S74A (p.Ser74Ala) variant of ATP6V1A (P38606)
S74A (p.Ser74Ala) in ATP6V1A (P38606) 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.
S74A (p.Ser74Ala) variant details
- p.Ser74Ala
- rs2549719151
- ClinGen CA354006995
- ClinVar RCV003030332
- Uncertain significance
- not provided
- Missense
- ClinVar: Uncertain significance (not provided)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available