Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
4 | g.125434331T>A | CA358135230 | FAT4 | c.7105T>A (p.Tyr2369Asn) c.1876T>A (p.Tyr626Asn) c.1999T>A (p.Tyr667Asn) | |
4 | g.125434331T>C | CA358135231 | FAT4 | c.7105T>C (p.Tyr2369His) c.1876T>C (p.Tyr626His) c.1999T>C (p.Tyr667His) | |
4 | g.125434331T>G | CA358135232 | FAT4 | c.7105T>G (p.Tyr2369Asp) c.1876T>G (p.Tyr626Asp) c.1999T>G (p.Tyr667Asp) | |
4 | g.125434332A= | CA1491646824 | FAT4 | c.7106A= (p.Tyr2369=) c.1877A= (p.Tyr626=) c.2000A= (p.Tyr667=) | |
4 | g.125434332A>C | CA358135234 | FAT4 | c.7106A>C (p.Tyr2369Ser) c.1877A>C (p.Tyr626Ser) c.2000A>C (p.Tyr667Ser) | |
4 | g.125434332A>G | CA3073096 | FAT4 | c.7106A>G (p.Tyr2369Cys) c.1877A>G (p.Tyr626Cys) c.2000A>G (p.Tyr667Cys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.125434332A>T | CA358135235 | FAT4 | c.7106A>T (p.Tyr2369Phe) c.1877A>T (p.Tyr626Phe) c.2000A>T (p.Tyr667Phe) | |
4 | g.125434333T>A | CA358135238 | FAT4 | c.7107T>A (p.Tyr2369Ter) c.1878T>A (p.Tyr626Ter) c.2001T>A (p.Tyr667Ter) | |
4 | g.125434333T>C | CA441205021 | FAT4 | c.7107T>C (p.Tyr2369=) c.1878T>C (p.Tyr626=) c.2001T>C (p.Tyr667=) | |
4 | g.125434333T>G | CA358135237 | FAT4 | c.7107T>G (p.Tyr2369Ter) c.1878T>G (p.Tyr626Ter) c.2001T>G (p.Tyr667Ter) | |
4 | g.125434334T>A | CA358135240 | FAT4 | c.7108T>A (p.Phe2370Ile) c.1879T>A (p.Phe627Ile) c.2002T>A (p.Phe668Ile) | |
4 | g.125434334T>C | CA358135241 | FAT4 | c.7108T>C (p.Phe2370Leu) c.1879T>C (p.Phe627Leu) c.2002T>C (p.Phe668Leu) | |
4 | g.125434334T>G | CA358135243 | FAT4 | c.7108T>G (p.Phe2370Val) c.1879T>G (p.Phe627Val) c.2002T>G (p.Phe668Val) | |
4 | g.125434335T>A | CA358135245 | FAT4 | c.7109T>A (p.Phe2370Tyr) c.1880T>A (p.Phe627Tyr) c.2003T>A (p.Phe668Tyr) | |
4 | g.125434335T>C | CA358135246 | FAT4 | c.7109T>C (p.Phe2370Ser) c.1880T>C (p.Phe627Ser) c.2003T>C (p.Phe668Ser) | |
4 | g.125434335T>G | CA358135247 | FAT4 | c.7109T>G (p.Phe2370Cys) c.1880T>G (p.Phe627Cys) c.2003T>G (p.Phe668Cys) | dbSNP gnomAD v2 gnomAD v4 |
4 | g.125434335T= | CA1491646825 | FAT4 | c.7109T= (p.Phe2370=) c.1880T= (p.Phe627=) c.2003T= (p.Phe668=) | |
4 | g.125434336C>A | CA358135251 | FAT4 | c.7110C>A (p.Phe2370Leu) c.1881C>A (p.Phe627Leu) c.2004C>A (p.Phe668Leu) | |
4 | g.125434336C= | CA1491646826 | FAT4 | c.7110C= (p.Phe2370=) c.1881C= (p.Phe627=) c.2004C= (p.Phe668=) | |
4 | g.125434336C>G | CA358135250 | FAT4 | c.7110C>G (p.Phe2370Leu) c.1881C>G (p.Phe627Leu) c.2004C>G (p.Phe668Leu) | |
4 | g.125434336C>T | CA104869333 | FAT4 | c.7110C>T (p.Phe2370=) c.1881C>T (p.Phe627=) c.2004C>T (p.Phe668=) | dbSNP COSMIC COSMIC |
4 | g.125434337A>C | CA358135252 | FAT4 | c.7111A>C (p.Thr2371Pro) c.1882A>C (p.Thr628Pro) c.2005A>C (p.Thr669Pro) | |
4 | g.125434337A>G | CA358135253 | FAT4 | c.7111A>G (p.Thr2371Ala) c.1882A>G (p.Thr628Ala) c.2005A>G (p.Thr669Ala) | |
4 | g.125434337A>T | CA358135255 | FAT4 | c.7111A>T (p.Thr2371Ser) c.1882A>T (p.Thr628Ser) c.2005A>T (p.Thr669Ser) | |
4 | g.125434341_125434343del | CA2672009890 | FAT4 | c.7115_7117del (p.Thr2372del) c.1886_1888del (p.Thr629del) c.2009_2011del (p.Thr670del) | gnomAD v4 |
4 | g.125434338C>A | CA358135257 | FAT4 | c.7112C>A (p.Thr2371Lys) c.1883C>A (p.Thr628Lys) c.2006C>A (p.Thr669Lys) | |
4 | g.125434338C>G | CA358135258 | FAT4 | c.7112C>G (p.Thr2371Arg) c.1883C>G (p.Thr628Arg) c.2006C>G (p.Thr669Arg) | |
4 | g.125434338C>T | CA358135260 | FAT4 | c.7112C>T (p.Thr2371Ile) c.1883C>T (p.Thr628Ile) c.2006C>T (p.Thr669Ile) | |
4 | g.125434339A>C | CA441205024 | FAT4 | c.7113A>C (p.Thr2371=) c.1884A>C (p.Thr628=) c.2007A>C (p.Thr669=) | |
4 | g.125434339A>G | CA441205023 | FAT4 | c.7113A>G (p.Thr2371=) c.1884A>G (p.Thr628=) c.2007A>G (p.Thr669=) | gnomAD v4 |
4 | g.125434339A>T | CA441205022 | FAT4 | c.7113A>T (p.Thr2371=) c.1884A>T (p.Thr628=) c.2007A>T (p.Thr669=) | |
4 | g.125434340A= | CA1491646827 | FAT4 | c.7114A= (p.Thr2372=) c.1885A= (p.Thr629=) c.2008A= (p.Thr670=) | |
4 | g.125434340A>C | CA104869339 | FAT4 | c.7114A>C (p.Thr2372Pro) c.1885A>C (p.Thr629Pro) c.2008A>C (p.Thr670Pro) | dbSNP gnomAD v3 gnomAD v4 |
4 | g.125434340A>G | CA358135262 | FAT4 | c.7114A>G (p.Thr2372Ala) c.1885A>G (p.Thr629Ala) c.2008A>G (p.Thr670Ala) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.125434340A>T | CA358135264 | FAT4 | c.7114A>T (p.Thr2372Ser) c.1885A>T (p.Thr629Ser) c.2008A>T (p.Thr670Ser) | |
4 | g.125434341C>A | CA358135266 | FAT4 | c.7115C>A (p.Thr2372Lys) c.1886C>A (p.Thr629Lys) c.2009C>A (p.Thr670Lys) | |
4 | g.125434341C= | CA1491646828 | FAT4 | c.7115C= (p.Thr2372=) c.1886C= (p.Thr629=) c.2009C= (p.Thr670=) | |
4 | g.125434341C>G | CA358135267 | FAT4 | c.7115C>G (p.Thr2372Arg) c.1886C>G (p.Thr629Arg) c.2009C>G (p.Thr670Arg) | |
4 | g.125434341C>T | CA358135269 | FAT4 | c.7115C>T (p.Thr2372Ile) c.1886C>T (p.Thr629Ile) c.2009C>T (p.Thr670Ile) | dbSNP gnomAD v3 gnomAD v4 |
4 | g.125434342A>C | CA441205027 | FAT4 | c.7116A>C (p.Thr2372=) c.1887A>C (p.Thr629=) c.2010A>C (p.Thr670=) | |
4 | g.125434342A>G | CA441205026 | FAT4 | c.7116A>G (p.Thr2372=) c.1887A>G (p.Thr629=) c.2010A>G (p.Thr670=) | |
4 | g.125434342A>T | CA441205025 | FAT4 | c.7116A>T (p.Thr2372=) c.1887A>T (p.Thr629=) c.2010A>T (p.Thr670=) | |
4 | g.125434343A>C | CA358135270 | FAT4 | c.7117A>C (p.Ile2373Leu) c.1888A>C (p.Ile630Leu) c.2011A>C (p.Ile671Leu) | |
4 | g.125434343A>G | CA358135272 | FAT4 | c.7117A>G (p.Ile2373Val) c.1888A>G (p.Ile630Val) c.2011A>G (p.Ile671Val) | gnomAD v4 |
4 | g.125434343A>T | CA358135274 | FAT4 | c.7117A>T (p.Ile2373Phe) c.1888A>T (p.Ile630Phe) c.2011A>T (p.Ile671Phe) | |
4 | g.125434344T>A | CA358135275 | FAT4 | c.7118T>A (p.Ile2373Asn) c.1889T>A (p.Ile630Asn) c.2012T>A (p.Ile671Asn) | |
4 | g.125434344T>C | CA358135276 | FAT4 | c.7118T>C (p.Ile2373Thr) c.1889T>C (p.Ile630Thr) c.2012T>C (p.Ile671Thr) | |
4 | g.125434344T>G | CA358135278 | FAT4 | c.7118T>G (p.Ile2373Ser) c.1889T>G (p.Ile630Ser) c.2012T>G (p.Ile671Ser) | |
4 | g.125434345T>A | CA441205028 | FAT4 | c.7119T>A (p.Ile2373=) c.1890T>A (p.Ile630=) c.2013T>A (p.Ile671=) | |
4 | g.125434345T>C | CA441205029 | FAT4 | c.7119T>C (p.Ile2373=) c.1890T>C (p.Ile630=) c.2013T>C (p.Ile671=) | dbSNP |
4 | g.125434345T>G | CA358135280 | FAT4 | c.7119T>G (p.Ile2373Met) c.1890T>G (p.Ile630Met) c.2013T>G (p.Ile671Met) | |
4 | g.125434345T= | CA1491646829 | FAT4 | c.7119T= (p.Ile2373=) c.1890T= (p.Ile630=) c.2013T= (p.Ile671=) | |
4 | g.125434346C>A | CA358135282 | FAT4 | c.7120C>A (p.Pro2374Thr) c.1891C>A (p.Pro631Thr) c.2014C>A (p.Pro672Thr) | |
4 | g.125434346C= | CA1491646830 | FAT4 | c.7120C= (p.Pro2374=) c.1891C= (p.Pro631=) c.2014C= (p.Pro672=) | |
4 | g.125434346C>G | CA358135283 | FAT4 | c.7120C>G (p.Pro2374Ala) c.1891C>G (p.Pro631Ala) c.2014C>G (p.Pro672Ala) | |
4 | g.125434346C>T | CA3073097 | FAT4 | c.7120C>T (p.Pro2374Ser) c.1891C>T (p.Pro631Ser) c.2014C>T (p.Pro672Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.125434347C>A | CA358135286 | FAT4 | c.7121C>A (p.Pro2374His) c.1892C>A (p.Pro631His) c.2015C>A (p.Pro672His) | |
4 | g.125434347C= | CA1491646831 | FAT4 | c.7121C= (p.Pro2374=) c.1892C= (p.Pro631=) c.2015C= (p.Pro672=) | |
4 | g.125434347C>G | CA358135288 | FAT4 | c.7121C>G (p.Pro2374Arg) c.1892C>G (p.Pro631Arg) c.2015C>G (p.Pro672Arg) | |
4 | g.125434347C>T | CA358135287 | FAT4 | c.7121C>T (p.Pro2374Leu) c.1892C>T (p.Pro631Leu) c.2015C>T (p.Pro672Leu) | dbSNP gnomAD v2 gnomAD v4 |
4 | g.125434348T>A | CA441205030 | FAT4 | c.7122T>A (p.Pro2374=) c.1893T>A (p.Pro631=) c.2016T>A (p.Pro672=) | |
4 | g.125434348T>C | CA441205031 | FAT4 | c.7122T>C (p.Pro2374=) c.1893T>C (p.Pro631=) c.2016T>C (p.Pro672=) | |
4 | g.125434348T>G | CA441205032 | FAT4 | c.7122T>G (p.Pro2374=) c.1893T>G (p.Pro631=) c.2016T>G (p.Pro672=) | |
4 | g.125434349G>A | CA145423 | FAT4 | c.7123G>A (p.Glu2375Lys) c.1894G>A (p.Glu632Lys) c.2017G>A (p.Glu673Lys) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
4 | g.125434349G>C | CA358135291 | FAT4 | c.7123G>C (p.Glu2375Gln) c.1894G>C (p.Glu632Gln) c.2017G>C (p.Glu673Gln) | COSMIC COSMIC |
4 | g.125434349G= | CA1491646832 | FAT4 | c.7123G= (p.Glu2375=) c.1894G= (p.Glu632=) c.2017G= (p.Glu673=) | |
4 | g.125434349G>T | CA358135289 | FAT4 | c.7123G>T (p.Glu2375Ter) c.1894G>T (p.Glu632Ter) c.2017G>T (p.Glu673Ter) | |
4 | g.125434350A>C | CA358135293 | FAT4 | c.7124A>C (p.Glu2375Ala) c.1895A>C (p.Glu632Ala) c.2018A>C (p.Glu673Ala) | |
4 | g.125434350A>G | CA358135294 | FAT4 | c.7124A>G (p.Glu2375Gly) c.1895A>G (p.Glu632Gly) c.2018A>G (p.Glu673Gly) | |
4 | g.125434350A>T | CA358135296 | FAT4 | c.7124A>T (p.Glu2375Val) c.1895A>T (p.Glu632Val) c.2018A>T (p.Glu673Val) | |
4 | g.125434351G>A | CA3073098 | FAT4 | c.7125G>A (p.Glu2375=) c.1896G>A (p.Glu632=) c.2019G>A (p.Glu673=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.125434351G>C | CA358135298 | FAT4 | c.7125G>C (p.Glu2375Asp) c.1896G>C (p.Glu632Asp) c.2019G>C (p.Glu673Asp) | |
4 | g.125434351G= | CA1491646833 | FAT4 | c.7125G= (p.Glu2375=) c.1896G= (p.Glu632=) c.2019G= (p.Glu673=) | |
4 | g.125434351G>T | CA358135300 | FAT4 | c.7125G>T (p.Glu2375Asp) c.1896G>T (p.Glu632Asp) c.2019G>T (p.Glu673Asp) | |
4 | g.125434352G>A | CA358135301 | FAT4 | c.7126G>A (p.Asp2376Asn) c.1897G>A (p.Asp633Asn) c.2020G>A (p.Asp674Asn) | |
4 | g.125434352G>C | CA358135302 | FAT4 | c.7126G>C (p.Asp2376His) c.1897G>C (p.Asp633His) c.2020G>C (p.Asp674His) | |
4 | g.125434352G>T | CA358135304 | FAT4 | c.7126G>T (p.Asp2376Tyr) c.1897G>T (p.Asp633Tyr) c.2020G>T (p.Asp674Tyr) | gnomAD v4 |
4 | g.125434353A= | CA1491646834 | FAT4 | c.7127A= (p.Asp2376=) c.1898A= (p.Asp633=) c.2021A= (p.Asp674=) | |
4 | g.125434353A>C | CA358135305 | FAT4 | c.7127A>C (p.Asp2376Ala) c.1898A>C (p.Asp633Ala) c.2021A>C (p.Asp674Ala) | |
4 | g.125434353A>G | CA358135306 | FAT4 | c.7127A>G (p.Asp2376Gly) c.1898A>G (p.Asp633Gly) c.2021A>G (p.Asp674Gly) | |
4 | g.125434353A>T | CA358135307 | FAT4 | c.7127A>T (p.Asp2376Val) c.1898A>T (p.Asp633Val) c.2021A>T (p.Asp674Val) | dbSNP gnomAD v2 gnomAD v4 |
4 | g.125434354T>A | CA358135308 | FAT4 | c.7128T>A (p.Asp2376Glu) c.1899T>A (p.Asp633Glu) c.2022T>A (p.Asp674Glu) | |
4 | g.125434354T>C | CA441205033 | FAT4 | c.7128T>C (p.Asp2376=) c.1899T>C (p.Asp633=) c.2022T>C (p.Asp674=) | dbSNP |
4 | g.125434354T>G | CA358135309 | FAT4 | c.7128T>G (p.Asp2376Glu) c.1899T>G (p.Asp633Glu) c.2022T>G (p.Asp674Glu) | |
4 | g.125434354T= | CA1491646835 | FAT4 | c.7128T= (p.Asp2376=) c.1899T= (p.Asp633=) c.2022T= (p.Asp674=) | |
4 | g.125434355G>A | CA358135310 | FAT4 | c.7129G>A (p.Ala2377Thr) c.1900G>A (p.Ala634Thr) c.2023G>A (p.Ala675Thr) | |
4 | g.125434355G>C | CA358135311 | FAT4 | c.7129G>C (p.Ala2377Pro) c.1900G>C (p.Ala634Pro) c.2023G>C (p.Ala675Pro) | |
4 | g.125434355G>T | CA358135313 | FAT4 | c.7129G>T (p.Ala2377Ser) c.1900G>T (p.Ala634Ser) c.2023G>T (p.Ala675Ser) | |
4 | g.125434356C>A | CA358135314 | FAT4 | c.7130C>A (p.Ala2377Glu) c.1901C>A (p.Ala634Glu) c.2024C>A (p.Ala675Glu) | |
4 | g.125434356C>G | CA358135316 | FAT4 | c.7130C>G (p.Ala2377Gly) c.1901C>G (p.Ala634Gly) c.2024C>G (p.Ala675Gly) | |
4 | g.125434356C>T | CA358135317 | FAT4 | c.7130C>T (p.Ala2377Val) c.1901C>T (p.Ala634Val) c.2024C>T (p.Ala675Val) | |
4 | g.125434357A= | CA1491646836 | FAT4 | c.7131A= (p.Ala2377=) c.1902A= (p.Ala634=) c.2025A= (p.Ala675=) | |
4 | g.125434357A>C | CA441205034 | FAT4 | c.7131A>C (p.Ala2377=) c.1902A>C (p.Ala634=) c.2025A>C (p.Ala675=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.125434357A>G | CA3073099 | FAT4 | c.7131A>G (p.Ala2377=) c.1902A>G (p.Ala634=) c.2025A>G (p.Ala675=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.125434357A>T | CA441205035 | FAT4 | c.7131A>T (p.Ala2377=) c.1902A>T (p.Ala634=) c.2025A>T (p.Ala675=) | |
4 | g.125434358C>A | CA358135320 | FAT4 | c.7132C>A (p.Pro2378Thr) c.1903C>A (p.Pro635Thr) c.2026C>A (p.Pro676Thr) | dbSNP |
4 | g.125434358C= | CA1491646837 | FAT4 | c.7132C= (p.Pro2378=) c.1903C= (p.Pro635=) c.2026C= (p.Pro676=) | |
4 | g.125434358C>G | CA358135321 | FAT4 | c.7132C>G (p.Pro2378Ala) c.1903C>G (p.Pro635Ala) c.2026C>G (p.Pro676Ala) | |
4 | g.125434358C>T | CA358135323 | FAT4 | c.7132C>T (p.Pro2378Ser) c.1903C>T (p.Pro635Ser) c.2026C>T (p.Pro676Ser) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
4 | g.125434359C>A | CA3073100 | FAT4 | c.7133C>A (p.Pro2378Gln) c.1904C>A (p.Pro635Gln) c.2027C>A (p.Pro676Gln) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.125434359C= | CA1491646838 | FAT4 | c.7133C= (p.Pro2378=) c.1904C= (p.Pro635=) c.2027C= (p.Pro676=) | |
4 | g.125434359C>G | CA358135325 | FAT4 | c.7133C>G (p.Pro2378Arg) c.1904C>G (p.Pro635Arg) c.2027C>G (p.Pro676Arg) | |
4 | g.125434359C>T | CA358135327 | FAT4 | c.7133C>T (p.Pro2378Leu) c.1904C>T (p.Pro635Leu) c.2027C>T (p.Pro676Leu) | |
4 | g.125434360A>C | CA441205036 | FAT4 | c.7134A>C (p.Pro2378=) c.1905A>C (p.Pro635=) c.2028A>C (p.Pro676=) | |
4 | g.125434360A>G | CA441205037 | FAT4 | c.7134A>G (p.Pro2378=) c.1905A>G (p.Pro635=) c.2028A>G (p.Pro676=) | |
4 | g.125434360A>T | CA441205038 | FAT4 | c.7134A>T (p.Pro2378=) c.1905A>T (p.Pro635=) c.2028A>T (p.Pro676=) | |
4 | g.125434361A= | CA1491646839 | FAT4 | c.7135A= (p.Thr2379=) c.1906A= (p.Thr636=) c.2029A= (p.Thr677=) | |
4 | g.125434361A>C | CA358135329 | FAT4 | c.7135A>C (p.Thr2379Pro) c.1906A>C (p.Thr636Pro) c.2029A>C (p.Thr677Pro) | |
4 | g.125434361A>G | CA104869378 | FAT4 | c.7135A>G (p.Thr2379Ala) c.1906A>G (p.Thr636Ala) c.2029A>G (p.Thr677Ala) | dbSNP gnomAD v2 gnomAD v4 |
4 | g.125434361A>T | CA358135330 | FAT4 | c.7135A>T (p.Thr2379Ser) c.1906A>T (p.Thr636Ser) c.2029A>T (p.Thr677Ser) | |
4 | g.125434362C>A | CA358135332 | FAT4 | c.7136C>A (p.Thr2379Asn) c.1907C>A (p.Thr636Asn) c.2030C>A (p.Thr677Asn) | |
4 | g.125434362C= | CA1491646840 | FAT4 | c.7136C= (p.Thr2379=) c.1907C= (p.Thr636=) c.2030C= (p.Thr677=) | |
4 | g.125434362C>G | CA358135334 | FAT4 | c.7136C>G (p.Thr2379Ser) c.1907C>G (p.Thr636Ser) c.2030C>G (p.Thr677Ser) | |
4 | g.125434362C>T | CA104869379 | FAT4 | c.7136C>T (p.Thr2379Ile) c.1907C>T (p.Thr636Ile) c.2030C>T (p.Thr677Ile) | dbSNP |
4 | g.125434363T>A | CA441205039 | FAT4 | c.7137T>A (p.Thr2379=) c.1908T>A (p.Thr636=) c.2031T>A (p.Thr677=) | |
4 | g.125434363T>C | CA441205040 | FAT4 | c.7137T>C (p.Thr2379=) c.1908T>C (p.Thr636=) c.2031T>C (p.Thr677=) | |
4 | g.125434363T>G | CA441205041 | FAT4 | c.7137T>G (p.Thr2379=) c.1908T>G (p.Thr636=) c.2031T>G (p.Thr677=) | |
4 | g.125434364G>A | CA358135337 | FAT4 | c.7138G>A (p.Gly2380Arg) c.1909G>A (p.Gly637Arg) c.2032G>A (p.Gly678Arg) | |
4 | g.125434364G>C | CA358135338 | FAT4 | c.7138G>C (p.Gly2380Arg) c.1909G>C (p.Gly637Arg) c.2032G>C (p.Gly678Arg) | |
4 | g.125434364G>T | CA358135340 | FAT4 | c.7138G>T (p.Gly2380Ter) c.1909G>T (p.Gly637Ter) c.2032G>T (p.Gly678Ter) | |
4 | g.125434365G>A | CA358135342 | FAT4 | c.7139G>A (p.Gly2380Glu) c.1910G>A (p.Gly637Glu) c.2033G>A (p.Gly678Glu) | dbSNP gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC |
4 | g.125434365G>C | CA358135343 | FAT4 | c.7139G>C (p.Gly2380Ala) c.1910G>C (p.Gly637Ala) c.2033G>C (p.Gly678Ala) | |
4 | g.125434365G>T | CA358135344 | FAT4 | c.7139G>T (p.Gly2380Val) c.1910G>T (p.Gly637Val) c.2033G>T (p.Gly678Val) | |
4 | g.125434366A>C | CA441205044 | FAT4 | c.7140A>C (p.Gly2380=) c.1911A>C (p.Gly637=) c.2034A>C (p.Gly678=) | ClinVar gnomAD v4 |
4 | g.125434366A>G | CA441205043 | FAT4 | c.7140A>G (p.Gly2380=) c.1911A>G (p.Gly637=) c.2034A>G (p.Gly678=) | |
4 | g.125434366A>T | CA441205042 | FAT4 | c.7140A>T (p.Gly2380=) c.1911A>T (p.Gly637=) c.2034A>T (p.Gly678=) | |
4 | g.125434367A>C | CA358135345 | FAT4 | c.7141A>C (p.Thr2381Pro) c.1912A>C (p.Thr638Pro) c.2035A>C (p.Thr679Pro) | |
4 | g.125434367A>G | CA358135346 | FAT4 | c.7141A>G (p.Thr2381Ala) c.1912A>G (p.Thr638Ala) c.2035A>G (p.Thr679Ala) | |
4 | g.125434367A>T | CA358135347 | FAT4 | c.7141A>T (p.Thr2381Ser) c.1912A>T (p.Thr638Ser) c.2035A>T (p.Thr679Ser) | |
4 | g.125434368C>A | CA358135352 | FAT4 | c.7142C>A (p.Thr2381Lys) c.1913C>A (p.Thr638Lys) c.2036C>A (p.Thr679Lys) | ClinVar gnomAD v4 |
4 | g.125434368C>G | CA358135351 | FAT4 | c.7142C>G (p.Thr2381Arg) c.1913C>G (p.Thr638Arg) c.2036C>G (p.Thr679Arg) | gnomAD v4 |
4 | g.125434368C>T | CA358135349 | FAT4 | c.7142C>T (p.Thr2381Ile) c.1913C>T (p.Thr638Ile) c.2036C>T (p.Thr679Ile) | gnomAD v4 |
4 | g.125434369A>C | CA441205045 | FAT4 | c.7143A>C (p.Thr2381=) c.1914A>C (p.Thr638=) c.2037A>C (p.Thr679=) | |
4 | g.125434369A>G | CA441205046 | FAT4 | c.7143A>G (p.Thr2381=) c.1914A>G (p.Thr638=) c.2037A>G (p.Thr679=) | |
4 | g.125434369A>T | CA441205047 | FAT4 | c.7143A>T (p.Thr2381=) c.1914A>T (p.Thr638=) c.2037A>T (p.Thr679=) | |
4 | g.125434370G>A | CA358135353 | FAT4 | c.7144G>A (p.Asp2382Asn) c.1915G>A (p.Asp639Asn) c.2038G>A (p.Asp680Asn) | |
4 | g.125434370G>C | CA358135354 | FAT4 | c.7144G>C (p.Asp2382His) c.1915G>C (p.Asp639His) c.2038G>C (p.Asp680His) | |
4 | g.125434370G>T | CA358135355 | FAT4 | c.7144G>T (p.Asp2382Tyr) c.1915G>T (p.Asp639Tyr) c.2038G>T (p.Asp680Tyr) | |
4 | g.125434371A>C | CA358135357 | FAT4 | c.7145A>C (p.Asp2382Ala) c.1916A>C (p.Asp639Ala) c.2039A>C (p.Asp680Ala) | |
4 | g.125434371A>G | CA358135359 | FAT4 | c.7145A>G (p.Asp2382Gly) c.1916A>G (p.Asp639Gly) c.2039A>G (p.Asp680Gly) | gnomAD v4 |
4 | g.125434371A>T | CA358135360 | FAT4 | c.7145A>T (p.Asp2382Val) c.1916A>T (p.Asp639Val) c.2039A>T (p.Asp680Val) | |
4 | g.125434372T>A | CA358135361 | FAT4 | c.7146T>A (p.Asp2382Glu) c.1917T>A (p.Asp639Glu) c.2040T>A (p.Asp680Glu) | |
4 | g.125434372T>C | CA3073101 | FAT4 | c.7146T>C (p.Asp2382=) c.1917T>C (p.Asp639=) c.2040T>C (p.Asp680=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
4 | g.125434372T>G | CA358135364 | FAT4 | c.7146T>G (p.Asp2382Glu) c.1917T>G (p.Asp639Glu) c.2040T>G (p.Asp680Glu) | |
4 | g.125434372T= | CA1491646841 | FAT4 | c.7146T= (p.Asp2382=) c.1917T= (p.Asp639=) c.2040T= (p.Asp680=) | |
4 | g.125434373G>A | CA3073102 | FAT4 | c.7147G>A (p.Val2383Ile) c.1918G>A (p.Val640Ile) c.2041G>A (p.Val681Ile) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.125434373G>C | CA358135366 | FAT4 | c.7147G>C (p.Val2383Leu) c.1918G>C (p.Val640Leu) c.2041G>C (p.Val681Leu) | |
4 | g.125434373G= | CA1491646842 | FAT4 | c.7147G= (p.Val2383=) c.1918G= (p.Val640=) c.2041G= (p.Val681=) | |
4 | g.125434373G>T | CA358135368 | FAT4 | c.7147G>T (p.Val2383Phe) c.1918G>T (p.Val640Phe) c.2041G>T (p.Val681Phe) | |
4 | g.125434374T>A | CA358135370 | FAT4 | c.7148T>A (p.Val2383Asp) c.1919T>A (p.Val640Asp) c.2042T>A (p.Val681Asp) | |
4 | g.125434374T>C | CA358135373 | FAT4 | c.7148T>C (p.Val2383Ala) c.1919T>C (p.Val640Ala) c.2042T>C (p.Val681Ala) | |
4 | g.125434374T>G | CA358135372 | FAT4 | c.7148T>G (p.Val2383Gly) c.1919T>G (p.Val640Gly) c.2042T>G (p.Val681Gly) | |
4 | g.125434375T>A | CA441205048 | FAT4 | c.7149T>A (p.Val2383=) c.1920T>A (p.Val640=) c.2043T>A (p.Val681=) | COSMIC COSMIC |
4 | g.125434375T>C | CA441205049 | FAT4 | c.7149T>C (p.Val2383=) c.1920T>C (p.Val640=) c.2043T>C (p.Val681=) | |
4 | g.125434375T>G | CA441205050 | FAT4 | c.7149T>G (p.Val2383=) c.1920T>G (p.Val640=) c.2043T>G (p.Val681=) | |
4 | g.125434376T>A | CA358135375 | FAT4 | c.7150T>A (p.Leu2384Ile) c.1921T>A (p.Leu641Ile) c.2044T>A (p.Leu682Ile) | |
4 | g.125434376T>C | CA441205051 | FAT4 | c.7150T>C (p.Leu2384=) c.1921T>C (p.Leu641=) c.2044T>C (p.Leu682=) | |
4 | g.125434376T>G | CA358135376 | FAT4 | c.7150T>G (p.Leu2384Val) c.1921T>G (p.Leu641Val) c.2044T>G (p.Leu682Val) | |
4 | g.125434377T>A | CA358135378 | FAT4 | c.7151T>A (p.Leu2384Ter) c.1922T>A (p.Leu641Ter) c.2045T>A (p.Leu682Ter) | |
4 | g.125434377T>C | CA3073103 | FAT4 | c.7151T>C (p.Leu2384Ser) c.1922T>C (p.Leu641Ser) c.2045T>C (p.Leu682Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.125434377T>G | CA358135379 | FAT4 | c.7151T>G (p.Leu2384Ter) c.1922T>G (p.Leu641Ter) c.2045T>G (p.Leu682Ter) | |
4 | g.125434377T= | CA1491646843 | FAT4 | c.7151T= (p.Leu2384=) c.1922T= (p.Leu641=) c.2045T= (p.Leu682=) | |
4 | g.125434378A>C | CA358135382 | FAT4 | c.7152A>C (p.Leu2384Phe) c.1923A>C (p.Leu641Phe) c.2046A>C (p.Leu682Phe) | |
4 | g.125434378A>G | CA441205052 | FAT4 | c.7152A>G (p.Leu2384=) c.1923A>G (p.Leu641=) c.2046A>G (p.Leu682=) | |
4 | g.125434378A>T | CA358135383 | FAT4 | c.7152A>T (p.Leu2384Phe) c.1923A>T (p.Leu641Phe) c.2046A>T (p.Leu682Phe) | |
4 | g.125434379T>A | CA358135385 | FAT4 | c.7153T>A (p.Leu2385Met) c.1924T>A (p.Leu642Met) c.2047T>A (p.Leu683Met) | |
4 | g.125434379T>C | CA441205053 | FAT4 | c.7153T>C (p.Leu2385=) c.1924T>C (p.Leu642=) c.2047T>C (p.Leu683=) | gnomAD v4 |
4 | g.125434379T>G | CA358135386 | FAT4 | c.7153T>G (p.Leu2385Val) c.1924T>G (p.Leu642Val) c.2047T>G (p.Leu683Val) | |
4 | g.125434380T>A | CA358135388 | FAT4 | c.7154T>A (p.Leu2385Ter) c.1925T>A (p.Leu642Ter) c.2048T>A (p.Leu683Ter) | |
4 | g.125434380T>C | CA358135389 | FAT4 | c.7154T>C (p.Leu2385Ser) c.1925T>C (p.Leu642Ser) c.2048T>C (p.Leu683Ser) | COSMIC COSMIC |
4 | g.125434380T>G | CA358135391 | FAT4 | c.7154T>G (p.Leu2385Trp) c.1925T>G (p.Leu642Trp) c.2048T>G (p.Leu683Trp) | |
4 | g.125434381G>A | CA441205054 | FAT4 | c.7155G>A (p.Leu2385=) c.1926G>A (p.Leu642=) c.2049G>A (p.Leu683=) | |
4 | g.125434381G>C | CA358135393 | FAT4 | c.7155G>C (p.Leu2385Phe) c.1926G>C (p.Leu642Phe) c.2049G>C (p.Leu683Phe) | |
4 | g.125434381G>T | CA358135394 | FAT4 | c.7155G>T (p.Leu2385Phe) c.1926G>T (p.Leu642Phe) c.2049G>T (p.Leu683Phe) | |
4 | g.125434382G>A | CA358135396 | FAT4 | c.7156G>A (p.Val2386Ile) c.1927G>A (p.Val643Ile) c.2050G>A (p.Val684Ile) | |
4 | g.125434382G>C | CA358135398 | FAT4 | c.7156G>C (p.Val2386Leu) c.1927G>C (p.Val643Leu) c.2050G>C (p.Val684Leu) | gnomAD v4 |
4 | g.125434382G>T | CA358135399 | FAT4 | c.7156G>T (p.Val2386Leu) c.1927G>T (p.Val643Leu) c.2050G>T (p.Val684Leu) | |
4 | g.125434383T>A | CA358135405 | FAT4 | c.7157T>A (p.Val2386Glu) c.1928T>A (p.Val643Glu) c.2051T>A (p.Val684Glu) | |
4 | g.125434383T>C | CA358135401 | FAT4 | c.7157T>C (p.Val2386Ala) c.1928T>C (p.Val643Ala) c.2051T>C (p.Val684Ala) | |
4 | g.125434383T>G | CA358135403 | FAT4 | c.7157T>G (p.Val2386Gly) c.1928T>G (p.Val643Gly) c.2051T>G (p.Val684Gly) | |
4 | g.125434384A>C | CA441205055 | FAT4 | c.7158A>C (p.Val2386=) c.1929A>C (p.Val643=) c.2052A>C (p.Val684=) | |
4 | g.125434384A>G | CA441205056 | FAT4 | c.7158A>G (p.Val2386=) c.1929A>G (p.Val643=) c.2052A>G (p.Val684=) | |
4 | g.125434384A>T | CA441205057 | FAT4 | c.7158A>T (p.Val2386=) c.1929A>T (p.Val643=) c.2052A>T (p.Val684=) | |
4 | g.125434385A>C | CA358135406 | FAT4 | c.7159A>C (p.Asn2387His) c.1930A>C (p.Asn644His) c.2053A>C (p.Asn685His) | |
4 | g.125434385A>G | CA358135408 | FAT4 | c.7159A>G (p.Asn2387Asp) c.1930A>G (p.Asn644Asp) c.2053A>G (p.Asn685Asp) | gnomAD v4 |
4 | g.125434385A>T | CA358135409 | FAT4 | c.7159A>T (p.Asn2387Tyr) c.1930A>T (p.Asn644Tyr) c.2053A>T (p.Asn685Tyr) | |
4 | g.125434386A>C | CA358135411 | FAT4 | c.7160A>C (p.Asn2387Thr) c.1931A>C (p.Asn644Thr) c.2054A>C (p.Asn685Thr) | |
4 | g.125434386A>G | CA358135413 | FAT4 | c.7160A>G (p.Asn2387Ser) c.1931A>G (p.Asn644Ser) c.2054A>G (p.Asn685Ser) | |
4 | g.125434386A>T | CA358135414 | FAT4 | c.7160A>T (p.Asn2387Ile) c.1931A>T (p.Asn644Ile) c.2054A>T (p.Asn685Ile) | |
4 | g.125434387T>A | CA358135416 | FAT4 | c.7161T>A (p.Asn2387Lys) c.1932T>A (p.Asn644Lys) c.2055T>A (p.Asn685Lys) | |
4 | g.125434387T>C | CA441205058 | FAT4 | c.7161T>C (p.Asn2387=) c.1932T>C (p.Asn644=) c.2055T>C (p.Asn685=) | |
4 | g.125434387T>G | CA358135418 | FAT4 | c.7161T>G (p.Asn2387Lys) c.1932T>G (p.Asn644Lys) c.2055T>G (p.Asn685Lys) | |
4 | g.125434388G>A | CA358135420 | FAT4 | c.7162G>A (p.Ala2388Thr) c.1933G>A (p.Ala645Thr) c.2056G>A (p.Ala686Thr) | gnomAD v4 |
4 | g.125434388G>C | CA358135421 | FAT4 | c.7162G>C (p.Ala2388Pro) c.1933G>C (p.Ala645Pro) c.2056G>C (p.Ala686Pro) | |
4 | g.125434388G>T | CA358135423 | FAT4 | c.7162G>T (p.Ala2388Ser) c.1933G>T (p.Ala645Ser) c.2056G>T (p.Ala686Ser) | |
4 | g.125434389C>A | CA358135425 | FAT4 | c.7163C>A (p.Ala2388Asp) c.1934C>A (p.Ala645Asp) c.2057C>A (p.Ala686Asp) | gnomAD v4 |
4 | g.125434389C= | CA1491646844 | FAT4 | c.7163C= (p.Ala2388=) c.1934C= (p.Ala645=) c.2057C= (p.Ala686=) | |
4 | g.125434389C>G | CA3073104 | FAT4 | c.7163C>G (p.Ala2388Gly) c.1934C>G (p.Ala645Gly) c.2057C>G (p.Ala686Gly) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.125434389C>T | CA3073105 | FAT4 | c.7163C>T (p.Ala2388Val) c.1934C>T (p.Ala645Val) c.2057C>T (p.Ala686Val) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.125434390C>A | CA441205059 | FAT4 | c.7164C>A (p.Ala2388=) c.1935C>A (p.Ala645=) c.2058C>A (p.Ala686=) | |
4 | g.125434390C= | CA1491646845 | FAT4 | c.7164C= (p.Ala2388=) c.1935C= (p.Ala645=) c.2058C= (p.Ala686=) | |
4 | g.125434390C>G | CA441205060 | FAT4 | c.7164C>G (p.Ala2388=) c.1935C>G (p.Ala645=) c.2058C>G (p.Ala686=) | |
4 | g.125434390C>T | CA3073106 | FAT4 | c.7164C>T (p.Ala2388=) c.1935C>T (p.Ala645=) c.2058C>T (p.Ala686=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
4 | g.125434391T>A | CA358135428 | FAT4 | c.7165T>A (p.Ser2389Thr) c.1936T>A (p.Ser646Thr) c.2059T>A (p.Ser687Thr) | |
4 | g.125434391T>C | CA358135429 | FAT4 | c.7165T>C (p.Ser2389Pro) c.1936T>C (p.Ser646Pro) c.2059T>C (p.Ser687Pro) | |
4 | g.125434391T>G | CA358135430 | FAT4 | c.7165T>G (p.Ser2389Ala) c.1936T>G (p.Ser646Ala) c.2059T>G (p.Ser687Ala) | |
4 | g.125434392C>A | CA358135432 | FAT4 | c.7166C>A (p.Ser2389Ter) c.1937C>A (p.Ser646Ter) c.2060C>A (p.Ser687Ter) | |
4 | g.125434392C>G | CA358135434 | FAT4 | c.7166C>G (p.Ser2389Ter) c.1937C>G (p.Ser646Ter) c.2060C>G (p.Ser687Ter) | |
4 | g.125434392C>T | CA358135435 | FAT4 | c.7166C>T (p.Ser2389Leu) c.1937C>T (p.Ser646Leu) c.2060C>T (p.Ser687Leu) | COSMIC COSMIC |
4 | g.125434393A= | CA1491646846 | FAT4 | c.7167A= (p.Ser2389=) c.1938A= (p.Ser646=) c.2061A= (p.Ser687=) | |
4 | g.125434393A>C | CA441205061 | FAT4 | c.7167A>C (p.Ser2389=) c.1938A>C (p.Ser646=) c.2061A>C (p.Ser687=) | dbSNP gnomAD v2 gnomAD v4 |
4 | g.125434393A>G | CA441205062 | FAT4 | c.7167A>G (p.Ser2389=) c.1938A>G (p.Ser646=) c.2061A>G (p.Ser687=) | |
4 | g.125434393A>T | CA441205063 | FAT4 | c.7167A>T (p.Ser2389=) c.1938A>T (p.Ser646=) c.2061A>T (p.Ser687=) | |
4 | g.125434394G>A | CA358135436 | FAT4 | c.7168G>A (p.Asp2390Asn) c.1939G>A (p.Asp647Asn) c.2062G>A (p.Asp688Asn) | |
4 | g.125434394G>C | CA358135437 | FAT4 | c.7168G>C (p.Asp2390His) c.1939G>C (p.Asp647His) c.2062G>C (p.Asp688His) | |
4 | g.125434394G>T | CA358135439 | FAT4 | c.7168G>T (p.Asp2390Tyr) c.1939G>T (p.Asp647Tyr) c.2062G>T (p.Asp688Tyr) | |
4 | g.125434395A>C | CA358135441 | FAT4 | c.7169A>C (p.Asp2390Ala) c.1940A>C (p.Asp647Ala) c.2063A>C (p.Asp688Ala) | |
4 | g.125434395A>G | CA358135443 | FAT4 | c.7169A>G (p.Asp2390Gly) c.1940A>G (p.Asp647Gly) c.2063A>G (p.Asp688Gly) | gnomAD v4 |
4 | g.125434395A>T | CA358135444 | FAT4 | c.7169A>T (p.Asp2390Val) c.1940A>T (p.Asp647Val) c.2063A>T (p.Asp688Val) | |
4 | g.125434396T>A | CA358135448 | FAT4 | c.7170T>A (p.Asp2390Glu) c.1941T>A (p.Asp647Glu) c.2064T>A (p.Asp688Glu) | |
4 | g.125434396T>C | CA3073107 | FAT4 | c.7170T>C (p.Asp2390=) c.1941T>C (p.Asp647=) c.2064T>C (p.Asp688=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.125434396T>G | CA358135446 | FAT4 | c.7170T>G (p.Asp2390Glu) c.1941T>G (p.Asp647Glu) c.2064T>G (p.Asp688Glu) | |
4 | g.125434396T= | CA1491646847 | FAT4 | c.7170T= (p.Asp2390=) c.1941T= (p.Asp647=) c.2064T= (p.Asp688=) | |
4 | g.125434397G>A | CA358135450 | FAT4 | c.7171G>A (p.Ala2391Thr) c.1942G>A (p.Ala648Thr) c.2065G>A (p.Ala689Thr) | dbSNP gnomAD v3 gnomAD v4 |
4 | g.125434397G>C | CA358135451 | FAT4 | c.7171G>C (p.Ala2391Pro) c.1942G>C (p.Ala648Pro) c.2065G>C (p.Ala689Pro) | |
4 | g.125434397G= | CA1491646848 | FAT4 | c.7171G= (p.Ala2391=) c.1942G= (p.Ala648=) c.2065G= (p.Ala689=) | |
4 | g.125434397G>T | CA358135452 | FAT4 | c.7171G>T (p.Ala2391Ser) c.1942G>T (p.Ala648Ser) c.2065G>T (p.Ala689Ser) | |
4 | g.125434398C>A | CA358135454 | FAT4 | c.7172C>A (p.Ala2391Asp) c.1943C>A (p.Ala648Asp) c.2066C>A (p.Ala689Asp) | |
4 | g.125434398C>G | CA358135456 | FAT4 | c.7172C>G (p.Ala2391Gly) c.1943C>G (p.Ala648Gly) c.2066C>G (p.Ala689Gly) | |
4 | g.125434398C>T | CA358135457 | FAT4 | c.7172C>T (p.Ala2391Val) c.1943C>T (p.Ala648Val) c.2066C>T (p.Ala689Val) | gnomAD v4 |
4 | g.125434399T>A | CA441205064 | FAT4 | c.7173T>A (p.Ala2391=) c.1944T>A (p.Ala648=) c.2067T>A (p.Ala689=) | |
4 | g.125434399T>C | CA441205065 | FAT4 | c.7173T>C (p.Ala2391=) c.1944T>C (p.Ala648=) c.2067T>C (p.Ala689=) | dbSNP |
4 | g.125434399T>G | CA441205066 | FAT4 | c.7173T>G (p.Ala2391=) c.1944T>G (p.Ala648=) c.2067T>G (p.Ala689=) | |
4 | g.125434399T= | CA1491646849 | FAT4 | c.7173T= (p.Ala2391=) c.1944T= (p.Ala648=) c.2067T= (p.Ala689=) | |
4 | g.125434400G>A | CA358135459 | FAT4 | c.7174G>A (p.Asp2392Asn) c.1945G>A (p.Asp649Asn) c.2068G>A (p.Asp690Asn) | |
4 | g.125434400G>C | CA358135460 | FAT4 | c.7174G>C (p.Asp2392His) c.1945G>C (p.Asp649His) c.2068G>C (p.Asp690His) | |
4 | g.125434400G>T | CA358135461 | FAT4 | c.7174G>T (p.Asp2392Tyr) c.1945G>T (p.Asp649Tyr) c.2068G>T (p.Asp690Tyr) | |
4 | g.125434401A>C | CA358135463 | FAT4 | c.7175A>C (p.Asp2392Ala) c.1946A>C (p.Asp649Ala) c.2069A>C (p.Asp690Ala) | |
4 | g.125434401A>G | CA358135465 | FAT4 | c.7175A>G (p.Asp2392Gly) c.1946A>G (p.Asp649Gly) c.2069A>G (p.Asp690Gly) | gnomAD v4 |
4 | g.125434401A>T | CA358135466 | FAT4 | c.7175A>T (p.Asp2392Val) c.1946A>T (p.Asp649Val) c.2069A>T (p.Asp690Val) | |
4 | g.125434402T>A | CA358135468 | FAT4 | c.7176T>A (p.Asp2392Glu) c.1947T>A (p.Asp649Glu) c.2070T>A (p.Asp690Glu) | |
4 | g.125434402T>C | CA441205067 | FAT4 | c.7176T>C (p.Asp2392=) c.1947T>C (p.Asp649=) c.2070T>C (p.Asp690=) | |
4 | g.125434402T>G | CA358135469 | FAT4 | c.7176T>G (p.Asp2392Glu) c.1947T>G (p.Asp649Glu) c.2070T>G (p.Asp690Glu) | |
4 | g.125434403G>A | CA358135471 | FAT4 | c.7177G>A (p.Ala2393Thr) c.1948G>A (p.Ala650Thr) c.2071G>A (p.Ala691Thr) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
4 | g.125434403G>C | CA358135474 | FAT4 | c.7177G>C (p.Ala2393Pro) c.1948G>C (p.Ala650Pro) c.2071G>C (p.Ala691Pro) | |
4 | g.125434403G= | CA1491646850 | FAT4 | c.7177G= (p.Ala2393=) c.1948G= (p.Ala650=) c.2071G= (p.Ala691=) | |
4 | g.125434403G>T | CA358135473 | FAT4 | c.7177G>T (p.Ala2393Ser) c.1948G>T (p.Ala650Ser) c.2071G>T (p.Ala691Ser) | |
4 | g.125434404C>A | CA358135475 | FAT4 | c.7178C>A (p.Ala2393Asp) c.1949C>A (p.Ala650Asp) c.2072C>A (p.Ala691Asp) | |
4 | g.125434404C>G | CA358135476 | FAT4 | c.7178C>G (p.Ala2393Gly) c.1949C>G (p.Ala650Gly) c.2072C>G (p.Ala691Gly) | |
4 | g.125434404C>T | CA358135477 | FAT4 | c.7178C>T (p.Ala2393Val) c.1949C>T (p.Ala650Val) c.2072C>T (p.Ala691Val) | |
4 | g.125434405T>A | CA441205068 | FAT4 | c.7179T>A (p.Ala2393=) c.1950T>A (p.Ala650=) c.2073T>A (p.Ala691=) | |
4 | g.125434405T>C | CA441205069 | FAT4 | c.7179T>C (p.Ala2393=) c.1950T>C (p.Ala650=) c.2073T>C (p.Ala691=) | dbSNP |
4 | g.125434405T>G | CA441205070 | FAT4 | c.7179T>G (p.Ala2393=) c.1950T>G (p.Ala650=) c.2073T>G (p.Ala691=) | gnomAD v4 |
4 | g.125434405T= | CA1491646851 | FAT4 | c.7179T= (p.Ala2393=) c.1950T= (p.Ala650=) c.2073T= (p.Ala691=) | |
4 | g.125434406T>A | CA358135478 | FAT4 | c.7180T>A (p.Ser2394Thr) c.1951T>A (p.Ser651Thr) c.2074T>A (p.Ser692Thr) | |
4 | g.125434406T>C | CA358135479 | FAT4 | c.7180T>C (p.Ser2394Pro) c.1951T>C (p.Ser651Pro) c.2074T>C (p.Ser692Pro) | |
4 | g.125434406T>G | CA358135481 | FAT4 | c.7180T>G (p.Ser2394Ala) c.1951T>G (p.Ser651Ala) c.2074T>G (p.Ser692Ala) | |
4 | g.125434407C>A | CA358135482 | FAT4 | c.7181C>A (p.Ser2394Ter) c.1952C>A (p.Ser651Ter) c.2075C>A (p.Ser692Ter) | |
4 | g.125434407C>G | CA358135483 | FAT4 | c.7181C>G (p.Ser2394Ter) c.1952C>G (p.Ser651Ter) c.2075C>G (p.Ser692Ter) | |
4 | g.125434407C>T | CA358135484 | FAT4 | c.7181C>T (p.Ser2394Leu) c.1952C>T (p.Ser651Leu) c.2075C>T (p.Ser692Leu) | COSMIC COSMIC |
4 | g.125434408A>C | CA441205073 | FAT4 | c.7182A>C (p.Ser2394=) c.1953A>C (p.Ser651=) c.2076A>C (p.Ser692=) | gnomAD v4 |
4 | g.125434408A>G | CA441205071 | FAT4 | c.7182A>G (p.Ser2394=) c.1953A>G (p.Ser651=) c.2076A>G (p.Ser692=) | gnomAD v4 |
4 | g.125434408A>T | CA441205072 | FAT4 | c.7182A>T (p.Ser2394=) c.1953A>T (p.Ser651=) c.2076A>T (p.Ser692=) | |
4 | g.125434409A= | CA1491646852 | FAT4 | c.7183A= (p.Lys2395=) c.1954A= (p.Lys652=) c.2077A= (p.Lys693=) | |
4 | g.125434409A>C | CA358135485 | FAT4 | c.7183A>C (p.Lys2395Gln) c.1954A>C (p.Lys652Gln) c.2077A>C (p.Lys693Gln) | |
4 | g.125434409A>G | CA358135486 | FAT4 | c.7183A>G (p.Lys2395Glu) c.1954A>G (p.Lys652Glu) c.2077A>G (p.Lys693Glu) | dbSNP gnomAD v2 gnomAD v4 |
4 | g.125434409A>T | CA358135488 | FAT4 | c.7183A>T (p.Lys2395Ter) c.1954A>T (p.Lys652Ter) c.2077A>T (p.Lys693Ter) | |
4 | g.125434410A>C | CA358135490 | FAT4 | c.7184A>C (p.Lys2395Thr) c.1955A>C (p.Lys652Thr) c.2078A>C (p.Lys693Thr) | dbSNP |
4 | g.125434410A>G | CA358135492 | FAT4 | c.7184A>G (p.Lys2395Arg) c.1955A>G (p.Lys652Arg) c.2078A>G (p.Lys693Arg) | |
4 | g.125434410A>T | CA358135491 | FAT4 | c.7184A>T (p.Lys2395Met) c.1955A>T (p.Lys652Met) c.2078A>T (p.Lys693Met) | |
4 | g.125434411G>A | CA441205074 | FAT4 | c.7185G>A (p.Lys2395=) c.1956G>A (p.Lys652=) c.2079G>A (p.Lys693=) | |
4 | g.125434411G>C | CA358135494 | FAT4 | c.7185G>C (p.Lys2395Asn) c.1956G>C (p.Lys652Asn) c.2079G>C (p.Lys693Asn) | |
4 | g.125434411G= | CA1491646853 | FAT4 | c.7185G= (p.Lys2395=) c.1956G= (p.Lys652=) c.2079G= (p.Lys693=) | |
4 | g.125434411G>T | CA3073108 | FAT4 | c.7185G>T (p.Lys2395Asn) c.1956G>T (p.Lys652Asn) c.2079G>T (p.Lys693Asn) | dbSNP ExAC gnomAD v2 COSMIC COSMIC |
4 | g.125434412A>C | CA358135497 | FAT4 | c.7186A>C (p.Asn2396His) c.1957A>C (p.Asn653His) c.2080A>C (p.Asn694His) | |
4 | g.125434412A>G | CA358135498 | FAT4 | c.7186A>G (p.Asn2396Asp) c.1957A>G (p.Asn653Asp) c.2080A>G (p.Asn694Asp) | |
4 | g.125434412A>T | CA358135499 | FAT4 | c.7186A>T (p.Asn2396Tyr) c.1957A>T (p.Asn653Tyr) c.2080A>T (p.Asn694Tyr) | |
4 | g.125434413A= | CA1491646854 | FAT4 | c.7187A= (p.Asn2396=) c.1958A= (p.Asn653=) c.2081A= (p.Asn694=) | |
4 | g.125434413A>C | CA104869427 | FAT4 | c.7187A>C (p.Asn2396Thr) c.1958A>C (p.Asn653Thr) c.2081A>C (p.Asn694Thr) | dbSNP |
4 | g.125434413A>G | CA3073109 | FAT4 | c.7187A>G (p.Asn2396Ser) c.1958A>G (p.Asn653Ser) c.2081A>G (p.Asn694Ser) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.125434413A>T | CA358135503 | FAT4 | c.7187A>T (p.Asn2396Ile) c.1958A>T (p.Asn653Ile) c.2081A>T (p.Asn694Ile) | |
4 | g.125434414T>A | CA358135504 | FAT4 | c.7188T>A (p.Asn2396Lys) c.1959T>A (p.Asn653Lys) c.2082T>A (p.Asn694Lys) | |
4 | g.125434414T>C | CA441205075 | FAT4 | c.7188T>C (p.Asn2396=) c.1959T>C (p.Asn653=) c.2082T>C (p.Asn694=) | gnomAD v4 |
4 | g.125434414T>G | CA358135506 | FAT4 | c.7188T>G (p.Asn2396Lys) c.1959T>G (p.Asn653Lys) c.2082T>G (p.Asn694Lys) | |
4 | g.125434415G>A | CA358135510 | FAT4 | c.7189G>A (p.Ala2397Thr) c.1960G>A (p.Ala654Thr) c.2083G>A (p.Ala695Thr) | ClinVar dbSNP gnomAD v4 |
4 | g.125434415G>C | CA358135511 | FAT4 | c.7189G>C (p.Ala2397Pro) c.1960G>C (p.Ala654Pro) c.2083G>C (p.Ala695Pro) | |
4 | g.125434415G= | CA1491646855 | FAT4 | c.7189G= (p.Ala2397=) c.1960G= (p.Ala654=) c.2083G= (p.Ala695=) | |
4 | g.125434415G>T | CA358135508 | FAT4 | c.7189G>T (p.Ala2397Ser) c.1960G>T (p.Ala654Ser) c.2083G>T (p.Ala695Ser) | |
4 | g.125434416C>A | CA358135512 | FAT4 | c.7190C>A (p.Ala2397Glu) c.1961C>A (p.Ala654Glu) c.2084C>A (p.Ala695Glu) | |
4 | g.125434416C>G | CA358135513 | FAT4 | c.7190C>G (p.Ala2397Gly) c.1961C>G (p.Ala654Gly) c.2084C>G (p.Ala695Gly) | |
4 | g.125434416C>T | CA358135515 | FAT4 | c.7190C>T (p.Ala2397Val) c.1961C>T (p.Ala654Val) c.2084C>T (p.Ala695Val) | ClinVar gnomAD v4 |
4 | g.125434417A= | CA1491646856 | FAT4 | c.7191A= (p.Ala2397=) c.1962A= (p.Ala654=) c.2085A= (p.Ala695=) | |
4 | g.125434417A>C | CA441205076 | FAT4 | c.7191A>C (p.Ala2397=) c.1962A>C (p.Ala654=) c.2085A>C (p.Ala695=) | |
4 | g.125434417A>G | CA3073110 | FAT4 | c.7191A>G (p.Ala2397=) c.1962A>G (p.Ala654=) c.2085A>G (p.Ala695=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.125434417A>T | CA441205077 | FAT4 | c.7191A>T (p.Ala2397=) c.1962A>T (p.Ala654=) c.2085A>T (p.Ala695=) | |
4 | g.125434418G>A | CA358135517 | FAT4 | c.7192G>A (p.Val2398Ile) c.1963G>A (p.Val655Ile) c.2086G>A (p.Val696Ile) | gnomAD v4 |
4 | g.125434418G>C | CA358135519 | FAT4 | c.7192G>C (p.Val2398Leu) c.1963G>C (p.Val655Leu) c.2086G>C (p.Val696Leu) | |
4 | g.125434418G>T | CA358135520 | FAT4 | c.7192G>T (p.Val2398Phe) c.1963G>T (p.Val655Phe) c.2086G>T (p.Val696Phe) | |
4 | g.125434419T>A | CA358135523 | FAT4 | c.7193T>A (p.Val2398Asp) c.1964T>A (p.Val655Asp) c.2087T>A (p.Val696Asp) | |
4 | g.125434419T>C | CA358135524 | FAT4 | c.7193T>C (p.Val2398Ala) c.1964T>C (p.Val655Ala) c.2087T>C (p.Val696Ala) | |
4 | g.125434419T>G | CA358135525 | FAT4 | c.7193T>G (p.Val2398Gly) c.1964T>G (p.Val655Gly) c.2087T>G (p.Val696Gly) | COSMIC COSMIC |
4 | g.125434420T>A | CA441205078 | FAT4 | c.7194T>A (p.Val2398=) c.1965T>A (p.Val655=) c.2088T>A (p.Val696=) | |
4 | g.125434420T>C | CA441205079 | FAT4 | c.7194T>C (p.Val2398=) c.1965T>C (p.Val655=) c.2088T>C (p.Val696=) | |
4 | g.125434420T>G | CA441205080 | FAT4 | c.7194T>G (p.Val2398=) c.1965T>G (p.Val655=) c.2088T>G (p.Val696=) | |
4 | g.125434421A= | CA1491646857 | FAT4 | c.7195A= (p.Ile2399=) c.1966A= (p.Ile656=) c.2089A= (p.Ile697=) | |
4 | g.125434421A>C | CA358135526 | FAT4 | c.7195A>C (p.Ile2399Leu) c.1966A>C (p.Ile656Leu) c.2089A>C (p.Ile697Leu) | gnomAD v4 |
4 | g.125434421A>G | CA3073111 | FAT4 | c.7195A>G (p.Ile2399Val) c.1966A>G (p.Ile656Val) c.2089A>G (p.Ile697Val) | dbSNP ExAC gnomAD v2 gnomAD v4 |
4 | g.125434421A>T | CA358135527 | FAT4 | c.7195A>T (p.Ile2399Leu) c.1966A>T (p.Ile656Leu) c.2089A>T (p.Ile697Leu) | |
4 | g.125434422T>A | CA358135529 | FAT4 | c.7196T>A (p.Ile2399Lys) c.1967T>A (p.Ile656Lys) c.2090T>A (p.Ile697Lys) | dbSNP gnomAD v4 |
4 | g.125434422T>C | CA3073112 | FAT4 | c.7196T>C (p.Ile2399Thr) c.1967T>C (p.Ile656Thr) c.2090T>C (p.Ile697Thr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.125434422T>G | CA358135528 | FAT4 | c.7196T>G (p.Ile2399Arg) c.1967T>G (p.Ile656Arg) c.2090T>G (p.Ile697Arg) | |
4 | g.125434422T= | CA1491646858 | FAT4 | c.7196T= (p.Ile2399=) c.1967T= (p.Ile656=) c.2090T= (p.Ile697=) | |
4 | g.125434423A>C | CA441205081 | FAT4 | c.7197A>C (p.Ile2399=) c.1968A>C (p.Ile656=) c.2091A>C (p.Ile697=) | gnomAD v4 |
4 | g.125434423A>G | CA358135531 | FAT4 | c.7197A>G (p.Ile2399Met) c.1968A>G (p.Ile656Met) c.2091A>G (p.Ile697Met) | |
4 | g.125434423A>T | CA441205082 | FAT4 | c.7197A>T (p.Ile2399=) c.1968A>T (p.Ile656=) c.2091A>T (p.Ile697=) | |
4 | g.125434424A>C | CA441205083 | FAT4 | c.7198A>C (p.Ser2400Arg) c.1969A>C (p.Ser657Arg) c.2092A>C (p.Arg698=) c.7198A>C (p.Arg2400=) | |
4 | g.125434424A>G | CA358135532 | FAT4 | c.7198A>G (p.Ser2400Gly) c.1969A>G (p.Ser657Gly) c.2092A>G (p.Arg698Gly) c.7198A>G (p.Arg2400Gly) | |
4 | g.125434424A>T | CA358135534 | FAT4 | c.7198A>T (p.Ser2400Cys) c.1969A>T (p.Ser657Cys) c.2092A>T (p.Arg698Trp) c.7198A>T (p.Arg2400Trp) | |
4 | g.125434425G>A | CA358135536 | FAT4 | c.7199G>A (p.Ser2400Asn) c.1970G>A (p.Ser657Asn) c.2093G>A (p.Arg698Lys) c.7199G>A (p.Arg2400Lys) | gnomAD v4 |
4 | g.125434425G>C | CA358135537 | FAT4 | c.7199G>C (p.Ser2400Thr) c.1970G>C (p.Ser657Thr) c.2093G>C (p.Arg698Thr) c.7199G>C (p.Arg2400Thr) | |
4 | g.125434425G>T | CA358135538 | FAT4 | c.7199G>T (p.Ser2400Ile) c.1970G>T (p.Ser657Ile) c.2093G>T (p.Arg698Met) c.7199G>T (p.Arg2400Met) | |
4 | g.125434426G>A | CA358135540 | FAT4 | c.7199+1G>A (n.7199+1G>A) c.1970+1G>A (n.1970+1G>A) c.2093+1G>A (n.2093+1G>A) | |
4 | g.125434426G>C | CA358135542 | FAT4 | c.7199+1G>C (n.7199+1G>C) c.1970+1G>C (n.1970+1G>C) c.2093+1G>C (n.2093+1G>C) | |
4 | g.125434426G>T | CA358135543 | FAT4 | c.7199+1G>T (n.7199+1G>T) c.1970+1G>T (n.1970+1G>T) c.2093+1G>T (n.2093+1G>T) | gnomAD v4 |
4 | g.125434427T>A | CA358135545 | FAT4 | c.7199+2T>A (n.7199+2T>A) c.1970+2T>A (n.1970+2T>A) c.2093+2T>A (n.2093+2T>A) | |
4 | g.125434427T>C | CA358135546 | FAT4 | c.7199+2T>C (n.7199+2T>C) c.1970+2T>C (n.1970+2T>C) c.2093+2T>C (n.2093+2T>C) | |
4 | g.125434427T>G | CA358135548 | FAT4 | c.7199+2T>G (n.7199+2T>G) c.1970+2T>G (n.1970+2T>G) c.2093+2T>G (n.2093+2T>G) | |
4 | g.125434428C>A | CA2672009891 | FAT4 | c.7199+3C>A (n.7199+3C>A) c.1970+3C>A (n.1970+3C>A) c.2093+3C>A (n.2093+3C>A) | gnomAD v4 |
4 | g.125434428C= | CA1491646859 | FAT4 | c.7199+3C= (n.7199+3C=) c.1970+3C= (n.1970+3C=) c.2093+3C= (n.2093+3C=) | |
4 | g.125434428C>T | CA3073113 | FAT4 | c.7199+3C>T (n.7199+3C>T) c.1970+3C>T (n.1970+3C>T) c.2093+3C>T (n.2093+3C>T) | dbSNP ExAC gnomAD v2 gnomAD v4 |