W14S (p.Trp14Ser) variant of GABRA1 (P14867)
W14S (p.Trp14Ser) in GABRA1 (P14867) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of not provided. The record also includes structural context.
W14S (p.Trp14Ser) variant details
- p.Trp14Ser
- rs2532198229
- ClinGen CA362181129
- ClinVar RCV002306427
- Uncertain significance
- not provided
- Missense
- ClinVar: Uncertain significance (not provided)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available