Paralogue Annotation for SCN5A residue 1842

Residue details

Gene: SCN5A
Reference Sequences: LRG: LRG_289, Ensembl variant: ENST00000333535 / ENSP00000328968
Amino Acid Position: 1842
Reference Amino Acid: M - Methionine
Protein Domain: C-terminus


Paralogue Variants mapped to SCN5A residue 1842

ParalogueVariantAssociated DiseaseMapping QualityConsensusPubmed
SCN1AM1856TGeneralized epilepsy with febrile seizures plusHigh8 18076640

To assess whether the paralogue annotation here confidently predicts that variation at this residue is pathogenic, it is important to check the reports in the Pubmed links above to ascertain that the mutations in these paralogues have been proved likely to be disease-causing. It is also important to check that the direction of effect of the variant in the paralogue is compatible with your observed phenotype in SCN5A.



SCN5ADALSEPLR--IAK--PNQI---SLINMDLP>M<VSGD-RIHCMDILFAFTKRVLGES--G---1866
SCN1AAALEPPLN--LPQ--PNKL---QLIAMDLP>M<VSGD-RIHCLDILFAFTKRVLGES--G---1880
SCN2ADALDPPLL--IAK--PNKV---QLIAMDLP>M<VSGD-RIHCLDILFAFTKRVLGES--G---1870
SCN3AAALDPPLL--IAK--PNKV---QLIAMDLP>M<VSGD-RIHCLDILFAFTKRVLGES--G---1865
SCN4ADTLQEPLR--IAK--PNKI---KLITLDLP>M<VPGD-KIHCLDILFALTKEVLGDS--G---1692
SCN7AAALDPPLF--MAK--PNKG---QLIALDLP>M<AVGD-RIHCLDILLAFTKRVMGQD--V---1590
SCN8ADALEHPLR--VPK--PNTI---ELIAMDLP>M<VSGD-RIHCLDILFAFTKRVLGDS--G---1860
SCN9AAALDPPLL--IAK--PNKV---QLIAMDLP>M<VSGD-RIHCLDILFAFTKRVLGES--G---1843
SCN10ADTLSGPLR--IPK--PNRN---ILIQMDLP>L<VPGD-KIHCLDILFAFTKNVLGES--G---1816
SCN11ADALPEPLR--VAK--PNKY---QFLVMDLP>M<VSED-RLHCMDILFAFTARVLGGS--D---1698
CACNA1ARVISPPLG--LGKKCPHRVACKRLLRMDLP>V<ADD-NTVHFNSTLMALIRTALDIKIAKGGA1914
CACNA1BKHMSPPLG--LGKKCPARVAYKRLVRMNMP>I<SNEDMTVHFTSTLMALIRTALEIKLAPAGT1813
CACNA1CRRIQPPLG--FGKLCPHRVACKRLVSMNMP>L<NSDG-TVMFNATLFALVRTALRIKTEG---1576
CACNA1DRRIQPPLG--FGKLCPHRVACKRLVAMNMP>L<NSDG-TVMFNATLFALVRTALKIKTEG---1584
CACNA1ETLMSPPLG--LGKRCPSKVAYKRLVLMNMP>V<AED-MTVHFTSTLMALIRTALDIKIAKGGA1826
CACNA1FRRIQPPLG--FGKLCPHRVACKRLVAMNMP>L<NSDG-TVTFNATLFALVRTSLKIKTEG---1541
CACNA1GPGVEGPDS--PDSPKPGAL---------HP>A<AHA-RSASHFSLEHPTDRQLFDTI---S--1936
CACNA1H-----PLP--QESPG--AR--------DAP>N<---------------LVARKV---------1919
CACNA1IR---GPGGAGGGGDT--EG---GLCRRCYS>P<AQE-N--LWLDSVSLIIKDSL---------1814
CACNA1SRRIQPPLG--FGKFCPHRVACKRLVGMNMP>L<NSDG-TVTFNATLFALVRTALKIKTEG---1481
cons                              > <                              

See full Alignment of Paralogues


Known Variants in SCN5A

ProteinCDSDisease ClassificationDiseasedbSNP linksEffect Prediction
p.M1842Lc.5524A>T Putative BenignSIFT: tolerated
Polyphen: benign
p.M1842Tc.5525T>C Putative BenignSIFT:
Polyphen:
p.M1842Vc.5524A>G Putative BenignSIFT:
Polyphen: