NM_002180.3(IGHMBP2):c.1515C>T (p.Asp505=) AND Inborn genetic diseases
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jul 11, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002395396.2
Allele description [Variation Report for NM_002180.3(IGHMBP2):c.1515C>T (p.Asp505=)]
NM_002180.3(IGHMBP2):c.1515C>T (p.Asp505=)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
Cpgi9468 AND (alive[prop]) (0)
Gene
-
178602[uid] AND (alive[prop]) (1)
Gene
-
ergo-1 Piwi domain-containing protein;Piwi-like protein ergo-1 [Caenorhabditis e...
ergo-1 Piwi domain-containing protein;Piwi-like protein ergo-1 [Caenorhabditis elegans]Gene ID:178602Gene
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Last Updated: May 1, 2024