NM_139057.4(ADAMTS17):c.771C>T (p.Ile257=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 17, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002196866.6
Allele description [Variation Report for NM_139057.4(ADAMTS17):c.771C>T (p.Ile257=)]
NM_139057.4(ADAMTS17):c.771C>T (p.Ile257=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 29, 2024