View genomic variant #0000015334

Chromosome 1
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Probably does not affect function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.53679229A>G
Published as -
GERP -
Segregation -
DB-ID CPT2_000032
MSCV MSCV_0015334
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 0.16738 View details
Owner LOVD




Variant on transcripts

1 entry on 1 page. Showing entry 1.
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Gene     

Transcript ID     

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Variant ID     

Affects function     

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DNA change (cDNA)     

Protein     

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GVS function     

Splice distance     

SIFT     
CPT2 00000665 NM_000098.2 0000015334 ./. - - c.1939A>G p.(Met647Val) - - - -
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ClinVar @ MSeqDR

RCVaccession RCV000078120; RCV000202533; RCV000578093; RCV000986323; RCV001533573; RCV001811357;
Chromosome 1:53679229..53679229
Allele frequencies from ESP 0.16738
Allele frequencies from ExAC 0.16197
Allele frequencies from TGP 0.10044
ClinVar Allele ID 98342
Disease database name and identifier MONDO:MONDO:0012136, MedGen:C1833518, OMIM:608836, Orphanet:228308|MONDO:MONDO:0010914, MedGen:C1833511, OMIM:600649, Orphanet:228305|MONDO:MONDO:0015515, MedGen:C0342790, Orphanet:157|MedGen:CN169374|MedGen:C3661900
ClinVar preferred disease name Carnitine palmitoyl transferase II deficiency, neonatal form|Carnitine palmitoyl transferase II deficiency, severe infantile form|Carnitine palmitoyltransferase II deficiency|not specified|not provided
HGVS variant names NC 000001.10:g.53679229A>G
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Benign
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA285315|UniProtKB:P23786#VAR 001400
Gene symbol:Gene id. CPT2:1376
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 1799822
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