NM_000018.4(ACADVL):c.1678+23C>T AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Aug 27, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001559679.2
Allele description [Variation Report for NM_000018.4(ACADVL):c.1678+23C>T]
NM_000018.4(ACADVL):c.1678+23C>T
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
Homo sapiens RAD51 paralog B (RAD51B), transcript variant 2, mRNA
Homo sapiens RAD51 paralog B (RAD51B), transcript variant 2, mRNAgi|1677475267|ref|NM_133510.4|Nucleotide
-
Coccidiosis
CoccidiosisMedGen
-
C0009187[conceptid] (1)
MedGen
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See more...Assertion and evidence details
Last Updated: Oct 13, 2024