A17T (p.Ala17Thr) variant of DNMT1 (P26358)
A17T (p.Ala17Thr) in DNMT1 (P26358) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.42 / 1. The record also includes population frequency data and structural context.
A17T (p.Ala17Thr) variant details
- p.Ala17Thr
- cosmic curated COSV61577
- Missense
- Variant Prioritization Score for Impact Estimate 0.416
- REVEL 0.15
- CADD 26.20
- PolyPhen-2 0.99
- SIFT 0.04
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Structural context available