NM_017680.6(ASPN):c.89T>C (p.Met30Thr) AND ASPN-related disorder
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Apr 28, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003956891.1
Allele description
NM_017680.6(ASPN):c.89T>C (p.Met30Thr)
Condition(s)
- Name:
- ASPN-related disorder
- Synonyms:
- ASPN-related condition
- Identifiers:
Assertion and evidence details
Last Updated: Sep 1, 2024