T38T (p.Thr38Thr) variant of SLC18A2 (Q05940)
T38T (p.Thr38Thr) in SLC18A2 (Q05940) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.68 / 1. The record also includes population frequency data, published literature, and structural context.
T38T (p.Thr38Thr) variant details
- p.Thr38Thr
- gnomAD 10-117241807-T-C
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.683
- CADD 11.10
- Most common in the South Asian population (allele frequency 1.2e-05)
- Structural context available
- Literature evidence available