Q160H (p.Gln160His) variant of REN (Renin)
Q160H (p.Gln160His) in REN (Renin) 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 0.28 / 1. The record also includes population frequency data and structural context.
Q160H (p.Gln160His) variant details
- p.Gln160His
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.281
- REVEL 0.24
- MetaLR 0.18
- MetaSVM -0.92
- CADD 15.30
- PolyPhen-2 0.02
- SIFT 0.00
- UniProt: Variant assessed as somatic; moderate impact. (in dbSNP:rs11571083)
- Most common in the Non-Finnish European population (allele frequency 3.6e-06)
- Structural context available