GRCh38/hg38 22q11.21(chr22:18178957-18997006)x3 AND See cases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- May 27, 2010
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000133705.5
Allele description [Variation Report for GRCh38/hg38 22q11.21(chr22:18178957-18997006)x3]
GRCh38/hg38 22q11.21(chr22:18178957-18997006)x3
Condition(s)
- Name:
- See cases [See the Variation display for details]
- Identifiers:
-
C10orf55 chromosome 10 putative open reading frame 55 [Homo sapiens]
C10orf55 chromosome 10 putative open reading frame 55 [Homo sapiens]Gene ID:414236Gene
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See more...Assertion and evidence details
Last Updated: May 7, 2024