NM_012123.4(MTO1):c.1368T>C (p.Thr456=) AND not provided
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- May 1, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003430695.9
Allele description [Variation Report for NM_012123.4(MTO1):c.1368T>C (p.Thr456=)]
NM_012123.4(MTO1):c.1368T>C (p.Thr456=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Oct 8, 2024