No paralogue variants have been mapped to residue 1439 for SCN5A.
SCN5A | YLALLQVATFKGWMDIMYAAVDSRGYEEQP>Q<WEYNLYMYIYFVIFIIFGSFFTLNLFIGVI | 1469 |
SCN1A | YLSLLQVATFKGWMDIMYAAVDSRNVELQP>K<YEESLYMYLYFVIFIIFGSFFTLNLFIGVI | 1482 |
SCN2A | YLSLLQVATFKGWMDIMYAAVDSRNVELQP>K<YEDNLYMYLYFVIFIIFGSFFTLNLFIGVI | 1472 |
SCN3A | YLALLQVATFKGWMDIMYAAVDSRDVKLQP>V<YEENLYMYLYFVIFIIFGSFFTLNLFIGVI | 1467 |
SCN4A | YLSLLQVATFKGWMDIMYAAVDSREKEEQP>Q<YEVNLYMYLYFVIFIIFGSFFTLNLFIGVI | 1294 |
SCN7A | FLSLLQVATFNGWITIMNSAIDSVAVNIQP>H<FEVNIYMYCYFINFIIFGVFLPLSMLITVI | 1192 |
SCN8A | YLALLQVATFKGWMDIMYAAVDSRKPDEQP>K<YEDNIYMYIYFVIFIIFGSFFTLNLFIGVI | 1463 |
SCN9A | YLSLLQVATFKGWTIIMYAAVDSVNVDKQP>K<YEYSLYMYIYFVVFIIFGSFFTLNLFIGVI | 1445 |
SCN10A | YLALLQVATFKGWMDIMYAAVDSREVNMQP>K<WEDNVYMYLYFVIFIIFGGFFTLNLFVGVI | 1417 |
SCN11A | YLALLQVATFKGWMDIIYAAVDSTEKEQQP>E<FESNSLGYIYFVVFIIFGSFFTLNLFIGVI | 1307 |
CACNA1A | LLTLFTVSTGEGWPQVLKHSVDATFENQGP>S<PGYRMEMSIFYVVYFVVFPFFFVNIFVALI | 1510 |
CACNA1B | LLTLFTVSTGEGWPMVLKHSVDATYEEQGP>S<PGYRMELSIFYVVYFVVFPFFFVNIFVALI | 1416 |
CACNA1C | MMALFTVSTFEGWPELLYRSIDSHTEDKGP>I<YNYRVEISIFFIIYIIIIAFFMMNIFVGFV | 1165 |
CACNA1D | MMALFTVSTFEGWPALLYKAIDSNGENIGP>I<YNHRVEISIFFIIYIIIVAFFMMNIFVGFV | 1171 |
CACNA1E | LLTLFTVSTGEGWPQVLQHSVDVTEEDRGP>S<RSNRMEMSIFYVVYFVVFPFFFVNIFVALI | 1422 |
CACNA1F | MMALFTVSTFEGWPALLYKAIDAYAEDHGP>I<YNYRVEISVFFIVYIIIIAFFMMNIFVGFV | 1136 |
CACNA1G | LMSLFVLASKDGWVDIMYDGLDAVGVDQQP>I<MNHNPWMLLYFISFLLIVAFFVLNMFVGVV | 1536 |
CACNA1H | LMSLFVLSSKDGWVNIMYDGLDAVGVDQQP>V<QNHNPWMLLYFISFLLIVSFFVLNMFVGVV | 1554 |
CACNA1I | LMSLFVLASKDGWVNIMYNGLDAVAVDQQP>V<TNHNPWMLLYFISFLLIVSFFVLNMFVGVV | 1430 |
CACNA1S | MMSLFTVSTFEGWPQLLYKAIDSNAEDVGP>I<YNNRVEMAIFFIIYIILIAFFMMNIFVGFV | 1064 |
cons | > < |
Protein | CDS | Disease Classification | Disease | dbSNP links | Effect Prediction |
---|---|---|---|---|---|
p.Q1439H | c.4317G>C | Putative Benign | SIFT: Polyphen: |