NM_182914.3(SYNE2):c.9974C>T (p.Ala3325Val) AND not specified
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Sep 3, 2015
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000264733.4
Allele description [Variation Report for NM_182914.3(SYNE2):c.9974C>T (p.Ala3325Val)]
NM_182914.3(SYNE2):c.9974C>T (p.Ala3325Val)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Feb 28, 2024