S15F (p.Ser15Phe) variant of GALT (P07902)
S15F (p.Ser15Phe) in GALT (P07902) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.14 / 1. The record also includes population frequency data, published literature, and structural context.
S15F (p.Ser15Phe) variant details
- p.Ser15Phe
- rs960526230
- gnomAD 9-34647243-C-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.135
- CADD 7.71
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available
- Literature evidence available