P17T (p.Pro17Thr) variant of GABRG2 (P18507)
P17T (p.Pro17Thr) in GABRG2 (P18507) is a missense change. Clinical records from ClinVar and UniProt describe it as uncertain significance in the context of not provided. The record also includes structural context.
P17T (p.Pro17Thr) variant details
- p.Pro17Thr
- NCI-TCGA Cosmic COSV6271
- cosmic curated COSV62717
- Uncertain significance
- not provided
- Missense
- ClinVar: Uncertain significance (not provided)
- UniProt: Uncertain significance
- Structural context available