WARNING - Protein Allele ID and Protein Sequence HGVS API Requests Temporarily Disabled:
We are investigating the periodic unresponsiveness in the Registry.
Although replication attempts were unsuccessful, there is a high correlation with protein alleles. And with haplotype HGVS queries.
This temporarily affects the API and the UI.
We are investigating the periodic unresponsiveness in the Registry.
Although replication attempts were unsuccessful, there is a high correlation with protein alleles. And with haplotype HGVS queries.
This temporarily affects the API and the UI.
| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 9 | g.114404006_114408890del | CA916084278 | WHRN | c.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 |
| 9 | g.114406401G>A | CA5205722 | WHRN | c.534C>T (p.Asp178=) c.2190C>T (p.Asp730=) c.1163C>T n.2071C>T c.1041C>T (p.Asp347=) c.1137C>T (p.Asp379=) c.1527C>T (p.Asp509=) c.2223C>T (p.Asp741=) c.2097C>T (p.Asp699=) c.1980C>T (p.Asp660=) c.900C>T (p.Asp300=) n.3127C>T n.3025C>T n.2438C>T n.2336C>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 9 | g.114406401G>C | CA374620110 | WHRN | c.534C>G (p.Asp178Glu) c.2190C>G (p.Asp730Glu) c.1163C>G n.2071C>G c.1041C>G (p.Asp347Glu) c.1137C>G (p.Asp379Glu) c.1527C>G (p.Asp509Glu) c.2223C>G (p.Asp741Glu) c.2097C>G (p.Asp699Glu) c.1980C>G (p.Asp660Glu) c.900C>G (p.Asp300Glu) n.3127C>G n.3025C>G n.2438C>G n.2336C>G | gnomAD v4 |
| 9 | g.114406401G= | CA1873827073 | WHRN | c.534C= (p.Asp178=) c.2190C= (p.Asp730=) c.1163C= n.2071C= c.1041C= (p.Asp347=) c.1137C= (p.Asp379=) c.1527C= (p.Asp509=) c.2223C= (p.Asp741=) c.2097C= (p.Asp699=) c.1980C= (p.Asp660=) c.900C= (p.Asp300=) n.3127C= n.3025C= n.2438C= n.2336C= | |
| 9 | g.114406401G>T | CA374620111 | WHRN | c.534C>A (p.Asp178Glu) c.2190C>A (p.Asp730Glu) c.1163C>A n.2071C>A c.1041C>A (p.Asp347Glu) c.1137C>A (p.Asp379Glu) c.1527C>A (p.Asp509Glu) c.2223C>A (p.Asp741Glu) c.2097C>A (p.Asp699Glu) c.1980C>A (p.Asp660Glu) c.900C>A (p.Asp300Glu) n.3127C>A n.3025C>A n.2438C>A n.2336C>A | |
| 9 | g.114406402T>A | CA374620112 | WHRN | c.533A>T (p.Asp178Val) c.2189A>T (p.Asp730Val) c.1162A>T n.2070A>T c.1040A>T (p.Asp347Val) c.1136A>T (p.Asp379Val) c.1526A>T (p.Asp509Val) c.2222A>T (p.Asp741Val) c.2096A>T (p.Asp699Val) c.1979A>T (p.Asp660Val) c.899A>T (p.Asp300Val) n.3126A>T n.3024A>T n.2437A>T n.2335A>T | |
| 9 | g.114406402T>C | CA5205723 | WHRN | c.533A>G (p.Asp178Gly) c.2189A>G (p.Asp730Gly) c.1162A>G n.2070A>G c.1040A>G (p.Asp347Gly) c.1136A>G (p.Asp379Gly) c.1526A>G (p.Asp509Gly) c.2222A>G (p.Asp741Gly) c.2096A>G (p.Asp699Gly) c.1979A>G (p.Asp660Gly) c.899A>G (p.Asp300Gly) n.3126A>G n.3024A>G n.2437A>G n.2335A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 9 | g.114406402T>G | CA374620113 | WHRN | c.533A>C (p.Asp178Ala) c.2189A>C (p.Asp730Ala) c.1162A>C n.2070A>C c.1040A>C (p.Asp347Ala) c.1136A>C (p.Asp379Ala) c.1526A>C (p.Asp509Ala) c.2222A>C (p.Asp741Ala) c.2096A>C (p.Asp699Ala) c.1979A>C (p.Asp660Ala) c.899A>C (p.Asp300Ala) n.3126A>C n.3024A>C n.2437A>C n.2335A>C | |
| 9 | g.114406402T= | CA1873827074 | WHRN | c.533A= (p.Asp178=) c.2189A= (p.Asp730=) c.1162A= n.2070A= c.1040A= (p.Asp347=) c.1136A= (p.Asp379=) c.1526A= (p.Asp509=) c.2222A= (p.Asp741=) c.2096A= (p.Asp699=) c.1979A= (p.Asp660=) c.899A= (p.Asp300=) n.3126A= n.3024A= n.2437A= n.2335A= | |
| 9 | g.114406403C>A | CA374620114 | WHRN | c.532G>T (p.Asp178Tyr) c.2188G>T (p.Asp730Tyr) c.1161G>T n.2069G>T c.1039G>T (p.Asp347Tyr) c.1135G>T (p.Asp379Tyr) c.1525G>T (p.Asp509Tyr) c.2221G>T (p.Asp741Tyr) c.2095G>T (p.Asp699Tyr) c.1978G>T (p.Asp660Tyr) c.898G>T (p.Asp300Tyr) n.3125G>T n.3023G>T n.2436G>T n.2334G>T | gnomAD v4 |
| 9 | g.114406403C= | CA1873827075 | WHRN | c.532G= (p.Asp178=) c.2188G= (p.Asp730=) c.1161G= n.2069G= c.1039G= (p.Asp347=) c.1135G= (p.Asp379=) c.1525G= (p.Asp509=) c.2221G= (p.Asp741=) c.2095G= (p.Asp699=) c.1978G= (p.Asp660=) c.898G= (p.Asp300=) n.3125G= n.3023G= n.2436G= n.2334G= | |
| 9 | g.114406403C>G | CA374620115 | WHRN | c.532G>C (p.Asp178His) c.2188G>C (p.Asp730His) c.1161G>C n.2069G>C c.1039G>C (p.Asp347His) c.1135G>C (p.Asp379His) c.1525G>C (p.Asp509His) c.2221G>C (p.Asp741His) c.2095G>C (p.Asp699His) c.1978G>C (p.Asp660His) c.898G>C (p.Asp300His) n.3125G>C n.3023G>C n.2436G>C n.2334G>C | gnomAD v4 |
| 9 | g.114406403C>T | CA5205724 | WHRN | c.532G>A (p.Asp178Asn) c.2188G>A (p.Asp730Asn) c.1161G>A n.2069G>A c.1039G>A (p.Asp347Asn) c.1135G>A (p.Asp379Asn) c.1525G>A (p.Asp509Asn) c.2221G>A (p.Asp741Asn) c.2095G>A (p.Asp699Asn) c.1978G>A (p.Asp660Asn) c.898G>A (p.Asp300Asn) n.3125G>A n.3023G>A n.2436G>A n.2334G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.114406403_114406404delinsCG | CA1873827076 | WHRN | c.531_532delinsCG (p.Pro177=) c.2187_2188delinsCG (p.Pro729=) c.1160_1161delinsCG n.2068_2069delinsCG c.1038_1039delinsCG (p.Pro346=) c.1134_1135delinsCG (p.Pro378=) c.1524_1525delinsCG (p.Pro508=) c.2220_2221delinsCG (p.Pro740=) c.2094_2095delinsCG (p.Pro698=) c.1977_1978delinsCG (p.Pro659=) c.897_898delinsCG (p.Pro299=) n.3124_3125delinsCG n.3022_3023delinsCG n.2435_2436delinsCG n.2333_2334delinsCG | |
| 9 | g.114406404G>A | CA5205725 | WHRN | c.531C>T (p.Pro177=) c.2187C>T (p.Pro729=) c.1160C>T n.2068C>T c.1038C>T (p.Pro346=) c.1134C>T (p.Pro378=) c.1524C>T (p.Pro508=) c.2220C>T (p.Pro740=) c.2094C>T (p.Pro698=) c.1977C>T (p.Pro659=) c.897C>T (p.Pro299=) n.3124C>T n.3022C>T n.2435C>T n.2333C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.114406404G>C | CA466911419 | WHRN | c.531C>G (p.Pro177=) c.2187C>G (p.Pro729=) c.1160C>G n.2068C>G c.1038C>G (p.Pro346=) c.1134C>G (p.Pro378=) c.1524C>G (p.Pro508=) c.2220C>G (p.Pro740=) c.2094C>G (p.Pro698=) c.1977C>G (p.Pro659=) c.897C>G (p.Pro299=) n.3124C>G n.3022C>G n.2435C>G n.2333C>G | gnomAD v4 |
| 9 | g.114406404G= | CA1873827077 | WHRN | c.531C= (p.Pro177=) c.2187C= (p.Pro729=) c.1160C= n.2068C= c.1038C= (p.Pro346=) c.1134C= (p.Pro378=) c.1524C= (p.Pro508=) c.2220C= (p.Pro740=) c.2094C= (p.Pro698=) c.1977C= (p.Pro659=) c.897C= (p.Pro299=) n.3124C= n.3022C= n.2435C= n.2333C= | |
| 9 | g.114406404G>T | CA466911418 | WHRN | c.531C>A (p.Pro177=) c.2187C>A (p.Pro729=) c.1160C>A n.2068C>A c.1038C>A (p.Pro346=) c.1134C>A (p.Pro378=) c.1524C>A (p.Pro508=) c.2220C>A (p.Pro740=) c.2094C>A (p.Pro698=) c.1977C>A (p.Pro659=) c.897C>A (p.Pro299=) n.3124C>A n.3022C>A n.2435C>A n.2333C>A | |
| 9 | g.114406407del | CA1139661140 | WHRN | c.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 |
| 9 | g.114406405G>A | CA374620116 | WHRN | c.530C>T (p.Pro177Leu) c.2186C>T (p.Pro729Leu) c.1159C>T n.2067C>T c.1037C>T (p.Pro346Leu) c.1133C>T (p.Pro378Leu) c.1523C>T (p.Pro508Leu) c.2219C>T (p.Pro740Leu) c.2093C>T (p.Pro698Leu) c.1976C>T (p.Pro659Leu) c.896C>T (p.Pro299Leu) n.3123C>T n.3021C>T n.2434C>T n.2332C>T | |
| 9 | g.114406405G>C | CA374620117 | WHRN | c.530C>G (p.Pro177Arg) c.2186C>G (p.Pro729Arg) c.1159C>G n.2067C>G c.1037C>G (p.Pro346Arg) c.1133C>G (p.Pro378Arg) c.1523C>G (p.Pro508Arg) c.2219C>G (p.Pro740Arg) c.2093C>G (p.Pro698Arg) c.1976C>G (p.Pro659Arg) c.896C>G (p.Pro299Arg) n.3123C>G n.3021C>G n.2434C>G n.2332C>G | |
| 9 | g.114406405G>T | CA374620118 | WHRN | c.530C>A (p.Pro177His) c.2186C>A (p.Pro729His) c.1159C>A n.2067C>A c.1037C>A (p.Pro346His) c.1133C>A (p.Pro378His) c.1523C>A (p.Pro508His) c.2219C>A (p.Pro740His) c.2093C>A (p.Pro698His) c.1976C>A (p.Pro659His) c.896C>A (p.Pro299His) n.3123C>A n.3021C>A n.2434C>A n.2332C>A | |
| 9 | g.114406406G>A | CA374620119 | WHRN | c.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 | |
| 9 | g.114406406G>C | CA374620120 | WHRN | c.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 | |
| 9 | g.114406406G>T | CA374620121 | WHRN | c.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 | |
| 9 | g.114406407G>A | CA466911424 | WHRN | c.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 | |
| 9 | g.114406407G>C | CA466911427 | WHRN | c.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 | |
| 9 | g.114406407G>T | CA466911430 | WHRN | c.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 | |
| 9 | g.114406408C>A | CA374620123 | WHRN | c.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 | |
| 9 | g.114406408C= | CA1873827078 | WHRN | c.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= | |
| 9 | g.114406408C>G | CA374620122 | WHRN | c.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 | |
| 9 | g.114406408C>T | CA223187 | WHRN | c.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 |
| 9 | g.114406409G>A | CA5205726 | WHRN | c.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 |
| 9 | g.114406409G>C | CA374620124 | WHRN | c.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 | |
| 9 | g.114406409G= | CA1873827079 | WHRN | c.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= | |
| 9 | g.114406409G>T | CA374620125 | WHRN | c.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 | |
| 9 | g.114406410G>A | CA466911435 | WHRN | c.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 | |
| 9 | g.114406410G>C | CA374620126 | WHRN | c.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 |
| 9 | g.114406410G>T | CA374620127 | WHRN | c.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 | |
| 9 | g.114406411T>A | CA374620128 | WHRN | c.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 | |
| 9 | g.114406411T>C | CA374620129 | WHRN | c.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 | |
| 9 | g.114406411T>G | CA374620130 | WHRN | c.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 |
| 9 | g.114406411T= | CA1873827080 | WHRN | c.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= | |
| 9 | g.114406412G>A | CA198649882 | WHRN | c.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 |
| 9 | g.114406412G>C | CA374620131 | WHRN | c.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 |
| 9 | g.114406412G= | CA1873827081 | WHRN | c.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= | |
| 9 | g.114406412G>T | CA374620132 | WHRN | c.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 | |
| 9 | g.114406413G>A | CA466911445 | WHRN | c.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 | |
| 9 | g.114406413G>C | CA466911447 | WHRN | c.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 | |
| 9 | g.114406413G>T | CA466911449 | WHRN | c.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 |