Gene entry
BRAT1
BRCA1 associated ATM activator 1
- Chromosome
- 7
- Cytoband
- 7p22.3
- Variants (rsID)
- 12
BRAT1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 7 (region 7p22.3). Its official name is “BRCA1 associated ATM activator 1”. The reference table lists 12 variants (rsID) for this gene.
Clinically classified variants
7 reference-table entries with clinical significance.
- rs150942467Benignsingle nucleotide variantNeonatal-onset encephalopathy with rigidity and seizures
- rs56727079Benignsingle nucleotide variantNeonatal-onset encephalopathy with rigidity and seizures
- rs61740320Benignsingle nucleotide variantNeonatal-onset encephalopathy with rigidity and seizures
- rs77213198Benignsingle nucleotide variantNeonatal-onset encephalopathy with rigidity and seizures
- rs79263074Conflicting interpretationssingle nucleotide variantNeonatal-onset encephalopathy with rigidity and seizures
- rs730880324PathogenicDuplicationNeonatal-onset encephalopathy with rigidity and seizures|Inborn genetic diseases|Neurodevelopmental disorder with cerebellar atrophy and with or without seizures
- rs148923187Uncertain significancesingle nucleotide variantNeonatal-onset encephalopathy with rigidity and seizures
Other listed variants
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.