Q38Q (p.Gln38Gln) variant of GALT (P07902)
Q38Q (p.Gln38Gln) in GALT (P07902) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.27 / 1. The record also includes population frequency data, published literature, and structural context.
Q38Q (p.Gln38Gln) variant details
- p.Gln38Gln
- gnomAD 9-34647120-G-A
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.267
- CADD 15.90
- Most common in the South Asian population (allele frequency 2.3e-05)
- Structural context available
- Literature evidence available