View genomic variant #0000000032

Chromosome 1
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Type subst
DNA change (genomic) (Relative to hg19 / GRCh37) g.53676706G>T
Published as -
GERP 4.870
Segregation -
DB-ID CPT2_000005 See all 2 reported entries
MSCV MSCV_0000032
dbSNP ID rs74315299
Frequency -
Sources ; clinvar; ensembl;
Reference 15622536
Variant remarks -
Genetic origin -
Average frequency (large NGS studies) Variant not found in online data sets
Owner LOVD




Variant on transcripts

1 entry on 1 page. Showing entry 1.
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Gene     

Transcript ID     

AscendingTranscript     

Variant ID     

Affects function     

Location     

Exon     

DNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
CPT2 00000665 NM_000098.2 0000000032 +/+ - 4/5 c.1360G>T p.(Glu454*) - stop_gained - -
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ClinVar @ MSeqDR

RCVaccession RCV000009528;
Chromosome 1:53676706..53676706
ClinVar Allele ID 24005
Disease database name and identifier MedGen:C1833508, OMIM:255110, Orphanet:ORPHA228302
ClinVar preferred disease name Carnitine palmitoyltransferase II deficiency, myopathic, stress-induced
HGVS variant names NC 000001.10:g.53676706G>T
ClinVar review status no assertion criteria provided
Clinical Significance Pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported OMIM Allelic Variant:600650.0015
Gene symbol:Gene id. CPT2:1376
Molecular consequence SO:0001587|nonsense
Allele origin germline
dbSNP ID 74315299
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

MSeqDR View Variant at Gbrowse

Mitomap Mitochondrial Variant Phenotype Information:

None

Ensembl Variant Phenotype Information:

variation_namechromseq_region_startseq_region_endallele_stringminor_alleleminor_allele_freqvariation_setPhenotype_description
rs7431529915367670653676706G/TOMIM phenotype variantsCARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LATE-ONSET
CM05024115367670653676706HGMD_MUTATIONHGMD-PUBLIC variantsAnnotated by HGMD but no phenotype description is publicly available