This section shows a general overview of the selected mutation. It describes the source of the mutation i.e gene name/sample name/tissue name with unique ID, and also shows the mutation syntax at the amino acid and nucleotide sequence level. You can see more information on our help pages.
- Mutation ID
- Gene name
- AA mutation
p.E88K (Substitution - Missense, position 88, E➞K)
- CDS mutation
c.262G>A (Substitution, position 262, G➞A)
- Nucleotides inserted
- Genomic coordinates
- GRCh38, X:101371680..101371680, view Ensembl contig
- 30953, view the multiple sequence alignment
- Ever confirmed somatic?
- FATHMM prediction
- Pathogenic (score 0.83)
- Drug resistance