NM_018177.6(N4BP2):c.1864A>G (p.Ile622Val) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Nov 12, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004115741.1
Allele description [Variation Report for NM_018177.6(N4BP2):c.1864A>G (p.Ile622Val)]
NM_018177.6(N4BP2):c.1864A>G (p.Ile622Val)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Jun 9, 2024