NM_000018.4(ACADVL):c.1678+9G>A AND Very long chain acyl-CoA dehydrogenase deficiency
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 28, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001503308.6
Allele description [Variation Report for NM_000018.4(ACADVL):c.1678+9G>A]
NM_000018.4(ACADVL):c.1678+9G>A
Condition(s)
-
Homo sapiens leukocyte associated immunoglobulin like receptor 2 (LAIR2), transc...
Homo sapiens leukocyte associated immunoglobulin like receptor 2 (LAIR2), transcript variant 1, mRNAgi|543173170|ref|NM_002288.5|Nucleotide
-
Rheocles wrightae brain super conserved receptor (sreb2) gene, partial cds
Rheocles wrightae brain super conserved receptor (sreb2) gene, partial cdsgi|394799619|gb|JX189945.1|Nucleotide
-
Rheocles wrightae hypothetical protein (ptr) gene, partial cds
Rheocles wrightae hypothetical protein (ptr) gene, partial cdsgi|394767550|gb|JX190082.1|Nucleotide
-
Rheocles wrightae histone H3a gene, partial cds
Rheocles wrightae histone H3a gene, partial cdsgi|56089756|gb|AY655558.1|Nucleotide
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Feb 28, 2024