G77A (p.Gly77Ala) variant of HSPG2 (P98160)
G77A (p.Gly77Ala) in HSPG2 (P98160) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact.
G77A (p.Gly77Ala) variant details
- p.Gly77Ala
- NCI-TCGA Cosmic COSV1010
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.