NM_000117.3(EMD):c.423T>G (p.Ser141=) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Oct 11, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000597174.5
Allele description [Variation Report for NM_000117.3(EMD):c.423T>G (p.Ser141=)]
NM_000117.3(EMD):c.423T>G (p.Ser141=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 28, 2024