View genomic variant #0000015302

Chromosome 1
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.53662764C>A
Published as -
GERP -
Segregation -
DB-ID CPT2_000011 See all 2 reported entries
MSCV MSCV_0000023
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
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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SIFT     
CPT2 00000665 NM_000098.2 0000015302 ./. - - c.149C>A p.(Pro50His) - - - -
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ClinVar @ MSeqDR

RCVaccession RCV000009511; RCV000009512; RCV000202440; RCV000440440; RCV000735345; RCV000762941; RCV003473063;
Chromosome 1:53662764..53662764
Allele frequencies from ExAC 0.00017
ClinVar Allele ID 23993
Disease database name and identifier 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|MONDO:MONDO:0012136, MedGen:C1833518, OMIM:608836, Orphanet:228308|MONDO:MONDO:0015515, MedGen:C0342790, Orphanet:157|MedGen:C3661900|Human Phenotype Ontology:HP:0002387, Human Phenotype Ontology:HP:0002459, Human Phenotype Ontology:HP:0007310, Human Phenotype Ontology:HP:0012332, MONDO:MONDO:0044872, MedGen:C0013363|Human Phenotype Ontology:HP:0005764, MONDO:MONDO:0024280, MedGen:C0162323|Human Phenotype Ontology:HP:0001369, MONDO:MONDO:0005578, MedGen:C0003864|Human Phenotype Ontology:HP:0012532, MedGen:C0150055|Human Phenotype Ontology:HP:0011703, MedGen:C0039239|Human Phenotype Ontology:HP:0040182, MedGen:C1881170|Human Phenotype Ontology:HP:0002579, MedGen:C1836923|Human Phenotype Ontology:HP:0001876, MONDO:MONDO:0001529, MedGen:C0030312
ClinVar preferred disease name Carnitine palmitoyl transferase II deficiency, severe infantile form|Carnitine palmitoyl transferase II deficiency, myopathic form|Encephalopathy, acute, infection-induced, susceptibility to, 4|Carnitine palmitoyl transferase II deficiency, neonatal form|Carnitine palmitoyltransferase II deficiency|not provided|Abnormal autonomic nervous system physiology|Polyarticular arthritis|Arthritis|Chronic pain|Sinus tachycardia|Inappropriate sinus tachycardia|Gastrointestinal dysmotility|Pancytopenia
HGVS variant names NC 000001.10:g.53662764C>A
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA254606|Genetic Testing Registry (GTR):GTR000604056|OMIM:600650.0003|UniProtKB:P23786#VAR 001391
Gene symbol:Gene id. CPT2:1376|LOC129930561:129930561
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 28936375
Variant Flags
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ClinVar @ MSeqDR as full content XML tree

MSeqDR View Variant at Gbrowse

Mitomap Mitochondrial Variant Phenotype Information:

None

Ensembl Variant Phenotype Information:

None