Paralogue Annotation for RYR2 residue 3869
Residue detailsGene: RYR2Reference Sequences:
, Ensembl variant:
ENSP00000355533Amino Acid Position:
3869Reference Amino Acid:
N - AsparagineProtein Domain:
Paralogue Variants mapped to RYR2 residue 3869
|Paralogue||Variant||Associated Disease||Mapping Quality||Consensus||Pubmed|
|RYR1||N3913D||Myopathy, congenital, RYR1-related||High||9
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 RYR2.
|cons|| > < |
Known Variants in RYR2
|Protein||CDS||Disease Classification||Disease||dbSNP links||Effect Prediction|