| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 5 | g.177097533G>A | CA3576772 | FGFR4 | c.2266G>A (p.Asp756Asn) c.2146G>A (p.Asp716Asn) c.2062G>A (p.Asp688Asn) n.214G>A c.2359G>A (p.Asp787Asn) c.1948G>A (p.Asp650Asn) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
| 5 | g.177097533G>C | CA362299626 | FGFR4 | c.2266G>C (p.Asp756His) c.2146G>C (p.Asp716His) c.2062G>C (p.Asp688His) n.214G>C c.2359G>C (p.Asp787His) c.1948G>C (p.Asp650His) | |
| 5 | g.177097533G= | CA1603407682 | FGFR4 | c.2266G= (p.Asp756=) c.2146G= (p.Asp716=) c.2062G= (p.Asp688=) n.214G= c.2359G= (p.Asp787=) c.1948G= (p.Asp650=) | |
| 5 | g.177097533G>T | CA362299627 | FGFR4 | c.2266G>T (p.Asp756Tyr) c.2146G>T (p.Asp716Tyr) c.2062G>T (p.Asp688Tyr) n.214G>T c.2359G>T (p.Asp787Tyr) c.1948G>T (p.Asp650Tyr) | |
| 5 | g.177097534A>C | CA362299630 | FGFR4 | c.2267A>C (p.Asp756Ala) c.2147A>C (p.Asp716Ala) c.2063A>C (p.Asp688Ala) n.215A>C c.2360A>C (p.Asp787Ala) c.1949A>C (p.Asp650Ala) | dbSNP |
| 5 | g.177097534A>G | CA362299631 | FGFR4 | c.2267A>G (p.Asp756Gly) c.2147A>G (p.Asp716Gly) c.2063A>G (p.Asp688Gly) n.215A>G c.2360A>G (p.Asp787Gly) c.1949A>G (p.Asp650Gly) | dbSNP |
| 5 | g.177097534A>T | CA362299632 | FGFR4 | c.2267A>T (p.Asp756Val) c.2147A>T (p.Asp716Val) c.2063A>T (p.Asp688Val) n.215A>T c.2360A>T (p.Asp787Val) c.1949A>T (p.Asp650Val) | dbSNP |
| 5 | g.177097535C>A | CA362299637 | FGFR4 | c.2268C>A (p.Asp756Glu) c.2148C>A (p.Asp716Glu) c.2064C>A (p.Asp688Glu) n.216C>A c.2361C>A (p.Asp787Glu) c.1950C>A (p.Asp650Glu) | |
| 5 | g.177097535C>G | CA362299635 | FGFR4 | c.2268C>G (p.Asp756Glu) c.2148C>G (p.Asp716Glu) c.2064C>G (p.Asp688Glu) n.216C>G c.2361C>G (p.Asp787Glu) c.1950C>G (p.Asp650Glu) | dbSNP |
| 5 | g.177097535C>T | CA447959126 | FGFR4 | c.2268C>T (p.Asp756=) c.2148C>T (p.Asp716=) c.2064C>T (p.Asp688=) n.216C>T c.2361C>T (p.Asp787=) c.1950C>T (p.Asp650=) | |
| 5 | g.177097536del | CA2676683929 | FGFR4 | c.2269del (p.Leu757SerfsTer3) c.2149del (p.Leu717SerfsTer3) c.2065del (p.Leu689SerfsTer3) n.217del c.2362del (p.Leu788SerfsTer3) c.1951del (p.Leu651SerfsTer3) | gnomAD v4 |
| 5 | g.177097536C>A | CA362299638 | FGFR4 | c.2269C>A (p.Leu757Ile) c.2149C>A (p.Leu717Ile) c.2065C>A (p.Leu689Ile) n.217C>A c.2362C>A (p.Leu788Ile) c.1951C>A (p.Leu651Ile) | |
| 5 | g.177097536C= | CA1603407686 | FGFR4 | c.2269C= (p.Leu757=) c.2149C= (p.Leu717=) c.2065C= (p.Leu689=) n.217C= c.2362C= (p.Leu788=) c.1951C= (p.Leu651=) | |
| 5 | g.177097536C>G | CA362299639 | FGFR4 | c.2269C>G (p.Leu757Val) c.2149C>G (p.Leu717Val) c.2065C>G (p.Leu689Val) n.217C>G c.2362C>G (p.Leu788Val) c.1951C>G (p.Leu651Val) | |
| 5 | g.177097536C>T | CA3576773 | FGFR4 | c.2269C>T (p.Leu757Phe) c.2149C>T (p.Leu717Phe) c.2065C>T (p.Leu689Phe) n.217C>T c.2362C>T (p.Leu788Phe) c.1951C>T (p.Leu651Phe) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 5 | g.177097537T>A | CA362299642 | FGFR4 | c.2270T>A (p.Leu757His) c.2150T>A (p.Leu717His) c.2066T>A (p.Leu689His) n.218T>A c.2363T>A (p.Leu788His) c.1952T>A (p.Leu651His) | |
| 5 | g.177097537T>C | CA362299643 | FGFR4 | c.2270T>C (p.Leu757Pro) c.2150T>C (p.Leu717Pro) c.2066T>C (p.Leu689Pro) n.218T>C c.2363T>C (p.Leu788Pro) c.1952T>C (p.Leu651Pro) | dbSNP gnomAD v4 |
| 5 | g.177097537T>G | CA132835141 | FGFR4 | c.2270T>G (p.Leu757Arg) c.2150T>G (p.Leu717Arg) c.2066T>G (p.Leu689Arg) n.218T>G c.2363T>G (p.Leu788Arg) c.1952T>G (p.Leu651Arg) | dbSNP gnomAD v4 |
| 5 | g.177097537T= | CA1603407708 | FGFR4 | c.2270T= (p.Leu757=) c.2150T= (p.Leu717=) c.2066T= (p.Leu689=) n.218T= c.2363T= (p.Leu788=) c.1952T= (p.Leu651=) | |
| 5 | g.177097538C>A | CA447959130 | FGFR4 | c.2271C>A (p.Leu757=) c.2151C>A (p.Leu717=) c.2067C>A (p.Leu689=) n.219C>A c.2364C>A (p.Leu788=) c.1953C>A (p.Leu651=) | |
| 5 | g.177097538C= | CA1603407710 | FGFR4 | c.2271C= (p.Leu757=) c.2151C= (p.Leu717=) c.2067C= (p.Leu689=) n.219C= c.2364C= (p.Leu788=) c.1953C= (p.Leu651=) | |
| 5 | g.177097538C>G | CA447959133 | FGFR4 | c.2271C>G (p.Leu757=) c.2151C>G (p.Leu717=) c.2067C>G (p.Leu689=) n.219C>G c.2364C>G (p.Leu788=) c.1953C>G (p.Leu651=) | |
| 5 | g.177097538C>T | CA3576774 | FGFR4 | c.2271C>T (p.Leu757=) c.2151C>T (p.Leu717=) c.2067C>T (p.Leu689=) n.219C>T c.2364C>T (p.Leu788=) c.1953C>T (p.Leu651=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 5 | g.177097539C>A | CA362299646 | FGFR4 | c.2272C>A (p.Arg758Ser) c.2152C>A (p.Arg718Ser) c.2068C>A (p.Arg690Ser) n.220C>A c.2365C>A (p.Arg789Ser) c.1954C>A (p.Arg652Ser) | |
| 5 | g.177097539C= | CA1603407714 | FGFR4 | c.2272C= (p.Arg758=) c.2152C= (p.Arg718=) c.2068C= (p.Arg690=) n.220C= c.2365C= (p.Arg789=) c.1954C= (p.Arg652=) | |
| 5 | g.177097539C>G | CA362299647 | FGFR4 | c.2272C>G (p.Arg758Gly) c.2152C>G (p.Arg718Gly) c.2068C>G (p.Arg690Gly) n.220C>G c.2365C>G (p.Arg789Gly) c.1954C>G (p.Arg652Gly) | |
| 5 | g.177097539C>T | CA3576775 | FGFR4 | c.2272C>T (p.Arg758Cys) c.2152C>T (p.Arg718Cys) c.2068C>T (p.Arg690Cys) n.220C>T c.2365C>T (p.Arg789Cys) c.1954C>T (p.Arg652Cys) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 5 | g.177097540G>A | CA3576776 | FGFR4 | c.2273G>A (p.Arg758His) c.2153G>A (p.Arg718His) c.2069G>A (p.Arg690His) n.221G>A c.2366G>A (p.Arg789His) c.1955G>A (p.Arg652His) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 5 | g.177097540G>C | CA362299650 | FGFR4 | c.2273G>C (p.Arg758Pro) c.2153G>C (p.Arg718Pro) c.2069G>C (p.Arg690Pro) n.221G>C c.2366G>C (p.Arg789Pro) c.1955G>C (p.Arg652Pro) | |
| 5 | g.177097540G= | CA1603407717 | FGFR4 | c.2273G= (p.Arg758=) c.2153G= (p.Arg718=) c.2069G= (p.Arg690=) n.221G= c.2366G= (p.Arg789=) c.1955G= (p.Arg652=) | |
| 5 | g.177097540G>T | CA362299651 | FGFR4 | c.2273G>T (p.Arg758Leu) c.2153G>T (p.Arg718Leu) c.2069G>T (p.Arg690Leu) n.221G>T c.2366G>T (p.Arg789Leu) c.1955G>T (p.Arg652Leu) | gnomAD v4 |
| 5 | g.177097541C>A | CA447959153 | FGFR4 | c.2274C>A (p.Arg758=) c.2154C>A (p.Arg718=) c.2070C>A (p.Arg690=) n.222C>A c.2367C>A (p.Arg789=) c.1956C>A (p.Arg652=) | |
| 5 | g.177097541C>G | CA447959156 | FGFR4 | c.2274C>G (p.Arg758=) c.2154C>G (p.Arg718=) c.2070C>G (p.Arg690=) n.222C>G c.2367C>G (p.Arg789=) c.1956C>G (p.Arg652=) | |
| 5 | g.177097541C>T | CA447959154 | FGFR4 | c.2274C>T (p.Arg758=) c.2154C>T (p.Arg718=) c.2070C>T (p.Arg690=) n.222C>T c.2367C>T (p.Arg789=) c.1956C>T (p.Arg652=) | |
| 5 | g.177097542C>A | CA362299657 | FGFR4 | c.2275C>A (p.Leu759Met) c.2155C>A (p.Leu719Met) c.2071C>A (p.Leu691Met) n.223C>A c.2368C>A (p.Leu790Met) c.1957C>A (p.Leu653Met) | |
| 5 | g.177097542C= | CA1603407724 | FGFR4 | c.2275C= (p.Leu759=) c.2155C= (p.Leu719=) c.2071C= (p.Leu691=) n.223C= c.2368C= (p.Leu790=) c.1957C= (p.Leu653=) | |
| 5 | g.177097542C>G | CA362299654 | FGFR4 | c.2275C>G (p.Leu759Val) c.2155C>G (p.Leu719Val) c.2071C>G (p.Leu691Val) n.223C>G c.2368C>G (p.Leu790Val) c.1957C>G (p.Leu653Val) | |
| 5 | g.177097542C>T | CA3576777 | FGFR4 | c.2275C>T (p.Leu759=) c.2155C>T (p.Leu719=) c.2071C>T (p.Leu691=) n.223C>T c.2368C>T (p.Leu790=) c.1957C>T (p.Leu653=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 5 | g.177097543T>A | CA362299659 | FGFR4 | c.2276T>A (p.Leu759Gln) c.2156T>A (p.Leu719Gln) c.2072T>A (p.Leu691Gln) n.224T>A c.2369T>A (p.Leu790Gln) c.1958T>A (p.Leu653Gln) | |
| 5 | g.177097543T>C | CA362299660 | FGFR4 | c.2276T>C (p.Leu759Pro) c.2156T>C (p.Leu719Pro) c.2072T>C (p.Leu691Pro) n.224T>C c.2369T>C (p.Leu790Pro) c.1958T>C (p.Leu653Pro) | |
| 5 | g.177097543T>G | CA362299662 | FGFR4 | c.2276T>G (p.Leu759Arg) c.2156T>G (p.Leu719Arg) c.2072T>G (p.Leu691Arg) n.224T>G c.2369T>G (p.Leu790Arg) c.1958T>G (p.Leu653Arg) | |
| 5 | g.177097544G>A | CA447959160 | FGFR4 | c.2277G>A (p.Leu759=) c.2157G>A (p.Leu719=) c.2073G>A (p.Leu691=) n.225G>A c.2370G>A (p.Leu790=) c.1959G>A (p.Leu653=) | gnomAD v4 |
| 5 | g.177097544G>C | CA447959161 | FGFR4 | c.2277G>C (p.Leu759=) c.2157G>C (p.Leu719=) c.2073G>C (p.Leu691=) n.225G>C c.2370G>C (p.Leu790=) c.1959G>C (p.Leu653=) | |
| 5 | g.177097544G>T | CA447959162 | FGFR4 | c.2277G>T (p.Leu759=) c.2157G>T (p.Leu719=) c.2073G>T (p.Leu691=) n.225G>T c.2370G>T (p.Leu790=) c.1959G>T (p.Leu653=) | |
| 5 | g.177097545A>C | CA362299663 | FGFR4 | c.2278A>C (p.Thr760Pro) c.2158A>C (p.Thr720Pro) c.2074A>C (p.Thr692Pro) n.226A>C c.2371A>C (p.Thr791Pro) c.1960A>C (p.Thr654Pro) | |
| 5 | g.177097545A>G | CA362299665 | FGFR4 | c.2278A>G (p.Thr760Ala) c.2158A>G (p.Thr720Ala) c.2074A>G (p.Thr692Ala) n.226A>G c.2371A>G (p.Thr791Ala) c.1960A>G (p.Thr654Ala) | |
| 5 | g.177097545A>T | CA362299667 | FGFR4 | c.2278A>T (p.Thr760Ser) c.2158A>T (p.Thr720Ser) c.2074A>T (p.Thr692Ser) n.226A>T c.2371A>T (p.Thr791Ser) c.1960A>T (p.Thr654Ser) | dbSNP |
| 5 | g.177097546C>A | CA362299673 | FGFR4 | c.2279C>A (p.Thr760Asn) c.2159C>A (p.Thr720Asn) c.2075C>A (p.Thr692Asn) n.227C>A c.2372C>A (p.Thr791Asn) c.1961C>A (p.Thr654Asn) | |
| 5 | g.177097546C>G | CA362299671 | FGFR4 | c.2279C>G (p.Thr760Ser) c.2159C>G (p.Thr720Ser) c.2075C>G (p.Thr692Ser) n.227C>G c.2372C>G (p.Thr791Ser) c.1961C>G (p.Thr654Ser) | |
| 5 | g.177097546C>T | CA362299669 | FGFR4 | c.2279C>T (p.Thr760Ile) c.2159C>T (p.Thr720Ile) c.2075C>T (p.Thr692Ile) n.227C>T c.2372C>T (p.Thr791Ile) c.1961C>T (p.Thr654Ile) |