NM_001256071.3(RNF213):c.14566T>C (p.Cys4856Arg) AND not provided
- Germline classification:
- Conflicting interpretations of pathogenicity (2 submissions)
- Last evaluated:
- Jan 1, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001218019.17
Allele description [Variation Report for NM_001256071.3(RNF213):c.14566T>C (p.Cys4856Arg)]
NM_001256071.3(RNF213):c.14566T>C (p.Cys4856Arg)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Apr 15, 2024