| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 14 | g.23423939C>A | CA389046688 | MYH7 | c.2890G>T (p.Val964Leu) n.2996G>T | |
| 14 | g.23423939C= | CA2123453975 | MYH7 | c.2890G= (p.Val964=) n.2996G= | |
| 14 | g.23423939C>G | CA013168 | MYH7 | c.2890G>C (p.Val964Leu) n.2996G>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23423939C>T | CA389046690 | MYH7 | c.2890G>A (p.Val964Met) n.2996G>A | |
| 14 | g.23423940T>A | CA389046693 | MYH7 | c.2889A>T (p.Lys963Asn) n.2995A>T | |
| 14 | g.23423940T>C | CA034515 | MYH7 | c.2889A>G (p.Lys963=) n.2995A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.23423940T>G | CA389046696 | MYH7 | c.2889A>C (p.Lys963Asn) n.2995A>C | |
| 14 | g.23423940T= | CA2123453977 | MYH7 | c.2889A= (p.Lys963=) n.2995A= | |
| 14 | g.23423941T>A | CA389046697 | MYH7 | c.2888A>T (p.Lys963Ile) n.2994A>T | |
| 14 | g.23423941T>C | CA389046698 | MYH7 | c.2888A>G (p.Lys963Arg) n.2994A>G | |
| 14 | g.23423941T>G | CA389046700 | MYH7 | c.2888A>C (p.Lys963Thr) n.2994A>C | |
| 14 | g.23423942T>A | CA389046702 | MYH7 | c.2887A>T (p.Lys963Ter) n.2993A>T | |
| 14 | g.23423942T>C | CA389046705 | MYH7 | c.2887A>G (p.Lys963Glu) n.2993A>G | |
| 14 | g.23423942T>G | CA389046704 | MYH7 | c.2887A>C (p.Lys963Gln) n.2993A>C | |
| 14 | g.23423942_23423943delinsTG | CA2123453979 | MYH7 | c.2886_2887delinsCA (p.Ala962=) n.2992_2993delinsCA | |
| 14 | g.23423943G>A | CA485766804 | MYH7 | c.2886C>T (p.Ala962=) n.2992C>T | |
| 14 | g.23423943G>C | CA485766803 | MYH7 | c.2886C>G (p.Ala962=) n.2992C>G | |
| 14 | g.23423943G>T | CA485766802 | MYH7 | c.2886C>A (p.Ala962=) n.2992C>A | |
| 14 | g.23423944del | CA10587768 | MYH7 | c.2886del (p.Val964TrpfsTer12) n.2992del | ClinVar dbSNP |
| 14 | g.23423944G>A | CA389046707 | MYH7 | c.2885C>T (p.Ala962Val) n.2991C>T | |
| 14 | g.23423944G>C | CA389046709 | MYH7 | c.2885C>G (p.Ala962Gly) n.2991C>G | |
| 14 | g.23423944G>T | CA389046710 | MYH7 | c.2885C>A (p.Ala962Asp) n.2991C>A | gnomAD v4 |
| 14 | g.23423945C>A | CA389046712 | MYH7 | c.2884G>T (p.Ala962Ser) n.2990G>T | gnomAD v4 |
| 14 | g.23423945C= | CA2123453983 | MYH7 | c.2884G= (p.Ala962=) n.2990G= | |
| 14 | g.23423945C>G | CA389046713 | MYH7 | c.2884G>C (p.Ala962Pro) n.2990G>C | ClinVar |
| 14 | g.23423945C>T | CA389046715 | MYH7 | c.2884G>A (p.Ala962Thr) n.2990G>A | dbSNP |
| 14 | g.23423946C>A | CA485766807 | MYH7 | c.2883G>T (p.Leu961=) n.2989G>T | |
| 14 | g.23423946C>G | CA485766810 | MYH7 | c.2883G>C (p.Leu961=) n.2989G>C | |
| 14 | g.23423946C>T | CA485766809 | MYH7 | c.2883G>A (p.Leu961=) n.2989G>A | |
| 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 |