View genomic variant #0000000329

Chromosome 11
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Type del
DNA change (genomic) (Relative to hg19 / GRCh37) g.68528997_68529000del
Published as -
GERP -
Segregation -
DB-ID CPT1A_000026 See all 2 reported entries
MSCV MSCV_0000329
dbSNP ID rs80356799
Frequency -
Sources ; ensembl;
Reference 20301700;12111367
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 0000000329 +?/+? - - c.2028+3_2028+6del p.? - - - -
CPT1A 00000662 NM_001876.3 0000000329 +?/+? - - c.2028+3_2028+6del p.? - - - -
CPT1A 00000664 XM_005273762.1 0000000329 +?/+? - - c.2124+3_2124+6del p.? - - - -
CPT1A 00000661 XM_005273763.1 0000000329 +?/+? - - c.2124+3_2124+6del p.? - - - -
CPT1A 00000663 XM_005273764.1 0000000329 +?/+? - - c.2028+3_2028+6del p.? - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV001279745;
Chromosome 11:68528996..68528996
Allele frequencies from ExAC 0.00006
ClinVar Allele ID 979116
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.68528996G>C
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. CPT1A:1374
Molecular consequence SO:0001627|intron variant
Allele origin germline
dbSNP ID 768465007
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR

RCVaccession RCV000055864;
Chromosome 11:68528997..68529000
ClinVar Allele ID 76559
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.68528997ACTT[1]
ClinVar review status no assertion provided
Clinical Significance not provided
Variant type Microsatellite
Sequence Ontology for variant type SO:0000289
Variant clinical sources reported ClinGen:CA344980
Gene symbol:Gene id. CPT1A:1374
Molecular consequence SO:0001575|splice donor variant
Allele origin unknown
dbSNP ID 80356799
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