NM_178857.6(RP1L1):c.420C>A (p.Gly140=) 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:
- RCV001700099.2
Allele description [Variation Report for NM_178857.6(RP1L1):c.420C>A (p.Gly140=)]
NM_178857.6(RP1L1):c.420C>A (p.Gly140=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Sep 29, 2024