No paralogue variants have been mapped to residue 1445 for SCN5A.
SCN5A | VATFKGWMDIMYAAVDSRGYEEQPQWEYNL>Y<MYIYFVIFIIFGSFFTLNLFIGVIIDNFNQ | 1475 |
SCN1A | VATFKGWMDIMYAAVDSRNVELQPKYEESL>Y<MYLYFVIFIIFGSFFTLNLFIGVIIDNFNQ | 1488 |
SCN2A | VATFKGWMDIMYAAVDSRNVELQPKYEDNL>Y<MYLYFVIFIIFGSFFTLNLFIGVIIDNFNQ | 1478 |
SCN3A | VATFKGWMDIMYAAVDSRDVKLQPVYEENL>Y<MYLYFVIFIIFGSFFTLNLFIGVIIDNFNQ | 1473 |
SCN4A | VATFKGWMDIMYAAVDSREKEEQPQYEVNL>Y<MYLYFVIFIIFGSFFTLNLFIGVIIDNFNQ | 1300 |
SCN7A | VATFNGWITIMNSAIDSVAVNIQPHFEVNI>Y<MYCYFINFIIFGVFLPLSMLITVIIDNFNK | 1198 |
SCN8A | VATFKGWMDIMYAAVDSRKPDEQPKYEDNI>Y<MYIYFVIFIIFGSFFTLNLFIGVIIDNFNQ | 1469 |
SCN9A | VATFKGWTIIMYAAVDSVNVDKQPKYEYSL>Y<MYIYFVVFIIFGSFFTLNLFIGVIIDNFNQ | 1451 |
SCN10A | VATFKGWMDIMYAAVDSREVNMQPKWEDNV>Y<MYLYFVIFIIFGGFFTLNLFVGVIIDNFNQ | 1423 |
SCN11A | VATFKGWMDIIYAAVDSTEKEQQPEFESNS>L<GYIYFVVFIIFGSFFTLNLFIGVIIDNFNQ | 1313 |
CACNA1A | VSTGEGWPQVLKHSVDATFENQGPSPGYRM>E<MSIFYVVYFVVFPFFFVNIFVALIIITFQE | 1516 |
CACNA1B | VSTGEGWPMVLKHSVDATYEEQGPSPGYRM>E<LSIFYVVYFVVFPFFFVNIFVALIIITFQE | 1422 |
CACNA1C | VSTFEGWPELLYRSIDSHTEDKGPIYNYRV>E<ISIFFIIYIIIIAFFMMNIFVGFVIVTFQE | 1171 |
CACNA1D | VSTFEGWPALLYKAIDSNGENIGPIYNHRV>E<ISIFFIIYIIIVAFFMMNIFVGFVIVTFQE | 1177 |
CACNA1E | VSTGEGWPQVLQHSVDVTEEDRGPSRSNRM>E<MSIFYVVYFVVFPFFFVNIFVALIIITFQE | 1428 |
CACNA1F | VSTFEGWPALLYKAIDAYAEDHGPIYNYRV>E<ISVFFIVYIIIIAFFMMNIFVGFVIITFRA | 1142 |
CACNA1G | LASKDGWVDIMYDGLDAVGVDQQPIMNHNP>W<MLLYFISFLLIVAFFVLNMFVGVVVENFHK | 1542 |
CACNA1H | LSSKDGWVNIMYDGLDAVGVDQQPVQNHNP>W<MLLYFISFLLIVSFFVLNMFVGVVVENFHK | 1560 |
CACNA1I | LASKDGWVNIMYNGLDAVAVDQQPVTNHNP>W<MLLYFISFLLIVSFFVLNMFVGVVVENFHK | 1436 |
CACNA1S | VSTFEGWPQLLYKAIDSNAEDVGPIYNNRV>E<MAIFFIIYIILIAFFMMNIFVGFVIVTFQE | 1070 |
cons | > < |
Protein | CDS | Disease Classification | Disease | dbSNP links | Effect Prediction |
---|---|---|---|---|---|
p.Y1445H | c.4333T>C | Putative Benign | SIFT: Polyphen: |