L13P (p.Leu13Pro) variant of HNRNPA1 (P09651)
L13P (p.Leu13Pro) in HNRNPA1 (P09651) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
L13P (p.Leu13Pro) variant details
- p.Leu13Pro
- NCI-TCGA Cosmic COSV9926
- cosmic curated COSV99267
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available