Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
19 | g.48703317A= | CA2340029967 | FUT2 | c.361A= (p.Arg121=) n.532T= | |
19 | g.48703317A>C | CA508272290 | FUT2 | c.361A>C (p.Arg121=) n.532T>G | dbSNP gnomAD v4 |
19 | g.48703317A>G | CA406709803 | FUT2 | c.361A>G (p.Arg121Gly) n.532T>C | |
19 | g.48703317A>T | CA406709811 | FUT2 | c.361A>T (p.Arg121Trp) n.532T>A | |
19 | g.48703318G>A | CA406709816 | FUT2 | c.362G>A (p.Arg121Lys) n.531C>T | |
19 | g.48703318G>C | CA406709819 | FUT2 | c.362G>C (p.Arg121Thr) n.531C>G | |
19 | g.48703318G>T | CA406709821 | FUT2 | c.362G>T (p.Arg121Met) n.531C>A | |
19 | g.48703319G>A | CA508272294 | FUT2 | c.363G>A (p.Arg121=) n.530C>T | COSMIC |
19 | g.48703319G>C | CA406709825 | FUT2 | c.363G>C (p.Arg121Ser) n.530C>G | |
19 | g.48703319G= | CA2340029968 | FUT2 | c.363G= (p.Arg121=) n.530C= | |
19 | g.48703319G>T | CA309352393 | FUT2 | c.363G>T (p.Arg121Ser) n.530C>A | dbSNP gnomAD v3 gnomAD v4 |
19 | g.48703320A>C | CA406709832 | FUT2 | c.364A>C (p.Ile122Leu) n.529T>G | |
19 | g.48703320A>G | CA406709835 | FUT2 | c.364A>G (p.Ile122Val) n.529T>C | |
19 | g.48703320A>T | CA406709838 | FUT2 | c.364A>T (p.Ile122Phe) n.529T>A | |
19 | g.48703321T>A | CA406709850 | FUT2 | c.365T>A (p.Ile122Asn) n.528A>T | |
19 | g.48703321T>C | CA406709845 | FUT2 | c.365T>C (p.Ile122Thr) n.528A>G | gnomAD v4 |
19 | g.48703321T>G | CA406709842 | FUT2 | c.365T>G (p.Ile122Ser) n.528A>C | |
19 | g.48703322C>A | CA508272297 | FUT2 | c.366C>A (p.Ile122=) n.527G>T | |
19 | g.48703322C= | CA2340029969 | FUT2 | c.366C= (p.Ile122=) n.527G= | |
19 | g.48703322C>G | CA406709854 | FUT2 | c.366C>G (p.Ile122Met) n.527G>C | |
19 | g.48703322C>T | CA508272298 | FUT2 | c.366C>T (p.Ile122=) n.527G>A | dbSNP gnomAD v2 gnomAD v4 |
19 | g.48703323C>A | CA406709864 | FUT2 | c.367C>A (p.Pro123Thr) n.526G>T | |
19 | g.48703323C= | CA2340029970 | FUT2 | c.367C= (p.Pro123=) n.526G= | |
19 | g.48703323C>G | CA406709859 | FUT2 | c.367C>G (p.Pro123Ala) n.526G>C | dbSNP |
19 | g.48703323C>T | CA9556224 | FUT2 | c.367C>T (p.Pro123Ser) n.526G>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
19 | g.48703324C>A | CA406709866 | FUT2 | c.368C>A (p.Pro123His) n.525G>T | |
19 | g.48703324C= | CA2340029971 | FUT2 | c.368C= (p.Pro123=) n.525G= | |
19 | g.48703324C>G | CA406709868 | FUT2 | c.368C>G (p.Pro123Arg) n.525G>C | |
19 | g.48703324C>T | CA406709870 | FUT2 | c.368C>T (p.Pro123Leu) n.525G>A | dbSNP gnomAD v4 |
19 | g.48703325C>A | CA508272300 | FUT2 | c.369C>A (p.Pro123=) n.524G>T | |
19 | g.48703325C= | CA2340029972 | FUT2 | c.369C= (p.Pro123=) n.524G= | |
19 | g.48703325C>G | CA508272301 | FUT2 | c.369C>G (p.Pro123=) n.524G>C | |
19 | g.48703325C>T | CA9556225 | FUT2 | c.369C>T (p.Pro123=) n.524G>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
19 | g.48703326T>A | CA406709877 | FUT2 | c.370T>A (p.Trp124Arg) n.523A>T | |
19 | g.48703326T>C | CA406709880 | FUT2 | c.370T>C (p.Trp124Arg) n.523A>G | dbSNP gnomAD v2 gnomAD v4 |
19 | g.48703326T>G | CA406709883 | FUT2 | c.370T>G (p.Trp124Gly) n.523A>C | |
19 | g.48703326T= | CA2340029973 | FUT2 | c.370T= (p.Trp124=) n.523A= | |
19 | g.48703327G>A | CA406709887 | FUT2 | c.371G>A (p.Trp124Ter) n.522C>T | |
19 | g.48703327G>C | CA406709894 | FUT2 | c.371G>C (p.Trp124Ser) n.522C>G | gnomAD v4 |
19 | g.48703327G>T | CA406709897 | FUT2 | c.371G>T (p.Trp124Leu) n.522C>A | |
19 | g.48703328G>A | CA9556227 | FUT2 | c.372G>A (p.Trp124Ter) n.521C>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
19 | g.48703328G>C | CA406709902 | FUT2 | c.372G>C (p.Trp124Cys) n.521C>G | |
19 | g.48703328G= | CA2340029974 | FUT2 | c.372G= (p.Trp124=) n.521C= | |
19 | g.48703328G>T | CA9556226 | FUT2 | c.372G>T (p.Trp124Cys) n.521C>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.48703329C>A | CA406709913 | FUT2 | c.373C>A (p.Gln125Lys) n.520G>T | COSMIC |
19 | g.48703329C>G | CA406709916 | FUT2 | c.373C>G (p.Gln125Glu) n.520G>C | |
19 | g.48703329C>T | CA406709919 | FUT2 | c.373C>T (p.Gln125Ter) n.520G>A | |
19 | g.48703330A>C | CA406709924 | FUT2 | c.374A>C (p.Gln125Pro) n.519T>G | |
19 | g.48703330A>G | CA406709926 | FUT2 | c.374A>G (p.Gln125Arg) n.519T>C | |
19 | g.48703330A>T | CA406709931 | FUT2 | c.374A>T (p.Gln125Leu) n.519T>A | |
19 | g.48703331G>A | CA508272305 | FUT2 | c.375G>A (p.Gln125=) n.518C>T | |
19 | g.48703331G>C | CA406709935 | FUT2 | c.375G>C (p.Gln125His) n.518C>G | |
19 | g.48703331G>T | CA406709938 | FUT2 | c.375G>T (p.Gln125His) n.518C>A | |
19 | g.48703332A>C | CA406709944 | FUT2 | c.376A>C (p.Asn126His) n.517T>G | |
19 | g.48703332A>G | CA406709946 | FUT2 | c.376A>G (p.Asn126Asp) n.517T>C | |
19 | g.48703332A>T | CA406709949 | FUT2 | c.376A>T (p.Asn126Tyr) n.517T>A | |
19 | g.48703333A>C | CA406709956 | FUT2 | c.377A>C (p.Asn126Thr) n.516T>G | |
19 | g.48703333A>G | CA406709959 | FUT2 | c.377A>G (p.Asn126Ser) n.516T>C | |
19 | g.48703333A>T | CA406709954 | FUT2 | c.377A>T (p.Asn126Ile) n.516T>A | gnomAD v4 |
19 | g.48703334C>A | CA406709962 | FUT2 | c.378C>A (p.Asn126Lys) n.515G>T | |
19 | g.48703334C= | CA2340029975 | FUT2 | c.378C= (p.Asn126=) n.515G= | |
19 | g.48703334C>G | CA406709965 | FUT2 | c.378C>G (p.Asn126Lys) n.515G>C | |
19 | g.48703334C>T | CA309352399 | FUT2 | c.378C>T (p.Asn126=) n.515G>A | dbSNP gnomAD v3 gnomAD v4 |
19 | g.48703335T>A | CA406709982 | FUT2 | c.379T>A (p.Tyr127Asn) n.514A>T | |
19 | g.48703335T>C | CA406709984 | FUT2 | c.379T>C (p.Tyr127His) n.514A>G | |
19 | g.48703335T>G | CA406709987 | FUT2 | c.379T>G (p.Tyr127Asp) n.514A>C | |
19 | g.48703336A>C | CA406709997 | FUT2 | c.380A>C (p.Tyr127Ser) n.513T>G | dbSNP |
19 | g.48703336A>G | CA406709992 | FUT2 | c.380A>G (p.Tyr127Cys) n.513T>C | |
19 | g.48703336A>T | CA406709994 | FUT2 | c.380A>T (p.Tyr127Phe) n.513T>A | |
19 | g.48703337C>A | CA406710002 | FUT2 | c.381C>A (p.Tyr127Ter) n.512G>T | dbSNP gnomAD v2 |
19 | g.48703337C= | CA2340029976 | FUT2 | c.381C= (p.Tyr127=) n.512G= | |
19 | g.48703337C>G | CA406710006 | FUT2 | c.381C>G (p.Tyr127Ter) n.512G>C | |
19 | g.48703337C>T | CA508272309 | FUT2 | c.381C>T (p.Tyr127=) n.512G>A | |
19 | g.48703338C>A | CA406710011 | FUT2 | c.382C>A (p.His128Asn) n.511G>T | dbSNP gnomAD v3 gnomAD v4 |
19 | g.48703338C= | CA2340029977 | FUT2 | c.382C= (p.His128=) n.511G= | |
19 | g.48703338C>G | CA406710014 | FUT2 | c.382C>G (p.His128Asp) n.511G>C | |
19 | g.48703338C>T | CA406710018 | FUT2 | c.382C>T (p.His128Tyr) n.511G>A | dbSNP gnomAD v2 gnomAD v4 |
19 | g.48703339A>C | CA406710023 | FUT2 | c.383A>C (p.His128Pro) n.510T>G | dbSNP gnomAD v3 gnomAD v4 |
19 | g.48703339A>G | CA406710028 | FUT2 | c.383A>G (p.His128Arg) n.510T>C | |
19 | g.48703339A>T | CA406710026 | FUT2 | c.383A>T (p.His128Leu) n.510T>A | |
19 | g.48703340C>A | CA406710033 | FUT2 | c.384C>A (p.His128Gln) n.509G>T | |
19 | g.48703340C>G | CA406710035 | FUT2 | c.384C>G (p.His128Gln) n.509G>C | |
19 | g.48703340C>T | CA508272314 | FUT2 | c.384C>T (p.His128=) n.509G>A | |
19 | g.48703341C>A | CA406710040 | FUT2 | c.385C>A (p.Leu129Met) n.508G>T | |
19 | g.48703341C= | CA2340029978 | FUT2 | c.385C= (p.Leu129=) n.508G= | |
19 | g.48703341C>G | CA406710043 | FUT2 | c.385C>G (p.Leu129Val) n.508G>C | dbSNP gnomAD v2 |
19 | g.48703341C>T | CA309352401 | FUT2 | c.385C>T (p.Leu129=) n.508G>A | dbSNP |
19 | g.48703342T>A | CA406710048 | FUT2 | c.386T>A (p.Leu129Gln) n.507A>T | |
19 | g.48703342T>C | CA406710050 | FUT2 | c.386T>C (p.Leu129Pro) n.507A>G | |
19 | g.48703342T>G | CA9556228 | FUT2 | c.386T>G (p.Leu129Arg) n.507A>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
19 | g.48703342T= | CA2340029979 | FUT2 | c.386T= (p.Leu129=) n.507A= | |
19 | g.48703343G>A | CA508272318 | FUT2 | c.387G>A (p.Leu129=) n.506C>T | |
19 | g.48703343G>C | CA508272319 | FUT2 | c.387G>C (p.Leu129=) n.506C>G | dbSNP |
19 | g.48703343G= | CA2340029980 | FUT2 | c.387G= (p.Leu129=) n.506C= | |
19 | g.48703343G>T | CA508272320 | FUT2 | c.387G>T (p.Leu129=) n.506C>A | |
19 | g.48703344A>C | CA406710057 | FUT2 | c.388A>C (p.Asn130His) n.505T>G | |
19 | g.48703344A>G | CA406710060 | FUT2 | c.388A>G (p.Asn130Asp) n.505T>C | |
19 | g.48703344A>T | CA406710062 | FUT2 | c.388A>T (p.Asn130Tyr) n.505T>A | |
19 | g.48703345A>C | CA406710073 | FUT2 | c.389A>C (p.Asn130Thr) n.504T>G | |
19 | g.48703345A>G | CA406710070 | FUT2 | c.389A>G (p.Asn130Ser) n.504T>C | |
19 | g.48703345A>T | CA406710067 | FUT2 | c.389A>T (p.Asn130Ile) n.504T>A | |
19 | g.48703346C>A | CA406710078 | FUT2 | c.390C>A (p.Asn130Lys) n.503G>T | |
19 | g.48703346C= | CA2340029981 | FUT2 | c.390C= (p.Asn130=) n.503G= | |
19 | g.48703346C>G | CA406710084 | FUT2 | c.390C>G (p.Asn130Lys) n.503G>C | dbSNP |
19 | g.48703346C>T | CA9556229 | FUT2 | c.390C>T (p.Asn130=) n.503G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.48703347G>A | CA406710093 | FUT2 | c.391G>A (p.Asp131Asn) n.502C>T | dbSNP gnomAD v3 gnomAD v4 |
19 | g.48703347G>C | CA406710095 | FUT2 | c.391G>C (p.Asp131His) n.502C>G | |
19 | g.48703347G= | CA2340029982 | FUT2 | c.391G= (p.Asp131=) n.502C= | |
19 | g.48703347G>T | CA406710097 | FUT2 | c.391G>T (p.Asp131Tyr) n.502C>A | gnomAD v4 |
19 | g.48703348A>C | CA406710100 | FUT2 | c.392A>C (p.Asp131Ala) n.501T>G | |
19 | g.48703348A>G | CA406710102 | FUT2 | c.392A>G (p.Asp131Gly) n.501T>C | |
19 | g.48703348A>T | CA406710103 | FUT2 | c.392A>T (p.Asp131Val) n.501T>A | |
19 | g.48703349C>A | CA406710108 | FUT2 | c.393C>A (p.Asp131Glu) n.500G>T | |
19 | g.48703349C>G | CA406710105 | FUT2 | c.393C>G (p.Asp131Glu) n.500G>C | |
19 | g.48703349C>T | CA508272323 | FUT2 | c.393C>T (p.Asp131=) n.500G>A | |
19 | g.48703350T>A | CA406710111 | FUT2 | c.394T>A (p.Trp132Arg) n.499A>T | |
19 | g.48703350T>C | CA9556230 | FUT2 | c.394T>C (p.Trp132Arg) n.499A>G | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.48703350T>G | CA406710114 | FUT2 | c.394T>G (p.Trp132Gly) n.499A>C | |
19 | g.48703350T= | CA2340029983 | FUT2 | c.394T= (p.Trp132=) n.499A= | |
19 | g.48703351G>A | CA406710117 | FUT2 | c.395G>A (p.Trp132Ter) n.498C>T | |
19 | g.48703351G>C | CA406710119 | FUT2 | c.395G>C (p.Trp132Ser) n.498C>G | |
19 | g.48703351G>T | CA406710121 | FUT2 | c.395G>T (p.Trp132Leu) n.498C>A | |
19 | g.48703352G>A | CA406710128 | FUT2 | c.396G>A (p.Trp132Ter) n.497C>T | |
19 | g.48703352G>C | CA406710123 | FUT2 | c.396G>C (p.Trp132Cys) n.497C>G | |
19 | g.48703352G>T | CA406710126 | FUT2 | c.396G>T (p.Trp132Cys) n.497C>A | |
19 | g.48703353A= | CA2340029984 | FUT2 | c.397A= (p.Met133=) n.496T= | |
19 | g.48703353A>C | CA406710131 | FUT2 | c.397A>C (p.Met133Leu) n.496T>G | |
19 | g.48703353A>G | CA9556231 | FUT2 | c.397A>G (p.Met133Val) n.496T>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
19 | g.48703353A>T | CA406710134 | FUT2 | c.397A>T (p.Met133Leu) n.496T>A | |
19 | g.48703354T>A | CA406710142 | FUT2 | c.398T>A (p.Met133Lys) n.495A>T | |
19 | g.48703354T>C | CA406710144 | FUT2 | c.398T>C (p.Met133Thr) n.495A>G | |
19 | g.48703354T>G | CA406710146 | FUT2 | c.398T>G (p.Met133Arg) n.495A>C | |
19 | g.48703355G>A | CA406710149 | FUT2 | c.399G>A (p.Met133Ile) n.494C>T | |
19 | g.48703355G>C | CA406710151 | FUT2 | c.399G>C (p.Met133Ile) n.494C>G | |
19 | g.48703355G>T | CA406710153 | FUT2 | c.399G>T (p.Met133Ile) n.494C>A | |
19 | g.48703356G>A | CA406710157 | FUT2 | c.400G>A (p.Glu134Lys) n.493C>T | dbSNP |
19 | g.48703356G>C | CA406710158 | FUT2 | c.400G>C (p.Glu134Gln) n.493C>G | |
19 | g.48703356G= | CA2340029985 | FUT2 | c.400G= (p.Glu134=) n.493C= | |
19 | g.48703356G>T | CA406710160 | FUT2 | c.400G>T (p.Glu134Ter) n.493C>A | |
19 | g.48703357A>C | CA406710164 | FUT2 | c.401A>C (p.Glu134Ala) n.492T>G | |
19 | g.48703357A>G | CA406710169 | FUT2 | c.401A>G (p.Glu134Gly) n.492T>C | |
19 | g.48703357A>T | CA406710167 | FUT2 | c.401A>T (p.Glu134Val) n.492T>A | gnomAD v4 |
19 | g.48703357_48703358insT | CA2586240156 | FUT2 | c.401_402insT (p.Glu134AspfsTer?) n.491_492insA | gnomAD v4 |
19 | g.48703358G>A | CA9556232 | FUT2 | c.402G>A (p.Glu134=) n.491C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.48703358G>C | CA406710175 | FUT2 | c.402G>C (p.Glu134Asp) n.491C>G | |
19 | g.48703358G= | CA2340029986 | FUT2 | c.402G= (p.Glu134=) n.491C= | |
19 | g.48703358G>T | CA406710177 | FUT2 | c.402G>T (p.Glu134Asp) n.491C>A | |
19 | g.48703359G>A | CA9556233 | FUT2 | c.403G>A (p.Glu135Lys) n.490C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.48703359G>C | CA406710181 | FUT2 | c.403G>C (p.Glu135Gln) n.490C>G | |
19 | g.48703359G= | CA2340029987 | FUT2 | c.403G= (p.Glu135=) n.490C= | |
19 | g.48703359G>T | CA406710183 | FUT2 | c.403G>T (p.Glu135Ter) n.490C>A | |
19 | g.48703360A>C | CA406710186 | FUT2 | c.404A>C (p.Glu135Ala) n.489T>G | |
19 | g.48703360A>G | CA406710189 | FUT2 | c.404A>G (p.Glu135Gly) n.489T>C | gnomAD v4 |
19 | g.48703360A>T | CA406710191 | FUT2 | c.404A>T (p.Glu135Val) n.489T>A | |
19 | g.48703361G>A | CA508272332 | FUT2 | c.405G>A (p.Glu135=) n.488C>T | dbSNP gnomAD v2 gnomAD v4 |
19 | g.48703361G>C | CA309352410 | FUT2 | c.405G>C (p.Glu135Asp) n.488C>G | dbSNP |
19 | g.48703361G= | CA2340029988 | FUT2 | c.405G= (p.Glu135=) n.488C= | |
19 | g.48703361G>T | CA406710198 | FUT2 | c.405G>T (p.Glu135Asp) n.488C>A | |
19 | g.48703361_48703362insCG | CA2517881269 | FUT2 | c.405_406insCG (p.Glu136ArgfsTer?) n.488_489insGC | |
19 | g.48703362G>A | CA406710205 | FUT2 | c.406G>A (p.Glu136Lys) n.487C>T | |
19 | g.48703362G>C | CA406710204 | FUT2 | c.406G>C (p.Glu136Gln) n.487C>G | |
19 | g.48703362G>T | CA406710202 | FUT2 | c.406G>T (p.Glu136Ter) n.487C>A | |
19 | g.48703362_48703364delinsGAA | CA2340029989 | FUT2 | c.406_408delinsGAA (p.Glu136=) n.485_487delinsTTC | |
19 | g.48703363A>C | CA406710207 | FUT2 | c.407A>C (p.Glu136Ala) n.486T>G | |
19 | g.48703363A>G | CA406710208 | FUT2 | c.407A>G (p.Glu136Gly) n.486T>C | |
19 | g.48703363A>T | CA406710209 | FUT2 | c.407A>T (p.Glu136Val) n.486T>A | |
19 | g.48703363_48703364del | CA2340029990 | FUT2 | c.407_408del (p.Glu136ValfsTer?) n.485_486del | dbSNP |
19 | g.48703364A= | CA2340029991 | FUT2 | c.408A= (p.Glu136=) n.485T= | |
19 | g.48703364A>C | CA406710212 | FUT2 | c.408A>C (p.Glu136Asp) n.485T>G | |
19 | g.48703364A>G | CA9556234 | FUT2 | c.408A>G (p.Glu136=) n.485T>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.48703364A>T | CA406710215 | FUT2 | c.408A>T (p.Glu136Asp) n.485T>A | |
19 | g.48703365del | CA645614262 | FUT2 | c.409del (p.Tyr137ThrfsTer?) n.484del | COSMIC |
19 | g.48703365T>A | CA406710218 | FUT2 | c.409T>A (p.Tyr137Asn) n.484A>T | |
19 | g.48703365T>C | CA406710220 | FUT2 | c.409T>C (p.Tyr137His) n.484A>G | |
19 | g.48703365T>G | CA406710222 | FUT2 | c.409T>G (p.Tyr137Asp) n.484A>C | |
19 | g.48703366A= | CA2340029992 | FUT2 | c.410A= (p.Tyr137=) n.483T= | |
19 | g.48703366A>C | CA406710225 | FUT2 | c.410A>C (p.Tyr137Ser) n.483T>G | dbSNP gnomAD v4 |
19 | g.48703366A>G | CA406710226 | FUT2 | c.410A>G (p.Tyr137Cys) n.483T>C | |
19 | g.48703366A>T | CA406710229 | FUT2 | c.410A>T (p.Tyr137Phe) n.483T>A | |
19 | g.48703366_48703367insACCC | CA309352413 | FUT2 | c.410_411insACCC (p.Tyr137Ter) n.482_483insGGGT | dbSNP |
19 | g.48703367C>A | CA406710233 | FUT2 | c.411C>A (p.Tyr137Ter) n.482G>T | |
19 | g.48703367C>G | CA406710232 | FUT2 | c.411C>G (p.Tyr137Ter) n.482G>C | |
19 | g.48703367C>T | CA508272338 | FUT2 | c.411C>T (p.Tyr137=) n.482G>A | gnomAD v4 |
19 | g.48703368C>A | CA406710236 | FUT2 | c.412C>A (p.Arg138Ser) n.481G>T | |
19 | g.48703368C= | CA2340029993 | FUT2 | c.412C= (p.Arg138=) n.481G= | |
19 | g.48703368C>G | CA406710239 | FUT2 | c.412C>G (p.Arg138Gly) n.481G>C | |
19 | g.48703368C>T | CA9556235 | FUT2 | c.412C>T (p.Arg138Cys) n.481G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.48703369G>A | CA9556236 | FUT2 | c.413G>A (p.Arg138His) n.480C>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
19 | g.48703369G>C | CA406710242 | FUT2 | c.413G>C (p.Arg138Pro) n.480C>G | COSMIC |
19 | g.48703369G= | CA2340029994 | FUT2 | c.413G= (p.Arg138=) n.480C= | |
19 | g.48703369G>T | CA406710244 | FUT2 | c.413G>T (p.Arg138Leu) n.480C>A | |
19 | g.48703370C>A | CA508272341 | FUT2 | c.414C>A (p.Arg138=) n.479G>T | |
19 | g.48703370C= | CA2340029995 | FUT2 | c.414C= (p.Arg138=) n.479G= | |
19 | g.48703370C>G | CA508272343 | FUT2 | c.414C>G (p.Arg138=) n.479G>C | |
19 | g.48703370C>T | CA9556237 | FUT2 | c.414C>T (p.Arg138=) n.479G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.48703371C>A | CA406710250 | FUT2 | c.415C>A (p.His139Asn) n.478G>T | |
19 | g.48703371C>G | CA406710252 | FUT2 | c.415C>G (p.His139Asp) n.478G>C | |
19 | g.48703371C>T | CA406710254 | FUT2 | c.415C>T (p.His139Tyr) n.478G>A | gnomAD v4 |
19 | g.48703372A>C | CA406710256 | FUT2 | c.416A>C (p.His139Pro) n.477T>G | |
19 | g.48703372A>G | CA406710258 | FUT2 | c.416A>G (p.His139Arg) n.477T>C | |
19 | g.48703372A>T | CA406710260 | FUT2 | c.416A>T (p.His139Leu) n.477T>A | |
19 | g.48703373C>A | CA406710263 | FUT2 | c.417C>A (p.His139Gln) n.476G>T | |
19 | g.48703373C= | CA2340029996 | FUT2 | c.417C= (p.His139=) n.476G= | |
19 | g.48703373C>G | CA406710264 | FUT2 | c.417C>G (p.His139Gln) n.476G>C | dbSNP |
19 | g.48703373C>T | CA508272350 | FUT2 | c.417C>T (p.His139=) n.476G>A | |
19 | g.48703374A= | CA2340029997 | FUT2 | c.418A= (p.Ile140=) n.475T= | |
19 | g.48703374A>C | CA406710268 | FUT2 | c.418A>C (p.Ile140Leu) n.475T>G | dbSNP |
19 | g.48703374A>G | CA406710271 | FUT2 | c.418A>G (p.Ile140Val) n.475T>C | |
19 | g.48703374A>T | CA122800 | FUT2 | c.418A>T (p.Ile140Phe) n.475T>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.48703375T>A | CA406710274 | FUT2 | c.419T>A (p.Ile140Asn) n.474A>T | dbSNP |
19 | g.48703375T>C | CA406710276 | FUT2 | c.419T>C (p.Ile140Thr) n.474A>G | |
19 | g.48703375T>G | CA406710277 | FUT2 | c.419T>G (p.Ile140Ser) n.474A>C | |
19 | g.48703375T= | CA2340029998 | FUT2 | c.419T= (p.Ile140=) n.474A= | |
19 | g.48703376C>A | CA508272354 | FUT2 | c.420C>A (p.Ile140=) n.473G>T | |
19 | g.48703376C= | CA2340029999 | FUT2 | c.420C= (p.Ile140=) n.473G= | |
19 | g.48703376C>G | CA406710280 | FUT2 | c.420C>G (p.Ile140Met) n.473G>C | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.48703376C>T | CA508272353 | FUT2 | c.420C>T (p.Ile140=) n.473G>A | dbSNP gnomAD v3 gnomAD v4 |
19 | g.48703377C>A | CA406710283 | FUT2 | c.421C>A (p.Pro141Thr) n.472G>T | gnomAD v4 |
19 | g.48703377C>G | CA406710285 | FUT2 | c.421C>G (p.Pro141Ala) n.472G>C | |
19 | g.48703377C>T | CA406710287 | FUT2 | c.421C>T (p.Pro141Ser) n.472G>A | |
19 | g.48703378C>A | CA406710290 | FUT2 | c.422C>A (p.Pro141Gln) n.471G>T | gnomAD v4 |
19 | g.48703378C= | CA2340030000 | FUT2 | c.422C= (p.Pro141=) n.471G= | |
19 | g.48703378C>G | CA9556238 | FUT2 | c.422C>G (p.Pro141Arg) n.471G>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
19 | g.48703378C>T | CA9556239 | FUT2 | c.422C>T (p.Pro141Leu) n.471G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.48703379G>A | CA9556241 | FUT2 | c.423G>A (p.Pro141=) n.470C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
19 | g.48703379G>C | CA9556242 | FUT2 | c.423G>C (p.Pro141=) n.470C>G | dbSNP ExAC gnomAD v2 gnomAD v4 |
19 | g.48703379G= | CA2340030001 | FUT2 | c.423G= (p.Pro141=) n.470C= | |
19 | g.48703379G>T | CA9556240 | FUT2 | c.423G>T (p.Pro141=) n.470C>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.48703383dup | CA2340030002 | FUT2 | c.427dup (p.Glu143GlyfsTer?) n.470dup | dbSNP |
19 | g.48703383del | CA645614263 | FUT2 | c.427del (p.Glu143SerfsTer?) n.470del | COSMIC |
19 | g.48703380G>A | CA406710302 | FUT2 | c.424G>A (p.Gly142Arg) n.469C>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.48703380G>C | CA406710304 | FUT2 | c.424G>C (p.Gly142Arg) n.469C>G | gnomAD v4 |
19 | g.48703380G= | CA2340030003 | FUT2 | c.424G= (p.Gly142=) n.469C= | |
19 | g.48703380G>T | CA406710306 | FUT2 | c.424G>T (p.Gly142Trp) n.469C>A | |
19 | g.48703381G>A | CA406710307 | FUT2 | c.425G>A (p.Gly142Glu) n.468C>T | COSMIC |
19 | g.48703381G>C | CA406710309 | FUT2 | c.425G>C (p.Gly142Ala) n.468C>G | dbSNP gnomAD v2 |
19 | g.48703381G= | CA2340030004 | FUT2 | c.425G= (p.Gly142=) n.468C= | |
19 | g.48703381G>T | CA406710310 | FUT2 | c.425G>T (p.Gly142Val) n.468C>A | |
19 | g.48703382G>A | CA508272367 | FUT2 | c.426G>A (p.Gly142=) n.467C>T | gnomAD v4 |
19 | g.48703382G>C | CA508272368 | FUT2 | c.426G>C (p.Gly142=) n.467C>G | |
19 | g.48703382G>T | CA508272369 | FUT2 | c.426G>T (p.Gly142=) n.467C>A | |
19 | g.48703382_48703383insC | CA2586240159 | FUT2 | c.426_427insC (p.Glu143ArgfsTer?) n.466_467insG | gnomAD v4 |
19 | g.48703382_48703383insCGCT | CA2586240157 | FUT2 | c.426_427insCGCT (p.Glu143ArgfsTer2) n.466_467insAGCG | gnomAD v4 |
19 | g.48703382_48703383insCGCTGT | CA2586240158 | FUT2 | c.426_427insCGCTGT (p.Gly142_Glu143insArgCys) n.466_467insACAGCG | gnomAD v4 |
19 | g.48703383G>A | CA406710311 | FUT2 | c.427G>A (p.Glu143Lys) n.466C>T | |
19 | g.48703383G>C | CA406710313 | FUT2 | c.427G>C (p.Glu143Gln) n.466C>G | gnomAD v4 |
19 | g.48703383G= | CA2340030005 | FUT2 | c.427G= (p.Glu143=) n.466C= | |
19 | g.48703383G>T | CA406710314 | FUT2 | c.427G>T (p.Glu143Ter) n.466C>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.48703383_48703384insC | CA2340030006 | FUT2 | c.427_428insC (p.Glu143AlafsTer?) n.465_466insG | dbSNP gnomAD v4 |
19 | g.48703384A= | CA2340030007 | FUT2 | c.428A= (p.Glu143=) n.465T= | |
19 | g.48703384A>C | CA406710316 | FUT2 | c.428A>C (p.Glu143Ala) n.465T>G | |
19 | g.48703384A>G | CA406710318 | FUT2 | c.428A>G (p.Glu143Gly) n.465T>C | |
19 | g.48703384A>T | CA406710320 | FUT2 | c.428A>T (p.Glu143Val) n.465T>A | dbSNP gnomAD v4 |
19 | g.48703385G>A | CA9556243 | FUT2 | c.429G>A (p.Glu143=) n.464C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.48703385G>C | CA406710324 | FUT2 | c.429G>C (p.Glu143Asp) n.464C>G | |
19 | g.48703385G= | CA2340030008 | FUT2 | c.429G= (p.Glu143=) n.464C= | |
19 | g.48703385G>T | CA406710322 | FUT2 | c.429G>T (p.Glu143Asp) n.464C>A | |
19 | g.48703386T>A | CA406710327 | FUT2 | c.430T>A (p.Tyr144Asn) n.463A>T | |
19 | g.48703386T>C | CA406710329 | FUT2 | c.430T>C (p.Tyr144His) n.463A>G | |
19 | g.48703386T>G | CA406710330 | FUT2 | c.430T>G (p.Tyr144Asp) n.463A>C | dbSNP gnomAD v3 gnomAD v4 |
19 | g.48703386T= | CA2340030009 | FUT2 | c.430T= (p.Tyr144=) n.463A= | |
19 | g.48703386_48703388delinsTAC | CA2340030010 | FUT2 | c.430_432delinsTAC (p.Tyr144=) n.461_463delinsGTA | |
19 | g.48703387A>C | CA406710333 | FUT2 | c.431A>C (p.Tyr144Ser) n.462T>G | |
19 | g.48703387A>G | CA406710335 | FUT2 | c.431A>G (p.Tyr144Cys) n.462T>C | |
19 | g.48703387A>T | CA406710337 | FUT2 | c.431A>T (p.Tyr144Phe) n.462T>A | ClinVar |
19 | g.48703387_48703388del | CA2340030011 | FUT2 | c.431_432del (p.Tyr144CysfsTer?) n.461_462del | dbSNP gnomAD v4 |
19 | g.48703388C>A | CA406710342 | FUT2 | c.432C>A (p.Tyr144Ter) n.461G>T | |
19 | g.48703388C= | CA2340030012 | FUT2 | c.432C= (p.Tyr144=) n.461G= | |
19 | g.48703388C>G | CA406710340 | FUT2 | c.432C>G (p.Tyr144Ter) n.461G>C | |
19 | g.48703388C>T | CA508272379 | FUT2 | c.432C>T (p.Tyr144=) n.461G>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.48703389G>A | CA9556244 | FUT2 | c.433G>A (p.Val145Ile) n.460C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
19 | g.48703389G>C | CA406710349 | FUT2 | c.433G>C (p.Val145Leu) n.460C>G | |
19 | g.48703389G= | CA2340030013 | FUT2 | c.433G= (p.Val145=) n.460C= | |
19 | g.48703389G>T | CA406710351 | FUT2 | c.433G>T (p.Val145Phe) n.460C>A | |
19 | g.48703390T>A | CA406710355 | FUT2 | c.434T>A (p.Val145Asp) n.459A>T | |
19 | g.48703390T>C | CA406710356 | FUT2 | c.434T>C (p.Val145Ala) n.459A>G | dbSNP gnomAD v4 |
19 | g.48703390T>G | CA406710358 | FUT2 | c.434T>G (p.Val145Gly) n.459A>C | gnomAD v3 gnomAD v4 |
19 | g.48703390T= | CA2340030014 | FUT2 | c.434T= (p.Val145=) n.459A= | |
19 | g.48703391C>A | CA508272382 | FUT2 | c.435C>A (p.Val145=) n.458G>T | |
19 | g.48703391C>G | CA508272383 | FUT2 | c.435C>G (p.Val145=) n.458G>C | |
19 | g.48703391C>T | CA508272384 | FUT2 | c.435C>T (p.Val145=) n.458G>A | |
19 | g.48703392C>A | CA406710363 | FUT2 | c.436C>A (p.Arg146Ser) n.457G>T | |
19 | g.48703392C= | CA2340030015 | FUT2 | c.436C= (p.Arg146=) n.457G= | |
19 | g.48703392C>G | CA406710362 | FUT2 | c.436C>G (p.Arg146Gly) n.457G>C | |
19 | g.48703392C>T | CA9556245 | FUT2 | c.436C>T (p.Arg146Cys) n.457G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.48703393G>A | CA9556246 | FUT2 | c.437G>A (p.Arg146His) n.456C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.48703393G>C | CA406710368 | FUT2 | c.437G>C (p.Arg146Pro) n.456C>G | dbSNP gnomAD v3 gnomAD v4 |
19 | g.48703393G= | CA2340030016 | FUT2 | c.437G= (p.Arg146=) n.456C= | |
19 | g.48703393G>T | CA406710366 | FUT2 | c.437G>T (p.Arg146Leu) n.456C>A | |
19 | g.48703394C>A | CA508272387 | FUT2 | c.438C>A (p.Arg146=) n.455G>T | |
19 | g.48703394C= | CA2340030017 | FUT2 | c.438C= (p.Arg146=) n.455G= | |
19 | g.48703394C>G | CA508272389 | FUT2 | c.438C>G (p.Arg146=) n.455G>C | |
19 | g.48703394C>T | CA309352426 | FUT2 | c.438C>T (p.Arg146=) n.455G>A | dbSNP gnomAD v3 gnomAD v4 |
19 | g.48703395T>A | CA406710371 | FUT2 | c.439T>A (p.Phe147Ile) n.454A>T | |
19 | g.48703395T>C | CA406710375 | FUT2 | c.439T>C (p.Phe147Leu) n.454A>G | dbSNP gnomAD v4 |
19 | g.48703395T>G | CA406710373 | FUT2 | c.439T>G (p.Phe147Val) n.454A>C | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.48703395T= | CA2340030018 | FUT2 | c.439T= (p.Phe147=) n.454A= | |
19 | g.48703396T>A | CA406710378 | FUT2 | c.440T>A (p.Phe147Tyr) n.453A>T | gnomAD v4 |
19 | g.48703396T>C | CA406710382 | FUT2 | c.440T>C (p.Phe147Ser) n.453A>G | dbSNP |
19 | g.48703396T>G | CA406710380 | FUT2 | c.440T>G (p.Phe147Cys) n.453A>C | |
19 | g.48703396T= | CA2340030019 | FUT2 | c.440T= (p.Phe147=) n.453A= | |
19 | g.48703397C>A | CA406710385 | FUT2 | c.441C>A (p.Phe147Leu) n.452G>T | |
19 | g.48703397C>G | CA406710386 | FUT2 | c.441C>G (p.Phe147Leu) n.452G>C | |
19 | g.48703397C>T | CA508272391 | FUT2 | c.441C>T (p.Phe147=) n.452G>A | |
19 | g.48703398A>C | CA406710389 | FUT2 | c.442A>C (p.Thr148Pro) n.451T>G | |
19 | g.48703398A>G | CA406710393 | FUT2 | c.442A>G (p.Thr148Ala) n.451T>C | |
19 | g.48703398A>T | CA406710391 | FUT2 | c.442A>T (p.Thr148Ser) n.451T>A | |
19 | g.48703399C>A | CA406710396 | FUT2 | c.443C>A (p.Thr148Asn) n.450G>T | |
19 | g.48703399C>G | CA406710399 | FUT2 | c.443C>G (p.Thr148Ser) n.450G>C | |
19 | g.48703399C>T | CA406710397 | FUT2 | c.443C>T (p.Thr148Ile) n.450G>A | |
19 | g.48703400C>A | CA508272397 | FUT2 | c.444C>A (p.Thr148=) n.449G>T | |
19 | g.48703400C= | CA2340030020 | FUT2 | c.444C= (p.Thr148=) n.449G= | |
19 | g.48703400C>G | CA9556247 | FUT2 | c.444C>G (p.Thr148=) n.449G>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
19 | g.48703400C>T | CA9556248 | FUT2 | c.444C>T (p.Thr148=) n.449G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.48703401G>A | CA9556249 | FUT2 | c.445G>A (p.Gly149Ser) n.448C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
19 | g.48703401G>C | CA406710404 | FUT2 | c.445G>C (p.Gly149Arg) n.448C>G | |
19 | g.48703401G= | CA2340030021 | FUT2 | c.445G= (p.Gly149=) n.448C= | |
19 | g.48703401G>T | CA406710402 | FUT2 | c.445G>T (p.Gly149Cys) n.448C>A | |
19 | g.48703402G>A | CA406710407 | FUT2 | c.446G>A (p.Gly149Asp) n.447C>T | |
19 | g.48703402G>C | CA406710410 | FUT2 | c.446G>C (p.Gly149Ala) n.447C>G | |
19 | g.48703402G>T | CA406710412 | FUT2 | c.446G>T (p.Gly149Val) n.447C>A | |
19 | g.48703403C>A | CA508272403 | FUT2 | c.447C>A (p.Gly149=) n.446G>T | |
19 | g.48703403C>G | CA508272405 | FUT2 | c.447C>G (p.Gly149=) n.446G>C | |
19 | g.48703403C>T | CA508272404 | FUT2 | c.447C>T (p.Gly149=) n.446G>A | |
19 | g.48703404T>A | CA406710416 | FUT2 | c.448T>A (p.Tyr150Asn) n.445A>T | |
19 | g.48703404T>C | CA406710418 | FUT2 | c.448T>C (p.Tyr150His) n.445A>G | |
19 | g.48703404T>G | CA406710420 | FUT2 | c.448T>G (p.Tyr150Asp) n.445A>C | |
19 | g.48703405A>C | CA406710421 | FUT2 | c.449A>C (p.Tyr150Ser) n.444T>G | |
19 | g.48703405A>G | CA406710422 | FUT2 | c.449A>G (p.Tyr150Cys) n.444T>C | |
19 | g.48703405A>T | CA406710424 | FUT2 | c.449A>T (p.Tyr150Phe) n.444T>A | |
19 | g.48703406C>A | CA9556250 | FUT2 | c.450C>A (p.Tyr150Ter) n.443G>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
19 | g.48703406C= | CA2340030022 | FUT2 | c.450C= (p.Tyr150=) n.443G= | |
19 | g.48703406C>G | CA406710428 | FUT2 | c.450C>G (p.Tyr150Ter) n.443G>C | |
19 | g.48703406C>T | CA508272408 | FUT2 | c.450C>T (p.Tyr150=) n.443G>A | |
19 | g.48703407C>A | CA406710430 | FUT2 | c.451C>A (p.Pro151Thr) n.442G>T | gnomAD v3 gnomAD v4 |
19 | g.48703407C= | CA2340030023 | FUT2 | c.451C= (p.Pro151=) n.442G= | |
19 | g.48703407C>G | CA406710432 | FUT2 | c.451C>G (p.Pro151Ala) n.442G>C | |
19 | g.48703407C>T | CA406710434 | FUT2 | c.451C>T (p.Pro151Ser) n.442G>A | dbSNP gnomAD v4 |
19 | g.48703408C>A | CA406710440 | FUT2 | c.452C>A (p.Pro151His) n.441G>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.48703408C= | CA2340030024 | FUT2 | c.452C= (p.Pro151=) n.441G= | |
19 | g.48703408C>G | CA406710439 | FUT2 | c.452C>G (p.Pro151Arg) n.441G>C | |
19 | g.48703408C>T | CA406710437 | FUT2 | c.452C>T (p.Pro151Leu) n.441G>A | COSMIC |
19 | g.48703409C>A | CA508272537 | FUT2 | c.453C>A (p.Pro151=) n.440G>T | |
19 | g.48703409C>G | CA508272540 | FUT2 | c.453C>G (p.Pro151=) n.440G>C | |
19 | g.48703409C>T | CA508272544 | FUT2 | c.453C>T (p.Pro151=) n.440G>A | gnomAD v4 |
19 | g.48703410T>A | CA406710443 | FUT2 | c.454T>A (p.Cys152Ser) n.439A>T | |
19 | g.48703410T>C | CA406710445 | FUT2 | c.454T>C (p.Cys152Arg) n.439A>G | dbSNP |
19 | g.48703410T>G | CA406710447 | FUT2 | c.454T>G (p.Cys152Gly) n.439A>C | |
19 | g.48703410T= | CA2340030025 | FUT2 | c.454T= (p.Cys152=) n.439A= | |
19 | g.48703411G>A | CA406710450 | FUT2 | c.455G>A (p.Cys152Tyr) n.438C>T | |
19 | g.48703411G>C | CA406710451 | FUT2 | c.455G>C (p.Cys152Ser) n.438C>G | gnomAD v4 |
19 | g.48703411G>T | CA406710453 | FUT2 | c.455G>T (p.Cys152Phe) n.438C>A | |
19 | g.48703412C>A | CA406710456 | FUT2 | c.456C>A (p.Cys152Ter) n.437G>T | |
19 | g.48703412C= | CA2340030026 | FUT2 | c.456C= (p.Cys152=) n.437G= | |
19 | g.48703412C>G | CA406710458 | FUT2 | c.456C>G (p.Cys152Trp) n.437G>C | dbSNP gnomAD v2 |
19 | g.48703412C>T | CA508272550 | FUT2 | c.456C>T (p.Cys152=) n.437G>A | dbSNP gnomAD v2 gnomAD v4 |
19 | g.48703413T>A | CA406710461 | FUT2 | c.457T>A (p.Ser153Thr) n.436A>T | |
19 | g.48703413T>C | CA406710462 | FUT2 | c.457T>C (p.Ser153Pro) n.436A>G | |
19 | g.48703413T>G | CA406710463 | FUT2 | c.457T>G (p.Ser153Ala) n.436A>C | |
19 | g.48703414C>A | CA406710465 | FUT2 | c.458C>A (p.Ser153Tyr) n.435G>T | |
19 | g.48703414C= | CA2340030027 | FUT2 | c.458C= (p.Ser153=) n.435G= | |
19 | g.48703414C>G | CA406710467 | FUT2 | c.458C>G (p.Ser153Cys) n.435G>C | dbSNP |
19 | g.48703414C>T | CA406710468 | FUT2 | c.458C>T (p.Ser153Phe) n.435G>A | gnomAD v4 |
19 | g.48703415C>A | CA508272551 | FUT2 | c.459C>A (p.Ser153=) n.434G>T | |
19 | g.48703415C= | CA2340030028 | FUT2 | c.459C= (p.Ser153=) n.434G= | |
19 | g.48703415C>G | CA508272552 | FUT2 | c.459C>G (p.Ser153=) n.434G>C | dbSNP gnomAD v2 gnomAD v4 |
19 | g.48703415C>T | CA508272553 | FUT2 | c.459C>T (p.Ser153=) n.434G>A | |
19 | g.48703417_48703425del | CA2586240160 | FUT2 | c.461_469del (p.Trp154_Phe156del) n.426_434del | gnomAD v4 |
19 | g.48703416T>A | CA406710473 | FUT2 | c.460T>A (p.Trp154Arg) n.433A>T | |
19 | g.48703416T>C | CA406710474 | FUT2 | c.460T>C (p.Trp154Arg) n.433A>G | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.48703416T>G | CA406710472 | FUT2 | c.460T>G (p.Trp154Gly) n.433A>C | |
19 | g.48703416T= | CA2340030029 | FUT2 | c.460T= (p.Trp154=) n.433A= | |
19 | g.48703417G>A | CA122797 | FUT2 | c.461G>A (p.Trp154Ter) n.432C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.48703417G>C | CA406710483 | FUT2 | c.461G>C (p.Trp154Ser) n.432C>G | |
19 | g.48703417G= | CA2340030030 | FUT2 | c.461G= (p.Trp154=) n.432C= | |
19 | g.48703417G>T | CA406710485 | FUT2 | c.461G>T (p.Trp154Leu) n.432C>A |