G86D (p.Gly86Asp) variant of RELN (Reelin)
G86D (p.Gly86Asp) in RELN (Reelin) is a missense change. Clinical records from ClinVar and UniProt describe it as uncertain significance in the context of Inborn genetic diseases. The record also includes variant effect predictions.
G86D (p.Gly86Asp) variant details
- p.Gly86Asp
- NCI-TCGA Cosmic COSV1006
- NCI-TCGA Cosmic COSV5903
- cosmic curated COSV59036
- Uncertain significance
- Inborn genetic diseases
- Missense
- MetaLR 0.12
- MetaSVM -0.99
- SIFT 0.02
- ClinVar: Uncertain significance (Inborn genetic diseases)
- UniProt: Uncertain significance