NM_015272.5(RPGRIP1L):c.3738C>T (p.Asp1246=) AND multiple conditions
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Feb 15, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002495745.1
Allele description [Variation Report for NM_015272.5(RPGRIP1L):c.3738C>T (p.Asp1246=)]
NM_015272.5(RPGRIP1L):c.3738C>T (p.Asp1246=)
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024