GRCh38/hg38 5p14.1(chr5:26620589-27232606)x3 AND See cases
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 10, 2011
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000139800.5
Allele description [Variation Report for GRCh38/hg38 5p14.1(chr5:26620589-27232606)x3]
GRCh38/hg38 5p14.1(chr5:26620589-27232606)x3
Condition(s)
- Name:
- See cases [See the Variation display for details]
- Identifiers:
-
za75h08.s1 Soares_fetal_lung_NbHL19W Homo sapiens cDNA clone IMAGE:298431 3', mR...
za75h08.s1 Soares_fetal_lung_NbHL19W Homo sapiens cDNA clone IMAGE:298431 3', mRNA sequencegi|1231420|gnl|dbEST|480272|gb|N741Nucleotide
-
Homo sapiens casein alpha s1 (CSN1S1), transcript variant 2, mRNA
Homo sapiens casein alpha s1 (CSN1S1), transcript variant 2, mRNAgi|1675116695|ref|NM_001025104.2|Nucleotide
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See more...Assertion and evidence details
Last Updated: May 7, 2024