NM_206933.4(USH2A):c.3725C>T (p.Pro1242Leu) AND Retinitis pigmentosa
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 12, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000386343.5
Allele description [Variation Report for NM_206933.4(USH2A):c.3725C>T (p.Pro1242Leu)]
NM_206933.4(USH2A):c.3725C>T (p.Pro1242Leu)
Condition(s)
Assertion and evidence details
Last Updated: Mar 16, 2024