N22T (p.Asn22Thr) variant of CUX1 (Homeobox protein cut-like 1)
N22T (p.Asn22Thr) in CUX1 (Homeobox protein cut-like 1) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.40 / 1. The record also includes population frequency data, experimental measurements, published literature, and structural context.
N22T (p.Asn22Thr) variant details
- p.Asn22Thr
- gnomAD 7-101816041-A-C
- Missense
- Variant Prioritization Score for Impact Estimate 0.403
- CADD 23.40
- SIFT 0.02
- Most common in the Non-Finnish European population (allele frequency 1e-06)
- Structural context available
- CUX1 CUT domain domainome 1.0: score -0.916
- Literature evidence available