U.S. flag

An official website of the United States government

NM_000018.4(ACADVL):c.602_603del (p.Tyr201fs) AND Very long chain acyl-CoA dehydrogenase deficiency

Germline classification:
Pathogenic (1 submission)
Last evaluated:
May 10, 2023
Review status:
1 star out of maximum of 4 stars
criteria provided, single submitter
Somatic classification
of clinical impact:
None
Review status:
(0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided
Somatic classification
of oncogenicity:
None
Review status:
(0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided
Record status:
current
Accession:
RCV003322775.1

Allele description [Variation Report for NM_000018.4(ACADVL):c.602_603del (p.Tyr201fs)]

NM_000018.4(ACADVL):c.602_603del (p.Tyr201fs)

Gene:
ACADVL:acyl-CoA dehydrogenase very long chain [Gene - OMIM - HGNC]
Variant type:
Deletion
Cytogenetic location:
17p13.1
Genomic location:
Preferred name:
NM_000018.4(ACADVL):c.602_603del (p.Tyr201fs)
Other names:
p.Tyr201Serfs*51
HGVS:
  • NC_000017.11:g.7221662_7221663del
  • NG_007975.1:g.6829_6830del
  • NG_008391.2:g.3388_3389del
  • NM_000018.3:c.602_603del
  • NM_000018.4:c.602_603delMANE SELECT
  • NM_001033859.3:c.536_537del
  • NM_001270447.2:c.671_672del
  • NM_001270448.2:c.374_375del
  • NP_000009.1:p.Tyr201fs
  • NP_001029031.1:p.Tyr179fs
  • NP_001257376.1:p.Tyr224fs
  • NP_001257377.1:p.Tyr125fs
  • NC_000017.10:g.7124981_7124982del
  • NM_000018.2:c.602_603delAC
Protein change:
Y125fs
Links:
dbSNP: rs1064796104
NCBI 1000 Genomes Browser:
rs1064796104
Molecular consequence:
  • NM_000018.4:c.602_603del - frameshift variant - [Sequence Ontology: SO:0001589]
  • NM_001033859.3:c.536_537del - frameshift variant - [Sequence Ontology: SO:0001589]
  • NM_001270447.2:c.671_672del - frameshift variant - [Sequence Ontology: SO:0001589]
  • NM_001270448.2:c.374_375del - frameshift variant - [Sequence Ontology: SO:0001589]

Condition(s)

Name:
Very long chain acyl-CoA dehydrogenase deficiency (ACADVLD)
Synonyms:
VLCAD deficiency
Identifiers:
MONDO: MONDO:0008723; MedGen: C3887523; Orphanet: 26793; OMIM: 201475

Recent activity

Clear Turn Off Turn On

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...

Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV004028496Molecular Diagnostics Laboratory, M Health Fairview: University of Minnesota
criteria provided, single submitter

(ACMG Guidelines, 2015)		Pathogenic
(May 10, 2023) 		germlineclinical testing

PubMed (1)
[See all records that cite this PMID]

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineyesnot providednot providednot providednot providednot providedclinical testing

Citations

PubMed

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.

Richards S, Aziz N, Bale S, Bick D, Das S, Gastier-Foster J, Grody WW, Hegde M, Lyon E, Spector E, Voelkerding K, Rehm HL; ACMG Laboratory Quality Assurance Committee..

Genet Med. 2015 May;17(5):405-24. doi: 10.1038/gim.2015.30. Epub 2015 Mar 5.

PubMed [citation]
PMID:
25741868
PMCID:
PMC4544753

Details of each submission

From Molecular Diagnostics Laboratory, M Health Fairview: University of Minnesota, SCV004028496.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testing PubMed (1)
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineyesnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Aug 26, 2023