K13Q (p.Lys13Gln) variant of CREBBP (CREB-binding protein)
K13Q (p.Lys13Gln) in CREBBP (CREB-binding protein) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Rubinstein-Taybi syndrome. The available variant effect predictions contribute to a CATVariant prioritization score of 0.76 / 1. The record also includes published literature and structural context.
K13Q (p.Lys13Gln) variant details
- p.Lys13Gln
- rs587783484
- ClinGen CA394567872
- ClinVar RCV001220894
- Ensembl rs587783484
- Uncertain significance
- Rubinstein-Taybi syndrome
- Missense
- Variant Prioritization Score for Impact Estimate 0.76
- AlphaMissense 0.44
- MetaLR 0.85
- MetaSVM 0.84
- PolyPhen-2 1.00
- SIFT 0.00
- MutPred 0.30
- ClinVar: Uncertain significance (Rubinstein-Taybi syndrome)
- EBI: Likely pathogenic
- UniProt: Likely pathogenic
- Structural context available
- Cited in: Rubinstein-Taybi Syndrome. (PMID 20301699)