| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 14 | g.23430894G>A | CA704268993 | MYH7 | c.895+7C>T (n.895+7C>T) n.1001+7C>T | dbSNP gnomAD v3 gnomAD v4 |
| 14 | g.23430894G= | CA2123450270 | MYH7 | c.895+7C= (n.895+7C=) n.1001+7C= | |
| 14 | g.23430894G>T | CA2624250547 | MYH7 | c.895+7C>A (n.895+7C>A) n.1001+7C>A | gnomAD v4 |
| 14 | g.23430895A>T | CA2575486691 | MYH7 | c.895+6T>A (n.895+6T>A) n.1001+6T>A | |
| 14 | g.23430896C= | CA2123450274 | MYH7 | c.895+5G= (n.895+5G=) n.1001+5G= | |
| 14 | g.23430896C>G | CA2499222597 | MYH7 | c.895+5G>C (n.895+5G>C) n.1001+5G>C | ClinVar dbSNP |
| 14 | g.23430896C>T | CA049524 | MYH7 | c.895+5G>A (n.895+5G>A) n.1001+5G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.23430897T>G | CA257825584 | MYH7 | c.895+4A>C (n.895+4A>C) n.1001+4A>C | dbSNP |
| 14 | g.23430897T= | CA2123450284 | MYH7 | c.895+4A= (n.895+4A=) n.1001+4A= | |
| 14 | g.23430898C>A | CA2580087876 | MYH7 | c.895+3G>T (n.895+3G>T) n.1001+3G>T | ClinVar gnomAD v4 |
| 14 | g.23430898C= | CA2123450291 | MYH7 | c.895+3G= (n.895+3G=) n.1001+3G= | |
| 14 | g.23430898C>T | CA612938305 | MYH7 | c.895+3G>A (n.895+3G>A) n.1001+3G>A | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.23430899A= | CA2123450304 | MYH7 | c.895+2T= (n.895+2T=) n.1001+2T= | |
| 14 | g.23430899A>C | CA389051808 | MYH7 | c.895+2T>G (n.895+2T>G) n.1001+2T>G | |
| 14 | g.23430899A>G | CA257825586 | MYH7 | c.895+2T>C (n.895+2T>C) n.1001+2T>C | dbSNP |
| 14 | g.23430899A>T | CA257825588 | MYH7 | c.895+2T>A (n.895+2T>A) n.1001+2T>A | dbSNP |
| 14 | g.23430900C>A | CA389051809 | MYH7 | c.895+1G>T (n.895+1G>T) n.1001+1G>T | |
| 14 | g.23430900C= | CA2123450312 | MYH7 | c.895+1G= (n.895+1G=) n.1001+1G= | |
| 14 | g.23430900C>G | CA257825590 | MYH7 | c.895+1G>C (n.895+1G>C) n.1001+1G>C | dbSNP |
| 14 | g.23430900C>T | CA257825592 | MYH7 | c.895+1G>A (n.895+1G>A) n.1001+1G>A | ClinVar dbSNP COSMIC |
| 14 | g.23430901C>A | CA389051810 | MYH7 | c.895G>T (p.Asp299Tyr) n.1001G>T | |
| 14 | g.23430901C= | CA2123450326 | MYH7 | c.895G= (p.Asp299=) n.1001G= | |
| 14 | g.23430901C>G | CA389051811 | MYH7 | c.895G>C (p.Asp299His) n.1001G>C | ClinVar dbSNP |
| 14 | g.23430901C>T | CA16614097 | MYH7 | c.895G>A (p.Asp299Asn) n.1001G>A | ClinVar dbSNP gnomAD v4 |
| 14 | g.23430902C>A | CA485626153 | MYH7 | c.894G>T (p.Leu298=) n.1000G>T | |
| 14 | g.23430902C= | CA2123450332 | MYH7 | c.894G= (p.Leu298=) n.1000G= | |
| 14 | g.23430902C>G | CA485626154 | MYH7 | c.894G>C (p.Leu298=) n.1000G>C | |
| 14 | g.23430902C>T | CA049428 | MYH7 | c.894G>A (p.Leu298=) n.1000G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23430903A>C | CA389051812 | MYH7 | c.893T>G (p.Leu298Arg) n.999T>G | |
| 14 | g.23430903A>G | CA389051813 | MYH7 | c.893T>C (p.Leu298Pro) n.999T>C | |
| 14 | g.23430903A>T | CA389051814 | MYH7 | c.893T>A (p.Leu298Gln) n.999T>A | gnomAD v4 |
| 14 | g.23430904G>A | CA485626155 | MYH7 | c.892C>T (p.Leu298=) n.998C>T | |
| 14 | g.23430904G>C | CA389051815 | MYH7 | c.892C>G (p.Leu298Val) n.998C>G | |
| 14 | g.23430904G>T | CA389051816 | MYH7 | c.892C>A (p.Leu298Met) n.998C>A | |
| 14 | g.23430905C>A | CA485626156 | MYH7 | c.891G>T (p.Leu297=) n.997G>T | |
| 14 | g.23430905C>G | CA485626158 | MYH7 | c.891G>C (p.Leu297=) n.997G>C | |
| 14 | g.23430905C>T | CA485626157 | MYH7 | c.891G>A (p.Leu297=) n.997G>A | |
| 14 | g.23430906A>C | CA389051817 | MYH7 | c.890T>G (p.Leu297Arg) n.996T>G | |
| 14 | g.23430906A>G | CA389051818 | MYH7 | c.890T>C (p.Leu297Pro) n.996T>C | |
| 14 | g.23430906A>T | CA389051819 | MYH7 | c.890T>A (p.Leu297Gln) n.996T>A | COSMIC |
| 14 | g.23430907G>A | CA485626159 | MYH7 | c.889C>T (p.Leu297=) n.995C>T | |
| 14 | g.23430907G>C | CA389051820 | MYH7 | c.889C>G (p.Leu297Val) n.995C>G | |
| 14 | g.23430907G>T | CA389051821 | MYH7 | c.889C>A (p.Leu297Met) n.995C>A | gnomAD v4 COSMIC |
| 14 | g.23430908C>A | CA389051822 | MYH7 | c.888G>T (p.Glu296Asp) n.994G>T | |
| 14 | g.23430908C>G | CA389051823 | MYH7 | c.888G>C (p.Glu296Asp) n.994G>C | |
| 14 | g.23430908C>T | CA485626161 | MYH7 | c.888G>A (p.Glu296=) n.994G>A | |
| 14 | g.23430909T>A | CA389051824 | MYH7 | c.887A>T (p.Glu296Val) n.993A>T | |
| 14 | g.23430909T>C | CA389051826 | MYH7 | c.887A>G (p.Glu296Gly) n.993A>G | |
| 14 | g.23430909T>G | CA389051825 | MYH7 | c.887A>C (p.Glu296Ala) n.993A>C | |
| 14 | g.23430910C>A | CA389051827 | MYH7 | c.886G>T (p.Glu296Ter) n.992G>T | |
| 14 | g.23430910C>G | CA389051828 | MYH7 | c.886G>C (p.Glu296Gln) n.992G>C | |
| 14 | g.23430910C>T | CA389051829 | MYH7 | c.886G>A (p.Glu296Lys) n.992G>A | |
| 14 | g.23430911A= | CA2123450338 | MYH7 | c.885T= (p.Pro295=) n.991T= | |
| 14 | g.23430911A>C | CA485626164 | MYH7 | c.885T>G (p.Pro295=) n.991T>G | |
| 14 | g.23430911A>G | CA257825596 | MYH7 | c.885T>C (p.Pro295=) n.991T>C | dbSNP |
| 14 | g.23430911A>T | CA485626166 | MYH7 | c.885T>A (p.Pro295=) n.991T>A | |
| 14 | g.23430912G>A | CA389051830 | MYH7 | c.884C>T (p.Pro295Leu) n.990C>T | |
| 14 | g.23430912G>C | CA389051831 | MYH7 | c.884C>G (p.Pro295Arg) n.990C>G | |
| 14 | g.23430912G>T | CA389051832 | MYH7 | c.884C>A (p.Pro295His) n.990C>A | |
| 14 | g.23430913G>A | CA389051833 | MYH7 | c.883C>T (p.Pro295Ser) n.989C>T | |
| 14 | g.23430913G>C | CA389051834 | MYH7 | c.883C>G (p.Pro295Ala) n.989C>G | |
| 14 | g.23430913G= | CA2123450344 | MYH7 | c.883C= (p.Pro295=) n.989C= | |
| 14 | g.23430913G>T | CA16614498 | MYH7 | c.883C>A (p.Pro295Thr) n.989C>A | ClinVar dbSNP gnomAD v2 |
| 14 | g.23430914C>A | CA389051835 | MYH7 | c.882G>T (p.Lys294Asn) n.988G>T | |
| 14 | g.23430914C>G | CA389051836 | MYH7 | c.882G>C (p.Lys294Asn) n.988G>C | |
| 14 | g.23430914C>T | CA485626169 | MYH7 | c.882G>A (p.Lys294=) n.988G>A | |
| 14 | g.23430914_23430915delinsCT | CA2123450349 | MYH7 | c.881_882delinsAG (p.Lys294=) n.987_988delinsAG | |
| 14 | g.23430915T>A | CA389051837 | MYH7 | c.881A>T (p.Lys294Met) n.987A>T | |
| 14 | g.23430915T>C | CA389051838 | MYH7 | c.881A>G (p.Lys294Arg) n.987A>G | |
| 14 | g.23430915T>G | CA389051839 | MYH7 | c.881A>C (p.Lys294Thr) n.987A>C | |
| 14 | g.23430919del | CA257825598 | MYH7 | c.881del (p.Lys294SerfsTer9) n.987del | dbSNP |
| 14 | g.23430916T>A | CA389051840 | MYH7 | c.880A>T (p.Lys294Ter) n.986A>T | |
| 14 | g.23430916T>C | CA389051841 | MYH7 | c.880A>G (p.Lys294Glu) n.986A>G | gnomAD v4 |
| 14 | g.23430916T>G | CA389051842 | MYH7 | c.880A>C (p.Lys294Gln) n.986A>C | |
| 14 | g.23430917T>A | CA389051843 | MYH7 | c.879A>T (p.Lys293Asn) n.985A>T | |
| 14 | g.23430917T>C | CA485626173 | MYH7 | c.879A>G (p.Lys293=) n.985A>G | |
| 14 | g.23430917T>G | CA389051844 | MYH7 | c.879A>C (p.Lys293Asn) n.985A>C | |
| 14 | g.23430918T>A | CA389051845 | MYH7 | c.878A>T (p.Lys293Ile) n.984A>T | |
| 14 | g.23430918T>C | CA389051846 | MYH7 | c.878A>G (p.Lys293Arg) n.984A>G | ClinVar dbSNP |
| 14 | g.23430918T>G | CA389051847 | MYH7 | c.878A>C (p.Lys293Thr) n.984A>C | |
| 14 | g.23430918T= | CA2123450355 | MYH7 | c.878A= (p.Lys293=) n.984A= | |
| 14 | g.23430919T>A | CA389051848 | MYH7 | c.877A>T (p.Lys293Ter) n.983A>T | |
| 14 | g.23430919T>C | CA389051849 | MYH7 | c.877A>G (p.Lys293Glu) n.983A>G | |
| 14 | g.23430919T>G | CA389051850 | MYH7 | c.877A>C (p.Lys293Gln) n.983A>C | |
| 14 | g.23430920G>A | CA485626175 | MYH7 | c.876C>T (p.Asn292=) n.982C>T | |
| 14 | g.23430920G>C | CA389051851 | MYH7 | c.876C>G (p.Asn292Lys) n.982C>G | |
| 14 | g.23430920G>T | CA389051852 | MYH7 | c.876C>A (p.Asn292Lys) n.982C>A | |
| 14 | g.23430921T>A | CA389051853 | MYH7 | c.875A>T (p.Asn292Ile) n.981A>T | |
| 14 | g.23430921T>C | CA389051854 | MYH7 | c.875A>G (p.Asn292Ser) n.981A>G | |
| 14 | g.23430921T>G | CA049402 | MYH7 | c.875A>C (p.Asn292Thr) n.981A>C | dbSNP ExAC gnomAD v2 |
| 14 | g.23430921T= | CA2123450366 | MYH7 | c.875A= (p.Asn292=) n.981A= | |
| 14 | g.23430922del | CA2575486693 | MYH7 | c.875del (p.Asn292ThrfsTer11) n.981del | |
| 14 | g.23430922T>A | CA389051855 | MYH7 | c.874A>T (p.Asn292Tyr) n.980A>T | |
| 14 | g.23430922T>C | CA389051856 | MYH7 | c.874A>G (p.Asn292Asp) n.980A>G | |
| 14 | g.23430922T>G | CA389051857 | MYH7 | c.874A>C (p.Asn292His) n.980A>C | |
| 14 | g.23430923A>C | CA485626178 | MYH7 | c.873T>G (p.Ser291=) n.979T>G | |
| 14 | g.23430923A>G | CA485626179 | MYH7 | c.873T>C (p.Ser291=) n.979T>C | dbSNP |
| 14 | g.23430923A>T | CA485626180 | MYH7 | c.873T>A (p.Ser291=) n.979T>A | |
| 14 | g.23430925_23430928del | CA2573149872 | MYH7 | c.870_873del (p.Ser291ThrfsTer11) n.976_979del | ClinVar dbSNP |
| 14 | g.23430924G>A | CA016918 | MYH7 | c.872C>T (p.Ser291Phe) n.978C>T | ClinVar dbSNP gnomAD v4 |
| 14 | g.23430924G>C | CA389051858 | MYH7 | c.872C>G (p.Ser291Cys) n.978C>G | |
| 14 | g.23430924G= | CA2123450374 | MYH7 | c.872C= (p.Ser291=) n.978C= | |
| 14 | g.23430924G>T | CA389051859 | MYH7 | c.872C>A (p.Ser291Tyr) n.978C>A | |
| 14 | g.23430925A= | CA2123450385 | MYH7 | c.871T= (p.Ser291=) n.977T= | |
| 14 | g.23430925A>C | CA389051860 | MYH7 | c.871T>G (p.Ser291Ala) n.977T>G | |
| 14 | g.23430925A>G | CA016911 | MYH7 | c.871T>C (p.Ser291Pro) n.977T>C | ClinVar dbSNP |
| 14 | g.23430925A>T | CA389051861 | MYH7 | c.871T>A (p.Ser291Thr) n.977T>A | |
| 14 | g.23430926C>A | CA485626187 | MYH7 | c.870G>T (p.Leu290=) n.976G>T | |
| 14 | g.23430926C= | CA2123450396 | MYH7 | c.870G= (p.Leu290=) n.976G= | |
| 14 | g.23430926C>G | CA049393 | MYH7 | c.870G>C (p.Leu290=) n.976G>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.23430926C>T | CA10587177 | MYH7 | c.870G>A (p.Leu290=) n.976G>A | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 14 | g.23430927A>C | CA389051862 | MYH7 | c.869T>G (p.Leu290Arg) n.975T>G | |
| 14 | g.23430927A>G | CA389051864 | MYH7 | c.869T>C (p.Leu290Pro) n.975T>C | |
| 14 | g.23430927A>T | CA389051863 | MYH7 | c.869T>A (p.Leu290Gln) n.975T>A | |
| 14 | g.23430928G>A | CA485626189 | MYH7 | c.868C>T (p.Leu290=) n.974C>T | dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.23430928G>C | CA389051865 | MYH7 | c.868C>G (p.Leu290Val) n.974C>G | |
| 14 | g.23430928G= | CA2123450404 | MYH7 | c.868C= (p.Leu290=) n.974C= | |
| 14 | g.23430928G>T | CA389051866 | MYH7 | c.868C>A (p.Leu290Met) n.974C>A | |
| 14 | g.23430929G>A | CA485626190 | MYH7 | c.867C>T (p.Ile289=) n.973C>T | COSMIC |
| 14 | g.23430929G>C | CA389051867 | MYH7 | c.867C>G (p.Ile289Met) n.973C>G | |
| 14 | g.23430929G= | CA2123450410 | MYH7 | c.867C= (p.Ile289=) n.973C= | |
| 14 | g.23430929G>T | CA485626191 | MYH7 | c.867C>A (p.Ile289=) n.973C>A | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.23430930A>C | CA389051868 | MYH7 | c.866T>G (p.Ile289Ser) n.972T>G | |
| 14 | g.23430930A>G | CA389051869 | MYH7 | c.866T>C (p.Ile289Thr) n.972T>C | |
| 14 | g.23430930A>T | CA389051870 | MYH7 | c.866T>A (p.Ile289Asn) n.972T>A | |
| 14 | g.23430931T>A | CA389051871 | MYH7 | c.865A>T (p.Ile289Phe) n.971A>T | |
| 14 | g.23430931T>C | CA389051872 | MYH7 | c.865A>G (p.Ile289Val) n.971A>G | dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.23430931T>G | CA389051873 | MYH7 | c.865A>C (p.Ile289Leu) n.971A>C | |
| 14 | g.23430931T= | CA2123450413 | MYH7 | c.865A= (p.Ile289=) n.971A= | |
| 14 | g.23430932T>A | CA389051874 | MYH7 | c.864A>T (p.Gln288His) n.970A>T | |
| 14 | g.23430932T>C | CA485626192 | MYH7 | c.864A>G (p.Gln288=) n.970A>G | |
| 14 | g.23430932T>G | CA389051875 | MYH7 | c.864A>C (p.Gln288His) n.970A>C | |
| 14 | g.23430933T>A | CA389051876 | MYH7 | c.863A>T (p.Gln288Leu) n.969A>T | |
| 14 | g.23430933T>C | CA389051877 | MYH7 | c.863A>G (p.Gln288Arg) n.969A>G | ClinVar |
| 14 | g.23430933T>G | CA389051878 | MYH7 | c.863A>C (p.Gln288Pro) n.969A>C | |
| 14 | g.23430934G>A | CA389051879 | MYH7 | c.862C>T (p.Gln288Ter) n.968C>T | ClinVar |
| 14 | g.23430934G>C | CA389051881 | MYH7 | c.862C>G (p.Gln288Glu) n.968C>G | dbSNP |
| 14 | g.23430934G= | CA2123450421 | MYH7 | c.862C= (p.Gln288=) n.968C= | |
| 14 | g.23430934G>T | CA389051880 | MYH7 | c.862C>A (p.Gln288Lys) n.968C>A | |
| 14 | g.23430935G>A | CA485626193 | MYH7 | c.861C>T (p.Tyr287=) n.967C>T | dbSNP gnomAD v4 |
| 14 | g.23430935G>C | CA389051882 | MYH7 | c.861C>G (p.Tyr287Ter) n.967C>G | |
| 14 | g.23430935G= | CA2123450424 | MYH7 | c.861C= (p.Tyr287=) n.967C= | |
| 14 | g.23430935G>T | CA389051883 | MYH7 | c.861C>A (p.Tyr287Ter) n.967C>A | |
| 14 | g.23430936T>A | CA389051884 | MYH7 | c.860A>T (p.Tyr287Phe) n.966A>T | |
| 14 | g.23430936T>C | CA016907 | MYH7 | c.860A>G (p.Tyr287Cys) n.966A>G | ClinVar dbSNP |
| 14 | g.23430936T>G | CA389051885 | MYH7 | c.860A>C (p.Tyr287Ser) n.966A>C | |
| 14 | g.23430936T= | CA2123450429 | MYH7 | c.860A= (p.Tyr287=) n.966A= | |
| 14 | g.23430937A= | CA2123450435 | MYH7 | c.859T= (p.Tyr287=) n.965T= | |
| 14 | g.23430937A>C | CA389051886 | MYH7 | c.859T>G (p.Tyr287Asp) n.965T>G | |
| 14 | g.23430937A>G | CA016905 | MYH7 | c.859T>C (p.Tyr287His) n.965T>C | ClinVar dbSNP |
| 14 | g.23430937A>T | CA389051887 | MYH7 | c.859T>A (p.Tyr287Asn) n.965T>A | |
| 14 | g.23430938G>A | CA485626195 | MYH7 | c.858C>T (p.Phe286=) n.964C>T | |
| 14 | g.23430938G>C | CA389051888 | MYH7 | c.858C>G (p.Phe286Leu) n.964C>G | |
| 14 | g.23430938G>T | CA389051889 | MYH7 | c.858C>A (p.Phe286Leu) n.964C>A | |
| 14 | g.23430939A= | CA2123450441 | MYH7 | c.857T= (p.Phe286=) n.963T= | |
| 14 | g.23430939A>C | CA389051891 | MYH7 | c.857T>G (p.Phe286Cys) n.963T>G | ClinVar dbSNP |
| 14 | g.23430939A>G | CA389051892 | MYH7 | c.857T>C (p.Phe286Ser) n.963T>C | ClinVar dbSNP |
| 14 | g.23430939A>T | CA389051890 | MYH7 | c.857T>A (p.Phe286Tyr) n.963T>A | |
| 14 | g.23430940A>C | CA389051893 | MYH7 | c.856T>G (p.Phe286Val) n.962T>G | |
| 14 | g.23430940A>G | CA389051894 | MYH7 | c.856T>C (p.Phe286Leu) n.962T>C | |
| 14 | g.23430940A>T | CA389051895 | MYH7 | c.856T>A (p.Phe286Ile) n.962T>A | gnomAD v4 |
| 14 | g.23430941A>C | CA389051896 | MYH7 | c.855T>G (p.Ile285Met) n.961T>G | |
| 14 | g.23430941A>G | CA485626196 | MYH7 | c.855T>C (p.Ile285=) n.961T>C | |
| 14 | g.23430941A>T | CA485626197 | MYH7 | c.855T>A (p.Ile285=) n.961T>A | |
| 14 | g.23430942A= | CA2123450448 | MYH7 | c.854T= (p.Ile285=) n.960T= | |
| 14 | g.23430942A>C | CA389051897 | MYH7 | c.854T>G (p.Ile285Ser) n.960T>G | |
| 14 | g.23430942A>G | CA389051898 | MYH7 | c.854T>C (p.Ile285Thr) n.960T>C | ClinVar dbSNP |
| 14 | g.23430942A>T | CA389051899 | MYH7 | c.854T>A (p.Ile285Asn) n.960T>A | |
| 14 | g.23430943T>A | CA389051900 | MYH7 | c.853A>T (p.Ile285Phe) n.959A>T | |
| 14 | g.23430943T>C | CA049384 | MYH7 | c.853A>G (p.Ile285Val) n.959A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23430943T>G | CA389051901 | MYH7 | c.853A>C (p.Ile285Leu) n.959A>C | ClinVar |
| 14 | g.23430943T= | CA2123450460 | MYH7 | c.853A= (p.Ile285=) n.959A= | |
| 14 | g.23430944G>A | CA485626198 | MYH7 | c.852C>T (p.His284=) n.958C>T | gnomAD v4 |
| 14 | g.23430944G>C | CA389051902 | MYH7 | c.852C>G (p.His284Gln) n.958C>G | |
| 14 | g.23430944G>T | CA389051903 | MYH7 | c.852C>A (p.His284Gln) n.958C>A | |
| 14 | g.23430945T>A | CA389051906 | MYH7 | c.851A>T (p.His284Leu) n.957A>T | |
| 14 | g.23430945T>C | CA389051904 | MYH7 | c.851A>G (p.His284Arg) n.957A>G | |
| 14 | g.23430945T>G | CA389051905 | MYH7 | c.851A>C (p.His284Pro) n.957A>C | |
| 14 | g.23430946G>A | CA389051907 | MYH7 | c.850C>T (p.His284Tyr) n.956C>T | ClinVar |
| 14 | g.23430946G>C | CA389051908 | MYH7 | c.850C>G (p.His284Asp) n.956C>G | |
| 14 | g.23430946G>T | CA389051909 | MYH7 | c.850C>A (p.His284Asn) n.956C>A | |
| 14 | g.23430947A>C | CA389051910 | MYH7 | c.849T>G (p.Tyr283Ter) n.955T>G | |
| 14 | g.23430947A>G | CA485626199 | MYH7 | c.849T>C (p.Tyr283=) n.955T>C | gnomAD v4 |
| 14 | g.23430947A>T | CA389051911 | MYH7 | c.849T>A (p.Tyr283Ter) n.955T>A | |
| 14 | g.23430948T>A | CA389051912 | MYH7 | c.848A>T (p.Tyr283Phe) n.954A>T | |
| 14 | g.23430948T>C | CA016898 | MYH7 | c.848A>G (p.Tyr283Cys) n.954A>G | ClinVar dbSNP |
| 14 | g.23430948T>G | CA389051913 | MYH7 | c.848A>C (p.Tyr283Ser) n.954A>C | |
| 14 | g.23430948T= | CA2123450469 | MYH7 | c.848A= (p.Tyr283=) n.954A= | |
| 14 | g.23430949A= | CA2123450473 | MYH7 | c.847T= (p.Tyr283=) n.953T= | |
| 14 | g.23430949A>C | CA016893 | MYH7 | c.847T>G (p.Tyr283Asp) n.953T>G | ClinVar dbSNP |
| 14 | g.23430949A>G | CA389051914 | MYH7 | c.847T>C (p.Tyr283His) n.953T>C | |
| 14 | g.23430949A>T | CA389051915 | MYH7 | c.847T>A (p.Tyr283Asn) n.953T>A | ClinVar |
| 14 | g.23430950A>C | CA389051916 | MYH7 | c.846T>G (p.Asp282Glu) n.952T>G | |
| 14 | g.23430950A>G | CA485626200 | MYH7 | c.846T>C (p.Asp282=) n.952T>C | |
| 14 | g.23430950A>T | CA389051917 | MYH7 | c.846T>A (p.Asp282Glu) n.952T>A | |
| 14 | g.23430951T>A | CA389051919 | MYH7 | c.845A>T (p.Asp282Val) n.951A>T | |
| 14 | g.23430951T>C | CA389051920 | MYH7 | c.845A>G (p.Asp282Gly) n.951A>G | |
| 14 | g.23430951T>G | CA389051918 | MYH7 | c.845A>C (p.Asp282Ala) n.951A>C | |
| 14 | g.23430952C>A | CA016885 | MYH7 | c.844G>T (p.Asp282Tyr) n.950G>T | ClinVar dbSNP |
| 14 | g.23430952C= | CA2123450484 | MYH7 | c.844G= (p.Asp282=) n.950G= | |
| 14 | g.23430952C>G | CA389051921 | MYH7 | c.844G>C (p.Asp282His) n.950G>C | |
| 14 | g.23430952C>T | CA389051922 | MYH7 | c.844G>A (p.Asp282Asn) n.950G>A | gnomAD v4 |
| 14 | g.23430953T>A | CA389051923 | MYH7 | c.843A>T (p.Arg281Ser) n.949A>T | |
| 14 | g.23430953T>C | CA485626201 | MYH7 | c.843A>G (p.Arg281=) n.949A>G | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23430953T>G | CA389051924 | MYH7 | c.843A>C (p.Arg281Ser) n.949A>C | |
| 14 | g.23430953T= | CA2123450490 | MYH7 | c.843A= (p.Arg281=) n.949A= | |
| 14 | g.23430954C>A | CA389051925 | MYH7 | c.842G>T (p.Arg281Ile) n.948G>T | |
| 14 | g.23430954C= | CA2123450499 | MYH7 | c.842G= (p.Arg281=) n.948G= | |
| 14 | g.23430954C>G | CA016879 | MYH7 | c.842G>C (p.Arg281Thr) n.948G>C | ClinVar dbSNP gnomAD v4 |
| 14 | g.23430954C>T | CA389051926 | MYH7 | c.842G>A (p.Arg281Lys) n.948G>A | ClinVar dbSNP |
| 14 | g.23430955T>A | CA389051927 | MYH7 | c.841A>T (p.Arg281Ter) n.947A>T | |
| 14 | g.23430955T>C | CA389051928 | MYH7 | c.841A>G (p.Arg281Gly) n.947A>G | |
| 14 | g.23430955T>G | CA485626202 | MYH7 | c.841A>C (p.Arg281=) n.947A>C | |
| 14 | g.23430956C>A | CA389051929 | MYH7 | c.840G>T (p.Glu280Asp) n.946G>T | |
| 14 | g.23430956C>G | CA389051930 | MYH7 | c.840G>C (p.Glu280Asp) n.946G>C | |
| 14 | g.23430956C>T | CA485626203 | MYH7 | c.840G>A (p.Glu280=) n.946G>A | |
| 14 | g.23430957del | CA2573149873 | MYH7 | c.839del (p.Glu280GlyfsTer23) n.945del | ClinVar dbSNP |
| 14 | g.23430957T>A | CA389051931 | MYH7 | c.839A>T (p.Glu280Val) n.945A>T | |
| 14 | g.23430957T>C | CA389051932 | MYH7 | c.839A>G (p.Glu280Gly) n.945A>G | ClinVar |
| 14 | g.23430957T>G | CA389051933 | MYH7 | c.839A>C (p.Glu280Ala) n.945A>C | |
| 14 | g.23430958C>A | CA389051934 | MYH7 | c.838G>T (p.Glu280Ter) n.944G>T | |
| 14 | g.23430958C>G | CA389051936 | MYH7 | c.838G>C (p.Glu280Gln) n.944G>C | |
| 14 | g.23430958C>T | CA389051935 | MYH7 | c.838G>A (p.Glu280Lys) n.944G>A | ClinVar COSMIC |
| 14 | g.23430959T>A | CA485626204 | MYH7 | c.837A>T (p.Ala279=) n.943A>T | ClinVar dbSNP |
| 14 | g.23430959T>C | CA257825612 | MYH7 | c.837A>G (p.Ala279=) n.943A>G | dbSNP |
| 14 | g.23430959T>G | CA485626205 | MYH7 | c.837A>C (p.Ala279=) n.943A>C | |
| 14 | g.23430959T= | CA2123450505 | MYH7 | c.837A= (p.Ala279=) n.943A= | |
| 14 | g.23430960G>A | CA389051937 | MYH7 | c.836C>T (p.Ala279Val) n.942C>T | ClinVar |
| 14 | g.23430960G>C | CA389051938 | MYH7 | c.836C>G (p.Ala279Gly) n.942C>G | |
| 14 | g.23430960G>T | CA389051939 | MYH7 | c.836C>A (p.Ala279Glu) n.942C>A | |
| 14 | g.23430961C>A | CA389051940 | MYH7 | c.835G>T (p.Ala279Ser) n.941G>T | |
| 14 | g.23430961C= | CA2123450512 | MYH7 | c.835G= (p.Ala279=) n.941G= | |
| 14 | g.23430961C>G | CA389051941 | MYH7 | c.835G>C (p.Ala279Pro) n.941G>C | |
| 14 | g.23430961C>T | CA016872 | MYH7 | c.835G>A (p.Ala279Thr) n.941G>A | ClinVar dbSNP |
| 14 | g.23430962T>A | CA389051942 | MYH7 | c.834A>T (p.Lys278Asn) n.940A>T | |
| 14 | g.23430962T>C | CA485626206 | MYH7 | c.834A>G (p.Lys278=) n.940A>G | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23430962T>G | CA389051943 | MYH7 | c.834A>C (p.Lys278Asn) n.940A>C | |
| 14 | g.23430962T= | CA2123450519 | MYH7 | c.834A= (p.Lys278=) n.940A= | |
| 14 | g.23430963T>A | CA389051944 | MYH7 | c.833A>T (p.Lys278Ile) n.939A>T | |
| 14 | g.23430963T>C | CA389051945 | MYH7 | c.833A>G (p.Lys278Arg) n.939A>G | |
| 14 | g.23430963T>G | CA389051946 | MYH7 | c.833A>C (p.Lys278Thr) n.939A>C | |
| 14 | g.23430964T>A | CA389051949 | MYH7 | c.832A>T (p.Lys278Ter) n.938A>T | |
| 14 | g.23430964T>C | CA389051948 | MYH7 | c.832A>G (p.Lys278Glu) n.938A>G | |
| 14 | g.23430964T>G | CA389051947 | MYH7 | c.832A>C (p.Lys278Gln) n.938A>C | |
| 14 | g.23430965C>A | CA485626207 | MYH7 | c.831G>T (p.Leu277=) n.937G>T | |
| 14 | g.23430965C>G | CA485626208 | MYH7 | c.831G>C (p.Leu277=) n.937G>C | |
| 14 | g.23430965C>T | CA485626209 | MYH7 | c.831G>A (p.Leu277=) n.937G>A | gnomAD v4 |
| 14 | g.23430966A= | CA2123450523 | MYH7 | c.830T= (p.Leu277=) n.936T= | |
| 14 | g.23430966A>C | CA389051950 | MYH7 | c.830T>G (p.Leu277Arg) n.936T>G | |
| 14 | g.23430966A>G | CA016867 | MYH7 | c.830T>C (p.Leu277Pro) n.936T>C | ClinVar dbSNP |
| 14 | g.23430966A>T | CA389051951 | MYH7 | c.830T>A (p.Leu277Gln) n.936T>A | |
| 14 | g.23430967G>A | CA485626210 | MYH7 | c.829C>T (p.Leu277=) n.935C>T | |
| 14 | g.23430967G>C | CA016861 | MYH7 | c.829C>G (p.Leu277Val) n.935C>G | ClinVar dbSNP |
| 14 | g.23430967G= | CA2123450530 | MYH7 | c.829C= (p.Leu277=) n.935C= | |
| 14 | g.23430967G>T | CA389051952 | MYH7 | c.829C>A (p.Leu277Met) n.935C>A | |
| 14 | g.23430968C>A | CA389051953 | MYH7 | c.828G>T (p.Gln276His) n.934G>T | |
| 14 | g.23430968C= | CA2123450536 | MYH7 | c.828G= (p.Gln276=) n.934G= | |
| 14 | g.23430968C>G | CA389051954 | MYH7 | c.828G>C (p.Gln276His) n.934G>C | |
| 14 | g.23430968C>T | CA257825620 | MYH7 | c.828G>A (p.Gln276=) n.934G>A | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.23430969T>A | CA389051955 | MYH7 | c.827A>T (p.Gln276Leu) n.933A>T | |
| 14 | g.23430969T>C | CA389051956 | MYH7 | c.827A>G (p.Gln276Arg) n.933A>G | dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.23430969T>G | CA389051957 | MYH7 | c.827A>C (p.Gln276Pro) n.933A>C | |
| 14 | g.23430969T= | CA2123450541 | MYH7 | c.827A= (p.Gln276=) n.933A= | |
| 14 | g.23430970G>A | CA389051958 | MYH7 | c.826C>T (p.Gln276Ter) n.932C>T | |
| 14 | g.23430970G>C | CA389051959 | MYH7 | c.826C>G (p.Gln276Glu) n.932C>G | |
| 14 | g.23430970G>T | CA389051960 | MYH7 | c.826C>A (p.Gln276Lys) n.932C>A | |
| 14 | g.23430971G>A | CA049334 | MYH7 | c.825C>T (p.Phe275=) n.931C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 14 | g.23430971G>C | CA389051962 | MYH7 | c.825C>G (p.Phe275Leu) n.931C>G | |
| 14 | g.23430971G= | CA2123450547 | MYH7 | c.825C= (p.Phe275=) n.931C= | |
| 14 | g.23430971G>T | CA389051961 | MYH7 | c.825C>A (p.Phe275Leu) n.931C>A | gnomAD v4 |
| 14 | g.23430972A>C | CA389051963 | MYH7 | c.824T>G (p.Phe275Cys) n.930T>G | |
| 14 | g.23430972A>G | CA389051964 | MYH7 | c.824T>C (p.Phe275Ser) n.930T>C | ClinVar |
| 14 | g.23430972A>T | CA389051965 | MYH7 | c.824T>A (p.Phe275Tyr) n.930T>A | |
| 14 | g.23430973A>C | CA389051966 | MYH7 | c.823T>G (p.Phe275Val) n.929T>G | |
| 14 | g.23430973A>G | CA389051967 | MYH7 | c.823T>C (p.Phe275Leu) n.929T>C | |
| 14 | g.23430973A>T | CA389051968 | MYH7 | c.823T>A (p.Phe275Ile) n.929T>A | |
| 14 | g.23430974A>C | CA389051969 | MYH7 | c.822T>G (p.Ile274Met) n.928T>G | |
| 14 | g.23430974A>G | CA485626211 | MYH7 | c.822T>C (p.Ile274=) n.928T>C | |
| 14 | g.23430974A>T | CA485626212 | MYH7 | c.822T>A (p.Ile274=) n.928T>A | |
| 14 | g.23430975A= | CA2123450554 | MYH7 | c.821T= (p.Ile274=) n.927T= | |
| 14 | g.23430975A>C | CA389051970 | MYH7 | c.821T>G (p.Ile274Ser) n.927T>G | |
| 14 | g.23430975A>G | CA049321 | MYH7 | c.821T>C (p.Ile274Thr) n.927T>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.23430975A>T | CA389051971 | MYH7 | c.821T>A (p.Ile274Asn) n.927T>A | |
| 14 | g.23430976T>A | CA389051972 | MYH7 | c.820A>T (p.Ile274Phe) n.926A>T | |
| 14 | g.23430976T>C | CA389051973 | MYH7 | c.820A>G (p.Ile274Val) n.926A>G | gnomAD v4 |
| 14 | g.23430976T>G | CA389051974 | MYH7 | c.820A>C (p.Ile274Leu) n.926A>C | |
| 14 | g.23430977A>C | CA485626213 | MYH7 | c.819T>G (p.Val273=) n.925T>G | |
| 14 | g.23430977A>G | CA485626214 | MYH7 | c.819T>C (p.Val273=) n.925T>C | ClinVar dbSNP gnomAD v4 |
| 14 | g.23430977A>T | CA485626215 | MYH7 | c.819T>A (p.Val273=) n.925T>A | |
| 14 | g.23430978A>C | CA389051977 | MYH7 | c.818T>G (p.Val273Gly) n.924T>G | |
| 14 | g.23430978A>G | CA389051975 | MYH7 | c.818T>C (p.Val273Ala) n.924T>C | |
| 14 | g.23430978A>T | CA389051976 | MYH7 | c.818T>A (p.Val273Asp) n.924T>A | |
| 14 | g.23430978_23430980delinsACT | CA2123450558 | MYH7 | c.816_818delinsAGT (p.Arg272=) n.922_924delinsAGT | |
| 14 | g.23430979C>A | CA389051978 | MYH7 | c.817G>T (p.Val273Phe) n.923G>T | ClinVar dbSNP |
| 14 | g.23430979C= | CA2123450569 | MYH7 | c.817G= (p.Val273=) n.923G= | |
| 14 | g.23430979C>G | CA389051980 | MYH7 | c.817G>C (p.Val273Leu) n.923G>C | |
| 14 | g.23430979C>T | CA389051979 | MYH7 | c.817G>A (p.Val273Ile) n.923G>A | ClinVar dbSNP |
| 14 | g.23430981_23430982del | CA704269098 | MYH7 | c.816_817del (p.Arg272SerfsTer20) n.922_923del | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 14 | g.23430980T>A | CA389051981 | MYH7 | c.816A>T (p.Arg272Ser) n.922A>T | ClinVar |
| 14 | g.23430980T>C | CA485626216 | MYH7 | c.816A>G (p.Arg272=) n.922A>G | dbSNP gnomAD v4 |
| 14 | g.23430980T>G | CA389051982 | MYH7 | c.816A>C (p.Arg272Ser) n.922A>C | |
| 14 | g.23430980T= | CA2123450577 | MYH7 | c.816A= (p.Arg272=) n.922A= | |
| 14 | g.23430981C>A | CA389051983 | MYH7 | c.815G>T (p.Arg272Ile) n.921G>T | |
| 14 | g.23430981C= | CA2123450583 | MYH7 | c.815G= (p.Arg272=) n.921G= | |
| 14 | g.23430981C>G | CA389051985 | MYH7 | c.815G>C (p.Arg272Thr) n.921G>C | ClinVar dbSNP gnomAD v4 |
| 14 | g.23430981C>T | CA389051984 | MYH7 | c.815G>A (p.Arg272Lys) n.921G>A | |
| 14 | g.23430982T>A | CA389051986 | MYH7 | c.814A>T (p.Arg272Ter) n.920A>T | |
| 14 | g.23430982T>C | CA389051987 | MYH7 | c.814A>G (p.Arg272Gly) n.920A>G | |
| 14 | g.23430982T>G | CA485626217 | MYH7 | c.814A>C (p.Arg272=) n.920A>C | |
| 14 | g.23430983G>A | CA257825626 | MYH7 | c.813C>T (p.Ser271=) n.919C>T | ClinVar dbSNP gnomAD v4 |
| 14 | g.23430983G>C | CA485626219 | MYH7 | c.813C>G (p.Ser271=) n.919C>G | |
| 14 | g.23430983G= | CA2123450587 | MYH7 | c.813C= (p.Ser271=) n.919C= | |
| 14 | g.23430983G>T | CA485626218 | MYH7 | c.813C>A (p.Ser271=) n.919C>A | |
| 14 | g.23430984G>A | CA389051988 | MYH7 | c.812C>T (p.Ser271Phe) n.918C>T | |
| 14 | g.23430984G>C | CA389051989 | MYH7 | c.812C>G (p.Ser271Cys) n.918C>G | |
| 14 | g.23430984G>T | CA389051990 | MYH7 | c.812C>A (p.Ser271Tyr) n.918C>A | |
| 14 | g.23430985A>C | CA389051991 | MYH7 | c.811T>G (p.Ser271Ala) n.917T>G | |
| 14 | g.23430985A>G | CA389051992 | MYH7 | c.811T>C (p.Ser271Pro) n.917T>C | |
| 14 | g.23430985A>T | CA389051993 | MYH7 | c.811T>A (p.Ser271Thr) n.917T>A | |
| 14 | g.23430986T>A | CA389051994 | MYH7 | c.810A>T (p.Lys270Asn) n.916A>T | |
| 14 | g.23430986T>C | CA485626220 | MYH7 | c.810A>G (p.Lys270=) n.916A>G | |
| 14 | g.23430986T>G | CA389051995 | MYH7 | c.810A>C (p.Lys270Asn) n.916A>C | gnomAD v4 |
| 14 | g.23430990dup | CA2573149874 | MYH7 | c.810dup (p.Ser271IlefsTer22) n.916dup | ClinVar dbSNP |
| 14 | g.23430987T>A | CA389051996 | MYH7 | c.809A>T (p.Lys270Ile) n.915A>T | |
| 14 | g.23430987T>C | CA389051997 | MYH7 | c.809A>G (p.Lys270Arg) n.915A>G | dbSNP gnomAD v4 |
| 14 | g.23430987T>G | CA389051998 | MYH7 | c.809A>C (p.Lys270Thr) n.915A>C | |
| 14 | g.23430987T= | CA2123450589 | MYH7 | c.809A= (p.Lys270=) n.915A= | |
| 14 | g.23430988T>A | CA389051999 | MYH7 | c.808A>T (p.Lys270Ter) n.914A>T | |
| 14 | g.23430988T>C | CA389052000 | MYH7 | c.808A>G (p.Lys270Glu) n.914A>G | |
| 14 | g.23430988T>G | CA389052001 | MYH7 | c.808A>C (p.Lys270Gln) n.914A>C | |
| 14 | g.23430989T>A | CA389052002 | MYH7 | c.807A>T (p.Glu269Asp) n.913A>T | |
| 14 | g.23430989T>C | CA485626221 | MYH7 | c.807A>G (p.Glu269=) n.913A>G | dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.23430989T>G | CA389052003 | MYH7 | c.807A>C (p.Glu269Asp) n.913A>C | |
| 14 | g.23430989T= | CA2123450599 | MYH7 | c.807A= (p.Glu269=) n.913A= | |
| 14 | g.23430990T>A | CA389052004 | MYH7 | c.806A>T (p.Glu269Val) n.912A>T | |
| 14 | g.23430990T>C | CA389052005 | MYH7 | c.806A>G (p.Glu269Gly) n.912A>G | ClinVar |
| 14 | g.23430990T>G | CA389052006 | MYH7 | c.806A>C (p.Glu269Ala) n.912A>C | |
| 14 | g.23430991C>A | CA389052007 | MYH7 | c.805G>T (p.Glu269Ter) n.911G>T | |
| 14 | g.23430991C>G | CA389052008 | MYH7 | c.805G>C (p.Glu269Gln) n.911G>C | |
| 14 | g.23430991C>T | CA389052009 | MYH7 | c.805G>A (p.Glu269Lys) n.911G>A | COSMIC |
| 14 | g.23430992C>A | CA485626222 | MYH7 | c.804G>T (p.Leu268=) n.910G>T | dbSNP |
| 14 | g.23430992C= | CA2123450605 | MYH7 | c.804G= (p.Leu268=) n.910G= | |
| 14 | g.23430992C>G | CA485626223 | MYH7 | c.804G>C (p.Leu268=) n.910G>C | |
| 14 | g.23430992C>T | CA485626224 | MYH7 | c.804G>A (p.Leu268=) n.910G>A | ClinVar dbSNP |
| 14 | g.23430993A= | CA2123450611 | MYH7 | c.803T= (p.Leu268=) n.909T= | |
| 14 | g.23430993A>C | CA389052010 | MYH7 | c.803T>G (p.Leu268Arg) n.909T>G | ClinVar dbSNP |
| 14 | g.23430993A>G | CA389052011 | MYH7 | c.803T>C (p.Leu268Pro) n.909T>C | ClinVar dbSNP |
| 14 | g.23430993A>T | CA389052012 | MYH7 | c.803T>A (p.Leu268Gln) n.909T>A |