NM_000352.6(ABCC8):c.4588C>T (p.Arg1530Cys) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Apr 15, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000503292.6
Allele description [Variation Report for NM_000352.6(ABCC8):c.4588C>T (p.Arg1530Cys)]
NM_000352.6(ABCC8):c.4588C>T (p.Arg1530Cys)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Jul 22, 2023