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 |