V37V (p.Val37Val) variant of SLC22A1 (O15245)
V37V (p.Val37Val) in SLC22A1 (O15245) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.41 / 1. The record also includes population frequency data, published literature, and structural context.
V37V (p.Val37Val) variant details
- p.Val37Val
- rs750016388
- gnomAD 6-160122046-G-A
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.409
- CADD 4.92
- Most common in the Finnish in Finland (FIN) population (allele frequency 7.5e-05)
- Structural context available
- Literature evidence available