L16P (p.Leu16Pro) variant of TNFRSF1A (P19438)
L16P (p.Leu16Pro) in TNFRSF1A (P19438) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
L16P (p.Leu16Pro) variant details
- p.Leu16Pro
- NCI-TCGA Cosmic COSV9936
- cosmic curated COSV99369
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available