View genomic variant #0000016623

Chromosome 11
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.68562381T>C
Published as -
GERP -
Segregation -
DB-ID CPT1A_000041
MSCV MSCV_0016623
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

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 0000016623 ./. - - c.772-2A>G p.? - - - -
CPT1A 00000662 NM_001876.3 0000016623 ./. - - c.772-2A>G p.? - - - -
CPT1A 00000664 XM_005273762.1 0000016623 ./. - - c.868-2A>G p.? - - - -
CPT1A 00000661 XM_005273763.1 0000016623 ./. - - c.868-2A>G p.? - - - -
CPT1A 00000663 XM_005273764.1 0000016623 ./. - - c.772-2A>G p.? - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000409488;
Chromosome 11:68562381..68562381
ClinVar Allele ID 358060
Disease database name and identifier MONDO:MONDO:0009705, MedGen:C1829703, OMIM:255120, Orphanet:156
ClinVar preferred disease name Carnitine palmitoyl transferase 1A deficiency
HGVS variant names NC 000011.9:g.68562381T>C
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:CA16041540
Gene symbol:Gene id. CPT1A:1374
Molecular consequence SO:0001574|splice acceptor variant
Allele origin unknown
dbSNP ID 1057517245
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