NM_020882.4(COL20A1):c.1168T>A (p.Ser390Thr) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 2, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004194999.1
Allele description [Variation Report for NM_020882.4(COL20A1):c.1168T>A (p.Ser390Thr)]
NM_020882.4(COL20A1):c.1168T>A (p.Ser390Thr)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Oct 13, 2024