Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
4 | g.125317817A= | CA1491600812 | FAT4 | c.1406A= (p.Asn469=) c.-55+1840A= (n.-55+1840A=) | |
4 | g.125317817A>C | CA358117831 | FAT4 | c.1406A>C (p.Asn469Thr) c.-55+1840A>C (n.-55+1840A>C) | |
4 | g.125317817A>G | CA358117832 | FAT4 | c.1406A>G (p.Asn469Ser) c.-55+1840A>G (n.-55+1840A>G) | dbSNP gnomAD v3 gnomAD v4 |
4 | g.125317817A>T | CA358117833 | FAT4 | c.1406A>T (p.Asn469Ile) c.-55+1840A>T (n.-55+1840A>T) | |
4 | g.125317818T>A | CA358117834 | FAT4 | c.1407T>A (p.Asn469Lys) c.-55+1841T>A (n.-55+1841T>A) | |
4 | g.125317818T>C | CA441366617 | FAT4 | c.1407T>C (p.Asn469=) c.-55+1841T>C (n.-55+1841T>C) | |
4 | g.125317818T>G | CA358117835 | FAT4 | c.1407T>G (p.Asn469Lys) c.-55+1841T>G (n.-55+1841T>G) | |
4 | g.125317819G>A | CA358117838 | FAT4 | c.1408G>A (p.Asp470Asn) c.-55+1842G>A (n.-55+1842G>A) | |
4 | g.125317819G>C | CA358117837 | FAT4 | c.1408G>C (p.Asp470His) c.-55+1842G>C (n.-55+1842G>C) | |
4 | g.125317819G>T | CA358117836 | FAT4 | c.1408G>T (p.Asp470Tyr) c.-55+1842G>T (n.-55+1842G>T) | |
4 | g.125317820A= | CA1491600819 | FAT4 | c.1409A= (p.Asp470=) c.-55+1843A= (n.-55+1843A=) | |
4 | g.125317820A>C | CA3071984 | FAT4 | c.1409A>C (p.Asp470Ala) c.-55+1843A>C (n.-55+1843A>C) | dbSNP ExAC gnomAD v2 gnomAD v4 |
4 | g.125317820A>G | CA358117840 | FAT4 | c.1409A>G (p.Asp470Gly) c.-55+1843A>G (n.-55+1843A>G) | |
4 | g.125317820A>T | CA358117839 | FAT4 | c.1409A>T (p.Asp470Val) c.-55+1843A>T (n.-55+1843A>T) | dbSNP gnomAD v2 gnomAD v4 |
4 | g.125317821C>A | CA358117841 | FAT4 | c.1410C>A (p.Asp470Glu) c.-55+1844C>A (n.-55+1844C>A) | |
4 | g.125317821C>G | CA358117842 | FAT4 | c.1410C>G (p.Asp470Glu) c.-55+1844C>G (n.-55+1844C>G) | |
4 | g.125317821C>T | CA441366627 | FAT4 | c.1410C>T (p.Asp470=) c.-55+1844C>T (n.-55+1844C>T) | |
4 | g.125317822C>A | CA358117843 | FAT4 | c.1411C>A (p.His471Asn) c.-55+1845C>A (n.-55+1845C>A) | |
4 | g.125317822C>G | CA358117844 | FAT4 | c.1411C>G (p.His471Asp) c.-55+1845C>G (n.-55+1845C>G) | |
4 | g.125317822C>T | CA358117845 | FAT4 | c.1411C>T (p.His471Tyr) c.-55+1845C>T (n.-55+1845C>T) | |
4 | g.125317823A= | CA1491600824 | FAT4 | c.1412A= (p.His471=) c.-55+1846A= (n.-55+1846A=) | |
4 | g.125317823A>C | CA358117846 | FAT4 | c.1412A>C (p.His471Pro) c.-55+1846A>C (n.-55+1846A>C) | |
4 | g.125317823A>G | CA358117847 | FAT4 | c.1412A>G (p.His471Arg) c.-55+1846A>G (n.-55+1846A>G) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
4 | g.125317823A>T | CA358117848 | FAT4 | c.1412A>T (p.His471Leu) c.-55+1846A>T (n.-55+1846A>T) | |
4 | g.125317824T>A | CA3071985 | FAT4 | c.1413T>A (p.His471Gln) c.-55+1847T>A (n.-55+1847T>A) | dbSNP ExAC gnomAD v2 gnomAD v4 |
4 | g.125317824T>C | CA441366630 | FAT4 | c.1413T>C (p.His471=) c.-55+1847T>C (n.-55+1847T>C) | gnomAD v4 |
4 | g.125317824T>G | CA358117849 | FAT4 | c.1413T>G (p.His471Gln) c.-55+1847T>G (n.-55+1847T>G) | COSMIC COSMIC |
4 | g.125317824T= | CA1491600831 | FAT4 | c.1413T= (p.His471=) c.-55+1847T= (n.-55+1847T=) | |
4 | g.125317825C>A | CA358117850 | FAT4 | c.1414C>A (p.Pro472Thr) c.-55+1848C>A (n.-55+1848C>A) | |
4 | g.125317825C= | CA1491600836 | FAT4 | c.1414C= (p.Pro472=) c.-55+1848C= (n.-55+1848C=) | |
4 | g.125317825C>G | CA358117851 | FAT4 | c.1414C>G (p.Pro472Ala) c.-55+1848C>G (n.-55+1848C>G) | |
4 | g.125317825C>T | CA358117852 | FAT4 | c.1414C>T (p.Pro472Ser) c.-55+1848C>T (n.-55+1848C>T) | dbSNP gnomAD v2 gnomAD v4 |
4 | g.125317826C>A | CA358117853 | FAT4 | c.1415C>A (p.Pro472His) c.-55+1849C>A (n.-55+1849C>A) | gnomAD v4 |
4 | g.125317826C= | CA1491600841 | FAT4 | c.1415C= (p.Pro472=) c.-55+1849C= (n.-55+1849C=) | |
4 | g.125317826C>G | CA358117855 | FAT4 | c.1415C>G (p.Pro472Arg) c.-55+1849C>G (n.-55+1849C>G) | |
4 | g.125317826C>T | CA358117854 | FAT4 | c.1415C>T (p.Pro472Leu) c.-55+1849C>T (n.-55+1849C>T) | dbSNP gnomAD v2 gnomAD v4 COSMIC COSMIC |
4 | g.125317827T>A | CA441366637 | FAT4 | c.1416T>A (p.Pro472=) c.-55+1850T>A (n.-55+1850T>A) | |
4 | g.125317827T>C | CA441366639 | FAT4 | c.1416T>C (p.Pro472=) c.-55+1850T>C (n.-55+1850T>C) | |
4 | g.125317827T>G | CA441366642 | FAT4 | c.1416T>G (p.Pro472=) c.-55+1850T>G (n.-55+1850T>G) | |
4 | g.125317828C>A | CA358117856 | FAT4 | c.1417C>A (p.Pro473Thr) c.-55+1851C>A (n.-55+1851C>A) | |
4 | g.125317828C>G | CA358117857 | FAT4 | c.1417C>G (p.Pro473Ala) c.-55+1851C>G (n.-55+1851C>G) | |
4 | g.125317828C>T | CA358117858 | FAT4 | c.1417C>T (p.Pro473Ser) c.-55+1851C>T (n.-55+1851C>T) | gnomAD v4 |
4 | g.125317829C>A | CA358117859 | FAT4 | c.1418C>A (p.Pro473His) c.-55+1852C>A (n.-55+1852C>A) | |
4 | g.125317829C>G | CA358117860 | FAT4 | c.1418C>G (p.Pro473Arg) c.-55+1852C>G (n.-55+1852C>G) | |
4 | g.125317829C>T | CA358117861 | FAT4 | c.1418C>T (p.Pro473Leu) c.-55+1852C>T (n.-55+1852C>T) | |
4 | g.125317830T>A | CA441366645 | FAT4 | c.1419T>A (p.Pro473=) c.-55+1853T>A (n.-55+1853T>A) | |
4 | g.125317830T>C | CA3071986 | FAT4 | c.1419T>C (p.Pro473=) c.-55+1853T>C (n.-55+1853T>C) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.125317830T>G | CA441366646 | FAT4 | c.1419T>G (p.Pro473=) c.-55+1853T>G (n.-55+1853T>G) | |
4 | g.125317830T= | CA1491600846 | FAT4 | c.1419T= (p.Pro473=) c.-55+1853T= (n.-55+1853T=) | |
4 | g.125317831G>A | CA3071987 | FAT4 | c.1420G>A (p.Val474Ile) c.-55+1854G>A (n.-55+1854G>A) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.125317831G>C | CA358117862 | FAT4 | c.1420G>C (p.Val474Leu) c.-55+1854G>C (n.-55+1854G>C) | dbSNP gnomAD v4 |
4 | g.125317831G= | CA1491600854 | FAT4 | c.1420G= (p.Val474=) c.-55+1854G= (n.-55+1854G=) | |
4 | g.125317831G>T | CA358117863 | FAT4 | c.1420G>T (p.Val474Phe) c.-55+1854G>T (n.-55+1854G>T) | |
4 | g.125317832T>A | CA358117866 | FAT4 | c.1421T>A (p.Val474Asp) c.-55+1855T>A (n.-55+1855T>A) | |
4 | g.125317832T>C | CA358117865 | FAT4 | c.1421T>C (p.Val474Ala) c.-55+1855T>C (n.-55+1855T>C) | |
4 | g.125317832T>G | CA358117864 | FAT4 | c.1421T>G (p.Val474Gly) c.-55+1855T>G (n.-55+1855T>G) | ClinVar |
4 | g.125317833C>A | CA441366655 | FAT4 | c.1422C>A (p.Val474=) c.-55+1856C>A (n.-55+1856C>A) | |
4 | g.125317833C= | CA1491600858 | FAT4 | c.1422C= (p.Val474=) c.-55+1856C= (n.-55+1856C=) | |
4 | g.125317833C>G | CA441366654 | FAT4 | c.1422C>G (p.Val474=) c.-55+1856C>G (n.-55+1856C>G) | dbSNP gnomAD v2 gnomAD v4 |
4 | g.125317833C>T | CA441366653 | FAT4 | c.1422C>T (p.Val474=) c.-55+1856C>T (n.-55+1856C>T) | |
4 | g.125317834T>A | CA358117869 | FAT4 | c.1423T>A (p.Phe475Ile) c.-55+1857T>A (n.-55+1857T>A) | |
4 | g.125317834T>C | CA358117867 | FAT4 | c.1423T>C (p.Phe475Leu) c.-55+1857T>C (n.-55+1857T>C) | |
4 | g.125317834T>G | CA358117868 | FAT4 | c.1423T>G (p.Phe475Val) c.-55+1857T>G (n.-55+1857T>G) | |
4 | g.125317835T>A | CA358117870 | FAT4 | c.1424T>A (p.Phe475Tyr) c.-55+1858T>A (n.-55+1858T>A) | |
4 | g.125317835T>C | CA358117871 | FAT4 | c.1424T>C (p.Phe475Ser) c.-55+1858T>C (n.-55+1858T>C) | |
4 | g.125317835T>G | CA358117872 | FAT4 | c.1424T>G (p.Phe475Cys) c.-55+1858T>G (n.-55+1858T>G) | |
4 | g.125317836T>A | CA358117873 | FAT4 | c.1425T>A (p.Phe475Leu) c.-55+1859T>A (n.-55+1859T>A) | |
4 | g.125317836T>C | CA441366661 | FAT4 | c.1425T>C (p.Phe475=) c.-55+1859T>C (n.-55+1859T>C) | |
4 | g.125317836T>G | CA358117874 | FAT4 | c.1425T>G (p.Phe475Leu) c.-55+1859T>G (n.-55+1859T>G) | |
4 | g.125317837T>A | CA358117875 | FAT4 | c.1426T>A (p.Ser476Thr) c.-55+1860T>A (n.-55+1860T>A) | |
4 | g.125317837T>C | CA358117876 | FAT4 | c.1426T>C (p.Ser476Pro) c.-55+1860T>C (n.-55+1860T>C) | |
4 | g.125317837T>G | CA358117877 | FAT4 | c.1426T>G (p.Ser476Ala) c.-55+1860T>G (n.-55+1860T>G) | |
4 | g.125317838C>A | CA358117878 | FAT4 | c.1427C>A (p.Ser476Ter) c.-55+1861C>A (n.-55+1861C>A) | |
4 | g.125317838C>G | CA358117879 | FAT4 | c.1427C>G (p.Ser476Ter) c.-55+1861C>G (n.-55+1861C>G) | COSMIC COSMIC |
4 | g.125317838C>T | CA358117880 | FAT4 | c.1427C>T (p.Ser476Leu) c.-55+1861C>T (n.-55+1861C>T) | |
4 | g.125317839A>C | CA441366666 | FAT4 | c.1428A>C (p.Ser476=) c.-55+1862A>C (n.-55+1862A>C) | |
4 | g.125317839A>G | CA441366672 | FAT4 | c.1428A>G (p.Ser476=) c.-55+1862A>G (n.-55+1862A>G) | |
4 | g.125317839A>T | CA441366669 | FAT4 | c.1428A>T (p.Ser476=) c.-55+1862A>T (n.-55+1862A>T) | |
4 | g.125317840C>A | CA358117883 | FAT4 | c.1429C>A (p.Gln477Lys) c.-55+1863C>A (n.-55+1863C>A) | |
4 | g.125317840C>G | CA358117881 | FAT4 | c.1429C>G (p.Gln477Glu) c.-55+1863C>G (n.-55+1863C>G) | |
4 | g.125317840C>T | CA358117882 | FAT4 | c.1429C>T (p.Gln477Ter) c.-55+1863C>T (n.-55+1863C>T) | |
4 | g.125317841A>C | CA358117884 | FAT4 | c.1430A>C (p.Gln477Pro) c.-55+1864A>C (n.-55+1864A>C) | |
4 | g.125317841A>G | CA358117885 | FAT4 | c.1430A>G (p.Gln477Arg) c.-55+1864A>G (n.-55+1864A>G) | |
4 | g.125317841A>T | CA358117886 | FAT4 | c.1430A>T (p.Gln477Leu) c.-55+1864A>T (n.-55+1864A>T) | |
4 | g.125317842G>A | CA441366677 | FAT4 | c.1431G>A (p.Gln477=) c.-55+1865G>A (n.-55+1865G>A) | |
4 | g.125317842G>C | CA358117887 | FAT4 | c.1431G>C (p.Gln477His) c.-55+1865G>C (n.-55+1865G>C) | |
4 | g.125317842G>T | CA358117888 | FAT4 | c.1431G>T (p.Gln477His) c.-55+1865G>T (n.-55+1865G>T) | |
4 | g.125317843C>A | CA358117889 | FAT4 | c.1432C>A (p.Gln478Lys) c.-55+1866C>A (n.-55+1866C>A) | COSMIC COSMIC |
4 | g.125317843C= | CA1491600863 | FAT4 | c.1432C= (p.Gln478=) c.-55+1866C= (n.-55+1866C=) | |
4 | g.125317843C>G | CA3071988 | FAT4 | c.1432C>G (p.Gln478Glu) c.-55+1866C>G (n.-55+1866C>G) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.125317843C>T | CA358117890 | FAT4 | c.1432C>T (p.Gln478Ter) c.-55+1866C>T (n.-55+1866C>T) | |
4 | g.125317844A>C | CA358117891 | FAT4 | c.1433A>C (p.Gln478Pro) c.-55+1867A>C (n.-55+1867A>C) | |
4 | g.125317844A>G | CA358117892 | FAT4 | c.1433A>G (p.Gln478Arg) c.-55+1867A>G (n.-55+1867A>G) | |
4 | g.125317844A>T | CA358117893 | FAT4 | c.1433A>T (p.Gln478Leu) c.-55+1867A>T (n.-55+1867A>T) | |
4 | g.125317845A>C | CA358117894 | FAT4 | c.1434A>C (p.Gln478His) c.-55+1868A>C (n.-55+1868A>C) | |
4 | g.125317845A>G | CA441366683 | FAT4 | c.1434A>G (p.Gln478=) c.-55+1868A>G (n.-55+1868A>G) | gnomAD v4 |
4 | g.125317845A>T | CA358117895 | FAT4 | c.1434A>T (p.Gln478His) c.-55+1868A>T (n.-55+1868A>T) | |
4 | g.125317846G>A | CA358117897 | FAT4 | c.1435G>A (p.Val479Met) c.-55+1869G>A (n.-55+1869G>A) | ClinVar |
4 | g.125317846G>C | CA358117898 | FAT4 | c.1435G>C (p.Val479Leu) c.-55+1869G>C (n.-55+1869G>C) | |
4 | g.125317846G>T | CA358117896 | FAT4 | c.1435G>T (p.Val479Leu) c.-55+1869G>T (n.-55+1869G>T) | gnomAD v4 |
4 | g.125317847T>A | CA358117899 | FAT4 | c.1436T>A (p.Val479Glu) c.-55+1870T>A (n.-55+1870T>A) | |
4 | g.125317847T>C | CA358117900 | FAT4 | c.1436T>C (p.Val479Ala) c.-55+1870T>C (n.-55+1870T>C) | |
4 | g.125317847T>G | CA358117901 | FAT4 | c.1436T>G (p.Val479Gly) c.-55+1870T>G (n.-55+1870T>G) | |
4 | g.125317848G>A | CA441366689 | FAT4 | c.1437G>A (p.Val479=) c.-55+1871G>A (n.-55+1871G>A) | gnomAD v4 |
4 | g.125317848G>C | CA441366690 | FAT4 | c.1437G>C (p.Val479=) c.-55+1871G>C (n.-55+1871G>C) | |
4 | g.125317848G>T | CA441366691 | FAT4 | c.1437G>T (p.Val479=) c.-55+1871G>T (n.-55+1871G>T) | |
4 | g.125317849T>A | CA358117902 | FAT4 | c.1438T>A (p.Tyr480Asn) c.-55+1872T>A (n.-55+1872T>A) | |
4 | g.125317849T>C | CA358117903 | FAT4 | c.1438T>C (p.Tyr480His) c.-55+1872T>C (n.-55+1872T>C) | |
4 | g.125317849T>G | CA358117904 | FAT4 | c.1438T>G (p.Tyr480Asp) c.-55+1872T>G (n.-55+1872T>G) | |
4 | g.125317850A>C | CA358117905 | FAT4 | c.1439A>C (p.Tyr480Ser) c.-55+1873A>C (n.-55+1873A>C) | |
4 | g.125317850A>G | CA358117906 | FAT4 | c.1439A>G (p.Tyr480Cys) c.-55+1873A>G (n.-55+1873A>G) | |
4 | g.125317850A>T | CA358117907 | FAT4 | c.1439A>T (p.Tyr480Phe) c.-55+1873A>T (n.-55+1873A>T) | |
4 | g.125317851C>A | CA358117908 | FAT4 | c.1440C>A (p.Tyr480Ter) c.-55+1874C>A (n.-55+1874C>A) | |
4 | g.125317851C>G | CA358117909 | FAT4 | c.1440C>G (p.Tyr480Ter) c.-55+1874C>G (n.-55+1874C>G) | |
4 | g.125317851C>T | CA441366701 | FAT4 | c.1440C>T (p.Tyr480=) c.-55+1874C>T (n.-55+1874C>T) | |
4 | g.125317852A= | CA1491600867 | FAT4 | c.1441A= (p.Arg481=) c.-55+1875A= (n.-55+1875A=) | |
4 | g.125317852A>C | CA441366702 | FAT4 | c.1441A>C (p.Arg481=) c.-55+1875A>C (n.-55+1875A>C) | |
4 | g.125317852A>G | CA358117910 | FAT4 | c.1441A>G (p.Arg481Gly) c.-55+1875A>G (n.-55+1875A>G) | dbSNP gnomAD v4 |
4 | g.125317852A>T | CA358117911 | FAT4 | c.1441A>T (p.Arg481Ter) c.-55+1875A>T (n.-55+1875A>T) | gnomAD v4 |
4 | g.125317853G>A | CA358117914 | FAT4 | c.1442G>A (p.Arg481Lys) c.-55+1876G>A (n.-55+1876G>A) | |
4 | g.125317853G>C | CA358117913 | FAT4 | c.1442G>C (p.Arg481Thr) c.-55+1876G>C (n.-55+1876G>C) | |
4 | g.125317853G>T | CA358117912 | FAT4 | c.1442G>T (p.Arg481Ile) c.-55+1876G>T (n.-55+1876G>T) | |
4 | g.125317854A= | CA1491600874 | FAT4 | c.1443A= (p.Arg481=) c.-55+1877A= (n.-55+1877A=) | |
4 | g.125317854A>C | CA358117915 | FAT4 | c.1443A>C (p.Arg481Ser) c.-55+1877A>C (n.-55+1877A>C) | |
4 | g.125317854A>G | CA104864067 | FAT4 | c.1443A>G (p.Arg481=) c.-55+1877A>G (n.-55+1877A>G) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.125317854A>T | CA358117916 | FAT4 | c.1443A>T (p.Arg481Ser) c.-55+1877A>T (n.-55+1877A>T) | |
4 | g.125317855G>A | CA358117917 | FAT4 | c.1444G>A (p.Val482Met) c.-55+1878G>A (n.-55+1878G>A) | dbSNP gnomAD v4 |
4 | g.125317855G>C | CA358117918 | FAT4 | c.1444G>C (p.Val482Leu) c.-55+1878G>C (n.-55+1878G>C) | |
4 | g.125317855G= | CA1491600882 | FAT4 | c.1444G= (p.Val482=) c.-55+1878G= (n.-55+1878G=) | |
4 | g.125317855G>T | CA358117919 | FAT4 | c.1444G>T (p.Val482Leu) c.-55+1878G>T (n.-55+1878G>T) | |
4 | g.125317856T>A | CA358117920 | FAT4 | c.1445T>A (p.Val482Glu) c.-55+1879T>A (n.-55+1879T>A) | |
4 | g.125317856T>C | CA358117921 | FAT4 | c.1445T>C (p.Val482Ala) c.-55+1879T>C (n.-55+1879T>C) | dbSNP gnomAD v2 gnomAD v4 |
4 | g.125317856T>G | CA358117922 | FAT4 | c.1445T>G (p.Val482Gly) c.-55+1879T>G (n.-55+1879T>G) | |
4 | g.125317856T= | CA1491600885 | FAT4 | c.1445T= (p.Val482=) c.-55+1879T= (n.-55+1879T=) | |
4 | g.125317857G>A | CA441366711 | FAT4 | c.1446G>A (p.Val482=) c.-55+1880G>A (n.-55+1880G>A) | |
4 | g.125317857G>C | CA441366713 | FAT4 | c.1446G>C (p.Val482=) c.-55+1880G>C (n.-55+1880G>C) | |
4 | g.125317857G>T | CA441366714 | FAT4 | c.1446G>T (p.Val482=) c.-55+1880G>T (n.-55+1880G>T) | |
4 | g.125317858A>C | CA358117923 | FAT4 | c.1447A>C (p.Asn483His) c.-55+1881A>C (n.-55+1881A>C) | |
4 | g.125317858A>G | CA358117924 | FAT4 | c.1447A>G (p.Asn483Asp) c.-55+1881A>G (n.-55+1881A>G) | |
4 | g.125317858A>T | CA358117925 | FAT4 | c.1447A>T (p.Asn483Tyr) c.-55+1881A>T (n.-55+1881A>T) | |
4 | g.125317859A>C | CA358117926 | FAT4 | c.1448A>C (p.Asn483Thr) c.-55+1882A>C (n.-55+1882A>C) | |
4 | g.125317859A>G | CA358117927 | FAT4 | c.1448A>G (p.Asn483Ser) c.-55+1882A>G (n.-55+1882A>G) | ClinVar dbSNP gnomAD v4 |
4 | g.125317859A>T | CA358117928 | FAT4 | c.1448A>T (p.Asn483Ile) c.-55+1882A>T (n.-55+1882A>T) | |
4 | g.125317860C>A | CA358117929 | FAT4 | c.1449C>A (p.Asn483Lys) c.-55+1883C>A (n.-55+1883C>A) | |
4 | g.125317860C= | CA1491600886 | FAT4 | c.1449C= (p.Asn483=) c.-55+1883C= (n.-55+1883C=) | |
4 | g.125317860C>G | CA358117930 | FAT4 | c.1449C>G (p.Asn483Lys) c.-55+1883C>G (n.-55+1883C>G) | |
4 | g.125317860C>T | CA3071989 | FAT4 | c.1449C>T (p.Asn483=) c.-55+1883C>T (n.-55+1883C>T) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.125317861C>A | CA3071990 | FAT4 | c.1450C>A (p.Leu484Met) c.-55+1884C>A (n.-55+1884C>A) | dbSNP ExAC gnomAD v2 gnomAD v4 |
4 | g.125317861C= | CA1491600888 | FAT4 | c.1450C= (p.Leu484=) c.-55+1884C= (n.-55+1884C=) | |
4 | g.125317861C>G | CA358117931 | FAT4 | c.1450C>G (p.Leu484Val) c.-55+1884C>G (n.-55+1884C>G) | |
4 | g.125317861C>T | CA441366725 | FAT4 | c.1450C>T (p.Leu484=) c.-55+1884C>T (n.-55+1884C>T) | |
4 | g.125317862T>A | CA358117932 | FAT4 | c.1451T>A (p.Leu484Gln) c.-55+1885T>A (n.-55+1885T>A) | ClinVar gnomAD v4 |
4 | g.125317862T>C | CA3071991 | FAT4 | c.1451T>C (p.Leu484Pro) c.-55+1885T>C (n.-55+1885T>C) | dbSNP ExAC gnomAD v2 |
4 | g.125317862T>G | CA358117933 | FAT4 | c.1451T>G (p.Leu484Arg) c.-55+1885T>G (n.-55+1885T>G) | dbSNP gnomAD v2 gnomAD v4 |
4 | g.125317862T= | CA1491600890 | FAT4 | c.1451T= (p.Leu484=) c.-55+1885T= (n.-55+1885T=) | |
4 | g.125317863G>A | CA441366727 | FAT4 | c.1452G>A (p.Leu484=) c.-55+1886G>A (n.-55+1886G>A) | ClinVar |
4 | g.125317863G>C | CA441366728 | FAT4 | c.1452G>C (p.Leu484=) c.-55+1886G>C (n.-55+1886G>C) | |
4 | g.125317863G>T | CA441366729 | FAT4 | c.1452G>T (p.Leu484=) c.-55+1886G>T (n.-55+1886G>T) | |
4 | g.125317864A= | CA1491600896 | FAT4 | c.1453A= (p.Ser485=) c.-55+1887A= (n.-55+1887A=) | |
4 | g.125317864A>C | CA358117934 | FAT4 | c.1453A>C (p.Ser485Arg) c.-55+1887A>C (n.-55+1887A>C) | |
4 | g.125317864A>G | CA3071992 | FAT4 | c.1453A>G (p.Ser485Gly) c.-55+1887A>G (n.-55+1887A>G) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.125317864A>T | CA358117935 | FAT4 | c.1453A>T (p.Ser485Cys) c.-55+1887A>T (n.-55+1887A>T) | |
4 | g.125317865G>A | CA358117936 | FAT4 | c.1454G>A (p.Ser485Asn) c.-55+1888G>A (n.-55+1888G>A) | |
4 | g.125317865G>C | CA358117937 | FAT4 | c.1454G>C (p.Ser485Thr) c.-55+1888G>C (n.-55+1888G>C) | gnomAD v4 |
4 | g.125317865G>T | CA358117938 | FAT4 | c.1454G>T (p.Ser485Ile) c.-55+1888G>T (n.-55+1888G>T) | |
4 | g.125317866C>A | CA358117939 | FAT4 | c.1455C>A (p.Ser485Arg) c.-55+1889C>A (n.-55+1889C>A) | |
4 | g.125317866C>G | CA358117940 | FAT4 | c.1455C>G (p.Ser485Arg) c.-55+1889C>G (n.-55+1889C>G) | |
4 | g.125317866C>T | CA441366738 | FAT4 | c.1455C>T (p.Ser485=) c.-55+1889C>T (n.-55+1889C>T) | COSMIC COSMIC |
4 | g.125317867G>A | CA3071993 | FAT4 | c.1456G>A (p.Glu486Lys) c.-55+1890G>A (n.-55+1890G>A) | dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC COSMIC |
4 | g.125317867G>C | CA358117942 | FAT4 | c.1456G>C (p.Glu486Gln) c.-55+1890G>C (n.-55+1890G>C) | |
4 | g.125317867G= | CA1491600907 | FAT4 | c.1456G= (p.Glu486=) c.-55+1890G= (n.-55+1890G=) | |
4 | g.125317867G>T | CA358117941 | FAT4 | c.1456G>T (p.Glu486Ter) c.-55+1890G>T (n.-55+1890G>T) | |
4 | g.125317868A>C | CA358117943 | FAT4 | c.1457A>C (p.Glu486Ala) c.-55+1891A>C (n.-55+1891A>C) | |
4 | g.125317868A>G | CA358117944 | FAT4 | c.1457A>G (p.Glu486Gly) c.-55+1891A>G (n.-55+1891A>G) | |
4 | g.125317868A>T | CA358117945 | FAT4 | c.1457A>T (p.Glu486Val) c.-55+1891A>T (n.-55+1891A>T) | |
4 | g.125317869G>A | CA441366743 | FAT4 | c.1458G>A (p.Glu486=) c.-55+1892G>A (n.-55+1892G>A) | |
4 | g.125317869G>C | CA358117946 | FAT4 | c.1458G>C (p.Glu486Asp) c.-55+1892G>C (n.-55+1892G>C) | |
4 | g.125317869G>T | CA358117947 | FAT4 | c.1458G>T (p.Glu486Asp) c.-55+1892G>T (n.-55+1892G>T) | |
4 | g.125317870G>A | CA358117948 | FAT4 | c.1459G>A (p.Glu487Lys) c.-55+1893G>A (n.-55+1893G>A) | ClinVar |
4 | g.125317870G>C | CA358117949 | FAT4 | c.1459G>C (p.Glu487Gln) c.-55+1893G>C (n.-55+1893G>C) | |
4 | g.125317870G>T | CA358117950 | FAT4 | c.1459G>T (p.Glu487Ter) c.-55+1893G>T (n.-55+1893G>T) | |
4 | g.125317871A>C | CA358117951 | FAT4 | c.1460A>C (p.Glu487Ala) c.-55+1894A>C (n.-55+1894A>C) | |
4 | g.125317871A>G | CA358117952 | FAT4 | c.1460A>G (p.Glu487Gly) c.-55+1894A>G (n.-55+1894A>G) | |
4 | g.125317871A>T | CA358117953 | FAT4 | c.1460A>T (p.Glu487Val) c.-55+1894A>T (n.-55+1894A>T) | |
4 | g.125317872G>A | CA441366748 | FAT4 | c.1461G>A (p.Glu487=) c.-55+1895G>A (n.-55+1895G>A) | |
4 | g.125317872G>C | CA358117954 | FAT4 | c.1461G>C (p.Glu487Asp) c.-55+1895G>C (n.-55+1895G>C) | |
4 | g.125317872G>T | CA358117955 | FAT4 | c.1461G>T (p.Glu487Asp) c.-55+1895G>T (n.-55+1895G>T) | |
4 | g.125317873G>A | CA3071994 | FAT4 | c.1462G>A (p.Ala488Thr) c.-55+1896G>A (n.-55+1896G>A) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.125317873G>C | CA358117956 | FAT4 | c.1462G>C (p.Ala488Pro) c.-55+1896G>C (n.-55+1896G>C) | |
4 | g.125317873G= | CA1491600911 | FAT4 | c.1462G= (p.Ala488=) c.-55+1896G= (n.-55+1896G=) | |
4 | g.125317873G>T | CA358117957 | FAT4 | c.1462G>T (p.Ala488Ser) c.-55+1896G>T (n.-55+1896G>T) | gnomAD v4 |
4 | g.125317874C>A | CA358117958 | FAT4 | c.1463C>A (p.Ala488Glu) c.-55+1897C>A (n.-55+1897C>A) | |
4 | g.125317874C>G | CA358117959 | FAT4 | c.1463C>G (p.Ala488Gly) c.-55+1897C>G (n.-55+1897C>G) | |
4 | g.125317874C>T | CA358117960 | FAT4 | c.1463C>T (p.Ala488Val) c.-55+1897C>T (n.-55+1897C>T) | gnomAD v4 |
4 | g.125317875G>A | CA3071995 | FAT4 | c.1464G>A (p.Ala488=) c.-55+1898G>A (n.-55+1898G>A) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
4 | g.125317875G>C | CA441366755 | FAT4 | c.1464G>C (p.Ala488=) c.-55+1898G>C (n.-55+1898G>C) | dbSNP gnomAD v2 gnomAD v4 |
4 | g.125317875G= | CA1491600917 | FAT4 | c.1464G= (p.Ala488=) c.-55+1898G= (n.-55+1898G=) | |
4 | g.125317875G>T | CA441366754 | FAT4 | c.1464G>T (p.Ala488=) c.-55+1898G>T (n.-55+1898G>T) | |
4 | g.125317876C>A | CA358117961 | FAT4 | c.1465C>A (p.Pro489Thr) c.-55+1899C>A (n.-55+1899C>A) | |
4 | g.125317876C= | CA1491600924 | FAT4 | c.1465C= (p.Pro489=) c.-55+1899C= (n.-55+1899C=) | |
4 | g.125317876C>G | CA358117962 | FAT4 | c.1465C>G (p.Pro489Ala) c.-55+1899C>G (n.-55+1899C>G) | dbSNP gnomAD v4 |
4 | g.125317876C>T | CA358117963 | FAT4 | c.1465C>T (p.Pro489Ser) c.-55+1899C>T (n.-55+1899C>T) | |
4 | g.125317877C>A | CA358117964 | FAT4 | c.1466C>A (p.Pro489His) c.-55+1900C>A (n.-55+1900C>A) | |
4 | g.125317877C>G | CA358117965 | FAT4 | c.1466C>G (p.Pro489Arg) c.-55+1900C>G (n.-55+1900C>G) | |
4 | g.125317877C>T | CA358117966 | FAT4 | c.1466C>T (p.Pro489Leu) c.-55+1900C>T (n.-55+1900C>T) | |
4 | g.125317878T>A | CA3071996 | FAT4 | c.1467T>A (p.Pro489=) c.-55+1901T>A (n.-55+1901T>A) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
4 | g.125317878T>C | CA441366758 | FAT4 | c.1467T>C (p.Pro489=) c.-55+1901T>C (n.-55+1901T>C) | |
4 | g.125317878T>G | CA441366759 | FAT4 | c.1467T>G (p.Pro489=) c.-55+1901T>G (n.-55+1901T>G) | |
4 | g.125317878T= | CA1491600929 | FAT4 | c.1467T= (p.Pro489=) c.-55+1901T= (n.-55+1901T=) | |
4 | g.125317879C>A | CA358117969 | FAT4 | c.1468C>A (p.Pro490Thr) c.-55+1902C>A (n.-55+1902C>A) | dbSNP gnomAD v4 |
4 | g.125317879C= | CA1491600931 | FAT4 | c.1468C= (p.Pro490=) c.-55+1902C= (n.-55+1902C=) | |
4 | g.125317879C>G | CA358117968 | FAT4 | c.1468C>G (p.Pro490Ala) c.-55+1902C>G (n.-55+1902C>G) | |
4 | g.125317879C>T | CA358117967 | FAT4 | c.1468C>T (p.Pro490Ser) c.-55+1902C>T (n.-55+1902C>T) | |
4 | g.125317880C>A | CA358117970 | FAT4 | c.1469C>A (p.Pro490Gln) c.-55+1903C>A (n.-55+1903C>A) | |
4 | g.125317880C>G | CA358117971 | FAT4 | c.1469C>G (p.Pro490Arg) c.-55+1903C>G (n.-55+1903C>G) | |
4 | g.125317880C>T | CA358117972 | FAT4 | c.1469C>T (p.Pro490Leu) c.-55+1903C>T (n.-55+1903C>T) | gnomAD v4 |
4 | g.125317881G>A | CA3071997 | FAT4 | c.1470G>A (p.Pro490=) c.-55+1904G>A (n.-55+1904G>A) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.125317881G>C | CA441366768 | FAT4 | c.1470G>C (p.Pro490=) c.-55+1904G>C (n.-55+1904G>C) | |
4 | g.125317881G= | CA1491600933 | FAT4 | c.1470G= (p.Pro490=) c.-55+1904G= (n.-55+1904G=) | |
4 | g.125317881G>T | CA441366765 | FAT4 | c.1470G>T (p.Pro490=) c.-55+1904G>T (n.-55+1904G>T) | |
4 | g.125317882G>A | CA358117973 | FAT4 | c.1471G>A (p.Gly491Arg) c.-55+1905G>A (n.-55+1905G>A) | dbSNP gnomAD v2 gnomAD v4 |
4 | g.125317882G>C | CA358117974 | FAT4 | c.1471G>C (p.Gly491Arg) c.-55+1905G>C (n.-55+1905G>C) | |
4 | g.125317882G= | CA1491600939 | FAT4 | c.1471G= (p.Gly491=) c.-55+1905G= (n.-55+1905G=) | |
4 | g.125317882G>T | CA358117975 | FAT4 | c.1471G>T (p.Gly491Ter) c.-55+1905G>T (n.-55+1905G>T) | |
4 | g.125317883G>A | CA358117976 | FAT4 | c.1472G>A (p.Gly491Glu) c.-55+1906G>A (n.-55+1906G>A) | |
4 | g.125317883G>C | CA358117977 | FAT4 | c.1472G>C (p.Gly491Ala) c.-55+1906G>C (n.-55+1906G>C) | |
4 | g.125317883G>T | CA358117978 | FAT4 | c.1472G>T (p.Gly491Val) c.-55+1906G>T (n.-55+1906G>T) | |
4 | g.125317884A= | CA1491600940 | FAT4 | c.1473A= (p.Gly491=) c.-55+1907A= (n.-55+1907A=) | |
4 | g.125317884A>C | CA441366774 | FAT4 | c.1473A>C (p.Gly491=) c.-55+1907A>C (n.-55+1907A>C) | |
4 | g.125317884A>G | CA441366775 | FAT4 | c.1473A>G (p.Gly491=) c.-55+1907A>G (n.-55+1907A>G) | |
4 | g.125317884A>T | CA104864101 | FAT4 | c.1473A>T (p.Gly491=) c.-55+1907A>T (n.-55+1907A>T) | dbSNP |
4 | g.125317885A>C | CA358117979 | FAT4 | c.1474A>C (p.Ser492Arg) c.-55+1908A>C (n.-55+1908A>C) | |
4 | g.125317885A>G | CA358117980 | FAT4 | c.1474A>G (p.Ser492Gly) c.-55+1908A>G (n.-55+1908A>G) | gnomAD v4 |
4 | g.125317885A>T | CA358117981 | FAT4 | c.1474A>T (p.Ser492Cys) c.-55+1908A>T (n.-55+1908A>T) | |
4 | g.125317886G>A | CA358117983 | FAT4 | c.1475G>A (p.Ser492Asn) c.-55+1909G>A (n.-55+1909G>A) | |
4 | g.125317886G>C | CA358117984 | FAT4 | c.1475G>C (p.Ser492Thr) c.-55+1909G>C (n.-55+1909G>C) | |
4 | g.125317886G>T | CA358117982 | FAT4 | c.1475G>T (p.Ser492Ile) c.-55+1909G>T (n.-55+1909G>T) | |
4 | g.125317887C>A | CA358117985 | FAT4 | c.1476C>A (p.Ser492Arg) c.-55+1910C>A (n.-55+1910C>A) | |
4 | g.125317887C>G | CA358117986 | FAT4 | c.1476C>G (p.Ser492Arg) c.-55+1910C>G (n.-55+1910C>G) | |
4 | g.125317887C>T | CA441366786 | FAT4 | c.1476C>T (p.Ser492=) c.-55+1910C>T (n.-55+1910C>T) | |
4 | g.125317888T>A | CA358117987 | FAT4 | c.1477T>A (p.Tyr493Asn) c.-55+1911T>A (n.-55+1911T>A) | |
4 | g.125317888T>C | CA3071998 | FAT4 | c.1477T>C (p.Tyr493His) c.-55+1911T>C (n.-55+1911T>C) | dbSNP ExAC gnomAD v2 gnomAD v4 |
4 | g.125317888T>G | CA358117988 | FAT4 | c.1477T>G (p.Tyr493Asp) c.-55+1911T>G (n.-55+1911T>G) | |
4 | g.125317888T= | CA1491600945 | FAT4 | c.1477T= (p.Tyr493=) c.-55+1911T= (n.-55+1911T=) | |
4 | g.125317889A>C | CA358117989 | FAT4 | c.1478A>C (p.Tyr493Ser) c.-55+1912A>C (n.-55+1912A>C) | |
4 | g.125317889A>G | CA358117990 | FAT4 | c.1478A>G (p.Tyr493Cys) c.-55+1912A>G (n.-55+1912A>G) | |
4 | g.125317889A>T | CA358117991 | FAT4 | c.1478A>T (p.Tyr493Phe) c.-55+1912A>T (n.-55+1912A>T) | |
4 | g.125317890T>A | CA358117992 | FAT4 | c.1479T>A (p.Tyr493Ter) c.-55+1913T>A (n.-55+1913T>A) | |
4 | g.125317890T>C | CA441366793 | FAT4 | c.1479T>C (p.Tyr493=) c.-55+1913T>C (n.-55+1913T>C) | ClinVar |
4 | g.125317890T>G | CA358117993 | FAT4 | c.1479T>G (p.Tyr493Ter) c.-55+1913T>G (n.-55+1913T>G) | |
4 | g.125317891G>A | CA358117994 | FAT4 | c.1480G>A (p.Val494Met) c.-55+1914G>A (n.-55+1914G>A) | |
4 | g.125317891G>C | CA358117995 | FAT4 | c.1480G>C (p.Val494Leu) c.-55+1914G>C (n.-55+1914G>C) | |
4 | g.125317891G= | CA1491600950 | FAT4 | c.1480G= (p.Val494=) c.-55+1914G= (n.-55+1914G=) | |
4 | g.125317891G>T | CA358117996 | FAT4 | c.1480G>T (p.Val494Leu) c.-55+1914G>T (n.-55+1914G>T) | dbSNP gnomAD v3 gnomAD v4 |
4 | g.125317892T>A | CA358117998 | FAT4 | c.1481T>A (p.Val494Glu) c.-55+1915T>A (n.-55+1915T>A) | |
4 | g.125317892T>C | CA3071999 | FAT4 | c.1481T>C (p.Val494Ala) c.-55+1915T>C (n.-55+1915T>C) | dbSNP ExAC gnomAD v2 gnomAD v4 |
4 | g.125317892T>G | CA358117997 | FAT4 | c.1481T>G (p.Val494Gly) c.-55+1915T>G (n.-55+1915T>G) | dbSNP gnomAD v3 gnomAD v4 |
4 | g.125317892T= | CA1491600955 | FAT4 | c.1481T= (p.Val494=) c.-55+1915T= (n.-55+1915T=) | |
4 | g.125317893G>A | CA441366801 | FAT4 | c.1482G>A (p.Val494=) c.-55+1916G>A (n.-55+1916G>A) | |
4 | g.125317893G>C | CA441366803 | FAT4 | c.1482G>C (p.Val494=) c.-55+1916G>C (n.-55+1916G>C) | |
4 | g.125317893G= | CA1491600978 | FAT4 | c.1482G= (p.Val494=) c.-55+1916G= (n.-55+1916G=) | |
4 | g.125317893G>T | CA441366802 | FAT4 | c.1482G>T (p.Val494=) c.-55+1916G>T (n.-55+1916G>T) | ClinVar dbSNP gnomAD v4 |
4 | g.125317894A>C | CA358117999 | FAT4 | c.1483A>C (p.Ser495Arg) c.-55+1917A>C (n.-55+1917A>C) | |
4 | g.125317894A>G | CA358118000 | FAT4 | c.1483A>G (p.Ser495Gly) c.-55+1917A>G (n.-55+1917A>G) | |
4 | g.125317894A>T | CA358118001 | FAT4 | c.1483A>T (p.Ser495Cys) c.-55+1917A>T (n.-55+1917A>T) | |
4 | g.125317895G>A | CA358118002 | FAT4 | c.1484G>A (p.Ser495Asn) c.-55+1918G>A (n.-55+1918G>A) | dbSNP gnomAD v3 gnomAD v4 |
4 | g.125317895G>C | CA358118003 | FAT4 | c.1484G>C (p.Ser495Thr) c.-55+1918G>C (n.-55+1918G>C) | |
4 | g.125317895G= | CA1491600982 | FAT4 | c.1484G= (p.Ser495=) c.-55+1918G= (n.-55+1918G=) | |
4 | g.125317895G>T | CA358118004 | FAT4 | c.1484G>T (p.Ser495Ile) c.-55+1918G>T (n.-55+1918G>T) | |
4 | g.125317896T>A | CA358118005 | FAT4 | c.1485T>A (p.Ser495Arg) c.-55+1919T>A (n.-55+1919T>A) | |
4 | g.125317896T>C | CA3072000 | FAT4 | c.1485T>C (p.Ser495=) c.-55+1919T>C (n.-55+1919T>C) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.125317896T>G | CA358118006 | FAT4 | c.1485T>G (p.Ser495Arg) c.-55+1919T>G (n.-55+1919T>G) | |
4 | g.125317896T= | CA1491600988 | FAT4 | c.1485T= (p.Ser495=) c.-55+1919T= (n.-55+1919T=) | |
4 | g.125317897G>A | CA358118007 | FAT4 | c.1486G>A (p.Gly496Arg) c.-55+1920G>A (n.-55+1920G>A) | gnomAD v4 |
4 | g.125317897G>C | CA358118008 | FAT4 | c.1486G>C (p.Gly496Arg) c.-55+1920G>C (n.-55+1920G>C) | |
4 | g.125317897G>T | CA358118009 | FAT4 | c.1486G>T (p.Gly496Trp) c.-55+1920G>T (n.-55+1920G>T) | |
4 | g.125317898G>A | CA358118012 | FAT4 | c.1487G>A (p.Gly496Glu) c.-55+1921G>A (n.-55+1921G>A) | |
4 | g.125317898G>C | CA358118010 | FAT4 | c.1487G>C (p.Gly496Ala) c.-55+1921G>C (n.-55+1921G>C) | gnomAD v4 |
4 | g.125317898G>T | CA358118011 | FAT4 | c.1487G>T (p.Gly496Val) c.-55+1921G>T (n.-55+1921G>T) | gnomAD v4 |
4 | g.125317899G>A | CA441366820 | FAT4 | c.1488G>A (p.Gly496=) c.-55+1922G>A (n.-55+1922G>A) | dbSNP |
4 | g.125317899G>C | CA441366821 | FAT4 | c.1488G>C (p.Gly496=) c.-55+1922G>C (n.-55+1922G>C) | dbSNP |
4 | g.125317899G= | CA1491600996 | FAT4 | c.1488G= (p.Gly496=) c.-55+1922G= (n.-55+1922G=) | |
4 | g.125317899G>T | CA441366822 | FAT4 | c.1488G>T (p.Gly496=) c.-55+1922G>T (n.-55+1922G>T) | |
4 | g.125317900A= | CA1491601002 | FAT4 | c.1489A= (p.Ile497=) c.-55+1923A= (n.-55+1923A=) | |
4 | g.125317900A>C | CA3072001 | FAT4 | c.1489A>C (p.Ile497Leu) c.-55+1923A>C (n.-55+1923A>C) | dbSNP ExAC gnomAD v2 |
4 | g.125317900A>G | CA358118013 | FAT4 | c.1489A>G (p.Ile497Val) c.-55+1923A>G (n.-55+1923A>G) | ClinVar gnomAD v4 |
4 | g.125317900A>T | CA358118014 | FAT4 | c.1489A>T (p.Ile497Leu) c.-55+1923A>T (n.-55+1923A>T) | |
4 | g.125317901T>A | CA358118015 | FAT4 | c.1490T>A (p.Ile497Lys) c.-55+1924T>A (n.-55+1924T>A) | |
4 | g.125317901T>C | CA358118016 | FAT4 | c.1490T>C (p.Ile497Thr) c.-55+1924T>C (n.-55+1924T>C) | |
4 | g.125317901T>G | CA358118017 | FAT4 | c.1490T>G (p.Ile497Arg) c.-55+1924T>G (n.-55+1924T>G) | |
4 | g.125317902A>C | CA441366828 | FAT4 | c.1491A>C (p.Ile497=) c.-55+1925A>C (n.-55+1925A>C) | |
4 | g.125317902A>G | CA358118018 | FAT4 | c.1491A>G (p.Ile497Met) c.-55+1925A>G (n.-55+1925A>G) | gnomAD v4 |
4 | g.125317902A>T | CA441366835 | FAT4 | c.1491A>T (p.Ile497=) c.-55+1925A>T (n.-55+1925A>T) | |
4 | g.125317903T>A | CA358118019 | FAT4 | c.1492T>A (p.Ser498Thr) c.-55+1926T>A (n.-55+1926T>A) | |
4 | g.125317903T>C | CA358118020 | FAT4 | c.1492T>C (p.Ser498Pro) c.-55+1926T>C (n.-55+1926T>C) | |
4 | g.125317903T>G | CA358118021 | FAT4 | c.1492T>G (p.Ser498Ala) c.-55+1926T>G (n.-55+1926T>G) | |
4 | g.125317904C>A | CA358118022 | FAT4 | c.1493C>A (p.Ser498Tyr) c.-55+1927C>A (n.-55+1927C>A) | |
4 | g.125317904C= | CA1491601007 | FAT4 | c.1493C= (p.Ser498=) c.-55+1927C= (n.-55+1927C=) | |
4 | g.125317904C>G | CA358118023 | FAT4 | c.1493C>G (p.Ser498Cys) c.-55+1927C>G (n.-55+1927C>G) | dbSNP gnomAD v3 gnomAD v4 |
4 | g.125317904C>T | CA358118024 | FAT4 | c.1493C>T (p.Ser498Phe) c.-55+1927C>T (n.-55+1927C>T) | |
4 | g.125317905T>A | CA441366845 | FAT4 | c.1494T>A (p.Ser498=) c.-55+1928T>A (n.-55+1928T>A) | |
4 | g.125317905T>C | CA441366846 | FAT4 | c.1494T>C (p.Ser498=) c.-55+1928T>C (n.-55+1928T>C) | |
4 | g.125317905T>G | CA441366848 | FAT4 | c.1494T>G (p.Ser498=) c.-55+1928T>G (n.-55+1928T>G) | |
4 | g.125317906G>A | CA104864124 | FAT4 | c.1495G>A (p.Ala499Thr) c.-55+1929G>A (n.-55+1929G>A) | dbSNP |
4 | g.125317906G>C | CA358118026 | FAT4 | c.1495G>C (p.Ala499Pro) c.-55+1929G>C (n.-55+1929G>C) | |
4 | g.125317906G= | CA1491601011 | FAT4 | c.1495G= (p.Ala499=) c.-55+1929G= (n.-55+1929G=) | |
4 | g.125317906G>T | CA358118025 | FAT4 | c.1495G>T (p.Ala499Ser) c.-55+1929G>T (n.-55+1929G>T) | |
4 | g.125317907C>A | CA358118027 | FAT4 | c.1496C>A (p.Ala499Asp) c.-55+1930C>A (n.-55+1930C>A) | |
4 | g.125317907C>G | CA358118028 | FAT4 | c.1496C>G (p.Ala499Gly) c.-55+1930C>G (n.-55+1930C>G) | |
4 | g.125317907C>T | CA358118029 | FAT4 | c.1496C>T (p.Ala499Val) c.-55+1930C>T (n.-55+1930C>T) | |
4 | g.125317908C>A | CA441366857 | FAT4 | c.1497C>A (p.Ala499=) c.-55+1931C>A (n.-55+1931C>A) | |
4 | g.125317908C= | CA1491601015 | FAT4 | c.1497C= (p.Ala499=) c.-55+1931C= (n.-55+1931C=) | |
4 | g.125317908C>G | CA441366859 | FAT4 | c.1497C>G (p.Ala499=) c.-55+1931C>G (n.-55+1931C>G) | |
4 | g.125317908C>T | CA3072002 | FAT4 | c.1497C>T (p.Ala499=) c.-55+1931C>T (n.-55+1931C>T) | ClinVar dbSNP ExAC |
4 | g.125317909A>C | CA358118030 | FAT4 | c.1498A>C (p.Thr500Pro) c.-55+1932A>C (n.-55+1932A>C) | |
4 | g.125317909A>G | CA358118031 | FAT4 | c.1498A>G (p.Thr500Ala) c.-55+1932A>G (n.-55+1932A>G) | |
4 | g.125317909A>T | CA358118032 | FAT4 | c.1498A>T (p.Thr500Ser) c.-55+1932A>T (n.-55+1932A>T) | |
4 | g.125317910C>A | CA358118033 | FAT4 | c.1499C>A (p.Thr500Asn) c.-55+1933C>A (n.-55+1933C>A) | |
4 | g.125317910C>G | CA358118034 | FAT4 | c.1499C>G (p.Thr500Ser) c.-55+1933C>G (n.-55+1933C>G) | |
4 | g.125317910C>T | CA358118035 | FAT4 | c.1499C>T (p.Thr500Ile) c.-55+1933C>T (n.-55+1933C>T) | |
4 | g.125317911T>A | CA441366869 | FAT4 | c.1500T>A (p.Thr500=) c.-55+1934T>A (n.-55+1934T>A) | gnomAD v4 |
4 | g.125317911T>C | CA441366870 | FAT4 | c.1500T>C (p.Thr500=) c.-55+1934T>C (n.-55+1934T>C) | |
4 | g.125317911T>G | CA3072003 | FAT4 | c.1500T>G (p.Thr500=) c.-55+1934T>G (n.-55+1934T>G) | dbSNP ExAC gnomAD v2 gnomAD v4 |
4 | g.125317911T= | CA1491601018 | FAT4 | c.1500T= (p.Thr500=) c.-55+1934T= (n.-55+1934T=) | |
4 | g.125317912G>A | CA358118036 | FAT4 | c.1501G>A (p.Asp501Asn) c.-55+1935G>A (n.-55+1935G>A) | |
4 | g.125317912G>C | CA358118037 | FAT4 | c.1501G>C (p.Asp501His) c.-55+1935G>C (n.-55+1935G>C) | |
4 | g.125317912G>T | CA358118038 | FAT4 | c.1501G>T (p.Asp501Tyr) c.-55+1935G>T (n.-55+1935G>T) | |
4 | g.125317913A>C | CA358118041 | FAT4 | c.1502A>C (p.Asp501Ala) c.-55+1936A>C (n.-55+1936A>C) | |
4 | g.125317913A>G | CA358118040 | FAT4 | c.1502A>G (p.Asp501Gly) c.-55+1936A>G (n.-55+1936A>G) | |
4 | g.125317913A>T | CA358118039 | FAT4 | c.1502A>T (p.Asp501Val) c.-55+1936A>T (n.-55+1936A>T) | |
4 | g.125317914T>A | CA358118042 | FAT4 | c.1503T>A (p.Asp501Glu) c.-55+1937T>A (n.-55+1937T>A) | |
4 | g.125317914T>C | CA441366883 | FAT4 | c.1503T>C (p.Asp501=) c.-55+1937T>C (n.-55+1937T>C) | gnomAD v4 |
4 | g.125317914T>G | CA358118043 | FAT4 | c.1503T>G (p.Asp501Glu) c.-55+1937T>G (n.-55+1937T>G) | |
4 | g.125317915G>A | CA358118044 | FAT4 | c.1504G>A (p.Gly502Ser) c.-55+1938G>A (n.-55+1938G>A) | |
4 | g.125317915G>C | CA358118045 | FAT4 | c.1504G>C (p.Gly502Arg) c.-55+1938G>C (n.-55+1938G>C) | |
4 | g.125317915G>T | CA358118046 | FAT4 | c.1504G>T (p.Gly502Cys) c.-55+1938G>T (n.-55+1938G>T) | |
4 | g.125317916G>A | CA358118047 | FAT4 | c.1505G>A (p.Gly502Asp) c.-55+1939G>A (n.-55+1939G>A) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
4 | g.125317916G>C | CA358118048 | FAT4 | c.1505G>C (p.Gly502Ala) c.-55+1939G>C (n.-55+1939G>C) | |
4 | g.125317916G= | CA1491601021 | FAT4 | c.1505G= (p.Gly502=) c.-55+1939G= (n.-55+1939G=) | |
4 | g.125317916G>T | CA358118049 | FAT4 | c.1505G>T (p.Gly502Val) c.-55+1939G>T (n.-55+1939G>T) | |
4 | g.125317917C>A | CA441366893 | FAT4 | c.1506C>A (p.Gly502=) c.-55+1940C>A (n.-55+1940C>A) | dbSNP gnomAD v2 gnomAD v4 |
4 | g.125317917C= | CA1491601023 | FAT4 | c.1506C= (p.Gly502=) c.-55+1940C= (n.-55+1940C=) | |
4 | g.125317917C>G | CA441366894 | FAT4 | c.1506C>G (p.Gly502=) c.-55+1940C>G (n.-55+1940C>G) | |
4 | g.125317917C>T | CA441366895 | FAT4 | c.1506C>T (p.Gly502=) c.-55+1940C>T (n.-55+1940C>T) | gnomAD v4 |