No paralogue variants have been mapped to residue 1442 for SCN5A.
SCN5A | LLQVATFKGWMDIMYAAVDSRGYEEQPQWE>Y<NLYMYIYFVIFIIFGSFFTLNLFIGVIIDN | 1472 |
SCN1A | LLQVATFKGWMDIMYAAVDSRNVELQPKYE>E<SLYMYLYFVIFIIFGSFFTLNLFIGVIIDN | 1485 |
SCN2A | LLQVATFKGWMDIMYAAVDSRNVELQPKYE>D<NLYMYLYFVIFIIFGSFFTLNLFIGVIIDN | 1475 |
SCN3A | LLQVATFKGWMDIMYAAVDSRDVKLQPVYE>E<NLYMYLYFVIFIIFGSFFTLNLFIGVIIDN | 1470 |
SCN4A | LLQVATFKGWMDIMYAAVDSREKEEQPQYE>V<NLYMYLYFVIFIIFGSFFTLNLFIGVIIDN | 1297 |
SCN7A | LLQVATFNGWITIMNSAIDSVAVNIQPHFE>V<NIYMYCYFINFIIFGVFLPLSMLITVIIDN | 1195 |
SCN8A | LLQVATFKGWMDIMYAAVDSRKPDEQPKYE>D<NIYMYIYFVIFIIFGSFFTLNLFIGVIIDN | 1466 |
SCN9A | LLQVATFKGWTIIMYAAVDSVNVDKQPKYE>Y<SLYMYIYFVVFIIFGSFFTLNLFIGVIIDN | 1448 |
SCN10A | LLQVATFKGWMDIMYAAVDSREVNMQPKWE>D<NVYMYLYFVIFIIFGGFFTLNLFVGVIIDN | 1420 |
SCN11A | LLQVATFKGWMDIIYAAVDSTEKEQQPEFE>S<NSLGYIYFVVFIIFGSFFTLNLFIGVIIDN | 1310 |
CACNA1A | LFTVSTGEGWPQVLKHSVDATFENQGPSPG>Y<RMEMSIFYVVYFVVFPFFFVNIFVALIIIT | 1513 |
CACNA1B | LFTVSTGEGWPMVLKHSVDATYEEQGPSPG>Y<RMELSIFYVVYFVVFPFFFVNIFVALIIIT | 1419 |
CACNA1C | LFTVSTFEGWPELLYRSIDSHTEDKGPIYN>Y<RVEISIFFIIYIIIIAFFMMNIFVGFVIVT | 1168 |
CACNA1D | LFTVSTFEGWPALLYKAIDSNGENIGPIYN>H<RVEISIFFIIYIIIVAFFMMNIFVGFVIVT | 1174 |
CACNA1E | LFTVSTGEGWPQVLQHSVDVTEEDRGPSRS>N<RMEMSIFYVVYFVVFPFFFVNIFVALIIIT | 1425 |
CACNA1F | LFTVSTFEGWPALLYKAIDAYAEDHGPIYN>Y<RVEISVFFIVYIIIIAFFMMNIFVGFVIIT | 1139 |
CACNA1G | LFVLASKDGWVDIMYDGLDAVGVDQQPIMN>H<NPWMLLYFISFLLIVAFFVLNMFVGVVVEN | 1539 |
CACNA1H | LFVLSSKDGWVNIMYDGLDAVGVDQQPVQN>H<NPWMLLYFISFLLIVSFFVLNMFVGVVVEN | 1557 |
CACNA1I | LFVLASKDGWVNIMYNGLDAVAVDQQPVTN>H<NPWMLLYFISFLLIVSFFVLNMFVGVVVEN | 1433 |
CACNA1S | LFTVSTFEGWPQLLYKAIDSNAEDVGPIYN>N<RVEMAIFFIIYIILIAFFMMNIFVGFVIVT | 1067 |
cons | > < |
Protein | CDS | Disease Classification | Disease | dbSNP links | Effect Prediction |
---|---|---|---|---|---|
p.Y1442C | c.4325A>G | Putative Benign | SIFT: Polyphen: | ||
p.Y1442N | c.4324T>A | Putative Benign | SIFT: Polyphen: |