NM_001844.5(COL2A1):c.3084G>T (p.Thr1028=) AND not provided
- Germline classification:
- Likely benign (3 submissions)
- Last evaluated:
- Apr 1, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000991607.13
Allele description [Variation Report for NM_001844.5(COL2A1):c.3084G>T (p.Thr1028=)]
NM_001844.5(COL2A1):c.3084G>T (p.Thr1028=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Oct 8, 2024