NM_024642.5(GALNT12):c.25C>G (p.Arg9Gly) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- May 28, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004022804.1
Allele description [Variation Report for NM_024642.5(GALNT12):c.25C>G (p.Arg9Gly)]
NM_024642.5(GALNT12):c.25C>G (p.Arg9Gly)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
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Last Updated: Oct 13, 2024