P87H (p.Pro87His) variant of HCN1 (O60741)
P87H (p.Pro87His) in HCN1 (O60741) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The available variant effect predictions contribute to a CATVariant prioritization score of 0.46 / 1. The record also includes population frequency data and structural context.
P87H (p.Pro87His) variant details
- p.Pro87His
- rs1397144091
- NCI-TCGA Cosmic COSV1003
- cosmic curated COSV10030
- Ensembl rs1397144091
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.46
- REVEL 0.30
- CADD 22.70
- PolyPhen-2 0.09
- SIFT 0.12
- UniProt: Variant assessed as somatic; moderate impact.
- Population evidence available
- Structural context available