NM_000901.5(NR3C2):c.*813G>A AND Autosomal dominant pseudohypoaldosteronism type 1
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 13, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001148961.4
Allele description [Variation Report for NM_000901.5(NR3C2):c.*813G>A]
NM_000901.5(NR3C2):c.*813G>A
Condition(s)
-
Homo sapiens family with sequence similarity 72 member A (FAM72A), transcript va...
Homo sapiens family with sequence similarity 72 member A (FAM72A), transcript variant 5, mRNAgi|1869284215|ref|NM_001385241.1|Nucleotide
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Last Updated: Apr 9, 2023