T27S (p.Thr27Ser) variant of ERBB2 (P04626)
T27S (p.Thr27Ser) in ERBB2 (P04626) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes structural context.
T27S (p.Thr27Ser) variant details
- p.Thr27Ser
- NCI-TCGA Cosmic COSV9950
- cosmic curated COSV99506
- ExAC rs779913120
- TOPMed rs779913120
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available