NM_032634.4(PIGO):c.2166G>C (p.Ala722=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Aug 28, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000441071.2
Allele description
NM_032634.4(PIGO):c.2166G>C (p.Ala722=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Jun 15, 2021