NM_178857.6(RP1L1):c.3022C>T (p.Gln1008Ter) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 1, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000762488.17
Allele description [Variation Report for NM_178857.6(RP1L1):c.3022C>T (p.Gln1008Ter)]
NM_178857.6(RP1L1):c.3022C>T (p.Gln1008Ter)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Apr 15, 2024