NM_001306215.2(ZNF827):c.2316A>T (p.Pro772=) AND not provided
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Mar 30, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000960846.3
Allele description [Variation Report for NM_001306215.2(ZNF827):c.2316A>T (p.Pro772=)]
NM_001306215.2(ZNF827):c.2316A>T (p.Pro772=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Dec 24, 2023