NM_022132.5(MCCC2):c.114C>G (p.Gly38=) AND not provided
- Germline classification:
- Likely benign (2 submissions)
- Last evaluated:
- May 1, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004569813.5
Allele description [Variation Report for NM_022132.5(MCCC2):c.114C>G (p.Gly38=)]
NM_022132.5(MCCC2):c.114C>G (p.Gly38=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
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Last Updated: Oct 13, 2024