NM_000018.4(ACADVL):c.1751+7_1751+9del AND Very long chain acyl-CoA dehydrogenase deficiency
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 14, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002823678.3
Allele description [Variation Report for NM_000018.4(ACADVL):c.1751+7_1751+9del]
NM_000018.4(ACADVL):c.1751+7_1751+9del
Condition(s)
-
Homo sapiens solute carrier family 12 member 2 (SLC12A2), transcript variant 1, ...
Homo sapiens solute carrier family 12 member 2 (SLC12A2), transcript variant 1, mRNAgi|1519314779|ref|NM_001046.3|Nucleotide
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024