NM_014000.2(VCL):c.2802C>T (p.Ala934=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jul 10, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000614117.1
Allele description
NM_014000.2(VCL):c.2802C>T (p.Ala934=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Jul 10, 2021