NM_004523.4(KIF11):c.1344C>T (p.Asp448=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Aug 16, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000935826.6
Allele description [Variation Report for NM_004523.4(KIF11):c.1344C>T (p.Asp448=)]
NM_004523.4(KIF11):c.1344C>T (p.Asp448=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 20, 2024