No paralogue variants have been mapped to residue 1678 for SCN5A.
SCN5A | FALMMSLPALFNIGLLLFLVMFIYSIFGMA>N<FAYVKW-----EAG-----IDDMFNFQTFA | 1698 |
SCN1A | FALMMSLPALFNIGLLLFLVMFIYAIFGMS>N<FAYVKR-----EVG-----IDDMFNFETFG | 1711 |
SCN2A | FALMMSLPALFNIGLLLFLVMFIYAIFGMS>N<FAYVKR-----EVG-----IDDMFNFETFG | 1701 |
SCN3A | FALMMSLPALFNIGLLLFLVMFIYAIFGMS>N<FAYVKK-----EAG-----IDDMFNFETFG | 1696 |
SCN4A | FALMMSLPALFNIGLLLFLVMFIYSIFGMS>N<FAYVKK-----ESG-----IDDMFNFETFG | 1523 |
SCN7A | LPLMLSLPALLNIILLIFLVMFIYAVFGMY>N<FAYVKK-----EAG-----INDVSNFETFG | 1421 |
SCN8A | FALMMSLPALFNIGLLLFLVMFIFSIFGMS>N<FAYVKH-----EAG-----IDDMFNFETFG | 1692 |
SCN9A | FALMMSLPALFNIGLLLFLVMFIYAIFGMS>N<FAYVKK-----EDG-----INDMFNFETFG | 1674 |
SCN10A | FALMMSLPALFNIGLLLFLVMFIYSIFGMS>S<FPHVRW-----EAG-----IDDMFNFQTFA | 1648 |
SCN11A | FALMMSLPSLFNIGLLLFLIMFIYAILGMN>W<FSKVNP-----ESG-----IDDIFNFKTFA | 1538 |
CACNA1A | WTFVQSFKALPYVCLLIAMLFFIYAIIGMQ>V<FGNIGIDVEDEDSDEDEFQITEHNNFRTFF | 1743 |
CACNA1B | WTFVQSFKALPYVCLLIAMLFFIYAIIGMQ>V<FGNIALDD---DTS-----INRHNNFRTFL | 1643 |
CACNA1C | WTFIKSFQALPYVALLIVMLFFIYAVIGMQ>V<FGKIALND---TTE-----INRNNNFQTFP | 1403 |
CACNA1D | WTFIKSFQALPYVALLIAMLFFIYAVIGMQ>M<FGKVAMRD---NNQ-----INRNNNFQTFP | 1413 |
CACNA1E | WTFVQSFKALPYVCLLIAMLFFIYAIIGMQ>V<FGNIKLDE---ESH-----INRHNNFRSFF | 1650 |
CACNA1F | WTFIKSFQALPYVALLIAMIFFIYAVIGMQ>M<FGKVALQD---GTQ-----INRNNNFQTFP | 1370 |
CACNA1G | DTVMQALPQVGNLGLLFMLLFFIFAALGVE>L<FGDLECDET---HP--CEGLGRHATFRNFG | 1789 |
CACNA1H | DTVVQALPQVGNLGLLFMLLFFIYAALGVE>L<FGRLECSED---NP--CEGLSRHATFSNFG | 1795 |
CACNA1I | DTVVQALPQVGNLGLLFMLLFFIYAALGVE>L<FGKLVCNDE---NP--CEGMSRHATFENFG | 1665 |
CACNA1S | WTFIKSFQALPYVALLIVMLFFIYAVIGMQ>M<FGKIALVD---GTQ-----INRNNNFQTFP | 1310 |
cons | > < |
Protein | CDS | Disease Classification | Disease | dbSNP links | Effect Prediction |
---|---|---|---|---|---|
p.N1678S | c.5033A>G | Putative Benign | SIFT: Polyphen: |