S13* (p.Ser13Ter) variant of MECP2 (Methyl-CpG-binding protein 2)
S13* (p.Ser13Ter) in MECP2 (Methyl-CpG-binding protein 2) is a protein-truncating change. Clinical records from EBI and UniProt describe it as pathogenic. The record also includes experimental measurements, published literature, and structural context.
S13* (p.Ser13Ter) variant details
- p.Ser13Ter
- rs2148667313
- ClinGen CA415179115
- ClinVar RCV001384305
- ClinVar RCV004698352
- Pathogenic
- Stop Gained
- EBI: Pathogenic
- UniProt: Pathogenic
- Structural context available
- MECP2 Methyl-CpG DNA binding domain domainome 1.0: score -0.824
- Cited in: MECP2 Disorders. (PMID 20301670)
- Cited in: Clinical genetics evaluation in identifying the etiology of autism spectrum disorders: 2013 guideline revisions. (PMID 23519317)