NM_018960.6(GNMT):c.25C>G (p.Arg9Gly) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Feb 14, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001052288.7
Allele description [Variation Report for NM_018960.6(GNMT):c.25C>G (p.Arg9Gly)]
NM_018960.6(GNMT):c.25C>G (p.Arg9Gly)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
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Last Updated: Sep 29, 2024