NM_001042424.3(NSD2):c.51G>C (p.Lys17Asn) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 21, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004493712.1
Allele description [Variation Report for NM_001042424.3(NSD2):c.51G>C (p.Lys17Asn)]
NM_001042424.3(NSD2):c.51G>C (p.Lys17Asn)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
LOC129664323 [Homo sapiens]
LOC129664323 [Homo sapiens]Gene ID:129664323Gene
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Last Updated: May 7, 2024