Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
14 | g.23423701A= | CA2123453455 | MYH7 | c.2945T= (p.Met982=) n.3051T= | |
14 | g.23423701A>C | CA389046461 | MYH7 | c.2945T>G (p.Met982Arg) n.3051T>G | |
14 | g.23423701A>G | CA013227 | MYH7 | c.2945T>C (p.Met982Thr) n.3051T>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.23423701A>T | CA389046463 | MYH7 | c.2945T>A (p.Met982Lys) n.3051T>A | ClinVar |
14 | g.23423702T>A | CA389046465 | MYH7 | c.2944A>T (p.Met982Leu) n.3050A>T | |
14 | g.23423702T>C | CA389046467 | MYH7 | c.2944A>G (p.Met982Val) n.3050A>G | |
14 | g.23423702T>G | CA389046466 | MYH7 | c.2944A>C (p.Met982Leu) n.3050A>C | |
14 | g.23423703C>A | CA389046469 | MYH7 | c.2943G>T (p.Glu981Asp) n.3049G>T | |
14 | g.23423703C>G | CA389046470 | MYH7 | c.2943G>C (p.Glu981Asp) n.3049G>C | |
14 | g.23423703C>T | CA485766607 | MYH7 | c.2943G>A (p.Glu981=) n.3049G>A | |
14 | g.23423704T>A | CA389046472 | MYH7 | c.2942A>T (p.Glu981Val) n.3048A>T | |
14 | g.23423704T>C | CA389046474 | MYH7 | c.2942A>G (p.Glu981Gly) n.3048A>G | |
14 | g.23423704T>G | CA389046475 | MYH7 | c.2942A>C (p.Glu981Ala) n.3048A>C | |
14 | g.23423705C>A | CA389046477 | MYH7 | c.2941G>T (p.Glu981Ter) n.3047G>T | |
14 | g.23423705C= | CA2123453461 | MYH7 | c.2941G= (p.Glu981=) n.3047G= | |
14 | g.23423705C>G | CA389046478 | MYH7 | c.2941G>C (p.Glu981Gln) n.3047G>C | |
14 | g.23423705C>T | CA257818761 | MYH7 | c.2941G>A (p.Glu981Lys) n.3047G>A | dbSNP |
14 | g.23423706C>A | CA389046480 | MYH7 | c.2940G>T (p.Glu980Asp) n.3046G>T | |
14 | g.23423706C>G | CA389046482 | MYH7 | c.2940G>C (p.Glu980Asp) n.3046G>C | |
14 | g.23423706C>T | CA485766608 | MYH7 | c.2940G>A (p.Glu980=) n.3046G>A | ClinVar |
14 | g.23423707T>A | CA389046484 | MYH7 | c.2939A>T (p.Glu980Val) n.3045A>T | |
14 | g.23423707T>C | CA389046485 | MYH7 | c.2939A>G (p.Glu980Gly) n.3045A>G | |
14 | g.23423707T>G | CA389046483 | MYH7 | c.2939A>C (p.Glu980Ala) n.3045A>C | |
14 | g.23423708C>A | CA389046487 | MYH7 | c.2938G>T (p.Glu980Ter) n.3044G>T | |
14 | g.23423708C= | CA2123453465 | MYH7 | c.2938G= (p.Glu980=) n.3044G= | |
14 | g.23423708C>G | CA389046488 | MYH7 | c.2938G>C (p.Glu980Gln) n.3044G>C | |
14 | g.23423708C>T | CA389046490 | MYH7 | c.2938G>A (p.Glu980Lys) n.3044G>A | dbSNP gnomAD v4 |
14 | g.23423709T>A | CA485766609 | MYH7 | c.2937A>T (p.Thr979=) n.3043A>T | |
14 | g.23423709T>C | CA485766610 | MYH7 | c.2937A>G (p.Thr979=) n.3043A>G | dbSNP gnomAD v4 |
14 | g.23423709T>G | CA485766611 | MYH7 | c.2937A>C (p.Thr979=) n.3043A>C | gnomAD v4 |
14 | g.23423709T= | CA2123453468 | MYH7 | c.2937A= (p.Thr979=) n.3043A= | |
14 | g.23423710G>A | CA389046491 | MYH7 | c.2936C>T (p.Thr979Ile) n.3042C>T | |
14 | g.23423710G>C | CA10643997 | MYH7 | c.2936C>G (p.Thr979Arg) n.3042C>G | ClinVar dbSNP |
14 | g.23423710G= | CA2123453471 | MYH7 | c.2936C= (p.Thr979=) n.3042C= | |
14 | g.23423710G>T | CA389046493 | MYH7 | c.2936C>A (p.Thr979Lys) n.3042C>A | |
14 | g.23423711T>A | CA389046498 | MYH7 | c.2935A>T (p.Thr979Ser) n.3041A>T | |
14 | g.23423711T>C | CA389046494 | MYH7 | c.2935A>G (p.Thr979Ala) n.3041A>G | |
14 | g.23423711T>G | CA389046496 | MYH7 | c.2935A>C (p.Thr979Pro) n.3041A>C | |
14 | g.23423712C>A | CA485766612 | MYH7 | c.2934G>T (p.Leu978=) n.3040G>T | |
14 | g.23423712C= | CA2123453478 | MYH7 | c.2934G= (p.Leu978=) n.3040G= | |
14 | g.23423712C>G | CA485766613 | MYH7 | c.2934G>C (p.Leu978=) n.3040G>C | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.23423712C>T | CA485766614 | MYH7 | c.2934G>A (p.Leu978=) n.3040G>A | |
14 | g.23423713A>C | CA389046499 | MYH7 | c.2933T>G (p.Leu978Arg) n.3039T>G | |
14 | g.23423713A>G | CA389046501 | MYH7 | c.2933T>C (p.Leu978Pro) n.3039T>C | ClinVar |
14 | g.23423713A>T | CA389046502 | MYH7 | c.2933T>A (p.Leu978Gln) n.3039T>A | |
14 | g.23423714G>A | CA485766615 | MYH7 | c.2932C>T (p.Leu978=) n.3038C>T | |
14 | g.23423714G>C | CA389046503 | MYH7 | c.2932C>G (p.Leu978Val) n.3038C>G | |
14 | g.23423714G>T | CA389046504 | MYH7 | c.2932C>A (p.Leu978Met) n.3038C>A | |
14 | g.23423715G>A | CA034951 | MYH7 | c.2931C>T (p.Asn977=) n.3037C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
14 | g.23423715G>C | CA389046509 | MYH7 | c.2931C>G (p.Asn977Lys) n.3037C>G |