View genomic variant #0000015317

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.53676584_53676585del
Published as -
GERP -
Segregation -
DB-ID CPT2_000003 See all 2 reported entries
MSCV MSCV_0000030
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 0000015317 ./. - - c.1238_1239del p.(Lys414Thrfs*7) - - - -
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ClinVar @ MSeqDR

RCVaccession RCV000185837; RCV000202516; RCV000576522; RCV002225079; RCV002490673; RCV003474675;
Chromosome 1:53676584..53676585
ClinVar Allele ID 98339
Disease database name and identifier MONDO:MONDO:0015515, MedGen:C0342790, Orphanet:157|MONDO:MONDO:0012136, MedGen:C1833518, OMIM:608836, Orphanet:228308|MONDO:MONDO:0013633, MedGen:C3280160, OMIM:614212, Orphanet:263524|MONDO:MONDO:0010914, MedGen:C1833511, OMIM:600649, Orphanet:228305|MONDO:MONDO:0009704, MedGen:C1833508, OMIM:255110, Orphanet:157, Orphanet:228302|MedGen:C3661900
ClinVar preferred disease name Carnitine palmitoyltransferase II deficiency|Carnitine palmitoyl transferase II deficiency, neonatal form|Encephalopathy, acute, infection-induced, susceptibility to, 4|Carnitine palmitoyl transferase II deficiency, severe infantile form|Carnitine palmitoyl transferase II deficiency, myopathic form|not provided
HGVS variant names NC 000001.10:g.53676585 53676586del
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Pathogenic
Variant type Deletion
Sequence Ontology for variant type SO:0000159
Variant clinical sources reported ClinGen:CA266757|Genetic Testing Registry (GTR):GTR000604056|OMIM:600650.0009
Gene symbol:Gene id. CPT2:1376
Molecular consequence SO:0001589|frameshift variant
Allele origin germline
dbSNP ID 397509431
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