M46T (p.Met46Thr) variant of HNRNPA1 (P09651)
M46T (p.Met46Thr) 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.
M46T (p.Met46Thr) variant details
- p.Met46Thr
- NCI-TCGA Cosmic COSV9926
- cosmic curated COSV99267
- TOPMed rs1944177420
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available