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.114406499C>ACA374620315WHRNc.436G>T (p.Val146Leu)
c.2092G>T (p.Val698Leu)
c.1065G>T
n.1973G>T
c.943G>T (p.Val315Leu)
c.1039G>T (p.Val347Leu)
c.1429G>T (p.Val477Leu)
c.2125G>T (p.Val709Leu)
c.1999G>T (p.Val667Leu)
c.1882G>T (p.Val628Leu)
c.802G>T (p.Val268Leu)
n.3029G>T
n.2927G>T
n.2340G>T
n.2238G>T
9g.114406499C>GCA374620316WHRNc.436G>C (p.Val146Leu)
c.2092G>C (p.Val698Leu)
c.1065G>C
n.1973G>C
c.943G>C (p.Val315Leu)
c.1039G>C (p.Val347Leu)
c.1429G>C (p.Val477Leu)
c.2125G>C (p.Val709Leu)
c.1999G>C (p.Val667Leu)
c.1882G>C (p.Val628Leu)
c.802G>C (p.Val268Leu)
n.3029G>C
n.2927G>C
n.2340G>C
n.2238G>C
9g.114406499C>TCA374620317WHRNc.436G>A (p.Val146Met)
c.2092G>A (p.Val698Met)
c.1065G>A
n.1973G>A
c.943G>A (p.Val315Met)
c.1039G>A (p.Val347Met)
c.1429G>A (p.Val477Met)
c.2125G>A (p.Val709Met)
c.1999G>A (p.Val667Met)
c.1882G>A (p.Val628Met)
c.802G>A (p.Val268Met)
n.3029G>A
n.2927G>A
n.2340G>A
n.2238G>A
9g.114406500T>ACA466911624WHRNc.435A>T (p.Thr145=)
c.2091A>T (p.Thr697=)
c.1064A>T
n.1972A>T
c.942A>T (p.Thr314=)
c.1038A>T (p.Thr346=)
c.1428A>T (p.Thr476=)
c.2124A>T (p.Thr708=)
c.1998A>T (p.Thr666=)
c.1881A>T (p.Thr627=)
c.801A>T (p.Thr267=)
n.3028A>T
n.2926A>T
n.2339A>T
n.2237A>T
9g.114406500T>CCA466911626WHRNc.435A>G (p.Thr145=)
c.2091A>G (p.Thr697=)
c.1064A>G
n.1972A>G
c.942A>G (p.Thr314=)
c.1038A>G (p.Thr346=)
c.1428A>G (p.Thr476=)
c.2124A>G (p.Thr708=)
c.1998A>G (p.Thr666=)
c.1881A>G (p.Thr627=)
c.801A>G (p.Thr267=)
n.3028A>G
n.2926A>G
n.2339A>G
n.2237A>G
gnomAD v4
9g.114406500T>GCA466911625WHRNc.435A>C (p.Thr145=)
c.2091A>C (p.Thr697=)
c.1064A>C
n.1972A>C
c.942A>C (p.Thr314=)
c.1038A>C (p.Thr346=)
c.1428A>C (p.Thr476=)
c.2124A>C (p.Thr708=)
c.1998A>C (p.Thr666=)
c.1881A>C (p.Thr627=)
c.801A>C (p.Thr267=)
n.3028A>C
n.2926A>C
n.2339A>C
n.2237A>C
9g.114406501G>ACA374620320WHRNc.434C>T (p.Thr145Ile)
c.2090C>T (p.Thr697Ile)
c.1063C>T
n.1971C>T
c.941C>T (p.Thr314Ile)
c.1037C>T (p.Thr346Ile)
c.1427C>T (p.Thr476Ile)
c.2123C>T (p.Thr708Ile)
c.1997C>T (p.Thr666Ile)
c.1880C>T (p.Thr627Ile)
c.800C>T (p.Thr267Ile)
n.3027C>T
n.2925C>T
n.2338C>T
n.2236C>T
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
9g.114406501G>CCA374620319WHRNc.434C>G (p.Thr145Arg)
c.2090C>G (p.Thr697Arg)
c.1063C>G
n.1971C>G
c.941C>G (p.Thr314Arg)
c.1037C>G (p.Thr346Arg)
c.1427C>G (p.Thr476Arg)
c.2123C>G (p.Thr708Arg)
c.1997C>G (p.Thr666Arg)
c.1880C>G (p.Thr627Arg)
c.800C>G (p.Thr267Arg)
n.3027C>G
n.2925C>G
n.2338C>G
n.2236C>G
9g.114406501G=CA1873827117WHRNc.434C= (p.Thr145=)
c.2090C= (p.Thr697=)
c.1063C=
n.1971C=
c.941C= (p.Thr314=)
c.1037C= (p.Thr346=)
c.1427C= (p.Thr476=)
c.2123C= (p.Thr708=)
c.1997C= (p.Thr666=)
c.1880C= (p.Thr627=)
c.800C= (p.Thr267=)
n.3027C=
n.2925C=
n.2338C=
n.2236C=
9g.114406501G>TCA374620318WHRNc.434C>A (p.Thr145Lys)
c.2090C>A (p.Thr697Lys)
c.1063C>A
n.1971C>A
c.941C>A (p.Thr314Lys)
c.1037C>A (p.Thr346Lys)
c.1427C>A (p.Thr476Lys)
c.2123C>A (p.Thr708Lys)
c.1997C>A (p.Thr666Lys)
c.1880C>A (p.Thr627Lys)
c.800C>A (p.Thr267Lys)
n.3027C>A
n.2925C>A
n.2338C>A
n.2236C>A
9g.114406502T>ACA374620321WHRNc.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
9g.114406502T>CCA374620322WHRNc.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
9g.114406502T>GCA374620323WHRNc.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
9g.114406502T=CA1873827118WHRNc.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=
9g.114406503G>ACA466911632WHRNc.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
9g.114406503G>CCA466911633WHRNc.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
9g.114406503G>TCA466911634WHRNc.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
9g.114406504G>ACA374620324WHRNc.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
9g.114406504G>CCA374620325WHRNc.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
9g.114406504G>TCA374620326WHRNc.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
9g.114406505C>ACA374620327WHRNc.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
9g.114406505C>GCA374620329WHRNc.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
9g.114406505C>TCA374620328WHRNc.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
9g.114406506C>ACA374620330WHRNc.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
9g.114406506C=CA1873827119WHRNc.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=
9g.114406506C>GCA374620331WHRNc.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
9g.114406506C>TCA136904WHRNc.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
9g.114406507T>ACA374620332WHRNc.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
9g.114406507T>CCA374620333WHRNc.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
9g.114406507T>GCA374620334WHRNc.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
9g.114406508C>ACA374620335WHRNc.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
9g.114406508C>GCA374620336WHRNc.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
9g.114406508C>TCA374620337WHRNc.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
9g.114406509T>ACA466911639WHRNc.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
9g.114406509T>CCA466911640WHRNc.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
9g.114406509T>GCA466911641WHRNc.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
9g.114406510G>ACA374620338WHRNc.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
9g.114406510G>CCA374620339WHRNc.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
9g.114406510G=CA1873827120WHRNc.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=
9g.114406510G>TCA374620340WHRNc.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
9g.114406511C>ACA374620342WHRNc.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
9g.114406511C=CA1873827121WHRNc.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=
9g.114406511C>GCA374620343WHRNc.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
9g.114406511C>TCA374620341WHRNc.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
9g.114406512A>CCA466911646WHRNc.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
9g.114406512A>GCA466911648WHRNc.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
9g.114406512A>TCA466911650WHRNc.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
9g.114406513G>ACA374620344WHRNc.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
9g.114406513G>CCA374620346WHRNc.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

Number of alleles fetched