H16Q (p.His16Gln) variant of SLC22A2 (O15244)
H16Q (p.His16Gln) in SLC22A2 (O15244) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.21 / 1. The record also includes population frequency data and structural context.
H16Q (p.His16Gln) variant details
- p.His16Gln
- ExAC rs776630141
- gnomAD rs776630141
- Missense
- Variant Prioritization Score for Impact Estimate 0.21
- REVEL 0.15
- CADD 17.20
- PolyPhen-2 0.08
- SIFT 0.00
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Structural context available