NM_000875.5(IGF1R):c.246C>T (p.Thr82=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 6, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003814337.2
Allele description [Variation Report for NM_000875.5(IGF1R):c.246C>T (p.Thr82=)]
NM_000875.5(IGF1R):c.246C>T (p.Thr82=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 29, 2024