GRCh37/hg19 9p24.3-24.1(chr9:203862-8548307)x1 AND not specified
- Germline classification:
- Pathogenic (1 submission)
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003986852.1
Allele description [Variation Report for GRCh37/hg19 9p24.3-24.1(chr9:203862-8548307)x1]
GRCh37/hg19 9p24.3-24.1(chr9:203862-8548307)x1
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
PREDICTED: Homo sapiens torsin family 1 member B (TOR1B), transcript variant X1,...
PREDICTED: Homo sapiens torsin family 1 member B (TOR1B), transcript variant X1, mRNAgi|2462624229|ref|XM_054362751.1|Nucleotide
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Last Updated: Sep 1, 2024