NM_000018.4(ACADVL):c.1678+23C>T AND ACADVL-related disorder
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jun 25, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003937977.2
Allele description [Variation Report for NM_000018.4(ACADVL):c.1678+23C>T]
NM_000018.4(ACADVL):c.1678+23C>T
Condition(s)
- Name:
- ACADVL-related disorder
- Synonyms:
- ACADVL-related condition
- Identifiers:
-
Homo sapiens BRCA1 DNA repair associated (BRCA1), transcript variant 299, mRNA
Homo sapiens BRCA1 DNA repair associated (BRCA1), transcript variant 299, mRNAgi|2255452522|ref|NM_001408439.1|Nucleotide
-
Godartiana byses voucher MGCL:MGCLLOAN523 putative Ngg1 interacting factor 3 lik...
Godartiana byses voucher MGCL:MGCLLOAN523 putative Ngg1 interacting factor 3 like 1 binding protein 1 gene, partial cdsgi|2569198810|gb|OL167100.1|Nucleotide
-
Lib 0
Lib 0biosample
-
LOC101930296 [Homo sapiens]
LOC101930296 [Homo sapiens]Gene ID:101930296Gene
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Last Updated: Oct 13, 2024