| Paralogue | Variant | Associated Disease | Mapping Quality | Consensus | Pubmed |
|---|---|---|---|---|---|
| CACNA1F | N746T | Night blindness, congenital stationary 2 | High | 9 | 25472526 |
To assess whether the paralogue annotation here confidently predicts that variation at this residue is pathogenic, it is important to check the reports in the Pubmed links above to ascertain that the mutations in these paralogues have been proved likely to be disease-causing. It is also important to check that the direction of effect of the variant in the paralogue is compatible with your observed phenotype in SCN5A.
| SCN5A | TMWDCMEV-----SGQSLCLLVFLLVMVIG>N<LVVLNLFLALLLSSFS-ADNLTAP-DEDRE | 955 |
| SCN1A | TMWDCMEV-----AGQAMCLTVFMMVMVIG>N<LVVLNLFLALLLSSFS-ADNLAAT-DDDNE | 1008 |
| SCN2A | TMWDCMEV-----AGQTMCLTVFMMVMVIG>N<LVVLNLFLALLLSSFS-SDNLAAT-DDDNE | 999 |
| SCN3A | TMWDCMEV-----AGQTMCLIVFMLVMVIG>N<LVVLNLFLALLLSSFS-SDNLAAT-DDDNE | 1000 |
| SCN4A | TMWDCMEV-----AGQAMCLTVFLMVMVIG>N<LVVLNLFLALLLSSFS-ADSLAAS-DEDGE | 818 |
| SCN7A | TLWDCMEV-----AGQSWCIPFYLMVILIG>N<LLVLYLFLA-LVSSFS-SCKDVTA-EENNE | 744 |
| SCN8A | TMWDCMEV-----AGQAMCLIVFMMVMVIG>N<LVVLNLFLALLLSSFS-ADNLAAT-DDDGE | 993 |
| SCN9A | TMWDCMEV-----AGQAMCLIVYMMVMVIG>N<LVVLNLFLALLLSSFS-SDNLTAI-EEDPD | 973 |
| SCN10A | NMWACMEV-----GQKSICLILFLTVMVLG>N<LVVLNLFIALLLNSFS-ADNLTAP-EDDGE | 906 |
| SCN11A | NMWECMQEAN---ASSSLCVIVFILITVIG>K<LVVLNLFIALLLNSFS-NEERNGNLEGEAR | 828 |
| CACNA1A | VMYDGIKSQGGV-QGGMVFSIYFIVLTLFG>N<YTLLNVFLAIAVDNLANAQELTKDEQEEEE | 732 |
| CACNA1B | VMYHGIESQGGV-SKGMFSSFYFIVLTLFG>N<YTLLNVFLAIAVDNLANAQELTKDEEEMEE | 728 |
| CACNA1C | VMYDGIMAYGGPSFPGMLVCIYFIILFICG>N<YILLNVFLAIAVDNLADAESLTSAQKEEEE | 771 |
| CACNA1D | VMYDGIMAYGGPSSSGMIVCIYFIILFICG>N<YILLNVFLAIAVDNLADAESLNTAQKEEAE | 790 |
| CACNA1E | VMYNGIRSQGGV-SSGMWSAIYFIVLTLFG>N<YTLLNVFLAIAVDNLANAQELTKDEQEEEE | 721 |
| CACNA1F | VMYDGIMAYGGPFFPGMLVCIYFIILFICG>N<YILLNVFLAIAVDNLASGDA-GTAKDKGGE | 775 |
| CACNA1G | VLYNGMAS-T-S----SWAALYFIALMTFG>N<YVLFNLLVAILVEGFQ-AEEISKREDASGQ | 981 |
| CACNA1H | VLYNGMAS-T-S----SWAALYFVALMTFG>N<YVLFNLLVAILVEGFQ-AEGDANRSDTDED | 1032 |
| CACNA1I | VLYNGMAS-T-S----PWASLYFVALMTFG>N<YVLFNLLVAILVEGFQAEGDAN-RSYSDED | 879 |
| CACNA1S | MMYNGIMAYGGPSYPGMLVCIYFIILFVCG>N<YILLNVFLAIAVDNLAEAESLTSAQKAKAE | 679 |
| cons | > < |
| Protein | CDS | Disease Classification | Disease | dbSNP links | Effect Prediction |
|---|---|---|---|---|---|
| p.N927S | c.2780A>G | Inherited Arrhythmia | BrS | rs199473589 | SIFT: deleterious Polyphen: benign |
| Reports | Inherited Arrhythmia | BrS | Diagnostic value of flecainide testing in unmasking SCN5A-related Brugada syndrome. J Cardiovasc Electrophysiol. 2006 17(8):857-64. 16764707 | ||
| Inherited Arrhythmia | BrS | An international compendium of mutations in the SCN5A-encoded cardiac sodium channel in patients referred for Brugada syndrome genetic testing. Heart Rhythm. 2010 7(1):33-46. 20129283 | |||
| p.N927K | c.2781C>G | Putative Benign | SIFT: Polyphen: | ||