M46I (p.Met46Ile) variant of HSPG2 (P98160)
M46I (p.Met46Ile) in HSPG2 (P98160) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact.
M46I (p.Met46Ile) variant details
- p.Met46Ile
- NCI-TCGA Cosmic COSV1010
- NCI-TCGA Cosmic COSV6597
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.