View genomic variant #0000024156

Chromosome 11
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.68582843A>G
Published as -
GERP -
Segregation -
DB-ID CPT1A_000054
MSCV -
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 Lishuang Shen




Variant on transcripts

5 entries on 1 page. Showing entries 1 - 5.
Legend  

Gene     

Transcript ID     

AscendingTranscript     

Variant ID     

Affects function     

Location     

Exon     

DNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
CPT1A 00000660 NM_001031847.2 0000024156 ./. - - c.100T>C p.(Ser34Pro) - - - -
CPT1A 00000662 NM_001876.3 0000024156 ./. - - c.100T>C p.(Ser34Pro) - - - -
CPT1A 00000664 XM_005273762.1 0000024156 ./. - - c.196T>C p.(Ser66Pro) - - - -
CPT1A 00000661 XM_005273763.1 0000024156 ./. - - c.196T>C p.(Ser66Pro) - - - -
CPT1A 00000663 XM_005273764.1 0000024156 ./. - - c.100T>C p.(Ser34Pro) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000693588; RCV000723488; RCV003407458;
Chromosome 11:68582843..68582843
ClinVar Allele ID 99873
Disease database name and identifier .|MONDO:MONDO:0009705, MedGen:C1829703, OMIM:255120, Orphanet:156|MedGen:C3661900
ClinVar preferred disease name CPT1A-related condition|Carnitine palmitoyl transferase 1A deficiency|not provided
HGVS variant names NC 000011.9:g.68582843A>G
ClinVar review status criteria provided, conflicting interpretations
Clinical Significance Conflicting interpretations of pathogenicity
Conflicting clinical significance Likely pathogenic(2)|Uncertain significance(3)
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA221850
Gene symbol:Gene id. CPT1A:1374
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 398123653
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