T118= variant of HSPG2 (P98160)
T118= in HSPG2 (P98160) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; low impact.
T118= variant details
- NCI-TCGA Cosmic COSV6593
- Variant assessed as somatic; low impact.
- Missense
- UniProt: Variant assessed as somatic; low impact.