A36V (p.Ala36Val) variant of FGFR1 (P11362)
A36V (p.Ala36Val) in FGFR1 (P11362) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.28 / 1. The record also includes population frequency data and structural context.
A36V (p.Ala36Val) variant details
- p.Ala36Val
- gnomAD rs1424869652
- Missense
- Variant Prioritization Score for Impact Estimate 0.279
- REVEL 0.21
- CADD 19.80
- PolyPhen-2 0.00
- SIFT 0.28
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available