NM_000117.3(EMD):c.646G>A (p.Gly216Arg) AND not provided
- Germline classification:
- Conflicting interpretations of pathogenicity (2 submissions)
- Last evaluated:
- Nov 5, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000732781.11
Allele description [Variation Report for NM_000117.3(EMD):c.646G>A (p.Gly216Arg)]
NM_000117.3(EMD):c.646G>A (p.Gly216Arg)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 29, 2024