NM_001206744.2(TPO):c.2052T>C (p.Arg684=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jul 24, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000971102.4
Allele description [Variation Report for NM_001206744.2(TPO):c.2052T>C (p.Arg684=)]
NM_001206744.2(TPO):c.2052T>C (p.Arg684=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 29, 2024