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.K451K (Substitution - coding silent, position 451, K➞K)
- CDS mutation
c.1353G>A (Substitution, position 1353, G➞A)
- Nucleotides inserted
- Genomic coordinates
- GRCh38, 8:97713742..97713742, view Ensembl contig
- 12089, view the multiple sequence alignment
- Ever confirmed somatic?
- FATHMM prediction
- Pathogenic (score 0.92)
- Drug resistance