View genomic variant #0000015300

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.53662709del
Published as -
GERP -
Segregation -
DB-ID CPT2_000017
MSCV MSCV_0015300
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 0000015300 ./. - - c.94del p.(Gly32Alafs*41) - - - -
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ClinVar @ MSeqDR

RCVaccession RCV002141144;
Chromosome 1:53662708..53662708
ClinVar Allele ID 1535036
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.53662708C>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|LOC129930561:129930561
Molecular consequence SO:0001819|synonymous variant
Allele origin germline
dbSNP ID 1056264696
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR

RCVaccession RCV000409193; RCV000410121; RCV000411223;
Chromosome 1:53662709..53662709
ClinVar Allele ID 357115
Disease database name and identifier MONDO:MONDO:0009704, MedGen:C1833508, OMIM:255110, Orphanet:157, Orphanet:228302|MONDO:MONDO:0012136, MedGen:C1833518, OMIM:608836, Orphanet:228308|MONDO:MONDO:0010914, MedGen:C1833511, OMIM:600649, Orphanet:228305
ClinVar preferred disease name Carnitine palmitoyl transferase II deficiency, myopathic form|Carnitine palmitoyl transferase II deficiency, neonatal form|Carnitine palmitoyl transferase II deficiency, severe infantile form
HGVS variant names NC 000001.10:g.53662710del
ClinVar review status criteria provided, single submitter
Clinical Significance Likely pathogenic
Variant type Deletion
Sequence Ontology for variant type SO:0000159
Variant clinical sources reported ClinGen:CA16040762
Gene symbol:Gene id. CPT2:1376|LOC129930561:129930561
Molecular consequence SO:0001589|frameshift variant
Allele origin unknown
dbSNP ID 1057517494
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