Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
14 | g.23396316_23396350del | CA2624246239 | MYH6 | c.2366_2400del (p.Arg789HisfsTer2) | gnomAD v4 |
14 | g.23396329C>A | CA389016189 | MYH6 | c.2384G>T (p.Arg795Leu) | |
14 | g.23396329C= | CA2123417897 | MYH6 | c.2384G= (p.Arg795=) | |
14 | g.23396329C>G | CA389016190 | MYH6 | c.2384G>C (p.Arg795Pro) | gnomAD v4 |
14 | g.23396329C>T | CA123764 | MYH6 | c.2384G>A (p.Arg795Gln) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
14 | g.23396330G>A | CA7115483 | MYH6 | c.2383C>T (p.Arg795Trp) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.23396330G>C | CA389016194 | MYH6 | c.2383C>G (p.Arg795Gly) | |
14 | g.23396330G= | CA2123417903 | MYH6 | c.2383C= (p.Arg795=) | |
14 | g.23396330G>T | CA485609947 | MYH6 | c.2383C>A (p.Arg795=) | gnomAD v4 |
14 | g.23396331G>A | CA485609948 | MYH6 | c.2382C>T (p.Ala794=) | |
14 | g.23396331G>C | CA485609949 | MYH6 | c.2382C>G (p.Ala794=) | |
14 | g.23396331G>T | CA485609950 | MYH6 | c.2382C>A (p.Ala794=) | |
14 | g.23396332G>A | CA389016197 | MYH6 | c.2381C>T (p.Ala794Val) | gnomAD v4 |
14 | g.23396332G>C | CA389016198 | MYH6 | c.2381C>G (p.Ala794Gly) | |
14 | g.23396332G>T | CA389016200 | MYH6 | c.2381C>A (p.Ala794Asp) | |
14 | g.23396333C>A | CA389016202 | MYH6 | c.2380G>T (p.Ala794Ser) | |
14 | g.23396333C>G | CA389016203 | MYH6 | c.2380G>C (p.Ala794Pro) | |
14 | g.23396333C>T | CA389016205 | MYH6 | c.2380G>A (p.Ala794Thr) | |
14 | g.23396334T>A | CA389016209 | MYH6 | c.2379A>T (p.Gln793His) | |
14 | g.23396334T>C | CA7115484 | MYH6 | c.2379A>G (p.Gln793=) | ClinVar dbSNP ExAC gnomAD v4 COSMIC |
14 | g.23396334T>G | CA389016207 | MYH6 | c.2379A>C (p.Gln793His) | |
14 | g.23396334T= | CA2123417911 | MYH6 | c.2379A= (p.Gln793=) | |
14 | g.23396335T>A | CA389016212 | MYH6 | c.2378A>T (p.Gln793Leu) | |
14 | g.23396335T>C | CA389016213 | MYH6 | c.2378A>G (p.Gln793Arg) | |
14 | g.23396335T>G | CA389016214 | MYH6 | c.2378A>C (p.Gln793Pro) | |
14 | g.23396336G>A | CA389016217 | MYH6 | c.2377C>T (p.Gln793Ter) | gnomAD v4 |
14 | g.23396336G>C | CA389016218 | MYH6 | c.2377C>G (p.Gln793Glu) | |
14 | g.23396336G>T | CA389016220 | MYH6 | c.2377C>A (p.Gln793Lys) | gnomAD v4 |
14 | g.23396337G>A | CA485609955 | MYH6 | c.2376C>T (p.Ala792=) | dbSNP |
14 | g.23396337G>C | CA485609954 | MYH6 | c.2376C>G (p.Ala792=) | |
14 | g.23396337G= | CA2123417915 | MYH6 | c.2376C= (p.Ala792=) | |
14 | g.23396337G>T | CA485609953 | MYH6 | c.2376C>A (p.Ala792=) | |
14 | g.23396338G>A | CA389016222 | MYH6 | c.2375C>T (p.Ala792Val) | |
14 | g.23396338G>C | CA389016224 | MYH6 | c.2375C>G (p.Ala792Gly) | |
14 | g.23396338G>T | CA389016223 | MYH6 | c.2375C>A (p.Ala792Asp) | |
14 | g.23396339C>A | CA389016225 | MYH6 | c.2374G>T (p.Ala792Ser) | |
14 | g.23396339C>G | CA389016227 | MYH6 | c.2374G>C (p.Ala792Pro) | |
14 | g.23396339C>T | CA389016229 | MYH6 | c.2374G>A (p.Ala792Thr) | ClinVar |
14 | g.23396340C>A | CA389016231 | MYH6 | c.2373G>T (p.Gln791His) | dbSNP |
14 | g.23396340C= | CA2123417918 | MYH6 | c.2373G= (p.Gln791=) | |
14 | g.23396340C>G | CA389016232 | MYH6 | c.2373G>C (p.Gln791His) | |
14 | g.23396340C>T | CA485609958 | MYH6 | c.2373G>A (p.Gln791=) | |
14 | g.23396341T>A | CA389016234 | MYH6 | c.2372A>T (p.Gln791Leu) | |
14 | g.23396341T>C | CA389016236 | MYH6 | c.2372A>G (p.Gln791Arg) | gnomAD v4 |
14 | g.23396341T>G | CA389016238 | MYH6 | c.2372A>C (p.Gln791Pro) | |
14 | g.23396342G>A | CA257789181 | MYH6 | c.2371C>T (p.Gln791Ter) | dbSNP gnomAD v2 gnomAD v4 |
14 | g.23396342G>C | CA7115485 | MYH6 | c.2371C>G (p.Gln791Glu) | dbSNP ExAC gnomAD v2 gnomAD v4 |
14 | g.23396342G= | CA2123417924 | MYH6 | c.2371C= (p.Gln791=) | |
14 | g.23396342G>T | CA389016241 | MYH6 | c.2371C>A (p.Gln791Lys) | |
14 | g.23396343C>A | CA389016243 | MYH6 | c.2370G>T (p.Met790Ile) |