NM_000388.4(CASR):c.2356A>G (p.Ile786Val) AND Nephrolithiasis/nephrocalcinosis
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 31, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004028659.1
Allele description [Variation Report for NM_000388.4(CASR):c.2356A>G (p.Ile786Val)]
NM_000388.4(CASR):c.2356A>G (p.Ile786Val)
Condition(s)
- Name:
- Nephrolithiasis/nephrocalcinosis
- Identifiers:
- MedGen: CN580796
-
Homo sapiens chromosome 17 open reading frame 42, mRNA (cDNA clone IMAGE:5739804...
Homo sapiens chromosome 17 open reading frame 42, mRNA (cDNA clone IMAGE:5739804), with apparent retained introngi|40555776|gb|BC064631.1|Nucleotide
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Last Updated: Nov 3, 2024