P65Q (p.Pro65Gln) variant of TGFB2 (P61812)
P65Q (p.Pro65Gln) in TGFB2 (P61812) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
P65Q (p.Pro65Gln) variant details
- p.Pro65Gln
- NCI-TCGA Cosmic COSV6511
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available