P79S (p.Pro79Ser) variant of INSR (Insulin receptor)
P79S (p.Pro79Ser) in INSR (Insulin receptor) 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 0.72 / 1. The record also includes population frequency data and structural context.
P79S (p.Pro79Ser) variant details
- p.Pro79Ser
- NCI-TCGA Cosmic COSV5715
- cosmic curated COSV57158
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.718
- REVEL 0.72
- MetaLR 0.59
- MetaSVM 0.26
- CADD 26.00
- PolyPhen-2 1.00
- SIFT 0.02
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available