NM_005120.3(MED12):c.934G>C (p.Val312Leu) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jul 15, 2013
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000117597.16
Allele description [Variation Report for NM_005120.3(MED12):c.934G>C (p.Val312Leu)]
NM_005120.3(MED12):c.934G>C (p.Val312Leu)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
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Last Updated: Jun 9, 2024