NM_006269.2(RP1):c.2991T>C (p.Asn997=) AND Retinitis pigmentosa
- Germline classification:
- 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:
- RCV000376223.5
Allele description [Variation Report for NM_006269.2(RP1):c.2991T>C (p.Asn997=)]
NM_006269.2(RP1):c.2991T>C (p.Asn997=)
Condition(s)
Assertion and evidence details
Last Updated: Feb 28, 2024