NM_000208.4(INSR):c.3255C>T (p.His1085=) AND Rabson-Mendenhall syndrome
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jan 15, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000278910.13
Allele description [Variation Report for NM_000208.4(INSR):c.3255C>T (p.His1085=)]
NM_000208.4(INSR):c.3255C>T (p.His1085=)
Condition(s)
Assertion and evidence details
Last Updated: Aug 18, 2024