No paralogue variants have been mapped to residue 866 for SCN5A.
| SCN5A | VGALGNLTLVLAIIVFIFAVVGMQLFGKNY>S<EL-RDS----D-SG---LLPRWHMMDFFHA | 887 |
| SCN1A | VGALGNLTLVLAIIVFIFAVVGMQLFGKSY>K<DC-VCK----I-AS-DCQLPRWHMNDFFHS | 940 |
| SCN2A | VGALGNLTLVLAIIVFIFAVVGMQLFGKSY>K<EC-VCK----I-SN-DCELPRWHMHDFFHS | 931 |
| SCN3A | VGALGNLTLVLAIIVFIFAVVGMQLFGKSY>K<EC-VCK----I-ND-DCTLPRWHMNDFFHS | 932 |
| SCN4A | VGALGNLTLVLAIIVFIFAVVGMQLFGKSY>K<EC-VCK----I-AL-DCNLPRWHMHDFFHS | 750 |
| SCN7A | WVALKDLVLLLFTFIFFSAAFGMKLFGKNY>E<EF-VCH----I-DK-DCQLPRWHMHDFFHS | 677 |
| SCN8A | VGALGNLTLVLAIIVFIFAVVGMQLFGKSY>K<EC-VCK----I-NQ-DCELPRWHMHDFFHS | 925 |
| SCN9A | VGALGNLTLVLAIIVFIFAVVGMQLFGKSY>K<EC-VCK----I-ND-DCTLPRWHMNDFFHS | 905 |
| SCN10A | VGALGNLTIILAIIVFVFALVGKQLLGENY>R<NN-RKN----I-SAPHEDWPRWHMHDFFHS | 838 |
| SCN11A | VGALGSLTVVLVIVIFIFSVVGMQLFGRSF>N<SQ-KSPKLCNPTGPTVSCLRHWHMGDFWHS | 757 |
| CACNA1A | MKSIISLLFLLFLFIVVFALLGMQLFGGQF>N<FD-E------------G-TPPTNFDTFPAA | 657 |
| CACNA1B | MKSIISLLFLLFLFIVVFALLGMQLFGGQF>N<FQ-D------------E-TPTTNFDTFPAA | 653 |
| CACNA1C | VRSIASLLLLLFLFIIIFSLLGMQLFGGKF>N<FD-E------------MQTRRSTFDNFPQS | 695 |
| CACNA1D | MKSIASLLLLLFLFIIIFSLLGMQLFGGKF>N<FD-E------------TQTKRSTFDNFPQA | 714 |
| CACNA1E | MKSIISLLFLLFLFIVVFALLGMQLFGGRF>N<FN-D------------G-TPSANFDTFPAA | 646 |
| CACNA1F | MKSIASLLLLLFLFIIIFSLLGMQLFGGKF>N<FD-Q------------THTKRSTFDTFPQA | 700 |
| CACNA1G | MDNVATFCMLLMLFIFIFSILGMHLFGCKF>A<SER---------DG-DTLPDRKNFDSLLWA | 912 |
| CACNA1H | MDNVATFCTLLMLFIFIFSILGMHLFGCKF>S<LKTD--------TG-DTVPDRKNFDSLLWA | 963 |
| CACNA1I | MDNVATFCMLLMLFIFIFSILGMHIFGCKF>S<LRTD--------TG-DTVPDRKNFDSLLWA | 810 |
| CACNA1S | IRSIASLLLLLFLFIVIFALLGMQLFGGRY>D<FE-D------------TEVRRSNFDNFPQA | 603 |
| cons | > < |
| Protein | CDS | Disease Classification | Disease | dbSNP links | Effect Prediction |
|---|---|---|---|---|---|
| p.S866L | c.2597C>T | Putative Benign | SIFT: Polyphen: | ||
| p.S866P | c.2596T>C | Putative Benign | SIFT: Polyphen: |