G86V (p.Gly86Val) variant of RELN (Reelin)
G86V (p.Gly86Val) in RELN (Reelin) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes variant effect predictions and population frequency data.
G86V (p.Gly86Val) variant details
- p.Gly86Val
- NCI-TCGA Cosmic COSV1006
- cosmic curated COSV10063
- NCI-TCGA Cosmic COSV5903
- Variant assessed as somatic; moderate impact.
- Missense
- REVEL 0.41
- MetaLR 0.12
- MetaSVM -0.99
- CADD 24.40
- PolyPhen-2 1.00
- SIFT 0.00
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the African/African-American population (allele frequency 3e-05)