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.K89N (Substitution - Missense, position 89, K➞N)
- CDS mutation
c.267G>C (Substitution, position 267, G➞C)
- Nucleotides inserted
- Genomic coordinates
- GRCh38, X:15803751..15803751, view Ensembl contig
- 21061, view the multiple sequence alignment
- Ever confirmed somatic?
- FATHMM prediction
- Pathogenic (score 0.93)
- Drug resistance