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.S1842P (Substitution - Missense, position 1842, S➞P)
- CDS mutation
c.5524T>C (Substitution, position 5524, T➞C)
- Nucleotides inserted
- Genomic coordinates
- GRCh38, 1:119919569..119919569, view Ensembl contig
- 7865, view the multiple sequence alignment
- Ever confirmed somatic?
- FATHMM prediction
- Pathogenic (score 0.83)
- Drug resistance