GRCh38/hg38 18q22.1(chr18:66379346-67471172)x3 AND See cases
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Sep 27, 2013
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000140917.6
Allele description [Variation Report for GRCh38/hg38 18q22.1(chr18:66379346-67471172)x3]
GRCh38/hg38 18q22.1(chr18:66379346-67471172)x3
Condition(s)
- Name:
- See cases [See the Variation display for details]
- Identifiers:
-
PREDICTED: Cataglyphis hispanica U1 spliceosomal RNA (LOC126848524), ncRNA
PREDICTED: Cataglyphis hispanica U1 spliceosomal RNA (LOC126848524), ncRNAgi|2296780661|ref|XR_007687276.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: May 7, 2024