NM_080680.3(COL11A2):c.4854C>T (p.Asp1618=) AND not provided
- Germline classification:
- Benign/Likely benign (3 submissions)
- Last evaluated:
- Mar 1, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001569222.13
Allele description [Variation Report for NM_080680.3(COL11A2):c.4854C>T (p.Asp1618=)]
NM_080680.3(COL11A2):c.4854C>T (p.Asp1618=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Aug 4, 2024