NM_152592.6(SYNE3):c.55T>C (p.Trp19Arg) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Oct 3, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004159094.1
Allele description [Variation Report for NM_152592.6(SYNE3):c.55T>C (p.Trp19Arg)]
NM_152592.6(SYNE3):c.55T>C (p.Trp19Arg)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Aug 11, 2024