No paralogue variants have been mapped to residue 1170 for CACNA1C.
| CACNA1C | VEISIFFIIYIIIIAFFMMNIFVGFVIVTF>Q<EQGEQE----YKNCELDKNQR------QCV | 1190 |
| CACNA1A | MEMSIFYVVYFVVFPFFFVNIFVALIIITF>Q<EQGDKM----MEEYSLEKNER------ACI | 1535 |
| CACNA1B | MELSIFYVVYFVVFPFFFVNIFVALIIITF>Q<EQGDKV----MSECSLEKNER------ACI | 1441 |
| CACNA1D | VEISIFFIIYIIIVAFFMMNIFVGFVIVTF>Q<EQGEKE----YKNCELDKNQR------QCV | 1196 |
| CACNA1E | MEMSIFYVVYFVVFPFFFVNIFVALIIITF>Q<EQGDKM----MEECSLEKNER------ACI | 1447 |
| CACNA1F | VEISVFFIVYIIIIAFFMMNIFVGFVIITF>R<AQGEQE----YQNCELDKNQR------QCV | 1161 |
| CACNA1G | PWMLLYFISFLLIVAFFVLNMFVGVVVENF>H<KCRQHQEEEEARRREEKRLRRLEKKRRNLM | 1571 |
| CACNA1H | PWMLLYFISFLLIVSFFVLNMFVGVVVENF>H<KCRQHQEAEEARRREEK----------RLR | 1579 |
| CACNA1I | PWMLLYFISFLLIVSFFVLNMFVGVVVENF>H<KCRQHQEAEEARRREEK----------RLR | 1455 |
| CACNA1S | VEMAIFFIIYIILIAFFMMNIFVGFVIVTF>Q<EQGETE----YKNCELDKNQR------QCV | 1089 |
| SCN10A | VYMYLYFVIFIIFGGFFTLNLFVGVIIDNF>N<QQKKKLGGQDIFMTEEQKKYY------NAM | 1446 |
| SCN11A | SLGYIYFVVFIIFGSFFTLNLFIGVIIDNF>N<QQQKKLGGQDIFMTEEQKKYY------NAM | 1336 |
| SCN1A | LYMYLYFVIFIIFGSFFTLNLFIGVIIDNF>N<QQKKKFGGQDIFMTEEQKKYY------NAM | 1511 |
| SCN2A | LYMYLYFVIFIIFGSFFTLNLFIGVIIDNF>N<QQKKKFGGQDIFMTEEQKKYY------NAM | 1501 |
| SCN3A | LYMYLYFVIFIIFGSFFTLNLFIGVIIDNF>N<QQKKKFGGQDIFMTEEQKKYY------NAM | 1496 |
| SCN4A | LYMYLYFVIFIIFGSFFTLNLFIGVIIDNF>N<QQKKKLGGKDIFMTEEQKKYY------NAM | 1323 |
| SCN5A | LYMYIYFVIFIIFGSFFTLNLFIGVIIDNF>N<QQKKKLGGQDIFMTEEQKKYY------NAM | 1498 |
| SCN7A | IYMYCYFINFIIFGVFLPLSMLITVIIDNF>N<KHKIKLGGSNIFITVKQRKQY------RRL | 1221 |
| SCN8A | IYMYIYFVIFIIFGSFFTLNLFIGVIIDNF>N<QQKKKFGGQDIFMTEEQKKYY------NAM | 1492 |
| SCN9A | LYMYIYFVVFIIFGSFFTLNLFIGVIIDNF>N<QQKKKLGGQDIFMTEEQKKYY------NAM | 1474 |
| cons | > < |
| Protein | CDS | Disease Classification | Disease | dbSNP links | Effect Prediction |
|---|---|---|---|---|---|
| p.Q1170R | c.3509A>G | Putative Benign | rs200634867 | SIFT: tolerated Polyphen: possibly damaging |