NM_203304.4(MEX3D):c.495C>G (p.Asp165Glu) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Apr 7, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004310574.1
Allele description [Variation Report for NM_203304.4(MEX3D):c.495C>G (p.Asp165Glu)]
NM_203304.4(MEX3D):c.495C>G (p.Asp165Glu)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
LOC127892369 [Homo sapiens]
LOC127892369 [Homo sapiens]Gene ID:127892369Gene
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Last Updated: Jun 2, 2024