A26T (p.Ala26Thr) variant of GFAP (Glial fibrillary acidic protein)
A26T (p.Ala26Thr) in GFAP (Glial fibrillary acidic protein) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as likely benign in the context of not provided. The available variant effect predictions contribute to a CATVariant prioritization score of 0.57 / 1. The record also includes population frequency data.
A26T (p.Ala26Thr) variant details
- p.Ala26Thr
- rs1231379140
- ClinGen CA399849134
- ClinVar RCV003419756
- TOPMed rs1231379140
- Likely benign
- not provided
- Missense
- Variant Prioritization Score for Impact Estimate 0.566
- CADD 12.60
- PolyPhen-2 0.00
- SIFT 0.30
- ClinVar: Likely benign (not provided)
- EBI: Likely benign
- UniProt: Likely benign
- Most common in the Non-Finnish European population (allele frequency 8.8e-05)