Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
12 | g.5045943_5045944delinsGT | CA645578791 | KCNA5 | c.1796_1797delinsGT (p.Ser599Cys) | COSMIC |
12 | g.5045944C>A | CA478095977 | KCNA5 | c.1797C>A (p.Ser599=) | COSMIC |
12 | g.5045944C= | CA2013431470 | KCNA5 | c.1797C= (p.Ser599=) | |
12 | g.5045944C>G | CA6399951 | KCNA5 | c.1797C>G (p.Ser599=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.5045944C>T | CA478095978 | KCNA5 | c.1797C>T (p.Ser599=) | |
12 | g.5045945C>A | CA383467243 | KCNA5 | c.1798C>A (p.Leu600Ile) | gnomAD v4 |
12 | g.5045945C>G | CA383467241 | KCNA5 | c.1798C>G (p.Leu600Val) | |
12 | g.5045945C>T | CA383467242 | KCNA5 | c.1798C>T (p.Leu600Phe) | |
12 | g.5045946T>A | CA383467244 | KCNA5 | c.1799T>A (p.Leu600His) | |
12 | g.5045946T>C | CA383467245 | KCNA5 | c.1799T>C (p.Leu600Pro) | |
12 | g.5045946T>G | CA383467246 | KCNA5 | c.1799T>G (p.Leu600Arg) | |
12 | g.5045947T>A | CA478095982 | KCNA5 | c.1800T>A (p.Leu600=) | |
12 | g.5045947T>C | CA478095983 | KCNA5 | c.1800T>C (p.Leu600=) | |
12 | g.5045947T>G | CA478095981 | KCNA5 | c.1800T>G (p.Leu600=) | |
12 | g.5045948T>A | CA383467247 | KCNA5 | c.1801T>A (p.Tyr601Asn) | gnomAD v4 |
12 | g.5045948T>C | CA383467248 | KCNA5 | c.1801T>C (p.Tyr601His) | |
12 | g.5045948T>G | CA383467249 | KCNA5 | c.1801T>G (p.Tyr601Asp) | |
12 | g.5045949A= | CA2013431471 | KCNA5 | c.1802A= (p.Tyr601=) | |
12 | g.5045949A>C | CA383467250 | KCNA5 | c.1802A>C (p.Tyr601Ser) | |
12 | g.5045949A>G | CA383467251 | KCNA5 | c.1802A>G (p.Tyr601Cys) | |
12 | g.5045949A>T | CA383467252 | KCNA5 | c.1802A>T (p.Tyr601Phe) | dbSNP gnomAD v3 gnomAD v4 |
12 | g.5045950T>A | CA383467254 | KCNA5 | c.1803T>A (p.Tyr601Ter) | |
12 | g.5045950T>C | CA478095987 | KCNA5 | c.1803T>C (p.Tyr601=) | dbSNP gnomAD v4 |
12 | g.5045950T>G | CA383467253 | KCNA5 | c.1803T>G (p.Tyr601Ter) | |
12 | g.5045950T= | CA2013431472 | KCNA5 | c.1803T= (p.Tyr601=) | |
12 | g.5045951G>A | CA383467255 | KCNA5 | c.1804G>A (p.Ala602Thr) | |
12 | g.5045951G>C | CA383467256 | KCNA5 | c.1804G>C (p.Ala602Pro) | |
12 | g.5045951G>T | CA383467257 | KCNA5 | c.1804G>T (p.Ala602Ser) | |
12 | g.5045952C>A | CA383467258 | KCNA5 | c.1805C>A (p.Ala602Asp) | |
12 | g.5045952C>G | CA383467259 | KCNA5 | c.1805C>G (p.Ala602Gly) | |
12 | g.5045952C>T | CA383467260 | KCNA5 | c.1805C>T (p.Ala602Val) | gnomAD v4 |
12 | g.5045953C>A | CA478095991 | KCNA5 | c.1806C>A (p.Ala602=) | |
12 | g.5045953C>G | CA478095992 | KCNA5 | c.1806C>G (p.Ala602=) | gnomAD v4 |
12 | g.5045953C>T | CA478095994 | KCNA5 | c.1806C>T (p.Ala602=) | |
12 | g.5045954C>A | CA383467261 | KCNA5 | c.1807C>A (p.Leu603Ile) | |
12 | g.5045954C>G | CA383467262 | KCNA5 | c.1807C>G (p.Leu603Val) | |
12 | g.5045954C>T | CA383467263 | KCNA5 | c.1807C>T (p.Leu603Phe) | |
12 | g.5045955T>A | CA383467264 | KCNA5 | c.1808T>A (p.Leu603His) | |
12 | g.5045955T>C | CA383467265 | KCNA5 | c.1808T>C (p.Leu603Pro) | |
12 | g.5045955T>G | CA383467266 | KCNA5 | c.1808T>G (p.Leu603Arg) | |
12 | g.5045956C>A | CA478095996 | KCNA5 | c.1809C>A (p.Leu603=) | |
12 | g.5045956C>G | CA478095997 | KCNA5 | c.1809C>G (p.Leu603=) | |
12 | g.5045956C>T | CA478095998 | KCNA5 | c.1809C>T (p.Leu603=) | |
12 | g.5045957T>A | CA383467268 | KCNA5 | c.1810T>A (p.Cys604Ser) | |
12 | g.5045957T>C | CA383467269 | KCNA5 | c.1810T>C (p.Cys604Arg) | |
12 | g.5045957T>G | CA383467267 | KCNA5 | c.1810T>G (p.Cys604Gly) | |
12 | g.5045958G>A | CA383467270 | KCNA5 | c.1811G>A (p.Cys604Tyr) | |
12 | g.5045958G>C | CA383467271 | KCNA5 | c.1811G>C (p.Cys604Ser) | |
12 | g.5045958G>T | CA383467272 | KCNA5 | c.1811G>T (p.Cys604Phe) | gnomAD v4 |
12 | g.5045959C>A | CA383467273 | KCNA5 | c.1812C>A (p.Cys604Ter) |