Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
14 | g.23423947A= | CA2123453988 | MYH7 | c.2882T= (p.Leu961=) n.2988T= | |
14 | g.23423947A>C | CA10587769 | MYH7 | c.2882T>G (p.Leu961Arg) n.2988T>G | ClinVar dbSNP gnomAD v4 |
14 | g.23423947A>G | CA013164 | MYH7 | c.2882T>C (p.Leu961Pro) n.2988T>C | ClinVar dbSNP |
14 | g.23423947A>T | CA389046717 | MYH7 | c.2882T>A (p.Leu961Gln) n.2988T>A | |
14 | g.23423948G>A | CA485766812 | MYH7 | c.2881C>T (p.Leu961=) n.2987C>T | ClinVar dbSNP |
14 | g.23423948G>C | CA389046721 | MYH7 | c.2881C>G (p.Leu961Val) n.2987C>G | ClinVar dbSNP gnomAD v4 |
14 | g.23423948G= | CA2123453996 | MYH7 | c.2881C= (p.Leu961=) n.2987C= | |
14 | g.23423948G>T | CA389046719 | MYH7 | c.2881C>A (p.Leu961Met) n.2987C>A | |
14 | g.23423949T>A | CA485766815 | MYH7 | c.2880A>T (p.Thr960=) n.2986A>T | |
14 | g.23423949T>C | CA485766816 | MYH7 | c.2880A>G (p.Thr960=) n.2986A>G | |
14 | g.23423949T>G | CA485766817 | MYH7 | c.2880A>C (p.Thr960=) n.2986A>C | |
14 | g.23423950G>A | CA389046722 | MYH7 | c.2879C>T (p.Thr960Ile) n.2985C>T | |
14 | g.23423950G>C | CA389046724 | MYH7 | c.2879C>G (p.Thr960Arg) n.2985C>G | |
14 | g.23423950G>T | CA389046725 | MYH7 | c.2879C>A (p.Thr960Lys) n.2985C>A | |
14 | g.23423951T>A | CA389046726 | MYH7 | c.2878A>T (p.Thr960Ser) n.2984A>T | |
14 | g.23423951T>C | CA389046728 | MYH7 | c.2878A>G (p.Thr960Ala) n.2984A>G | |
14 | g.23423951T>G | CA389046730 | MYH7 | c.2878A>C (p.Thr960Pro) n.2984A>C | |
14 | g.23423952C>A | CA485766821 | MYH7 | c.2877G>T (p.Leu959=) n.2983G>T | |
14 | g.23423952C= | CA2123454001 | MYH7 | c.2877G= (p.Leu959=) n.2983G= | |
14 | g.23423952C>G | CA485766822 | MYH7 | c.2877G>C (p.Leu959=) n.2983G>C | COSMIC |
14 | g.23423952C>T | CA10587772 | MYH7 | c.2877G>A (p.Leu959=) n.2983G>A | ClinVar dbSNP gnomAD v4 |
14 | g.23423953A>C | CA389046732 | MYH7 | c.2876T>G (p.Leu959Arg) n.2982T>G | |
14 | g.23423953A>G | CA389046735 | MYH7 | c.2876T>C (p.Leu959Pro) n.2982T>C | |
14 | g.23423953A>T | CA389046734 | MYH7 | c.2876T>A (p.Leu959Gln) n.2982T>A | |
14 | g.23423954G>A | CA485766825 | MYH7 | c.2875C>T (p.Leu959=) n.2981C>T | |
14 | g.23423954G>C | CA389046737 | MYH7 | c.2875C>G (p.Leu959Val) n.2981C>G | |
14 | g.23423954G>T | CA389046738 | MYH7 | c.2875C>A (p.Leu959Met) n.2981C>A | |
14 | g.23423955C>A | CA389046739 | MYH7 | c.2874G>T (p.Glu958Asp) n.2980G>T | |
14 | g.23423955C= | CA2123454004 | MYH7 | c.2874G= (p.Glu958=) n.2980G= | |
14 | g.23423955C>G | CA389046740 | MYH7 | c.2874G>C (p.Glu958Asp) n.2980G>C | |
14 | g.23423955C>T | CA257818889 | MYH7 | c.2874G>A (p.Glu958=) n.2980G>A | dbSNP gnomAD v2 gnomAD v4 |
14 | g.23423956T>A | CA389046742 | MYH7 | c.2873A>T (p.Glu958Val) n.2979A>T | |
14 | g.23423956T>C | CA389046745 | MYH7 | c.2873A>G (p.Glu958Gly) n.2979A>G | |
14 | g.23423956T>G | CA389046744 | MYH7 | c.2873A>C (p.Glu958Ala) n.2979A>C | |
14 | g.23423957C>A | CA389046747 | MYH7 | c.2872G>T (p.Glu958Ter) n.2978G>T | |
14 | g.23423957C>G | CA389046748 | MYH7 | c.2872G>C (p.Glu958Gln) n.2978G>C | gnomAD v4 |
14 | g.23423957C>T | CA389046750 | MYH7 | c.2872G>A (p.Glu958Lys) n.2978G>A | ClinVar dbSNP gnomAD v4 |
14 | g.23423958C>A | CA485766828 | MYH7 | c.2871G>T (p.Leu957=) n.2977G>T | |
14 | g.23423958C>G | CA485766830 | MYH7 | c.2871G>C (p.Leu957=) n.2977G>C | |
14 | g.23423958C>T | CA485766831 | MYH7 | c.2871G>A (p.Leu957=) n.2977G>A | |
14 | g.23423958_23423959delinsCA | CA2123454010 | MYH7 | c.2870_2871delinsTG (p.Leu957=) n.2976_2977delinsTG | |
14 | g.23423959del | CA2123454013 | MYH7 | c.2870del (p.Leu957ArgfsTer3) n.2976del | dbSNP |
14 | g.23423959A>C | CA389046752 | MYH7 | c.2870T>G (p.Leu957Arg) n.2976T>G | |
14 | g.23423959A>G | CA389046753 | MYH7 | c.2870T>C (p.Leu957Pro) n.2976T>C | |
14 | g.23423959A>T | CA389046754 | MYH7 | c.2870T>A (p.Leu957Gln) n.2976T>A | |
14 | g.23423960G>A | CA485766832 | MYH7 | c.2869C>T (p.Leu957=) n.2975C>T | gnomAD v4 |
14 | g.23423960G>C | CA389046755 | MYH7 | c.2869C>G (p.Leu957Val) n.2975C>G | |
14 | g.23423960G>T | CA389046757 | MYH7 | c.2869C>A (p.Leu957Met) n.2975C>A | |
14 | g.23423961A= | CA2123454017 | MYH7 | c.2868T= (p.Asp956=) n.2974T= | |
14 | g.23423961A>C | CA389046759 | MYH7 | c.2868T>G (p.Asp956Glu) n.2974T>G |