P38S (p.Pro38Ser) variant of FGFR2 (P21802)
P38S (p.Pro38Ser) in FGFR2 (P21802) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.40 / 1. The record also includes population frequency data and structural context.
P38S (p.Pro38Ser) variant details
- p.Pro38Ser
- cosmic curated COSV60649
- ExAC rs775973432
- gnomAD rs775973432
- Missense
- Variant Prioritization Score for Impact Estimate 0.397
- REVEL 0.30
- CADD 23.90
- PolyPhen-2 0.22
- SIFT 0.11
- Most common in the 1KG:GIH population (allele frequency 0.0053)
- Structural context available