NM_000018.4(ACADVL):c.1566C>T (p.Ser522=) AND Inborn genetic diseases
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jul 6, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002405182.2
Allele description [Variation Report for NM_000018.4(ACADVL):c.1566C>T (p.Ser522=)]
NM_000018.4(ACADVL):c.1566C>T (p.Ser522=)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
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POTE ankyrin domain family member E isoform X4 [Homo sapiens]
POTE ankyrin domain family member E isoform X4 [Homo sapiens]gi|2217328136|ref|XP_047300377.1|Protein
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SLC35E2B [Papio anubis]
SLC35E2B [Papio anubis]Gene ID:103886161Gene
-
SLC35E4 [Papio anubis]
SLC35E4 [Papio anubis]Gene ID:101008998Gene
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LOC102611099 [Citrus sinensis]
LOC102611099 [Citrus sinensis]Gene ID:102611099Gene
-
LOC111225169 [Seriola dumerili]
LOC111225169 [Seriola dumerili]Gene ID:111225169Gene
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See more...Assertion and evidence details
Last Updated: May 1, 2024