) | |
4 | g.154569602_154569603delinsAG | CA1504935320 | FGB | c.1047_1048delinsAG (p.Gly349=) n.939+295_939+296delinsAG c.390_391delinsAG (p.Gly130=) c.870_871delinsAG (p.Gly290=) c.915_916delinsAG (p.Gly305=) c.747_748delinsAG (p.Gly249=) c.1038_1039delinsAG (p.Gly346=) | |
4 | g.154569603del | CA555971632 | FGB | c.1048del (p.Asp350ThrfsTer3) n.939+296del c.391del (p.Asp131ThrfsTer3) c.871del (p.Asp291ThrfsTer3) c.916del (p.Asp306ThrfsTer3) c.748del (p.Asp250ThrfsTer3) c.1039del (p.Asp347ThrfsTer3) | dbSNP gnomAD v2 gnomAD v4 |
4 | g.154569603G>A | CA358514911 | FGB | c.1048G>A (p.Asp350Asn) n.939+296G>A c.391G>A (p.Asp131Asn) c.871G>A (p.Asp291Asn) c.916G>A (p.Asp306Asn) c.748G>A (p.Asp250Asn) c.1039G>A (p.Asp347Asn) | dbSNP gnomAD v4 |
4 | g.154569603G>C | CA358514912 | FGB | c.1048G>C (p.Asp350His) n.939+296G>C c.391G>C (p.Asp131His) c.871G>C (p.Asp291His) c.916G>C (p.Asp306His) c.748G>C (p.Asp250His) c.1039G>C (p.Asp347His) | |
4 | g.154569603G= | CA1504935322 | FGB | c.1048G= (p.Asp350=) n.939+296G= c.391G= (p.Asp131=) c.871G= (p.Asp291=) c.916G= (p.Asp306=) c.748G= (p.Asp250=) c.1039G= (p.Asp347=) | |
4 | g.154569603G>T | CA358514913 | FGB | c.1048G>T (p.Asp350Tyr) n.939+296G>T c.391G>T (p.Asp131Tyr) c.871G>T (p.Asp291Tyr) c.916G>T (p.Asp306Tyr) c.748G>T (p.Asp250Tyr) c.1039G>T (p.Asp347Tyr) | |
4 | g.154569604A>C | CA358514915 | FGB | c.1049A>C (p.Asp350Ala) n.939+297A>C c.392A>C (p.Asp131Ala) c.872A>C (p.Asp291Ala) c.917A>C (p.Asp306Ala) c.749A>C (p.Asp250Ala) c.1040A>C (p.Asp347Ala) | |
4 | g.154569604A>G | CA358514916 | FGB | c.1049A>G (p.Asp350Gly) n.939+297A>G c.392A>G (p.Asp131Gly) c.872A>G (p.Asp291Gly) c.917A>G (p.Asp306Gly) c.749A>G (p.Asp250Gly) c.1040A>G (p.Asp347Gly) | gnomAD v4 |
4 | g.154569604A>T | CA358514918 | FGB | c.1049A>T (p.Asp350Val) n.939+297A>T c.392A>T (p.Asp131Val) c.872A>T (p.Asp291Val) c.917A>T (p.Asp306Val) c.749A>T (p.Asp250Val) c.1040A>T (p.Asp347Val) | |
4 | g.154569605C>A | CA358514920 | FGB | c.1050C>A (p.Asp350Glu) n.939+298C>A c.393C>A (p.Asp131Glu) c.873C>A (p.Asp291Glu) c.918C>A (p.Asp306Glu) c.750C>A (p.Asp250Glu) c.1041C>A (p.Asp347Glu) | dbSNP |
4 | g.154569605C= | CA1504935324 | FGB | c.1050C= (p.Asp350=) n.939+298C= c.393C= (p.Asp131=) c.873C= (p.Asp291=) c.918C= (p.Asp306=) c.750C= (p.Asp250=) c.1041C= (p.Asp347=) | |
4 | g.154569605C>G | CA358514921 | FGB | c.1050C>G (p.Asp350Glu) n.939+298C>G c.393C>G (p.Asp131Glu) c.873C>G (p.Asp291Glu) c.918C>G (p.Asp306Glu) c.750C>G (p.Asp250Glu) c.1041C>G (p.Asp347Glu) | |
4 | g.154569605C>T | CA3114709 | FGB | c.1050C>T (p.Asp350=) n.939+298C>T c.393C>T (p.Asp131=) c.873C>T (p.Asp291=) c.918C>T (p.Asp306=) c.750C>T (p.Asp250=) c.1041C>T (p.Asp347=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.154569605_154569610delinsCAAAGT | CA1504935326 | FGB | c.1050_1055delinsCAAAGT (p.Asp350=) n.939+298_939+303delinsCAAAGT c.393_398delinsCAAAGT (p.Asp131=) c.873_878delinsCAAAGT (p.Asp291=) c.918_923delinsCAAAGT (p.Asp306=) c.750_755delinsCAAAGT (p.Asp250=) c.1041_1046delinsCAAAGT (p.Asp347=) | |
4 | g.154569606A>C | CA358514923 | FGB | c.1051A>C (p.Lys351Gln) n.939+299A>C c.394A>C (p.Lys132Gln) c.874A>C (p.Lys292Gln) c.919A>C (p.Lys307Gln) c.751A>C (p.Lys251Gln) c.1042A>C (p.Lys348Gln) | |
4 | g.154569606A>G | CA358514924 | FGB | c.1051A>G (p.Lys351Glu) n.939+299A>G c.394A>G (p.Lys132Glu) c.874A>G (p.Lys292Glu) c.919A>G (p.Lys307Glu) c.751A>G (p.Lys251Glu) c.1042A>G (p.Lys348Glu) | gnomAD v4 |
4 | g.154569606A>T | CA358514922 | FGB | c.1051A>T (p.Lys351Ter) n.939+299A>T c.394A>T (p.Lys132Ter) c.874A>T (p.Lys292Ter) c.919A>T (p.Lys307Ter) c.751A>T (p.Lys251Ter) c.1042A>T (p.Lys348Ter) | |
4 | g.154569610_154569614del | CA3114708 | FGB | c.1055_1059del (p.Val352GlyfsTer11) n.939+303_939+307del c.398_402del (p.Val133GlyfsTer11) c.878_882del (p.Val293GlyfsTer11) c.923_927del (p.Val308GlyfsTer11) c.755_759del (p.Val252GlyfsTer11) c.1046_1050del (p.Val349GlyfsTer11) c.1055_1059del (p.Val352GlyfsTer18) | dbSNP ExAC gnomAD v2 |
4 | g.154569607A>C | CA358514926 | FGB | c.1052A>C (p.Lys351Thr) n.939+300A>C c.395A>C (p.Lys132Thr) c.875A>C (p.Lys292Thr) c.920A>C (p.Lys307Thr) c.752A>C (p.Lys251Thr) c.1043A>C (p.Lys348Thr) | |
4 | g.154569607A>G | CA358514928 | FGB | c.1052A>G (p.Lys351Arg) n.939+300A>G c.395A>G (p.Lys132Arg) c.875A>G (p.Lys292Arg) c.920A>G (p.Lys307Arg) c.752A>G (p.Lys251Arg) c.1043A>G (p.Lys348Arg) | |
4 | g.154569607A>T | CA358514930 | FGB | c.1052A>T (p.Lys351Ile) n.939+300A>T c.395A>T (p.Lys132Ile) c.875A>T (p.Lys292Ile) c.920A>T (p.Lys307Ile) c.752A>T (p.Lys251Ile) c.1043A>T (p.Lys348Ile) | |
4 | g.154569608A= | CA1504935329 | FGB | c.1053A= (p.Lys351=) n.939+301A= c.396A= (p.Lys132=) c.876A= (p.Lys292=) c.921A= (p.Lys307=) c.753A= (p.Lys251=) c.1044A= (p.Lys348=) | |
4 | g.154569608A>C | CA358514931 | FGB | c.1053A>C (p.Lys351Asn) n.939+301A>C c.396A>C (p.Lys132Asn) c.876A>C (p.Lys292Asn) c.921A>C (p.Lys307Asn) c.753A>C (p.Lys251Asn) c.1044A>C (p.Lys348Asn) | gnomAD v4 |
4 | g.154569608A>G | CA442013285 | FGB | c.1053A>G (p.Lys351=) n.939+301A>G c.396A>G (p.Lys132=) c.876A>G (p.Lys292=) c.921A>G (p.Lys307=) c.753A>G (p.Lys251=) c.1044A>G (p.Lys348=) | dbSNP |
4 | g.154569608A>T | CA358514932 | FGB | c.1053A>T (p.Lys351Asn) n.939+301A>T c.396A>T (p.Lys132Asn) c.876A>T (p.Lys292Asn) c.921A>T (p.Lys307Asn) c.753A>T (p.Lys251Asn) c.1044A>T (p.Lys348Asn) | |
4 | g.154569609G>A | CA358514935 | FGB | c.1054G>A (p.Val352Ile) n.939+302G>A c.397G>A (p.Val133Ile) c.877G>A (p.Val293Ile) c.922G>A (p.Val308Ile) c.754G>A (p.Val252Ile) c.1045G>A (p.Val349Ile) | |
4 | g.154569609G>C | CA358514937 | FGB | c.1054G>C (p.Val352Leu) n.939+302G>C c.397G>C (p.Val133Leu) c.877G>C (p.Val293Leu) c.922G>C (p.Val308Leu) c.754G>C (p.Val252Leu) c.1045G>C (p.Val349Leu) | |
4 | g.154569609G>T | CA358514938 | FGB | c.1054G>T (p.Val352Leu) n.939+302G>T c.397G>T (p.Val133Leu) c.877G>T (p.Val293Leu) c.922G>T (p.Val308Leu) c.754G>T (p.Val252Leu) c.1045G>T (p.Val349Leu) | |
4 | g.154569610T>A | CA358514940 | FGB | c.1055T>A (p.Val352Glu) n.939+303T>A c.398T>A (p.Val133Glu) c.878T>A (p.Val293Glu) c.923T>A (p.Val308Glu) c.755T>A (p.Val252Glu) c.1046T>A (p.Val349Glu) | |
4 | g.154569610T>C | CA358514942 | FGB | c.1055T>C (p.Val352Ala) n.939+303T>C c.398T>C (p.Val133Ala) c.878T>C (p.Val293Ala) c.923T>C (p.Val308Ala) c.755T>C (p.Val252Ala) c.1046T>C (p.Val349Ala) | |
4 | g.154569610T>G | CA358514943 | FGB | c.1055T>G (p.Val352Gly) n.939+303T>G c.398T>G (p.Val133Gly) c.878T>G (p.Val293Gly) c.923T>G (p.Val308Gly) c.755T>G (p.Val252Gly) c.1046T>G (p.Val349Gly) | |
4 | g.154569611A= | CA1504935331 | FGB | c.1056A= (p.Val352=) n.939+304A= c.399A= (p.Val133=) c.879A= (p.Val293=) c.924A= (p.Val308=) c.756A= (p.Val252=) c.1047A= (p.Val349=) | |
4 | g.154569611A>C | CA442013293 | FGB | c.1056A>C (p.Val352=) n.939+304A>C c.399A>C (p.Val133=) c.879A>C (p.Val293=) c.924A>C (p.Val308=) c.756A>C (p.Val252=) c.1047A>C (p.Val349=) | |
4 | g.154569611A>G | CA442013294 | FGB | c.1056A>G (p.Val352=) n.939+304A>G c.399A>G (p.Val133=) c.879A>G (p.Val293=) c.924A>G (p.Val308=) c.756A>G (p.Val252=) c.1047A>G (p.Val349=) | dbSNP |
4 | g.154569611A>T | CA442013295 | FGB | c.1056A>T (p.Val352=) n.939+304A>T c.399A>T (p.Val133=) c.879A>T (p.Val293=) c.924A>T (p.Val308=) c.756A>T (p.Val252=) c.1047A>T (p.Val349=) | |
4 | g.154569612A>C | CA358514947 | FGB | c.1057A>C (p.Lys353Gln) n.939+305A>C c.400A>C (p.Lys134Gln) c.880A>C (p.Lys294Gln) c.925A>C (p.Lys309Gln) c.757A>C (p.Lys253Gln) c.1048A>C (p.Lys350Gln) | |
4 | g.154569612A>G | CA358514948 | FGB | c.1057A>G (p.Lys353Glu) n.939+305A>G c.400A>G (p.Lys134Glu) c.880A>G (p.Lys294Glu) c.925A>G (p.Lys309Glu) c.757A>G (p.Lys253Glu) c.1048A>G (p.Lys350Glu) | |
4 | g.154569612A>T | CA358514945 | FGB | c.1057A>T (p.Lys353Ter) n.939+305A>T c.400A>T (p.Lys134Ter) c.880A>T (p.Lys294Ter) c.925A>T (p.Lys309Ter) c.757A>T (p.Lys253Ter) c.1048A>T (p.Lys350Ter) | |
4 | g.154569613A= | CA1504935334 | FGB | c.1058A= (p.Lys353=) n.939+306A= c.401A= (p.Lys134=) c.881A= (p.Lys294=) c.926A= (p.Lys309=) c.758A= (p.Lys253=) c.1049A= (p.Lys350=) | |
4 | g.154569613A>C | CA358514949 | FGB | c.1058A>C (p.Lys353Thr) n.939+306A>C c.401A>C (p.Lys134Thr) c.881A>C (p.Lys294Thr) c.926A>C (p.Lys309Thr) c.758A>C (p.Lys253Thr) c.1049A>C (p.Lys350Thr) | gnomAD v4 |
4 | g.154569613A>G | CA3114710 | FGB | c.1058A>G (p.Lys353Arg) n.939+306A>G c.401A>G (p.Lys134Arg) c.881A>G (p.Lys294Arg) c.926A>G (p.Lys309Arg) c.758A>G (p.Lys253Arg) c.1049A>G (p.Lys350Arg) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.154569613A>T | CA358514951 | FGB | c.1058A>T (p.Lys353Met) n.939+306A>T c.401A>T (p.Lys134Met) c.881A>T (p.Lys294Met) c.926A>T (p.Lys309Met) c.758A>T (p.Lys253Met) c.1049A>T (p.Lys350Met) | |
4 | g.154569614G>A | CA442013297 | FGB | c.1059G>A (p.Lys353=) n.939+307G>A c.402G>A (p.Lys134=) c.882G>A (p.Lys294=) c.927G>A (p.Lys309=) c.759G>A (p.Lys253=) c.1050G>A (p.Lys350=) | gnomAD v4 |
4 | g.154569614G>C | CA3114711 | FGB | c.1059G>C (p.Lys353Asn) n.939+307G>C c.402G>C (p.Lys134Asn) c.882G>C (p.Lys294Asn) c.927G>C (p.Lys309Asn) c.759G>C (p.Lys253Asn) c.1050G>C (p.Lys350Asn) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.154569614G= | CA1504935336 | FGB | c.1059G= (p.Lys353=) n.939+307G= c.402G= (p.Lys134=) c.882G= (p.Lys294=) c.927G= (p.Lys309=) c.759G= (p.Lys253=) c.1050G= (p.Lys350=) | |
4 | g.154569614G>T | CA358514953 | FGB | c.1059G>T (p.Lys353Asn) n.939+307G>T c.402G>T (p.Lys134Asn) c.882G>T (p.Lys294Asn) c.927G>T (p.Lys309Asn) c.759G>T (p.Lys253Asn) c.1050G>T (p.Lys350Asn) | |
4 | g.154569615G>A | CA358514957 | FGB | c.1060G>A (p.Ala354Thr) n.939+308G>A c.403G>A (p.Ala135Thr) c.883G>A (p.Ala295Thr) c.928G>A (p.Ala310Thr) c.760G>A (p.Ala254Thr) c.1051G>A (p.Ala351Thr) | dbSNP gnomAD v3 gnomAD v4 |
4 | g.154569615G>C | CA358514954 | FGB | c.1060G>C (p.Ala354Pro) n.939+308G>C c.403G>C (p.Ala135Pro) c.883G>C (p.Ala295Pro) c.928G>C (p.Ala310Pro) c.760G>C (p.Ala254Pro) c.1051G>C (p.Ala351Pro) | gnomAD v4 |
4 | g.154569615G>T | CA358514955 | FGB | c.1060G>T (p.Ala354Ser) n.939+308G>T c.403G>T (p.Ala135Ser) c.883G>T (p.Ala295Ser) c.928G>T (p.Ala310Ser) c.760G>T (p.Ala254Ser) c.1051G>T (p.Ala351Ser) | |
4 | g.154569616C>A | CA358514959 | FGB | c.1061C>A (p.Ala354Asp) n.939+309C>A c.404C>A (p.Ala135Asp) c.884C>A (p.Ala295Asp) c.929C>A (p.Ala310Asp) c.761C>A (p.Ala254Asp) c.1052C>A (p.Ala351Asp) | |
4 | g.154569616C>G | CA358514960 | FGB | c.1061C>G (p.Ala354Gly) n.939+309C>G c.404C>G (p.Ala135Gly) c.884C>G (p.Ala295Gly) c.929C>G (p.Ala310Gly) c.761C>G (p.Ala254Gly) c.1052C>G (p.Ala351Gly) | |
4 | g.154569616C>T | CA358514962 | FGB | c.1061C>T (p.Ala354Val) n.939+309C>T c.404C>T (p.Ala135Val) c.884C>T (p.Ala295Val) c.929C>T (p.Ala310Val) c.761C>T (p.Ala254Val) c.1052C>T (p.Ala351Val) | gnomAD v4 |
4 | g.154569617T>A | CA442013307 | FGB | c.1062T>A (p.Ala354=) n.939+310T>A c.405T>A (p.Ala135=) c.885T>A (p.Ala295=) c.930T>A (p.Ala310=) c.762T>A (p.Ala254=) c.1053T>A (p.Ala351=) | dbSNP |
4 | g.154569617T>C | CA442013309 | FGB | c.1062T>C (p.Ala354=) n.939+310T>C c.405T>C (p.Ala135=) c.885T>C (p.Ala295=) c.930T>C (p.Ala310=) c.762T>C (p.Ala254=) c.1053T>C (p.Ala351=) | |
4 | g.154569617T>G | CA442013306 | FGB | c.1062T>G (p.Ala354=) n.939+310T>G c.405T>G (p.Ala135=) c.885T>G (p.Ala295=) c.930T>G (p.Ala310=) c.762T>G (p.Ala254=) c.1053T>G (p.Ala351=) | |
4 | g.154569617T= | CA1504935338 | FGB | c.1062T= (p.Ala354=) n.939+310T= c.405T= (p.Ala135=) c.885T= (p.Ala295=) c.930T= (p.Ala310=) c.762T= (p.Ala254=) c.1053T= (p.Ala351=) | |
4 | g.154569618C>A | CA358514964 | FGB | c.1063C>A (p.His355Asn) n.939+311C>A c.406C>A (p.His136Asn) c.886C>A (p.His296Asn) c.931C>A (p.His311Asn) c.763C>A (p.His255Asn) c.1054C>A (p.His352Asn) | |
4 | g.154569618C>G | CA358514966 | FGB | c.1063C>G (p.His355Asp) n.939+311C>G c.406C>G (p.His136Asp) c.886C>G (p.His296Asp) c.931C>G (p.His311Asp) c.763C>G (p.His255Asp) c.1054C>G (p.His352Asp) | |
4 | g.154569618C>T | CA358514967 | FGB | c.1063C>T (p.His355Tyr) n.939+311C>T c.406C>T (p.His136Tyr) c.886C>T (p.His296Tyr) c.931C>T (p.His311Tyr) c.763C>T (p.His255Tyr) c.1054C>T (p.His352Tyr) | |
4 | g.154569619A>C | CA358514973 | FGB | c.1064A>C (p.His355Pro) n.939+312A>C c.407A>C (p.His136Pro) c.887A>C (p.His296Pro) c.932A>C (p.His311Pro) c.764A>C (p.His255Pro) c.1055A>C (p.His352Pro) | gnomAD v4 |
4 | g.154569619A>G | CA358514971 | FGB | c.1064A>G (p.His355Arg) n.939+312A>G c.407A>G (p.His136Arg) c.887A>G (p.His296Arg) c.932A>G (p.His311Arg) c.764A>G (p.His255Arg) c.1055A>G (p.His352Arg) | |
4 | g.154569619A>T | CA358514969 | FGB | c.1064A>T (p.His355Leu) n.939+312A>T c.407A>T (p.His136Leu) c.887A>T (p.His296Leu) c.932A>T (p.His311Leu) c.764A>T (p.His255Leu) c.1055A>T (p.His352Leu) | |
4 | g.154569620C>A | CA358514976 | FGB | c.1065C>A (p.His355Gln) n.939+313C>A c.408C>A (p.His136Gln) c.888C>A (p.His296Gln) c.933C>A (p.His311Gln) c.765C>A (p.His255Gln) c.1056C>A (p.His352Gln) | |
4 | g.154569620C= | CA1504935340 | FGB | c.1065C= (p.His355=) n.939+313C= c.408C= (p.His136=) c.888C= (p.His296=) c.933C= (p.His311=) c.765C= (p.His255=) c.1056C= (p.His352=) | |
4 | g.154569620C>G | CA358514975 | FGB | c.1065C>G (p.His355Gln) n.939+313C>G c.408C>G (p.His136Gln) c.888C>G (p.His296Gln) c.933C>G (p.His311Gln) c.765C>G (p.His255Gln) c.1056C>G (p.His352Gln) | gnomAD v4 |
4 | g.154569620C>T | CA442013314 | FGB | c.1065C>T (p.His355=) n.939+313C>T c.408C>T (p.His136=) c.888C>T (p.His296=) c.933C>T (p.His311=) c.765C>T (p.His255=) c.1056C>T (p.His352=) | dbSNP gnomAD v4 |
4 | g.154569620_154569621insCAAAAA | CA3114713 | FGB | c.1065_1066insCAAAAA (p.His355_Tyr356insGlnLys) n.939+313_939+314insCAAAAA c.408_409insCAAAAA (p.His136_Tyr137insGlnLys) c.888_889insCAAAAA (p.His296_Tyr297insGlnLys) c.933_934insCAAAAA (p.His311_Tyr312insGlnLys) c.765_766insCAAAAA (p.His255_Tyr256insGlnLys) c.1056_1057insCAAAAA (p.His352_Tyr353insGlnLys) | dbSNP ExAC gnomAD v2 |
4 | g.154569620_154569621insCAAAAATAAAATTT | CA3114712 | FGB | c.1065_1066insCAAAAATAAAATTT (p.Tyr356GlnfsTer3) n.939+313_939+314insCAAAAATAAAATTT c.408_409insCAAAAATAAAATTT (p.Tyr137GlnfsTer3) c.888_889insCAAAAATAAAATTT (p.Tyr297GlnfsTer3) c.933_934insCAAAAATAAAATTT (p.Tyr312GlnfsTer3) c.765_766insCAAAAATAAAATTT (p.Tyr256GlnfsTer3) c.1056_1057insCAAAAATAAAATTT (p.Tyr353GlnfsTer3) | dbSNP ExAC |
4 | g.154569621T>A | CA358514978 | FGB | c.1066T>A (p.Tyr356Asn) n.939+314T>A c.409T>A (p.Tyr137Asn) c.889T>A (p.Tyr297Asn) c.934T>A (p.Tyr312Asn) c.766T>A (p.Tyr256Asn) c.1057T>A (p.Tyr353Asn) | |
4 | g.154569621T>C | CA358514980 | FGB | c.1066T>C (p.Tyr356His) n.939+314T>C c.409T>C (p.Tyr137His) c.889T>C (p.Tyr297His) c.934T>C (p.Tyr312His) c.766T>C (p.Tyr256His) c.1057T>C (p.Tyr353His) | |
4 | g.154569621T>G | CA358514982 | FGB | c.1066T>G (p.Tyr356Asp) n.939+314T>G c.409T>G (p.Tyr137Asp) c.889T>G (p.Tyr297Asp) c.934T>G (p.Tyr312Asp) c.766T>G (p.Tyr256Asp) c.1057T>G (p.Tyr353Asp) | |
4 | g.154569622A= | CA1504935344 | FGB | c.1067A= (p.Tyr356=) n.939+315A= c.410A= (p.Tyr137=) c.890A= (p.Tyr297=) c.935A= (p.Tyr312=) c.767A= (p.Tyr256=) c.1058A= (p.Tyr353=) | |
4 | g.154569622A>C | CA358514985 | FGB | c.1067A>C (p.Tyr356Ser) n.939+315A>C c.410A>C (p.Tyr137Ser) c.890A>C (p.Tyr297Ser) c.935A>C (p.Tyr312Ser) c.767A>C (p.Tyr256Ser) c.1058A>C (p.Tyr353Ser) | |
4 | g.154569622A>G | CA358514987 | FGB | c.1067A>G (p.Tyr356Cys) n.939+315A>G c.410A>G (p.Tyr137Cys) c.890A>G (p.Tyr297Cys) c.935A>G (p.Tyr312Cys) c.767A>G (p.Tyr256Cys) c.1058A>G (p.Tyr353Cys) | gnomAD v4 |
4 | g.154569622A>T | CA358514989 | FGB | c.1067A>T (p.Tyr356Phe) n.939+315A>T c.410A>T (p.Tyr137Phe) c.890A>T (p.Tyr297Phe) c.935A>T (p.Tyr312Phe) c.767A>T (p.Tyr256Phe) c.1058A>T (p.Tyr353Phe) | |
4 | g.154569622_154569623insAAATTT | CA3114714 | FGB | c.1067_1068insAAATTT (p.Tyr356Ter) n.939+315_939+316insAAATTT c.410_411insAAATTT (p.Tyr137Ter) c.890_891insAAATTT (p.Tyr297Ter) c.935_936insAAATTT (p.Tyr312Ter) c.767_768insAAATTT (p.Tyr256Ter) c.1058_1059insAAATTT (p.Tyr353Ter) | dbSNP ExAC gnomAD v2 |
4 | g.154569623T>A | CA358514990 | FGB | c.1068T>A (p.Tyr356Ter) n.939+316T>A c.411T>A (p.Tyr137Ter) c.891T>A (p.Tyr297Ter) c.936T>A (p.Tyr312Ter) c.768T>A (p.Tyr256Ter) c.1059T>A (p.Tyr353Ter) | |
4 | g.154569623T>C | CA442013320 | FGB | c.1068T>C (p.Tyr356=) n.939+316T>C c.411T>C (p.Tyr137=) c.891T>C (p.Tyr297=) c.936T>C (p.Tyr312=) c.768T>C (p.Tyr256=) c.1059T>C (p.Tyr353=) | dbSNP gnomAD v2 gnomAD v4 |
4 | g.154569623T>G | CA358514992 | FGB | c.1068T>G (p.Tyr356Ter) n.939+316T>G c.411T>G (p.Tyr137Ter) c.891T>G (p.Tyr297Ter) c.936T>G (p.Tyr312Ter) c.768T>G (p.Tyr256Ter) c.1059T>G (p.Tyr353Ter) | |
4 | g.154569623T= | CA1504935348 | FGB | c.1068T= (p.Tyr356=) n.939+316T= c.411T= (p.Tyr137=) c.891T= (p.Tyr297=) c.936T= (p.Tyr312=) c.768T= (p.Tyr256=) c.1059T= (p.Tyr353=) | |
4 | g.154569624G>A | CA3114715 | FGB | c.1069G>A (p.Gly357Arg) n.939+317G>A c.412G>A (p.Gly138Arg) c.892G>A (p.Gly298Arg) c.937G>A (p.Gly313Arg) c.769G>A (p.Gly257Arg) c.1060G>A (p.Gly354Arg) | dbSNP ExAC gnomAD v2 gnomAD v4 |
4 | g.154569624G>C | CA358514994 | FGB | c.1069G>C (p.Gly357Arg) n.939+317G>C c.412G>C (p.Gly138Arg) c.892G>C (p.Gly298Arg) c.937G>C (p.Gly313Arg) c.769G>C (p.Gly257Arg) c.1060G>C (p.Gly354Arg) | |
4 | g.154569624G= | CA1504935352 | FGB | c.1069G= (p.Gly357=) n.939+317G= c.412G= (p.Gly138=) c.892G= (p.Gly298=) c.937G= (p.Gly313=) c.769G= (p.Gly257=) c.1060G= (p.Gly354=) | |
4 | g.154569624G>T | CA358514996 | FGB | c.1069G>T (p.Gly357Ter) n.939+317G>T c.412G>T (p.Gly138Ter) c.892G>T (p.Gly298Ter) c.937G>T (p.Gly313Ter) c.769G>T (p.Gly257Ter) c.1060G>T (p.Gly354Ter) | |
4 | g.154569625G>A | CA358515000 | FGB | c.1070G>A (p.Gly357Glu) n.939+318G>A c.413G>A (p.Gly138Glu) c.893G>A (p.Gly298Glu) c.938G>A (p.Gly313Glu) c.770G>A (p.Gly257Glu) c.1061G>A (p.Gly354Glu) | |
4 | g.154569625G>C | CA358514998 | FGB | c.1070G>C (p.Gly357Ala) n.939+318G>C c.413G>C (p.Gly138Ala) c.893G>C (p.Gly298Ala) c.938G>C (p.Gly313Ala) c.770G>C (p.Gly257Ala) c.1061G>C (p.Gly354Ala) | |
4 | g.154569625G>T | CA358514999 | FGB | c.1070G>T (p.Gly357Val) n.939+318G>T c.413G>T (p.Gly138Val) c.893G>T (p.Gly298Val) c.938G>T (p.Gly313Val) c.770G>T (p.Gly257Val) c.1061G>T (p.Gly354Val) | |
4 | g.154569626A>C | CA442013328 | FGB | c.1071A>C (p.Gly357=) n.939+319A>C c.414A>C (p.Gly138=) c.894A>C (p.Gly298=) c.939A>C (p.Gly313=) c.771A>C (p.Gly257=) c.1062A>C (p.Gly354=) | |
4 | g.154569626A>G | CA442013329 | FGB | c.1071A>G (p.Gly357=) n.939+319A>G c.414A>G (p.Gly138=) c.894A>G (p.Gly298=) c.939A>G (p.Gly313=) c.771A>G (p.Gly257=) c.1062A>G (p.Gly354=) | |
4 | g.154569626A>T | CA442013327 | FGB | c.1071A>T (p.Gly357=) n.939+319A>T c.414A>T (p.Gly138=) c.894A>T (p.Gly298=) c.939A>T (p.Gly313=) c.771A>T (p.Gly257=) c.1062A>T (p.Gly354=) | |
4 | g.154569627G>A | CA3114716 | FGB | c.1072G>A (p.Gly358Arg) n.939+320G>A c.415G>A (p.Gly139Arg) c.895G>A (p.Gly299Arg) c.940G>A (p.Gly314Arg) c.772G>A (p.Gly258Arg) c.1063G>A (p.Gly355Arg) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.154569627G>C | CA358515002 | FGB | c.1072G>C (p.Gly358Arg) n.939+320G>C c.415G>C (p.Gly139Arg) c.895G>C (p.Gly299Arg) c.940G>C (p.Gly314Arg) c.772G>C (p.Gly258Arg) c.1063G>C (p.Gly355Arg) | |
4 | g.154569627G= | CA1504935356 | FGB | c.1072G= (p.Gly358=) n.939+320G= c.415G= (p.Gly139=) c.895G= (p.Gly299=) c.940G= (p.Gly314=) c.772G= (p.Gly258=) c.1063G= (p.Gly355=) | |
4 | g.154569627G>T | CA358515004 | FGB | c.1072G>T (p.Gly358Ter) n.939+320G>T c.415G>T (p.Gly139Ter) c.895G>T (p.Gly299Ter) c.940G>T (p.Gly314Ter) c.772G>T (p.Gly258Ter) c.1063G>T (p.Gly355Ter) | |
4 | g.154569628G>A | CA358515006 | FGB | c.1073G>A (p.Gly358Glu) n.939+321G>A c.416G>A (p.Gly139Glu) c.896G>A (p.Gly299Glu) c.941G>A (p.Gly314Glu) c.773G>A (p.Gly258Glu) c.1064G>A (p.Gly355Glu) | gnomAD v4 |
4 | g.154569628G>C | CA358515007 | FGB | c.1073G>C (p.Gly358Ala) n.939+321G>C c.416G>C (p.Gly139Ala) c.896G>C (p.Gly299Ala) c.941G>C (p.Gly314Ala) c.773G>C (p.Gly258Ala) c.1064G>C (p.Gly355Ala) | |
4 | g.154569628G>T | CA358515009 | FGB | c.1073G>T (p.Gly358Val) n.939+321G>T c.416G>T (p.Gly139Val) c.896G>T (p.Gly299Val) c.941G>T (p.Gly314Val) c.773G>T (p.Gly258Val) c.1064G>T (p.Gly355Val) | |
4 | g.154569629A= | CA1504935361 | FGB | c.1074A= (p.Gly358=) n.939+322A= c.417A= (p.Gly139=) c.897A= (p.Gly299=) c.942A= (p.Gly314=) c.774A= (p.Gly258=) c.1065A= (p.Gly355=) | |
4 | g.154569629A>C | CA442013336 | FGB | c.1074A>C (p.Gly358=) n.939+322A>C c.417A>C (p.Gly139=) c.897A>C (p.Gly299=) c.942A>C (p.Gly314=) c.774A>C (p.Gly258=) c.1065A>C (p.Gly355=) | dbSNP |
4 | g.154569629A>G | CA442013338 | FGB | c.1074A>G (p.Gly358=) n.939+322A>G c.417A>G (p.Gly139=) c.897A>G (p.Gly299=) c.942A>G (p.Gly314=) c.774A>G (p.Gly258=) c.1065A>G (p.Gly355=) | |
4 | g.154569629A>T | CA442013341 | FGB | c.1074A>T (p.Gly358=) n.939+322A>T c.417A>T (p.Gly139=) c.897A>T (p.Gly299=) c.942A>T (p.Gly314=) c.774A>T (p.Gly258=) c.1065A>T (p.Gly355=) | |
4 | g.154569630T>A | CA358515011 | FGB | c.1075T>A (p.Phe359Ile) n.939+323T>A c.418T>A (p.Phe140Ile) c.898T>A (p.Phe300Ile) c.943T>A (p.Phe315Ile) c.775T>A (p.Phe259Ile) c.1066T>A (p.Phe356Ile) | |
4 | g.154569630T>C | CA358515013 | FGB | c.1075T>C (p.Phe359Leu) n.939+323T>C c.418T>C (p.Phe140Leu) c.898T>C (p.Phe300Leu) c.943T>C (p.Phe315Leu) c.775T>C (p.Phe259Leu) c.1066T>C (p.Phe356Leu) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.154569630T>G | CA358515014 | FGB | c.1075T>G (p.Phe359Val) n.939+323T>G c.418T>G (p.Phe140Val) c.898T>G (p.Phe300Val) c.943T>G (p.Phe315Val) c.775T>G (p.Phe259Val) c.1066T>G (p.Phe356Val) | |
4 | g.154569630T= | CA1504935364 | FGB | c.1075T= (p.Phe359=) n.939+323T= c.418T= (p.Phe140=) c.898T= (p.Phe300=) c.943T= (p.Phe315=) c.775T= (p.Phe259=) c.1066T= (p.Phe356=) | |
4 | g.154569631T>A | CA358515015 | FGB | c.1076T>A (p.Phe359Tyr) n.939+324T>A c.419T>A (p.Phe140Tyr) c.899T>A (p.Phe300Tyr) c.944T>A (p.Phe315Tyr) c.776T>A (p.Phe259Tyr) c.1067T>A (p.Phe356Tyr) | |
4 | g.154569631T>C | CA358515017 | FGB | c.1076T>C (p.Phe359Ser) n.939+324T>C c.419T>C (p.Phe140Ser) c.899T>C (p.Phe300Ser) c.944T>C (p.Phe315Ser) c.776T>C (p.Phe259Ser) c.1067T>C (p.Phe356Ser) | |
4 | g.154569631T>G | CA358515020 | FGB | c.1076T>G (p.Phe359Cys) n.939+324T>G c.419T>G (p.Phe140Cys) c.899T>G (p.Phe300Cys) c.944T>G (p.Phe315Cys) c.776T>G (p.Phe259Cys) c.1067T>G (p.Phe356Cys) | |
4 | g.154569632C>A | CA358515022 | FGB | c.1077C>A (p.Phe359Leu) n.939+325C>A c.420C>A (p.Phe140Leu) c.900C>A (p.Phe300Leu) c.945C>A (p.Phe315Leu) c.777C>A (p.Phe259Leu) c.1068C>A (p.Phe356Leu) | |
4 | g.154569632C>G | CA358515024 | FGB | c.1077C>G (p.Phe359Leu) n.939+325C>G c.420C>G (p.Phe140Leu) c.900C>G (p.Phe300Leu) c.945C>G (p.Phe315Leu) c.777C>G (p.Phe259Leu) c.1068C>G (p.Phe356Leu) | |
4 | g.154569632C>T | CA442013348 | FGB | c.1077C>T (p.Phe359=) n.939+325C>T c.420C>T (p.Phe140=) c.900C>T (p.Phe300=) c.945C>T (p.Phe315=) c.777C>T (p.Phe259=) c.1068C>T (p.Phe356=) | |
4 | g.154569633A= | CA1504935368 | FGB | c.1078A= (p.Thr360=) n.939+326A= c.421A= (p.Thr141=) c.901A= (p.Thr301=) c.946A= (p.Thr316=) c.778A= (p.Thr260=) c.1069A= (p.Thr357=) | |
4 | g.154569633A>C | CA358515029 | FGB | c.1078A>C (p.Thr360Pro) n.939+326A>C c.421A>C (p.Thr141Pro) c.901A>C (p.Thr301Pro) c.946A>C (p.Thr316Pro) c.778A>C (p.Thr260Pro) c.1069A>C (p.Thr357Pro) | |
4 | g.154569633A>G | CA358515031 | FGB | c.1078A>G (p.Thr360Ala) n.939+326A>G c.421A>G (p.Thr141Ala) c.901A>G (p.Thr301Ala) c.946A>G (p.Thr316Ala) c.778A>G (p.Thr260Ala) c.1069A>G (p.Thr357Ala) | dbSNP gnomAD v2 gnomAD v4 |
4 | g.154569633A>T | CA358515032 | FGB | c.1078A>T (p.Thr360Ser) n.939+326A>T c.421A>T (p.Thr141Ser) c.901A>T (p.Thr301Ser) c.946A>T (p.Thr316Ser) c.778A>T (p.Thr260Ser) c.1069A>T (p.Thr357Ser) | |
4 | g.154569634C>A | CA358515034 | FGB | c.1079C>A (p.Thr360Asn) n.939+327C>A c.422C>A (p.Thr141Asn) c.902C>A (p.Thr301Asn) c.947C>A (p.Thr316Asn) c.779C>A (p.Thr260Asn) c.1070C>A (p.Thr357Asn) | |
4 | g.154569634C= | CA1504935371 | FGB | c.1079C= (p.Thr360=) n.939+327C= c.422C= (p.Thr141=) c.902C= (p.Thr301=) c.947C= (p.Thr316=) c.779C= (p.Thr260=) c.1070C= (p.Thr357=) | |
4 | g.154569634C>G | CA358515036 | FGB | c.1079C>G (p.Thr360Ser) n.939+327C>G c.422C>G (p.Thr141Ser) c.902C>G (p.Thr301Ser) c.947C>G (p.Thr316Ser) c.779C>G (p.Thr260Ser) c.1070C>G (p.Thr357Ser) | |
4 | g.154569634C>T | CA3114717 | FGB | c.1079C>T (p.Thr360Ile) n.939+327C>T c.422C>T (p.Thr141Ile) c.902C>T (p.Thr301Ile) c.947C>T (p.Thr316Ile) c.779C>T (p.Thr260Ile) c.1070C>T (p.Thr357Ile) | dbSNP ExAC gnomAD v2 gnomAD v4 |
4 | g.154569635T>A | CA442013353 | FGB | c.1080T>A (p.Thr360=) n.939+328T>A c.423T>A (p.Thr141=) c.903T>A (p.Thr301=) c.948T>A (p.Thr316=) c.780T>A (p.Thr260=) c.1071T>A (p.Thr357=) | |
4 | g.154569635T>C | CA442013354 | FGB | c.1080T>C (p.Thr360=) n.939+328T>C c.423T>C (p.Thr141=) c.903T>C (p.Thr301=) c.948T>C (p.Thr316=) c.780T>C (p.Thr260=) c.1071T>C (p.Thr357=) | gnomAD v4 |
4 | g.154569635T>G | CA442013355 | FGB | c.1080T>G (p.Thr360=) n.939+328T>G c.423T>G (p.Thr141=) c.903T>G (p.Thr301=) c.948T>G (p.Thr316=) c.780T>G (p.Thr260=) c.1071T>G (p.Thr357=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.154569635T= | CA1504935375 | FGB | c.1080T= (p.Thr360=) n.939+328T= c.423T= (p.Thr141=) c.903T= (p.Thr301=) c.948T= (p.Thr316=) c.780T= (p.Thr260=) c.1071T= (p.Thr357=) | |
4 | g.154569636G>A | CA358515038 | FGB | c.1081G>A (p.Val361Ile) n.939+329G>A c.424G>A (p.Val142Ile) c.904G>A (p.Val302Ile) c.949G>A (p.Val317Ile) c.781G>A (p.Val261Ile) c.1072G>A (p.Val358Ile) c.1080+1G>A (n.1080+1G>A) | dbSNP gnomAD v4 |
4 | g.154569636G>C | CA358515040 | FGB | c.1081G>C (p.Val361Leu) n.939+329G>C c.424G>C (p.Val142Leu) c.904G>C (p.Val302Leu) c.949G>C (p.Val317Leu) c.781G>C (p.Val261Leu) c.1072G>C (p.Val358Leu) c.1080+1G>C (n.1080+1G>C) | |
4 | g.154569636G= | CA1504935378 | FGB | c.1081G= (p.Val361=) n.939+329G= c.424G= (p.Val142=) c.904G= (p.Val302=) c.949G= (p.Val317=) c.781G= (p.Val261=) c.1072G= (p.Val358=) c.1080+1G= (n.1080+1G=) | |
4 | g.154569636G>T | CA3114718 | FGB | c.1081G>T (p.Val361Leu) n.939+329G>T c.424G>T (p.Val142Leu) c.904G>T (p.Val302Leu) c.949G>T (p.Val317Leu) c.781G>T (p.Val261Leu) c.1072G>T (p.Val358Leu) c.1080+1G>T (n.1080+1G>T) | dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
4 | g.154569637T>A | CA358515042 | FGB | c.1082T>A (p.Val361Glu) n.939+330T>A c.425T>A (p.Val142Glu) c.905T>A (p.Val302Glu) c.950T>A (p.Val317Glu) c.782T>A (p.Val261Glu) c.1073T>A (p.Val358Glu) c.1080+2T>A (n.1080+2T>A) | |
4 | g.154569637T>C | CA358515043 | FGB | c.1082T>C (p.Val361Ala) n.939+330T>C c.425T>C (p.Val142Ala) c.905T>C (p.Val302Ala) c.950T>C (p.Val317Ala) c.782T>C (p.Val261Ala) c.1073T>C (p.Val358Ala) c.1080+2T>C (n.1080+2T>C) | |
4 | g.154569637T>G | CA358515045 | FGB | c.1082T>G (p.Val361Gly) n.939+330T>G c.425T>G (p.Val142Gly) c.905T>G (p.Val302Gly) c.950T>G (p.Val317Gly) c.782T>G (p.Val261Gly) c.1073T>G (p.Val358Gly) c.1080+2T>G (n.1080+2T>G) | |
4 | g.154569638A= | CA1504935381 | FGB | c.1083A= (p.Val361=) n.939+331A= c.426A= (p.Val142=) c.906A= (p.Val302=) c.951A= (p.Val317=) c.783A= (p.Val261=) c.1074A= (p.Val358=) c.1080+3A= (n.1080+3A=) | |
4 | g.154569638A>C | CA442013362 | FGB | c.1083A>C (p.Val361=) n.939+331A>C c.426A>C (p.Val142=) c.906A>C (p.Val302=) c.951A>C (p.Val317=) c.783A>C (p.Val261=) c.1074A>C (p.Val358=) c.1080+3A>C (n.1080+3A>C) | |
4 | g.154569638A>G | CA442013360 | FGB | c.1083A>G (p.Val361=) n.939+331A>G c.426A>G (p.Val142=) c.906A>G (p.Val302=) c.951A>G (p.Val317=) c.783A>G (p.Val261=) c.1074A>G (p.Val358=) c.1080+3A>G (n.1080+3A>G) | dbSNP gnomAD v2 gnomAD v4 |
4 | g.154569638A>T | CA442013361 | FGB | c.1083A>T (p.Val361=) n.939+331A>T c.426A>T (p.Val142=) c.906A>T (p.Val302=) c.951A>T (p.Val317=) c.783A>T (p.Val261=) c.1074A>T (p.Val358=) c.1080+3A>T (n.1080+3A>T) | |
4 | g.154569639C>A | CA358515049 | FGB | c.1084C>A (p.Gln362Lys) n.939+332C>A c.427C>A (p.Gln143Lys) c.907C>A (p.Gln303Lys) c.952C>A (p.Gln318Lys) c.784C>A (p.Gln262Lys) c.1075C>A (p.Gln359Lys) c.1080+4C>A (n.1080+4C>A) | |
4 | g.154569639C= | CA1504935386 | FGB | c.1084C= (p.Gln362=) n.939+332C= c.427C= (p.Gln143=) c.907C= (p.Gln303=) c.952C= (p.Gln318=) c.784C= (p.Gln262=) c.1075C= (p.Gln359=) c.1080+4C= (n.1080+4C=) | |
4 | g.154569639C>G | CA358515048 | FGB | c.1084C>G (p.Gln362Glu) n.939+332C>G c.427C>G (p.Gln143Glu) c.907C>G (p.Gln303Glu) c.952C>G (p.Gln318Glu) c.784C>G (p.Gln262Glu) c.1075C>G (p.Gln359Glu) c.1080+4C>G (n.1080+4C>G) | |
4 | g.154569639C>T | CA108751650 | FGB | c.1084C>T (p.Gln362Ter) n.939+332C>T c.427C>T (p.Gln143Ter) c.907C>T (p.Gln303Ter) c.952C>T (p.Gln318Ter) c.784C>T (p.Gln262Ter) c.1075C>T (p.Gln359Ter) c.1080+4C>T (n.1080+4C>T) | dbSNP |
4 | g.154569640A= | CA1504935389 | FGB | c.1085A= (p.Gln362=) n.939+333A= c.428A= (p.Gln143=) c.908A= (p.Gln303=) c.953A= (p.Gln318=) c.785A= (p.Gln262=) c.1076A= (p.Gln359=) c.1080+5A= (n.1080+5A=) | |
4 | g.154569640A>C | CA358515051 | FGB | c.1085A>C (p.Gln362Pro) n.939+333A>C c.428A>C (p.Gln143Pro) c.908A>C (p.Gln303Pro) c.953A>C (p.Gln318Pro) c.785A>C (p.Gln262Pro) c.1076A>C (p.Gln359Pro) c.1080+5A>C (n.1080+5A>C) | |
4 | g.154569640A>G | CA358515053 | FGB | c.1085A>G (p.Gln362Arg) n.939+333A>G c.428A>G (p.Gln143Arg) c.908A>G (p.Gln303Arg) c.953A>G (p.Gln318Arg) c.785A>G (p.Gln262Arg) c.1076A>G (p.Gln359Arg) c.1080+5A>G (n.1080+5A>G) | dbSNP gnomAD v2 gnomAD v4 |
4 | g.154569640A>T | CA358515055 | FGB | c.1085A>T (p.Gln362Leu) n.939+333A>T c.428A>T (p.Gln143Leu) c.908A>T (p.Gln303Leu) c.953A>T (p.Gln318Leu) c.785A>T (p.Gln262Leu) c.1076A>T (p.Gln359Leu) c.1080+5A>T (n.1080+5A>T) | |
4 | g.154569641G>A | CA442013366 | FGB | c.1086G>A (p.Gln362=) n.939+334G>A c.429G>A (p.Gln143=) c.909G>A (p.Gln303=) c.954G>A (p.Gln318=) c.786G>A (p.Gln262=) c.1077G>A (p.Gln359=) c.1080+6G>A (n.1080+6G>A) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.154569641G>C | CA358515056 | FGB | c.1086G>C (p.Gln362His) n.939+334G>C c.429G>C (p.Gln143His) c.909G>C (p.Gln303His) c.954G>C (p.Gln318His) c.786G>C (p.Gln262His) c.1077G>C (p.Gln359His) c.1080+6G>C (n.1080+6G>C) | |
4 | g.154569641G= | CA1504935391 | FGB | c.1086G= (p.Gln362=) n.939+334G= c.429G= (p.Gln143=) c.909G= (p.Gln303=) c.954G= (p.Gln318=) c.786G= (p.Gln262=) c.1077G= (p.Gln359=) c.1080+6G= (n.1080+6G=) | |
4 | g.154569641G>T | CA358515058 | FGB | c.1086G>T (p.Gln362His) n.939+334G>T c.429G>T (p.Gln143His) c.909G>T (p.Gln303His) c.954G>T (p.Gln318His) c.786G>T (p.Gln262His) c.1077G>T (p.Gln359His) c.1080+6G>T (n.1080+6G>T) | gnomAD v4 COSMIC |
4 | g.154569642A>C | CA358515059 | FGB | c.1087A>C (p.Asn363His) n.939+335A>C c.430A>C (p.Asn144His) c.910A>C (p.Asn304His) c.955A>C (p.Asn319His) c.787A>C (p.Asn263His) c.1078A>C (p.Asn360His) c.1080+7A>C (n.1080+7A>C) | |
4 | g.154569642A>G | CA358515060 | FGB | c.1087A>G (p.Asn363Asp) n.939+335A>G c.430A>G (p.Asn144Asp) c.910A>G (p.Asn304Asp) c.955A>G (p.Asn319Asp) c.787A>G (p.Asn263Asp) c.1078A>G (p.Asn360Asp) c.1080+7A>G (n.1080+7A>G) | |
4 | g.154569642A>T | CA358515061 | FGB | c.1087A>T (p.Asn363Tyr) n.939+335A>T c.430A>T (p.Asn144Tyr) c.910A>T (p.Asn304Tyr) c.955A>T (p.Asn319Tyr) c.787A>T (p.Asn263Tyr) c.1078A>T (p.Asn360Tyr) c.1080+7A>T (n.1080+7A>T) | |
4 | g.154569643A>C | CA358515064 | FGB | c.1088A>C (p.Asn363Thr) n.939+336A>C c.431A>C (p.Asn144Thr) c.911A>C (p.Asn304Thr) c.956A>C (p.Asn319Thr) c.788A>C (p.Asn263Thr) c.1079A>C (p.Asn360Thr) c.1080+8A>C (n.1080+8A>C) | |
4 | g.154569643A>G | CA358515065 | FGB | c.1088A>G (p.Asn363Ser) n.939+336A>G c.431A>G (p.Asn144Ser) c.911A>G (p.Asn304Ser) c.956A>G (p.Asn319Ser) c.788A>G (p.Asn263Ser) c.1079A>G (p.Asn360Ser) c.1080+8A>G (n.1080+8A>G) | |
4 | g.154569643A>T | CA358515066 | FGB | c.1088A>T (p.Asn363Ile) n.939+336A>T c.431A>T (p.Asn144Ile) c.911A>T (p.Asn304Ile) c.956A>T (p.Asn319Ile) c.788A>T (p.Asn263Ile) c.1079A>T (p.Asn360Ile) c.1080+8A>T (n.1080+8A>T) | |
4 | g.154569644T>A | CA358515067 | FGB | c.1089T>A (p.Asn363Lys) n.939+337T>A c.432T>A (p.Asn144Lys) c.912T>A (p.Asn304Lys) c.957T>A (p.Asn319Lys) c.789T>A (p.Asn263Lys) c.1080T>A (p.Asn360Lys) c.1080+9T>A (n.1080+9T>A) | |
4 | g.154569644T>C | CA442013370 | FGB | c.1089T>C (p.Asn363=) n.939+337T>C c.432T>C (p.Asn144=) c.912T>C (p.Asn304=) c.957T>C (p.Asn319=) c.789T>C (p.Asn263=) c.1080T>C (p.Asn360=) c.1080+9T>C (n.1080+9T>C) | dbSNP gnomAD v3 gnomAD v4 |
4 | g.154569644T>G | CA358515068 | FGB | c.1089T>G (p.Asn363Lys) n.939+337T>G c.432T>G (p.Asn144Lys) c.912T>G (p.Asn304Lys) c.957T>G (p.Asn319Lys) c.789T>G (p.Asn263Lys) c.1080T>G (p.Asn360Lys) c.1080+9T>G (n.1080+9T>G) | dbSNP |
4 | g.154569644T= | CA1504935394 | FGB | c.1089T= (p.Asn363=) n.939+337T= c.432T= (p.Asn144=) c.912T= (p.Asn304=) c.957T= (p.Asn319=) c.789T= (p.Asn263=) c.1080T= (p.Asn360=) c.1080+9T= (n.1080+9T=) | |
4 | g.154569645G>A | CA358515071 | FGB | c.1090G>A (p.Glu364Lys) n.939+338G>A c.433G>A (p.Glu145Lys) c.913G>A (p.Glu305Lys) c.958G>A (p.Glu320Lys) c.790G>A (p.Glu264Lys) c.1081G>A (p.Glu361Lys) c.1080+10G>A (n.1080+10G>A) | COSMIC |
4 | g.154569645G>C | CA358515073 | FGB | c.1090G>C (p.Glu364Gln) n.939+338G>C c.433G>C (p.Glu145Gln) c.913G>C (p.Glu305Gln) c.958G>C (p.Glu320Gln) c.790G>C (p.Glu264Gln) c.1081G>C (p.Glu361Gln) c.1080+10G>C (n.1080+10G>C) | |
4 | g.154569645G>T | CA358515070 | FGB | c.1090G>T (p.Glu364Ter) n.939+338G>T c.433G>T (p.Glu145Ter) c.913G>T (p.Glu305Ter) c.958G>T (p.Glu320Ter) c.790G>T (p.Glu264Ter) c.1081G>T (p.Glu361Ter) c.1080+10G>T (n.1080+10G>T) | |
4 | g.154569646A>C | CA358515075 | FGB | c.1091A>C (p.Glu364Ala) n.939+339A>C c.434A>C (p.Glu145Ala) c.914A>C (p.Glu305Ala) c.959A>C (p.Glu320Ala) c.791A>C (p.Glu264Ala) c.1082A>C (p.Glu361Ala) c.1080+11A>C (n.1080+11A>C) | |
4 | g.154569646A>G | CA358515078 | FGB | c.1091A>G (p.Glu364Gly) n.939+339A>G c.434A>G (p.Glu145Gly) c.914A>G (p.Glu305Gly) c.959A>G (p.Glu320Gly) c.791A>G (p.Glu264Gly) c.1082A>G (p.Glu361Gly) c.1080+11A>G (n.1080+11A>G) | |
4 | g.154569646A>T | CA358515076 | FGB | c.1091A>T (p.Glu364Val) n.939+339A>T c.434A>T (p.Glu145Val) c.914A>T (p.Glu305Val) c.959A>T (p.Glu320Val) c.791A>T (p.Glu264Val) c.1082A>T (p.Glu361Val) c.1080+11A>T (n.1080+11A>T) | |
4 | g.154569647A= | CA1504935397 | FGB | c.1092A= (p.Glu364=) n.939+340A= c.435A= (p.Glu145=) c.915A= (p.Glu305=) c.960A= (p.Glu320=) c.792A= (p.Glu264=) c.1083A= (p.Glu361=) c.1080+12A= (n.1080+12A=) | |
4 | g.154569647A>C | CA358515080 | FGB | c.1092A>C (p.Glu364Asp) n.939+340A>C c.435A>C (p.Glu145Asp) c.915A>C (p.Glu305Asp) c.960A>C (p.Glu320Asp) c.792A>C (p.Glu264Asp) c.1083A>C (p.Glu361Asp) c.1080+12A>C (n.1080+12A>C) | |
4 | g.154569647A>G | CA108751653 | FGB | c.1092A>G (p.Glu364=) n.939+340A>G c.435A>G (p.Glu145=) c.915A>G (p.Glu305=) c.960A>G (p.Glu320=) c.792A>G (p.Glu264=) c.1083A>G (p.Glu361=) c.1080+12A>G (n.1080+12A>G) | dbSNP |
4 | g.154569647A>T | CA358515081 | FGB | c.1092A>T (p.Glu364Asp) n.939+340A>T c.435A>T (p.Glu145Asp) c.915A>T (p.Glu305Asp) c.960A>T (p.Glu320Asp) c.792A>T (p.Glu264Asp) c.1083A>T (p.Glu361Asp) c.1080+12A>T (n.1080+12A>T) | |
4 | g.154569648G>A | CA126431 | FGB | c.1093G>A (p.Ala365Thr) n.939+341G>A c.436G>A (p.Ala146Thr) c.916G>A (p.Ala306Thr) c.961G>A (p.Ala321Thr) c.793G>A (p.Ala265Thr) c.1084G>A (p.Ala362Thr) c.1080+13G>A (n.1080+13G>A) | ClinVar dbSNP |
4 | g.154569648G>C | CA358515084 | FGB | c.1093G>C (p.Ala365Pro) n.939+341G>C c.436G>C (p.Ala146Pro) c.916G>C (p.Ala306Pro) c.961G>C (p.Ala321Pro) c.793G>C (p.Ala265Pro) c.1084G>C (p.Ala362Pro) c.1080+13G>C (n.1080+13G>C) | |
4 | g.154569648G= | CA1504935402 | FGB | c.1093G= (p.Ala365=) n.939+341G= c.436G= (p.Ala146=) c.916G= (p.Ala306=) c.961G= (p.Ala321=) c.793G= (p.Ala265=) c.1084G= (p.Ala362=) c.1080+13G= (n.1080+13G=) | |
4 | g.154569648G>T | CA358515085 | FGB | c.1093G>T (p.Ala365Ser) n.939+341G>T c.436G>T (p.Ala146Ser) c.916G>T (p.Ala306Ser) c.961G>T (p.Ala321Ser) c.793G>T (p.Ala265Ser) c.1084G>T (p.Ala362Ser) c.1080+13G>T (n.1080+13G>T) | |
4 | g.154569649C>A | CA358515087 | FGB | c.1094C>A (p.Ala365Asp) n.939+342C>A c.437C>A (p.Ala146Asp) c.917C>A (p.Ala306Asp) c.962C>A (p.Ala321Asp) c.794C>A (p.Ala265Asp) c.1085C>A (p.Ala362Asp) c.1080+14C>A (n.1080+14C>A) | |
4 | g.154569649C>G | CA358515088 | FGB | c.1094C>G (p.Ala365Gly) n.939+342C>G c.437C>G (p.Ala146Gly) c.917C>G (p.Ala306Gly) c.962C>G (p.Ala321Gly) c.794C>G (p.Ala265Gly) c.1085C>G (p.Ala362Gly) c.1080+14C>G (n.1080+14C>G) | |
4 | g.154569649C>T | CA358515090 | FGB | c.1094C>T (p.Ala365Val) n.939+342C>T c.437C>T (p.Ala146Val) c.917C>T (p.Ala306Val) c.962C>T (p.Ala321Val) c.794C>T (p.Ala265Val) c.1085C>T (p.Ala362Val) c.1080+14C>T (n.1080+14C>T) | |
4 | g.154569650C>A | CA442013385 | FGB | c.1095C>A (p.Ala365=) n.939+343C>A c.438C>A (p.Ala146=) c.918C>A (p.Ala306=) c.963C>A (p.Ala321=) c.795C>A (p.Ala265=) c.1086C>A (p.Ala362=) c.1080+15C>A (n.1080+15C>A) | |
4 | g.154569650C>G | CA442013386 | FGB | c.1095C>G (p.Ala365=) n.939+343C>G c.438C>G (p.Ala146=) c.918C>G (p.Ala306=) c.963C>G (p.Ala321=) c.795C>G (p.Ala265=) c.1086C>G (p.Ala362=) c.1080+15C>G (n.1080+15C>G) | |
4 | g.154569650C>T | CA442013387 | FGB | c.1095C>T (p.Ala365=) n.939+343C>T c.438C>T (p.Ala146=) c.918C>T (p.Ala306=) c.963C>T (p.Ala321=) c.795C>T (p.Ala265=) c.1086C>T (p.Ala362=) c.1080+15C>T (n.1080+15C>T) | gnomAD v4 |
4 | g.154569651A>C | CA358515092 | FGB | c.1096A>C (p.Asn366His) n.939+344A>C c.439A>C (p.Asn147His) c.919A>C (p.Asn307His) c.964A>C (p.Asn322His) c.796A>C (p.Asn266His) c.1087A>C (p.Asn363His) c.1080+16A>C (n.1080+16A>C) | |
4 | g.154569651A>G | CA358515094 | FGB | c.1096A>G (p.Asn366Asp) n.939+344A>G c.439A>G (p.Asn147Asp) c.919A>G (p.Asn307Asp) c.964A>G (p.Asn322Asp) c.796A>G (p.Asn266Asp) c.1087A>G (p.Asn363Asp) c.1080+16A>G (n.1080+16A>G) | |
4 | g.154569651A>T | CA358515095 | FGB | c.1096A>T (p.Asn366Tyr) n.939+344A>T c.439A>T (p.Asn147Tyr) c.919A>T (p.Asn307Tyr) c.964A>T (p.Asn322Tyr) c.796A>T (p.Asn266Tyr) c.1087A>T (p.Asn363Tyr) c.1080+16A>T (n.1080+16A>T) | |
4 | g.154569652A= | CA1504935408 | FGB | c.1097A= (p.Asn366=) n.939+345A= c.440A= (p.Asn147=) c.920A= (p.Asn307=) c.965A= (p.Asn322=) c.797A= (p.Asn266=) c.1088A= (p.Asn363=) c.1080+17A= (n.1080+17A=) | |
4 | g.154569652A>C | CA358515100 | FGB | c.1097A>C (p.Asn366Thr) n.939+345A>C c.440A>C (p.Asn147Thr) c.920A>C (p.Asn307Thr) c.965A>C (p.Asn322Thr) c.797A>C (p.Asn266Thr) c.1088A>C (p.Asn363Thr) c.1080+17A>C (n.1080+17A>C) | |
4 | g.154569652A>G | CA358515098 | FGB | c.1097A>G (p.Asn366Ser) n.939+345A>G c.440A>G (p.Asn147Ser) c.920A>G (p.Asn307Ser) c.965A>G (p.Asn322Ser) c.797A>G (p.Asn266Ser) c.1088A>G (p.Asn363Ser) c.1080+17A>G (n.1080+17A>G) | dbSNP gnomAD v4 COSMIC |
4 | g.154569652A>T | CA358515097 | FGB | c.1097A>T (p.Asn366Ile) n.939+345A>T c.440A>T (p.Asn147Ile) c.920A>T (p.Asn307Ile) c.965A>T (p.Asn322Ile) c.797A>T (p.Asn266Ile) c.1088A>T (p.Asn363Ile) c.1080+17A>T (n.1080+17A>T) | |
4 | g.154569653C>A | CA358515101 | FGB | c.1098C>A (p.Asn366Lys) n.939+346C>A c.441C>A (p.Asn147Lys) c.921C>A (p.Asn307Lys) c.966C>A (p.Asn322Lys) c.798C>A (p.Asn266Lys) c.1089C>A (p.Asn363Lys) c.1080+18C>A (n.1080+18C>A) | dbSNP |
4 | g.154569653C= | CA1504935412 | FGB | c.1098C= (p.Asn366=) n.939+346C= c.441C= (p.Asn147=) c.921C= (p.Asn307=) c.966C= (p.Asn322=) c.798C= (p.Asn266=) c.1089C= (p.Asn363=) c.1080+18C= (n.1080+18C=) | |
4 | g.154569653C>G | CA358515103 | FGB | c.1098C>G (p.Asn366Lys) n.939+346C>G c.441C>G (p.Asn147Lys) c.921C>G (p.Asn307Lys) c.966C>G (p.Asn322Lys) c.798C>G (p.Asn266Lys) c.1089C>G (p.Asn363Lys) c.1080+18C>G (n.1080+18C>G) | |
4 | g.154569653C>T | CA442013390 | FGB | c.1098C>T (p.Asn366=) n.939+346C>T c.441C>T (p.Asn147=) c.921C>T (p.Asn307=) c.966C>T (p.Asn322=) c.798C>T (p.Asn266=) c.1089C>T (p.Asn363=) c.1080+18C>T (n.1080+18C>T) | dbSNP |
4 | g.154569654A>C | CA358515105 | FGB | c.1099A>C (p.Lys367Gln) n.939+347A>C c.442A>C (p.Lys148Gln) c.922A>C (p.Lys308Gln) c.967A>C (p.Lys323Gln) c.799A>C (p.Lys267Gln) c.1090A>C (p.Lys364Gln) c.1080+19A>C (n.1080+19A>C) | |
4 | g.154569654A>G | CA358515107 | FGB | c.1099A>G (p.Lys367Glu) n.939+347A>G c.442A>G (p.Lys148Glu) c.922A>G (p.Lys308Glu) c.967A>G (p.Lys323Glu) c.799A>G (p.Lys267Glu) c.1090A>G (p.Lys364Glu) c.1080+19A>G (n.1080+19A>G) | |
4 | g.154569654A>T | CA358515108 | FGB | c.1099A>T (p.Lys367Ter) n.939+347A>T c.442A>T (p.Lys148Ter) c.922A>T (p.Lys308Ter) c.967A>T (p.Lys323Ter) c.799A>T (p.Lys267Ter) c.1090A>T (p.Lys364Ter) c.1080+19A>T (n.1080+19A>T) | |
4 | g.154569655A= | CA1504935416 | FGB | c.1100A= (p.Lys367=) n.939+348A= c.443A= (p.Lys148=) c.923A= (p.Lys308=) c.968A= (p.Lys323=) c.800A= (p.Lys267=) c.1091A= (p.Lys364=) c.1080+20A= (n.1080+20A=) | |
4 | g.154569655A>C | CA358515110 | FGB | c.1100A>C (p.Lys367Thr) n.939+348A>C c.443A>C (p.Lys148Thr) c.923A>C (p.Lys308Thr) c.968A>C (p.Lys323Thr) c.800A>C (p.Lys267Thr) c.1091A>C (p.Lys364Thr) c.1080+20A>C (n.1080+20A>C) | |
4 | g.154569655A>G | CA358515111 | FGB | c.1100A>G (p.Lys367Arg) n.939+348A>G c.443A>G (p.Lys148Arg) c.923A>G (p.Lys308Arg) c.968A>G (p.Lys323Arg) c.800A>G (p.Lys267Arg) c.1091A>G (p.Lys364Arg) c.1080+20A>G (n.1080+20A>G) | dbSNP gnomAD v3 gnomAD v4 |
4 | g.154569655A>T | CA358515112 | FGB | c.1100A>T (p.Lys367Ile) n.939+348A>T c.443A>T (p.Lys148Ile) c.923A>T (p.Lys308Ile) c.968A>T (p.Lys323Ile) c.800A>T (p.Lys267Ile) c.1091A>T (p.Lys364Ile) c.1080+20A>T (n.1080+20A>T) | |
4 | g.154569656A= | CA1504935419 | FGB | c.1101A= (p.Lys367=) n.939+349A= c.444A= (p.Lys148=) c.924A= (p.Lys308=) c.969A= (p.Lys323=) c.801A= (p.Lys267=) c.1092A= (p.Lys364=) c.1080+21A= (n.1080+21A=) | |
4 | g.154569656A>C | CA358515114 | FGB | c.1101A>C (p.Lys367Asn) n.939+349A>C c.444A>C (p.Lys148Asn) c.924A>C (p.Lys308Asn) c.969A>C (p.Lys323Asn) c.801A>C (p.Lys267Asn) c.1092A>C (p.Lys364Asn) c.1080+21A>C (n.1080+21A>C) | |
4 | g.154569656A>G | CA442013396 | FGB | c.1101A>G (p.Lys367=) n.939+349A>G c.444A>G (p.Lys148=) c.924A>G (p.Lys308=) c.969A>G (p.Lys323=) c.801A>G (p.Lys267=) c.1092A>G (p.Lys364=) c.1080+21A>G (n.1080+21A>G) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.154569656A>T | CA358515115 | FGB | c.1101A>T (p.Lys367Asn) n.939+349A>T c.444A>T (p.Lys148Asn) c.924A>T (p.Lys308Asn) c.969A>T (p.Lys323Asn) c.801A>T (p.Lys267Asn) c.1092A>T (p.Lys364Asn) c.1080+21A>T (n.1080+21A>T) | |
4 | g.154569657T>A | CA358515117 | FGB | c.1102T>A (p.Tyr368Asn) n.939+350T>A c.445T>A (p.Tyr149Asn) c.925T>A (p.Tyr309Asn) c.970T>A (p.Tyr324Asn) c.802T>A (p.Tyr268Asn) c.1093T>A (p.Tyr365Asn) c.1080+22T>A (n.1080+22T>A) | |
4 | g.154569657T>C | CA358515119 | FGB | c.1102T>C (p.Tyr368His) n.939+350T>C c.445T>C (p.Tyr149His) c.925T>C (p.Tyr309His) c.970T>C (p.Tyr324His) c.802T>C (p.Tyr268His) c.1093T>C (p.Tyr365His) c.1080+22T>C (n.1080+22T>C) | gnomAD v4 |
4 | g.154569657T>G | CA358515120 | FGB | c.1102T>G (p.Tyr368Asp) n.939+350T>G c.445T>G (p.Tyr149Asp) c.925T>G (p.Tyr309Asp) c.970T>G (p.Tyr324Asp) c.802T>G (p.Tyr268Asp) c.1093T>G (p.Tyr365Asp) c.1080+22T>G (n.1080+22T>G) | |
4 | g.154569658A>C | CA358515123 | FGB | c.1103A>C (p.Tyr368Ser) n.939+351A>C c.446A>C (p.Tyr149Ser) c.926A>C (p.Tyr309Ser) c.971A>C (p.Tyr324Ser) c.803A>C (p.Tyr268Ser) c.1094A>C (p.Tyr365Ser) c.1080+23A>C (n.1080+23A>C) | |
4 | g.154569658A>G | CA358515125 | FGB | c.1103A>G (p.Tyr368Cys) n.939+351A>G c.446A>G (p.Tyr149Cys) c.926A>G (p.Tyr309Cys) c.971A>G (p.Tyr324Cys) c.803A>G (p.Tyr268Cys) c.1094A>G (p.Tyr365Cys) c.1080+23A>G (n.1080+23A>G) | COSMIC |
4 | g.154569658A>T | CA358515121 | FGB | c.1103A>T (p.Tyr368Phe) n.939+351A>T c.446A>T (p.Tyr149Phe) c.926A>T (p.Tyr309Phe) c.971A>T (p.Tyr324Phe) c.803A>T (p.Tyr268Phe) c.1094A>T (p.Tyr365Phe) c.1080+23A>T (n.1080+23A>T) | |
4 | g.154569659C>A | CA358515126 | FGB | c.1104C>A (p.Tyr368Ter) n.939+352C>A c.447C>A (p.Tyr149Ter) c.927C>A (p.Tyr309Ter) c.972C>A (p.Tyr324Ter) c.804C>A (p.Tyr268Ter) c.1095C>A (p.Tyr365Ter) c.1080+24C>A (n.1080+24C>A) | |
4 | g.154569659C>G | CA358515127 | FGB | c.1104C>G (p.Tyr368Ter) n.939+352C>G c.447C>G (p.Tyr149Ter) c.927C>G (p.Tyr309Ter) c.972C>G (p.Tyr324Ter) c.804C>G (p.Tyr268Ter) c.1095C>G (p.Tyr365Ter) c.1080+24C>G (n.1080+24C>G) | dbSNP |
4 | g.154569659C>T | CA442013400 | FGB | c.1104C>T (p.Tyr368=) n.939+352C>T c.447C>T (p.Tyr149=) c.927C>T (p.Tyr309=) c.972C>T (p.Tyr324=) c.804C>T (p.Tyr268=) c.1095C>T (p.Tyr365=) c.1080+24C>T (n.1080+24C>T) | |
4 | g.154569660C>A | CA358515129 | FGB | c.1105C>A (p.Gln369Lys) n.939+353C>A c.448C>A (p.Gln150Lys) c.928C>A (p.Gln310Lys) c.973C>A (p.Gln325Lys) c.805C>A (p.Gln269Lys) c.1096C>A (p.Gln366Lys) c.1080+25C>A (n.1080+25C>A) | |
4 | g.154569660C= | CA1504935421 | FGB | c.1105C= (p.Gln369=) n.939+353C= c.448C= (p.Gln150=) c.928C= (p.Gln310=) c.973C= (p.Gln325=) c.805C= (p.Gln269=) c.1096C= (p.Gln366=) c.1080+25C= (n.1080+25C=) | |
4 | g.154569660C>G | CA358515131 | FGB | c.1105C>G (p.Gln369Glu) n.939+353C>G c.448C>G (p.Gln150Glu) c.928C>G (p.Gln310Glu) c.973C>G (p.Gln325Glu) c.805C>G (p.Gln269Glu) c.1096C>G (p.Gln366Glu) c.1080+25C>G (n.1080+25C>G) | |
4 | g.154569660C>T | CA108751657 | FGB | c.1105C>T (p.Gln369Ter) n.939+353C>T c.448C>T (p.Gln150Ter) c.928C>T (p.Gln310Ter) c.973C>T (p.Gln325Ter) c.805C>T (p.Gln269Ter) c.1096C>T (p.Gln366Ter) c.1080+25C>T (n.1080+25C>T) | dbSNP |
4 | g.154569661A>C | CA358515135 | FGB | c.1106A>C (p.Gln369Pro) n.939+354A>C c.449A>C (p.Gln150Pro) c.929A>C (p.Gln310Pro) c.974A>C (p.Gln325Pro) c.806A>C (p.Gln269Pro) c.1097A>C (p.Gln366Pro) c.1080+26A>C (n.1080+26A>C) | |
4 | g.154569661A>G | CA358515136 | FGB | c.1106A>G (p.Gln369Arg) n.939+354A>G c.449A>G (p.Gln150Arg) c.929A>G (p.Gln310Arg) c.974A>G (p.Gln325Arg) c.806A>G (p.Gln269Arg) c.1097A>G (p.Gln366Arg) c.1080+26A>G (n.1080+26A>G) | |
4 | g.154569661A>T | CA358515137 | FGB | c.1106A>T (p.Gln369Leu) n.939+354A>T c.449A>T (p.Gln150Leu) c.929A>T (p.Gln310Leu) c.974A>T (p.Gln325Leu) c.806A>T (p.Gln269Leu) c.1097A>T (p.Gln366Leu) c.1080+26A>T (n.1080+26A>T) | |
4 | g.154569662G>A | CA442013403 | FGB | c.1107G>A (p.Gln369=) n.939+355G>A c.450G>A (p.Gln150=) c.930G>A (p.Gln310=) c.975G>A (p.Gln325=) c.807G>A (p.Gln269=) c.1098G>A (p.Gln366=) c.1080+27G>A (n.1080+27G>A) | dbSNP |
4 | g.154569662G>C | CA358515139 | FGB | c.1107G>C (p.Gln369His) n.939+355G>C c.450G>C (p.Gln150His) c.930G>C (p.Gln310His) c.975G>C (p.Gln325His) c.807G>C (p.Gln269His) c.1098G>C (p.Gln366His) c.1080+27G>C (n.1080+27G>C) | |
4 | g.154569662G= | CA1504935425 | FGB | c.1107G= (p.Gln369=) n.939+355G= c.450G= (p.Gln150=) c.930G= (p.Gln310=) c.975G= (p.Gln325=) c.807G= (p.Gln269=) c.1098G= (p.Gln366=) c.1080+27G= (n.1080+27G=) | |
4 | g.154569662G>T | CA358515141 | FGB | c.1107G>T (p.Gln369His) n.939+355G>T c.450G>T (p.Gln150His) c.930G>T (p.Gln310His) c.975G>T (p.Gln325His) c.807G>T (p.Gln269His) c.1098G>T (p.Gln366His) c.1080+27G>T (n.1080+27G>T) | |
4 | g.154569663A= | CA1504935429 | FGB | c.1108A= (p.Ile370=) n.939+356A= c.451A= (p.Ile151=) c.931A= (p.Ile311=) c.976A= (p.Ile326=) c.808A= (p.Ile270=) c.1099A= (p.Ile367=) c.1080+28A= (n.1080+28A=) | |
4 | g.154569663A>C | CA358515146 | FGB | c.1108A>C (p.Ile370Leu) n.939+356A>C c.451A>C (p.Ile151Leu) c.931A>C (p.Ile311Leu) c.976A>C (p.Ile326Leu) c.808A>C (p.Ile270Leu) c.1099A>C (p.Ile367Leu) c.1080+28A>C (n.1080+28A>C) | |
4 | g.154569663A>G | CA358515144 | FGB | c.1108A>G (p.Ile370Val) n.939+356A>G c.451A>G (p.Ile151Val) c.931A>G (p.Ile311Val) c.976A>G (p.Ile326Val) c.808A>G (p.Ile270Val) c.1099A>G (p.Ile367Val) c.1080+28A>G (n.1080+28A>G) | dbSNP |
4 | g.154569663A>T | CA358515143 | FGB | c.1108A>T (p.Ile370Phe) n.939+356A>T c.451A>T (p.Ile151Phe) c.931A>T (p.Ile311Phe) c.976A>T (p.Ile326Phe) c.808A>T (p.Ile270Phe) c.1099A>T (p.Ile367Phe) c.1080+28A>T (n.1080+28A>T) | |
4 | g.154569664T>A | CA358515147 | FGB | c.1109T>A (p.Ile370Asn) n.939+357T>A c.452T>A (p.Ile151Asn) c.932T>A (p.Ile311Asn) c.977T>A (p.Ile326Asn) c.809T>A (p.Ile270Asn) c.1100T>A (p.Ile367Asn) c.1080+29T>A (n.1080+29T>A) | |
4 | g.154569664T>C | CA358515148 | FGB | c.1109T>C (p.Ile370Thr) n.939+357T>C c.452T>C (p.Ile151Thr) c.932T>C (p.Ile311Thr) c.977T>C (p.Ile326Thr) c.809T>C (p.Ile270Thr) c.1100T>C (p.Ile367Thr) c.1080+29T>C (n.1080+29T>C) | COSMIC |
4 | g.154569664T>G | CA358515149 | FGB | c.1109T>G (p.Ile370Ser) n.939+357T>G c.452T>G (p.Ile151Ser) c.932T>G (p.Ile311Ser) c.977T>G (p.Ile326Ser) c.809T>G (p.Ile270Ser) c.1100T>G (p.Ile367Ser) c.1080+29T>G (n.1080+29T>G) | |
4 | g.154569665C>A | CA442013408 | FGB | c.1110C>A (p.Ile370=) n.939+358C>A c.453C>A (p.Ile151=) c.933C>A (p.Ile311=) c.978C>A (p.Ile326=) c.810C>A (p.Ile270=) c.1101C>A (p.Ile367=) c.1080+30C>A (n.1080+30C>A) | |
4 | g.154569665C= | CA1504935432 | FGB | c.1110C= (p.Ile370=) n.939+358C= c.453C= (p.Ile151=) c.933C= (p.Ile311=) c.978C= (p.Ile326=) c.810C= (p.Ile270=) c.1101C= (p.Ile367=) c.1080+30C= (n.1080+30C=) | |
4 | g.154569665C>G | CA3114719 | FGB | c.1110C>G (p.Ile370Met) n.939+358C>G c.453C>G (p.Ile151Met) c.933C>G (p.Ile311Met) c.978C>G (p.Ile326Met) c.810C>G (p.Ile270Met) c.1101C>G (p.Ile367Met) c.1080+30C>G (n.1080+30C>G) | dbSNP ExAC gnomAD v2 gnomAD v4 |
4 | g.154569665C>T | CA3114720 | FGB | c.1110C>T (p.Ile370=) n.939+358C>T c.453C>T (p.Ile151=) c.933C>T (p.Ile311=) c.978C>T (p.Ile326=) c.810C>T (p.Ile270=) c.1101C>T (p.Ile367=) c.1080+30C>T (n.1080+30C>T) | dbSNP ExAC gnomAD v2 gnomAD v4 |
4 | g.154569666T>A | CA358515151 | FGB | c.1111T>A (p.Ser371Thr) n.939+359T>A c.454T>A (p.Ser152Thr) c.934T>A (p.Ser312Thr) c.979T>A (p.Ser327Thr) c.811T>A (p.Ser271Thr) c.1102T>A (p.Ser368Thr) c.1080+31T>A (n.1080+31T>A) | gnomAD v4 |
4 | g.154569666T>C | CA358515152 | FGB | c.1111T>C (p.Ser371Pro) n.939+359T>C c.454T>C (p.Ser152Pro) c.934T>C (p.Ser312Pro) c.979T>C (p.Ser327Pro) c.811T>C (p.Ser271Pro) c.1102T>C (p.Ser368Pro) c.1080+31T>C (n.1080+31T>C) | |
4 | g.154569666T>G | CA358515154 | FGB | c.1111T>G (p.Ser371Ala) n.939+359T>G c.454T>G (p.Ser152Ala) c.934T>G (p.Ser312Ala) c.979T>G (p.Ser327Ala) c.811T>G (p.Ser271Ala) c.1102T>G (p.Ser368Ala) c.1080+31T>G (n.1080+31T>G) | |
4 | g.154569667C>A | CA358515156 | FGB | c.1112C>A (p.Ser371Ter) n.939+360C>A c.455C>A (p.Ser152Ter) c.935C>A (p.Ser312Ter) c.980C>A (p.Ser327Ter) c.812C>A (p.Ser271Ter) c.1103C>A (p.Ser368Ter) c.1080+32C>A (n.1080+32C>A) | |
4 | g.154569667C>G | CA358515157 | FGB | c.1112C>G (p.Ser371Ter) n.939+360C>G c.455C>G (p.Ser152Ter) c.935C>G (p.Ser312Ter) c.980C>G (p.Ser327Ter) c.812C>G (p.Ser271Ter) c.1103C>G (p.Ser368Ter) c.1080+32C>G (n.1080+32C>G) | |
4 | g.154569667C>T | CA358515158 | FGB | c.1112C>T (p.Ser371Leu) n.939+360C>T c.455C>T (p.Ser152Leu) c.935C>T (p.Ser312Leu) c.980C>T (p.Ser327Leu) c.812C>T (p.Ser271Leu) c.1103C>T (p.Ser368Leu) c.1080+32C>T (n.1080+32C>T) | COSMIC |
4 | g.154569668A= | CA1504935436 | FGB | c.1113A= (p.Ser371=) n.939+361A= c.456A= (p.Ser152=) c.936A= (p.Ser312=) c.981A= (p.Ser327=) c.813A= (p.Ser271=) c.1104A= (p.Ser368=) c.1080+33A= (n.1080+33A=) | |
4 | g.154569668A>C | CA442013413 | FGB | c.1113A>C (p.Ser371=) n.939+361A>C c.456A>C (p.Ser152=) c.936A>C (p.Ser312=) c.981A>C (p.Ser327=) c.813A>C (p.Ser271=) c.1104A>C (p.Ser368=) c.1080+33A>C (n.1080+33A>C) | |
4 | g.154569668A>G | CA3114721 | FGB | c.1113A>G (p.Ser371=) n.939+361A>G c.456A>G (p.Ser152=) c.936A>G (p.Ser312=) c.981A>G (p.Ser327=) c.813A>G (p.Ser271=) c.1104A>G (p.Ser368=) c.1080+33A>G (n.1080+33A>G) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.154569668A>T | CA442013414 | FGB | c.1113A>T (p.Ser371=) n.939+361A>T c.456A>T (p.Ser152=) c.936A>T (p.Ser312=) c.981A>T (p.Ser327=) c.813A>T (p.Ser271=) c.1104A>T (p.Ser368=) c.1080+33A>T (n.1080+33A>T) | gnomAD v4 |
4 | g.154569668_154569669del | CA2672441406 | FGB | c.1113_1114del (p.Val372GlufsTer9) n.939+361_939+362del c.456_457del (p.Val153GlufsTer9) c.936_937del (p.Val313GlufsTer9) c.981_982del (p.Val328GlufsTer9) c.813_814del (p.Val272GlufsTer9) c.1104_1105del (p.Val369GlufsTer9) c.1080+33_1080+34del (n.1080+33_1080+34del) | gnomAD v4 |
4 | g.154569669G>A | CA108751677 | FGB | c.1114G>A (p.Val372Met) n.939+362G>A c.457G>A (p.Val153Met) c.937G>A (p.Val313Met) c.982G>A (p.Val328Met) c.814G>A (p.Val272Met) c.1105G>A (p.Val369Met) c.1080+34G>A (n.1080+34G>A) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.154569669G>C | CA358515163 | FGB | c.1114G>C (p.Val372Leu) n.939+362G>C c.457G>C (p.Val153Leu) c.937G>C (p.Val313Leu) c.982G>C (p.Val328Leu) c.814G>C (p.Val272Leu) c.1105G>C (p.Val369Leu) c.1080+34G>C (n.1080+34G>C) | |
4 | g.154569669G= | CA1504935441 | FGB | c.1114G= (p.Val372=) n.939+362G= c.457G= (p.Val153=) c.937G= (p.Val313=) c.982G= (p.Val328=) c.814G= (p.Val272=) c.1105G= (p.Val369=) c.1080+34G= (n.1080+34G=) | |
4 | g.154569669G>T | CA358515161 | FGB | c.1114G>T (p.Val372Leu) n.939+362G>T c.457G>T (p.Val153Leu) c.937G>T (p.Val313Leu) c.982G>T (p.Val328Leu) c.814G>T (p.Val272Leu) c.1105G>T (p.Val369Leu) c.1080+34G>T (n.1080+34G>T) | |
4 | g.154569670T>A | CA358515164 | FGB | c.1115T>A (p.Val372Glu) n.939+363T>A c.458T>A (p.Val153Glu) c.938T>A (p.Val313Glu) c.983T>A (p.Val328Glu) c.815T>A (p.Val272Glu) c.1106T>A (p.Val369Glu) c.1080+35T>A (n.1080+35T>A) | |
4 | g.154569670T>C | CA358515166 | FGB | c.1115T>C (p.Val372Ala) n.939+363T>C c.458T>C (p.Val153Ala) c.938T>C (p.Val313Ala) c.983T>C (p.Val328Ala) c.815T>C (p.Val272Ala) c.1106T>C (p.Val369Ala) c.1080+35T>C (n.1080+35T>C) | |
4 | g.154569670T>G | CA358515167 | FGB | c.1115T>G (p.Val372Gly) n.939+363T>G c.458T>G (p.Val153Gly) c.938T>G (p.Val313Gly) c.983T>G (p.Val328Gly) c.815T>G (p.Val272Gly) c.1106T>G (p.Val369Gly) c.1080+35T>G (n.1080+35T>G) | |
4 | g.154569671G>A | CA442013416 | FGB | c.1116G>A (p.Val372=) n.939+364G>A c.459G>A (p.Val153=) c.939G>A (p.Val313=) c.984G>A (p.Val328=) c.816G>A (p.Val272=) c.1107G>A (p.Val369=) c.1080+36G>A (n.1080+36G>A) | |
4 | g.154569671G>C | CA442013417 | FGB | c.1116G>C (p.Val372=) n.939+364G>C c.459G>C (p.Val153=) c.939G>C (p.Val313=) c.984G>C (p.Val328=) c.816G>C (p.Val272=) c.1107G>C (p.Val369=) c.1080+36G>C (n.1080+36G>C) | |
4 | g.154569671G>T | CA442013418 | FGB | c.1116G>T (p.Val372=) n.939+364G>T c.459G>T (p.Val153=) c.939G>T (p.Val313=) c.984G>T (p.Val328=) c.816G>T (p.Val272=) c.1107G>T (p.Val369=) c.1080+36G>T (n.1080+36G>T) | |
4 | g.154569672A= | CA1504935449 | FGB | c.1117A= (p.Asn373=) n.939+365A= c.460A= (p.Asn154=) c.940A= (p.Asn314=) c.985A= (p.Asn329=) c.817A= (p.Asn273=) c.1108A= (p.Asn370=) c.1080+37A= (n.1080+37A=) | |
4 | g.154569672A>C | CA358515169 | FGB | c.1117A>C (p.Asn373His) n.939+365A>C c.460A>C (p.Asn154His) c.940A>C (p.Asn314His) c.985A>C (p.Asn329His) c.817A>C (p.Asn273His) c.1108A>C (p.Asn370His) c.1080+37A>C (n.1080+37A>C) | |
4 | g.154569672A>G | CA358515170 | FGB | c.1117A>G (p.Asn373Asp) n.939+365A>G c.460A>G (p.Asn154Asp) c.940A>G (p.Asn314Asp) c.985A>G (p.Asn329Asp) c.817A>G (p.Asn273Asp) c.1108A>G (p.Asn370Asp) c.1080+37A>G (n.1080+37A>G) | |
4 | g.154569672A>T | CA3114722 | FGB | c.1117A>T (p.Asn373Tyr) n.939+365A>T c.460A>T (p.Asn154Tyr) c.940A>T (p.Asn314Tyr) c.985A>T (p.Asn329Tyr) c.817A>T (p.Asn273Tyr) c.1108A>T (p.Asn370Tyr) c.1080+37A>T (n.1080+37A>T) | dbSNP ExAC gnomAD v2 gnomAD v4 |
4 | g.154569673A= | CA1504935453 | FGB | c.1118A= (p.Asn373=) n.939+366A= c.461A= (p.Asn154=) c.941A= (p.Asn314=) c.986A= (p.Asn329=) c.818A= (p.Asn273=) c.1109A= (p.Asn370=) c.1080+38A= (n.1080+38A=) | |
4 | g.154569673A>C | CA358515176 | FGB | c.1118A>C (p.Asn373Thr) n.939+366A>C c.461A>C (p.Asn154Thr) c.941A>C (p.Asn314Thr) c.986A>C (p.Asn329Thr) c.818A>C (p.Asn273Thr) c.1109A>C (p.Asn370Thr) c.1080+38A>C (n.1080+38A>C) | |
4 | g.154569673A>G | CA358515173 | FGB | c.1118A>G (p.Asn373Ser) n.939+366A>G c.461A>G (p.Asn154Ser) c.941A>G (p.Asn314Ser) c.986A>G (p.Asn329Ser) c.818A>G (p.Asn273Ser) c.1109A>G (p.Asn370Ser) c.1080+38A>G (n.1080+38A>G) | dbSNP gnomAD v3 gnomAD v4 |
4 | g.154569673A>T | CA358515174 | FGB | c.1118A>T (p.Asn373Ile) n.939+366A>T c.461A>T (p.Asn154Ile) c.941A>T (p.Asn314Ile) c.986A>T (p.Asn329Ile) c.818A>T (p.Asn273Ile) c.1109A>T (p.Asn370Ile) c.1080+38A>T (n.1080+38A>T) | |
4 | g.154569674C>A | CA358515178 | FGB | c.1119C>A (p.Asn373Lys) n.939+367C>A c.462C>A (p.Asn154Lys) c.942C>A (p.Asn314Lys) c.987C>A (p.Asn329Lys) c.819C>A (p.Asn273Lys) c.1110C>A (p.Asn370Lys) c.1080+39C>A (n.1080+39C>A) | |
4 | g.154569674C>G | CA358515179 | FGB | c.1119C>G (p.Asn373Lys) n.939+367C>G c.462C>G (p.Asn154Lys) c.942C>G (p.Asn314Lys) c.987C>G (p.Asn329Lys) c.819C>G (p.Asn273Lys) c.1110C>G (p.Asn370Lys) c.1080+39C>G (n.1080+39C>G) | |
4 | g.154569674C>T | CA442013423 | FGB | c.1119C>T (p.Asn373=) n.939+367C>T c.462C>T (p.Asn154=) c.942C>T (p.Asn314=) c.987C>T (p.Asn329=) c.819C>T (p.Asn273=) c.1110C>T (p.Asn370=) c.1080+39C>T (n.1080+39C>T) | |
4 | g.154569675A>C | CA358515181 | FGB | c.1120A>C (p.Lys374Gln) n.939+368A>C c.463A>C (p.Lys155Gln) c.943A>C (p.Lys315Gln) c.988A>C (p.Lys330Gln) c.820A>C (p.Lys274Gln) c.1111A>C (p.Lys371Gln) c.1080+40A>C (n.1080+40A>C) | |
4 | g.154569675A>G | CA358515183 | FGB | c.1120A>G (p.Lys374Glu) n.939+368A>G c.463A>G (p.Lys155Glu) c.943A>G (p.Lys315Glu) c.988A>G (p.Lys330Glu) c.820A>G (p.Lys274Glu) c.1111A>G (p.Lys371Glu) c.1080+40A>G (n.1080+40A>G) | |
4 | g.154569675A>T | CA358515185 | FGB | c.1120A>T (p.Lys374Ter) n.939+368A>T c.463A>T (p.Lys155Ter) c.943A>T (p.Lys315Ter) c.988A>T (p.Lys330Ter) c.820A>T (p.Lys274Ter) c.1111A>T (p.Lys371Ter) c.1080+40A>T (n.1080+40A>T) | |
4 | g.154569676A= | CA1504935456 | FGB | c.1121A= (p.Lys374=) n.939+369A= c.464A= (p.Lys155=) c.944A= (p.Lys315=) c.989A= (p.Lys330=) c.821A= (p.Lys274=) c.1112A= (p.Lys371=) c.1080+41A= (n.1080+41A=) | |
4 | g.154569676A>C | CA3114723 | FGB | c.1121A>C (p.Lys374Thr) n.939+369A>C c.464A>C (p.Lys155Thr) c.944A>C (p.Lys315Thr) c.989A>C (p.Lys330Thr) c.821A>C (p.Lys274Thr) c.1112A>C (p.Lys371Thr) c.1080+41A>C (n.1080+41A>C) | dbSNP ExAC gnomAD v2 gnomAD v4 |
4 | g.154569676A>G | CA358515186 | FGB | c.1121A>G (p.Lys374Arg) n.939+369A>G c.464A>G (p.Lys155Arg) c.944A>G (p.Lys315Arg) c.989A>G (p.Lys330Arg) c.821A>G (p.Lys274Arg) c.1112A>G (p.Lys371Arg) c.1080+41A>G (n.1080+41A>G) | dbSNP gnomAD v4 |
4 | g.154569676A>T | CA358515188 | FGB | c.1121A>T (p.Lys374Ile) n.939+369A>T c.464A>T (p.Lys155Ile) c.944A>T (p.Lys315Ile) c.989A>T (p.Lys330Ile) c.821A>T (p.Lys274Ile) c.1112A>T (p.Lys371Ile) c.1080+41A>T (n.1080+41A>T) | |
4 | g.154569677A>C | CA358515191 | FGB | c.1122A>C (p.Lys374Asn) n.939+370A>C c.465A>C (p.Lys155Asn) c.945A>C (p.Lys315Asn) c.990A>C (p.Lys330Asn) c.822A>C (p.Lys274Asn) c.1113A>C (p.Lys371Asn) c.1080+42A>C (n.1080+42A>C) | |
4 | g.154569677A>G | CA442013429 | FGB | c.1122A>G (p.Lys374=) n.939+370A>G c.465A>G (p.Lys155=) c.945A>G (p.Lys315=) c.990A>G (p.Lys330=) c.822A>G (p.Lys274=) c.1113A>G (p.Lys371=) c.1080+42A>G (n.1080+42A>G) | |
4 | g.154569677A>T | CA358515192 | FGB | c.1122A>T (p.Lys374Asn) n.939+370A>T c.465A>T (p.Lys155Asn) c.945A>T (p.Lys315Asn) c.990A>T (p.Lys330Asn) c.822A>T (p.Lys274Asn) c.1113A>T (p.Lys371Asn) c.1080+42A>T (n.1080+42A>T) | |
4 | g.154569678T>A | CA358515194 | FGB | c.1123T>A (p.Tyr375Asn) n.939+371T>A c.466T>A (p.Tyr156Asn) c.946T>A (p.Tyr316Asn) c.991T>A (p.Tyr331Asn) c.823T>A (p.Tyr275Asn) c.1114T>A (p.Tyr372Asn) c.1080+43T>A (n.1080+43T>A) | |
4 | g.154569678T>C | CA358515195 | FGB | c.1123T>C (p.Tyr375His) n.939+371T>C c.466T>C (p.Tyr156His) c.946T>C (p.Tyr316His) c.991T>C (p.Tyr331His) c.823T>C (p.Tyr275His) c.1114T>C (p.Tyr372His) c.1080+43T>C (n.1080+43T>C) | |
4 | g.154569678T>G | CA358515197 | FGB | c.1123T>G (p.Tyr375Asp) n.939+371T>G c.466T>G (p.Tyr156Asp) c.946T>G (p.Tyr316Asp) c.991T>G (p.Tyr331Asp) c.823T>G (p.Tyr275Asp) c.1114T>G (p.Tyr372Asp) c.1080+43T>G (n.1080+43T>G) | |
4 | g.154569679A= | CA1504935460 | FGB | c.1124A= (p.Tyr375=) n.939+372A= c.467A= (p.Tyr156=) c.947A= (p.Tyr316=) c.992A= (p.Tyr331=) c.824A= (p.Tyr275=) c.1115A= (p.Tyr372=) c.1080+44A= (n.1080+44A=) | |
4 | g.154569679A>C | CA358515199 | FGB | c.1124A>C (p.Tyr375Ser) n.939+372A>C c.467A>C (p.Tyr156Ser) c.947A>C (p.Tyr316Ser) c.992A>C (p.Tyr331Ser) c.824A>C (p.Tyr275Ser) c.1115A>C (p.Tyr372Ser) c.1080+44A>C (n.1080+44A>C) | |
4 | g.154569679A>G | CA358515201 | FGB | c.1124A>G (p.Tyr375Cys) n.939+372A>G c.467A>G (p.Tyr156Cys) c.947A>G (p.Tyr316Cys) c.992A>G (p.Tyr331Cys) c.824A>G (p.Tyr275Cys) c.1115A>G (p.Tyr372Cys) c.1080+44A>G (n.1080+44A>G) | ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC |
4 | g.154569679A>T | CA358515203 | FGB | c.1124A>T (p.Tyr375Phe) n.939+372A>T c.467A>T (p.Tyr156Phe) c.947A>T (p.Tyr316Phe) c.992A>T (p.Tyr331Phe) c.824A>T (p.Tyr275Phe) c.1115A>T (p.Tyr372Phe) c.1080+44A>T (n.1080+44A>T) | |
4 | g.154569680C>A | CA358515204 | FGB | c.1125C>A (p.Tyr375Ter) n.939+373C>A c.468C>A (p.Tyr156Ter) c.948C>A (p.Tyr316Ter) c.993C>A (p.Tyr331Ter) c.825C>A (p.Tyr275Ter) c.1116C>A (p.Tyr372Ter) c.1080+45C>A (n.1080+45C>A) | |
4 | g.154569680C= | CA1504935470 | FGB | c.1125C= (p.Tyr375=) n.939+373C= c.468C= (p.Tyr156=) c.948C= (p.Tyr316=) c.993C= (p.Tyr331=) c.825C= (p.Tyr275=) c.1116C= (p.Tyr372=) c.1080+45C= (n.1080+45C=) | |
4 | g.154569680C>G | CA358515205 | FGB | c.1125C>G (p.Tyr375Ter) n.939+373C>G c.468C>G (p.Tyr156Ter) c.948C>G (p.Tyr316Ter) c.993C>G (p.Tyr331Ter) c.825C>G (p.Tyr275Ter) c.1116C>G (p.Tyr372Ter) c.1080+45C>G (n.1080+45C>G) | |
4 | g.154569680C>T | CA3114724 | FGB | c.1125C>T (p.Tyr375=) n.939+373C>T c.468C>T (p.Tyr156=) c.948C>T (p.Tyr316=) c.993C>T (p.Tyr331=) c.825C>T (p.Tyr275=) c.1116C>T (p.Tyr372=) c.1080+45C>T (n.1080+45C>T) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.154569681A= | CA1504935477 | FGB | c.1126A= (p.Arg376=) n.939+374A= c.469A= (p.Arg157=) c.949A= (p.Arg317=) c.994A= (p.Arg332=) c.826A= (p.Arg276=) c.1117A= (p.Arg373=) c.1080+46A= (n.1080+46A=) | |
4 | g.154569681A>C | CA442013437 | FGB | c.1126A>C (p.Arg376=) n.939+374A>C c.469A>C (p.Arg157=) c.949A>C (p.Arg317=) c.994A>C (p.Arg332=) c.826A>C (p.Arg276=) c.1117A>C (p.Arg373=) c.1080+46A>C (n.1080+46A>C) | |
4 | g.154569681A>G | CA358515206 | FGB | c.1126A>G (p.Arg376Gly) n.939+374A>G c.469A>G (p.Arg157Gly) c.949A>G (p.Arg317Gly) c.994A>G (p.Arg332Gly) c.826A>G (p.Arg276Gly) c.1117A>G (p.Arg373Gly) c.1080+46A>G (n.1080+46A>G) | dbSNP gnomAD v2 gnomAD v4 |
4 | g.154569681A>T | CA358515208 | FGB | c.1126A>T (p.Arg376Ter) n.939+374A>T c.469A>T (p.Arg157Ter) c.949A>T (p.Arg317Ter) c.994A>T (p.Arg332Ter) c.826A>T (p.Arg276Ter) c.1117A>T (p.Arg373Ter) c.1080+46A>T (n.1080+46A>T) | |
4 | g.154569682G>A | CA358515209 | FGB | c.1127G>A (p.Arg376Lys) n.939+375G>A c.470G>A (p.Arg157Lys) c.950G>A (p.Arg317Lys) c.995G>A (p.Arg332Lys) c.827G>A (p.Arg276Lys) c.1118G>A (p.Arg373Lys) c.1080+47G>A (n.1080+47G>A) | dbSNP gnomAD v4 |
4 | g.154569682G>C | CA358515211 | FGB | c.1127G>C (p.Arg376Thr) n.939+375G>C c.470G>C (p.Arg157Thr) c.950G>C (p.Arg317Thr) c.995G>C (p.Arg332Thr) c.827G>C (p.Arg276Thr) c.1118G>C (p.Arg373Thr) c.1080+47G>C (n.1080+47G>C) | |
4 | g.154569682G= | CA1504935480 | FGB | c.1127G= (p.Arg376=) n.939+375G= c.470G= (p.Arg157=) c.950G= (p.Arg317=) c.995G= (p.Arg332=) c.827G= (p.Arg276=) c.1118G= (p.Arg373=) c.1080+47G= (n.1080+47G=) | |
4 | g.154569682G>T | CA358515210 | FGB | c.1127G>T (p.Arg376Ile) n.939+375G>T c.470G>T (p.Arg157Ile) c.950G>T (p.Arg317Ile) c.995G>T (p.Arg332Ile) c.827G>T (p.Arg276Ile) c.1118G>T (p.Arg373Ile) c.1080+47G>T (n.1080+47G>T) | |
4 | g.154569683A= | CA1504935482 | FGB | c.1128A= (p.Arg376=) n.939+376A= c.471A= (p.Arg157=) c.951A= (p.Arg317=) c.996A= (p.Arg332=) c.828A= (p.Arg276=) c.1119A= (p.Arg373=) c.1080+48A= (n.1080+48A=) | |
4 | g.154569683A>C | CA358515212 | FGB | c.1128A>C (p.Arg376Ser) n.939+376A>C c.471A>C (p.Arg157Ser) c.951A>C (p.Arg317Ser) c.996A>C (p.Arg332Ser) c.828A>C (p.Arg276Ser) c.1119A>C (p.Arg373Ser) c.1080+48A>C (n.1080+48A>C) | |
4 | g.154569683A>G | CA3114725 | FGB | c.1128A>G (p.Arg376=) n.939+376A>G c.471A>G (p.Arg157=) c.951A>G (p.Arg317=) c.996A>G (p.Arg332=) c.828A>G (p.Arg276=) c.1119A>G (p.Arg373=) c.1080+48A>G (n.1080+48A>G) | dbSNP ExAC gnomAD v2 gnomAD v4 |
4 | g.154569683A>T | CA358515214 | FGB | c.1128A>T (p.Arg376Ser) n.939+376A>T c.471A>T (p.Arg157Ser) c.951A>T (p.Arg317Ser) c.996A>T (p.Arg332Ser) c.828A>T (p.Arg276Ser) c.1119A>T (p.Arg373Ser) c.1080+48A>T (n.1080+48A>T) | |
4 | g.154569684G>A | CA358515216 | FGB | c.1129G>A (p.Gly377Arg) n.939+377G>A c.472G>A (p.Gly158Arg) c.952G>A (p.Gly318Arg) c.997G>A (p.Gly333Arg) c.829G>A (p.Gly277Arg) c.1120G>A (p.Gly374Arg) c.1080+49G>A (n.1080+49G>A) | gnomAD v4 |
4 | g.154569684G>C | CA358515217 | FGB | c.1129G>C (p.Gly377Arg) n.939+377G>C c.472G>C (p.Gly158Arg) c.952G>C (p.Gly318Arg) c.997G>C (p.Gly333Arg) c.829G>C (p.Gly277Arg) c.1120G>C (p.Gly374Arg) c.1080+49G>C (n.1080+49G>C) | gnomAD v4 |
4 | g.154569684G>T | CA358515219 | FGB | c.1129G>T (p.Gly377Ter) n.939+377G>T c.472G>T (p.Gly158Ter) c.952G>T (p.Gly318Ter) c.997G>T (p.Gly333Ter) c.829G>T (p.Gly277Ter) c.1120G>T (p.Gly374Ter) c.1080+49G>T (n.1080+49G>T) | |
4 | g.154569685G>A | CA358515221 | FGB | c.1130G>A (p.Gly377Glu) n.939+378G>A c.473G>A (p.Gly158Glu) c.953G>A (p.Gly318Glu) c.998G>A (p.Gly333Glu) c.830G>A (p.Gly277Glu) c.1121G>A (p.Gly374Glu) c.1080+50G>A (n.1080+50G>A) | |
4 | g.154569685G>C | CA358515223 | FGB | c.1130G>C (p.Gly377Ala) n.939+378G>C c.473G>C (p.Gly158Ala) c.953G>C (p.Gly318Ala) c.998G>C (p.Gly333Ala) c.830G>C (p.Gly277Ala) c.1121G>C (p.Gly374Ala) c.1080+50G>C (n.1080+50G>C) | |
4 | g.154569685G>T | CA358515224 | FGB | c.1130G>T (p.Gly377Val) n.939+378G>T c.473G>T (p.Gly158Val) c.953G>T (p.Gly318Val) c.998G>T (p.Gly333Val) c.830G>T (p.Gly277Val) c.1121G>T (p.Gly374Val) c.1080+50G>T (n.1080+50G>T) | |
4 | g.154569686A= | CA1504935485 | FGB | c.1131A= (p.Gly377=) n.939+379A= c.474A= (p.Gly158=) c.954A= (p.Gly318=) c.999A= (p.Gly333=) c.831A= (p.Gly277=) c.1122A= (p.Gly374=) c.1080+51A= (n.1080+51A=) | |
4 | g.154569686A>C | CA442013445 | FGB | c.1131A>C (p.Gly377=) n.939+379A>C c.474A>C (p.Gly158=) c.954A>C (p.Gly318=) c.999A>C (p.Gly333=) c.831A>C (p.Gly277=) c.1122A>C (p.Gly374=) c.1080+51A>C (n.1080+51A>C) | |
4 | g.154569686A>G | CA442013446 | FGB | c.1131A>G (p.Gly377=) n.939+379A>G c.474A>G (p.Gly158=) c.954A>G (p.Gly318=) c.999A>G (p.Gly333=) c.831A>G (p.Gly277=) c.1122A>G (p.Gly374=) c.1080+51A>G (n.1080+51A>G) | dbSNP |
4 | g.154569686A>T | CA442013448 | FGB | c.1131A>T (p.Gly377=) n.939+379A>T c.474A>T (p.Gly158=) c.954A>T (p.Gly318=) c.999A>T (p.Gly333=) c.831A>T (p.Gly277=) c.1122A>T (p.Gly374=) c.1080+51A>T (n.1080+51A>T) | |
4 | g.154569687A= | CA1504935489 | FGB | c.1132A= (p.Thr378=) n.939+380A= c.475A= (p.Thr159=) c.955A= (p.Thr319=) c.1000A= (p.Thr334=) c.832A= (p.Thr278=) c.1123A= (p.Thr375=) c.1080+52A= (n.1080+52A=) | |
4 | g.154569687A>C | CA3114726 | FGB | c.1132A>C (p.Thr378Pro) n.939+380A>C c.475A>C (p.Thr159Pro) c.955A>C (p.Thr319Pro) c.1000A>C (p.Thr334Pro) c.832A>C (p.Thr278Pro) c.1123A>C (p.Thr375Pro) c.1080+52A>C (n.1080+52A>C) | dbSNP ExAC gnomAD v2 gnomAD v4 |
4 | g.154569687A>G | CA358515227 | FGB | c.1132A>G (p.Thr378Ala) n.939+380A>G c.475A>G (p.Thr159Ala) c.955A>G (p.Thr319Ala) c.1000A>G (p.Thr334Ala) c.832A>G (p.Thr278Ala) c.1123A>G (p.Thr375Ala) c.1080+52A>G (n.1080+52A>G) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.154569687A>T | CA358515228 | FGB | c.1132A>T (p.Thr378Ser) n.939+380A>T c.475A>T (p.Thr159Ser) c.955A>T (p.Thr319Ser) c.1000A>T (p.Thr334Ser) c.832A>T (p.Thr278Ser) c.1123A>T (p.Thr375Ser) c.1080+52A>T (n.1080+52A>T) | |
4 | g.154569688C>A | CA358515234 | FGB | c.1133C>A (p.Thr378Lys) n.939+381C>A c.476C>A (p.Thr159Lys) c.956C>A (p.Thr319Lys) c.1001C>A (p.Thr334Lys) c.833C>A (p.Thr278Lys) c.1124C>A (p.Thr375Lys) c.1080+53C>A (n.1080+53C>A) | |
4 | g.154569688C>G | CA358515233 | FGB | c.1133C>G (p.Thr378Arg) n.939+381C>G c.476C>G (p.Thr159Arg) c.956C>G (p.Thr319Arg) c.1001C>G (p.Thr334Arg) c.833C>G (p.Thr278Arg) c.1124C>G (p.Thr375Arg) c.1080+53C>G (n.1080+53C>G) | |
4 | g.154569688C>T | CA358515231 | FGB | c.1133C>T (p.Thr378Ile) n.939+381C>T c.476C>T (p.Thr159Ile) c.956C>T (p.Thr319Ile) c.1001C>T (p.Thr334Ile) c.833C>T (p.Thr278Ile) c.1124C>T (p.Thr375Ile) c.1080+53C>T (n.1080+53C>T) | ClinVar gnomAD v4 |
4 | g.154569689A= | CA1504935494 | FGB | c.1134A= (p.Thr378=) n.939+382A= c.477A= (p.Thr159=) c.957A= (p.Thr319=) c.1002A= (p.Thr334=) c.834A= (p.Thr278=) c.1125A= (p.Thr375=) c.1080+54A= (n.1080+54A=) | |
4 | g.154569689A>C | CA442013453 | FGB | c.1134A>C (p.Thr378=) n.939+382A>C c.477A>C (p.Thr159=) c.957A>C (p.Thr319=) c.1002A>C (p.Thr334=) c.834A>C (p.Thr278=) c.1125A>C (p.Thr375=) c.1080+54A>C (n.1080+54A>C) | |
4 | g.154569689A>G | CA442013454 | FGB | c.1134A>G (p.Thr378=) n.939+382A>G c.477A>G (p.Thr159=) c.957A>G (p.Thr319=) c.1002A>G (p.Thr334=) c.834A>G (p.Thr278=) c.1125A>G (p.Thr375=) c.1080+54A>G (n.1080+54A>G) | dbSNP |
4 | g.154569689A>T | CA442013456 | FGB | c.1134A>T (p.Thr378=) n.939+382A>T c.477A>T (p.Thr159=) c.957A>T (p.Thr319=) c.1002A>T (p.Thr334=) c.834A>T (p.Thr278=) c.1125A>T (p.Thr375=) c.1080+54A>T (n.1080+54A>T) | |
4 | g.154569690G>A | CA358515237 | FGB | c.1135G>A (p.Ala379Thr) n.939+383G>A c.478G>A (p.Ala160Thr) c.958G>A (p.Ala320Thr) c.1003G>A (p.Ala335Thr) c.835G>A (p.Ala279Thr) c.1126G>A (p.Ala376Thr) c.1080+55G>A (n.1080+55G>A) | gnomAD v4 |
4 | g.154569690G>C | CA358515238 | FGB | c.1135G>C (p.Ala379Pro) n.939+383G>C c.478G>C (p.Ala160Pro) c.958G>C (p.Ala320Pro) c.1003G>C (p.Ala335Pro) c.835G>C (p.Ala279Pro) c.1126G>C (p.Ala376Pro) c.1080+55G>C (n.1080+55G>C) | |
4 | g.154569690G>T | CA358515239 | FGB | c.1135G>T (p.Ala379Ser) n.939+383G>T c.478G>T (p.Ala160Ser) c.958G>T (p.Ala320Ser) c.1003G>T (p.Ala335Ser) c.835G>T (p.Ala279Ser) c.1126G>T (p.Ala376Ser) c.1080+55G>T (n.1080+55G>T) | |
4 | g.154569691C>A | CA358515241 | FGB | c.1136C>A (p.Ala379Asp) n.939+384C>A c.479C>A (p.Ala160Asp) c.959C>A (p.Ala320Asp) c.1004C>A (p.Ala335Asp) c.836C>A (p.Ala279Asp) c.1127C>A (p.Ala376Asp) c.1080+56C>A (n.1080+56C>A) | |
4 | g.154569691C>G | CA358515242 | FGB | c.1136C>G (p.Ala379Gly) n.939+384C>G c.479C>G (p.Ala160Gly) c.959C>G (p.Ala320Gly) c.1004C>G (p.Ala335Gly) c.836C>G (p.Ala279Gly) c.1127C>G (p.Ala376Gly) c.1080+56C>G (n.1080+56C>G) | |
4 | g.154569691C>T | CA358515243 | FGB | c.1136C>T (p.Ala379Val) n.939+384C>T c.479C>T (p.Ala160Val) c.959C>T (p.Ala320Val) c.1004C>T (p.Ala335Val) c.836C>T (p.Ala279Val) c.1127C>T (p.Ala376Val) c.1080+56C>T (n.1080+56C>T) | |
4 | g.154569692C>A | CA442013459 | FGB | c.1137C>A (p.Ala379=) n.939+385C>A c.480C>A (p.Ala160=) c.960C>A (p.Ala320=) c.1005C>A (p.Ala335=) c.837C>A (p.Ala279=) c.1128C>A (p.Ala376=) c.1080+57C>A (n.1080+57C>A) | dbSNP gnomAD v2 gnomAD v4 |
4 | g.154569692C= | CA1504935498 | FGB | c.1137C= (p.Ala379=) n.939+385C= c.480C= (p.Ala160=) c.960C= (p.Ala320=) c.1005C= (p.Ala335=) c.837C= (p.Ala279=) c.1128C= (p.Ala376=) c.1080+57C= (n.1080+57C=) | |
4 | g.154569692C>G | CA442013461 | FGB | c.1137C>G (p.Ala379=) n.939+385C>G c.480C>G (p.Ala160=) c.960C>G (p.Ala320=) c.1005C>G (p.Ala335=) c.837C>G (p.Ala279=) c.1128C>G (p.Ala376=) c.1080+57C>G (n.1080+57C>G) | |
4 | g.154569692C>T | CA3114727 | FGB | c.1137C>T (p.Ala379=) n.939+385C>T c.480C>T (p.Ala160=) c.960C>T (p.Ala320=) c.1005C>T (p.Ala335=) c.837C>T (p.Ala279=) c.1128C>T (p.Ala376=) c.1080+57C>T (n.1080+57C>T) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.154569693G>A | CA3114728 | FGB | c.1138G>A (p.Gly380Ser) n.939+386G>A c.481G>A (p.Gly161Ser) c.961G>A (p.Gly321Ser) c.1006G>A (p.Gly336Ser) c.838G>A (p.Gly280Ser) c.1129G>A (p.Gly377Ser) c.1080+58G>A (n.1080+58G>A) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
4 | g.154569693G>C | CA358515247 | FGB | c.1138G>C (p.Gly380Arg) n.939+386G>C c.481G>C (p.Gly161Arg) c.961G>C (p.Gly321Arg) c.1006G>C (p.Gly336Arg) c.838G>C (p.Gly280Arg) c.1129G>C (p.Gly377Arg) c.1080+58G>C (n.1080+58G>C) | |
4 | g.154569693G= | CA1504935504 | FGB | c.1138G= (p.Gly380=) n.939+386G= c.481G= (p.Gly161=) c.961G= (p.Gly321=) c.1006G= (p.Gly336=) c.838G= (p.Gly280=) c.1129G= (p.Gly377=) c.1080+58G= (n.1080+58G=) | |
4 | g.154569693G>T | CA358515248 | FGB | c.1138G>T (p.Gly380Cys) n.939+386G>T c.481G>T (p.Gly161Cys) c.961G>T (p.Gly321Cys) c.1006G>T (p.Gly336Cys) c.838G>T (p.Gly280Cys) c.1129G>T (p.Gly377Cys) c.1080+58G>T (n.1080+58G>T) | |
4 | g.154569694G>A | CA358515250 | FGB | c.1139G>A (p.Gly380Asp) n.939+387G>A c.482G>A (p.Gly161Asp) c.962G>A (p.Gly321Asp) c.1007G>A (p.Gly336Asp) c.839G>A (p.Gly280Asp) c.1130G>A (p.Gly377Asp) c.1080+59G>A (n.1080+59G>A) | |
4 | g.154569694G>C | CA358515252 | FGB | c.1139G>C (p.Gly380Ala) n.939+387G>C c.482G>C (p.Gly161Ala) c.962G>C (p.Gly321Ala) c.1007G>C (p.Gly336Ala) c.839G>C (p.Gly280Ala) c.1130G>C (p.Gly377Ala) c.1080+59G>C (n.1080+59G>C) | |
4 | g.154569694G>T | CA358515254 | FGB | c.1139G>T (p.Gly380Val) n.939+387G>T c.482G>T (p.Gly161Val) c.962G>T (p.Gly321Val) c.1007G>T (p.Gly336Val) c.839G>T (p.Gly280Val) c.1130G>T (p.Gly377Val) c.1080+59G>T (n.1080+59G>T) | |
4 | g.154569695T>A | CA442013467 | FGB | c.1140T>A (p.Gly380=) n.939+388T>A c.483T>A (p.Gly161=) c.963T>A (p.Gly321=) c.1008T>A (p.Gly336=) c.840T>A (p.Gly280=) c.1131T>A (p.Gly377=) c.1080+60T>A (n.1080+60T>A) | |
4 | g.154569695T>C | CA108751698 | FGB | c.1140T>C (p.Gly380=) n.939+388T>C c.483T>C (p.Gly161=) c.963T>C (p.Gly321=) c.1008T>C (p.Gly336=) c.840T>C (p.Gly280=) c.1131T>C (p.Gly377=) c.1080+60T>C (n.1080+60T>C) | dbSNP |
4 | g.154569695T>G | CA442013468 | FGB | c.1140T>G (p.Gly380=) n.939+388T>G c.483T>G (p.Gly161=) c.963T>G (p.Gly321=) c.1008T>G (p.Gly336=) c.840T>G (p.Gly280=) c.1131T>G (p.Gly377=) c.1080+60T>G (n.1080+60T>G) | |
4 | g.154569695T= | CA1504935506 | FGB | c.1140T= (p.Gly380=) n.939+388T= c.483T= (p.Gly161=) c.963T= (p.Gly321=) c.1008T= (p.Gly336=) c.840T= (p.Gly280=) c.1131T= (p.Gly377=) c.1080+60T= (n.1080+60T=) | |
4 | g.154569696A>C | CA358515258 | FGB | c.1141A>C (p.Asn381His) n.939+389A>C c.484A>C (p.Asn162His) c.964A>C (p.Asn322His) c.1009A>C (p.Asn337His) c.841A>C (p.Asn281His) c.1132A>C (p.Asn378His) c.1080+61A>C (n.1080+61A>C) | |
4 | g.154569696A>G | CA358515257 | FGB | c.1141A>G (p.Asn381Asp) n.939+389A>G c.484A>G (p.Asn162Asp) c.964A>G (p.Asn322Asp) c.1009A>G (p.Asn337Asp) c.841A>G (p.Asn281Asp) c.1132A>G (p.Asn378Asp) c.1080+61A>G (n.1080+61A>G) | |
4 | g.154569696A>T | CA358515260 | FGB | c.1141A>T (p.Asn381Tyr) n.939+389A>T c.484A>T (p.Asn162Tyr) c.964A>T (p.Asn322Tyr) c.1009A>T (p.Asn337Tyr) c.841A>T (p.Asn281Tyr) c.1132A>T (p.Asn378Tyr) c.1080+61A>T (n.1080+61A>T) |