NM_001365536.1(SCN9A):c.1980G>A (p.Thr660=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- May 25, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000423461.2
Allele description
NM_001365536.1(SCN9A):c.1980G>A (p.Thr660=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Jun 8, 2021