NM_178857.6(RP1L1):c.416dup (p.Gly140fs) AND not specified
- Germline classification:
- Benign (2 submissions)
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001729566.3
Allele description [Variation Report for NM_178857.6(RP1L1):c.416dup (p.Gly140fs)]
NM_178857.6(RP1L1):c.416dup (p.Gly140fs)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Sep 29, 2024