NM_001008537.3(NEXMIF):c.4346G>A (p.Arg1449His) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Dec 16, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000792949.6
Allele description [Variation Report for NM_001008537.3(NEXMIF):c.4346G>A (p.Arg1449His)]
NM_001008537.3(NEXMIF):c.4346G>A (p.Arg1449His)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Jun 9, 2024