NM_003900.5(SQSTM1):c.183C>T (p.Gly61=) AND Paget disease of bone 3
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 13, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000372389.6
Allele description [Variation Report for NM_003900.5(SQSTM1):c.183C>T (p.Gly61=)]
NM_003900.5(SQSTM1):c.183C>T (p.Gly61=)
Condition(s)
Assertion and evidence details
Last Updated: Oct 8, 2024