NM_080680.3(COL11A2):c.4767C>T (p.Asp1589=) AND not provided
- Germline classification:
- Conflicting interpretations of pathogenicity (2 submissions)
- Last evaluated:
- Mar 9, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000405179.10
Allele description [Variation Report for NM_080680.3(COL11A2):c.4767C>T (p.Asp1589=)]
NM_080680.3(COL11A2):c.4767C>T (p.Asp1589=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 20, 2024