No paralogue variants have been mapped to residue 1676 for SCN5A.
SCN5A | LLFALMMSLPALFNIGLLLFLVMFIYSIFG>M<ANFAYVKW-----EAG-----IDDMFNFQT | 1696 |
SCN1A | LLFALMMSLPALFNIGLLLFLVMFIYAIFG>M<SNFAYVKR-----EVG-----IDDMFNFET | 1709 |
SCN2A | LLFALMMSLPALFNIGLLLFLVMFIYAIFG>M<SNFAYVKR-----EVG-----IDDMFNFET | 1699 |
SCN3A | LLFALMMSLPALFNIGLLLFLVMFIYAIFG>M<SNFAYVKK-----EAG-----IDDMFNFET | 1694 |
SCN4A | LLFALMMSLPALFNIGLLLFLVMFIYSIFG>M<SNFAYVKK-----ESG-----IDDMFNFET | 1521 |
SCN7A | LMLPLMLSLPALLNIILLIFLVMFIYAVFG>M<YNFAYVKK-----EAG-----INDVSNFET | 1419 |
SCN8A | LLFALMMSLPALFNIGLLLFLVMFIFSIFG>M<SNFAYVKH-----EAG-----IDDMFNFET | 1690 |
SCN9A | LLFALMMSLPALFNIGLLLFLVMFIYAIFG>M<SNFAYVKK-----EDG-----INDMFNFET | 1672 |
SCN10A | LLFALMMSLPALFNIGLLLFLVMFIYSIFG>M<SSFPHVRW-----EAG-----IDDMFNFQT | 1646 |
SCN11A | LLFALMMSLPSLFNIGLLLFLIMFIYAILG>M<NWFSKVNP-----ESG-----IDDIFNFKT | 1536 |
CACNA1A | LLWTFVQSFKALPYVCLLIAMLFFIYAIIG>M<QVFGNIGIDVEDEDSDEDEFQITEHNNFRT | 1741 |
CACNA1B | LLWTFVQSFKALPYVCLLIAMLFFIYAIIG>M<QVFGNIALDD---DTS-----INRHNNFRT | 1641 |
CACNA1C | LLWTFIKSFQALPYVALLIVMLFFIYAVIG>M<QVFGKIALND---TTE-----INRNNNFQT | 1401 |
CACNA1D | LLWTFIKSFQALPYVALLIAMLFFIYAVIG>M<QMFGKVAMRD---NNQ-----INRNNNFQT | 1411 |
CACNA1E | LLWTFVQSFKALPYVCLLIAMLFFIYAIIG>M<QVFGNIKLDE---ESH-----INRHNNFRS | 1648 |
CACNA1F | LLWTFIKSFQALPYVALLIAMIFFIYAVIG>M<QMFGKVALQD---GTQ-----INRNNNFQT | 1368 |
CACNA1G | LLDTVMQALPQVGNLGLLFMLLFFIFAALG>V<ELFGDLECDET---HP--CEGLGRHATFRN | 1787 |
CACNA1H | LLDTVVQALPQVGNLGLLFMLLFFIYAALG>V<ELFGRLECSED---NP--CEGLSRHATFSN | 1793 |
CACNA1I | LLDTVVQALPQVGNLGLLFMLLFFIYAALG>V<ELFGKLVCNDE---NP--CEGMSRHATFEN | 1663 |
CACNA1S | LLWTFIKSFQALPYVALLIVMLFFIYAVIG>M<QMFGKIALVD---GTQ-----INRNNNFQT | 1308 |
cons | > < |
Protein | CDS | Disease Classification | Disease | dbSNP links | Effect Prediction |
---|---|---|---|---|---|
p.M1676I | c.5028G>A | Putative Benign | SIFT: Polyphen: | ||
p.M1676T | c.5027T>C | Putative Benign | SIFT: Polyphen: | ||
p.Met1676Val | c.5026A>G | Unknown | SIFT: Polyphen: |