M1T (p.Met1Thr) variant of HSPG2 (P98160)
M1T (p.Met1Thr) in HSPG2 (P98160) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of not provided. The record also includes variant effect predictions.
M1T (p.Met1Thr) variant details
- p.Met1Thr
- rs2152809609
- ClinGen CA338910129
- ClinVar RCV003712957
- Uncertain significance
- not provided
- Missense
- MetaLR 0.44
- MetaSVM -0.15
- PolyPhen-2 0.46
- SIFT 0.00
- MutPred 0.98
- ClinVar: Uncertain significance (not provided)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance