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.C772R (Substitution - Missense, position 772, C➞R)
- CDS mutation
c.2314T>C (Substitution, position 2314, T➞C)
- Nucleotides inserted
- Genomic coordinates
- GRCh38, 1:119953594..119953594, view Ensembl contig
- 7865, view the multiple sequence alignment
- Ever confirmed somatic?
- FATHMM prediction
- Pathogenic (score 1.00)
- Drug resistance