NM_004370.6(COL12A1):c.3092G>A (p.Arg1031His) AND multiple conditions
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Nov 1, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000815602.6
Allele description [Variation Report for NM_004370.6(COL12A1):c.3092G>A (p.Arg1031His)]
NM_004370.6(COL12A1):c.3092G>A (p.Arg1031His)
Condition(s)
Assertion and evidence details
Last Updated: Mar 5, 2024