View genomic variant #0000015328

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.53676960C>A
Published as -
GERP -
Segregation -
DB-ID CPT2_000037
MSCV MSCV_0015328
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.
Legend  

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 0000015328 ./. - - c.1614C>A p.(Tyr538*) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000409314; RCV000410441; RCV000411274;
Chromosome 1:53676960..53676960
ClinVar Allele ID 357125
Disease database name and identifier MONDO:MONDO:0012136, MedGen:C1833518, OMIM:608836, Orphanet:228308|MONDO:MONDO:0009704, MedGen:C1833508, OMIM:255110, Orphanet:157, Orphanet:228302|MONDO:MONDO:0010914, MedGen:C1833511, OMIM:600649, Orphanet:228305
ClinVar preferred disease name Carnitine palmitoyl transferase II deficiency, neonatal form|Carnitine palmitoyl transferase II deficiency, myopathic form|Carnitine palmitoyl transferase II deficiency, severe infantile form
HGVS variant names NC 000001.10:g.53676960C>A
ClinVar review status criteria provided, single submitter
Clinical Significance Likely pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA16040769
Gene symbol:Gene id. CPT2:1376
Molecular consequence SO:0001587|nonsense, SO:0001627|intron variant
Allele origin unknown
dbSNP ID 1057517517
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR

RCVaccession RCV003112741;
Chromosome 1:53676960..53676960
ClinVar Allele ID 1938625
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.53676960C>T
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
Molecular consequence SO:0001627|intron variant, SO:0001819|synonymous variant
Allele origin germline
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