GRCh38/hg38 1p36.33(chr1:844353-911241)x3 AND See cases
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Aug 30, 2010
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000134780.5
Allele description [Variation Report for GRCh38/hg38 1p36.33(chr1:844353-911241)x3]
GRCh38/hg38 1p36.33(chr1:844353-911241)x3
Condition(s)
- Name:
- See cases [See the Variation display for details]
- Identifiers:
-
PREDICTED: Homo sapiens uncharacterized protein (LOC112267992), transcript varia...
PREDICTED: Homo sapiens uncharacterized protein (LOC112267992), transcript variant X4, misc_RNAgi|2217369370|ref|XR_002956537.2|Nucleotide
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Last Updated: May 7, 2024