NM_001365276.2(TNXB):c.7704T>C (p.Val2568=) AND not provided
- Germline classification:
- Likely benign (2 submissions)
- Last evaluated:
- Dec 30, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001548668.3
Allele description [Variation Report for NM_001365276.2(TNXB):c.7704T>C (p.Val2568=)]
NM_001365276.2(TNXB):c.7704T>C (p.Val2568=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 29, 2024