NM_001379150.1(IRS4):c.2852C>T (p.Pro951Leu) AND not provided
- 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:
- RCV003457615.8
Allele description [Variation Report for NM_001379150.1(IRS4):c.2852C>T (p.Pro951Leu)]
NM_001379150.1(IRS4):c.2852C>T (p.Pro951Leu)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Oct 8, 2024