NM_182961.4(SYNE1):c.20646G>A (p.Ser6882=) AND multiple conditions
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jan 26, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000549032.12
Allele description [Variation Report for NM_182961.4(SYNE1):c.20646G>A (p.Ser6882=)]
NM_182961.4(SYNE1):c.20646G>A (p.Ser6882=)
Condition(s)
Assertion and evidence details
Last Updated: Mar 5, 2024