NM_000901.5(NR3C2):c.*86T>C AND Autosomal dominant pseudohypoaldosteronism type 1
- Germline classification:
- Benign (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:
- RCV000346724.5
Allele description [Variation Report for NM_000901.5(NR3C2):c.*86T>C]
NM_000901.5(NR3C2):c.*86T>C
Condition(s)
-
transcription factor E2F8 isoform X1 [Homo sapiens]
transcription factor E2F8 isoform X1 [Homo sapiens]gi|2462527612|ref|XP_054225931.1|Protein
-
hypothetical protein HMPREF1211_06961 [Streptomyces sp. HGB0020]
hypothetical protein HMPREF1211_06961 [Streptomyces sp. HGB0020]gi|512057744|gb|EPD57231.1||gnl|WGS |HMPREF1211_06961T0Protein
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Last Updated: Sep 29, 2024