Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
8 | g.132888018T>A | CA463216363 | TG | c.2211T>A (p.Ala737=) c.1950T>A (p.Ala650=) | |
8 | g.132888018T>C | CA463216364 | TG | c.2211T>C (p.Ala737=) c.1950T>C (p.Ala650=) | dbSNP gnomAD v2 gnomAD v4 |
8 | g.132888018T>G | CA463216365 | TG | c.2211T>G (p.Ala737=) c.1950T>G (p.Ala650=) | |
8 | g.132888018T= | CA1820989854 | TG | c.2211T= (p.Ala737=) c.1950T= (p.Ala650=) | |
8 | g.132888019T>A | CA372234882 | TG | c.2212T>A (p.Phe738Ile) c.1951T>A (p.Phe651Ile) | |
8 | g.132888019T>C | CA372234883 | TG | c.2212T>C (p.Phe738Leu) c.1951T>C (p.Phe651Leu) | gnomAD v4 |
8 | g.132888019T>G | CA372234884 | TG | c.2212T>G (p.Phe738Val) c.1951T>G (p.Phe651Val) | |
8 | g.132888020T>A | CA372234885 | TG | c.2213T>A (p.Phe738Tyr) c.1952T>A (p.Phe651Tyr) | |
8 | g.132888020T>C | CA372234886 | TG | c.2213T>C (p.Phe738Ser) c.1952T>C (p.Phe651Ser) | |
8 | g.132888020T>G | CA372234887 | TG | c.2213T>G (p.Phe738Cys) c.1952T>G (p.Phe651Cys) | |
8 | g.132888021C>A | CA372234888 | TG | c.2214C>A (p.Phe738Leu) c.1953C>A (p.Phe651Leu) | |
8 | g.132888021C= | CA1820989855 | TG | c.2214C= (p.Phe738=) c.1953C= (p.Phe651=) | |
8 | g.132888021C>G | CA372234889 | TG | c.2214C>G (p.Phe738Leu) c.1953C>G (p.Phe651Leu) | |
8 | g.132888021C>T | CA4883352 | TG | c.2214C>T (p.Phe738=) c.1953C>T (p.Phe651=) | dbSNP ExAC gnomAD v2 |
8 | g.132888022C>A | CA372234890 | TG | c.2215C>A (p.Leu739Ile) c.1954C>A (p.Leu652Ile) | |
8 | g.132888022C= | CA1820989856 | TG | c.2215C= (p.Leu739=) c.1954C= (p.Leu652=) | |
8 | g.132888022C>G | CA372234891 | TG | c.2215C>G (p.Leu739Val) c.1954C>G (p.Leu652Val) | dbSNP |
8 | g.132888022C>T | CA372234892 | TG | c.2215C>T (p.Leu739Phe) c.1954C>T (p.Leu652Phe) | dbSNP gnomAD v4 |
8 | g.132888023T>A | CA372234893 | TG | c.2216T>A (p.Leu739His) c.1955T>A (p.Leu652His) | |
8 | g.132888023T>C | CA372234894 | TG | c.2216T>C (p.Leu739Pro) c.1955T>C (p.Leu652Pro) | |
8 | g.132888023T>G | CA372234895 | TG | c.2216T>G (p.Leu739Arg) c.1955T>G (p.Leu652Arg) | |
8 | g.132888024C>A | CA4883353 | TG | c.2217C>A (p.Leu739=) c.1956C>A (p.Leu652=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.132888024C= | CA1820989857 | TG | c.2217C= (p.Leu739=) c.1956C= (p.Leu652=) | |
8 | g.132888024C>G | CA463216370 | TG | c.2217C>G (p.Leu739=) c.1956C>G (p.Leu652=) | |
8 | g.132888024C>T | CA463216369 | TG | c.2217C>T (p.Leu739=) c.1956C>T (p.Leu652=) | |
8 | g.132888025A>C | CA463216373 | TG | c.2218A>C (p.Arg740=) c.1957A>C (p.Arg653=) | |
8 | g.132888025A>G | CA372234896 | TG | c.2218A>G (p.Arg740Gly) c.1957A>G (p.Arg653Gly) | |
8 | g.132888025A>T | CA372234897 | TG | c.2218A>T (p.Arg740Trp) c.1957A>T (p.Arg653Trp) | |
8 | g.132888026G>A | CA372234898 | TG | c.2219G>A (p.Arg740Lys) c.1958G>A (p.Arg653Lys) | |
8 | g.132888026G>C | CA372234899 | TG | c.2219G>C (p.Arg740Thr) c.1958G>C (p.Arg653Thr) | |
8 | g.132888026G>T | CA372234900 | TG | c.2219G>T (p.Arg740Met) c.1958G>T (p.Arg653Met) | |
8 | g.132888027G>A | CA463216375 | TG | c.2220G>A (p.Arg740=) c.1959G>A (p.Arg653=) | COSMIC |
8 | g.132888027G>C | CA372234901 | TG | c.2220G>C (p.Arg740Ser) c.1959G>C (p.Arg653Ser) | |
8 | g.132888027G>T | CA372234902 | TG | c.2220G>T (p.Arg740Ser) c.1959G>T (p.Arg653Ser) | |
8 | g.132888028A>C | CA372234903 | TG | c.2221A>C (p.Thr741Pro) c.1960A>C (p.Thr654Pro) | |
8 | g.132888028A>G | CA372234905 | TG | c.2221A>G (p.Thr741Ala) c.1960A>G (p.Thr654Ala) | |
8 | g.132888028A>T | CA372234904 | TG | c.2221A>T (p.Thr741Ser) c.1960A>T (p.Thr654Ser) | |
8 | g.132888029C>A | CA372234906 | TG | c.2222C>A (p.Thr741Lys) c.1961C>A (p.Thr654Lys) | |
8 | g.132888029C= | CA1820989858 | TG | c.2222C= (p.Thr741=) c.1961C= (p.Thr654=) | |
8 | g.132888029C>G | CA372234907 | TG | c.2222C>G (p.Thr741Arg) c.1961C>G (p.Thr654Arg) | |
8 | g.132888029C>T | CA4883354 | TG | c.2222C>T (p.Thr741Met) c.1961C>T (p.Thr654Met) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.132888029dup | CA2579253783 | TG | c.2222dup (p.Val742GlyfsTer7) c.1961dup (p.Val655GlyfsTer7) | |
8 | g.132888030G>A | CA4883355 | TG | c.2223G>A (p.Thr741=) c.1962G>A (p.Thr654=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.132888030G>C | CA463216380 | TG | c.2223G>C (p.Thr741=) c.1962G>C (p.Thr654=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
8 | g.132888030G= | CA1820989859 | TG | c.2223G= (p.Thr741=) c.1962G= (p.Thr654=) | |
8 | g.132888030G>T | CA463216379 | TG | c.2223G>T (p.Thr741=) c.1962G>T (p.Thr654=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.132888031G>A | CA4883356 | TG | c.2224G>A (p.Val742Met) c.1963G>A (p.Val655Met) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.132888031G>C | CA372234908 | TG | c.2224G>C (p.Val742Leu) c.1963G>C (p.Val655Leu) | |
8 | g.132888031G= | CA1820989860 | TG | c.2224G= (p.Val742=) c.1963G= (p.Val655=) | |
8 | g.132888031G>T | CA186284308 | TG | c.2224G>T (p.Val742Leu) c.1963G>T (p.Val655Leu) | dbSNP |
8 | g.132888032T>A | CA372234909 | TG | c.2225T>A (p.Val742Glu) c.1964T>A (p.Val655Glu) | |
8 | g.132888032T>C | CA4883358 | TG | c.2225T>C (p.Val742Ala) c.1964T>C (p.Val655Ala) | dbSNP ExAC gnomAD v2 gnomAD v4 |
8 | g.132888032T>G | CA4883357 | TG | c.2225T>G (p.Val742Gly) c.1964T>G (p.Val655Gly) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.132888032T= | CA1820989861 | TG | c.2225T= (p.Val742=) c.1964T= (p.Val655=) | |
8 | g.132888033G>A | CA463216381 | TG | c.2226G>A (p.Val742=) c.1965G>A (p.Val655=) | COSMIC |
8 | g.132888033G>C | CA463216382 | TG | c.2226G>C (p.Val742=) c.1965G>C (p.Val655=) | |
8 | g.132888033G>T | CA463216383 | TG | c.2226G>T (p.Val742=) c.1965G>T (p.Val655=) | |
8 | g.132888034C>A | CA372234910 | TG | c.2227C>A (p.Gln743Lys) c.1966C>A (p.Gln656Lys) | |
8 | g.132888034C>G | CA372234912 | TG | c.2227C>G (p.Gln743Glu) c.1966C>G (p.Gln656Glu) | |
8 | g.132888034C>T | CA372234911 | TG | c.2227C>T (p.Gln743Ter) c.1966C>T (p.Gln656Ter) | gnomAD v4 |
8 | g.132888035A= | CA1820989862 | TG | c.2228A= (p.Gln743=) c.1967A= (p.Gln656=) | |
8 | g.132888035A>C | CA372234913 | TG | c.2228A>C (p.Gln743Pro) c.1967A>C (p.Gln656Pro) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.132888035A>G | CA372234915 | TG | c.2228A>G (p.Gln743Arg) c.1967A>G (p.Gln656Arg) | |
8 | g.132888035A>T | CA372234914 | TG | c.2228A>T (p.Gln743Leu) c.1967A>T (p.Gln656Leu) | |
8 | g.132888036G>A | CA463216385 | TG | c.2229G>A (p.Gln743=) c.1968G>A (p.Gln656=) | |
8 | g.132888036G>C | CA372234916 | TG | c.2229G>C (p.Gln743His) c.1968G>C (p.Gln656His) | |
8 | g.132888036G>T | CA372234917 | TG | c.2229G>T (p.Gln743His) c.1968G>T (p.Gln656His) | COSMIC |
8 | g.132888037G>A | CA372234918 | TG | c.2230G>A (p.Ala744Thr) c.1969G>A (p.Ala657Thr) | gnomAD v4 |
8 | g.132888037G>C | CA372234919 | TG | c.2230G>C (p.Ala744Pro) c.1969G>C (p.Ala657Pro) | gnomAD v4 |
8 | g.132888037G>T | CA372234920 | TG | c.2230G>T (p.Ala744Ser) c.1969G>T (p.Ala657Ser) | |
8 | g.132888038C>A | CA372234921 | TG | c.2231C>A (p.Ala744Asp) c.1970C>A (p.Ala657Asp) | gnomAD v4 |
8 | g.132888038C= | CA1820989863 | TG | c.2231C= (p.Ala744=) c.1970C= (p.Ala657=) | |
8 | g.132888038C>G | CA372234922 | TG | c.2231C>G (p.Ala744Gly) c.1970C>G (p.Ala657Gly) | gnomAD v4 |
8 | g.132888038C>T | CA372234923 | TG | c.2231C>T (p.Ala744Val) c.1970C>T (p.Ala657Val) | dbSNP gnomAD v4 COSMIC |
8 | g.132888039C>A | CA463216386 | TG | c.2232C>A (p.Ala744=) c.1971C>A (p.Ala657=) | |
8 | g.132888039C= | CA1820989864 | TG | c.2232C= (p.Ala744=) c.1971C= (p.Ala657=) | |
8 | g.132888039C>G | CA463216387 | TG | c.2232C>G (p.Ala744=) c.1971C>G (p.Ala657=) | |
8 | g.132888039C>T | CA463216388 | TG | c.2232C>T (p.Ala744=) c.1971C>T (p.Ala657=) | dbSNP gnomAD v3 gnomAD v4 |
8 | g.132888040C>A | CA372234924 | TG | c.2233C>A (p.Leu745Met) c.1972C>A (p.Leu658Met) | |
8 | g.132888040C= | CA1820989865 | TG | c.2233C= (p.Leu745=) c.1972C= (p.Leu658=) | |
8 | g.132888040C>G | CA372234925 | TG | c.2233C>G (p.Leu745Val) c.1972C>G (p.Leu658Val) | |
8 | g.132888040C>T | CA463216390 | TG | c.2233C>T (p.Leu745=) c.1972C>T (p.Leu658=) | |
8 | g.132888041T>A | CA372234926 | TG | c.2234T>A (p.Leu745Gln) c.1973T>A (p.Leu658Gln) | dbSNP gnomAD v2 gnomAD v4 |
8 | g.132888041T>C | CA372234927 | TG | c.2234T>C (p.Leu745Pro) c.1973T>C (p.Leu658Pro) | gnomAD v4 |
8 | g.132888041T>G | CA372234928 | TG | c.2234T>G (p.Leu745Arg) c.1973T>G (p.Leu658Arg) | |
8 | g.132888041T= | CA1820989866 | TG | c.2234T= (p.Leu745=) c.1973T= (p.Leu658=) | |
8 | g.132888041dup | CA463216391 | TG | c.2234dup (p.Leu746AlafsTer3) c.1973dup (p.Leu659AlafsTer3) | ClinVar dbSNP gnomAD v4 |
8 | g.132888042G>A | CA463216392 | TG | c.2235G>A (p.Leu745=) c.1974G>A (p.Leu658=) | dbSNP gnomAD v3 gnomAD v4 |
8 | g.132888042G>C | CA463216393 | TG | c.2235G>C (p.Leu745=) c.1974G>C (p.Leu658=) | gnomAD v4 |
8 | g.132888042G= | CA1820989867 | TG | c.2235G= (p.Leu745=) c.1974G= (p.Leu658=) | |
8 | g.132888042G>T | CA463216394 | TG | c.2235G>T (p.Leu745=) c.1974G>T (p.Leu658=) | COSMIC |
8 | g.132888043C>A | CA372234929 | TG | c.2236C>A (p.Leu746Ile) c.1975C>A (p.Leu659Ile) | gnomAD v4 |
8 | g.132888043C= | CA1820989868 | TG | c.2236C= (p.Leu746=) c.1975C= (p.Leu659=) | |
8 | g.132888043C>G | CA372234931 | TG | c.2236C>G (p.Leu746Val) c.1975C>G (p.Leu659Val) | dbSNP gnomAD v3 gnomAD v4 |
8 | g.132888043C>T | CA372234930 | TG | c.2236C>T (p.Leu746Phe) c.1975C>T (p.Leu659Phe) | |
8 | g.132888044T>A | CA372234932 | TG | c.2237T>A (p.Leu746His) c.1976T>A (p.Leu659His) | |
8 | g.132888044T>C | CA372234933 | TG | c.2237T>C (p.Leu746Pro) c.1976T>C (p.Leu659Pro) | |
8 | g.132888044T>G | CA372234934 | TG | c.2237T>G (p.Leu746Arg) c.1976T>G (p.Leu659Arg) | |
8 | g.132888045C>A | CA463216397 | TG | c.2238C>A (p.Leu746=) c.1977C>A (p.Leu659=) | |
8 | g.132888045C>G | CA463216399 | TG | c.2238C>G (p.Leu746=) c.1977C>G (p.Leu659=) | |
8 | g.132888045C>T | CA463216400 | TG | c.2238C>T (p.Leu746=) c.1977C>T (p.Leu659=) | |
8 | g.132888048_132888053del | CA2782271368 | TG | c.2241_2246del (p.Asn748_Ser749del) c.1980_1985del (p.Asn661_Ser662del) | |
8 | g.132888046T>A | CA4883359 | TG | c.2239T>A (p.Ser747Thr) c.1978T>A (p.Ser660Thr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
8 | g.132888046T>C | CA372234935 | TG | c.2239T>C (p.Ser747Pro) c.1978T>C (p.Ser660Pro) | |
8 | g.132888046T>G | CA372234936 | TG | c.2239T>G (p.Ser747Ala) c.1978T>G (p.Ser660Ala) | |
8 | g.132888046T= | CA1820989869 | TG | c.2239T= (p.Ser747=) c.1978T= (p.Ser660=) | |
8 | g.132888047C>A | CA372234937 | TG | c.2240C>A (p.Ser747Tyr) c.1979C>A (p.Ser660Tyr) | |
8 | g.132888047C>G | CA372234938 | TG | c.2240C>G (p.Ser747Cys) c.1979C>G (p.Ser660Cys) | |
8 | g.132888047C>T | CA372234939 | TG | c.2240C>T (p.Ser747Phe) c.1979C>T (p.Ser660Phe) | gnomAD v4 |
8 | g.132888048T>A | CA463216401 | TG | c.2241T>A (p.Ser747=) c.1980T>A (p.Ser660=) | |
8 | g.132888048T>C | CA463216402 | TG | c.2241T>C (p.Ser747=) c.1980T>C (p.Ser660=) | |
8 | g.132888048T>G | CA463216403 | TG | c.2241T>G (p.Ser747=) c.1980T>G (p.Ser660=) | |
8 | g.132888048dup | CA2579253784 | TG | c.2241dup (p.Asn748Ter) c.1980dup (p.Asn661Ter) | gnomAD v4 |
8 | g.132888049A>C | CA372234942 | TG | c.2242A>C (p.Asn748His) c.1981A>C (p.Asn661His) | |
8 | g.132888049A>G | CA372234941 | TG | c.2242A>G (p.Asn748Asp) c.1981A>G (p.Asn661Asp) | gnomAD v4 |
8 | g.132888049A>T | CA372234940 | TG | c.2242A>T (p.Asn748Tyr) c.1981A>T (p.Asn661Tyr) | |
8 | g.132888050A= | CA1820989870 | TG | c.2243A= (p.Asn748=) c.1982A= (p.Asn661=) | |
8 | g.132888050A>C | CA372234943 | TG | c.2243A>C (p.Asn748Thr) c.1982A>C (p.Asn661Thr) | |
8 | g.132888050A>G | CA372234944 | TG | c.2243A>G (p.Asn748Ser) c.1982A>G (p.Asn661Ser) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.132888050A>T | CA372234945 | TG | c.2243A>T (p.Asn748Ile) c.1982A>T (p.Asn661Ile) | |
8 | g.132888051C>A | CA372234946 | TG | c.2244C>A (p.Asn748Lys) c.1983C>A (p.Asn661Lys) | |
8 | g.132888051C= | CA1820989871 | TG | c.2244C= (p.Asn748=) c.1983C= (p.Asn661=) | |
8 | g.132888051C>G | CA372234947 | TG | c.2244C>G (p.Asn748Lys) c.1983C>G (p.Asn661Lys) | |
8 | g.132888051C>T | CA4883360 | TG | c.2244C>T (p.Asn748=) c.1983C>T (p.Asn661=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.132888052T>A | CA4883361 | TG | c.2245T>A (p.Ser749Thr) c.1984T>A (p.Ser662Thr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.132888052T>C | CA372234948 | TG | c.2245T>C (p.Ser749Pro) c.1984T>C (p.Ser662Pro) | |
8 | g.132888052T>G | CA372234949 | TG | c.2245T>G (p.Ser749Ala) c.1984T>G (p.Ser662Ala) | |
8 | g.132888052T= | CA1820989872 | TG | c.2245T= (p.Ser749=) c.1984T= (p.Ser662=) | |
8 | g.132888052_132888053delinsTC | CA1820989873 | TG | c.2245_2246delinsTC (p.Ser749=) c.1984_1985delinsTC (p.Ser662=) | |
8 | g.132888053C>A | CA372234950 | TG | c.2246C>A (p.Ser749Tyr) c.1985C>A (p.Ser662Tyr) | |
8 | g.132888053C= | CA1820989875 | TG | c.2246C= (p.Ser749=) c.1985C= (p.Ser662=) | |
8 | g.132888053C>G | CA186284320 | TG | c.2246C>G (p.Ser749Cys) c.1985C>G (p.Ser662Cys) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.132888053C>T | CA4883362 | TG | c.2246C>T (p.Ser749Phe) c.1985C>T (p.Ser662Phe) | dbSNP ExAC gnomAD v2 gnomAD v4 |
8 | g.132888054del | CA1820989874 | TG | c.2247del (p.Ser750AlafsTer?) c.1986del (p.Ser663AlafsTer?) | dbSNP |
8 | g.132888054C>A | CA463216405 | TG | c.2247C>A (p.Ser749=) c.1986C>A (p.Ser662=) | |
8 | g.132888054C= | CA1820989876 | TG | c.2247C= (p.Ser749=) c.1986C= (p.Ser662=) | |
8 | g.132888054C>G | CA463216406 | TG | c.2247C>G (p.Ser749=) c.1986C>G (p.Ser662=) | dbSNP |
8 | g.132888054C>T | CA186284324 | TG | c.2247C>T (p.Ser749=) c.1986C>T (p.Ser662=) | dbSNP |
8 | g.132888055A>C | CA372234953 | TG | c.2248A>C (p.Ser750Arg) c.1987A>C (p.Ser663Arg) | |
8 | g.132888055A>G | CA372234951 | TG | c.2248A>G (p.Ser750Gly) c.1987A>G (p.Ser663Gly) | gnomAD v4 |
8 | g.132888055A>T | CA372234952 | TG | c.2248A>T (p.Ser750Cys) c.1987A>T (p.Ser663Cys) | |
8 | g.132888056G>A | CA372234954 | TG | c.2249G>A (p.Ser750Asn) c.1988G>A (p.Ser663Asn) | |
8 | g.132888056G>C | CA372234955 | TG | c.2249G>C (p.Ser750Thr) c.1988G>C (p.Ser663Thr) | |
8 | g.132888056G>T | CA372234956 | TG | c.2249G>T (p.Ser750Ile) c.1988G>T (p.Ser663Ile) | |
8 | g.132888057C>A | CA372234957 | TG | c.2250C>A (p.Ser750Arg) c.1989C>A (p.Ser663Arg) | |
8 | g.132888057C>G | CA372234958 | TG | c.2250C>G (p.Ser750Arg) c.1989C>G (p.Ser663Arg) | |
8 | g.132888057C>T | CA463216408 | TG | c.2250C>T (p.Ser750=) c.1989C>T (p.Ser663=) | |
8 | g.132888058A= | CA1820989877 | TG | c.2251A= (p.Met751=) c.1990A= (p.Met664=) | |
8 | g.132888058A>C | CA186284328 | TG | c.2251A>C (p.Met751Leu) c.1990A>C (p.Met664Leu) | dbSNP gnomAD v4 |
8 | g.132888058A>G | CA4883363 | TG | c.2251A>G (p.Met751Val) c.1990A>G (p.Met664Val) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.132888058A>T | CA372234959 | TG | c.2251A>T (p.Met751Leu) c.1990A>T (p.Met664Leu) | dbSNP |
8 | g.132888059T>A | CA372234960 | TG | c.2252T>A (p.Met751Lys) c.1991T>A (p.Met664Lys) | |
8 | g.132888059T>C | CA372234961 | TG | c.2252T>C (p.Met751Thr) c.1991T>C (p.Met664Thr) | dbSNP |
8 | g.132888059T>G | CA372234962 | TG | c.2252T>G (p.Met751Arg) c.1991T>G (p.Met664Arg) | |
8 | g.132888059T= | CA1820989878 | TG | c.2252T= (p.Met751=) c.1991T= (p.Met664=) | |
8 | g.132888060G>A | CA372234965 | TG | c.2253G>A (p.Met751Ile) c.1992G>A (p.Met664Ile) | gnomAD v4 |
8 | g.132888060G>C | CA372234964 | TG | c.2253G>C (p.Met751Ile) c.1992G>C (p.Met664Ile) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.132888060G= | CA1820989879 | TG | c.2253G= (p.Met751=) c.1992G= (p.Met664=) | |
8 | g.132888060G>T | CA372234963 | TG | c.2253G>T (p.Met751Ile) c.1992G>T (p.Met664Ile) | |
8 | g.132888061C>A | CA372234966 | TG | c.2254C>A (p.Leu752Ile) c.1993C>A (p.Leu665Ile) | dbSNP gnomAD v2 gnomAD v4 |
8 | g.132888061C= | CA1820989880 | TG | c.2254C= (p.Leu752=) c.1993C= (p.Leu665=) | |
8 | g.132888061C>G | CA372234967 | TG | c.2254C>G (p.Leu752Val) c.1993C>G (p.Leu665Val) | gnomAD v4 |
8 | g.132888061C>T | CA186284331 | TG | c.2254C>T (p.Leu752=) c.1993C>T (p.Leu665=) | dbSNP gnomAD v3 gnomAD v4 |
8 | g.132888062T>A | CA372234968 | TG | c.2255T>A (p.Leu752Gln) c.1994T>A (p.Leu665Gln) | |
8 | g.132888062T>C | CA372234969 | TG | c.2255T>C (p.Leu752Pro) c.1994T>C (p.Leu665Pro) | gnomAD v4 |
8 | g.132888062T>G | CA372234970 | TG | c.2255T>G (p.Leu752Arg) c.1994T>G (p.Leu665Arg) | |
8 | g.132888063A>C | CA463216410 | TG | c.2256A>C (p.Leu752=) c.1995A>C (p.Leu665=) | |
8 | g.132888063A>G | CA463216412 | TG | c.2256A>G (p.Leu752=) c.1995A>G (p.Leu665=) | |
8 | g.132888063A>T | CA463216411 | TG | c.2256A>T (p.Leu752=) c.1995A>T (p.Leu665=) | |
8 | g.132888064C>A | CA372234971 | TG | c.2257C>A (p.Pro753Thr) c.1996C>A (p.Pro666Thr) | |
8 | g.132888064C= | CA1820989881 | TG | c.2257C= (p.Pro753=) c.1996C= (p.Pro666=) | |
8 | g.132888064C>G | CA372234972 | TG | c.2257C>G (p.Pro753Ala) c.1996C>G (p.Pro666Ala) | |
8 | g.132888064C>T | CA4883364 | TG | c.2257C>T (p.Pro753Ser) c.1996C>T (p.Pro666Ser) | dbSNP ExAC gnomAD v2 gnomAD v4 |
8 | g.132888065C>A | CA372234973 | TG | c.2258C>A (p.Pro753His) c.1997C>A (p.Pro666His) | |
8 | g.132888065C>G | CA372234974 | TG | c.2258C>G (p.Pro753Arg) c.1997C>G (p.Pro666Arg) | |
8 | g.132888065C>T | CA372234975 | TG | c.2258C>T (p.Pro753Leu) c.1997C>T (p.Pro666Leu) | |
8 | g.132888066C>A | CA463216414 | TG | c.2259C>A (p.Pro753=) c.1998C>A (p.Pro666=) | |
8 | g.132888066C>G | CA463216415 | TG | c.2259C>G (p.Pro753=) c.1998C>G (p.Pro666=) | |
8 | g.132888066C>T | CA463216416 | TG | c.2259C>T (p.Pro753=) c.1998C>T (p.Pro666=) | gnomAD v4 |
8 | g.132888067A= | CA1820989883 | TG | c.2260A= (p.Thr754=) c.1999A= (p.Thr667=) | |
8 | g.132888067A>C | CA372234976 | TG | c.2260A>C (p.Thr754Pro) c.1999A>C (p.Thr667Pro) | |
8 | g.132888067A>G | CA372234977 | TG | c.2260A>G (p.Thr754Ala) c.1999A>G (p.Thr667Ala) | dbSNP gnomAD v2 gnomAD v4 |
8 | g.132888067A>T | CA372234979 | TG | c.2260A>T (p.Thr754Ser) c.1999A>T (p.Thr667Ser) | gnomAD v4 |
8 | g.132888068C>A | CA372234984 | TG | c.2261C>A (p.Thr754Asn) c.2000C>A (p.Thr667Asn) | |
8 | g.132888068C>G | CA372234983 | TG | c.2261C>G (p.Thr754Ser) c.2000C>G (p.Thr667Ser) | gnomAD v4 |
8 | g.132888068C>T | CA372234981 | TG | c.2261C>T (p.Thr754Ile) c.2000C>T (p.Thr667Ile) | |
8 | g.132888070del | CA2688648743 | TG | c.2263del (p.Leu755PhefsTer?) c.2002del (p.Leu668PhefsTer?) | gnomAD v4 |
8 | g.132888069C>A | CA463216417 | TG | c.2262C>A (p.Thr754=) c.2001C>A (p.Thr667=) | dbSNP |
8 | g.132888069C= | CA1820989884 | TG | c.2262C= (p.Thr754=) c.2001C= (p.Thr667=) | |
8 | g.132888069C>G | CA463216418 | TG | c.2262C>G (p.Thr754=) c.2001C>G (p.Thr667=) | ClinVar |
8 | g.132888069C>T | CA463216419 | TG | c.2262C>T (p.Thr754=) c.2001C>T (p.Thr667=) | dbSNP |
8 | g.132888070C>A | CA372234986 | TG | c.2263C>A (p.Leu755Ile) c.2002C>A (p.Leu668Ile) | |
8 | g.132888070C>G | CA372234987 | TG | c.2263C>G (p.Leu755Val) c.2002C>G (p.Leu668Val) | |
8 | g.132888070C>T | CA372234989 | TG | c.2263C>T (p.Leu755Phe) c.2002C>T (p.Leu668Phe) | |
8 | g.132888071T>A | CA372234991 | TG | c.2264T>A (p.Leu755His) c.2003T>A (p.Leu668His) | |
8 | g.132888071T>C | CA372234993 | TG | c.2264T>C (p.Leu755Pro) c.2003T>C (p.Leu668Pro) | gnomAD v4 |
8 | g.132888071T>G | CA372234995 | TG | c.2264T>G (p.Leu755Arg) c.2003T>G (p.Leu668Arg) | |
8 | g.132888072T>A | CA463216423 | TG | c.2265T>A (p.Leu755=) c.2004T>A (p.Leu668=) | |
8 | g.132888072T>C | CA463216421 | TG | c.2265T>C (p.Leu755=) c.2004T>C (p.Leu668=) | gnomAD v4 |
8 | g.132888072T>G | CA463216422 | TG | c.2265T>G (p.Leu755=) c.2004T>G (p.Leu668=) | |
8 | g.132888073T>A | CA372234996 | TG | c.2266T>A (p.Ser756Thr) c.2005T>A (p.Ser669Thr) | |
8 | g.132888073T>C | CA372234997 | TG | c.2266T>C (p.Ser756Pro) c.2005T>C (p.Ser669Pro) | |
8 | g.132888073T>G | CA372234999 | TG | c.2266T>G (p.Ser756Ala) c.2005T>G (p.Ser669Ala) | |
8 | g.132888074C>A | CA372235001 | TG | c.2267C>A (p.Ser756Tyr) c.2006C>A (p.Ser669Tyr) | |
8 | g.132888074C= | CA1820989886 | TG | c.2267C= (p.Ser756=) c.2006C= (p.Ser669=) | |
8 | g.132888074C>G | CA372235003 | TG | c.2267C>G (p.Ser756Cys) c.2006C>G (p.Ser669Cys) | |
8 | g.132888074C>T | CA4883365 | TG | c.2267C>T (p.Ser756Phe) c.2006C>T (p.Ser669Phe) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.132888075dup | CA2688648744 | TG | c.2268dup (p.Asp757ArgfsTer23) c.2007dup (p.Asp670ArgfsTer23) | gnomAD v4 |
8 | g.132888075C>A | CA463216424 | TG | c.2268C>A (p.Ser756=) c.2007C>A (p.Ser669=) | |
8 | g.132888075C= | CA1820989888 | TG | c.2268C= (p.Ser756=) c.2007C= (p.Ser669=) | |
8 | g.132888075C>G | CA463216426 | TG | c.2268C>G (p.Ser756=) c.2007C>G (p.Ser669=) | |
8 | g.132888075C>T | CA4883366 | TG | c.2268C>T (p.Ser756=) c.2007C>T (p.Ser669=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
8 | g.132888076G>A | CA4883367 | TG | c.2269G>A (p.Asp757Asn) c.2008G>A (p.Asp670Asn) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.132888076G>C | CA372235009 | TG | c.2269G>C (p.Asp757His) c.2008G>C (p.Asp670His) | dbSNP gnomAD v3 gnomAD v4 |
8 | g.132888076G= | CA1820989890 | TG | c.2269G= (p.Asp757=) c.2008G= (p.Asp670=) | |
8 | g.132888076G>T | CA372235006 | TG | c.2269G>T (p.Asp757Tyr) c.2008G>T (p.Asp670Tyr) | |
8 | g.132888077A>C | CA372235011 | TG | c.2270A>C (p.Asp757Ala) c.2009A>C (p.Asp670Ala) | |
8 | g.132888077A>G | CA372235012 | TG | c.2270A>G (p.Asp757Gly) c.2009A>G (p.Asp670Gly) | |
8 | g.132888077A>T | CA372235013 | TG | c.2270A>T (p.Asp757Val) c.2009A>T (p.Asp670Val) | |
8 | g.132888078C>A | CA372235016 | TG | c.2271C>A (p.Asp757Glu) c.2010C>A (p.Asp670Glu) | |
8 | g.132888078C>G | CA372235017 | TG | c.2271C>G (p.Asp757Glu) c.2010C>G (p.Asp670Glu) | |
8 | g.132888078C>T | CA463216428 | TG | c.2271C>T (p.Asp757=) c.2010C>T (p.Asp670=) | |
8 | g.132888079A= | CA1820989892 | TG | c.2272A= (p.Thr758=) c.2011A= (p.Thr671=) | |
8 | g.132888079A>C | CA4883368 | TG | c.2272A>C (p.Thr758Pro) c.2011A>C (p.Thr671Pro) | dbSNP ExAC gnomAD v2 gnomAD v4 |
8 | g.132888079A>G | CA372235020 | TG | c.2272A>G (p.Thr758Ala) c.2011A>G (p.Thr671Ala) | |
8 | g.132888079A>T | CA372235022 | TG | c.2272A>T (p.Thr758Ser) c.2011A>T (p.Thr671Ser) | gnomAD v4 |
8 | g.132888080C>A | CA372235024 | TG | c.2273C>A (p.Thr758Asn) c.2012C>A (p.Thr671Asn) | |
8 | g.132888080C>G | CA372235026 | TG | c.2273C>G (p.Thr758Ser) c.2012C>G (p.Thr671Ser) | |
8 | g.132888080C>T | CA372235028 | TG | c.2273C>T (p.Thr758Ile) c.2012C>T (p.Thr671Ile) | |
8 | g.132888081C>A | CA463216432 | TG | c.2274C>A (p.Thr758=) c.2013C>A (p.Thr671=) | |
8 | g.132888081C>G | CA463216433 | TG | c.2274C>G (p.Thr758=) c.2013C>G (p.Thr671=) | |
8 | g.132888081C>T | CA463216434 | TG | c.2274C>T (p.Thr758=) c.2013C>T (p.Thr671=) | gnomAD v4 |
8 | g.132888082T>A | CA372235034 | TG | c.2275T>A (p.Tyr759Asn) c.2014T>A (p.Tyr672Asn) | |
8 | g.132888082T>C | CA372235032 | TG | c.2275T>C (p.Tyr759His) c.2014T>C (p.Tyr672His) | |
8 | g.132888082T>G | CA372235030 | TG | c.2275T>G (p.Tyr759Asp) c.2014T>G (p.Tyr672Asp) | |
8 | g.132888083A= | CA1820989894 | TG | c.2276A= (p.Tyr759=) c.2015A= (p.Tyr672=) | |
8 | g.132888083A>C | CA372235036 | TG | c.2276A>C (p.Tyr759Ser) c.2015A>C (p.Tyr672Ser) | |
8 | g.132888083A>G | CA4883369 | TG | c.2276A>G (p.Tyr759Cys) c.2015A>G (p.Tyr672Cys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.132888083A>T | CA372235038 | TG | c.2276A>T (p.Tyr759Phe) c.2015A>T (p.Tyr672Phe) | |
8 | g.132888084C>A | CA372235040 | TG | c.2277C>A (p.Tyr759Ter) c.2016C>A (p.Tyr672Ter) | |
8 | g.132888084C= | CA1820989896 | TG | c.2277C= (p.Tyr759=) c.2016C= (p.Tyr672=) | |
8 | g.132888084C>G | CA372235041 | TG | c.2277C>G (p.Tyr759Ter) c.2016C>G (p.Tyr672Ter) | |
8 | g.132888084C>T | CA463216439 | TG | c.2277C>T (p.Tyr759=) c.2016C>T (p.Tyr672=) | ClinVar dbSNP gnomAD v4 |
8 | g.132888085A>C | CA372235044 | TG | c.2278A>C (p.Ile760Leu) c.2017A>C (p.Ile673Leu) | |
8 | g.132888085A>G | CA372235046 | TG | c.2278A>G (p.Ile760Val) c.2017A>G (p.Ile673Val) | gnomAD v4 |
8 | g.132888085A>T | CA372235048 | TG | c.2278A>T (p.Ile760Phe) c.2017A>T (p.Ile673Phe) | |
8 | g.132888086T>A | CA372235049 | TG | c.2279T>A (p.Ile760Asn) c.2018T>A (p.Ile673Asn) | |
8 | g.132888086T>C | CA372235050 | TG | c.2279T>C (p.Ile760Thr) c.2018T>C (p.Ile673Thr) | |
8 | g.132888086T>G | CA372235052 | TG | c.2279T>G (p.Ile760Ser) c.2018T>G (p.Ile673Ser) | |
8 | g.132888087C>A | CA463216440 | TG | c.2280C>A (p.Ile760=) c.2019C>A (p.Ile673=) | |
8 | g.132888087C>G | CA372235054 | TG | c.2280C>G (p.Ile760Met) c.2019C>G (p.Ile673Met) | |
8 | g.132888087C>T | CA463216441 | TG | c.2280C>T (p.Ile760=) c.2019C>T (p.Ile673=) | gnomAD v4 |
8 | g.132888088C>A | CA372235057 | TG | c.2281C>A (p.Pro761Thr) c.2020C>A (p.Pro674Thr) | dbSNP gnomAD v2 gnomAD v4 COSMIC |
8 | g.132888088C= | CA1820989898 | TG | c.2281C= (p.Pro761=) c.2020C= (p.Pro674=) | |
8 | g.132888088C>G | CA372235059 | TG | c.2281C>G (p.Pro761Ala) c.2020C>G (p.Pro674Ala) | |
8 | g.132888088C>T | CA4883370 | TG | c.2281C>T (p.Pro761Ser) c.2020C>T (p.Pro674Ser) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.132888089C>A | CA372235065 | TG | c.2282C>A (p.Pro761Gln) c.2021C>A (p.Pro674Gln) | |
8 | g.132888089C>G | CA372235061 | TG | c.2282C>G (p.Pro761Arg) c.2021C>G (p.Pro674Arg) | |
8 | g.132888089C>T | CA372235063 | TG | c.2282C>T (p.Pro761Leu) c.2021C>T (p.Pro674Leu) | gnomAD v4 |
8 | g.132888090A= | CA1820989900 | TG | c.2283A= (p.Pro761=) c.2022A= (p.Pro674=) | |
8 | g.132888090A>C | CA4883371 | TG | c.2283A>C (p.Pro761=) c.2022A>C (p.Pro674=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.132888090A>G | CA463216444 | TG | c.2283A>G (p.Pro761=) c.2022A>G (p.Pro674=) | |
8 | g.132888090A>T | CA463216445 | TG | c.2283A>T (p.Pro761=) c.2022A>T (p.Pro674=) | |
8 | g.132888091C>A | CA372235067 | TG | c.2284C>A (p.Gln762Lys) c.2023C>A (p.Gln675Lys) | |
8 | g.132888091C>G | CA372235069 | TG | c.2284C>G (p.Gln762Glu) c.2023C>G (p.Gln675Glu) | |
8 | g.132888091C>T | CA372235070 | TG | c.2284C>T (p.Gln762Ter) c.2023C>T (p.Gln675Ter) | |
8 | g.132888092A= | CA1820989902 | TG | c.2285A= (p.Gln762=) c.2024A= (p.Gln675=) | |
8 | g.132888092A>C | CA186284356 | TG | c.2285A>C (p.Gln762Pro) c.2024A>C (p.Gln675Pro) | dbSNP |
8 | g.132888092A>G | CA372235077 | TG | c.2285A>G (p.Gln762Arg) c.2024A>G (p.Gln675Arg) | |
8 | g.132888092A>T | CA372235080 | TG | c.2285A>T (p.Gln762Leu) c.2024A>T (p.Gln675Leu) | |
8 | g.132888093del | CA2739268991 | TG | c.2286del (p.Gln762HisfsTer?) c.2025del (p.Gln675HisfsTer?) | ClinVar |
8 | g.132888093G>A | CA463216451 | TG | c.2286G>A (p.Gln762=) c.2025G>A (p.Gln675=) | gnomAD v4 |
8 | g.132888093G>C | CA372235082 | TG | c.2286G>C (p.Gln762His) c.2025G>C (p.Gln675His) | |
8 | g.132888093G>T | CA372235084 | TG | c.2286G>T (p.Gln762His) c.2025G>T (p.Gln675His) | gnomAD v4 |
8 | g.132888094T>A | CA372235090 | TG | c.2287T>A (p.Cys763Ser) c.2026T>A (p.Cys676Ser) | |
8 | g.132888094T>C | CA372235088 | TG | c.2287T>C (p.Cys763Arg) c.2026T>C (p.Cys676Arg) | |
8 | g.132888094T>G | CA372235086 | TG | c.2287T>G (p.Cys763Gly) c.2026T>G (p.Cys676Gly) | |
8 | g.132888095G>A | CA372235092 | TG | c.2288G>A (p.Cys763Tyr) c.2027G>A (p.Cys676Tyr) | |
8 | g.132888095G>C | CA372235094 | TG | c.2288G>C (p.Cys763Ser) c.2027G>C (p.Cys676Ser) | |
8 | g.132888095G>T | CA372235096 | TG | c.2288G>T (p.Cys763Phe) c.2027G>T (p.Cys676Phe) | |
8 | g.132888096C>A | CA372235098 | TG | c.2289C>A (p.Cys763Ter) c.2028C>A (p.Cys676Ter) | |
8 | g.132888096C= | CA1820989904 | TG | c.2289C= (p.Cys763=) c.2028C= (p.Cys676=) | |
8 | g.132888096C>G | CA372235100 | TG | c.2289C>G (p.Cys763Trp) c.2028C>G (p.Cys676Trp) | |
8 | g.132888096C>T | CA463216454 | TG | c.2289C>T (p.Cys763=) c.2028C>T (p.Cys676=) | ClinVar dbSNP gnomAD v4 |
8 | g.132888097A>C | CA372235102 | TG | c.2290A>C (p.Ser764Arg) c.2029A>C (p.Ser677Arg) | gnomAD v4 |
8 | g.132888097A>G | CA372235103 | TG | c.2290A>G (p.Ser764Gly) c.2029A>G (p.Ser677Gly) | gnomAD v4 |
8 | g.132888097A>T | CA372235105 | TG | c.2290A>T (p.Ser764Cys) c.2029A>T (p.Ser677Cys) | |
8 | g.132888098G>A | CA372235107 | TG | c.2291G>A (p.Ser764Asn) c.2030G>A (p.Ser677Asn) | |
8 | g.132888098G>C | CA372235108 | TG | c.2291G>C (p.Ser764Thr) c.2030G>C (p.Ser677Thr) | |
8 | g.132888098G>T | CA372235109 | TG | c.2291G>T (p.Ser764Ile) c.2030G>T (p.Ser677Ile) | |
8 | g.132888099C>A | CA372235112 | TG | c.2292C>A (p.Ser764Arg) c.2031C>A (p.Ser677Arg) | |
8 | g.132888099C>G | CA372235114 | TG | c.2292C>G (p.Ser764Arg) c.2031C>G (p.Ser677Arg) | |
8 | g.132888099C>T | CA463216461 | TG | c.2292C>T (p.Ser764=) c.2031C>T (p.Ser677=) | |
8 | g.132888100A= | CA1820989906 | TG | c.2293A= (p.Thr765=) c.2032A= (p.Thr678=) | |
8 | g.132888100A>C | CA372235118 | TG | c.2293A>C (p.Thr765Pro) c.2032A>C (p.Thr678Pro) | dbSNP gnomAD v3 gnomAD v4 |
8 | g.132888100A>G | CA372235119 | TG | c.2293A>G (p.Thr765Ala) c.2032A>G (p.Thr678Ala) | |
8 | g.132888100A>T | CA372235116 | TG | c.2293A>T (p.Thr765Ser) c.2032A>T (p.Thr678Ser) | |
8 | g.132888101C>A | CA372235121 | TG | c.2294C>A (p.Thr765Asn) c.2033C>A (p.Thr678Asn) | |
8 | g.132888101C= | CA1820989908 | TG | c.2294C= (p.Thr765=) c.2033C= (p.Thr678=) | |
8 | g.132888101C>G | CA372235124 | TG | c.2294C>G (p.Thr765Ser) c.2033C>G (p.Thr678Ser) | |
8 | g.132888101C>T | CA372235125 | TG | c.2294C>T (p.Thr765Ile) c.2033C>T (p.Thr678Ile) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.132888102C>A | CA4883373 | TG | c.2295C>A (p.Thr765=) c.2034C>A (p.Thr678=) | dbSNP ExAC gnomAD v2 |
8 | g.132888102C= | CA1820989910 | TG | c.2295C= (p.Thr765=) c.2034C= (p.Thr678=) | |
8 | g.132888102C>G | CA463216467 | TG | c.2295C>G (p.Thr765=) c.2034C>G (p.Thr678=) | |
8 | g.132888102C>T | CA4883372 | TG | c.2295C>T (p.Thr765=) c.2034C>T (p.Thr678=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.132888103G>A | CA372235131 | TG | c.2296G>A (p.Asp766Asn) c.2035G>A (p.Asp679Asn) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
8 | g.132888103G>C | CA372235132 | TG | c.2296G>C (p.Asp766His) c.2035G>C (p.Asp679His) | |
8 | g.132888103G= | CA1820989913 | TG | c.2296G= (p.Asp766=) c.2035G= (p.Asp679=) | |
8 | g.132888103G>T | CA372235134 | TG | c.2296G>T (p.Asp766Tyr) c.2035G>T (p.Asp679Tyr) | dbSNP |
8 | g.132888104A= | CA1820989915 | TG | c.2297A= (p.Asp766=) c.2036A= (p.Asp679=) | |
8 | g.132888104A>C | CA372235136 | TG | c.2297A>C (p.Asp766Ala) c.2036A>C (p.Asp679Ala) | |
8 | g.132888104A>G | CA4883374 | TG | c.2297A>G (p.Asp766Gly) c.2036A>G (p.Asp679Gly) | dbSNP ExAC gnomAD v2 gnomAD v4 |
8 | g.132888104A>T | CA372235138 | TG | c.2297A>T (p.Asp766Val) c.2036A>T (p.Asp679Val) | |
8 | g.132888105T>A | CA372235140 | TG | c.2298T>A (p.Asp766Glu) c.2037T>A (p.Asp679Glu) | dbSNP gnomAD v3 gnomAD v4 |
8 | g.132888105T>C | CA463216472 | TG | c.2298T>C (p.Asp766=) c.2037T>C (p.Asp679=) | dbSNP gnomAD v4 |
8 | g.132888105T>G | CA372235142 | TG | c.2298T>G (p.Asp766Glu) c.2037T>G (p.Asp679Glu) | |
8 | g.132888105T= | CA1820989917 | TG | c.2298T= (p.Asp766=) c.2037T= (p.Asp679=) | |
8 | g.132888106G>A | CA4883375 | TG | c.2299G>A (p.Gly767Arg) c.2038G>A (p.Gly680Arg) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.132888106G>C | CA372235146 | TG | c.2299G>C (p.Gly767Arg) c.2038G>C (p.Gly680Arg) | dbSNP gnomAD v3 gnomAD v4 |
8 | g.132888106G= | CA1820989918 | TG | c.2299G= (p.Gly767=) c.2038G= (p.Gly680=) | |
8 | g.132888106G>T | CA372235144 | TG | c.2299G>T (p.Gly767Trp) c.2038G>T (p.Gly680Trp) | dbSNP |
8 | g.132888107G>A | CA372235147 | TG | c.2300G>A (p.Gly767Glu) c.2039G>A (p.Gly680Glu) | gnomAD v4 |
8 | g.132888107G>C | CA372235149 | TG | c.2300G>C (p.Gly767Ala) c.2039G>C (p.Gly680Ala) | |
8 | g.132888107G>T | CA372235151 | TG | c.2300G>T (p.Gly767Val) c.2039G>T (p.Gly680Val) | |
8 | g.132888108G>A | CA463216478 | TG | c.2301G>A (p.Gly767=) c.2040G>A (p.Gly680=) | |
8 | g.132888108G>C | CA463216481 | TG | c.2301G>C (p.Gly767=) c.2040G>C (p.Gly680=) | |
8 | g.132888108G>T | CA463216479 | TG | c.2301G>T (p.Gly767=) c.2040G>T (p.Gly680=) | |
8 | g.132888109C>A | CA372235152 | TG | c.2302C>A (p.Gln768Lys) c.2041C>A (p.Gln681Lys) | |
8 | g.132888109C>G | CA372235153 | TG | c.2302C>G (p.Gln768Glu) c.2041C>G (p.Gln681Glu) | |
8 | g.132888109C>T | CA372235155 | TG | c.2302C>T (p.Gln768Ter) c.2041C>T (p.Gln681Ter) | |
8 | g.132888110A>C | CA372235158 | TG | c.2303A>C (p.Gln768Pro) c.2042A>C (p.Gln681Pro) | |
8 | g.132888110A>G | CA372235159 | TG | c.2303A>G (p.Gln768Arg) c.2042A>G (p.Gln681Arg) | |
8 | g.132888110A>T | CA372235161 | TG | c.2303A>T (p.Gln768Leu) c.2042A>T (p.Gln681Leu) | |
8 | g.132888111G>A | CA463216487 | TG | c.2304G>A (p.Gln768=) c.2043G>A (p.Gln681=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
8 | g.132888111G>C | CA372235163 | TG | c.2304G>C (p.Gln768His) c.2043G>C (p.Gln681His) | |
8 | g.132888111G= | CA1820989921 | TG | c.2304G= (p.Gln768=) c.2043G= (p.Gln681=) | |
8 | g.132888111G>T | CA372235164 | TG | c.2304G>T (p.Gln768His) c.2043G>T (p.Gln681His) | |
8 | g.132888112T>A | CA372235166 | TG | c.2305T>A (p.Trp769Arg) c.2044T>A (p.Trp682Arg) | |
8 | g.132888112T>C | CA372235168 | TG | c.2305T>C (p.Trp769Arg) c.2044T>C (p.Trp682Arg) | |
8 | g.132888112T>G | CA372235170 | TG | c.2305T>G (p.Trp769Gly) c.2044T>G (p.Trp682Gly) | |
8 | g.132888113G>A | CA372235175 | TG | c.2306G>A (p.Trp769Ter) c.2045G>A (p.Trp682Ter) | |
8 | g.132888113G>C | CA372235174 | TG | c.2306G>C (p.Trp769Ser) c.2045G>C (p.Trp682Ser) | |
8 | g.132888113G>T | CA372235172 | TG | c.2306G>T (p.Trp769Leu) c.2045G>T (p.Trp682Leu) | |
8 | g.132888114G>A | CA372235178 | TG | c.2307G>A (p.Trp769Ter) c.2046G>A (p.Trp682Ter) | |
8 | g.132888114G>C | CA372235176 | TG | c.2307G>C (p.Trp769Cys) c.2046G>C (p.Trp682Cys) | |
8 | g.132888114G>T | CA372235180 | TG | c.2307G>T (p.Trp769Cys) c.2046G>T (p.Trp682Cys) | |
8 | g.132888115A>C | CA463216492 | TG | c.2308A>C (p.Arg770=) c.2047A>C (p.Arg683=) | |
8 | g.132888115A>G | CA372235182 | TG | c.2308A>G (p.Arg770Gly) c.2047A>G (p.Arg683Gly) | |
8 | g.132888115A>T | CA372235184 | TG | c.2308A>T (p.Arg770Ter) c.2047A>T (p.Arg683Ter) | |
8 | g.132888116G>A | CA372235186 | TG | c.2309G>A (p.Arg770Lys) c.2048G>A (p.Arg683Lys) | dbSNP gnomAD v2 |
8 | g.132888116G>C | CA372235188 | TG | c.2309G>C (p.Arg770Thr) c.2048G>C (p.Arg683Thr) | |
8 | g.132888116G= | CA1820989924 | TG | c.2309G= (p.Arg770=) c.2048G= (p.Arg683=) | |
8 | g.132888116G>T | CA372235190 | TG | c.2309G>T (p.Arg770Ile) c.2048G>T (p.Arg683Ile) | |
8 | g.132888117A= | CA1820989926 | TG | c.2310A= (p.Arg770=) c.2049A= (p.Arg683=) | |
8 | g.132888117A>C | CA372235192 | TG | c.2310A>C (p.Arg770Ser) c.2049A>C (p.Arg683Ser) | gnomAD v4 |
8 | g.132888117A>G | CA4883376 | TG | c.2310A>G (p.Arg770=) c.2049A>G (p.Arg683=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.132888117A>T | CA372235194 | TG | c.2310A>T (p.Arg770Ser) c.2049A>T (p.Arg683Ser) | |
8 | g.132888118C>A | CA4883378 | TG | c.2311C>A (p.Gln771Lys) c.2050C>A (p.Gln684Lys) | dbSNP ExAC gnomAD v2 gnomAD v4 |
8 | g.132888118C= | CA1820989928 | TG | c.2311C= (p.Gln771=) c.2050C= (p.Gln684=) | |
8 | g.132888118C>G | CA372235197 | TG | c.2311C>G (p.Gln771Glu) c.2050C>G (p.Gln684Glu) | gnomAD v4 |
8 | g.132888118C>T | CA4883377 | TG | c.2311C>T (p.Gln771Ter) c.2050C>T (p.Gln684Ter) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |