View genomic variant #0000015297

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

1 entry on 1 page. Showing entry 1.

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Gene	Transcript ID	Transcript	Variant ID	Affects function	Location	Exon	DNA change (cDNA)	Protein	PolyPhen	GVS function	Splice distance	SIFT
CPT2	00000665	NM_000098.2	0000015297	./.	-	-	c.35del	p.(Gly13Alafs*60)	-	-	-	-

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ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR
RCVaccession	RCV000169434; RCV002515200;
Chromosome	1:53662650..53662650
ClinVar Allele ID	186625
Disease database name and identifier	MONDO:MONDO:0015515, MedGen:C0342790, Orphanet:157|MONDO:MONDO:0010914, MedGen:C1833511, OMIM:600649, Orphanet:228305
ClinVar preferred disease name	Carnitine palmitoyltransferase II deficiency|Carnitine palmitoyl transferase II deficiency, severe infantile form
HGVS variant names	NC 000001.10:g.53662653del
ClinVar review status	criteria provided, multiple submitters, no conflicts
Clinical Significance	Pathogenic/Likely pathogenic
Variant type	Deletion
Sequence Ontology for variant type	SO:0000159
Variant clinical sources reported	ClinGen:CA274312
Gene symbol:Gene id.	CPT2:1376|LOC129930561:129930561
Molecular consequence	SO:0001589|frameshift variant
Allele origin	germline
dbSNP ID	786204647
Variant Flags	:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR
RCVaccession	RCV000558197;
Chromosome	1:53662650..53662650
ClinVar Allele ID	448194
Disease database name and identifier	MONDO:MONDO:0015515, MedGen:C0342790, Orphanet:157
ClinVar preferred disease name	Carnitine palmitoyltransferase II deficiency
HGVS variant names	NC 000001.10:g.53662650G>A
ClinVar review status	criteria provided, single submitter
Clinical Significance	Uncertain significance
Variant type	single nucleotide variant
Sequence Ontology for variant type	SO:0001483
Variant clinical sources reported	ClinGen:CA22626369
Gene symbol:Gene id.	CPT2:1376|LOC129930561:129930561
Molecular consequence	SO:0001583|missense variant
Allele origin	germline
dbSNP ID	1044059386
Variant Flags	:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR
RCVaccession	RCV001272279;
Chromosome	1:53662651..53662651
ClinVar Allele ID	746556
Disease database name and identifier	MONDO:MONDO:0015515, MedGen:C0342790, Orphanet:157
ClinVar preferred disease name	Carnitine palmitoyltransferase II deficiency
HGVS variant names	NC 000001.10:g.53662651G>C
ClinVar review status	criteria provided, single submitter
Clinical Significance	Likely benign
Variant type	single nucleotide variant
Sequence Ontology for variant type	SO:0001483
Gene symbol:Gene id.	CPT2:1376|LOC129930561:129930561
Molecular consequence	SO:0001819|synonymous variant
Allele origin	germline
dbSNP ID	1350688021
Variant Flags	:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR
RCVaccession	RCV001956469;
Chromosome	1:53662651..53662652
ClinVar Allele ID	1490968
Disease database name and identifier	MONDO:MONDO:0015515, MedGen:C0342790, Orphanet:157
ClinVar preferred disease name	Carnitine palmitoyltransferase II deficiency
HGVS variant names	NC 000001.10:g.53662654 53662661dup
ClinVar review status	criteria provided, single submitter
Clinical Significance	Pathogenic
Variant type	Duplication
Sequence Ontology for variant type	SO:1000035
Gene symbol:Gene id.	CPT2:1376|LOC129930561:129930561
Molecular consequence	SO:0001589|frameshift variant
Allele origin	germline
dbSNP ID	2100254713
Variant Flags	:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR
RCVaccession	RCV000672860; RCV002499183; RCV002532136; RCV003453357; RCV003456125; RCV003453358;
Chromosome	1:53662652..53662654
ClinVar Allele ID	541302
Disease database name and identifier	MONDO:MONDO:0015515, MedGen:C0342790, Orphanet:157|MONDO:MONDO:0012136, MedGen:C1833518, OMIM:608836, Orphanet:228308|MONDO:MONDO:0010914, MedGen:C1833511, OMIM:600649, Orphanet:228305|MONDO:MONDO:0009704, MedGen:C1833508, OMIM:255110, Orphanet:157, Orphanet:228302|MONDO:MONDO:0013633, MedGen:C3280160, OMIM:614212, Orphanet:263524
ClinVar preferred disease name	Carnitine palmitoyltransferase II deficiency|Carnitine palmitoyl transferase II deficiency, neonatal form|Carnitine palmitoyl transferase II deficiency, severe infantile form|Carnitine palmitoyl transferase II deficiency, myopathic form|Encephalopathy, acute, infection-induced, susceptibility to, 4
HGVS variant names	NC 000001.10:g.53662652 53662654del
ClinVar review status	criteria provided, multiple submitters, no conflicts
Clinical Significance	Uncertain significance
Variant type	Deletion
Sequence Ontology for variant type	SO:0000159
Gene symbol:Gene id.	CPT2:1376|LOC129930561:129930561
Molecular consequence	SO:0001822|inframe deletion
Allele origin	germline
dbSNP ID	1553168847
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