NM_178857.6(RP1L1):c.1297C>T (p.Arg433Cys) AND not provided
- Germline classification:
- Benign/Likely benign (2 submissions)
- Last evaluated:
- Jul 1, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003430943.9
Allele description [Variation Report for NM_178857.6(RP1L1):c.1297C>T (p.Arg433Cys)]
NM_178857.6(RP1L1):c.1297C>T (p.Arg433Cys)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 29, 2024