NM_133261.3(GIPC3):c.57G>T (p.Ala19=) AND not specified
- Germline classification:
- Likely benign (2 submissions)
- Last evaluated:
- Aug 23, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000246163.9
Allele description [Variation Report for NM_133261.3(GIPC3):c.57G>T (p.Ala19=)]
NM_133261.3(GIPC3):c.57G>T (p.Ala19=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Aug 4, 2024