NM_000208.4(INSR):c.489C>A (p.Ile163=) AND not provided
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Sep 27, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000927016.8
Allele description [Variation Report for NM_000208.4(INSR):c.489C>A (p.Ile163=)]
NM_000208.4(INSR):c.489C>A (p.Ile163=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Apr 15, 2024