NM_000208.4(INSR):c.3775G>A (p.Asp1259Asn) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Dec 30, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000503966.2
Allele description
NM_000208.4(INSR):c.3775G>A (p.Asp1259Asn)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Nov 29, 2021