NM_000489.6(ATRX):c.4659T>C (p.His1553=) AND not provided
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Mar 3, 2015
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001650900.10
Allele description [Variation Report for NM_000489.6(ATRX):c.4659T>C (p.His1553=)]
NM_000489.6(ATRX):c.4659T>C (p.His1553=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 1, 2024