NM_001854.4(COL11A1):c.5056G>A (p.Val1686Ile) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Mar 26, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003027617.2
Allele description [Variation Report for NM_001854.4(COL11A1):c.5056G>A (p.Val1686Ile)]
NM_001854.4(COL11A1):c.5056G>A (p.Val1686Ile)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 20, 2024