View genomic variant #0000015318

Chromosome 1
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.53676688T>C
Published as -
GERP -
Segregation -
DB-ID CPT2_000004 See all 2 reported entries
MSCV MSCV_0000031
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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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 0000015318 ./. - - c.1342T>C p.(Phe448Leu) - - - -
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ClinVar @ MSeqDR

RCVaccession RCV000178040; RCV000202478; RCV000430397; RCV001810398;
Chromosome 1:53676688..53676688
Allele frequencies from ExAC 0.00011
ClinVar Allele ID 23999
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:0012136, MedGen:C1833518, OMIM:608836, Orphanet:228308|MedGen:CN169374|MONDO:MONDO:0015515, MedGen:C0342790, Orphanet:157|MedGen:C3661900
ClinVar preferred disease name Carnitine palmitoyl transferase II deficiency, severe infantile form|Carnitine palmitoyl transferase II deficiency, myopathic form|Carnitine palmitoyl transferase II deficiency, neonatal form|not specified|Carnitine palmitoyltransferase II deficiency|not provided
HGVS variant names NC 000001.10:g.53676688T>C
ClinVar review status criteria provided, conflicting interpretations
Clinical Significance Conflicting interpretations of pathogenicity|other
Conflicting clinical significance Uncertain significance(2)|Benign(1)
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA245063|OMIM:600650.0009|UniProtKB:P23786#VAR 007968
Gene symbol:Gene id. CPT2:1376
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 74315297
For included Variant: Tag-value pairs of disease database name and identifier, e.g. OMIM:NNNNNN MONDO:MONDO:0009704, MedGen:C1833508, OMIM:255110, Orphanet:157, Orphanet:228302|MONDO:MONDO:0015515, MedGen:C0342790, Orphanet:157
For included Variant : ClinVar preferred disease name for the concept specified by disease identifiers in CLNDISDB Carnitine palmitoyl transferase II deficiency, myopathic form|Carnitine palmitoyltransferase II deficiency
Clinical significance for a haplotype or genotype that includes this variant. Reported as pairs of VariationID:clinical significance. 60702:Pathogenic
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