NM_000431.4(MVK):c.942T>A (p.Ser314=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Apr 5, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001712197.10
Allele description [Variation Report for NM_000431.4(MVK):c.942T>A (p.Ser314=)]
NM_000431.4(MVK):c.942T>A (p.Ser314=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Aug 18, 2024