T23N (p.Thr23Asn) variant of SLC6A19 (Q695T7)
T23N (p.Thr23Asn) in SLC6A19 (Q695T7) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.09 / 1. The record also includes population frequency data and structural context.
T23N (p.Thr23Asn) variant details
- p.Thr23Asn
- gnomAD rs1444672095
- Missense
- Variant Prioritization Score for Impact Estimate 0.0928
- REVEL 0.09
- ESM-1b 0.00
- AlphaMissense 0.07
- CADD 0.00
- PolyPhen-2 0.00
- SIFT 0.49
- Most common in the Latino/Admixed American population (allele frequency 2.2e-05)
- Structural context available