NM_017948.6(NOL8):c.3461G>A (p.Arg1154Gln) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 4, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004139169.1
Allele description [Variation Report for NM_017948.6(NOL8):c.3461G>A (p.Arg1154Gln)]
NM_017948.6(NOL8):c.3461G>A (p.Arg1154Gln)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Nov 24, 2024