Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
4 | g.125434229T>A | CA555019373 | FAT4 | c.7019-16T>A (n.7019-16T>A) c.1790-16T>A (n.1790-16T>A) c.1913-16T>A (n.1913-16T>A) | dbSNP gnomAD v2 gnomAD v4 |
4 | g.125434229T>C | CA3073070 | FAT4 | c.7019-16T>C (n.7019-16T>C) c.1790-16T>C (n.1790-16T>C) c.1913-16T>C (n.1913-16T>C) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.125434229T>G | CA786680115 | FAT4 | c.7019-16T>G (n.7019-16T>G) c.1790-16T>G (n.1790-16T>G) c.1913-16T>G (n.1913-16T>G) | dbSNP gnomAD v4 |
4 | g.125434229T= | CA1491646774 | FAT4 | c.7019-16T= (n.7019-16T=) c.1790-16T= (n.1790-16T=) c.1913-16T= (n.1913-16T=) | |
4 | g.125434231T>G | CA104869181 | FAT4 | c.7019-14T>G (n.7019-14T>G) c.1790-14T>G (n.1790-14T>G) c.1913-14T>G (n.1913-14T>G) | dbSNP |
4 | g.125434231T= | CA1491646775 | FAT4 | c.7019-14T= (n.7019-14T=) c.1790-14T= (n.1790-14T=) c.1913-14T= (n.1913-14T=) | |
4 | g.125434232C= | CA1491646776 | FAT4 | c.7019-13C= (n.7019-13C=) c.1790-13C= (n.1790-13C=) c.1913-13C= (n.1913-13C=) | |
4 | g.125434232C>T | CA3073071 | FAT4 | c.7019-13C>T (n.7019-13C>T) c.1790-13C>T (n.1790-13C>T) c.1913-13C>T (n.1913-13C>T) | dbSNP ExAC gnomAD v2 gnomAD v4 |
4 | g.125434233T>A | CA1491646778 | FAT4 | c.7019-12T>A (n.7019-12T>A) c.1790-12T>A (n.1790-12T>A) c.1913-12T>A (n.1913-12T>A) | dbSNP |
4 | g.125434233T>G | CA2578191087 | FAT4 | c.7019-12T>G (n.7019-12T>G) c.1790-12T>G (n.1790-12T>G) c.1913-12T>G (n.1913-12T>G) | |
4 | g.125434233T= | CA1491646777 | FAT4 | c.7019-12T= (n.7019-12T=) c.1790-12T= (n.1790-12T=) c.1913-12T= (n.1913-12T=) | |
4 | g.125434235T>G | CA1491646780 | FAT4 | c.7019-10T>G (n.7019-10T>G) c.1790-10T>G (n.1790-10T>G) c.1913-10T>G (n.1913-10T>G) | dbSNP |
4 | g.125434235T= | CA1491646779 | FAT4 | c.7019-10T= (n.7019-10T=) c.1790-10T= (n.1790-10T=) c.1913-10T= (n.1913-10T=) | |
4 | g.125434236T>C | CA3073072 | FAT4 | c.7019-9T>C (n.7019-9T>C) c.1790-9T>C (n.1790-9T>C) c.1913-9T>C (n.1913-9T>C) | dbSNP ExAC gnomAD v2 gnomAD v4 |
4 | g.125434236T= | CA1491646781 | FAT4 | c.7019-9T= (n.7019-9T=) c.1790-9T= (n.1790-9T=) c.1913-9T= (n.1913-9T=) | |
4 | g.125434237C>A | CA1067682681 | FAT4 | c.7019-8C>A (n.7019-8C>A) c.1790-8C>A (n.1790-8C>A) c.1913-8C>A (n.1913-8C>A) | dbSNP gnomAD v3 gnomAD v4 |
4 | g.125434237C= | CA1491646782 | FAT4 | c.7019-8C= (n.7019-8C=) c.1790-8C= (n.1790-8C=) c.1913-8C= (n.1913-8C=) | |
4 | g.125434237C>G | CA2578191088 | FAT4 | c.7019-8C>G (n.7019-8C>G) c.1790-8C>G (n.1790-8C>G) c.1913-8C>G (n.1913-8C>G) | gnomAD v4 |
4 | g.125434237C>T | CA3073073 | FAT4 | c.7019-8C>T (n.7019-8C>T) c.1790-8C>T (n.1790-8C>T) c.1913-8C>T (n.1913-8C>T) | dbSNP ExAC gnomAD v2 gnomAD v4 |
4 | g.125434238T>G | CA3073075 | FAT4 | c.7019-7T>G (n.7019-7T>G) c.1790-7T>G (n.1790-7T>G) c.1913-7T>G (n.1913-7T>G) | dbSNP ExAC gnomAD v2 |
4 | g.125434238T= | CA1491646784 | FAT4 | c.7019-7T= (n.7019-7T=) c.1790-7T= (n.1790-7T=) c.1913-7T= (n.1913-7T=) | |
4 | g.125434242dup | CA1491646783 | FAT4 | c.7019-3dup (n.7019-3dup) c.1790-3dup (n.1790-3dup) c.1913-3dup (n.1913-3dup) | dbSNP |
4 | g.125434241_125434242dup | CA3073074 | FAT4 | c.7019-4_7019-3dup (n.7019-4_7019-3dup) c.1790-4_1790-3dup (n.1790-4_1790-3dup) c.1913-4_1913-3dup (n.1913-4_1913-3dup) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.125434239T>C | CA2707130912 | FAT4 | c.7019-6T>C (n.7019-6T>C) c.1790-6T>C (n.1790-6T>C) c.1913-6T>C (n.1913-6T>C) | dbSNP |
4 | g.125434239T>G | CA645538581 | FAT4 | c.7019-6T>G (n.7019-6T>G) c.1790-6T>G (n.1790-6T>G) c.1913-6T>G (n.1913-6T>G) | COSMIC COSMIC |
4 | g.125434242T>G | CA3073076 | FAT4 | c.7019-3T>G (n.7019-3T>G) c.1790-3T>G (n.1790-3T>G) c.1913-3T>G (n.1913-3T>G) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.125434242T= | CA1491646785 | FAT4 | c.7019-3T= (n.7019-3T=) c.1790-3T= (n.1790-3T=) c.1913-3T= (n.1913-3T=) | |
4 | g.125434243A>C | CA358134929 | FAT4 | c.7019-2A>C (n.7019-2A>C) c.1790-2A>C (n.1790-2A>C) c.1913-2A>C (n.1913-2A>C) | |
4 | g.125434243A>G | CA358134931 | FAT4 | c.7019-2A>G (n.7019-2A>G) c.1790-2A>G (n.1790-2A>G) c.1913-2A>G (n.1913-2A>G) | |
4 | g.125434243A>T | CA358134934 | FAT4 | c.7019-2A>T (n.7019-2A>T) c.1790-2A>T (n.1790-2A>T) c.1913-2A>T (n.1913-2A>T) | |
4 | g.125434244G>A | CA358134936 | FAT4 | c.7019-1G>A (n.7019-1G>A) c.1790-1G>A (n.1790-1G>A) c.1913-1G>A (n.1913-1G>A) | gnomAD v3 gnomAD v4 |
4 | g.125434244G>C | CA358134938 | FAT4 | c.7019-1G>C (n.7019-1G>C) c.1790-1G>C (n.1790-1G>C) c.1913-1G>C (n.1913-1G>C) | |
4 | g.125434244G>T | CA358134940 | FAT4 | c.7019-1G>T (n.7019-1G>T) c.1790-1G>T (n.1790-1G>T) c.1913-1G>T (n.1913-1G>T) | gnomAD v4 |
4 | g.125434245G>A | CA358134942 | FAT4 | c.7019G>A (p.Gly2340Glu) c.1790G>A (p.Gly597Glu) c.1913G>A (p.Gly638Glu) | gnomAD v4 |
4 | g.125434245G>C | CA358134943 | FAT4 | c.7019G>C (p.Gly2340Ala) c.1790G>C (p.Gly597Ala) c.1913G>C (p.Gly638Ala) | |
4 | g.125434245G>T | CA358134945 | FAT4 | c.7019G>T (p.Gly2340Val) c.1790G>T (p.Gly597Val) c.1913G>T (p.Gly638Val) | gnomAD v4 |
4 | g.125434246A= | CA1491646786 | FAT4 | c.7020A= (p.Gly2340=) c.1791A= (p.Gly597=) c.1914A= (p.Gly638=) | |
4 | g.125434246A>C | CA441204962 | FAT4 | c.7020A>C (p.Gly2340=) c.1791A>C (p.Gly597=) c.1914A>C (p.Gly638=) | |
4 | g.125434246A>G | CA3073077 | FAT4 | c.7020A>G (p.Gly2340=) c.1791A>G (p.Gly597=) c.1914A>G (p.Gly638=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
4 | g.125434246A>T | CA441204963 | FAT4 | c.7020A>T (p.Gly2340=) c.1791A>T (p.Gly597=) c.1914A>T (p.Gly638=) | |
4 | g.125434247T>A | CA358134950 | FAT4 | c.7021T>A (p.Ser2341Thr) c.1792T>A (p.Ser598Thr) c.1915T>A (p.Ser639Thr) | |
4 | g.125434247T>C | CA358134952 | FAT4 | c.7021T>C (p.Ser2341Pro) c.1792T>C (p.Ser598Pro) c.1915T>C (p.Ser639Pro) | dbSNP gnomAD v4 |
4 | g.125434247T>G | CA358134954 | FAT4 | c.7021T>G (p.Ser2341Ala) c.1792T>G (p.Ser598Ala) c.1915T>G (p.Ser639Ala) | |
4 | g.125434247T= | CA1491646787 | FAT4 | c.7021T= (p.Ser2341=) c.1792T= (p.Ser598=) c.1915T= (p.Ser639=) | |
4 | g.125434248C>A | CA358134957 | FAT4 | c.7022C>A (p.Ser2341Tyr) c.1793C>A (p.Ser598Tyr) c.1916C>A (p.Ser639Tyr) | dbSNP gnomAD v3 gnomAD v4 |
4 | g.125434248C= | CA1491646788 | FAT4 | c.7022C= (p.Ser2341=) c.1793C= (p.Ser598=) c.1916C= (p.Ser639=) | |
4 | g.125434248C>G | CA358134959 | FAT4 | c.7022C>G (p.Ser2341Cys) c.1793C>G (p.Ser598Cys) c.1916C>G (p.Ser639Cys) | |
4 | g.125434248C>T | CA358134961 | FAT4 | c.7022C>T (p.Ser2341Phe) c.1793C>T (p.Ser598Phe) c.1916C>T (p.Ser639Phe) | dbSNP gnomAD v4 COSMIC COSMIC |
4 | g.125434251del | CA2672009889 | FAT4 | c.7025del (p.Pro2342LeufsTer3) c.1796del (p.Pro599LeufsTer3) c.1919del (p.Pro640LeufsTer3) | gnomAD v4 |
4 | g.125434249C>A | CA441204964 | FAT4 | c.7023C>A (p.Ser2341=) c.1794C>A (p.Ser598=) c.1917C>A (p.Ser639=) | |
4 | g.125434249C>G | CA441204965 | FAT4 | c.7023C>G (p.Ser2341=) c.1794C>G (p.Ser598=) c.1917C>G (p.Ser639=) | |
4 | g.125434249C>T | CA441204966 | FAT4 | c.7023C>T (p.Ser2341=) c.1794C>T (p.Ser598=) c.1917C>T (p.Ser639=) | gnomAD v4 |
4 | g.125434250C>A | CA358134965 | FAT4 | c.7024C>A (p.Pro2342Thr) c.1795C>A (p.Pro599Thr) c.1918C>A (p.Pro640Thr) | |
4 | g.125434250C= | CA1491646789 | FAT4 | c.7024C= (p.Pro2342=) c.1795C= (p.Pro599=) c.1918C= (p.Pro640=) | |
4 | g.125434250C>G | CA358134966 | FAT4 | c.7024C>G (p.Pro2342Ala) c.1795C>G (p.Pro599Ala) c.1918C>G (p.Pro640Ala) | |
4 | g.125434250C>T | CA3073078 | FAT4 | c.7024C>T (p.Pro2342Ser) c.1795C>T (p.Pro599Ser) c.1918C>T (p.Pro640Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
4 | g.125434251C>A | CA358134967 | FAT4 | c.7025C>A (p.Pro2342His) c.1796C>A (p.Pro599His) c.1919C>A (p.Pro640His) | |
4 | g.125434251C>G | CA358134968 | FAT4 | c.7025C>G (p.Pro2342Arg) c.1796C>G (p.Pro599Arg) c.1919C>G (p.Pro640Arg) | |
4 | g.125434251C>T | CA358134969 | FAT4 | c.7025C>T (p.Pro2342Leu) c.1796C>T (p.Pro599Leu) c.1919C>T (p.Pro640Leu) | ClinVar gnomAD v4 |
4 | g.125434252T>A | CA441204967 | FAT4 | c.7026T>A (p.Pro2342=) c.1797T>A (p.Pro599=) c.1920T>A (p.Pro640=) | |
4 | g.125434252T>C | CA441204968 | FAT4 | c.7026T>C (p.Pro2342=) c.1797T>C (p.Pro599=) c.1920T>C (p.Pro640=) | dbSNP |
4 | g.125434252T>G | CA441204969 | FAT4 | c.7026T>G (p.Pro2342=) c.1797T>G (p.Pro599=) c.1920T>G (p.Pro640=) | |
4 | g.125434252T= | CA1491646790 | FAT4 | c.7026T= (p.Pro2342=) c.1797T= (p.Pro599=) c.1920T= (p.Pro640=) | |
4 | g.125434253G>A | CA358134971 | FAT4 | c.7027G>A (p.Ala2343Thr) c.1798G>A (p.Ala600Thr) c.1921G>A (p.Ala641Thr) | |
4 | g.125434253G>C | CA358134972 | FAT4 | c.7027G>C (p.Ala2343Pro) c.1798G>C (p.Ala600Pro) c.1921G>C (p.Ala641Pro) | |
4 | g.125434253G>T | CA358134970 | FAT4 | c.7027G>T (p.Ala2343Ser) c.1798G>T (p.Ala600Ser) c.1921G>T (p.Ala641Ser) | |
4 | g.125434254C>A | CA358134973 | FAT4 | c.7028C>A (p.Ala2343Asp) c.1799C>A (p.Ala600Asp) c.1922C>A (p.Ala641Asp) | ClinVar |
4 | g.125434254C= | CA1491646791 | FAT4 | c.7028C= (p.Ala2343=) c.1799C= (p.Ala600=) c.1922C= (p.Ala641=) | |
4 | g.125434254C>G | CA358134974 | FAT4 | c.7028C>G (p.Ala2343Gly) c.1799C>G (p.Ala600Gly) c.1922C>G (p.Ala641Gly) | |
4 | g.125434254C>T | CA3073079 | FAT4 | c.7028C>T (p.Ala2343Val) c.1799C>T (p.Ala600Val) c.1922C>T (p.Ala641Val) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.125434254_125434255delinsTT | CA645538582 | FAT4 | c.7028_7029delinsTT (p.Ala2343Val) c.1799_1800delinsTT (p.Ala600Val) c.1922_1923delinsTT (p.Ala641Val) | COSMIC COSMIC |
4 | g.125434255C>A | CA441204970 | FAT4 | c.7029C>A (p.Ala2343=) c.1800C>A (p.Ala600=) c.1923C>A (p.Ala641=) | |
4 | g.125434255C>G | CA441204971 | FAT4 | c.7029C>G (p.Ala2343=) c.1800C>G (p.Ala600=) c.1923C>G (p.Ala641=) | |
4 | g.125434255C>T | CA441204972 | FAT4 | c.7029C>T (p.Ala2343=) c.1800C>T (p.Ala600=) c.1923C>T (p.Ala641=) | |
4 | g.125434256T>A | CA358134975 | FAT4 | c.7030T>A (p.Leu2344Met) c.1801T>A (p.Leu601Met) c.1924T>A (p.Leu642Met) | |
4 | g.125434256T>C | CA441204973 | FAT4 | c.7030T>C (p.Leu2344=) c.1801T>C (p.Leu601=) c.1924T>C (p.Leu642=) | gnomAD v4 |
4 | g.125434256T>G | CA358134976 | FAT4 | c.7030T>G (p.Leu2344Val) c.1801T>G (p.Leu601Val) c.1924T>G (p.Leu642Val) | |
4 | g.125434257T>A | CA358134977 | FAT4 | c.7031T>A (p.Leu2344Ter) c.1802T>A (p.Leu601Ter) c.1925T>A (p.Leu642Ter) | |
4 | g.125434257T>C | CA358134978 | FAT4 | c.7031T>C (p.Leu2344Ser) c.1802T>C (p.Leu601Ser) c.1925T>C (p.Leu642Ser) | |
4 | g.125434257T>G | CA358134979 | FAT4 | c.7031T>G (p.Leu2344Trp) c.1802T>G (p.Leu601Trp) c.1925T>G (p.Leu642Trp) | |
4 | g.125434258G>A | CA441204974 | FAT4 | c.7032G>A (p.Leu2344=) c.1803G>A (p.Leu601=) c.1926G>A (p.Leu642=) | |
4 | g.125434258G>C | CA358134980 | FAT4 | c.7032G>C (p.Leu2344Phe) c.1803G>C (p.Leu601Phe) c.1926G>C (p.Leu642Phe) | |
4 | g.125434258G= | CA1491646792 | FAT4 | c.7032G= (p.Leu2344=) c.1803G= (p.Leu601=) c.1926G= (p.Leu642=) | |
4 | g.125434258G>T | CA358134981 | FAT4 | c.7032G>T (p.Leu2344Phe) c.1803G>T (p.Leu601Phe) c.1926G>T (p.Leu642Phe) | |
4 | g.125434259A>C | CA358134982 | FAT4 | c.7033A>C (p.Thr2345Pro) c.1804A>C (p.Thr602Pro) c.1927A>C (p.Thr643Pro) | |
4 | g.125434259A>G | CA358134983 | FAT4 | c.7033A>G (p.Thr2345Ala) c.1804A>G (p.Thr602Ala) c.1927A>G (p.Thr643Ala) | |
4 | g.125434259A>T | CA358134984 | FAT4 | c.7033A>T (p.Thr2345Ser) c.1804A>T (p.Thr602Ser) c.1927A>T (p.Thr643Ser) | gnomAD v4 |
4 | g.125434267_125434272dup | CA170760 | FAT4 | c.7041_7046dup (p.Thr2349_Ile2350insGlyThr) c.1812_1817dup (p.Thr606_Ile607insGlyThr) c.1935_1940dup (p.Thr647_Ile648insGlyThr) | ClinVar dbSNP gnomAD v4 |
4 | g.125434260C>A | CA358134987 | FAT4 | c.7034C>A (p.Thr2345Asn) c.1805C>A (p.Thr602Asn) c.1928C>A (p.Thr643Asn) | |
4 | g.125434260C= | CA1491646793 | FAT4 | c.7034C= (p.Thr2345=) c.1805C= (p.Thr602=) c.1928C= (p.Thr643=) | |
4 | g.125434260C>G | CA358134985 | FAT4 | c.7034C>G (p.Thr2345Ser) c.1805C>G (p.Thr602Ser) c.1928C>G (p.Thr643Ser) | |
4 | g.125434260C>T | CA358134986 | FAT4 | c.7034C>T (p.Thr2345Ile) c.1805C>T (p.Thr602Ile) c.1928C>T (p.Thr643Ile) | dbSNP gnomAD v2 gnomAD v4 |
4 | g.125434261T>A | CA441204975 | FAT4 | c.7035T>A (p.Thr2345=) c.1806T>A (p.Thr602=) c.1929T>A (p.Thr643=) | |
4 | g.125434261T>C | CA441204976 | FAT4 | c.7035T>C (p.Thr2345=) c.1806T>C (p.Thr602=) c.1929T>C (p.Thr643=) | |
4 | g.125434261T>G | CA441204977 | FAT4 | c.7035T>G (p.Thr2345=) c.1806T>G (p.Thr602=) c.1929T>G (p.Thr643=) | |
4 | g.125434262G>A | CA358134988 | FAT4 | c.7036G>A (p.Gly2346Arg) c.1807G>A (p.Gly603Arg) c.1930G>A (p.Gly644Arg) | |
4 | g.125434262G>C | CA358134989 | FAT4 | c.7036G>C (p.Gly2346Arg) c.1807G>C (p.Gly603Arg) c.1930G>C (p.Gly644Arg) | |
4 | g.125434262G>T | CA358134990 | FAT4 | c.7036G>T (p.Gly2346Ter) c.1807G>T (p.Gly603Ter) c.1930G>T (p.Gly644Ter) | |
4 | g.125434263G>A | CA358134991 | FAT4 | c.7037G>A (p.Gly2346Glu) c.1808G>A (p.Gly603Glu) c.1931G>A (p.Gly644Glu) | |
4 | g.125434263G>C | CA358134992 | FAT4 | c.7037G>C (p.Gly2346Ala) c.1808G>C (p.Gly603Ala) c.1931G>C (p.Gly644Ala) | |
4 | g.125434263G>T | CA358134993 | FAT4 | c.7037G>T (p.Gly2346Val) c.1808G>T (p.Gly603Val) c.1931G>T (p.Gly644Val) | |
4 | g.125434264A>C | CA441204980 | FAT4 | c.7038A>C (p.Gly2346=) c.1809A>C (p.Gly603=) c.1932A>C (p.Gly644=) | |
4 | g.125434264A>G | CA441204979 | FAT4 | c.7038A>G (p.Gly2346=) c.1809A>G (p.Gly603=) c.1932A>G (p.Gly644=) | gnomAD v4 |
4 | g.125434264A>T | CA441204978 | FAT4 | c.7038A>T (p.Gly2346=) c.1809A>T (p.Gly603=) c.1932A>T (p.Gly644=) | |
4 | g.125434265A= | CA1491646794 | FAT4 | c.7039A= (p.Thr2347=) c.1810A= (p.Thr604=) c.1933A= (p.Thr645=) | |
4 | g.125434265A>C | CA358134994 | FAT4 | c.7039A>C (p.Thr2347Pro) c.1810A>C (p.Thr604Pro) c.1933A>C (p.Thr645Pro) | |
4 | g.125434265A>G | CA3073080 | FAT4 | c.7039A>G (p.Thr2347Ala) c.1810A>G (p.Thr604Ala) c.1933A>G (p.Thr645Ala) | dbSNP ExAC gnomAD v2 gnomAD v4 |
4 | g.125434265A>T | CA358134995 | FAT4 | c.7039A>T (p.Thr2347Ser) c.1810A>T (p.Thr604Ser) c.1933A>T (p.Thr645Ser) | |
4 | g.125434266C>A | CA358134996 | FAT4 | c.7040C>A (p.Thr2347Asn) c.1811C>A (p.Thr604Asn) c.1934C>A (p.Thr645Asn) | COSMIC COSMIC |
4 | g.125434266C>G | CA358134997 | FAT4 | c.7040C>G (p.Thr2347Ser) c.1811C>G (p.Thr604Ser) c.1934C>G (p.Thr645Ser) | |
4 | g.125434266C>T | CA358134998 | FAT4 | c.7040C>T (p.Thr2347Ile) c.1811C>T (p.Thr604Ile) c.1934C>T (p.Thr645Ile) | |
4 | g.125434267T>A | CA441204981 | FAT4 | c.7041T>A (p.Thr2347=) c.1812T>A (p.Thr604=) c.1935T>A (p.Thr645=) | |
4 | g.125434267T>C | CA441204982 | FAT4 | c.7041T>C (p.Thr2347=) c.1812T>C (p.Thr604=) c.1935T>C (p.Thr645=) | |
4 | g.125434267T>G | CA441204983 | FAT4 | c.7041T>G (p.Thr2347=) c.1812T>G (p.Thr604=) c.1935T>G (p.Thr645=) | |
4 | g.125434268G>A | CA358134999 | FAT4 | c.7042G>A (p.Gly2348Arg) c.1813G>A (p.Gly605Arg) c.1936G>A (p.Gly646Arg) | |
4 | g.125434268G>C | CA358135001 | FAT4 | c.7042G>C (p.Gly2348Arg) c.1813G>C (p.Gly605Arg) c.1936G>C (p.Gly646Arg) | |
4 | g.125434268G>T | CA358135000 | FAT4 | c.7042G>T (p.Gly2348Ter) c.1813G>T (p.Gly605Ter) c.1936G>T (p.Gly646Ter) | |
4 | g.125434269G>A | CA358135002 | FAT4 | c.7043G>A (p.Gly2348Glu) c.1814G>A (p.Gly605Glu) c.1937G>A (p.Gly646Glu) | |
4 | g.125434269G>C | CA358135004 | FAT4 | c.7043G>C (p.Gly2348Ala) c.1814G>C (p.Gly605Ala) c.1937G>C (p.Gly646Ala) | dbSNP gnomAD v3 gnomAD v4 |
4 | g.125434269G= | CA1491646795 | FAT4 | c.7043G= (p.Gly2348=) c.1814G= (p.Gly605=) c.1937G= (p.Gly646=) | |
4 | g.125434269G>T | CA358135003 | FAT4 | c.7043G>T (p.Gly2348Val) c.1814G>T (p.Gly605Val) c.1937G>T (p.Gly646Val) | ClinVar dbSNP gnomAD v4 |
4 | g.125434270A>C | CA441204984 | FAT4 | c.7044A>C (p.Gly2348=) c.1815A>C (p.Gly605=) c.1938A>C (p.Gly646=) | |
4 | g.125434270A>G | CA441204985 | FAT4 | c.7044A>G (p.Gly2348=) c.1815A>G (p.Gly605=) c.1938A>G (p.Gly646=) | |
4 | g.125434270A>T | CA441204986 | FAT4 | c.7044A>T (p.Gly2348=) c.1815A>T (p.Gly605=) c.1938A>T (p.Gly646=) | |
4 | g.125434271A>C | CA358135005 | FAT4 | c.7045A>C (p.Thr2349Pro) c.1816A>C (p.Thr606Pro) c.1939A>C (p.Thr647Pro) | gnomAD v4 |
4 | g.125434271A>G | CA358135007 | FAT4 | c.7045A>G (p.Thr2349Ala) c.1816A>G (p.Thr606Ala) c.1939A>G (p.Thr647Ala) | gnomAD v4 |
4 | g.125434271A>T | CA358135006 | FAT4 | c.7045A>T (p.Thr2349Ser) c.1816A>T (p.Thr606Ser) c.1939A>T (p.Thr647Ser) | |
4 | g.125434272C>A | CA104869226 | FAT4 | c.7046C>A (p.Thr2349Lys) c.1817C>A (p.Thr606Lys) c.1940C>A (p.Thr647Lys) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.125434272C= | CA1491646796 | FAT4 | c.7046C= (p.Thr2349=) c.1817C= (p.Thr606=) c.1940C= (p.Thr647=) | |
4 | g.125434272C>G | CA358135008 | FAT4 | c.7046C>G (p.Thr2349Arg) c.1817C>G (p.Thr606Arg) c.1940C>G (p.Thr647Arg) | |
4 | g.125434272C>T | CA358135009 | FAT4 | c.7046C>T (p.Thr2349Ile) c.1817C>T (p.Thr606Ile) c.1940C>T (p.Thr647Ile) | |
4 | g.125434273A>C | CA441204987 | FAT4 | c.7047A>C (p.Thr2349=) c.1818A>C (p.Thr606=) c.1941A>C (p.Thr647=) | |
4 | g.125434273A>G | CA441204988 | FAT4 | c.7047A>G (p.Thr2349=) c.1818A>G (p.Thr606=) c.1941A>G (p.Thr647=) | |
4 | g.125434273A>T | CA441204989 | FAT4 | c.7047A>T (p.Thr2349=) c.1818A>T (p.Thr606=) c.1941A>T (p.Thr647=) | |
4 | g.125434274A>C | CA358135011 | FAT4 | c.7048A>C (p.Ile2350Leu) c.1819A>C (p.Ile607Leu) c.1942A>C (p.Ile648Leu) | |
4 | g.125434274A>G | CA358135013 | FAT4 | c.7048A>G (p.Ile2350Val) c.1819A>G (p.Ile607Val) c.1942A>G (p.Ile648Val) | gnomAD v4 |
4 | g.125434274A>T | CA358135015 | FAT4 | c.7048A>T (p.Ile2350Phe) c.1819A>T (p.Ile607Phe) c.1942A>T (p.Ile648Phe) | |
4 | g.125434275T>A | CA358135017 | FAT4 | c.7049T>A (p.Ile2350Asn) c.1820T>A (p.Ile607Asn) c.1943T>A (p.Ile648Asn) | |
4 | g.125434275T>C | CA358135019 | FAT4 | c.7049T>C (p.Ile2350Thr) c.1820T>C (p.Ile607Thr) c.1943T>C (p.Ile648Thr) | dbSNP gnomAD v3 gnomAD v4 |
4 | g.125434275T>G | CA358135021 | FAT4 | c.7049T>G (p.Ile2350Ser) c.1820T>G (p.Ile607Ser) c.1943T>G (p.Ile648Ser) | |
4 | g.125434275T= | CA1491646797 | FAT4 | c.7049T= (p.Ile2350=) c.1820T= (p.Ile607=) c.1943T= (p.Ile648=) | |
4 | g.125434276C>A | CA441204990 | FAT4 | c.7050C>A (p.Ile2350=) c.1821C>A (p.Ile607=) c.1944C>A (p.Ile648=) | |
4 | g.125434276C>G | CA358135024 | FAT4 | c.7050C>G (p.Ile2350Met) c.1821C>G (p.Ile607Met) c.1944C>G (p.Ile648Met) | |
4 | g.125434276C>T | CA441204991 | FAT4 | c.7050C>T (p.Ile2350=) c.1821C>T (p.Ile607=) c.1944C>T (p.Ile648=) | gnomAD v4 |
4 | g.125434277A>C | CA358135027 | FAT4 | c.7051A>C (p.Asn2351His) c.1822A>C (p.Asn608His) c.1945A>C (p.Asn649His) | |
4 | g.125434277A>G | CA358135028 | FAT4 | c.7051A>G (p.Asn2351Asp) c.1822A>G (p.Asn608Asp) c.1945A>G (p.Asn649Asp) | |
4 | g.125434277A>T | CA358135030 | FAT4 | c.7051A>T (p.Asn2351Tyr) c.1822A>T (p.Asn608Tyr) c.1945A>T (p.Asn649Tyr) | |
4 | g.125434278A= | CA1491646798 | FAT4 | c.7052A= (p.Asn2351=) c.1823A= (p.Asn608=) c.1946A= (p.Asn649=) | |
4 | g.125434278A>C | CA358135033 | FAT4 | c.7052A>C (p.Asn2351Thr) c.1823A>C (p.Asn608Thr) c.1946A>C (p.Asn649Thr) | |
4 | g.125434278A>G | CA3073081 | FAT4 | c.7052A>G (p.Asn2351Ser) c.1823A>G (p.Asn608Ser) c.1946A>G (p.Asn649Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.125434278A>T | CA358135035 | FAT4 | c.7052A>T (p.Asn2351Ile) c.1823A>T (p.Asn608Ile) c.1946A>T (p.Asn649Ile) | |
4 | g.125434279C>A | CA358135040 | FAT4 | c.7053C>A (p.Asn2351Lys) c.1824C>A (p.Asn608Lys) c.1947C>A (p.Asn649Lys) | |
4 | g.125434279C= | CA1491646799 | FAT4 | c.7053C= (p.Asn2351=) c.1824C= (p.Asn608=) c.1947C= (p.Asn649=) | |
4 | g.125434279C>G | CA3073082 | FAT4 | c.7053C>G (p.Asn2351Lys) c.1824C>G (p.Asn608Lys) c.1947C>G (p.Asn649Lys) | dbSNP ExAC gnomAD v2 gnomAD v4 |
4 | g.125434279C>T | CA3073083 | FAT4 | c.7053C>T (p.Asn2351=) c.1824C>T (p.Asn608=) c.1947C>T (p.Asn649=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.125434280G>A | CA3073084 | FAT4 | c.7054G>A (p.Val2352Ile) c.1825G>A (p.Val609Ile) c.1948G>A (p.Val650Ile) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
4 | g.125434280G>C | CA358135045 | FAT4 | c.7054G>C (p.Val2352Leu) c.1825G>C (p.Val609Leu) c.1948G>C (p.Val650Leu) | |
4 | g.125434280G= | CA1491646800 | FAT4 | c.7054G= (p.Val2352=) c.1825G= (p.Val609=) c.1948G= (p.Val650=) | |
4 | g.125434280G>T | CA358135047 | FAT4 | c.7054G>T (p.Val2352Phe) c.1825G>T (p.Val609Phe) c.1948G>T (p.Val650Phe) | |
4 | g.125434281T>A | CA358135048 | FAT4 | c.7055T>A (p.Val2352Asp) c.1826T>A (p.Val609Asp) c.1949T>A (p.Val650Asp) | |
4 | g.125434281T>C | CA358135049 | FAT4 | c.7055T>C (p.Val2352Ala) c.1826T>C (p.Val609Ala) c.1949T>C (p.Val650Ala) | |
4 | g.125434281T>G | CA358135050 | FAT4 | c.7055T>G (p.Val2352Gly) c.1826T>G (p.Val609Gly) c.1949T>G (p.Val650Gly) | |
4 | g.125434282C>A | CA441204994 | FAT4 | c.7056C>A (p.Val2352=) c.1827C>A (p.Val609=) c.1950C>A (p.Val650=) | |
4 | g.125434282C>G | CA441204992 | FAT4 | c.7056C>G (p.Val2352=) c.1827C>G (p.Val609=) c.1950C>G (p.Val650=) | |
4 | g.125434282C>T | CA441204993 | FAT4 | c.7056C>T (p.Val2352=) c.1827C>T (p.Val609=) c.1950C>T (p.Val650=) | |
4 | g.125434283A= | CA1491646801 | FAT4 | c.7057A= (p.Ile2353=) c.1828A= (p.Ile610=) c.1951A= (p.Ile651=) | |
4 | g.125434283A>C | CA358135054 | FAT4 | c.7057A>C (p.Ile2353Leu) c.1828A>C (p.Ile610Leu) c.1951A>C (p.Ile651Leu) | |
4 | g.125434283A>G | CA358135052 | FAT4 | c.7057A>G (p.Ile2353Val) c.1828A>G (p.Ile610Val) c.1951A>G (p.Ile651Val) | dbSNP gnomAD v2 gnomAD v4 |
4 | g.125434283A>T | CA358135051 | FAT4 | c.7057A>T (p.Ile2353Leu) c.1828A>T (p.Ile610Leu) c.1951A>T (p.Ile651Leu) | |
4 | g.125434284T>A | CA358135057 | FAT4 | c.7058T>A (p.Ile2353Lys) c.1829T>A (p.Ile610Lys) c.1952T>A (p.Ile651Lys) | |
4 | g.125434284T>C | CA358135059 | FAT4 | c.7058T>C (p.Ile2353Thr) c.1829T>C (p.Ile610Thr) c.1952T>C (p.Ile651Thr) | |
4 | g.125434284T>G | CA358135061 | FAT4 | c.7058T>G (p.Ile2353Arg) c.1829T>G (p.Ile610Arg) c.1952T>G (p.Ile651Arg) | |
4 | g.125434285A= | CA1491646802 | FAT4 | c.7059A= (p.Ile2353=) c.1830A= (p.Ile610=) c.1953A= (p.Ile651=) | |
4 | g.125434285A>C | CA441204996 | FAT4 | c.7059A>C (p.Ile2353=) c.1830A>C (p.Ile610=) c.1953A>C (p.Ile651=) | dbSNP gnomAD v3 gnomAD v4 |
4 | g.125434285A>G | CA358135064 | FAT4 | c.7059A>G (p.Ile2353Met) c.1830A>G (p.Ile610Met) c.1953A>G (p.Ile651Met) | |
4 | g.125434285A>T | CA441204995 | FAT4 | c.7059A>T (p.Ile2353=) c.1830A>T (p.Ile610=) c.1953A>T (p.Ile651=) | |
4 | g.125434286G>A | CA358135066 | FAT4 | c.7060G>A (p.Val2354Ile) c.1831G>A (p.Val611Ile) c.1954G>A (p.Val652Ile) | |
4 | g.125434286G>C | CA358135068 | FAT4 | c.7060G>C (p.Val2354Leu) c.1831G>C (p.Val611Leu) c.1954G>C (p.Val652Leu) | |
4 | g.125434286G>T | CA358135070 | FAT4 | c.7060G>T (p.Val2354Leu) c.1831G>T (p.Val611Leu) c.1954G>T (p.Val652Leu) | ClinVar gnomAD v4 |
4 | g.125434287T>A | CA358135072 | FAT4 | c.7061T>A (p.Val2354Glu) c.1832T>A (p.Val611Glu) c.1955T>A (p.Val652Glu) | |
4 | g.125434287T>C | CA358135074 | FAT4 | c.7061T>C (p.Val2354Ala) c.1832T>C (p.Val611Ala) c.1955T>C (p.Val652Ala) | |
4 | g.125434287T>G | CA358135076 | FAT4 | c.7061T>G (p.Val2354Gly) c.1832T>G (p.Val611Gly) c.1955T>G (p.Val652Gly) | |
4 | g.125434288A>C | CA441204997 | FAT4 | c.7062A>C (p.Val2354=) c.1833A>C (p.Val611=) c.1956A>C (p.Val652=) | |
4 | g.125434288A>G | CA441204998 | FAT4 | c.7062A>G (p.Val2354=) c.1833A>G (p.Val611=) c.1956A>G (p.Val652=) | COSMIC COSMIC COSMIC |
4 | g.125434288A>T | CA441204999 | FAT4 | c.7062A>T (p.Val2354=) c.1833A>T (p.Val611=) c.1956A>T (p.Val652=) | |
4 | g.125434289G>A | CA358135078 | FAT4 | c.7063G>A (p.Asp2355Asn) c.1834G>A (p.Asp612Asn) c.1957G>A (p.Asp653Asn) | |
4 | g.125434289G>C | CA358135080 | FAT4 | c.7063G>C (p.Asp2355His) c.1834G>C (p.Asp612His) c.1957G>C (p.Asp653His) | dbSNP gnomAD v2 gnomAD v4 |
4 | g.125434289G= | CA1491646803 | FAT4 | c.7063G= (p.Asp2355=) c.1834G= (p.Asp612=) c.1957G= (p.Asp653=) | |
4 | g.125434289G>T | CA358135082 | FAT4 | c.7063G>T (p.Asp2355Tyr) c.1834G>T (p.Asp612Tyr) c.1957G>T (p.Asp653Tyr) | |
4 | g.125434290A= | CA1491646804 | FAT4 | c.7064A= (p.Asp2355=) c.1835A= (p.Asp612=) c.1958A= (p.Asp653=) | |
4 | g.125434290A>C | CA358135084 | FAT4 | c.7064A>C (p.Asp2355Ala) c.1835A>C (p.Asp612Ala) c.1958A>C (p.Asp653Ala) | |
4 | g.125434290A>G | CA358135089 | FAT4 | c.7064A>G (p.Asp2355Gly) c.1835A>G (p.Asp612Gly) c.1958A>G (p.Asp653Gly) | |
4 | g.125434290A>T | CA358135087 | FAT4 | c.7064A>T (p.Asp2355Val) c.1835A>T (p.Asp612Val) c.1958A>T (p.Asp653Val) | dbSNP gnomAD v3 gnomAD v4 |
4 | g.125434291T>A | CA358135091 | FAT4 | c.7065T>A (p.Asp2355Glu) c.1836T>A (p.Asp612Glu) c.1959T>A (p.Asp653Glu) | |
4 | g.125434291T>C | CA441205000 | FAT4 | c.7065T>C (p.Asp2355=) c.1836T>C (p.Asp612=) c.1959T>C (p.Asp653=) | dbSNP gnomAD v4 |
4 | g.125434291T>G | CA358135092 | FAT4 | c.7065T>G (p.Asp2355Glu) c.1836T>G (p.Asp612Glu) c.1959T>G (p.Asp653Glu) | dbSNP gnomAD v2 gnomAD v4 |
4 | g.125434291T= | CA1491646805 | FAT4 | c.7065T= (p.Asp2355=) c.1836T= (p.Asp612=) c.1959T= (p.Asp653=) | |
4 | g.125434292G>A | CA358135094 | FAT4 | c.7066G>A (p.Asp2356Asn) c.1837G>A (p.Asp613Asn) c.1960G>A (p.Asp654Asn) | gnomAD v4 |
4 | g.125434292G>C | CA358135096 | FAT4 | c.7066G>C (p.Asp2356His) c.1837G>C (p.Asp613His) c.1960G>C (p.Asp654His) | |
4 | g.125434292G>T | CA358135097 | FAT4 | c.7066G>T (p.Asp2356Tyr) c.1837G>T (p.Asp613Tyr) c.1960G>T (p.Asp654Tyr) | |
4 | g.125434293A>C | CA358135099 | FAT4 | c.7067A>C (p.Asp2356Ala) c.1838A>C (p.Asp613Ala) c.1961A>C (p.Asp654Ala) | |
4 | g.125434293A>G | CA358135100 | FAT4 | c.7067A>G (p.Asp2356Gly) c.1838A>G (p.Asp613Gly) c.1961A>G (p.Asp654Gly) | |
4 | g.125434293A>T | CA358135101 | FAT4 | c.7067A>T (p.Asp2356Val) c.1838A>T (p.Asp613Val) c.1961A>T (p.Asp654Val) | |
4 | g.125434294T>A | CA358135103 | FAT4 | c.7068T>A (p.Asp2356Glu) c.1839T>A (p.Asp613Glu) c.1962T>A (p.Asp654Glu) | |
4 | g.125434294T>C | CA441205001 | FAT4 | c.7068T>C (p.Asp2356=) c.1839T>C (p.Asp613=) c.1962T>C (p.Asp654=) | |
4 | g.125434294T>G | CA3073085 | FAT4 | c.7068T>G (p.Asp2356Glu) c.1839T>G (p.Asp613Glu) c.1962T>G (p.Asp654Glu) | dbSNP ExAC gnomAD v2 |
4 | g.125434294T= | CA1491646806 | FAT4 | c.7068T= (p.Asp2356=) c.1839T= (p.Asp613=) c.1962T= (p.Asp654=) | |
4 | g.125434295G>A | CA358135109 | FAT4 | c.7069G>A (p.Val2357Ile) c.1840G>A (p.Val614Ile) c.1963G>A (p.Val655Ile) | |
4 | g.125434295G>C | CA358135108 | FAT4 | c.7069G>C (p.Val2357Leu) c.1840G>C (p.Val614Leu) c.1963G>C (p.Val655Leu) | |
4 | g.125434295G>T | CA358135107 | FAT4 | c.7069G>T (p.Val2357Phe) c.1840G>T (p.Val614Phe) c.1963G>T (p.Val655Phe) | |
4 | g.125434296T>A | CA358135111 | FAT4 | c.7070T>A (p.Val2357Asp) c.1841T>A (p.Val614Asp) c.1964T>A (p.Val655Asp) | COSMIC COSMIC |
4 | g.125434296T>C | CA358135114 | FAT4 | c.7070T>C (p.Val2357Ala) c.1841T>C (p.Val614Ala) c.1964T>C (p.Val655Ala) | |
4 | g.125434296T>G | CA358135113 | FAT4 | c.7070T>G (p.Val2357Gly) c.1841T>G (p.Val614Gly) c.1964T>G (p.Val655Gly) | |
4 | g.125434297C>A | CA441205004 | FAT4 | c.7071C>A (p.Val2357=) c.1842C>A (p.Val614=) c.1965C>A (p.Val655=) | |
4 | g.125434297C= | CA1491646807 | FAT4 | c.7071C= (p.Val2357=) c.1842C= (p.Val614=) c.1965C= (p.Val655=) | |
4 | g.125434297C>G | CA441205002 | FAT4 | c.7071C>G (p.Val2357=) c.1842C>G (p.Val614=) c.1965C>G (p.Val655=) | |
4 | g.125434297C>T | CA441205003 | FAT4 | c.7071C>T (p.Val2357=) c.1842C>T (p.Val614=) c.1965C>T (p.Val655=) | dbSNP |
4 | g.125434298A= | CA1491646808 | FAT4 | c.7072A= (p.Asn2358=) c.1843A= (p.Asn615=) c.1966A= (p.Asn656=) | |
4 | g.125434298A>C | CA358135116 | FAT4 | c.7072A>C (p.Asn2358His) c.1843A>C (p.Asn615His) c.1966A>C (p.Asn656His) | |
4 | g.125434298A>G | CA3073086 | FAT4 | c.7072A>G (p.Asn2358Asp) c.1843A>G (p.Asn615Asp) c.1966A>G (p.Asn656Asp) | dbSNP ExAC gnomAD v2 gnomAD v4 |
4 | g.125434298A>T | CA358135118 | FAT4 | c.7072A>T (p.Asn2358Tyr) c.1843A>T (p.Asn615Tyr) c.1966A>T (p.Asn656Tyr) | |
4 | g.125434299A>C | CA358135121 | FAT4 | c.7073A>C (p.Asn2358Thr) c.1844A>C (p.Asn615Thr) c.1967A>C (p.Asn656Thr) | |
4 | g.125434299A>G | CA358135122 | FAT4 | c.7073A>G (p.Asn2358Ser) c.1844A>G (p.Asn615Ser) c.1967A>G (p.Asn656Ser) | |
4 | g.125434299A>T | CA358135124 | FAT4 | c.7073A>T (p.Asn2358Ile) c.1844A>T (p.Asn615Ile) c.1967A>T (p.Asn656Ile) | |
4 | g.125434300T>A | CA358135127 | FAT4 | c.7074T>A (p.Asn2358Lys) c.1845T>A (p.Asn615Lys) c.1968T>A (p.Asn656Lys) | |
4 | g.125434300T>C | CA441205005 | FAT4 | c.7074T>C (p.Asn2358=) c.1845T>C (p.Asn615=) c.1968T>C (p.Asn656=) | gnomAD v4 COSMIC COSMIC |
4 | g.125434300T>G | CA358135129 | FAT4 | c.7074T>G (p.Asn2358Lys) c.1845T>G (p.Asn615Lys) c.1968T>G (p.Asn656Lys) | |
4 | g.125434301G>A | CA358135130 | FAT4 | c.7075G>A (p.Asp2359Asn) c.1846G>A (p.Asp616Asn) c.1969G>A (p.Asp657Asn) | |
4 | g.125434301G>C | CA358135131 | FAT4 | c.7075G>C (p.Asp2359His) c.1846G>C (p.Asp616His) c.1969G>C (p.Asp657His) | |
4 | g.125434301G>T | CA358135133 | FAT4 | c.7075G>T (p.Asp2359Tyr) c.1846G>T (p.Asp616Tyr) c.1969G>T (p.Asp657Tyr) | |
4 | g.125434302A>C | CA358135136 | FAT4 | c.7076A>C (p.Asp2359Ala) c.1847A>C (p.Asp616Ala) c.1970A>C (p.Asp657Ala) | |
4 | g.125434302A>G | CA358135135 | FAT4 | c.7076A>G (p.Asp2359Gly) c.1847A>G (p.Asp616Gly) c.1970A>G (p.Asp657Gly) | |
4 | g.125434302A>T | CA358135134 | FAT4 | c.7076A>T (p.Asp2359Val) c.1847A>T (p.Asp616Val) c.1970A>T (p.Asp657Val) | |
4 | g.125434303C>A | CA358135137 | FAT4 | c.7077C>A (p.Asp2359Glu) c.1848C>A (p.Asp616Glu) c.1971C>A (p.Asp657Glu) | |
4 | g.125434303C>G | CA358135138 | FAT4 | c.7077C>G (p.Asp2359Glu) c.1848C>G (p.Asp616Glu) c.1971C>G (p.Asp657Glu) | |
4 | g.125434303C>T | CA441205006 | FAT4 | c.7077C>T (p.Asp2359=) c.1848C>T (p.Asp616=) c.1971C>T (p.Asp657=) | |
4 | g.125434304A>C | CA358135139 | FAT4 | c.7078A>C (p.Asn2360His) c.1849A>C (p.Asn617His) c.1972A>C (p.Asn658His) | |
4 | g.125434304A>G | CA358135140 | FAT4 | c.7078A>G (p.Asn2360Asp) c.1849A>G (p.Asn617Asp) c.1972A>G (p.Asn658Asp) | |
4 | g.125434304A>T | CA358135141 | FAT4 | c.7078A>T (p.Asn2360Tyr) c.1849A>T (p.Asn617Tyr) c.1972A>T (p.Asn658Tyr) | |
4 | g.125434305A= | CA1491646809 | FAT4 | c.7079A= (p.Asn2360=) c.1850A= (p.Asn617=) c.1973A= (p.Asn658=) | |
4 | g.125434305A>C | CA358135142 | FAT4 | c.7079A>C (p.Asn2360Thr) c.1850A>C (p.Asn617Thr) c.1973A>C (p.Asn658Thr) | |
4 | g.125434305A>G | CA3073087 | FAT4 | c.7079A>G (p.Asn2360Ser) c.1850A>G (p.Asn617Ser) c.1973A>G (p.Asn658Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.125434305A>T | CA358135144 | FAT4 | c.7079A>T (p.Asn2360Ile) c.1850A>T (p.Asn617Ile) c.1973A>T (p.Asn658Ile) | |
4 | g.125434306T>A | CA358135145 | FAT4 | c.7080T>A (p.Asn2360Lys) c.1851T>A (p.Asn617Lys) c.1974T>A (p.Asn658Lys) | |
4 | g.125434306T>C | CA3073088 | FAT4 | c.7080T>C (p.Asn2360=) c.1851T>C (p.Asn617=) c.1974T>C (p.Asn658=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.125434306T>G | CA358135147 | FAT4 | c.7080T>G (p.Asn2360Lys) c.1851T>G (p.Asn617Lys) c.1974T>G (p.Asn658Lys) | |
4 | g.125434306T= | CA1491646810 | FAT4 | c.7080T= (p.Asn2360=) c.1851T= (p.Asn617=) c.1974T= (p.Asn658=) | |
4 | g.125434307G>A | CA358135152 | FAT4 | c.7081G>A (p.Val2361Ile) c.1852G>A (p.Val618Ile) c.1975G>A (p.Val659Ile) | dbSNP |
4 | g.125434307G>C | CA358135150 | FAT4 | c.7081G>C (p.Val2361Leu) c.1852G>C (p.Val618Leu) c.1975G>C (p.Val659Leu) | |
4 | g.125434307G= | CA1491646811 | FAT4 | c.7081G= (p.Val2361=) c.1852G= (p.Val618=) c.1975G= (p.Val659=) | |
4 | g.125434307G>T | CA358135149 | FAT4 | c.7081G>T (p.Val2361Phe) c.1852G>T (p.Val618Phe) c.1975G>T (p.Val659Phe) | |
4 | g.125434308T>A | CA358135153 | FAT4 | c.7082T>A (p.Val2361Asp) c.1853T>A (p.Val618Asp) c.1976T>A (p.Val659Asp) | |
4 | g.125434308T>C | CA358135155 | FAT4 | c.7082T>C (p.Val2361Ala) c.1853T>C (p.Val618Ala) c.1976T>C (p.Val659Ala) | COSMIC COSMIC |
4 | g.125434308T>G | CA358135156 | FAT4 | c.7082T>G (p.Val2361Gly) c.1853T>G (p.Val618Gly) c.1976T>G (p.Val659Gly) | |
4 | g.125434309C>A | CA3073089 | FAT4 | c.7083C>A (p.Val2361=) c.1854C>A (p.Val618=) c.1977C>A (p.Val659=) | dbSNP ExAC gnomAD v2 |
4 | g.125434309C= | CA1491646812 | FAT4 | c.7083C= (p.Val2361=) c.1854C= (p.Val618=) c.1977C= (p.Val659=) | |
4 | g.125434309C>G | CA441205007 | FAT4 | c.7083C>G (p.Val2361=) c.1854C>G (p.Val618=) c.1977C>G (p.Val659=) | |
4 | g.125434309C>T | CA441205008 | FAT4 | c.7083C>T (p.Val2361=) c.1854C>T (p.Val618=) c.1977C>T (p.Val659=) | |
4 | g.125434310C>A | CA358135161 | FAT4 | c.7084C>A (p.Pro2362Thr) c.1855C>A (p.Pro619Thr) c.1978C>A (p.Pro660Thr) | |
4 | g.125434310C>G | CA358135162 | FAT4 | c.7084C>G (p.Pro2362Ala) c.1855C>G (p.Pro619Ala) c.1978C>G (p.Pro660Ala) | gnomAD v4 |
4 | g.125434310C>T | CA358135163 | FAT4 | c.7084C>T (p.Pro2362Ser) c.1855C>T (p.Pro619Ser) c.1978C>T (p.Pro660Ser) | gnomAD v3 gnomAD v4 |
4 | g.125434311C>A | CA358135165 | FAT4 | c.7085C>A (p.Pro2362His) c.1856C>A (p.Pro619His) c.1979C>A (p.Pro660His) | |
4 | g.125434311C>G | CA358135167 | FAT4 | c.7085C>G (p.Pro2362Arg) c.1856C>G (p.Pro619Arg) c.1979C>G (p.Pro660Arg) | |
4 | g.125434311C>T | CA358135168 | FAT4 | c.7085C>T (p.Pro2362Leu) c.1856C>T (p.Pro619Leu) c.1979C>T (p.Pro660Leu) | |
4 | g.125434312C>A | CA441205009 | FAT4 | c.7086C>A (p.Pro2362=) c.1857C>A (p.Pro619=) c.1980C>A (p.Pro660=) | |
4 | g.125434312C>G | CA441205010 | FAT4 | c.7086C>G (p.Pro2362=) c.1857C>G (p.Pro619=) c.1980C>G (p.Pro660=) | |
4 | g.125434312C>T | CA441205011 | FAT4 | c.7086C>T (p.Pro2362=) c.1857C>T (p.Pro619=) c.1980C>T (p.Pro660=) | |
4 | g.125434313A>C | CA358135169 | FAT4 | c.7087A>C (p.Thr2363Pro) c.1858A>C (p.Thr620Pro) c.1981A>C (p.Thr661Pro) | |
4 | g.125434313A>G | CA358135170 | FAT4 | c.7087A>G (p.Thr2363Ala) c.1858A>G (p.Thr620Ala) c.1981A>G (p.Thr661Ala) | COSMIC COSMIC |
4 | g.125434313A>T | CA358135171 | FAT4 | c.7087A>T (p.Thr2363Ser) c.1858A>T (p.Thr620Ser) c.1981A>T (p.Thr661Ser) | |
4 | g.125434314C>A | CA358135175 | FAT4 | c.7088C>A (p.Thr2363Lys) c.1859C>A (p.Thr620Lys) c.1982C>A (p.Thr661Lys) | |
4 | g.125434314C= | CA1491646813 | FAT4 | c.7088C= (p.Thr2363=) c.1859C= (p.Thr620=) c.1982C= (p.Thr661=) | |
4 | g.125434314C>G | CA358135172 | FAT4 | c.7088C>G (p.Thr2363Arg) c.1859C>G (p.Thr620Arg) c.1982C>G (p.Thr661Arg) | gnomAD v4 |
4 | g.125434314C>T | CA3073090 | FAT4 | c.7088C>T (p.Thr2363Ile) c.1859C>T (p.Thr620Ile) c.1982C>T (p.Thr661Ile) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.125434315A>C | CA441205012 | FAT4 | c.7089A>C (p.Thr2363=) c.1860A>C (p.Thr620=) c.1983A>C (p.Thr661=) | |
4 | g.125434315A>G | CA441205013 | FAT4 | c.7089A>G (p.Thr2363=) c.1860A>G (p.Thr620=) c.1983A>G (p.Thr661=) | gnomAD v4 |
4 | g.125434315A>T | CA441205014 | FAT4 | c.7089A>T (p.Thr2363=) c.1860A>T (p.Thr620=) c.1983A>T (p.Thr661=) | |
4 | g.125434316T>A | CA358135176 | FAT4 | c.7090T>A (p.Phe2364Ile) c.1861T>A (p.Phe621Ile) c.1984T>A (p.Phe662Ile) | |
4 | g.125434316T>C | CA358135177 | FAT4 | c.7090T>C (p.Phe2364Leu) c.1861T>C (p.Phe621Leu) c.1984T>C (p.Phe662Leu) | |
4 | g.125434316T>G | CA358135179 | FAT4 | c.7090T>G (p.Phe2364Val) c.1861T>G (p.Phe621Val) c.1984T>G (p.Phe662Val) | |
4 | g.125434317T>A | CA104869251 | FAT4 | c.7091T>A (p.Phe2364Tyr) c.1862T>A (p.Phe621Tyr) c.1985T>A (p.Phe662Tyr) | dbSNP gnomAD v3 gnomAD v4 |
4 | g.125434317T>C | CA358135182 | FAT4 | c.7091T>C (p.Phe2364Ser) c.1862T>C (p.Phe621Ser) c.1985T>C (p.Phe662Ser) | |
4 | g.125434317T>G | CA358135183 | FAT4 | c.7091T>G (p.Phe2364Cys) c.1862T>G (p.Phe621Cys) c.1985T>G (p.Phe662Cys) | |
4 | g.125434317T= | CA1491646814 | FAT4 | c.7091T= (p.Phe2364=) c.1862T= (p.Phe621=) c.1985T= (p.Phe662=) | |
4 | g.125434318T>A | CA358135185 | FAT4 | c.7092T>A (p.Phe2364Leu) c.1863T>A (p.Phe621Leu) c.1986T>A (p.Phe662Leu) | |
4 | g.125434318T>C | CA3073091 | FAT4 | c.7092T>C (p.Phe2364=) c.1863T>C (p.Phe621=) c.1986T>C (p.Phe662=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.125434318T>G | CA358135187 | FAT4 | c.7092T>G (p.Phe2364Leu) c.1863T>G (p.Phe621Leu) c.1986T>G (p.Phe662Leu) | |
4 | g.125434318T= | CA1491646815 | FAT4 | c.7092T= (p.Phe2364=) c.1863T= (p.Phe621=) c.1986T= (p.Phe662=) | |
4 | g.125434319G>A | CA358135188 | FAT4 | c.7093G>A (p.Ala2365Thr) c.1864G>A (p.Ala622Thr) c.1987G>A (p.Ala663Thr) | |
4 | g.125434319G>C | CA358135189 | FAT4 | c.7093G>C (p.Ala2365Pro) c.1864G>C (p.Ala622Pro) c.1987G>C (p.Ala663Pro) | |
4 | g.125434319G= | CA1491646816 | FAT4 | c.7093G= (p.Ala2365=) c.1864G= (p.Ala622=) c.1987G= (p.Ala663=) | |
4 | g.125434319G>T | CA358135191 | FAT4 | c.7093G>T (p.Ala2365Ser) c.1864G>T (p.Ala622Ser) c.1987G>T (p.Ala663Ser) | dbSNP gnomAD v3 gnomAD v4 |
4 | g.125434320C>A | CA358135194 | FAT4 | c.7094C>A (p.Ala2365Asp) c.1865C>A (p.Ala622Asp) c.1988C>A (p.Ala663Asp) | |
4 | g.125434320C= | CA1491646817 | FAT4 | c.7094C= (p.Ala2365=) c.1865C= (p.Ala622=) c.1988C= (p.Ala663=) | |
4 | g.125434320C>G | CA3073092 | FAT4 | c.7094C>G (p.Ala2365Gly) c.1865C>G (p.Ala622Gly) c.1988C>G (p.Ala663Gly) | dbSNP ExAC gnomAD v2 |
4 | g.125434320C>T | CA358135192 | FAT4 | c.7094C>T (p.Ala2365Val) c.1865C>T (p.Ala622Val) c.1988C>T (p.Ala663Val) | |
4 | g.125434321C>A | CA441205015 | FAT4 | c.7095C>A (p.Ala2365=) c.1866C>A (p.Ala622=) c.1989C>A (p.Ala663=) | |
4 | g.125434321C>G | CA441205016 | FAT4 | c.7095C>G (p.Ala2365=) c.1866C>G (p.Ala622=) c.1989C>G (p.Ala663=) | |
4 | g.125434321C>T | CA441205017 | FAT4 | c.7095C>T (p.Ala2365=) c.1866C>T (p.Ala622=) c.1989C>T (p.Ala663=) | |
4 | g.125434322A= | CA1491646818 | FAT4 | c.7096A= (p.Ser2366=) c.1867A= (p.Ser623=) c.1990A= (p.Ser664=) | |
4 | g.125434322A>C | CA358135199 | FAT4 | c.7096A>C (p.Ser2366Arg) c.1867A>C (p.Ser623Arg) c.1990A>C (p.Ser664Arg) | dbSNP |
4 | g.125434322A>G | CA358135196 | FAT4 | c.7096A>G (p.Ser2366Gly) c.1867A>G (p.Ser623Gly) c.1990A>G (p.Ser664Gly) | |
4 | g.125434322A>T | CA358135198 | FAT4 | c.7096A>T (p.Ser2366Cys) c.1867A>T (p.Ser623Cys) c.1990A>T (p.Ser664Cys) | gnomAD v4 |
4 | g.125434323G>A | CA358135201 | FAT4 | c.7097G>A (p.Ser2366Asn) c.1868G>A (p.Ser623Asn) c.1991G>A (p.Ser664Asn) | |
4 | g.125434323G>C | CA358135203 | FAT4 | c.7097G>C (p.Ser2366Thr) c.1868G>C (p.Ser623Thr) c.1991G>C (p.Ser664Thr) | |
4 | g.125434323G>T | CA358135204 | FAT4 | c.7097G>T (p.Ser2366Ile) c.1868G>T (p.Ser623Ile) c.1991G>T (p.Ser664Ile) | COSMIC COSMIC |
4 | g.125434324T>A | CA358135205 | FAT4 | c.7098T>A (p.Ser2366Arg) c.1869T>A (p.Ser623Arg) c.1992T>A (p.Ser664Arg) | |
4 | g.125434324T>C | CA3073093 | FAT4 | c.7098T>C (p.Ser2366=) c.1869T>C (p.Ser623=) c.1992T>C (p.Ser664=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
4 | g.125434324T>G | CA358135207 | FAT4 | c.7098T>G (p.Ser2366Arg) c.1869T>G (p.Ser623Arg) c.1992T>G (p.Ser664Arg) | |
4 | g.125434324T= | CA1491646819 | FAT4 | c.7098T= (p.Ser2366=) c.1869T= (p.Ser623=) c.1992T= (p.Ser664=) | |
4 | g.125434325A= | CA1491646820 | FAT4 | c.7099A= (p.Lys2367=) c.1870A= (p.Lys624=) c.1993A= (p.Lys665=) | |
4 | g.125434325A>C | CA358135209 | FAT4 | c.7099A>C (p.Lys2367Gln) c.1870A>C (p.Lys624Gln) c.1993A>C (p.Lys665Gln) | |
4 | g.125434325A>G | CA358135211 | FAT4 | c.7099A>G (p.Lys2367Glu) c.1870A>G (p.Lys624Glu) c.1993A>G (p.Lys665Glu) | dbSNP gnomAD v4 COSMIC |
4 | g.125434325A>T | CA358135212 | FAT4 | c.7099A>T (p.Lys2367Ter) c.1870A>T (p.Lys624Ter) c.1993A>T (p.Lys665Ter) | |
4 | g.125434326A>C | CA358135213 | FAT4 | c.7100A>C (p.Lys2367Thr) c.1871A>C (p.Lys624Thr) c.1994A>C (p.Lys665Thr) | |
4 | g.125434326A>G | CA358135215 | FAT4 | c.7100A>G (p.Lys2367Arg) c.1871A>G (p.Lys624Arg) c.1994A>G (p.Lys665Arg) | |
4 | g.125434326A>T | CA358135217 | FAT4 | c.7100A>T (p.Lys2367Ile) c.1871A>T (p.Lys624Ile) c.1994A>T (p.Lys665Ile) | |
4 | g.125434327A= | CA1491646821 | FAT4 | c.7101A= (p.Lys2367=) c.1872A= (p.Lys624=) c.1995A= (p.Lys665=) | |
4 | g.125434327A>C | CA358135218 | FAT4 | c.7101A>C (p.Lys2367Asn) c.1872A>C (p.Lys624Asn) c.1995A>C (p.Lys665Asn) | |
4 | g.125434327A>G | CA441205018 | FAT4 | c.7101A>G (p.Lys2367=) c.1872A>G (p.Lys624=) c.1995A>G (p.Lys665=) | dbSNP gnomAD v2 gnomAD v4 |
4 | g.125434327A>T | CA358135220 | FAT4 | c.7101A>T (p.Lys2367Asn) c.1872A>T (p.Lys624Asn) c.1995A>T (p.Lys665Asn) | |
4 | g.125434328G>A | CA358135221 | FAT4 | c.7102G>A (p.Ala2368Thr) c.1873G>A (p.Ala625Thr) c.1996G>A (p.Ala666Thr) | |
4 | g.125434328G>C | CA358135222 | FAT4 | c.7102G>C (p.Ala2368Pro) c.1873G>C (p.Ala625Pro) c.1996G>C (p.Ala666Pro) | |
4 | g.125434328G>T | CA358135223 | FAT4 | c.7102G>T (p.Ala2368Ser) c.1873G>T (p.Ala625Ser) c.1996G>T (p.Ala666Ser) | |
4 | g.125434329C>A | CA3073094 | FAT4 | c.7103C>A (p.Ala2368Glu) c.1874C>A (p.Ala625Glu) c.1997C>A (p.Ala666Glu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.125434329C= | CA1491646822 | FAT4 | c.7103C= (p.Ala2368=) c.1874C= (p.Ala625=) c.1997C= (p.Ala666=) | |
4 | g.125434329C>G | CA358135226 | FAT4 | c.7103C>G (p.Ala2368Gly) c.1874C>G (p.Ala625Gly) c.1997C>G (p.Ala666Gly) | |
4 | g.125434329C>T | CA358135228 | FAT4 | c.7103C>T (p.Ala2368Val) c.1874C>T (p.Ala625Val) c.1997C>T (p.Ala666Val) | ClinVar dbSNP gnomAD v4 |