S137F (p.Ser137Phe) variant of FERMT1 (Fermitin family homolog 1)
S137F (p.Ser137Phe) in FERMT1 (Fermitin family homolog 1) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
S137F (p.Ser137Phe) variant details
- p.Ser137Phe
- NCI-TCGA Cosmic COSV5409
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available