NM_024949.6(WWC2):c.1570G>C (p.Gly524Arg) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Apr 13, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004311086.1
Allele description [Variation Report for NM_024949.6(WWC2):c.1570G>C (p.Gly524Arg)]
NM_024949.6(WWC2):c.1570G>C (p.Gly524Arg)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Jun 9, 2024