NM_018180.3(DHX32):c.2193G>T (p.Glu731Asp) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jul 3, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003677724.1
Allele description [Variation Report for NM_018180.3(DHX32):c.2193G>T (p.Glu731Asp)]
NM_018180.3(DHX32):c.2193G>T (p.Glu731Asp)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 16, 2024