KIT S709F

Variant type

missense mutation

Location

Chromosome 17

Exon

8

Protein change

p.S709F

cDNA change

-

Genomic coordinate

Chromosome 17

FATHMM prediction

-

Variant category

I

Variant description

Not important.

Variant frequence

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

Accoiciated drug