Chr Mutation (hg38) CAid Gene Transcript Linkouts
9g.114404006_114408890delCA916084278WHRNc.1627-868_2312del
c.600-868_1285del
n.1508-868_2193del
c.478-868_1163del
c.574-868_1259del
c.1627-868_2309del
c.964-868_1649del
c.1660-868_2345del
c.1660-868_2342del
c.1534-868_2219del
c.1417-868_2102del
c.337-868_1022del
n.2564-868_3249del
n.2462-868_3147del
n.1875-868_2560del
n.1773-868_2458del
ClinVar
9g.114406407delCA1139661140WHRNc.531del (p.Asp178ThrfsTer9)
c.2187del (p.Asp730ThrfsTer9)
c.1160del
n.2068del
c.1038del (p.Asp347ThrfsTer9)
c.1134del (p.Asp379ThrfsTer9)
c.1524del (p.Asp509ThrfsTer9)
c.2220del (p.Asp741ThrfsTer9)
c.2094del (p.Asp699ThrfsTer9)
c.1977del (p.Asp660ThrfsTer9)
c.897del (p.Asp300ThrfsTer9)
n.3124del
n.3022del
n.2435del
n.2333del
ClinVar dbSNP
9g.114406406G>ACA374620119WHRNc.529C>T (p.Pro177Ser)
c.2185C>T (p.Pro729Ser)
c.1158C>T
n.2066C>T
c.1036C>T (p.Pro346Ser)
c.1132C>T (p.Pro378Ser)
c.1522C>T (p.Pro508Ser)
c.2218C>T (p.Pro740Ser)
c.2092C>T (p.Pro698Ser)
c.1975C>T (p.Pro659Ser)
c.895C>T (p.Pro299Ser)
n.3122C>T
n.3020C>T
n.2433C>T
n.2331C>T
9g.114406406G>CCA374620120WHRNc.529C>G (p.Pro177Ala)
c.2185C>G (p.Pro729Ala)
c.1158C>G
n.2066C>G
c.1036C>G (p.Pro346Ala)
c.1132C>G (p.Pro378Ala)
c.1522C>G (p.Pro508Ala)
c.2218C>G (p.Pro740Ala)
c.2092C>G (p.Pro698Ala)
c.1975C>G (p.Pro659Ala)
c.895C>G (p.Pro299Ala)
n.3122C>G
n.3020C>G
n.2433C>G
n.2331C>G
9g.114406406G>TCA374620121WHRNc.529C>A (p.Pro177Thr)
c.2185C>A (p.Pro729Thr)
c.1158C>A
n.2066C>A
c.1036C>A (p.Pro346Thr)
c.1132C>A (p.Pro378Thr)
c.1522C>A (p.Pro508Thr)
c.2218C>A (p.Pro740Thr)
c.2092C>A (p.Pro698Thr)
c.1975C>A (p.Pro659Thr)
c.895C>A (p.Pro299Thr)
n.3122C>A
n.3020C>A
n.2433C>A
n.2331C>A
9g.114406407G>ACA466911424WHRNc.528C>T (p.Arg176=)
c.2184C>T (p.Arg728=)
c.1157C>T
n.2065C>T
c.1035C>T (p.Arg345=)
c.1131C>T (p.Arg377=)
c.1521C>T (p.Arg507=)
c.2217C>T (p.Arg739=)
c.2091C>T (p.Arg697=)
c.1974C>T (p.Arg658=)
c.894C>T (p.Arg298=)
n.3121C>T
n.3019C>T
n.2432C>T
n.2330C>T
9g.114406407G>CCA466911427WHRNc.528C>G (p.Arg176=)
c.2184C>G (p.Arg728=)
c.1157C>G
n.2065C>G
c.1035C>G (p.Arg345=)
c.1131C>G (p.Arg377=)
c.1521C>G (p.Arg507=)
c.2217C>G (p.Arg739=)
c.2091C>G (p.Arg697=)
c.1974C>G (p.Arg658=)
c.894C>G (p.Arg298=)
n.3121C>G
n.3019C>G
n.2432C>G
n.2330C>G
9g.114406407G>TCA466911430WHRNc.528C>A (p.Arg176=)
c.2184C>A (p.Arg728=)
c.1157C>A
n.2065C>A
c.1035C>A (p.Arg345=)
c.1131C>A (p.Arg377=)
c.1521C>A (p.Arg507=)
c.2217C>A (p.Arg739=)
c.2091C>A (p.Arg697=)
c.1974C>A (p.Arg658=)
c.894C>A (p.Arg298=)
n.3121C>A
n.3019C>A
n.2432C>A
n.2330C>A
9g.114406408C>ACA374620123WHRNc.527G>T (p.Arg176Leu)
c.2183G>T (p.Arg728Leu)
c.1156G>T
n.2064G>T
c.1034G>T (p.Arg345Leu)
c.1130G>T (p.Arg377Leu)
c.1520G>T (p.Arg507Leu)
c.2216G>T (p.Arg739Leu)
c.2090G>T (p.Arg697Leu)
c.1973G>T (p.Arg658Leu)
c.893G>T (p.Arg298Leu)
n.3120G>T
n.3018G>T
n.2431G>T
n.2329G>T
9g.114406408C=CA1873827078WHRNc.527G= (p.Arg176=)
c.2183G= (p.Arg728=)
c.1156G=
n.2064G=
c.1034G= (p.Arg345=)
c.1130G= (p.Arg377=)
c.1520G= (p.Arg507=)
c.2216G= (p.Arg739=)
c.2090G= (p.Arg697=)
c.1973G= (p.Arg658=)
c.893G= (p.Arg298=)
n.3120G=
n.3018G=
n.2431G=
n.2329G=
9g.114406408C>GCA374620122WHRNc.527G>C (p.Arg176Pro)
c.2183G>C (p.Arg728Pro)
c.1156G>C
n.2064G>C
c.1034G>C (p.Arg345Pro)
c.1130G>C (p.Arg377Pro)
c.1520G>C (p.Arg507Pro)
c.2216G>C (p.Arg739Pro)
c.2090G>C (p.Arg697Pro)
c.1973G>C (p.Arg658Pro)
c.893G>C (p.Arg298Pro)
n.3120G>C
n.3018G>C
n.2431G>C
n.2329G>C
9g.114406408C>TCA223187WHRNc.527G>A (p.Arg176His)
c.2183G>A (p.Arg728His)
c.1156G>A
n.2064G>A
c.1034G>A (p.Arg345His)
c.1130G>A (p.Arg377His)
c.1520G>A (p.Arg507His)
c.2216G>A (p.Arg739His)
c.2090G>A (p.Arg697His)
c.1973G>A (p.Arg658His)
c.893G>A (p.Arg298His)
n.3120G>A
n.3018G>A
n.2431G>A
n.2329G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC
9g.114406409G>ACA5205726WHRNc.526C>T (p.Arg176Cys)
c.2182C>T (p.Arg728Cys)
c.1155C>T
n.2063C>T
c.1033C>T (p.Arg345Cys)
c.1129C>T (p.Arg377Cys)
c.1519C>T (p.Arg507Cys)
c.2215C>T (p.Arg739Cys)
c.2089C>T (p.Arg697Cys)
c.1972C>T (p.Arg658Cys)
c.892C>T (p.Arg298Cys)
n.3119C>T
n.3017C>T
n.2430C>T
n.2328C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.114406409G>CCA374620124WHRNc.526C>G (p.Arg176Gly)
c.2182C>G (p.Arg728Gly)
c.1155C>G
n.2063C>G
c.1033C>G (p.Arg345Gly)
c.1129C>G (p.Arg377Gly)
c.1519C>G (p.Arg507Gly)
c.2215C>G (p.Arg739Gly)
c.2089C>G (p.Arg697Gly)
c.1972C>G (p.Arg658Gly)
c.892C>G (p.Arg298Gly)
n.3119C>G
n.3017C>G
n.2430C>G
n.2328C>G
9g.114406409G=CA1873827079WHRNc.526C= (p.Arg176=)
c.2182C= (p.Arg728=)
c.1155C=
n.2063C=
c.1033C= (p.Arg345=)
c.1129C= (p.Arg377=)
c.1519C= (p.Arg507=)
c.2215C= (p.Arg739=)
c.2089C= (p.Arg697=)
c.1972C= (p.Arg658=)
c.892C= (p.Arg298=)
n.3119C=
n.3017C=
n.2430C=
n.2328C=
9g.114406409G>TCA374620125WHRNc.526C>A (p.Arg176Ser)
c.2182C>A (p.Arg728Ser)
c.1155C>A
n.2063C>A
c.1033C>A (p.Arg345Ser)
c.1129C>A (p.Arg377Ser)
c.1519C>A (p.Arg507Ser)
c.2215C>A (p.Arg739Ser)
c.2089C>A (p.Arg697Ser)
c.1972C>A (p.Arg658Ser)
c.892C>A (p.Arg298Ser)
n.3119C>A
n.3017C>A
n.2430C>A
n.2328C>A
9g.114406410G>ACA466911435WHRNc.525C>T (p.His175=)
c.2181C>T (p.His727=)
c.1154C>T
n.2062C>T
c.1032C>T (p.His344=)
c.1128C>T (p.His376=)
c.1518C>T (p.His506=)
c.2214C>T (p.His738=)
c.2088C>T (p.His696=)
c.1971C>T (p.His657=)
c.891C>T (p.His297=)
n.3118C>T
n.3016C>T
n.2429C>T
n.2327C>T
9g.114406410G>CCA374620126WHRNc.525C>G (p.His175Gln)
c.2181C>G (p.His727Gln)
c.1154C>G
n.2062C>G
c.1032C>G (p.His344Gln)
c.1128C>G (p.His376Gln)
c.1518C>G (p.His506Gln)
c.2214C>G (p.His738Gln)
c.2088C>G (p.His696Gln)
c.1971C>G (p.His657Gln)
c.891C>G (p.His297Gln)
n.3118C>G
n.3016C>G
n.2429C>G
n.2327C>G
gnomAD v4
9g.114406410G>TCA374620127WHRNc.525C>A (p.His175Gln)
c.2181C>A (p.His727Gln)
c.1154C>A
n.2062C>A
c.1032C>A (p.His344Gln)
c.1128C>A (p.His376Gln)
c.1518C>A (p.His506Gln)
c.2214C>A (p.His738Gln)
c.2088C>A (p.His696Gln)
c.1971C>A (p.His657Gln)
c.891C>A (p.His297Gln)
n.3118C>A
n.3016C>A
n.2429C>A
n.2327C>A
9g.114406411T>ACA374620128WHRNc.524A>T (p.His175Leu)
c.2180A>T (p.His727Leu)
c.1153A>T
n.2061A>T
c.1031A>T (p.His344Leu)
c.1127A>T (p.His376Leu)
c.1517A>T (p.His506Leu)
c.2213A>T (p.His738Leu)
c.2087A>T (p.His696Leu)
c.1970A>T (p.His657Leu)
c.890A>T (p.His297Leu)
n.3117A>T
n.3015A>T
n.2428A>T
n.2326A>T
9g.114406411T>CCA374620129WHRNc.524A>G (p.His175Arg)
c.2180A>G (p.His727Arg)
c.1153A>G
n.2061A>G
c.1031A>G (p.His344Arg)
c.1127A>G (p.His376Arg)
c.1517A>G (p.His506Arg)
c.2213A>G (p.His738Arg)
c.2087A>G (p.His696Arg)
c.1970A>G (p.His657Arg)
c.890A>G (p.His297Arg)
n.3117A>G
n.3015A>G
n.2428A>G
n.2326A>G
9g.114406411T>GCA374620130WHRNc.524A>C (p.His175Pro)
c.2180A>C (p.His727Pro)
c.1153A>C
n.2061A>C
c.1031A>C (p.His344Pro)
c.1127A>C (p.His376Pro)
c.1517A>C (p.His506Pro)
c.2213A>C (p.His738Pro)
c.2087A>C (p.His696Pro)
c.1970A>C (p.His657Pro)
c.890A>C (p.His297Pro)
n.3117A>C
n.3015A>C
n.2428A>C
n.2326A>C
dbSNP
9g.114406411T=CA1873827080WHRNc.524A= (p.His175=)
c.2180A= (p.His727=)
c.1153A=
n.2061A=
c.1031A= (p.His344=)
c.1127A= (p.His376=)
c.1517A= (p.His506=)
c.2213A= (p.His738=)
c.2087A= (p.His696=)
c.1970A= (p.His657=)
c.890A= (p.His297=)
n.3117A=
n.3015A=
n.2428A=
n.2326A=
9g.114406412G>ACA198649882WHRNc.523C>T (p.His175Tyr)
c.2179C>T (p.His727Tyr)
c.1152C>T
n.2060C>T
c.1030C>T (p.His344Tyr)
c.1126C>T (p.His376Tyr)
c.1516C>T (p.His506Tyr)
c.2212C>T (p.His738Tyr)
c.2086C>T (p.His696Tyr)
c.1969C>T (p.His657Tyr)
c.889C>T (p.His297Tyr)
n.3116C>T
n.3014C>T
n.2427C>T
n.2325C>T
dbSNP gnomAD v3 gnomAD v4
9g.114406412G>CCA374620131WHRNc.523C>G (p.His175Asp)
c.2179C>G (p.His727Asp)
c.1152C>G
n.2060C>G
c.1030C>G (p.His344Asp)
c.1126C>G (p.His376Asp)
c.1516C>G (p.His506Asp)
c.2212C>G (p.His738Asp)
c.2086C>G (p.His696Asp)
c.1969C>G (p.His657Asp)
c.889C>G (p.His297Asp)
n.3116C>G
n.3014C>G
n.2427C>G
n.2325C>G
gnomAD v4
9g.114406412G=CA1873827081WHRNc.523C= (p.His175=)
c.2179C= (p.His727=)
c.1152C=
n.2060C=
c.1030C= (p.His344=)
c.1126C= (p.His376=)
c.1516C= (p.His506=)
c.2212C= (p.His738=)
c.2086C= (p.His696=)
c.1969C= (p.His657=)
c.889C= (p.His297=)
n.3116C=
n.3014C=
n.2427C=
n.2325C=
9g.114406412G>TCA374620132WHRNc.523C>A (p.His175Asn)
c.2179C>A (p.His727Asn)
c.1152C>A
n.2060C>A
c.1030C>A (p.His344Asn)
c.1126C>A (p.His376Asn)
c.1516C>A (p.His506Asn)
c.2212C>A (p.His738Asn)
c.2086C>A (p.His696Asn)
c.1969C>A (p.His657Asn)
c.889C>A (p.His297Asn)
n.3116C>A
n.3014C>A
n.2427C>A
n.2325C>A
9g.114406413G>ACA466911445WHRNc.522C>T (p.Val174=)
c.2178C>T (p.Val726=)
c.1151C>T
n.2059C>T
c.1029C>T (p.Val343=)
c.1125C>T (p.Val375=)
c.1515C>T (p.Val505=)
c.2211C>T (p.Val737=)
c.2085C>T (p.Val695=)
c.1968C>T (p.Val656=)
c.888C>T (p.Val296=)
n.3115C>T
n.3013C>T
n.2426C>T
n.2324C>T
9g.114406413G>CCA466911447WHRNc.522C>G (p.Val174=)
c.2178C>G (p.Val726=)
c.1151C>G
n.2059C>G
c.1029C>G (p.Val343=)
c.1125C>G (p.Val375=)
c.1515C>G (p.Val505=)
c.2211C>G (p.Val737=)
c.2085C>G (p.Val695=)
c.1968C>G (p.Val656=)
c.888C>G (p.Val296=)
n.3115C>G
n.3013C>G
n.2426C>G
n.2324C>G
9g.114406413G>TCA466911449WHRNc.522C>A (p.Val174=)
c.2178C>A (p.Val726=)
c.1151C>A
n.2059C>A
c.1029C>A (p.Val343=)
c.1125C>A (p.Val375=)
c.1515C>A (p.Val505=)
c.2211C>A (p.Val737=)
c.2085C>A (p.Val695=)
c.1968C>A (p.Val656=)
c.888C>A (p.Val296=)
n.3115C>A
n.3013C>A
n.2426C>A
n.2324C>A
9g.114406414A>CCA374620133WHRNc.521T>G (p.Val174Gly)
c.2177T>G (p.Val726Gly)
c.1150T>G
n.2058T>G
c.1028T>G (p.Val343Gly)
c.1124T>G (p.Val375Gly)
c.1514T>G (p.Val505Gly)
c.2210T>G (p.Val737Gly)
c.2084T>G (p.Val695Gly)
c.1967T>G (p.Val656Gly)
c.887T>G (p.Val296Gly)
n.3114T>G
n.3012T>G
n.2425T>G
n.2323T>G
gnomAD v4
9g.114406414A>GCA374620134WHRNc.521T>C (p.Val174Ala)
c.2177T>C (p.Val726Ala)
c.1150T>C
n.2058T>C
c.1028T>C (p.Val343Ala)
c.1124T>C (p.Val375Ala)
c.1514T>C (p.Val505Ala)
c.2210T>C (p.Val737Ala)
c.2084T>C (p.Val695Ala)
c.1967T>C (p.Val656Ala)
c.887T>C (p.Val296Ala)
n.3114T>C
n.3012T>C
n.2425T>C
n.2323T>C
9g.114406414A>TCA374620135WHRNc.521T>A (p.Val174Asp)
c.2177T>A (p.Val726Asp)
c.1150T>A
n.2058T>A
c.1028T>A (p.Val343Asp)
c.1124T>A (p.Val375Asp)
c.1514T>A (p.Val505Asp)
c.2210T>A (p.Val737Asp)
c.2084T>A (p.Val695Asp)
c.1967T>A (p.Val656Asp)
c.887T>A (p.Val296Asp)
n.3114T>A
n.3012T>A
n.2425T>A
n.2323T>A
9g.114406415C>ACA374620137WHRNc.520G>T (p.Val174Phe)
c.2176G>T (p.Val726Phe)
c.1149G>T
n.2057G>T
c.1027G>T (p.Val343Phe)
c.1123G>T (p.Val375Phe)
c.1513G>T (p.Val505Phe)
c.2209G>T (p.Val737Phe)
c.2083G>T (p.Val695Phe)
c.1966G>T (p.Val656Phe)
c.886G>T (p.Val296Phe)
n.3113G>T
n.3011G>T
n.2424G>T
n.2322G>T
9g.114406415C>GCA374620138WHRNc.520G>C (p.Val174Leu)
c.2176G>C (p.Val726Leu)
c.1149G>C
n.2057G>C
c.1027G>C (p.Val343Leu)
c.1123G>C (p.Val375Leu)
c.1513G>C (p.Val505Leu)
c.2209G>C (p.Val737Leu)
c.2083G>C (p.Val695Leu)
c.1966G>C (p.Val656Leu)
c.886G>C (p.Val296Leu)
n.3113G>C
n.3011G>C
n.2424G>C
n.2322G>C
9g.114406415C>TCA374620136WHRNc.520G>A (p.Val174Ile)
c.2176G>A (p.Val726Ile)
c.1149G>A
n.2057G>A
c.1027G>A (p.Val343Ile)
c.1123G>A (p.Val375Ile)
c.1513G>A (p.Val505Ile)
c.2209G>A (p.Val737Ile)
c.2083G>A (p.Val695Ile)
c.1966G>A (p.Val656Ile)
c.886G>A (p.Val296Ile)
n.3113G>A
n.3011G>A
n.2424G>A
n.2322G>A
COSMIC COSMIC
9g.114406416C>ACA5205727WHRNc.519G>T (p.Glu173Asp)
c.2175G>T (p.Glu725Asp)
c.1148G>T
n.2056G>T
c.1026G>T (p.Glu342Asp)
c.1122G>T (p.Glu374Asp)
c.1512G>T (p.Glu504Asp)
c.2208G>T (p.Glu736Asp)
c.2082G>T (p.Glu694Asp)
c.1965G>T (p.Glu655Asp)
c.885G>T (p.Glu295Asp)
n.3112G>T
n.3010G>T
n.2423G>T
n.2321G>T
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.114406416C=CA1873827082WHRNc.519G= (p.Glu173=)
c.2175G= (p.Glu725=)
c.1148G=
n.2056G=
c.1026G= (p.Glu342=)
c.1122G= (p.Glu374=)
c.1512G= (p.Glu504=)
c.2208G= (p.Glu736=)
c.2082G= (p.Glu694=)
c.1965G= (p.Glu655=)
c.885G= (p.Glu295=)
n.3112G=
n.3010G=
n.2423G=
n.2321G=
9g.114406416C>GCA374620139WHRNc.519G>C (p.Glu173Asp)
c.2175G>C (p.Glu725Asp)
c.1148G>C
n.2056G>C
c.1026G>C (p.Glu342Asp)
c.1122G>C (p.Glu374Asp)
c.1512G>C (p.Glu504Asp)
c.2208G>C (p.Glu736Asp)
c.2082G>C (p.Glu694Asp)
c.1965G>C (p.Glu655Asp)
c.885G>C (p.Glu295Asp)
n.3112G>C
n.3010G>C
n.2423G>C
n.2321G>C
9g.114406416C>TCA466911458WHRNc.519G>A (p.Glu173=)
c.2175G>A (p.Glu725=)
c.1148G>A
n.2056G>A
c.1026G>A (p.Glu342=)
c.1122G>A (p.Glu374=)
c.1512G>A (p.Glu504=)
c.2208G>A (p.Glu736=)
c.2082G>A (p.Glu694=)
c.1965G>A (p.Glu655=)
c.885G>A (p.Glu295=)
n.3112G>A
n.3010G>A
n.2423G>A
n.2321G>A
gnomAD v4
9g.114406417T>ACA374620140WHRNc.518A>T (p.Glu173Val)
c.2174A>T (p.Glu725Val)
c.1147A>T
n.2055A>T
c.1025A>T (p.Glu342Val)
c.1121A>T (p.Glu374Val)
c.1511A>T (p.Glu504Val)
c.2207A>T (p.Glu736Val)
c.2081A>T (p.Glu694Val)
c.1964A>T (p.Glu655Val)
c.884A>T (p.Glu295Val)
n.3111A>T
n.3009A>T
n.2422A>T
n.2320A>T
9g.114406417T>CCA374620141WHRNc.518A>G (p.Glu173Gly)
c.2174A>G (p.Glu725Gly)
c.1147A>G
n.2055A>G
c.1025A>G (p.Glu342Gly)
c.1121A>G (p.Glu374Gly)
c.1511A>G (p.Glu504Gly)
c.2207A>G (p.Glu736Gly)
c.2081A>G (p.Glu694Gly)
c.1964A>G (p.Glu655Gly)
c.884A>G (p.Glu295Gly)
n.3111A>G
n.3009A>G
n.2422A>G
n.2320A>G
9g.114406417T>GCA374620142WHRNc.518A>C (p.Glu173Ala)
c.2174A>C (p.Glu725Ala)
c.1147A>C
n.2055A>C
c.1025A>C (p.Glu342Ala)
c.1121A>C (p.Glu374Ala)
c.1511A>C (p.Glu504Ala)
c.2207A>C (p.Glu736Ala)
c.2081A>C (p.Glu694Ala)
c.1964A>C (p.Glu655Ala)
c.884A>C (p.Glu295Ala)
n.3111A>C
n.3009A>C
n.2422A>C
n.2320A>C
gnomAD v4
9g.114406418C>ACA374620143WHRNc.517G>T (p.Glu173Ter)
c.2173G>T (p.Glu725Ter)
c.1146G>T
n.2054G>T
c.1024G>T (p.Glu342Ter)
c.1120G>T (p.Glu374Ter)
c.1510G>T (p.Glu504Ter)
c.2206G>T (p.Glu736Ter)
c.2080G>T (p.Glu694Ter)
c.1963G>T (p.Glu655Ter)
c.883G>T (p.Glu295Ter)
n.3110G>T
n.3008G>T
n.2421G>T
n.2319G>T
9g.114406418C=CA1873827083WHRNc.517G= (p.Glu173=)
c.2173G= (p.Glu725=)
c.1146G=
n.2054G=
c.1024G= (p.Glu342=)
c.1120G= (p.Glu374=)
c.1510G= (p.Glu504=)
c.2206G= (p.Glu736=)
c.2080G= (p.Glu694=)
c.1963G= (p.Glu655=)
c.883G= (p.Glu295=)
n.3110G=
n.3008G=
n.2421G=
n.2319G=
9g.114406418C>GCA10628846WHRNc.517G>C (p.Glu173Gln)
c.2173G>C (p.Glu725Gln)
c.1146G>C
n.2054G>C
c.1024G>C (p.Glu342Gln)
c.1120G>C (p.Glu374Gln)
c.1510G>C (p.Glu504Gln)
c.2206G>C (p.Glu736Gln)
c.2080G>C (p.Glu694Gln)
c.1963G>C (p.Glu655Gln)
c.883G>C (p.Glu295Gln)
n.3110G>C
n.3008G>C
n.2421G>C
n.2319G>C
ClinVar dbSNP
9g.114406418C>TCA5205728WHRNc.517G>A (p.Glu173Lys)
c.2173G>A (p.Glu725Lys)
c.1146G>A
n.2054G>A
c.1024G>A (p.Glu342Lys)
c.1120G>A (p.Glu374Lys)
c.1510G>A (p.Glu504Lys)
c.2206G>A (p.Glu736Lys)
c.2080G>A (p.Glu694Lys)
c.1963G>A (p.Glu655Lys)
c.883G>A (p.Glu295Lys)
n.3110G>A
n.3008G>A
n.2421G>A
n.2319G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.114406419C>ACA466911468WHRNc.516G>T (p.Val172=)
c.2172G>T (p.Val724=)
c.1145G>T
n.2053G>T
c.1023G>T (p.Val341=)
c.1119G>T (p.Val373=)
c.1509G>T (p.Val503=)
c.2205G>T (p.Val735=)
c.2079G>T (p.Val693=)
c.1962G>T (p.Val654=)
c.882G>T (p.Val294=)
n.3109G>T
n.3007G>T
n.2420G>T
n.2318G>T
9g.114406419C=CA1873827084WHRNc.516G= (p.Val172=)
c.2172G= (p.Val724=)
c.1145G=
n.2053G=
c.1023G= (p.Val341=)
c.1119G= (p.Val373=)
c.1509G= (p.Val503=)
c.2205G= (p.Val735=)
c.2079G= (p.Val693=)
c.1962G= (p.Val654=)
c.882G= (p.Val294=)
n.3109G=
n.3007G=
n.2420G=
n.2318G=
9g.114406419C>GCA466911469WHRNc.516G>C (p.Val172=)
c.2172G>C (p.Val724=)
c.1145G>C
n.2053G>C
c.1023G>C (p.Val341=)
c.1119G>C (p.Val373=)
c.1509G>C (p.Val503=)
c.2205G>C (p.Val735=)
c.2079G>C (p.Val693=)
c.1962G>C (p.Val654=)
c.882G>C (p.Val294=)
n.3109G>C
n.3007G>C
n.2420G>C
n.2318G>C

Number of alleles fetched