A181T (p.Ala181Thr) variant of SPTBN2 (O15020)
A181T (p.Ala181Thr) in SPTBN2 (O15020) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of not provided.
A181T (p.Ala181Thr) variant details
- p.Ala181Thr
- rs2496528788
- ClinGen CA381483396
- ClinVar RCV003326837
- Uncertain significance
- not provided
- Missense
- ClinVar: Uncertain significance (not provided)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance