NM_003322.6(TULP1):c.776T>C (p.Ile259Thr) 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:
- RCV000318574.13
Allele description [Variation Report for NM_003322.6(TULP1):c.776T>C (p.Ile259Thr)]
NM_003322.6(TULP1):c.776T>C (p.Ile259Thr)
Condition(s)
Assertion and evidence details
Last Updated: Aug 18, 2024