NM_000388.4(CASR):c.1027G>A (p.Val343Ile) AND Nephrolithiasis/nephrocalcinosis
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Dec 23, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004026546.1
Allele description [Variation Report for NM_000388.4(CASR):c.1027G>A (p.Val343Ile)]
NM_000388.4(CASR):c.1027G>A (p.Val343Ile)
Condition(s)
- Name:
- Nephrolithiasis/nephrocalcinosis
- Identifiers:
- MedGen: CN580796
-
Homo sapiens NME/NM23 family member 5 (NME5), mRNA
Homo sapiens NME/NM23 family member 5 (NME5), mRNAgi|1519242694|ref|NM_003551.3|Nucleotide
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Last Updated: Sep 29, 2024