D27G (p.Asp27Gly) variant of HNRNPA1 (P09651)
D27G (p.Asp27Gly) 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.
D27G (p.Asp27Gly) variant details
- p.Asp27Gly
- NCI-TCGA Cosmic COSV5293
- cosmic curated COSV52939
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available