NM_002431.4(MNAT1):c.496C>G (p.Gln166Glu) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 2, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004327008.1
Allele description [Variation Report for NM_002431.4(MNAT1):c.496C>G (p.Gln166Glu)]
NM_002431.4(MNAT1):c.496C>G (p.Gln166Glu)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: May 26, 2024