NM_006186.4(NR4A2):c.325dup (p.Gln109fs) AND Inborn genetic diseases
- Germline classification:
- Pathogenic (1 submission)
- Last evaluated:
- Jan 15, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001266179.4
Allele description [Variation Report for NM_006186.4(NR4A2):c.325dup (p.Gln109fs)]
NM_006186.4(NR4A2):c.325dup (p.Gln109fs)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
peptidase S41 [Sediminicola sp. YIK13]
peptidase S41 [Sediminicola sp. YIK13]gi|946528511|gnl|PRJNA271050|SB49_1 gb|ALM08502.1|Protein
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See more...Assertion and evidence details
Last Updated: Sep 16, 2024