NM_001378457.1(DMXL2):c.7047T>G (p.Val2349=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Aug 31, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002152613.5
Allele description [Variation Report for NM_001378457.1(DMXL2):c.7047T>G (p.Val2349=)]
NM_001378457.1(DMXL2):c.7047T>G (p.Val2349=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Mar 16, 2024