Paralogue Annotation for SCN5A residue 1676

Residue details

Gene: SCN5A
Reference Sequences: LRG: LRG_289, Ensembl variant: ENST00000333535 / ENSP00000328968
Amino Acid Position: 1676
Reference Amino Acid: M - Methionine
Protein Domain: TM Domain 4


Paralogue Variants mapped to SCN5A residue 1676

No paralogue variants have been mapped to residue 1676 for SCN5A.



SCN5ALLFALMMSLPALFNIGLLLFLVMFIYSIFG>M<ANFAYVKW-----EAG-----IDDMFNFQT1696
SCN1ALLFALMMSLPALFNIGLLLFLVMFIYAIFG>M<SNFAYVKR-----EVG-----IDDMFNFET1709
SCN2ALLFALMMSLPALFNIGLLLFLVMFIYAIFG>M<SNFAYVKR-----EVG-----IDDMFNFET1699
SCN3ALLFALMMSLPALFNIGLLLFLVMFIYAIFG>M<SNFAYVKK-----EAG-----IDDMFNFET1694
SCN4ALLFALMMSLPALFNIGLLLFLVMFIYSIFG>M<SNFAYVKK-----ESG-----IDDMFNFET1521
SCN7ALMLPLMLSLPALLNIILLIFLVMFIYAVFG>M<YNFAYVKK-----EAG-----INDVSNFET1419
SCN8ALLFALMMSLPALFNIGLLLFLVMFIFSIFG>M<SNFAYVKH-----EAG-----IDDMFNFET1690
SCN9ALLFALMMSLPALFNIGLLLFLVMFIYAIFG>M<SNFAYVKK-----EDG-----INDMFNFET1672
SCN10ALLFALMMSLPALFNIGLLLFLVMFIYSIFG>M<SSFPHVRW-----EAG-----IDDMFNFQT1646
SCN11ALLFALMMSLPSLFNIGLLLFLIMFIYAILG>M<NWFSKVNP-----ESG-----IDDIFNFKT1536
CACNA1ALLWTFVQSFKALPYVCLLIAMLFFIYAIIG>M<QVFGNIGIDVEDEDSDEDEFQITEHNNFRT1741
CACNA1BLLWTFVQSFKALPYVCLLIAMLFFIYAIIG>M<QVFGNIALDD---DTS-----INRHNNFRT1641
CACNA1CLLWTFIKSFQALPYVALLIVMLFFIYAVIG>M<QVFGKIALND---TTE-----INRNNNFQT1401
CACNA1DLLWTFIKSFQALPYVALLIAMLFFIYAVIG>M<QMFGKVAMRD---NNQ-----INRNNNFQT1411
CACNA1ELLWTFVQSFKALPYVCLLIAMLFFIYAIIG>M<QVFGNIKLDE---ESH-----INRHNNFRS1648
CACNA1FLLWTFIKSFQALPYVALLIAMIFFIYAVIG>M<QMFGKVALQD---GTQ-----INRNNNFQT1368
CACNA1GLLDTVMQALPQVGNLGLLFMLLFFIFAALG>V<ELFGDLECDET---HP--CEGLGRHATFRN1787
CACNA1HLLDTVVQALPQVGNLGLLFMLLFFIYAALG>V<ELFGRLECSED---NP--CEGLSRHATFSN1793
CACNA1ILLDTVVQALPQVGNLGLLFMLLFFIYAALG>V<ELFGKLVCNDE---NP--CEGMSRHATFEN1663
CACNA1SLLWTFIKSFQALPYVALLIVMLFFIYAVIG>M<QMFGKIALVD---GTQ-----INRNNNFQT1308
cons                              > <                              

See full Alignment of Paralogues


Known Variants in SCN5A

ProteinCDSDisease ClassificationDiseasedbSNP linksEffect Prediction
p.M1676Ic.5028G>A Putative BenignSIFT:
Polyphen:
p.M1676Tc.5027T>C Putative BenignSIFT:
Polyphen:
p.Met1676Valc.5026A>G UnknownSIFT:
Polyphen: