NM_000939.4(POMC):c.389C>T (p.Pro130Leu) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- May 4, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003287394.2
Allele description [Variation Report for NM_000939.4(POMC):c.389C>T (p.Pro130Leu)]
NM_000939.4(POMC):c.389C>T (p.Pro130Leu)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
Mus musculus natriuretic peptide receptor 2 (Npr2), transcript variant 2, mRNA
Mus musculus natriuretic peptide receptor 2 (Npr2), transcript variant 2, mRNAgi|1243057584|ref|NM_001355466.1|Nucleotide
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Last Updated: May 1, 2024