Paralogue Annotation for SCN5A residue 866

Residue details

Gene: SCN5A
Reference Sequences: LRG: LRG_289, Ensembl variant: ENST00000333535 / ENSP00000328968
Amino Acid Position: 866
Reference Amino Acid: S - Serine
Protein Domain: TM Domain 2


Paralogue Variants mapped to SCN5A residue 866

No paralogue variants have been mapped to residue 866 for SCN5A.



SCN5AVGALGNLTLVLAIIVFIFAVVGMQLFGKNY>S<EL-RDS----D-SG---LLPRWHMMDFFHA887
SCN1AVGALGNLTLVLAIIVFIFAVVGMQLFGKSY>K<DC-VCK----I-AS-DCQLPRWHMNDFFHS940
SCN2AVGALGNLTLVLAIIVFIFAVVGMQLFGKSY>K<EC-VCK----I-SN-DCELPRWHMHDFFHS931
SCN3AVGALGNLTLVLAIIVFIFAVVGMQLFGKSY>K<EC-VCK----I-ND-DCTLPRWHMNDFFHS932
SCN4AVGALGNLTLVLAIIVFIFAVVGMQLFGKSY>K<EC-VCK----I-AL-DCNLPRWHMHDFFHS750
SCN7AWVALKDLVLLLFTFIFFSAAFGMKLFGKNY>E<EF-VCH----I-DK-DCQLPRWHMHDFFHS677
SCN8AVGALGNLTLVLAIIVFIFAVVGMQLFGKSY>K<EC-VCK----I-NQ-DCELPRWHMHDFFHS925
SCN9AVGALGNLTLVLAIIVFIFAVVGMQLFGKSY>K<EC-VCK----I-ND-DCTLPRWHMNDFFHS905
SCN10AVGALGNLTIILAIIVFVFALVGKQLLGENY>R<NN-RKN----I-SAPHEDWPRWHMHDFFHS838
SCN11AVGALGSLTVVLVIVIFIFSVVGMQLFGRSF>N<SQ-KSPKLCNPTGPTVSCLRHWHMGDFWHS757
CACNA1AMKSIISLLFLLFLFIVVFALLGMQLFGGQF>N<FD-E------------G-TPPTNFDTFPAA657
CACNA1BMKSIISLLFLLFLFIVVFALLGMQLFGGQF>N<FQ-D------------E-TPTTNFDTFPAA653
CACNA1CVRSIASLLLLLFLFIIIFSLLGMQLFGGKF>N<FD-E------------MQTRRSTFDNFPQS695
CACNA1DMKSIASLLLLLFLFIIIFSLLGMQLFGGKF>N<FD-E------------TQTKRSTFDNFPQA714
CACNA1EMKSIISLLFLLFLFIVVFALLGMQLFGGRF>N<FN-D------------G-TPSANFDTFPAA646
CACNA1FMKSIASLLLLLFLFIIIFSLLGMQLFGGKF>N<FD-Q------------THTKRSTFDTFPQA700
CACNA1GMDNVATFCMLLMLFIFIFSILGMHLFGCKF>A<SER---------DG-DTLPDRKNFDSLLWA912
CACNA1HMDNVATFCTLLMLFIFIFSILGMHLFGCKF>S<LKTD--------TG-DTVPDRKNFDSLLWA963
CACNA1IMDNVATFCMLLMLFIFIFSILGMHIFGCKF>S<LRTD--------TG-DTVPDRKNFDSLLWA810
CACNA1SIRSIASLLLLLFLFIVIFALLGMQLFGGRY>D<FE-D------------TEVRRSNFDNFPQA603
cons                              > <                              

See full Alignment of Paralogues


Known Variants in SCN5A

ProteinCDSDisease ClassificationDiseasedbSNP linksEffect Prediction
p.S866Lc.2597C>T Putative BenignSIFT:
Polyphen:
p.S866Pc.2596T>C Putative BenignSIFT:
Polyphen: