T38S (p.Thr38Ser) variant of SLC18A2 (Q05940)
T38S (p.Thr38Ser) in SLC18A2 (Q05940) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.61 / 1. The record also includes population frequency data and structural context.
T38S (p.Thr38Ser) variant details
- p.Thr38Ser
- TOPMed rs1286556004
- gnomAD rs1286556004
- Missense
- Variant Prioritization Score for Impact Estimate 0.612
- CADD 24.80
- PolyPhen-2 0.51
- SIFT 0.03
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available