NM_001365276.2(TNXB):c.7866C>T (p.Thr2622=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Feb 26, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001577962.3
Allele description [Variation Report for NM_001365276.2(TNXB):c.7866C>T (p.Thr2622=)]
NM_001365276.2(TNXB):c.7866C>T (p.Thr2622=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 1, 2024