NM_004260.4(RECQL4):c.801G>C (p.Glu267Asp) AND not provided
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- May 26, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000834333.9
Allele description [Variation Report for NM_004260.4(RECQL4):c.801G>C (p.Glu267Asp)]
NM_004260.4(RECQL4):c.801G>C (p.Glu267Asp)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 8, 2024