NM_004370.6(COL12A1):c.97T>G (p.Phe33Val) AND multiple conditions
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 3, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001246252.6
Allele description [Variation Report for NM_004370.6(COL12A1):c.97T>G (p.Phe33Val)]
NM_004370.6(COL12A1):c.97T>G (p.Phe33Val)
Condition(s)
Assertion and evidence details
Last Updated: Feb 28, 2024