S76N (p.Ser76Asn) variant of HSPG2 (P98160)
S76N (p.Ser76Asn) in HSPG2 (P98160) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact.
S76N (p.Ser76Asn) variant details
- p.Ser76Asn
- NCI-TCGA Cosmic COSV6597
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.