NM_058216.3(RAD51C):c.396A>C (p.Thr132=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Nov 24, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001269242.1
Allele description [Variation Report for NM_058216.3(RAD51C):c.396A>C (p.Thr132=)]
NM_058216.3(RAD51C):c.396A>C (p.Thr132=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
MED23 [Cotesia glomerata]
MED23 [Cotesia glomerata]Gene ID:123266823Gene
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See more...Assertion and evidence details
Last Updated: May 1, 2024