NM_001034853.2(RPGR):c.2606_2632dup (p.860EEGEEGEGE[3]) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Sep 1, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002464519.6
Allele description [Variation Report for NM_001034853.2(RPGR):c.2606_2632dup (p.860EEGEEGEGE[3])]
NM_001034853.2(RPGR):c.2606_2632dup (p.860EEGEEGEGE[3])
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 16, 2024