NM_178857.6(RP1L1):c.1317C>A (p.Gly439=) AND not specified
- Germline classification:
- Benign (1 submission)
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001699607.2
Allele description [Variation Report for NM_178857.6(RP1L1):c.1317C>A (p.Gly439=)]
NM_178857.6(RP1L1):c.1317C>A (p.Gly439=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Dec 24, 2023