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.114406502T>A | CA374620321 | WHRN | c.433A>T (p.Thr145Ser) c.2089A>T (p.Thr697Ser) c.1062A>T n.1970A>T c.940A>T (p.Thr314Ser) c.1036A>T (p.Thr346Ser) c.1426A>T (p.Thr476Ser) c.2122A>T (p.Thr708Ser) c.1996A>T (p.Thr666Ser) c.1879A>T (p.Thr627Ser) c.799A>T (p.Thr267Ser) n.3026A>T n.2924A>T n.2337A>T n.2235A>T | |
9 | g.114406502T>C | CA374620322 | WHRN | c.433A>G (p.Thr145Ala) c.2089A>G (p.Thr697Ala) c.1062A>G n.1970A>G c.940A>G (p.Thr314Ala) c.1036A>G (p.Thr346Ala) c.1426A>G (p.Thr476Ala) c.2122A>G (p.Thr708Ala) c.1996A>G (p.Thr666Ala) c.1879A>G (p.Thr627Ala) c.799A>G (p.Thr267Ala) n.3026A>G n.2924A>G n.2337A>G n.2235A>G | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.114406502T>G | CA374620323 | WHRN | c.433A>C (p.Thr145Pro) c.2089A>C (p.Thr697Pro) c.1062A>C n.1970A>C c.940A>C (p.Thr314Pro) c.1036A>C (p.Thr346Pro) c.1426A>C (p.Thr476Pro) c.2122A>C (p.Thr708Pro) c.1996A>C (p.Thr666Pro) c.1879A>C (p.Thr627Pro) c.799A>C (p.Thr267Pro) n.3026A>C n.2924A>C n.2337A>C n.2235A>C | |
9 | g.114406502T= | CA1873827118 | WHRN | c.433A= (p.Thr145=) c.2089A= (p.Thr697=) c.1062A= n.1970A= c.940A= (p.Thr314=) c.1036A= (p.Thr346=) c.1426A= (p.Thr476=) c.2122A= (p.Thr708=) c.1996A= (p.Thr666=) c.1879A= (p.Thr627=) c.799A= (p.Thr267=) n.3026A= n.2924A= n.2337A= n.2235A= | |
9 | g.114406503G>A | CA466911632 | WHRN | c.432C>T (p.Ala144=) c.2088C>T (p.Ala696=) c.1061C>T n.1969C>T c.939C>T (p.Ala313=) c.1035C>T (p.Ala345=) c.1425C>T (p.Ala475=) c.2121C>T (p.Ala707=) c.1995C>T (p.Ala665=) c.1878C>T (p.Ala626=) c.798C>T (p.Ala266=) n.3025C>T n.2923C>T n.2336C>T n.2234C>T | gnomAD v4 |
9 | g.114406503G>C | CA466911633 | WHRN | c.432C>G (p.Ala144=) c.2088C>G (p.Ala696=) c.1061C>G n.1969C>G c.939C>G (p.Ala313=) c.1035C>G (p.Ala345=) c.1425C>G (p.Ala475=) c.2121C>G (p.Ala707=) c.1995C>G (p.Ala665=) c.1878C>G (p.Ala626=) c.798C>G (p.Ala266=) n.3025C>G n.2923C>G n.2336C>G n.2234C>G | |
9 | g.114406503G>T | CA466911634 | WHRN | c.432C>A (p.Ala144=) c.2088C>A (p.Ala696=) c.1061C>A n.1969C>A c.939C>A (p.Ala313=) c.1035C>A (p.Ala345=) c.1425C>A (p.Ala475=) c.2121C>A (p.Ala707=) c.1995C>A (p.Ala665=) c.1878C>A (p.Ala626=) c.798C>A (p.Ala266=) n.3025C>A n.2923C>A n.2336C>A n.2234C>A | |
9 | g.114406504G>A | CA374620324 | WHRN | c.431C>T (p.Ala144Val) c.2087C>T (p.Ala696Val) c.1060C>T n.1968C>T c.938C>T (p.Ala313Val) c.1034C>T (p.Ala345Val) c.1424C>T (p.Ala475Val) c.2120C>T (p.Ala707Val) c.1994C>T (p.Ala665Val) c.1877C>T (p.Ala626Val) c.797C>T (p.Ala266Val) n.3024C>T n.2922C>T n.2335C>T n.2233C>T | |
9 | g.114406504G>C | CA374620325 | WHRN | c.431C>G (p.Ala144Gly) c.2087C>G (p.Ala696Gly) c.1060C>G n.1968C>G c.938C>G (p.Ala313Gly) c.1034C>G (p.Ala345Gly) c.1424C>G (p.Ala475Gly) c.2120C>G (p.Ala707Gly) c.1994C>G (p.Ala665Gly) c.1877C>G (p.Ala626Gly) c.797C>G (p.Ala266Gly) n.3024C>G n.2922C>G n.2335C>G n.2233C>G | |
9 | g.114406504G>T | CA374620326 | WHRN | c.431C>A (p.Ala144Asp) c.2087C>A (p.Ala696Asp) c.1060C>A n.1968C>A c.938C>A (p.Ala313Asp) c.1034C>A (p.Ala345Asp) c.1424C>A (p.Ala475Asp) c.2120C>A (p.Ala707Asp) c.1994C>A (p.Ala665Asp) c.1877C>A (p.Ala626Asp) c.797C>A (p.Ala266Asp) n.3024C>A n.2922C>A n.2335C>A n.2233C>A | |
9 | g.114406505C>A | CA374620327 | WHRN | c.430G>T (p.Ala144Ser) c.2086G>T (p.Ala696Ser) c.1059G>T n.1967G>T c.937G>T (p.Ala313Ser) c.1033G>T (p.Ala345Ser) c.1423G>T (p.Ala475Ser) c.2119G>T (p.Ala707Ser) c.1993G>T (p.Ala665Ser) c.1876G>T (p.Ala626Ser) c.796G>T (p.Ala266Ser) n.3023G>T n.2921G>T n.2334G>T n.2232G>T | |
9 | g.114406505C>G | CA374620329 | WHRN | c.430G>C (p.Ala144Pro) c.2086G>C (p.Ala696Pro) c.1059G>C n.1967G>C c.937G>C (p.Ala313Pro) c.1033G>C (p.Ala345Pro) c.1423G>C (p.Ala475Pro) c.2119G>C (p.Ala707Pro) c.1993G>C (p.Ala665Pro) c.1876G>C (p.Ala626Pro) c.796G>C (p.Ala266Pro) n.3023G>C n.2921G>C n.2334G>C n.2232G>C | |
9 | g.114406505C>T | CA374620328 | WHRN | c.430G>A (p.Ala144Thr) c.2086G>A (p.Ala696Thr) c.1059G>A n.1967G>A c.937G>A (p.Ala313Thr) c.1033G>A (p.Ala345Thr) c.1423G>A (p.Ala475Thr) c.2119G>A (p.Ala707Thr) c.1993G>A (p.Ala665Thr) c.1876G>A (p.Ala626Thr) c.796G>A (p.Ala266Thr) n.3023G>A n.2921G>A n.2334G>A n.2232G>A | |
9 | g.114406506C>A | CA374620330 | WHRN | c.429G>T (p.Glu143Asp) c.2085G>T (p.Glu695Asp) c.1058G>T n.1966G>T c.936G>T (p.Glu312Asp) c.1032G>T (p.Glu344Asp) c.1422G>T (p.Glu474Asp) c.2118G>T (p.Glu706Asp) c.1992G>T (p.Glu664Asp) c.1875G>T (p.Glu625Asp) c.795G>T (p.Glu265Asp) n.3022G>T n.2920G>T n.2333G>T n.2231G>T | |
9 | g.114406506C= | CA1873827119 | WHRN | c.429G= (p.Glu143=) c.2085G= (p.Glu695=) c.1058G= n.1966G= c.936G= (p.Glu312=) c.1032G= (p.Glu344=) c.1422G= (p.Glu474=) c.2118G= (p.Glu706=) c.1992G= (p.Glu664=) c.1875G= (p.Glu625=) c.795G= (p.Glu265=) n.3022G= n.2920G= n.2333G= n.2231G= | |
9 | g.114406506C>G | CA374620331 | WHRN | c.429G>C (p.Glu143Asp) c.2085G>C (p.Glu695Asp) c.1058G>C n.1966G>C c.936G>C (p.Glu312Asp) c.1032G>C (p.Glu344Asp) c.1422G>C (p.Glu474Asp) c.2118G>C (p.Glu706Asp) c.1992G>C (p.Glu664Asp) c.1875G>C (p.Glu625Asp) c.795G>C (p.Glu265Asp) n.3022G>C n.2920G>C n.2333G>C n.2231G>C | |
9 | g.114406506C>T | CA136904 | WHRN | c.429G>A (p.Glu143=) c.2085G>A (p.Glu695=) c.1058G>A n.1966G>A c.936G>A (p.Glu312=) c.1032G>A (p.Glu344=) c.1422G>A (p.Glu474=) c.2118G>A (p.Glu706=) c.1992G>A (p.Glu664=) c.1875G>A (p.Glu625=) c.795G>A (p.Glu265=) n.3022G>A n.2920G>A n.2333G>A n.2231G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.114406507T>A | CA374620332 | WHRN | c.428A>T (p.Glu143Val) c.2084A>T (p.Glu695Val) c.1057A>T n.1965A>T c.935A>T (p.Glu312Val) c.1031A>T (p.Glu344Val) c.1421A>T (p.Glu474Val) c.2117A>T (p.Glu706Val) c.1991A>T (p.Glu664Val) c.1874A>T (p.Glu625Val) c.794A>T (p.Glu265Val) n.3021A>T n.2919A>T n.2332A>T n.2230A>T | |
9 | g.114406507T>C | CA374620333 | WHRN | c.428A>G (p.Glu143Gly) c.2084A>G (p.Glu695Gly) c.1057A>G n.1965A>G c.935A>G (p.Glu312Gly) c.1031A>G (p.Glu344Gly) c.1421A>G (p.Glu474Gly) c.2117A>G (p.Glu706Gly) c.1991A>G (p.Glu664Gly) c.1874A>G (p.Glu625Gly) c.794A>G (p.Glu265Gly) n.3021A>G n.2919A>G n.2332A>G n.2230A>G | |
9 | g.114406507T>G | CA374620334 | WHRN | c.428A>C (p.Glu143Ala) c.2084A>C (p.Glu695Ala) c.1057A>C n.1965A>C c.935A>C (p.Glu312Ala) c.1031A>C (p.Glu344Ala) c.1421A>C (p.Glu474Ala) c.2117A>C (p.Glu706Ala) c.1991A>C (p.Glu664Ala) c.1874A>C (p.Glu625Ala) c.794A>C (p.Glu265Ala) n.3021A>C n.2919A>C n.2332A>C n.2230A>C | |
9 | g.114406508C>A | CA374620335 | WHRN | c.427G>T (p.Glu143Ter) c.2083G>T (p.Glu695Ter) c.1056G>T n.1964G>T c.934G>T (p.Glu312Ter) c.1030G>T (p.Glu344Ter) c.1420G>T (p.Glu474Ter) c.2116G>T (p.Glu706Ter) c.1990G>T (p.Glu664Ter) c.1873G>T (p.Glu625Ter) c.793G>T (p.Glu265Ter) n.3020G>T n.2918G>T n.2331G>T n.2229G>T | |
9 | g.114406508C>G | CA374620336 | WHRN | c.427G>C (p.Glu143Gln) c.2083G>C (p.Glu695Gln) c.1056G>C n.1964G>C c.934G>C (p.Glu312Gln) c.1030G>C (p.Glu344Gln) c.1420G>C (p.Glu474Gln) c.2116G>C (p.Glu706Gln) c.1990G>C (p.Glu664Gln) c.1873G>C (p.Glu625Gln) c.793G>C (p.Glu265Gln) n.3020G>C n.2918G>C n.2331G>C n.2229G>C | |
9 | g.114406508C>T | CA374620337 | WHRN | c.427G>A (p.Glu143Lys) c.2083G>A (p.Glu695Lys) c.1056G>A n.1964G>A c.934G>A (p.Glu312Lys) c.1030G>A (p.Glu344Lys) c.1420G>A (p.Glu474Lys) c.2116G>A (p.Glu706Lys) c.1990G>A (p.Glu664Lys) c.1873G>A (p.Glu625Lys) c.793G>A (p.Glu265Lys) n.3020G>A n.2918G>A n.2331G>A n.2229G>A | gnomAD v4 |
9 | g.114406509T>A | CA466911639 | WHRN | c.426A>T (p.Ala142=) c.2082A>T (p.Ala694=) c.1055A>T n.1963A>T c.933A>T (p.Ala311=) c.1029A>T (p.Ala343=) c.1419A>T (p.Ala473=) c.2115A>T (p.Ala705=) c.1989A>T (p.Ala663=) c.1872A>T (p.Ala624=) c.792A>T (p.Ala264=) n.3019A>T n.2917A>T n.2330A>T n.2228A>T | |
9 | g.114406509T>C | CA466911640 | WHRN | c.426A>G (p.Ala142=) c.2082A>G (p.Ala694=) c.1055A>G n.1963A>G c.933A>G (p.Ala311=) c.1029A>G (p.Ala343=) c.1419A>G (p.Ala473=) c.2115A>G (p.Ala705=) c.1989A>G (p.Ala663=) c.1872A>G (p.Ala624=) c.792A>G (p.Ala264=) n.3019A>G n.2917A>G n.2330A>G n.2228A>G | |
9 | g.114406509T>G | CA466911641 | WHRN | c.426A>C (p.Ala142=) c.2082A>C (p.Ala694=) c.1055A>C n.1963A>C c.933A>C (p.Ala311=) c.1029A>C (p.Ala343=) c.1419A>C (p.Ala473=) c.2115A>C (p.Ala705=) c.1989A>C (p.Ala663=) c.1872A>C (p.Ala624=) c.792A>C (p.Ala264=) n.3019A>C n.2917A>C n.2330A>C n.2228A>C | |
9 | g.114406510G>A | CA374620338 | WHRN | c.425C>T (p.Ala142Val) c.2081C>T (p.Ala694Val) c.1054C>T n.1962C>T c.932C>T (p.Ala311Val) c.1028C>T (p.Ala343Val) c.1418C>T (p.Ala473Val) c.2114C>T (p.Ala705Val) c.1988C>T (p.Ala663Val) c.1871C>T (p.Ala624Val) c.791C>T (p.Ala264Val) n.3018C>T n.2916C>T n.2329C>T n.2227C>T | dbSNP gnomAD v4 |
9 | g.114406510G>C | CA374620339 | WHRN | c.425C>G (p.Ala142Gly) c.2081C>G (p.Ala694Gly) c.1054C>G n.1962C>G c.932C>G (p.Ala311Gly) c.1028C>G (p.Ala343Gly) c.1418C>G (p.Ala473Gly) c.2114C>G (p.Ala705Gly) c.1988C>G (p.Ala663Gly) c.1871C>G (p.Ala624Gly) c.791C>G (p.Ala264Gly) n.3018C>G n.2916C>G n.2329C>G n.2227C>G | |
9 | g.114406510G= | CA1873827120 | WHRN | c.425C= (p.Ala142=) c.2081C= (p.Ala694=) c.1054C= n.1962C= c.932C= (p.Ala311=) c.1028C= (p.Ala343=) c.1418C= (p.Ala473=) c.2114C= (p.Ala705=) c.1988C= (p.Ala663=) c.1871C= (p.Ala624=) c.791C= (p.Ala264=) n.3018C= n.2916C= n.2329C= n.2227C= | |
9 | g.114406510G>T | CA374620340 | WHRN | c.425C>A (p.Ala142Glu) c.2081C>A (p.Ala694Glu) c.1054C>A n.1962C>A c.932C>A (p.Ala311Glu) c.1028C>A (p.Ala343Glu) c.1418C>A (p.Ala473Glu) c.2114C>A (p.Ala705Glu) c.1988C>A (p.Ala663Glu) c.1871C>A (p.Ala624Glu) c.791C>A (p.Ala264Glu) n.3018C>A n.2916C>A n.2329C>A n.2227C>A | |
9 | g.114406511C>A | CA374620342 | WHRN | c.424G>T (p.Ala142Ser) c.2080G>T (p.Ala694Ser) c.1053G>T n.1961G>T c.931G>T (p.Ala311Ser) c.1027G>T (p.Ala343Ser) c.1417G>T (p.Ala473Ser) c.2113G>T (p.Ala705Ser) c.1987G>T (p.Ala663Ser) c.1870G>T (p.Ala624Ser) c.790G>T (p.Ala264Ser) n.3017G>T n.2915G>T n.2328G>T n.2226G>T | |
9 | g.114406511C= | CA1873827121 | WHRN | c.424G= (p.Ala142=) c.2080G= (p.Ala694=) c.1053G= n.1961G= c.931G= (p.Ala311=) c.1027G= (p.Ala343=) c.1417G= (p.Ala473=) c.2113G= (p.Ala705=) c.1987G= (p.Ala663=) c.1870G= (p.Ala624=) c.790G= (p.Ala264=) n.3017G= n.2915G= n.2328G= n.2226G= | |
9 | g.114406511C>G | CA374620343 | WHRN | c.424G>C (p.Ala142Pro) c.2080G>C (p.Ala694Pro) c.1053G>C n.1961G>C c.931G>C (p.Ala311Pro) c.1027G>C (p.Ala343Pro) c.1417G>C (p.Ala473Pro) c.2113G>C (p.Ala705Pro) c.1987G>C (p.Ala663Pro) c.1870G>C (p.Ala624Pro) c.790G>C (p.Ala264Pro) n.3017G>C n.2915G>C n.2328G>C n.2226G>C | |
9 | g.114406511C>T | CA374620341 | WHRN | c.424G>A (p.Ala142Thr) c.2080G>A (p.Ala694Thr) c.1053G>A n.1961G>A c.931G>A (p.Ala311Thr) c.1027G>A (p.Ala343Thr) c.1417G>A (p.Ala473Thr) c.2113G>A (p.Ala705Thr) c.1987G>A (p.Ala663Thr) c.1870G>A (p.Ala624Thr) c.790G>A (p.Ala264Thr) n.3017G>A n.2915G>A n.2328G>A n.2226G>A | dbSNP |
9 | g.114406512A>C | CA466911646 | WHRN | c.423T>G (p.Ser141=) c.2079T>G (p.Ser693=) c.1052T>G n.1960T>G c.930T>G (p.Ser310=) c.1026T>G (p.Ser342=) c.1416T>G (p.Ser472=) c.2112T>G (p.Ser704=) c.1986T>G (p.Ser662=) c.1869T>G (p.Ser623=) c.789T>G (p.Ser263=) n.3016T>G n.2914T>G n.2327T>G n.2225T>G | |
9 | g.114406512A>G | CA466911648 | WHRN | c.423T>C (p.Ser141=) c.2079T>C (p.Ser693=) c.1052T>C n.1960T>C c.930T>C (p.Ser310=) c.1026T>C (p.Ser342=) c.1416T>C (p.Ser472=) c.2112T>C (p.Ser704=) c.1986T>C (p.Ser662=) c.1869T>C (p.Ser623=) c.789T>C (p.Ser263=) n.3016T>C n.2914T>C n.2327T>C n.2225T>C | |
9 | g.114406512A>T | CA466911650 | WHRN | c.423T>A (p.Ser141=) c.2079T>A (p.Ser693=) c.1052T>A n.1960T>A c.930T>A (p.Ser310=) c.1026T>A (p.Ser342=) c.1416T>A (p.Ser472=) c.2112T>A (p.Ser704=) c.1986T>A (p.Ser662=) c.1869T>A (p.Ser623=) c.789T>A (p.Ser263=) n.3016T>A n.2914T>A n.2327T>A n.2225T>A | |
9 | g.114406513G>A | CA374620344 | WHRN | c.422C>T (p.Ser141Phe) c.2078C>T (p.Ser693Phe) c.1051C>T n.1959C>T c.929C>T (p.Ser310Phe) c.1025C>T (p.Ser342Phe) c.1415C>T (p.Ser472Phe) c.2111C>T (p.Ser704Phe) c.1985C>T (p.Ser662Phe) c.1868C>T (p.Ser623Phe) c.788C>T (p.Ser263Phe) n.3015C>T n.2913C>T n.2326C>T n.2224C>T | |
9 | g.114406513G>C | CA374620346 | WHRN | c.422C>G (p.Ser141Cys) c.2078C>G (p.Ser693Cys) c.1051C>G n.1959C>G c.929C>G (p.Ser310Cys) c.1025C>G (p.Ser342Cys) c.1415C>G (p.Ser472Cys) c.2111C>G (p.Ser704Cys) c.1985C>G (p.Ser662Cys) c.1868C>G (p.Ser623Cys) c.788C>G (p.Ser263Cys) n.3015C>G n.2913C>G n.2326C>G n.2224C>G | |
9 | g.114406513G>T | CA374620345 | WHRN | c.422C>A (p.Ser141Tyr) c.2078C>A (p.Ser693Tyr) c.1051C>A n.1959C>A c.929C>A (p.Ser310Tyr) c.1025C>A (p.Ser342Tyr) c.1415C>A (p.Ser472Tyr) c.2111C>A (p.Ser704Tyr) c.1985C>A (p.Ser662Tyr) c.1868C>A (p.Ser623Tyr) c.788C>A (p.Ser263Tyr) n.3015C>A n.2913C>A n.2326C>A n.2224C>A | |
9 | g.114406514A>C | CA374620347 | WHRN | c.421T>G (p.Ser141Ala) c.2077T>G (p.Ser693Ala) c.1050T>G n.1958T>G c.928T>G (p.Ser310Ala) c.1024T>G (p.Ser342Ala) c.1414T>G (p.Ser472Ala) c.2110T>G (p.Ser704Ala) c.1984T>G (p.Ser662Ala) c.1867T>G (p.Ser623Ala) c.787T>G (p.Ser263Ala) n.3014T>G n.2912T>G n.2325T>G n.2223T>G | |
9 | g.114406514A>G | CA374620349 | WHRN | c.421T>C (p.Ser141Pro) c.2077T>C (p.Ser693Pro) c.1050T>C n.1958T>C c.928T>C (p.Ser310Pro) c.1024T>C (p.Ser342Pro) c.1414T>C (p.Ser472Pro) c.2110T>C (p.Ser704Pro) c.1984T>C (p.Ser662Pro) c.1867T>C (p.Ser623Pro) c.787T>C (p.Ser263Pro) n.3014T>C n.2912T>C n.2325T>C n.2223T>C | |
9 | g.114406514A>T | CA374620348 | WHRN | c.421T>A (p.Ser141Thr) c.2077T>A (p.Ser693Thr) c.1050T>A n.1958T>A c.928T>A (p.Ser310Thr) c.1024T>A (p.Ser342Thr) c.1414T>A (p.Ser472Thr) c.2110T>A (p.Ser704Thr) c.1984T>A (p.Ser662Thr) c.1867T>A (p.Ser623Thr) c.787T>A (p.Ser263Thr) n.3014T>A n.2912T>A n.2325T>A n.2223T>A | |
9 | g.114406515G>A | CA466911652 | WHRN | c.420C>T (p.Pro140=) c.2076C>T (p.Pro692=) c.1049C>T n.1957C>T c.927C>T (p.Pro309=) c.1023C>T (p.Pro341=) c.1413C>T (p.Pro471=) c.2109C>T (p.Pro703=) c.1983C>T (p.Pro661=) c.1866C>T (p.Pro622=) c.786C>T (p.Pro262=) n.3013C>T n.2911C>T n.2324C>T n.2222C>T | |
9 | g.114406515G>C | CA466911653 | WHRN | c.420C>G (p.Pro140=) c.2076C>G (p.Pro692=) c.1049C>G n.1957C>G c.927C>G (p.Pro309=) c.1023C>G (p.Pro341=) c.1413C>G (p.Pro471=) c.2109C>G (p.Pro703=) c.1983C>G (p.Pro661=) c.1866C>G (p.Pro622=) c.786C>G (p.Pro262=) n.3013C>G n.2911C>G n.2324C>G n.2222C>G | gnomAD v4 |
9 | g.114406515G= | CA1873827122 | WHRN | c.420C= (p.Pro140=) c.2076C= (p.Pro692=) c.1049C= n.1957C= c.927C= (p.Pro309=) c.1023C= (p.Pro341=) c.1413C= (p.Pro471=) c.2109C= (p.Pro703=) c.1983C= (p.Pro661=) c.1866C= (p.Pro622=) c.786C= (p.Pro262=) n.3013C= n.2911C= n.2324C= n.2222C= | |
9 | g.114406515G>T | CA5205739 | WHRN | c.420C>A (p.Pro140=) c.2076C>A (p.Pro692=) c.1049C>A n.1957C>A c.927C>A (p.Pro309=) c.1023C>A (p.Pro341=) c.1413C>A (p.Pro471=) c.2109C>A (p.Pro703=) c.1983C>A (p.Pro661=) c.1866C>A (p.Pro622=) c.786C>A (p.Pro262=) n.3013C>A n.2911C>A n.2324C>A n.2222C>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
9 | g.114406516G>A | CA5205740 | WHRN | c.419C>T (p.Pro140Leu) c.2075C>T (p.Pro692Leu) c.1048C>T n.1956C>T c.926C>T (p.Pro309Leu) c.1022C>T (p.Pro341Leu) c.1412C>T (p.Pro471Leu) c.2108C>T (p.Pro703Leu) c.1982C>T (p.Pro661Leu) c.1865C>T (p.Pro622Leu) c.785C>T (p.Pro262Leu) n.3012C>T n.2910C>T n.2323C>T n.2221C>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
9 | g.114406516G>C | CA374620350 | WHRN | c.419C>G (p.Pro140Arg) c.2075C>G (p.Pro692Arg) c.1048C>G n.1956C>G c.926C>G (p.Pro309Arg) c.1022C>G (p.Pro341Arg) c.1412C>G (p.Pro471Arg) c.2108C>G (p.Pro703Arg) c.1982C>G (p.Pro661Arg) c.1865C>G (p.Pro622Arg) c.785C>G (p.Pro262Arg) n.3012C>G n.2910C>G n.2323C>G n.2221C>G |