NM_006269.2(RP1):c.3826C>T (p.Pro1276Ser) AND Retinitis pigmentosa
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 13, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001163234.4
Allele description [Variation Report for NM_006269.2(RP1):c.3826C>T (p.Pro1276Ser)]
NM_006269.2(RP1):c.3826C>T (p.Pro1276Ser)
Condition(s)
Assertion and evidence details
Last Updated: Oct 8, 2024