NM_003900.5(SQSTM1):c.1151C>T (p.Pro384Leu) AND multiple conditions
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 18, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002918613.2
Allele description [Variation Report for NM_003900.5(SQSTM1):c.1151C>T (p.Pro384Leu)]
NM_003900.5(SQSTM1):c.1151C>T (p.Pro384Leu)
Condition(s)
Assertion and evidence details
Last Updated: Jun 17, 2024