NM_006721.4(ADK):c.1088G>A (p.Ter363=) AND not provided
- Germline classification:
- Benign/Likely benign (3 submissions)
- Last evaluated:
- Jan 25, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000963506.16
Allele description [Variation Report for NM_006721.4(ADK):c.1088G>A (p.Ter363=)]
NM_006721.4(ADK):c.1088G>A (p.Ter363=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Oct 8, 2024