Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
14 | g.23424118C>A | CA389047305 | MYH7 | c.2711G>T (p.Arg904Leu) n.2817G>T | ClinVar dbSNP |
14 | g.23424118C= | CA2123454658 | MYH7 | c.2711G= (p.Arg904=) n.2817G= | |
14 | g.23424118C>G | CA257819011 | MYH7 | c.2711G>C (p.Arg904Pro) n.2817G>C | ClinVar dbSNP |
14 | g.23424118C>T | CA012913 | MYH7 | c.2711G>A (p.Arg904His) n.2817G>A | ClinVar dbSNP gnomAD v4 |
14 | g.23424119G>A | CA012904 | MYH7 | c.2710C>T (p.Arg904Cys) n.2816C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
14 | g.23424119G>C | CA389047309 | MYH7 | c.2710C>G (p.Arg904Gly) n.2816C>G | ClinVar |
14 | g.23424119G= | CA2123454664 | MYH7 | c.2710C= (p.Arg904=) n.2816C= | |
14 | g.23424119G>T | CA389047311 | MYH7 | c.2710C>A (p.Arg904Ser) n.2816C>A | ClinVar |
14 | g.23424120C>A | CA389047314 | MYH7 | c.2709G>T (p.Glu903Asp) n.2815G>T | ClinVar dbSNP gnomAD v4 |
14 | g.23424120C= | CA2123454672 | MYH7 | c.2709G= (p.Glu903=) n.2815G= | |
14 | g.23424120C>G | CA389047313 | MYH7 | c.2709G>C (p.Glu903Asp) n.2815G>C | |
14 | g.23424120C>T | CA034095 | MYH7 | c.2709G>A (p.Glu903=) n.2815G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
14 | g.23424121T>A | CA389047316 | MYH7 | c.2708A>T (p.Glu903Val) n.2814A>T | |
14 | g.23424121T>C | CA012900 | MYH7 | c.2708A>G (p.Glu903Gly) n.2814A>G | ClinVar dbSNP |
14 | g.23424121T>G | CA389047318 | MYH7 | c.2708A>C (p.Glu903Ala) n.2814A>C | |
14 | g.23424121T= | CA2123454683 | MYH7 | c.2708A= (p.Glu903=) n.2814A= | |
14 | g.23424122C>A | CA389047319 | MYH7 | c.2707G>T (p.Glu903Ter) n.2813G>T | |
14 | g.23424122C= | CA2123454691 | MYH7 | c.2707G= (p.Glu903=) n.2813G= | |
14 | g.23424122C>G | CA389047321 | MYH7 | c.2707G>C (p.Glu903Gln) n.2813G>C | ClinVar dbSNP |
14 | g.23424122C>T | CA012894 | MYH7 | c.2707G>A (p.Glu903Lys) n.2813G>A | ClinVar dbSNP |
14 | g.23424123C>A | CA389047322 | MYH7 | c.2706G>T (p.Glu902Asp) n.2812G>T | |
14 | g.23424123C>G | CA389047324 | MYH7 | c.2706G>C (p.Glu902Asp) n.2812G>C | |
14 | g.23424123C>T | CA485767246 | MYH7 | c.2706G>A (p.Glu902=) n.2812G>A | |
14 | g.23424124T>A | CA389047326 | MYH7 | c.2705A>T (p.Glu902Val) n.2811A>T | |
14 | g.23424124T>C | CA389047328 | MYH7 | c.2705A>G (p.Glu902Gly) n.2811A>G | |
14 | g.23424124T>G | CA389047329 | MYH7 | c.2705A>C (p.Glu902Ala) n.2811A>C | |
14 | g.23424125C>A | CA389047330 | MYH7 | c.2704G>T (p.Glu902Ter) n.2810G>T | |
14 | g.23424125C= | CA2123454701 | MYH7 | c.2704G= (p.Glu902=) n.2810G= | |
14 | g.23424125C>G | CA389047332 | MYH7 | c.2704G>C (p.Glu902Gln) n.2810G>C | |
14 | g.23424125C>T | CA10576956 | MYH7 | c.2704G>A (p.Glu902Lys) n.2810G>A | ClinVar dbSNP |
14 | g.23424126A= | CA2123454707 | MYH7 | c.2703T= (p.Ala901=) n.2809T= | |
14 | g.23424126A>C | CA485767256 | MYH7 | c.2703T>G (p.Ala901=) n.2809T>G | |
14 | g.23424126A>G | CA485767257 | MYH7 | c.2703T>C (p.Ala901=) n.2809T>C | dbSNP gnomAD v4 |
14 | g.23424126A>T | CA485767258 | MYH7 | c.2703T>A (p.Ala901=) n.2809T>A | |
14 | g.23424127G>A | CA389047336 | MYH7 | c.2702C>T (p.Ala901Val) n.2808C>T | |
14 | g.23424127G>C | CA389047337 | MYH7 | c.2702C>G (p.Ala901Gly) n.2808C>G | dbSNP |
14 | g.23424127G= | CA2123454720 | MYH7 | c.2702C= (p.Ala901=) n.2808C= | |
14 | g.23424127G>T | CA389047334 | MYH7 | c.2702C>A (p.Ala901Asp) n.2808C>A | |
14 | g.23424128C>A | CA389047339 | MYH7 | c.2701G>T (p.Ala901Ser) n.2807G>T | gnomAD v4 |
14 | g.23424128C= | CA2123454723 | MYH7 | c.2701G= (p.Ala901=) n.2807G= | |
14 | g.23424128C>G | CA389047340 | MYH7 | c.2701G>C (p.Ala901Pro) n.2807G>C | dbSNP |
14 | g.23424128C>T | CA389047341 | MYH7 | c.2701G>A (p.Ala901Thr) n.2807G>A | |
14 | g.23424129A= | CA2123454726 | MYH7 | c.2700T= (p.Asp900=) n.2806T= | |
14 | g.23424129A>C | CA389047343 | MYH7 | c.2700T>G (p.Asp900Glu) n.2806T>G | ClinVar dbSNP |
14 | g.23424129A>G | CA485767263 | MYH7 | c.2700T>C (p.Asp900=) n.2806T>C | ClinVar gnomAD v4 |
14 | g.23424129A>T | CA012887 | MYH7 | c.2700T>A (p.Asp900Glu) n.2806T>A | ClinVar dbSNP |
14 | g.23424130T>A | CA389047347 | MYH7 | c.2699A>T (p.Asp900Val) n.2805A>T | ClinVar |
14 | g.23424130T>C | CA012883 | MYH7 | c.2699A>G (p.Asp900Gly) n.2805A>G | ClinVar dbSNP |
14 | g.23424130T>G | CA389047345 | MYH7 | c.2699A>C (p.Asp900Ala) n.2805A>C | |
14 | g.23424130T= | CA2123454737 | MYH7 | c.2699A= (p.Asp900=) n.2805A= |