I137M (p.Ile137Met) variant of HSPG2 (P98160)
I137M (p.Ile137Met) in HSPG2 (P98160) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact.
I137M (p.Ile137Met) variant details
- p.Ile137Met
- NCI-TCGA Cosmic COSV1010
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.