A69A (p.Ala69Ala) variant of FHL1 (Q13642)
A69A (p.Ala69Ala) in FHL1 (Q13642) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.10 / 1. The record also includes population frequency data, published literature, and structural context.
A69A (p.Ala69Ala) variant details
- p.Ala69Ala
- rs1394298803
- gnomAD X-136206579-G-A
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.102
- CADD 3.02
- Most common in the Latino/Admixed American population (allele frequency 5.7e-05)
- Structural context available
- Literature evidence available