NM_024505.4(NOX5):c.814G>C (p.Gly272Arg) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- May 26, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004229081.1
Allele description [Variation Report for NM_024505.4(NOX5):c.814G>C (p.Gly272Arg)]
NM_024505.4(NOX5):c.814G>C (p.Gly272Arg)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
RNF139-DT RNF139 divergent transcript [Homo sapiens]
RNF139-DT RNF139 divergent transcript [Homo sapiens]Gene ID:101927612Gene
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See more...Assertion and evidence details
Last Updated: Jun 2, 2024