Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
11 | g.1841477G>A | CA379106840 | TNNI2 | c.475G>A (p.Gly159Ser) | |
11 | g.1841477G>C | CA379106841 | TNNI2 | c.475G>C (p.Gly159Arg) | dbSNP gnomAD v2 gnomAD v4 |
11 | g.1841477G= | CA1947878691 | TNNI2 | c.475G= (p.Gly159=) | |
11 | g.1841477G>T | CA379106842 | TNNI2 | c.475G>T (p.Gly159Cys) | |
11 | g.1841478G>A | CA379106843 | TNNI2 | c.476G>A (p.Gly159Asp) | |
11 | g.1841478G>C | CA379106844 | TNNI2 | c.476G>C (p.Gly159Ala) | gnomAD v4 |
11 | g.1841478G>T | CA379106845 | TNNI2 | c.476G>T (p.Gly159Val) | |
11 | g.1841479T>A | CA471993054 | TNNI2 | c.477T>A (p.Gly159=) | |
11 | g.1841479T>C | CA471993052 | TNNI2 | c.477T>C (p.Gly159=) | gnomAD v4 |
11 | g.1841479T>G | CA471993055 | TNNI2 | c.477T>G (p.Gly159=) | |
11 | g.1841480G>A | CA5815314 | TNNI2 | c.478G>A (p.Asp160Asn) | dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.1841480G>C | CA379106847 | TNNI2 | c.478G>C (p.Asp160His) | |
11 | g.1841480G= | CA1947878695 | TNNI2 | c.478G= (p.Asp160=) | |
11 | g.1841480G>T | CA379106846 | TNNI2 | c.478G>T (p.Asp160Tyr) | |
11 | g.1841481A>C | CA379106850 | TNNI2 | c.479A>C (p.Asp160Ala) | |
11 | g.1841481A>G | CA379106848 | TNNI2 | c.479A>G (p.Asp160Gly) | |
11 | g.1841481A>T | CA379106849 | TNNI2 | c.479A>T (p.Asp160Val) | |
11 | g.1841482C>A | CA379106851 | TNNI2 | c.480C>A (p.Asp160Glu) | |
11 | g.1841482C>G | CA379106852 | TNNI2 | c.480C>G (p.Asp160Glu) | |
11 | g.1841482C>T | CA471993063 | TNNI2 | c.480C>T (p.Asp160=) | |
11 | g.1841483del | CA2611933187 | TNNI2 | c.481del (p.Trp161GlyfsTer?) | gnomAD v4 |
11 | g.1841483T>A | CA379106853 | TNNI2 | c.481T>A (p.Trp161Arg) | |
11 | g.1841483T>C | CA379106854 | TNNI2 | c.481T>C (p.Trp161Arg) | |
11 | g.1841483T>G | CA379106855 | TNNI2 | c.481T>G (p.Trp161Gly) | |
11 | g.1841484G>A | CA379106856 | TNNI2 | c.482G>A (p.Trp161Ter) | |
11 | g.1841484G>C | CA379106857 | TNNI2 | c.482G>C (p.Trp161Ser) | |
11 | g.1841484G>T | CA379106858 | TNNI2 | c.482G>T (p.Trp161Leu) | |
11 | g.1841485G>A | CA379106859 | TNNI2 | c.483G>A (p.Trp161Ter) | COSMIC |
11 | g.1841485G>C | CA379106860 | TNNI2 | c.483G>C (p.Trp161Cys) | |
11 | g.1841485G>T | CA379106861 | TNNI2 | c.483G>T (p.Trp161Cys) | |
11 | g.1841486A= | CA1947878701 | TNNI2 | c.484A= (p.Arg162=) | |
11 | g.1841486A>C | CA471993075 | TNNI2 | c.484A>C (p.Arg162=) | dbSNP |
11 | g.1841486A>G | CA379106863 | TNNI2 | c.484A>G (p.Arg162Gly) | |
11 | g.1841486A>T | CA379106862 | TNNI2 | c.484A>T (p.Arg162Trp) | |
11 | g.1841487G>A | CA379106864 | TNNI2 | c.485G>A (p.Arg162Lys) | gnomAD v4 |
11 | g.1841487G>C | CA379106865 | TNNI2 | c.485G>C (p.Arg162Thr) | |
11 | g.1841487G>T | CA379106866 | TNNI2 | c.485G>T (p.Arg162Met) | |
11 | g.1841488G>A | CA471993088 | TNNI2 | c.486G>A (p.Arg162=) | COSMIC |
11 | g.1841488G>C | CA379106867 | TNNI2 | c.486G>C (p.Arg162Ser) | |
11 | g.1841488G>T | CA379106868 | TNNI2 | c.486G>T (p.Arg162Ser) | ClinVar |
11 | g.1841489A>C | CA379106869 | TNNI2 | c.487A>C (p.Lys163Gln) | |
11 | g.1841489A>G | CA379106870 | TNNI2 | c.487A>G (p.Lys163Glu) | |
11 | g.1841489A>T | CA379106871 | TNNI2 | c.487A>T (p.Lys163Ter) | |
11 | g.1841490A>C | CA379106872 | TNNI2 | c.488A>C (p.Lys163Thr) | |
11 | g.1841490A>G | CA379106873 | TNNI2 | c.488A>G (p.Lys163Arg) | |
11 | g.1841490A>T | CA379106874 | TNNI2 | c.488A>T (p.Lys163Met) | |
11 | g.1841491G>A | CA471993103 | TNNI2 | c.489G>A (p.Lys163=) | dbSNP gnomAD v2 gnomAD v4 |
11 | g.1841491G>C | CA379106875 | TNNI2 | c.489G>C (p.Lys163Asn) | |
11 | g.1841491G= | CA1947878704 | TNNI2 | c.489G= (p.Lys163=) | |
11 | g.1841491G>T | CA379106876 | TNNI2 | c.489G>T (p.Lys163Asn) | |
11 | g.1841492A= | CA1947878708 | TNNI2 | c.490A= (p.Asn164=) | |
11 | g.1841492A>C | CA379106879 | TNNI2 | c.490A>C (p.Asn164His) | |
11 | g.1841492A>G | CA379106878 | TNNI2 | c.490A>G (p.Asn164Asp) | |
11 | g.1841492A>T | CA379106877 | TNNI2 | c.490A>T (p.Asn164Tyr) | dbSNP |
11 | g.1841493A>C | CA379106880 | TNNI2 | c.491A>C (p.Asn164Thr) | |
11 | g.1841493A>G | CA379106881 | TNNI2 | c.491A>G (p.Asn164Ser) | dbSNP |
11 | g.1841493A>T | CA379106882 | TNNI2 | c.491A>T (p.Asn164Ile) | |
11 | g.1841494C>A | CA379106883 | TNNI2 | c.492C>A (p.Asn164Lys) | |
11 | g.1841494C= | CA1947878711 | TNNI2 | c.492C= (p.Asn164=) | |
11 | g.1841494C>G | CA379106884 | TNNI2 | c.492C>G (p.Asn164Lys) | |
11 | g.1841494C>T | CA471993117 | TNNI2 | c.492C>T (p.Asn164=) | dbSNP gnomAD v2 gnomAD v4 |
11 | g.1841495A= | CA1947878716 | TNNI2 | c.493A= (p.Ile165=) | |
11 | g.1841495A>C | CA379106887 | TNNI2 | c.493A>C (p.Ile165Leu) | |
11 | g.1841495A>G | CA379106886 | TNNI2 | c.493A>G (p.Ile165Val) | |
11 | g.1841495A>T | CA379106885 | TNNI2 | c.493A>T (p.Ile165Phe) | ClinVar dbSNP |
11 | g.1841496T>A | CA379106888 | TNNI2 | c.494T>A (p.Ile165Asn) | |
11 | g.1841496T>C | CA379106889 | TNNI2 | c.494T>C (p.Ile165Thr) | |
11 | g.1841496T>G | CA379106890 | TNNI2 | c.494T>G (p.Ile165Ser) | |
11 | g.1841497C>A | CA5815316 | TNNI2 | c.495C>A (p.Ile165=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.1841497C= | CA1947878725 | TNNI2 | c.495C= (p.Ile165=) | |
11 | g.1841497C>G | CA379106891 | TNNI2 | c.495C>G (p.Ile165Met) | |
11 | g.1841497C>T | CA5815315 | TNNI2 | c.495C>T (p.Ile165=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
11 | g.1841497_1841500delinsCGAG | CA1947878723 | TNNI2 | c.495_498delinsCGAG (p.Ile165=) | |
11 | g.1841498G>A | CA379106892 | TNNI2 | c.496G>A (p.Glu166Lys) | dbSNP gnomAD v3 gnomAD v4 |
11 | g.1841498G>C | CA379106894 | TNNI2 | c.496G>C (p.Glu166Gln) | |
11 | g.1841498G= | CA1947878735 | TNNI2 | c.496G= (p.Glu166=) | |
11 | g.1841498G>T | CA379106893 | TNNI2 | c.496G>T (p.Glu166Ter) | ClinVar |
11 | g.1841501_1841503del | CA122388 | TNNI2 | c.499_501del (p.Glu167del) | ClinVar dbSNP |
11 | g.1841499A>C | CA379106895 | TNNI2 | c.497A>C (p.Glu166Ala) | |
11 | g.1841499A>G | CA379106896 | TNNI2 | c.497A>G (p.Glu166Gly) | |
11 | g.1841499A>T | CA379106897 | TNNI2 | c.497A>T (p.Glu166Val) | |
11 | g.1841500G>A | CA471993143 | TNNI2 | c.498G>A (p.Glu166=) | gnomAD v4 |
11 | g.1841500G>C | CA379106898 | TNNI2 | c.498G>C (p.Glu166Asp) | |
11 | g.1841500G>T | CA379106899 | TNNI2 | c.498G>T (p.Glu166Asp) | |
11 | g.1841501G>A | CA379106900 | TNNI2 | c.499G>A (p.Glu167Lys) | |
11 | g.1841501G>C | CA379106901 | TNNI2 | c.499G>C (p.Glu167Gln) | |
11 | g.1841501G>T | CA379106902 | TNNI2 | c.499G>T (p.Glu167Ter) | |
11 | g.1841502del | CA2842288396 | TNNI2 | c.500del (p.Glu167GlyfsTer?) | |
11 | g.1841502A>C | CA379106903 | TNNI2 | c.500A>C (p.Glu167Ala) | |
11 | g.1841502A>G | CA379106904 | TNNI2 | c.500A>G (p.Glu167Gly) | |
11 | g.1841502A>T | CA379106905 | TNNI2 | c.500A>T (p.Glu167Val) | |
11 | g.1841503G>A | CA471993154 | TNNI2 | c.501G>A (p.Glu167=) | gnomAD v4 |
11 | g.1841503G>C | CA379106906 | TNNI2 | c.501G>C (p.Glu167Asp) | |
11 | g.1841503G>T | CA379106907 | TNNI2 | c.501G>T (p.Glu167Asp) | |
11 | g.1841504A>C | CA379106908 | TNNI2 | c.502A>C (p.Lys168Gln) | |
11 | g.1841504A>G | CA379106910 | TNNI2 | c.502A>G (p.Lys168Glu) | |
11 | g.1841504A>T | CA379106909 | TNNI2 | c.502A>T (p.Lys168Ter) | |
11 | g.1841505A>C | CA379106911 | TNNI2 | c.503A>C (p.Lys168Thr) | |
11 | g.1841505A>G | CA379106913 | TNNI2 | c.503A>G (p.Lys168Arg) | gnomAD v4 |
11 | g.1841505A>T | CA379106912 | TNNI2 | c.503A>T (p.Lys168Met) | ClinVar |
11 | g.1841505_1841507dup | CA2580082584 | TNNI2 | c.503_505dup (p.Ser169Ter) | ClinVar |
11 | g.1841506G>A | CA471993168 | TNNI2 | c.504G>A (p.Lys168=) | dbSNP |
11 | g.1841506G>C | CA379106914 | TNNI2 | c.504G>C (p.Lys168Asn) | |
11 | g.1841506G= | CA1947878740 | TNNI2 | c.504G= (p.Lys168=) | |
11 | g.1841506G>T | CA379106915 | TNNI2 | c.504G>T (p.Lys168Asn) | |
11 | g.1841506dup | CA2839544707 | TNNI2 | c.504dup (p.Ser169ValfsTer11) | |
11 | g.1841507T>A | CA5815317 | TNNI2 | c.505T>A (p.Ser169Thr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.1841507T>C | CA379106916 | TNNI2 | c.505T>C (p.Ser169Pro) | |
11 | g.1841507T>G | CA379106917 | TNNI2 | c.505T>G (p.Ser169Ala) | |
11 | g.1841507T= | CA1947878745 | TNNI2 | c.505T= (p.Ser169=) | |
11 | g.1841507dup | CA2838961144 | TNNI2 | c.505dup (p.Ser169PhefsTer11) | |
11 | g.1841508C>A | CA379106918 | TNNI2 | c.506C>A (p.Ser169Tyr) | |
11 | g.1841508C= | CA1947878750 | TNNI2 | c.506C= (p.Ser169=) | |
11 | g.1841508C>G | CA379106919 | TNNI2 | c.506C>G (p.Ser169Cys) | |
11 | g.1841508C>T | CA379106920 | TNNI2 | c.506C>T (p.Ser169Phe) | dbSNP gnomAD v2 gnomAD v4 |
11 | g.1841509T>A | CA471993180 | TNNI2 | c.507T>A (p.Ser169=) | |
11 | g.1841509T>C | CA471993183 | TNNI2 | c.507T>C (p.Ser169=) | |
11 | g.1841509T>G | CA471993185 | TNNI2 | c.507T>G (p.Ser169=) | |
11 | g.1841510G>A | CA379106921 | TNNI2 | c.508G>A (p.Gly170Ser) | gnomAD v4 |
11 | g.1841510G>C | CA379106923 | TNNI2 | c.508G>C (p.Gly170Arg) | |
11 | g.1841510G>T | CA379106922 | TNNI2 | c.508G>T (p.Gly170Cys) | |
11 | g.1841511G>A | CA379106924 | TNNI2 | c.509G>A (p.Gly170Asp) | |
11 | g.1841511G>C | CA216206335 | TNNI2 | c.509G>C (p.Gly170Ala) | dbSNP gnomAD v4 |
11 | g.1841511G= | CA1947878753 | TNNI2 | c.509G= (p.Gly170=) | |
11 | g.1841511G>T | CA379106925 | TNNI2 | c.509G>T (p.Gly170Val) | |
11 | g.1841512C>A | CA471993199 | TNNI2 | c.510C>A (p.Gly170=) | |
11 | g.1841512C>G | CA471993193 | TNNI2 | c.510C>G (p.Gly170=) | |
11 | g.1841512C>T | CA471993196 | TNNI2 | c.510C>T (p.Gly170=) | |
11 | g.1841513A>C | CA379106926 | TNNI2 | c.511A>C (p.Met171Leu) | |
11 | g.1841513A>G | CA379106927 | TNNI2 | c.511A>G (p.Met171Val) | gnomAD v4 |
11 | g.1841513A>T | CA379106928 | TNNI2 | c.511A>T (p.Met171Leu) | |
11 | g.1841514T>A | CA379106930 | TNNI2 | c.512T>A (p.Met171Lys) | |
11 | g.1841514T>C | CA379106931 | TNNI2 | c.512T>C (p.Met171Thr) | |
11 | g.1841514T>G | CA379106929 | TNNI2 | c.512T>G (p.Met171Arg) | gnomAD v4 |
11 | g.1841515G>A | CA379106932 | TNNI2 | c.513G>A (p.Met171Ile) | |
11 | g.1841515G>C | CA379106933 | TNNI2 | c.513G>C (p.Met171Ile) | |
11 | g.1841515G>T | CA379106934 | TNNI2 | c.513G>T (p.Met171Ile) | |
11 | g.1841516G>A | CA379106935 | TNNI2 | c.514G>A (p.Glu172Lys) | |
11 | g.1841516G>C | CA379106936 | TNNI2 | c.514G>C (p.Glu172Gln) | dbSNP gnomAD v2 gnomAD v4 |
11 | g.1841516G= | CA1947878755 | TNNI2 | c.514G= (p.Glu172=) | |
11 | g.1841516G>T | CA379106937 | TNNI2 | c.514G>T (p.Glu172Ter) | |
11 | g.1841517A>C | CA379106938 | TNNI2 | c.515A>C (p.Glu172Ala) | |
11 | g.1841517A>G | CA379106939 | TNNI2 | c.515A>G (p.Glu172Gly) | gnomAD v4 |
11 | g.1841517A>T | CA379106940 | TNNI2 | c.515A>T (p.Glu172Val) | |
11 | g.1841518G>A | CA471993224 | TNNI2 | c.516G>A (p.Glu172=) | dbSNP gnomAD v3 gnomAD v4 |
11 | g.1841518G>C | CA379106942 | TNNI2 | c.516G>C (p.Glu172Asp) | |
11 | g.1841518G= | CA1947878760 | TNNI2 | c.516G= (p.Glu172=) | |
11 | g.1841518G>T | CA379106941 | TNNI2 | c.516G>T (p.Glu172Asp) | |
11 | g.1841519G>A | CA379106943 | TNNI2 | c.517G>A (p.Gly173Ser) | |
11 | g.1841519G>C | CA379106944 | TNNI2 | c.517G>C (p.Gly173Arg) | |
11 | g.1841519G>T | CA379106945 | TNNI2 | c.517G>T (p.Gly173Cys) | |
11 | g.1841520G>A | CA379106946 | TNNI2 | c.518G>A (p.Gly173Asp) | |
11 | g.1841520G>C | CA379106947 | TNNI2 | c.518G>C (p.Gly173Ala) | |
11 | g.1841520G>T | CA379106948 | TNNI2 | c.518G>T (p.Gly173Val) | |
11 | g.1841521C>A | CA471993237 | TNNI2 | c.519C>A (p.Gly173=) | |
11 | g.1841521C= | CA1947878764 | TNNI2 | c.519C= (p.Gly173=) | |
11 | g.1841521C>G | CA471993239 | TNNI2 | c.519C>G (p.Gly173=) | |
11 | g.1841521C>T | CA471993235 | TNNI2 | c.519C>T (p.Gly173=) | dbSNP gnomAD v2 gnomAD v4 |
11 | g.1841522C>A | CA471993241 | TNNI2 | c.520C>A (p.Arg174=) | dbSNP |
11 | g.1841522C= | CA1947878768 | TNNI2 | c.520C= (p.Arg174=) | |
11 | g.1841522C>G | CA379106949 | TNNI2 | c.520C>G (p.Arg174Gly) | |
11 | g.1841522C>T | CA379106950 | TNNI2 | c.520C>T (p.Arg174Trp) | ClinVar dbSNP gnomAD v4 COSMIC |
11 | g.1841523G>A | CA122377 | TNNI2 | c.521G>A (p.Arg174Gln) | ClinVar dbSNP |
11 | g.1841523G>C | CA379106951 | TNNI2 | c.521G>C (p.Arg174Pro) | |
11 | g.1841523G= | CA1947878771 | TNNI2 | c.521G= (p.Arg174=) | |
11 | g.1841523G>T | CA379106952 | TNNI2 | c.521G>T (p.Arg174Leu) | |
11 | g.1841523_1841526delinsGGAA | CA1947878773 | TNNI2 | c.521_524delinsGGAA (p.Arg174=) | |
11 | g.1841524G>A | CA471993249 | TNNI2 | c.522G>A (p.Arg174=) | gnomAD v4 |
11 | g.1841524G>C | CA471993246 | TNNI2 | c.522G>C (p.Arg174=) | |
11 | g.1841524G>T | CA471993247 | TNNI2 | c.522G>T (p.Arg174=) | |
11 | g.1841529_1841531del | CA122381 | TNNI2 | c.527_529del (p.Lys176del) | ClinVar dbSNP |
11 | g.1841525A>C | CA379106955 | TNNI2 | c.523A>C (p.Lys175Gln) | |
11 | g.1841525A>G | CA379106954 | TNNI2 | c.523A>G (p.Lys175Glu) | |
11 | g.1841525A>T | CA379106953 | TNNI2 | c.523A>T (p.Lys175Ter) | |
11 | g.1841526A>C | CA379106958 | TNNI2 | c.524A>C (p.Lys175Thr) | |
11 | g.1841526A>G | CA379106957 | TNNI2 | c.524A>G (p.Lys175Arg) | |
11 | g.1841526A>T | CA379106956 | TNNI2 | c.524A>T (p.Lys175Met) | |
11 | g.1841527G>A | CA471993255 | TNNI2 | c.525G>A (p.Lys175=) | dbSNP gnomAD v4 |
11 | g.1841527G>C | CA379106959 | TNNI2 | c.525G>C (p.Lys175Asn) | |
11 | g.1841527G= | CA1947878781 | TNNI2 | c.525G= (p.Lys175=) | |
11 | g.1841527G>T | CA206706 | TNNI2 | c.525G>T (p.Lys175Asn) | ClinVar dbSNP |
11 | g.1841528A>C | CA379106960 | TNNI2 | c.526A>C (p.Lys176Gln) | |
11 | g.1841528A>G | CA379106961 | TNNI2 | c.526A>G (p.Lys176Glu) | |
11 | g.1841528A>T | CA379106962 | TNNI2 | c.526A>T (p.Lys176Ter) | |
11 | g.1841529A>C | CA379106963 | TNNI2 | c.527A>C (p.Lys176Thr) | |
11 | g.1841529A>G | CA379106964 | TNNI2 | c.527A>G (p.Lys176Arg) | |
11 | g.1841529A>T | CA379106965 | TNNI2 | c.527A>T (p.Lys176Met) | |
11 | g.1841530G>A | CA471993261 | TNNI2 | c.528G>A (p.Lys176=) | |
11 | g.1841530G>C | CA379106966 | TNNI2 | c.528G>C (p.Lys176Asn) | |
11 | g.1841530G>T | CA379106967 | TNNI2 | c.528G>T (p.Lys176Asn) | |
11 | g.1841531A>C | CA379106968 | TNNI2 | c.529A>C (p.Met177Leu) | |
11 | g.1841531A>G | CA379106969 | TNNI2 | c.529A>G (p.Met177Val) | |
11 | g.1841531A>T | CA379106970 | TNNI2 | c.529A>T (p.Met177Leu) | |
11 | g.1841532T>A | CA379106973 | TNNI2 | c.530T>A (p.Met177Lys) | |
11 | g.1841532T>C | CA379106972 | TNNI2 | c.530T>C (p.Met177Thr) | ClinVar dbSNP |
11 | g.1841532T>G | CA379106971 | TNNI2 | c.530T>G (p.Met177Arg) | |
11 | g.1841532T= | CA1947878786 | TNNI2 | c.530T= (p.Met177=) | |
11 | g.1841533G>A | CA5815318 | TNNI2 | c.531G>A (p.Met177Ile) | dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.1841533G>C | CA379106974 | TNNI2 | c.531G>C (p.Met177Ile) | |
11 | g.1841533G= | CA1947878791 | TNNI2 | c.531G= (p.Met177=) | |
11 | g.1841533G>T | CA379106975 | TNNI2 | c.531G>T (p.Met177Ile) | |
11 | g.1841534T>A | CA379106976 | TNNI2 | c.532T>A (p.Phe178Ile) | ClinVar dbSNP |
11 | g.1841534T>C | CA379106977 | TNNI2 | c.532T>C (p.Phe178Leu) | |
11 | g.1841534T>G | CA379106978 | TNNI2 | c.532T>G (p.Phe178Val) | |
11 | g.1841535T>A | CA379106979 | TNNI2 | c.533T>A (p.Phe178Tyr) | |
11 | g.1841535T>C | CA379106980 | TNNI2 | c.533T>C (p.Phe178Ser) | |
11 | g.1841535T>G | CA379106981 | TNNI2 | c.533T>G (p.Phe178Cys) | |
11 | g.1841536T>A | CA379106982 | TNNI2 | c.534T>A (p.Phe178Leu) | |
11 | g.1841536T>C | CA471993277 | TNNI2 | c.534T>C (p.Phe178=) | |
11 | g.1841536T>G | CA379106983 | TNNI2 | c.534T>G (p.Phe178Leu) | |
11 | g.1841537G>A | CA379106984 | TNNI2 | c.535G>A (p.Glu179Lys) | gnomAD v4 |
11 | g.1841537G>C | CA379106985 | TNNI2 | c.535G>C (p.Glu179Gln) | |
11 | g.1841537G>T | CA379106986 | TNNI2 | c.535G>T (p.Glu179Ter) | |
11 | g.1841538A>C | CA379106988 | TNNI2 | c.536A>C (p.Glu179Ala) | |
11 | g.1841538A>G | CA379106989 | TNNI2 | c.536A>G (p.Glu179Gly) | |
11 | g.1841538A>T | CA379106987 | TNNI2 | c.536A>T (p.Glu179Val) | |
11 | g.1841539G>A | CA471993285 | TNNI2 | c.537G>A (p.Glu179=) | |
11 | g.1841539G>C | CA379106990 | TNNI2 | c.537G>C (p.Glu179Asp) | |
11 | g.1841539G>T | CA379106991 | TNNI2 | c.537G>T (p.Glu179Asp) | |
11 | g.1841540T>A | CA379106992 | TNNI2 | c.538T>A (p.Ser180Thr) | |
11 | g.1841540T>C | CA379106993 | TNNI2 | c.538T>C (p.Ser180Pro) | dbSNP |
11 | g.1841540T>G | CA379106994 | TNNI2 | c.538T>G (p.Ser180Ala) | |
11 | g.1841541C>A | CA379106995 | TNNI2 | c.539C>A (p.Ser180Tyr) | |
11 | g.1841541C>G | CA379106996 | TNNI2 | c.539C>G (p.Ser180Cys) | |
11 | g.1841541C>T | CA379106997 | TNNI2 | c.539C>T (p.Ser180Phe) | |
11 | g.1841542C>A | CA471993294 | TNNI2 | c.540C>A (p.Ser180=) | |
11 | g.1841542C= | CA1947878795 | TNNI2 | c.540C= (p.Ser180=) | |
11 | g.1841542C>G | CA471993296 | TNNI2 | c.540C>G (p.Ser180=) | |
11 | g.1841542C>T | CA5815319 | TNNI2 | c.540C>T (p.Ser180=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.1841543G>A | CA216206371 | TNNI2 | c.541G>A (p.Glu181Lys) | dbSNP gnomAD v2 gnomAD v4 |
11 | g.1841543G>C | CA379106998 | TNNI2 | c.541G>C (p.Glu181Gln) | COSMIC |
11 | g.1841543G= | CA1947878798 | TNNI2 | c.541G= (p.Glu181=) | |
11 | g.1841543G>T | CA379106999 | TNNI2 | c.541G>T (p.Glu181Ter) | |
11 | g.1841544A>C | CA379107000 | TNNI2 | c.542A>C (p.Glu181Ala) | |
11 | g.1841544A>G | CA379107001 | TNNI2 | c.542A>G (p.Glu181Gly) | |
11 | g.1841544A>T | CA379107002 | TNNI2 | c.542A>T (p.Glu181Val) | gnomAD v4 |
11 | g.1841545G>A | CA471993301 | TNNI2 | c.543G>A (p.Glu181=) | |
11 | g.1841545G>C | CA379107003 | TNNI2 | c.543G>C (p.Glu181Asp) | |
11 | g.1841545G>T | CA379107004 | TNNI2 | c.543G>T (p.Glu181Asp) | |
11 | g.1841546T>A | CA379107005 | TNNI2 | c.544T>A (p.Ser182Thr) | |
11 | g.1841546T>C | CA379107007 | TNNI2 | c.544T>C (p.Ser182Pro) | |
11 | g.1841546T>G | CA379107006 | TNNI2 | c.544T>G (p.Ser182Ala) | |
11 | g.1841547C>A | CA379107008 | TNNI2 | c.545C>A (p.Ser182Tyr) | |
11 | g.1841547C>G | CA379107009 | TNNI2 | c.545C>G (p.Ser182Cys) | |
11 | g.1841547C>T | CA379107010 | TNNI2 | c.545C>T (p.Ser182Phe) | |
11 | g.1841548C>A | CA471993308 | TNNI2 | c.546C>A (p.Ser182=) | |
11 | g.1841548C>G | CA471993309 | TNNI2 | c.546C>G (p.Ser182=) | |
11 | g.1841548C>T | CA471993311 | TNNI2 | c.546C>T (p.Ser182=) | |
11 | g.1841549T>A | CA379107011 | TNNI2 | c.547T>A (p.Ter183Lys) | |
11 | g.1841549T>C | CA379107012 | TNNI2 | c.547T>C (p.Ter183Gln) | |
11 | g.1841549T>G | CA379107013 | TNNI2 | c.547T>G (p.Ter183Glu) | |
11 | g.1841550A= | CA1947878801 | TNNI2 | c.548A= (p.Ter183=) | |
11 | g.1841550A>C | CA379107016 | TNNI2 | c.548A>C (p.Ter183Ser) | gnomAD v4 |
11 | g.1841550A>G | CA379107015 | TNNI2 | c.548A>G (p.Ter183Trp) | dbSNP gnomAD v4 |
11 | g.1841550A>T | CA379107014 | TNNI2 | c.548A>T (p.Ter183Leu) | |
11 | g.1841551G>A | CA5815320 | TNNI2 | c.549G>A (p.Ter183=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.1841551G>C | CA379107017 | TNNI2 | c.549G>C (p.Ter183Tyr) | |
11 | g.1841551G= | CA1947878805 | TNNI2 | c.549G= (p.Ter183=) | |
11 | g.1841551G>T | CA379107018 | TNNI2 | c.549G>T (p.Ter183Tyr) | |
11 | g.1841552G>A | CA2611933241 | TNNI2 | c.*1G>A (n.*1G>A) c.550G>A (n.550G>A) | gnomAD v4 |
11 | g.1841553C>A | CA2842288397 | TNNI2 | c.*2C>A (n.*2C>A) c.551C>A (n.551C>A) | |
11 | g.1841553C>T | CA2611933243 | TNNI2 | c.*2C>T (n.*2C>T) c.551C>T (n.551C>T) | gnomAD v4 |
11 | g.1841554C>T | CA2842288398 | TNNI2 | c.*3C>T (n.*3C>T) c.552C>T (n.552C>T) | |
11 | g.1841555A= | CA1947878808 | TNNI2 | c.*4A= (n.*4A=) c.553A= (n.553A=) | |
11 | g.1841555A>T | CA1947878810 | TNNI2 | c.*4A>T (n.*4A>T) c.553A>T (n.553A>T) | dbSNP gnomAD v4 |
11 | g.1841556C>T | CA2611933246 | TNNI2 | c.*5C>T (n.*5C>T) c.554C>T (n.554C>T) | gnomAD v4 |
11 | g.1841558C>A | CA2838961148 | TNNI2 | c.*7C>A (n.*7C>A) c.556C>A (n.556C>A) | |
11 | g.1841558C= | CA1947878811 | TNNI2 | c.*7C= (n.*7C=) c.556C= (n.556C=) | |
11 | g.1841558C>G | CA2842288399 | TNNI2 | c.*7C>G (n.*7C>G) c.556C>G (n.556C>G) | |
11 | g.1841558C>T | CA5815321 | TNNI2 | c.*7C>T (n.*7C>T) c.556C>T (n.556C>T) | dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.1841559G>A | CA5815322 | TNNI2 | c.*8G>A (n.*8G>A) c.557G>A (n.557G>A) | dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.1841559G= | CA1947878812 | TNNI2 | c.*8G= (n.*8G=) c.557G= (n.557G=) | |
11 | g.1841559G>T | CA2842288400 | TNNI2 | c.*8G>T (n.*8G>T) c.557G>T (n.557G>T) | |
11 | g.1841561del | CA2723166714 | TNNI2 | c.*10del (n.*10del) c.559del (n.559del) | dbSNP |
11 | g.1841562G= | CA1947878813 | TNNI2 | c.*11G= (n.*11G=) c.560G= (n.560G=) | |
11 | g.1841562G>T | CA2838961154 | TNNI2 | c.*11G>T (n.*11G>T) c.560G>T (n.560G>T) | |
11 | g.1841563C= | CA1947878815 | TNNI2 | c.*12C= (n.*12C=) c.561C= (n.561C=) | |
11 | g.1841563C>T | CA934399362 | TNNI2 | c.*12C>T (n.*12C>T) c.561C>T (n.561C>T) | dbSNP gnomAD v3 gnomAD v4 |
11 | g.1841566dup | CA5815323 | TNNI2 | c.*15dup (n.*15dup) c.564dup (n.564dup) | dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.1841564C>A | CA2574742249 | TNNI2 | c.*13C>A (n.*13C>A) c.562C>A (n.562C>A) | gnomAD v4 |
11 | g.1841564C>T | CA2611933252 | TNNI2 | c.*13C>T (n.*13C>T) c.562C>T (n.562C>T) | gnomAD v4 |
11 | g.1841565C>A | CA2574742250 | TNNI2 | c.*14C>A (n.*14C>A) c.563C>A (n.563C>A) | |
11 | g.1841565C>T | CA2842288401 | TNNI2 | c.*14C>T (n.*14C>T) c.563C>T (n.563C>T) | |
11 | g.1841567T>C | CA2842288402 | TNNI2 | c.*16T>C (n.*16T>C) c.565T>C (n.565T>C) | |
11 | g.1841569C>A | CA597075004 | TNNI2 | c.*18C>A (n.*18C>A) c.567C>A (n.567C>A) | dbSNP gnomAD v2 gnomAD v4 |
11 | g.1841569C= | CA1947878819 | TNNI2 | c.*18C= (n.*18C=) c.567C= (n.567C=) | |
11 | g.1841569C>G | CA1947878818 | TNNI2 | c.*18C>G (n.*18C>G) c.567C>G (n.567C>G) | dbSNP |
11 | g.1841569C>T | CA5815324 | TNNI2 | c.*18C>T (n.*18C>T) c.567C>T (n.567C>T) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.1841570G>A | CA5815325 | TNNI2 | c.*19G>A (n.*19G>A) c.568G>A (n.568G>A) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.1841570G= | CA1947878823 | TNNI2 | c.*19G= (n.*19G=) c.568G= (n.568G=) | |
11 | g.1841570G>T | CA5815326 | TNNI2 | c.*19G>T (n.*19G>T) c.568G>T (n.568G>T) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.1841571C>A | CA5815327 | TNNI2 | c.*20C>A (n.*20C>A) c.569C>A (n.569C>A) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.1841571C= | CA1947878826 | TNNI2 | c.*20C= (n.*20C=) c.569C= (n.569C=) | |
11 | g.1841571C>T | CA5815328 | TNNI2 | c.*20C>T (n.*20C>T) c.569C>T (n.569C>T) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.1841572C>G | CA2611933256 | TNNI2 | c.*21C>G (n.*21C>G) c.570C>G (n.570C>G) | gnomAD v4 |
11 | g.1841572C>T | CA2611933258 | TNNI2 | c.*21C>T (n.*21C>T) c.570C>T (n.570C>T) | gnomAD v4 |
11 | g.1841573_1841574delinsTG | CA1947878829 | TNNI2 | c.*22_*23delinsTG (n.*22_*23delinsTG) c.571_572delinsTG (n.571_572delinsTG) | |
11 | g.1841574del | CA934399368 | TNNI2 | c.*23del (n.*23del) c.572del (n.572del) | dbSNP gnomAD v3 gnomAD v4 |
11 | g.1841574G>T | CA2839180231 | TNNI2 | c.*23G>T (n.*23G>T) c.572G>T (n.572G>T) | |
11 | g.1841575C>G | CA2611933260 | TNNI2 | c.*24C>G (n.*24C>G) c.573C>G (n.573C>G) | dbSNP gnomAD v4 |
11 | g.1841575C>T | CA2611933261 | TNNI2 | c.*24C>T (n.*24C>T) c.573C>T (n.573C>T) | gnomAD v4 |
11 | g.1841578del | CA2611933259 | TNNI2 | c.*27del (n.*27del) c.576del (n.576del) | gnomAD v4 |
11 | g.1841576C>A | CA2611933263 | TNNI2 | c.*25C>A (n.*25C>A) c.574C>A (n.574C>A) | gnomAD v4 |
11 | g.1841576C>T | CA2838210459 | TNNI2 | c.*25C>T (n.*25C>T) c.574C>T (n.574C>T) | |
11 | g.1841577C>A | CA2611933265 | TNNI2 | c.*26C>A (n.*26C>A) c.575C>A (n.575C>A) | gnomAD v4 |