P9P (p.Pro9Pro) variant of SLC6A19 (Q695T7)
P9P (p.Pro9Pro) in SLC6A19 (Q695T7) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.08 / 1. The record also includes population frequency data, published literature, and structural context.
P9P (p.Pro9Pro) variant details
- p.Pro9Pro
- rs370311234
- gnomAD 5-1201677-C-A
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.0768
- CADD 0.12
- Most common in the Non-Finnish European population (allele frequency 4.4e-05)
- Structural context available
- Literature evidence available