NM_018238.4(AGK):c.1088C>T (p.Thr363Met) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Sep 17, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000200719.7
Allele description [Variation Report for NM_018238.4(AGK):c.1088C>T (p.Thr363Met)]
NM_018238.4(AGK):c.1088C>T (p.Thr363Met)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 29, 2024