NM_001113491.2(SEPTIN9):c.*1639C>G AND not provided
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- May 1, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003418029.6
Allele description
NM_001113491.2(SEPTIN9):c.*1639C>G
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Jun 17, 2024