| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 14 | g.23425716C>A | CA389048788 | MYH7 | c.2265G>T (p.Gln755His) n.2371G>T | |
| 14 | g.23425716C= | CA2123458185 | MYH7 | c.2265G= (p.Gln755=) n.2371G= | |
| 14 | g.23425716C>G | CA389048789 | MYH7 | c.2265G>C (p.Gln755His) n.2371G>C | |
| 14 | g.23425716C>T | CA485766880 | MYH7 | c.2265G>A (p.Gln755=) n.2371G>A | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 14 | g.23425717T>A | CA389048790 | MYH7 | c.2264A>T (p.Gln755Leu) n.2370A>T | gnomAD v4 |
| 14 | g.23425717T>C | CA389048791 | MYH7 | c.2264A>G (p.Gln755Arg) n.2370A>G | |
| 14 | g.23425717T>G | CA389048792 | MYH7 | c.2264A>C (p.Gln755Pro) n.2370A>C | |
| 14 | g.23425718G>A | CA031873 | MYH7 | c.2263C>T (p.Gln755Ter) n.2369C>T | dbSNP ExAC gnomAD v3 gnomAD v4 |
| 14 | g.23425718G>C | CA389048793 | MYH7 | c.2263C>G (p.Gln755Glu) n.2369C>G | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23425718G= | CA2123458187 | MYH7 | c.2263C= (p.Gln755=) n.2369C= | |
| 14 | g.23425718G>T | CA389048794 | MYH7 | c.2263C>A (p.Gln755Lys) n.2369C>A | |
| 14 | g.23425719G>A | CA485766883 | MYH7 | c.2262C>T (p.Asn754=) n.2368C>T | |
| 14 | g.23425719G>C | CA389048795 | MYH7 | c.2262C>G (p.Asn754Lys) n.2368C>G | ClinVar |
| 14 | g.23425719G>T | CA389048796 | MYH7 | c.2262C>A (p.Asn754Lys) n.2368C>A | |
| 14 | g.23425720T>A | CA389048797 | MYH7 | c.2261A>T (p.Asn754Ile) n.2367A>T | |
| 14 | g.23425720T>C | CA389048798 | MYH7 | c.2261A>G (p.Asn754Ser) n.2367A>G | ClinVar |
| 14 | g.23425720T>G | CA389048799 | MYH7 | c.2261A>C (p.Asn754Thr) n.2367A>C | |
| 14 | g.23425721T>A | CA389048800 | MYH7 | c.2260A>T (p.Asn754Tyr) n.2366A>T | |
| 14 | g.23425721T>C | CA389048802 | MYH7 | c.2260A>G (p.Asn754Asp) n.2366A>G | ClinVar dbSNP |
| 14 | g.23425721T>G | CA389048801 | MYH7 | c.2260A>C (p.Asn754His) n.2366A>C | ClinVar dbSNP gnomAD v2 |
| 14 | g.23425721T= | CA2123458190 | MYH7 | c.2260A= (p.Asn754=) n.2366A= | |
| 14 | g.23425722G>A | CA485766888 | MYH7 | c.2259C>T (p.His753=) n.2365C>T | gnomAD v4 |
| 14 | g.23425722G>C | CA389048803 | MYH7 | c.2259C>G (p.His753Gln) n.2365C>G | |
| 14 | g.23425722G>T | CA389048804 | MYH7 | c.2259C>A (p.His753Gln) n.2365C>A | |
| 14 | g.23425723T>A | CA389048805 | MYH7 | c.2258A>T (p.His753Leu) n.2364A>T | |
| 14 | g.23425723T>C | CA389048806 | MYH7 | c.2258A>G (p.His753Arg) n.2364A>G | dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.23425723T>G | CA389048807 | MYH7 | c.2258A>C (p.His753Pro) n.2364A>C | |
| 14 | g.23425723T= | CA2123458192 | MYH7 | c.2258A= (p.His753=) n.2364A= | |
| 14 | g.23425724G>A | CA389048808 | MYH7 | c.2257C>T (p.His753Tyr) n.2363C>T | |
| 14 | g.23425724G>C | CA257820658 | MYH7 | c.2257C>G (p.His753Asp) n.2363C>G | dbSNP |
| 14 | g.23425724G= | CA2123458196 | MYH7 | c.2257C= (p.His753=) n.2363C= | |
| 14 | g.23425724G>T | CA389048809 | MYH7 | c.2257C>A (p.His753Asn) n.2363C>A | |
| 14 | g.23425725A= | CA2123458198 | MYH7 | c.2256T= (p.Asp752=) n.2362T= | |
| 14 | g.23425725A>C | CA389048810 | MYH7 | c.2256T>G (p.Asp752Glu) n.2362T>G | |
| 14 | g.23425725A>G | CA257820663 | MYH7 | c.2256T>C (p.Asp752=) n.2362T>C | dbSNP gnomAD v4 |
| 14 | g.23425725A>T | CA389048811 | MYH7 | c.2256T>A (p.Asp752Glu) n.2362T>A | |
| 14 | g.23425726T>A | CA389048813 | MYH7 | c.2255A>T (p.Asp752Val) n.2361A>T | |
| 14 | g.23425726T>C | CA389048814 | MYH7 | c.2255A>G (p.Asp752Gly) n.2361A>G | |
| 14 | g.23425726T>G | CA389048812 | MYH7 | c.2255A>C (p.Asp752Ala) n.2361A>C | |
| 14 | g.23425727C>A | CA389048817 | MYH7 | c.2254G>T (p.Asp752Tyr) n.2360G>T | |
| 14 | g.23425727C= | CA2123458200 | MYH7 | c.2254G= (p.Asp752=) n.2360G= | |
| 14 | g.23425727C>G | CA389048815 | MYH7 | c.2254G>C (p.Asp752His) n.2360G>C | COSMIC |
| 14 | g.23425727C>T | CA389048816 | MYH7 | c.2254G>A (p.Asp752Asn) n.2360G>A | dbSNP |
| 14 | g.23425728A>C | CA389048818 | MYH7 | c.2253T>G (p.Ile751Met) n.2359T>G | |
| 14 | g.23425728A>G | CA485766906 | MYH7 | c.2253T>C (p.Ile751=) n.2359T>C | gnomAD v4 |
| 14 | g.23425728A>T | CA485766905 | MYH7 | c.2253T>A (p.Ile751=) n.2359T>A | |
| 14 | g.23425729A= | CA2123458202 | MYH7 | c.2252T= (p.Ile751=) n.2358T= | |
| 14 | g.23425729A>C | CA389048819 | MYH7 | c.2252T>G (p.Ile751Ser) n.2358T>G | |
| 14 | g.23425729A>G | CA389048820 | MYH7 | c.2252T>C (p.Ile751Thr) n.2358T>C | ClinVar dbSNP |
| 14 | g.23425729A>T | CA389048821 | MYH7 | c.2252T>A (p.Ile751Asn) n.2358T>A | |
| 14 | g.23425730T>A | CA389048822 | MYH7 | c.2251A>T (p.Ile751Phe) n.2357A>T | ClinVar dbSNP |
| 14 | g.23425730T>C | CA389048823 | MYH7 | c.2251A>G (p.Ile751Val) n.2357A>G | ClinVar dbSNP |
| 14 | g.23425730T>G | CA389048824 | MYH7 | c.2251A>C (p.Ile751Leu) n.2357A>C | |
| 14 | g.23425730T= | CA2123458213 | MYH7 | c.2251A= (p.Ile751=) n.2357A= | |
| 14 | g.23425731G>A | CA257820668 | MYH7 | c.2250C>T (p.Asp750=) n.2356C>T | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.23425731G>C | CA389048825 | MYH7 | c.2250C>G (p.Asp750Glu) n.2356C>G | |
| 14 | g.23425731G= | CA2123458222 | MYH7 | c.2250C= (p.Asp750=) n.2356C= | |
| 14 | g.23425731G>T | CA389048826 | MYH7 | c.2250C>A (p.Asp750Glu) n.2356C>A | |
| 14 | g.23425732T>A | CA389048828 | MYH7 | c.2249A>T (p.Asp750Val) n.2355A>T | |
| 14 | g.23425732T>C | CA389048829 | MYH7 | c.2249A>G (p.Asp750Gly) n.2355A>G | gnomAD v4 |
| 14 | g.23425732T>G | CA389048827 | MYH7 | c.2249A>C (p.Asp750Ala) n.2355A>C | |
| 14 | g.23425733C>A | CA389048830 | MYH7 | c.2248G>T (p.Asp750Tyr) n.2354G>T | |
| 14 | g.23425733C= | CA2123458226 | MYH7 | c.2248G= (p.Asp750=) n.2354G= | |
| 14 | g.23425733C>G | CA389048831 | MYH7 | c.2248G>C (p.Asp750His) n.2354G>C | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.23425733C>T | CA389048832 | MYH7 | c.2248G>A (p.Asp750Asn) n.2354G>A | dbSNP |
| 14 | g.23425734del | CA2624230225 | MYH7 | c.2248del (p.Asp750ThrfsTer27) n.2354del | gnomAD v4 |
| 14 | g.23425734C>A | CA485766916 | MYH7 | c.2247G>T (p.Leu749=) n.2353G>T | |
| 14 | g.23425734C>G | CA485766917 | MYH7 | c.2247G>C (p.Leu749=) n.2353G>C | ClinVar |
| 14 | g.23425734C>T | CA485766918 | MYH7 | c.2247G>A (p.Leu749=) n.2353G>A | ClinVar dbSNP |
| 14 | g.23425735A= | CA2123458230 | MYH7 | c.2246T= (p.Leu749=) n.2352T= | |
| 14 | g.23425735A>C | CA389048833 | MYH7 | c.2246T>G (p.Leu749Arg) n.2352T>G | |
| 14 | g.23425735A>G | CA389048834 | MYH7 | c.2246T>C (p.Leu749Pro) n.2352T>C | |
| 14 | g.23425735A>T | CA012055 | MYH7 | c.2246T>A (p.Leu749Gln) n.2352T>A | ClinVar dbSNP |
| 14 | g.23425736G>A | CA485766919 | MYH7 | c.2245C>T (p.Leu749=) n.2351C>T | ClinVar |
| 14 | g.23425736G>C | CA389048835 | MYH7 | c.2245C>G (p.Leu749Val) n.2351C>G | |
| 14 | g.23425736G>T | CA389048836 | MYH7 | c.2245C>A (p.Leu749Met) n.2351C>A | |
| 14 | g.23425737G>A | CA485766923 | MYH7 | c.2244C>T (p.Ser748=) n.2350C>T | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23425737G>C | CA485766924 | MYH7 | c.2244C>G (p.Ser748=) n.2350C>G | |
| 14 | g.23425737G= | CA2123458240 | MYH7 | c.2244C= (p.Ser748=) n.2350C= | |
| 14 | g.23425737G>T | CA485766925 | MYH7 | c.2244C>A (p.Ser748=) n.2350C>A | |
| 14 | g.23425738G>A | CA389048837 | MYH7 | c.2243C>T (p.Ser748Phe) n.2349C>T | |
| 14 | g.23425738G>C | CA389048838 | MYH7 | c.2243C>G (p.Ser748Cys) n.2349C>G | |
| 14 | g.23425738G>T | CA389048839 | MYH7 | c.2243C>A (p.Ser748Tyr) n.2349C>A | |
| 14 | g.23425738_23425739delinsAT | CA2580088002 | MYH7 | c.2242_2243delinsAT (p.Ser748Ile) n.2348_2349delinsAT | ClinVar |
| 14 | g.23425739A= | CA2123458246 | MYH7 | c.2242T= (p.Ser748=) n.2348T= | |
| 14 | g.23425739A>C | CA389048840 | MYH7 | c.2242T>G (p.Ser748Ala) n.2348T>G | |
| 14 | g.23425739A>G | CA10576958 | MYH7 | c.2242T>C (p.Ser748Pro) n.2348T>C | ClinVar dbSNP |
| 14 | g.23425739A>T | CA389048841 | MYH7 | c.2242T>A (p.Ser748Thr) n.2348T>A | gnomAD v4 |
| 14 | g.23425740G>A | CA485766930 | MYH7 | c.2241C>T (p.Ser747=) n.2347C>T | dbSNP gnomAD v4 |
| 14 | g.23425740G>C | CA389048842 | MYH7 | c.2241C>G (p.Ser747Arg) n.2347C>G | |
| 14 | g.23425740G= | CA2123458252 | MYH7 | c.2241C= (p.Ser747=) n.2347C= | |
| 14 | g.23425740G>T | CA389048843 | MYH7 | c.2241C>A (p.Ser747Arg) n.2347C>A | |
| 14 | g.23425741C>A | CA389048844 | MYH7 | c.2240G>T (p.Ser747Ile) n.2346G>T | |
| 14 | g.23425741C>G | CA389048845 | MYH7 | c.2240G>C (p.Ser747Thr) n.2346G>C | |
| 14 | g.23425741C>T | CA389048846 | MYH7 | c.2240G>A (p.Ser747Asn) n.2346G>A | |
| 14 | g.23425742T>A | CA389048847 | MYH7 | c.2239A>T (p.Ser747Cys) n.2345A>T | gnomAD v4 |
| 14 | g.23425742T>C | CA389048848 | MYH7 | c.2239A>G (p.Ser747Gly) n.2345A>G | dbSNP |
| 14 | g.23425742T>G | CA389048849 | MYH7 | c.2239A>C (p.Ser747Arg) n.2345A>C | |
| 14 | g.23425742T= | CA2123458256 | MYH7 | c.2239A= (p.Ser747=) n.2345A= | |
| 14 | g.23425743G>A | CA031861 | MYH7 | c.2238C>T (p.Leu746=) n.2344C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23425743G>C | CA485766938 | MYH7 | c.2238C>G (p.Leu746=) n.2344C>G | dbSNP |
| 14 | g.23425743G= | CA2123458259 | MYH7 | c.2238C= (p.Leu746=) n.2344C= | |
| 14 | g.23425743G>T | CA485766940 | MYH7 | c.2238C>A (p.Leu746=) n.2344C>A | gnomAD v4 |
| 14 | g.23425744A>C | CA389048850 | MYH7 | c.2237T>G (p.Leu746Arg) n.2343T>G | |
| 14 | g.23425744A>G | CA389048851 | MYH7 | c.2237T>C (p.Leu746Pro) n.2343T>C | |
| 14 | g.23425744A>T | CA389048852 | MYH7 | c.2237T>A (p.Leu746His) n.2343T>A | |
| 14 | g.23425745G>A | CA389048853 | MYH7 | c.2236C>T (p.Leu746Phe) n.2342C>T | ClinVar |
| 14 | g.23425745G>C | CA389048854 | MYH7 | c.2236C>G (p.Leu746Val) n.2342C>G | |
| 14 | g.23425745G>T | CA389048855 | MYH7 | c.2236C>A (p.Leu746Ile) n.2342C>A | |
| 14 | g.23425746C>A | CA485766945 | MYH7 | c.2235G>T (p.Leu745=) n.2341G>T | |
| 14 | g.23425746C= | CA2123458262 | MYH7 | c.2235G= (p.Leu745=) n.2341G= | |
| 14 | g.23425746C>G | CA257820684 | MYH7 | c.2235G>C (p.Leu745=) n.2341G>C | ClinVar dbSNP |
| 14 | g.23425746C>T | CA485766948 | MYH7 | c.2235G>A (p.Leu745=) n.2341G>A | |
| 14 | g.23425747A>C | CA389048858 | MYH7 | c.2234T>G (p.Leu745Arg) n.2340T>G | |
| 14 | g.23425747A>G | CA389048856 | MYH7 | c.2234T>C (p.Leu745Pro) n.2340T>C | |
| 14 | g.23425747A>T | CA389048857 | MYH7 | c.2234T>A (p.Leu745Gln) n.2340T>A | |
| 14 | g.23425748G>A | CA031847 | MYH7 | c.2233C>T (p.Leu745=) n.2339C>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.23425748G>C | CA389048859 | MYH7 | c.2233C>G (p.Leu745Val) n.2339C>G | |
| 14 | g.23425748G= | CA2123458264 | MYH7 | c.2233C= (p.Leu745=) n.2339C= | |
| 14 | g.23425748G>T | CA389048860 | MYH7 | c.2233C>A (p.Leu745Met) n.2339C>A | |
| 14 | g.23425749C>A | CA389048861 | MYH7 | c.2232G>T (p.Lys744Asn) n.2338G>T | dbSNP gnomAD v4 |
| 14 | g.23425749C= | CA2123458267 | MYH7 | c.2232G= (p.Lys744=) n.2338G= | |
| 14 | g.23425749C>G | CA389048862 | MYH7 | c.2232G>C (p.Lys744Asn) n.2338G>C | dbSNP |
| 14 | g.23425749C>T | CA031829 | MYH7 | c.2232G>A (p.Lys744=) n.2338G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23425750T>A | CA389048863 | MYH7 | c.2231A>T (p.Lys744Met) n.2337A>T | |
| 14 | g.23425750T>C | CA389048864 | MYH7 | c.2231A>G (p.Lys744Arg) n.2337A>G | |
| 14 | g.23425750T>G | CA389048865 | MYH7 | c.2231A>C (p.Lys744Thr) n.2337A>C | ClinVar dbSNP |
| 14 | g.23425751T>A | CA389048866 | MYH7 | c.2230A>T (p.Lys744Ter) n.2336A>T | ClinVar dbSNP gnomAD v4 |
| 14 | g.23425751T>C | CA389048867 | MYH7 | c.2230A>G (p.Lys744Glu) n.2336A>G | |
| 14 | g.23425751T>G | CA389048868 | MYH7 | c.2230A>C (p.Lys744Gln) n.2336A>C | dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.23425751T= | CA2123458276 | MYH7 | c.2230A= (p.Lys744=) n.2336A= | |
| 14 | g.23425752C>A | CA389048869 | MYH7 | c.2229G>T (p.Glu743Asp) n.2335G>T | |
| 14 | g.23425752C= | CA2123458288 | MYH7 | c.2229G= (p.Glu743=) n.2335G= | |
| 14 | g.23425752C>G | CA012046 | MYH7 | c.2229G>C (p.Glu743Asp) n.2335G>C | ClinVar dbSNP |
| 14 | g.23425752C>T | CA012039 | MYH7 | c.2229G>A (p.Glu743=) n.2335G>A | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 14 | g.23425753T>A | CA389048870 | MYH7 | c.2228A>T (p.Glu743Val) n.2334A>T | |
| 14 | g.23425753T>C | CA389048872 | MYH7 | c.2228A>G (p.Glu743Gly) n.2334A>G | ClinVar dbSNP |
| 14 | g.23425753T>G | CA389048871 | MYH7 | c.2228A>C (p.Glu743Ala) n.2334A>C | |
| 14 | g.23425753T= | CA2123458292 | MYH7 | c.2228A= (p.Glu743=) n.2334A= | |
| 14 | g.23425754C>A | CA389048873 | MYH7 | c.2227G>T (p.Glu743Ter) n.2333G>T | |
| 14 | g.23425754C>G | CA389048874 | MYH7 | c.2227G>C (p.Glu743Gln) n.2333G>C | COSMIC |
| 14 | g.23425754C>T | CA389048875 | MYH7 | c.2227G>A (p.Glu743Lys) n.2333G>A | gnomAD v4 |
| 14 | g.23425755T>A | CA485766954 | MYH7 | c.2226A>T (p.Ala742=) n.2332A>T | dbSNP |
| 14 | g.23425755T>C | CA485766955 | MYH7 | c.2226A>G (p.Ala742=) n.2332A>G | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.23425755T>G | CA485766957 | MYH7 | c.2226A>C (p.Ala742=) n.2332A>C | |
| 14 | g.23425755T= | CA2123458295 | MYH7 | c.2226A= (p.Ala742=) n.2332A= | |
| 14 | g.23425756G>A | CA389048876 | MYH7 | c.2225C>T (p.Ala742Val) n.2331C>T | |
| 14 | g.23425756G>C | CA389048877 | MYH7 | c.2225C>G (p.Ala742Gly) n.2331C>G | dbSNP |
| 14 | g.23425756G= | CA2123458299 | MYH7 | c.2225C= (p.Ala742=) n.2331C= | |
| 14 | g.23425756G>T | CA012029 | MYH7 | c.2225C>A (p.Ala742Glu) n.2331C>A | ClinVar dbSNP |
| 14 | g.23425757C>A | CA389048878 | MYH7 | c.2224G>T (p.Ala742Ser) n.2330G>T | |
| 14 | g.23425757C= | CA2123458305 | MYH7 | c.2224G= (p.Ala742=) n.2330G= | |
| 14 | g.23425757C>G | CA389048879 | MYH7 | c.2224G>C (p.Ala742Pro) n.2330G>C | ClinVar dbSNP |
| 14 | g.23425757C>T | CA031805 | MYH7 | c.2224G>A (p.Ala742Thr) n.2330G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.23425758C>A | CA485766962 | MYH7 | c.2223G>T (p.Gly741=) n.2329G>T | |
| 14 | g.23425758C>G | CA485766961 | MYH7 | c.2223G>C (p.Gly741=) n.2329G>C | |
| 14 | g.23425758C>T | CA485766960 | MYH7 | c.2223G>A (p.Gly741=) n.2329G>A | |
| 14 | g.23425758_23425762delinsCCCCT | CA2123458310 | MYH7 | c.2219_2223delinsAGGGG (p.Lys740=) n.2325_2329delinsAGGGG | |
| 14 | g.23425759C>A | CA389048880 | MYH7 | c.2222G>T (p.Gly741Val) n.2328G>T | |
| 14 | g.23425759C= | CA2123458313 | MYH7 | c.2222G= (p.Gly741=) n.2328G= | |
| 14 | g.23425759C>G | CA389048881 | MYH7 | c.2222G>C (p.Gly741Ala) n.2328G>C | |
| 14 | g.23425759C>T | CA16606949 | MYH7 | c.2222G>A (p.Gly741Glu) n.2328G>A | ClinVar dbSNP |
| 14 | g.23425759_23425762del | CA961068348 | MYH7 | c.2219_2222del (p.Lys740ArgfsTer?) n.2325_2328del | dbSNP gnomAD v3 gnomAD v4 |
| 14 | g.23425760C>A | CA012022 | MYH7 | c.2221G>T (p.Gly741Trp) n.2327G>T | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 14 | g.23425760C= | CA2123458327 | MYH7 | c.2221G= (p.Gly741=) n.2327G= | |
| 14 | g.23425760C>G | CA012013 | MYH7 | c.2221G>C (p.Gly741Arg) n.2327G>C | ClinVar dbSNP gnomAD v4 |
| 14 | g.23425760C>T | CA012004 | MYH7 | c.2221G>A (p.Gly741Arg) n.2327G>A | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23425760_23425761delinsAA | CA2580088004 | MYH7 | c.2220_2221delinsTT (p.Lys740_Gly741delinsAsnTrp) n.2326_2327delinsTT | ClinVar |
| 14 | g.23425761C>A | CA389048882 | MYH7 | c.2220G>T (p.Lys740Asn) n.2326G>T | ClinVar dbSNP gnomAD v4 |
| 14 | g.23425761C= | CA2123458359 | MYH7 | c.2220G= (p.Lys740=) n.2326G= | |
| 14 | g.23425761C>G | CA389048883 | MYH7 | c.2220G>C (p.Lys740Asn) n.2326G>C | ClinVar |
| 14 | g.23425761C>T | CA485766967 | MYH7 | c.2220G>A (p.Lys740=) n.2326G>A | dbSNP |
| 14 | g.23425762T>A | CA389048884 | MYH7 | c.2219A>T (p.Lys740Met) n.2325A>T | |
| 14 | g.23425762T>C | CA389048885 | MYH7 | c.2219A>G (p.Lys740Arg) n.2325A>G | |
| 14 | g.23425762T>G | CA389048886 | MYH7 | c.2219A>C (p.Lys740Thr) n.2325A>C | |
| 14 | g.23425763T>A | CA389048887 | MYH7 | c.2218A>T (p.Lys740Ter) n.2324A>T | |
| 14 | g.23425763T>C | CA389048888 | MYH7 | c.2218A>G (p.Lys740Glu) n.2324A>G | |
| 14 | g.23425763T>G | CA389048889 | MYH7 | c.2218A>C (p.Lys740Gln) n.2324A>C | |
| 14 | g.23425764C>A | CA011985 | MYH7 | c.2217G>T (p.Arg739Ser) n.2323G>T | ClinVar dbSNP |
| 14 | g.23425764C= | CA2123458372 | MYH7 | c.2217G= (p.Arg739=) n.2323G= | |
| 14 | g.23425764C>G | CA389048890 | MYH7 | c.2217G>C (p.Arg739Ser) n.2323G>C | ClinVar dbSNP |
| 14 | g.23425764C>T | CA257820727 | MYH7 | c.2217G>A (p.Arg739=) n.2323G>A | ClinVar dbSNP gnomAD v4 |
| 14 | g.23425765C>A | CA389048891 | MYH7 | c.2216G>T (p.Arg739Met) n.2322G>T | |
| 14 | g.23425765C>G | CA389048892 | MYH7 | c.2216G>C (p.Arg739Thr) n.2322G>C | |
| 14 | g.23425765C>T | CA389048893 | MYH7 | c.2216G>A (p.Arg739Lys) n.2322G>A | |
| 14 | g.23425766T>A | CA389048894 | MYH7 | c.2215A>T (p.Arg739Trp) n.2321A>T | |
| 14 | g.23425766T>C | CA389048895 | MYH7 | c.2215A>G (p.Arg739Gly) n.2321A>G | ClinVar dbSNP |
| 14 | g.23425766T>G | CA485766972 | MYH7 | c.2215A>C (p.Arg739=) n.2321A>C | |
| 14 | g.23425766T= | CA2123458387 | MYH7 | c.2215A= (p.Arg739=) n.2321A= | |
| 14 | g.23425767G>A | CA485766973 | MYH7 | c.2214C>T (p.Ser738=) n.2320C>T | |
| 14 | g.23425767G>C | CA389048896 | MYH7 | c.2214C>G (p.Ser738Arg) n.2320C>G | ClinVar dbSNP |
| 14 | g.23425767G= | CA2123458391 | MYH7 | c.2214C= (p.Ser738=) n.2320C= | |
| 14 | g.23425767G>T | CA389048897 | MYH7 | c.2214C>A (p.Ser738Arg) n.2320C>A | ClinVar |
| 14 | g.23425768C>A | CA389048898 | MYH7 | c.2213G>T (p.Ser738Ile) n.2319G>T | |
| 14 | g.23425768C= | CA2123458407 | MYH7 | c.2213G= (p.Ser738=) n.2319G= | |
| 14 | g.23425768C>G | CA011976 | MYH7 | c.2213G>C (p.Ser738Thr) n.2319G>C | ClinVar dbSNP |
| 14 | g.23425768C>T | CA389048899 | MYH7 | c.2213G>A (p.Ser738Asn) n.2319G>A | ClinVar dbSNP |
| 14 | g.23425769T>A | CA16619851 | MYH7 | c.2212A>T (p.Ser738Cys) n.2318A>T | ClinVar dbSNP |
| 14 | g.23425769T>C | CA389048900 | MYH7 | c.2212A>G (p.Ser738Gly) n.2318A>G | |
| 14 | g.23425769T>G | CA389048901 | MYH7 | c.2212A>C (p.Ser738Arg) n.2318A>C | |
| 14 | g.23425769T= | CA2123458415 | MYH7 | c.2212A= (p.Ser738=) n.2318A= | |
| 14 | g.23425770A= | CA2123458422 | MYH7 | c.2211T= (p.Asp737=) n.2317T= | |
| 14 | g.23425770A>C | CA389048902 | MYH7 | c.2211T>G (p.Asp737Glu) n.2317T>G | |
| 14 | g.23425770A>G | CA485766977 | MYH7 | c.2211T>C (p.Asp737=) n.2317T>C | ClinVar dbSNP gnomAD v4 |
| 14 | g.23425770A>T | CA389048903 | MYH7 | c.2211T>A (p.Asp737Glu) n.2317T>A | |
| 14 | g.23425771T>A | CA389048904 | MYH7 | c.2210A>T (p.Asp737Val) n.2316A>T | |
| 14 | g.23425771T>C | CA389048905 | MYH7 | c.2210A>G (p.Asp737Gly) n.2316A>G | |
| 14 | g.23425771T>G | CA389048906 | MYH7 | c.2210A>C (p.Asp737Ala) n.2316A>C | |
| 14 | g.23425772C>A | CA16619852 | MYH7 | c.2209G>T (p.Asp737Tyr) n.2315G>T | ClinVar dbSNP |
| 14 | g.23425772C= | CA2123458427 | MYH7 | c.2209G= (p.Asp737=) n.2315G= | |
| 14 | g.23425772C>G | CA389048908 | MYH7 | c.2209G>C (p.Asp737His) n.2315G>C | |
| 14 | g.23425772C>T | CA389048907 | MYH7 | c.2209G>A (p.Asp737Asn) n.2315G>A | |
| 14 | g.23425772_23425779del | CA2624230353 | MYH7 | c.2202_2209del (p.Phe735Ter) n.2308_2315del | gnomAD v4 |
| 14 | g.23425773A= | CA2123458433 | MYH7 | c.2208T= (p.Ile736=) n.2314T= | |
| 14 | g.23425773A>C | CA389048909 | MYH7 | c.2208T>G (p.Ile736Met) n.2314T>G | gnomAD v4 |
| 14 | g.23425773A>G | CA031791 | MYH7 | c.2208T>C (p.Ile736=) n.2314T>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23425773A>T | CA485766978 | MYH7 | c.2208T>A (p.Ile736=) n.2314T>A | dbSNP |
| 14 | g.23425774A= | CA2123458449 | MYH7 | c.2207T= (p.Ile736=) n.2313T= | |
| 14 | g.23425774A>C | CA389048910 | MYH7 | c.2207T>G (p.Ile736Ser) n.2313T>G | |
| 14 | g.23425774A>G | CA011970 | MYH7 | c.2207T>C (p.Ile736Thr) n.2313T>C | ClinVar dbSNP |
| 14 | g.23425774A>T | CA011964 | MYH7 | c.2207T>A (p.Ile736Asn) n.2313T>A | ClinVar dbSNP |
| 14 | g.23425775T>A | CA389048912 | MYH7 | c.2206A>T (p.Ile736Phe) n.2312A>T | ClinVar dbSNP |
| 14 | g.23425775T>C | CA011954 | MYH7 | c.2206A>G (p.Ile736Val) n.2312A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23425775T>G | CA389048911 | MYH7 | c.2206A>C (p.Ile736Leu) n.2312A>C | |
| 14 | g.23425775T= | CA2123458460 | MYH7 | c.2206A= (p.Ile736=) n.2312A= | |
| 14 | g.23425776G>A | CA485766981 | MYH7 | c.2205C>T (p.Phe735=) n.2311C>T | gnomAD v4 |
| 14 | g.23425776G>C | CA389048913 | MYH7 | c.2205C>G (p.Phe735Leu) n.2311C>G | ClinVar |
| 14 | g.23425776G>T | CA389048914 | MYH7 | c.2205C>A (p.Phe735Leu) n.2311C>A | |
| 14 | g.23425777A>C | CA389048915 | MYH7 | c.2204T>G (p.Phe735Cys) n.2310T>G | |
| 14 | g.23425777A>G | CA389048916 | MYH7 | c.2204T>C (p.Phe735Ser) n.2310T>C | |
| 14 | g.23425777A>T | CA389048917 | MYH7 | c.2204T>A (p.Phe735Tyr) n.2310T>A | |
| 14 | g.23425778A= | CA2123458464 | MYH7 | c.2203T= (p.Phe735=) n.2309T= | |
| 14 | g.23425778A>C | CA389048918 | MYH7 | c.2203T>G (p.Phe735Val) n.2309T>G | |
| 14 | g.23425778A>G | CA16614410 | MYH7 | c.2203T>C (p.Phe735Leu) n.2309T>C | ClinVar dbSNP |
| 14 | g.23425778A>T | CA389048919 | MYH7 | c.2203T>A (p.Phe735Ile) n.2309T>A | |
| 14 | g.23425779C>A | CA389048920 | MYH7 | c.2202G>T (p.Gln734His) n.2308G>T | |
| 14 | g.23425779C= | CA2123458466 | MYH7 | c.2202G= (p.Gln734=) n.2308G= | |
| 14 | g.23425779C>G | CA389048921 | MYH7 | c.2202G>C (p.Gln734His) n.2308G>C | |
| 14 | g.23425779C>T | CA485766986 | MYH7 | c.2202G>A (p.Gln734=) n.2308G>A | dbSNP gnomAD v4 |
| 14 | g.23425780T>A | CA389048922 | MYH7 | c.2201A>T (p.Gln734Leu) n.2307A>T | ClinVar |
| 14 | g.23425780T>C | CA389048923 | MYH7 | c.2201A>G (p.Gln734Arg) n.2307A>G | |
| 14 | g.23425780T>G | CA279297 | MYH7 | c.2201A>C (p.Gln734Pro) n.2307A>C | ClinVar dbSNP |
| 14 | g.23425780T= | CA2123458475 | MYH7 | c.2201A= (p.Gln734=) n.2307A= | |
| 14 | g.23425780dup | CA915947000 | MYH7 | c.2201dup (p.Phe735ValfsTer3) n.2307dup | ClinVar dbSNP gnomAD v4 |
| 14 | g.23425781G>A | CA389048924 | MYH7 | c.2200C>T (p.Gln734Ter) n.2306C>T | |
| 14 | g.23425781G>C | CA389048925 | MYH7 | c.2200C>G (p.Gln734Glu) n.2306C>G | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.23425781G= | CA2123458489 | MYH7 | c.2200C= (p.Gln734=) n.2306C= | |
| 14 | g.23425781G>T | CA389048926 | MYH7 | c.2200C>A (p.Gln734Lys) n.2306C>A | |
| 14 | g.23425781_23425783dup | CA011944 | MYH7 | c.2198_2200dup (p.Gly733_Gln734insArg) n.2304_2306dup | ClinVar dbSNP |
| 14 | g.23425782T>A | CA485766992 | MYH7 | c.2199A>T (p.Gly733=) n.2305A>T | ClinVar dbSNP gnomAD v4 |
| 14 | g.23425782T>C | CA485766993 | MYH7 | c.2199A>G (p.Gly733=) n.2305A>G | dbSNP |
| 14 | g.23425782T>G | CA485766995 | MYH7 | c.2199A>C (p.Gly733=) n.2305A>C | dbSNP |
| 14 | g.23425782T= | CA2123458498 | MYH7 | c.2199A= (p.Gly733=) n.2305A= | |
| 14 | g.23425783C>A | CA011936 | MYH7 | c.2198G>T (p.Gly733Val) n.2304G>T | ClinVar dbSNP |
| 14 | g.23425783C= | CA2123458503 | MYH7 | c.2198G= (p.Gly733=) n.2304G= | |
| 14 | g.23425783C>G | CA389048927 | MYH7 | c.2198G>C (p.Gly733Ala) n.2304G>C | |
| 14 | g.23425783C>T | CA011928 | MYH7 | c.2198G>A (p.Gly733Glu) n.2304G>A | ClinVar dbSNP |
| 14 | g.23425784C>A | CA389048930 | MYH7 | c.2197G>T (p.Gly733Ter) n.2303G>T | |
| 14 | g.23425784C>G | CA389048928 | MYH7 | c.2197G>C (p.Gly733Arg) n.2303G>C | gnomAD v4 |
| 14 | g.23425784C>T | CA389048929 | MYH7 | c.2197G>A (p.Gly733Arg) n.2303G>A | ClinVar gnomAD v4 |
| 14 | g.23425785C>A | CA389048931 | MYH7 | c.2196G>T (p.Glu732Asp) n.2302G>T | |
| 14 | g.23425785C= | CA2123458510 | MYH7 | c.2196G= (p.Glu732=) n.2302G= | |
| 14 | g.23425785C>G | CA389048932 | MYH7 | c.2196G>C (p.Glu732Asp) n.2302G>C | ClinVar dbSNP |
| 14 | g.23425785C>T | CA485766999 | MYH7 | c.2196G>A (p.Glu732=) n.2302G>A | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 14 | g.23425786T>A | CA389048933 | MYH7 | c.2195A>T (p.Glu732Val) n.2301A>T | |
| 14 | g.23425786T>C | CA389048934 | MYH7 | c.2195A>G (p.Glu732Gly) n.2301A>G | |
| 14 | g.23425786T>G | CA389048935 | MYH7 | c.2195A>C (p.Glu732Ala) n.2301A>C | |
| 14 | g.23425787C>A | CA389048936 | MYH7 | c.2194G>T (p.Glu732Ter) n.2300G>T | |
| 14 | g.23425787C= | CA2123458516 | MYH7 | c.2194G= (p.Glu732=) n.2300G= | |
| 14 | g.23425787C>G | CA389048937 | MYH7 | c.2194G>C (p.Glu732Gln) n.2300G>C | |
| 14 | g.23425787C>T | CA389048938 | MYH7 | c.2194G>A (p.Glu732Lys) n.2300G>A | dbSNP gnomAD v2 |
| 14 | g.23425788A= | CA2123458520 | MYH7 | c.2193T= (p.Pro731=) n.2299T= | |
| 14 | g.23425788A>C | CA485767000 | MYH7 | c.2193T>G (p.Pro731=) n.2299T>G | |
| 14 | g.23425788A>G | CA485767002 | MYH7 | c.2193T>C (p.Pro731=) n.2299T>C | dbSNP |
| 14 | g.23425788A>T | CA485767003 | MYH7 | c.2193T>A (p.Pro731=) n.2299T>A | gnomAD v4 |
| 14 | g.23425789G>A | CA389048939 | MYH7 | c.2192C>T (p.Pro731Leu) n.2298C>T | ClinVar dbSNP COSMIC |
| 14 | g.23425789G>C | CA389048940 | MYH7 | c.2192C>G (p.Pro731Arg) n.2298C>G | ClinVar dbSNP |
| 14 | g.23425789G= | CA2123458529 | MYH7 | c.2192C= (p.Pro731=) n.2298C= | |
| 14 | g.23425789G>T | CA389048941 | MYH7 | c.2192C>A (p.Pro731His) n.2298C>A | |
| 14 | g.23425790G>A | CA011922 | MYH7 | c.2191C>T (p.Pro731Ser) n.2297C>T | ClinVar dbSNP COSMIC |
| 14 | g.23425790G>C | CA011914 | MYH7 | c.2191C>G (p.Pro731Ala) n.2297C>G | ClinVar dbSNP |
| 14 | g.23425790G= | CA2123458539 | MYH7 | c.2191C= (p.Pro731=) n.2297C= | |
| 14 | g.23425790G>T | CA16603250 | MYH7 | c.2191C>A (p.Pro731Thr) n.2297C>A | ClinVar dbSNP |
| 14 | g.23425791G>A | CA485767005 | MYH7 | c.2190C>T (p.Ile730=) n.2296C>T | |
| 14 | g.23425791G>C | CA389048942 | MYH7 | c.2190C>G (p.Ile730Met) n.2296C>G | |
| 14 | g.23425791G>T | CA485767007 | MYH7 | c.2190C>A (p.Ile730=) n.2296C>A | |
| 14 | g.23425792A= | CA2123458550 | MYH7 | c.2189T= (p.Ile730=) n.2295T= | |
| 14 | g.23425792A>C | CA389048943 | MYH7 | c.2189T>G (p.Ile730Ser) n.2295T>G | |
| 14 | g.23425792A>G | CA16614089 | MYH7 | c.2189T>C (p.Ile730Thr) n.2295T>C | ClinVar dbSNP |
| 14 | g.23425792A>T | CA389048944 | MYH7 | c.2189T>A (p.Ile730Asn) n.2295T>A | ClinVar dbSNP |
| 14 | g.23425793T>A | CA389048945 | MYH7 | c.2188A>T (p.Ile730Phe) n.2294A>T | |
| 14 | g.23425793T>C | CA389048946 | MYH7 | c.2188A>G (p.Ile730Val) n.2294A>G | |
| 14 | g.23425793T>G | CA389048947 | MYH7 | c.2188A>C (p.Ile730Leu) n.2294A>C | |
| 14 | g.23425794G>A | CA485767012 | MYH7 | c.2187C>T (p.Ala729=) n.2293C>T | |
| 14 | g.23425794G>C | CA485767010 | MYH7 | c.2187C>G (p.Ala729=) n.2293C>G | |
| 14 | g.23425794G= | CA2123458585 | MYH7 | c.2187C= (p.Ala729=) n.2293C= | |
| 14 | g.23425794G>T | CA011910 | MYH7 | c.2187C>A (p.Ala729=) n.2293C>A | ClinVar dbSNP |
| 14 | g.23425795G>A | CA389048948 | MYH7 | c.2186C>T (p.Ala729Val) n.2292C>T | gnomAD v4 |
| 14 | g.23425795G>C | CA389048949 | MYH7 | c.2186C>G (p.Ala729Gly) n.2292C>G | |
| 14 | g.23425795G>T | CA389048950 | MYH7 | c.2186C>A (p.Ala729Asp) n.2292C>A | |
| 14 | g.23425796C>A | CA389048951 | MYH7 | c.2185G>T (p.Ala729Ser) n.2291G>T | |
| 14 | g.23425796C>G | CA389048952 | MYH7 | c.2185G>C (p.Ala729Pro) n.2291G>C | |
| 14 | g.23425796C>T | CA389048953 | MYH7 | c.2185G>A (p.Ala729Thr) n.2291G>A | |
| 14 | g.23425797C>A | CA485767013 | MYH7 | c.2184G>T (p.Ala728=) n.2290G>T | |
| 14 | g.23425797C= | CA2123458597 | MYH7 | c.2184G= (p.Ala728=) n.2290G= | |
| 14 | g.23425797C>G | CA16606950 | MYH7 | c.2184G>C (p.Ala728=) n.2290G>C | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 14 | g.23425797C>T | CA011905 | MYH7 | c.2184G>A (p.Ala728=) n.2290G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23425798G>A | CA011896 | MYH7 | c.2183C>T (p.Ala728Val) n.2289C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 14 | g.[23425798G>A;23427657C>T] | CA658682652 | MYH7 | c.[1816G>A;2183C>T] (p.[Val606Met;Ala728Val]) n.[1922G>A;2289C>T] | |
| 14 | g.23425798G>C | CA389048954 | MYH7 | c.2183C>G (p.Ala728Gly) n.2289C>G | |
| 14 | g.23425798G= | CA2123458608 | MYH7 | c.2183C= (p.Ala728=) n.2289C= | |
| 14 | g.23425798G>T | CA389048955 | MYH7 | c.2183C>A (p.Ala728Glu) n.2289C>A | |
| 14 | g.23425799C>A | CA389048956 | MYH7 | c.2182G>T (p.Ala728Ser) n.2288G>T | |
| 14 | g.23425799C>G | CA389048957 | MYH7 | c.2182G>C (p.Ala728Pro) n.2288G>C | |
| 14 | g.23425799C>T | CA389048958 | MYH7 | c.2182G>A (p.Ala728Thr) n.2288G>A | |
| 14 | g.23425800T>A | CA485767015 | MYH7 | c.2181A>T (p.Pro727=) n.2287A>T | |
| 14 | g.23425800T>C | CA011889 | MYH7 | c.2181A>G (p.Pro727=) n.2287A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.23425800T>G | CA485767016 | MYH7 | c.2181A>C (p.Pro727=) n.2287A>C | |
| 14 | g.23425800T= | CA2123458621 | MYH7 | c.2181A= (p.Pro727=) n.2287A= | |
| 14 | g.23425801G>A | CA389048959 | MYH7 | c.2180C>T (p.Pro727Leu) n.2286C>T | dbSNP |
| 14 | g.23425801G>C | CA389048960 | MYH7 | c.2180C>G (p.Pro727Arg) n.2286C>G | |
| 14 | g.23425801G= | CA2123458624 | MYH7 | c.2180C= (p.Pro727=) n.2286C= | |
| 14 | g.23425801G>T | CA389048961 | MYH7 | c.2180C>A (p.Pro727Gln) n.2286C>A | |
| 14 | g.23425802G>A | CA389048962 | MYH7 | c.2179C>T (p.Pro727Ser) n.2285C>T | |
| 14 | g.23425802G>C | CA389048963 | MYH7 | c.2179C>G (p.Pro727Ala) n.2285C>G | |
| 14 | g.23425802G>T | CA389048964 | MYH7 | c.2179C>A (p.Pro727Thr) n.2285C>A | |
| 14 | g.23425803G>A | CA485767023 | MYH7 | c.2178C>T (p.Asn726=) n.2284C>T | ClinVar dbSNP |
| 14 | g.23425803G>C | CA389048965 | MYH7 | c.2178C>G (p.Asn726Lys) n.2284C>G | |
| 14 | g.23425803G= | CA2123458631 | MYH7 | c.2178C= (p.Asn726=) n.2284C= | |
| 14 | g.23425803G>T | CA011879 | MYH7 | c.2178C>A (p.Asn726Lys) n.2284C>A | ClinVar dbSNP |
| 14 | g.23425804T>A | CA389048966 | MYH7 | c.2177A>T (p.Asn726Ile) n.2283A>T | |
| 14 | g.23425804T>C | CA031716 | MYH7 | c.2177A>G (p.Asn726Ser) n.2283A>G | dbSNP ExAC gnomAD v2 |
| 14 | g.23425804T>G | CA389048967 | MYH7 | c.2177A>C (p.Asn726Thr) n.2283A>C | |
| 14 | g.23425804T= | CA2123458636 | MYH7 | c.2177A= (p.Asn726=) n.2283A= | |
| 14 | g.23425805T>A | CA389048968 | MYH7 | c.2176A>T (p.Asn726Tyr) n.2282A>T | |
| 14 | g.23425805T>C | CA389048970 | MYH7 | c.2176A>G (p.Asn726Asp) n.2282A>G | |
| 14 | g.23425805T>G | CA389048969 | MYH7 | c.2176A>C (p.Asn726His) n.2282A>C | |
| 14 | g.23425806C>A | CA485767027 | MYH7 | c.2175G>T (p.Leu725=) n.2281G>T | |
| 14 | g.23425806C>G | CA485767029 | MYH7 | c.2175G>C (p.Leu725=) n.2281G>C | |
| 14 | g.23425806C>T | CA485767028 | MYH7 | c.2175G>A (p.Leu725=) n.2281G>A | gnomAD v4 |
| 14 | g.23425807A= | CA2123458642 | MYH7 | c.2174T= (p.Leu725=) n.2280T= | |
| 14 | g.23425807A>C | CA389048971 | MYH7 | c.2174T>G (p.Leu725Arg) n.2280T>G | |
| 14 | g.23425807A>G | CA011873 | MYH7 | c.2174T>C (p.Leu725Pro) n.2280T>C | ClinVar dbSNP |
| 14 | g.23425807A>T | CA389048972 | MYH7 | c.2174T>A (p.Leu725Gln) n.2280T>A | |
| 14 | g.23425808G>A | CA485767033 | MYH7 | c.2173C>T (p.Leu725=) n.2279C>T | |
| 14 | g.23425808G>C | CA389048973 | MYH7 | c.2173C>G (p.Leu725Val) n.2279C>G | |
| 14 | g.23425808G>T | CA389048974 | MYH7 | c.2173C>A (p.Leu725Met) n.2279C>A | |
| 14 | g.23425809G>A | CA257820818 | MYH7 | c.2172C>T (p.Ile724=) n.2278C>T | dbSNP COSMIC |
| 14 | g.23425809G>C | CA389048975 | MYH7 | c.2172C>G (p.Ile724Met) n.2278C>G | |
| 14 | g.23425809G= | CA2123458653 | MYH7 | c.2172C= (p.Ile724=) n.2278C= | |
| 14 | g.23425809G>T | CA031699 | MYH7 | c.2172C>A (p.Ile724=) n.2278C>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23425810A= | CA2123458659 | MYH7 | c.2171T= (p.Ile724=) n.2277T= | |
| 14 | g.23425810A>C | CA389048976 | MYH7 | c.2171T>G (p.Ile724Ser) n.2277T>G | |
| 14 | g.23425810A>G | CA389048977 | MYH7 | c.2171T>C (p.Ile724Thr) n.2277T>C | dbSNP |
| 14 | g.23425810A>T | CA011864 | MYH7 | c.2171T>A (p.Ile724Asn) n.2277T>A | ClinVar dbSNP |
| 14 | g.23425811T>A | CA389048980 | MYH7 | c.2170A>T (p.Ile724Phe) n.2276A>T | |
| 14 | g.23425811T>C | CA389048978 | MYH7 | c.2170A>G (p.Ile724Val) n.2276A>G | |
| 14 | g.23425811T>G | CA389048979 | MYH7 | c.2170A>C (p.Ile724Leu) n.2276A>C | |
| 14 | g.23425812G>A | CA485767036 | MYH7 | c.2169C>T (p.Arg723=) n.2275C>T | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23425812G>C | CA485767037 | MYH7 | c.2169C>G (p.Arg723=) n.2275C>G | |
| 14 | g.23425812G= | CA2123458663 | MYH7 | c.2169C= (p.Arg723=) n.2275C= | |
| 14 | g.23425812G>T | CA485767039 | MYH7 | c.2169C>A (p.Arg723=) n.2275C>A | ClinVar dbSNP gnomAD v4 |
| 14 | g.23425813C>A | CA389048981 | MYH7 | c.2168G>T (p.Arg723Leu) n.2274G>T | ClinVar |
| 14 | g.23425813C= | CA2123458669 | MYH7 | c.2168G= (p.Arg723=) n.2274G= | |
| 14 | g.23425813C>G | CA389048982 | MYH7 | c.2168G>C (p.Arg723Pro) n.2274G>C | dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.23425813C>T | CA011859 | MYH7 | c.2168G>A (p.Arg723His) n.2274G>A | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 14 | g.23425814G>A | CA011851 | MYH7 | c.2167C>T (p.Arg723Cys) n.2273C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23425814G>C | CA011843 | MYH7 | c.2167C>G (p.Arg723Gly) n.2273C>G | ClinVar dbSNP |
| 14 | g.23425814G= | CA2123458678 | MYH7 | c.2167C= (p.Arg723=) n.2273C= | |
| 14 | g.23425814G>T | CA389048983 | MYH7 | c.2167C>A (p.Arg723Ser) n.2273C>A | |
| 14 | g.23425815A= | CA2123458685 | MYH7 | c.2166T= (p.Tyr722=) n.2272T= | |
| 14 | g.23425815A>C | CA389048984 | MYH7 | c.2166T>G (p.Tyr722Ter) n.2272T>G | |
| 14 | g.23425815A>G | CA485767041 | MYH7 | c.2166T>C (p.Tyr722=) n.2272T>C | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 14 | g.23425815A>T | CA389048985 | MYH7 | c.2166T>A (p.Tyr722Ter) n.2272T>A | |
| 14 | g.23425816T>A | CA389048986 | MYH7 | c.2165A>T (p.Tyr722Phe) n.2271A>T | |
| 14 | g.23425816T>C | CA389048987 | MYH7 | c.2165A>G (p.Tyr722Cys) n.2271A>G | |
| 14 | g.23425816T>G | CA389048988 | MYH7 | c.2165A>C (p.Tyr722Ser) n.2271A>C |