No paralogue variants have been mapped to residue 387 for CACNA1C.
CACNA1C | FQCITMEGWTDVLYWVNDAVGRDWPWIYFV>T<LIIIGSFFVLNLVLGVLSGEFSKEREKAKA | 417 |
CACNA1A | FQCITMEGWTDLLYNSNDASGNTWNWLYFI>P<LIIIGSFFMLNLVLGVLSGEFAKERERVEN | 372 |
CACNA1B | FQCITMEGWTDILYNTNDAAGNTWNWLYFI>P<LIIIGSFFMLNLVLGVLSGEFAKERERVEN | 368 |
CACNA1D | FQCITMEGWTDVLYWVNDAIGWEWPWVYFV>S<LIILGSFFVLNLVLGVLSGEFSKEREKAKA | 418 |
CACNA1E | FQCITMEGWTTVLYNTNDALGATWNWLYFI>P<LIIIGSFFVLNLVLGVLSGEFAKERERVEN | 363 |
CACNA1F | FQCVTMEGWTDVLYWMQDAMGYELPWVYFV>S<LVIFGSFFVLNLVLGVLSGEFSKEREKAKA | 384 |
CACNA1G | FQVITLEGWVDIMYFVMDAHSF-YNFIYFI>L<LIIVGSFFMINLCLVVIATQFSETKQRESQ | 407 |
CACNA1H | FQVITLEGWVDIMYYVMDAHSF-YNFIYFI>L<LIIVGSFFMINLCLVVIATQFSETKQRESQ | 431 |
CACNA1I | FQVITLEGWVEIMYYVMDAHSF-YNFIYFI>L<LIIVGSFFMINLCLVVIATQFSETKQREHR | 410 |
CACNA1S | YQCITMEGWTDVLYWVNDAIGNEWPWIYFV>T<LILLGSFFILNLVLGVLSGEFTKEREKAKS | 346 |
SCN10A | FRLMTQDSWERLYQQTLRTSGKIY-MIFFV>L<VIFLGSFYLVNLILAVVTMAYEEQNQATTD | 409 |
SCN11A | FRLMTQDSWEKLYQQTLRTTGLYS-VFFFI>V<VIFLGSFYLINLTLAVVTMAYEEQNKNVAA | 412 |
SCN1A | FRLMTQDFWENLYQLTLRAAGKTY-MIFFV>L<VIFLGSFYLINLILAVVAMAYEEQNQATLE | 435 |
SCN2A | FRLMTQDFWENLYQLTLRAAGKTY-MIFFV>L<VIFLGSFYLINLILAVVAMAYEEQNQATLE | 437 |
SCN3A | FRLMTQDYWENLYQLTLRAAGKTY-MIFFV>L<VIFLGSFYLVNLILAVVAMAYEEQNQATLE | 436 |
SCN4A | FRLMTQDYWENLFQLTLRAAGKTY-MIFFV>V<IIFLGSFYLINLILAVVAMAYAEQNEATLA | 459 |
SCN5A | FRLMTQDCWERLYQQTLRSAGKIY-MIFFM>L<VIFLGSFYLVNLILAVVAMAYEEQNQATIA | 425 |
SCN7A | FRLMAQDYPEVLYHQILYASGKVY-MIFFV>V<VSFLFSFYMASLFLGILAMAYEEEKQRVGE | 406 |
SCN8A | FRLMTQDYWENLYQLTLRAAGKTY-MIFFV>L<VIFVGSFYLVNLILAVVAMAYEEQNQATLE | 423 |
SCN9A | FRLMTQDYWENLYQQTLRAAGKTY-MIFFV>V<VIFLGSFYLINLILAVVAMAYEEQNQANIE | 414 |
cons | > < |
Protein | CDS | Disease Classification | Disease | dbSNP links | Effect Prediction |
---|---|---|---|---|---|
p.T387R | c.1160C>G | Putative Benign | rs1051352 | SIFT: tolerated Polyphen: benign |