A61T (p.Ala61Thr) variant of HSPG2 (P98160)
A61T (p.Ala61Thr) in HSPG2 (P98160) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact.
A61T (p.Ala61Thr) variant details
- p.Ala61Thr
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.