P5H (p.Pro5His) variant of SCN9A (Q15858)
P5H (p.Pro5His) 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.
P5H (p.Pro5His) variant details
- p.Pro5His
- NCI-TCGA Cosmic COSV5761
- NCI-TCGA Cosmic COSV5762
- cosmic curated COSV57629
- Variant assessed as somatic; moderate impact.
- Missense
- MetaLR 0.78
- MetaSVM 0.46
- SIFT 0.00
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available