NM_002878.4(RAD51D):c.82+5_82+12del AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- May 29, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000828247.1
Allele description [Variation Report for NM_002878.4(RAD51D):c.82+5_82+12del]
NM_002878.4(RAD51D):c.82+5_82+12del
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: CN517202
-
TI_59393944 (0)
Nucleotide
-
Homo sapiens cDNA, FLJ98530
Homo sapiens cDNA, FLJ98530gi|164695837|dbj|AK308489.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Apr 23, 2022