NM_006122.4(MAN2A2):c.1378C>A (p.Gln460Lys) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Sep 12, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004362110.1
Allele description [Variation Report for NM_006122.4(MAN2A2):c.1378C>A (p.Gln460Lys)]
NM_006122.4(MAN2A2):c.1378C>A (p.Gln460Lys)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Oct 8, 2024