NM_005670.4(EPM2A):c.86T>C (p.Leu29Pro) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Dec 19, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002562127.2
Allele description [Variation Report for NM_005670.4(EPM2A):c.86T>C (p.Leu29Pro)]
NM_005670.4(EPM2A):c.86T>C (p.Leu29Pro)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
IFNGR2 [Lagopus muta]
IFNGR2 [Lagopus muta]Gene ID:125697195Gene
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Last Updated: May 1, 2024