T40A (p.Thr40Ala) variant of FGFR2 (P21802)
T40A (p.Thr40Ala) in FGFR2 (P21802) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.35 / 1. The record also includes population frequency data and structural context.
T40A (p.Thr40Ala) variant details
- p.Thr40Ala
- cosmic curated COSV10590
- Ensembl rs2135124714
- Missense
- Variant Prioritization Score for Impact Estimate 0.348
- REVEL 0.28
- CADD 22.00
- PolyPhen-2 0.00
- SIFT 0.50
- Most common in the Non-Finnish European population (allele frequency 3.4e-06)
- Structural context available