EGFR S781I

Variant type

missense mutation

Location

Chromosome 7

Exon

8

Protein change

p.S781I

cDNA change

-

Genomic coordinate

Chromosome 7

FATHMM prediction

-

Variant category

I

Variant description

The S768I mutation results in an amino acid substitution at position 768 of EGFR (exon 20), from a serine (S) to an isoleucine (I) (PMID: 22235099; 23922984).

Variant frequence

This section displays the distribution of mutated samples and tissue types (top 5).

Accoiciated drug