G69V (p.Gly69Val) variant of SCN9A (Q15858)
G69V (p.Gly69Val) in SCN9A (Q15858) 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 structural context.
G69V (p.Gly69Val) variant details
- p.Gly69Val
- NCI-TCGA Cosmic COSV5762
- cosmic curated COSV57621
- Variant assessed as somatic; moderate impact.
- Missense
- MetaLR 0.92
- MetaSVM 1.03
- SIFT 0.00
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available