V13I (p.Val13Ile) variant of FGFR2 (P21802)
V13I (p.Val13Ile) in FGFR2 (P21802) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.24 / 1. The record also includes population frequency data and structural context.
V13I (p.Val13Ile) variant details
- p.Val13Ile
- cosmic curated COSV10590
- Ensembl rs2135485083
- Missense
- Variant Prioritization Score for Impact Estimate 0.244
- REVEL 0.12
- CADD 16.30
- PolyPhen-2 0.00
- SIFT 0.39
- Most common in the Non-Finnish European population (allele frequency 9.9e-07)
- Structural context available