T14I (p.Thr14Ile) variant of FGFR2 (P21802)
T14I (p.Thr14Ile) in FGFR2 (P21802) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.50 / 1. The record also includes population frequency data and structural context.
T14I (p.Thr14Ile) variant details
- p.Thr14Ile
- cosmic curated COSV10740
- ExAC rs753987054
- gnomAD rs753987054
- Missense
- Variant Prioritization Score for Impact Estimate 0.501
- REVEL 0.40
- CADD 22.70
- PolyPhen-2 0.35
- SIFT 0.33
- Most common in the Non-Finnish European population (allele frequency 5.8e-05)
- Structural context available