NM_001365951.3(KIF1B):c.2664A>G (p.Lys888=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jun 21, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004042523.1
Allele description [Variation Report for NM_001365951.3(KIF1B):c.2664A>G (p.Lys888=)]
NM_001365951.3(KIF1B):c.2664A>G (p.Lys888=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Oct 26, 2024