NM_015655.4(ZNF337):c.1979T>C (p.Val660Ala) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Dec 7, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004122599.1
Allele description [Variation Report for NM_015655.4(ZNF337):c.1979T>C (p.Val660Ala)]
NM_015655.4(ZNF337):c.1979T>C (p.Val660Ala)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: May 26, 2024