View genomic variant #0000025364

Variant on transcripts

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Please note that a short description of a certain column can be displayed when you move your mouse cursor over the column's header and hold it still. Below, a more detailed description is shown per column.

Affects function: The variant's effect on the protein's function, in the format 'R/C' where R is the value reported by the source and C is the value concluded by the curator; '+' indicating the variant affects function, '+?' probably affects function, '+*' affects function, not associated with individual's disease phenotype, '#' affects function, not associated with any known disease phenotype, '-' does not affect function, '-?' probably does not affect function, '?' effect unknown, '.' effect not classified.

Location: Location of variant at DNA level; note that the variant location can also be derived from the variant description.
All options:

• 5' gene flanking
• 5' UTR
• Exon
• Intron
• 3' UTR
• 3' gene flanking

Exon: Number of exon/intron containing variant; 2 = exon 2, 12i = intron 12, 2i_7i = exons 3 to 7, 8i_9 = border intron 8/exon 9.

DNA change (cDNA): Description of variant at DNA level, based on a coding DNA reference sequence (following HGVS recommendations); e.g. c.123C>T, c.123_145del, c.123_126dup.

Protein: Description of variant at protein level (following HGVS recommendations).

• p.(Arg345Pro) = change predicted from DNA (RNA not analysed)
• p.Arg345Pro = change derived from RNA analysis
• p.? = unknown effect
• p.0? = probably no protein produced

PolyPhen: Effect of variant, predicted by PolyPhen.
All options:

• benign = Benign
• possiblyDamaging = Possibly damaging
• probablyDamaging = Probably damaging
• noPrediction = No prediction

GVS function: The functional annotation of this position from the Genome Variation Server.
All options:

• intergenic
• near-gene-5
• utr-5
• coding
• coding-near-splice
• coding-synonymous
• coding-synonymous-near-splice
• codingComplex
• codingComplex-near-splice
• frameshift
• frameshift-near-splice
• missense
• missense-near-splice
• splice-5
• intron
• splice-3
• stop-gained
• stop-gained-near-splice
• stop-lost
• stop-lost-near-splice
• utr-3
• near-gene-3

Splice distance: The distance to the nearest splice site.

SIFT: SIFT Annotation

4 entries on 1 page. Showing entries 1 - 4.

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Gene	Transcript ID	Transcript	Variant ID	Affects function	Location	Exon	DNA change (cDNA)	Protein	PolyPhen	GVS function	Splice distance	SIFT
ACADVL	00000390	NM_000018.3	0000025364	./.	-	-	c.138+1_138+2insT	p.?	-	-	-	-
ACADVL	00000391	NM_001033859.2	0000025364	./.	-	-	c.138+1_138+2insT	p.?	-	-	-	-
ACADVL	00000388	NM_001270447.1	0000025364	./.	-	-	c.207+1_207+2insT	p.?	-	-	-	-
ACADVL	00000389	NM_001270448.1	0000025364	./.	-	-	c.-91+1_-91+2insT	p.?	-	-	-	-

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ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR
RCVaccession	RCV000665642;
Chromosome	17:7123517..7123517
Allele frequencies from ExAC	0.00009
ClinVar Allele ID	548238
Disease database name and identifier	MONDO:MONDO:0008723, MedGen:C3887523, OMIM:201475, Orphanet:26793
ClinVar preferred disease name	Very long chain acyl-CoA dehydrogenase deficiency
HGVS variant names	NC 000017.10:g.7123517G>A
ClinVar review status	reviewed by expert panel
Clinical Significance	Likely pathogenic
Variant type	single nucleotide variant
Sequence Ontology for variant type	SO:0001483
Gene symbol:Gene id.	ACADVL:37|LOC130060113:130060113
Molecular consequence	SO:0001575|splice donor variant
Allele origin	germline
dbSNP ID	747351687
Variant Flags	:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR
RCVaccession	RCV000523516; RCV000666464;
Chromosome	17:7123517..7123518
ClinVar Allele ID	445883
Disease database name and identifier	MONDO:MONDO:0008723, MedGen:C3887523, OMIM:201475, Orphanet:26793|MedGen:CN517202
ClinVar preferred disease name	Very long chain acyl-CoA dehydrogenase deficiency|not provided
HGVS variant names	NC 000017.10:g.7123518dup
ClinVar review status	criteria provided, conflicting interpretations
Clinical Significance	Conflicting interpretations of pathogenicity
Conflicting clinical significance	Pathogenic(1)|Likely pathogenic(1)|Uncertain significance(2)
Variant type	Duplication
Sequence Ontology for variant type	SO:1000035
Variant clinical sources reported	ClinGen:CA658658531
Gene symbol:Gene id.	ACADVL:37|LOC130060113:130060113
Molecular consequence	SO:0001575|splice donor variant
Allele origin	germline
dbSNP ID	1555527548
Variant Flags	:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR
RCVaccession	RCV000410269;
Chromosome	17:7123518..7123518
ClinVar Allele ID	358459
Disease database name and identifier	MONDO:MONDO:0008723, MedGen:C3887523, OMIM:201475, Orphanet:26793
ClinVar preferred disease name	Very long chain acyl-CoA dehydrogenase deficiency
HGVS variant names	NC 000017.10:g.7123518T>C
ClinVar review status	criteria provided, multiple submitters, no conflicts
Clinical Significance	Likely pathogenic
Variant type	single nucleotide variant
Sequence Ontology for variant type	SO:0001483
Variant clinical sources reported	ClinGen:CA16041857
Gene symbol:Gene id.	ACADVL:37|LOC130060113:130060113
Molecular consequence	SO:0001575|splice donor variant
Allele origin	germline
dbSNP ID	1057516817
Variant Flags	:

ClinVar @ MSeqDR as full content XML tree

MSeqDR View Variant at Gbrowse

Mitomap Mitochondrial Variant Phenotype Information:

None

Ensembl Variant Phenotype Information:

None