F17= variant of CFTR (P13569)
F17= in CFTR (P13569) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; low impact. The record also includes structural context.
F17= variant details
- NCI-TCGA Cosmic COSV5004
- Variant assessed as somatic; low impact.
- Missense
- UniProt: Variant assessed as somatic; low impact.
- Structural context available