NM_001851.6(COL9A1):c.353G>A (p.Arg118Gln) AND multiple conditions
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Oct 31, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000764655.2
Allele description [Variation Report for NM_001851.6(COL9A1):c.353G>A (p.Arg118Gln)]
NM_001851.6(COL9A1):c.353G>A (p.Arg118Gln)
Condition(s)
Assertion and evidence details
Last Updated: Feb 20, 2024