L14F (p.Leu14Phe) variant of SPINK5 (Q9NQ38)
L14F (p.Leu14Phe) in SPINK5 (Q9NQ38) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact. The record also includes structural context.
L14F (p.Leu14Phe) variant details
- p.Leu14Phe
- NCI-TCGA Cosmic COSV5626
- NCI-TCGA Cosmic COSV9980
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.
- Structural context available