View genomic variant #0000002042

Chromosome 11
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Type del
DNA change (genomic) (Relative to hg19 / GRCh37) g.68527728_68527740del
Published as -
GERP -
Segregation -
DB-ID CPT1A_000032 See all 2 reported entries
MSCV MSCV_0002042
dbSNP ID rs80356797
Frequency -
Sources ; Ensembl;
Reference 20301700;12189492
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 0000002042 ./. - - c.2095_2107del p.(Leu699Glnfs*46) - - - -
CPT1A 00000662 NM_001876.3 0000002042 ?/? - - c.2095_2107del p.(Leu699Glnfs*52) - - - -
CPT1A 00000664 XM_005273762.1 0000002042 ./. - - c.2191_2203del p.(Leu731Glnfs*52) - - - -
CPT1A 00000661 XM_005273763.1 0000002042 ./. - - c.2191_2203del p.(Leu731Glnfs*46) - - - -
CPT1A 00000663 XM_005273764.1 0000002042 ./. - - c.2095_2107del p.(Leu699Glnfs*52) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV003083323;
Chromosome 11:68527727..68527727
ClinVar Allele ID 1881502
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.68527727G>A
ClinVar review status criteria provided, single submitter
Clinical Significance Uncertain significance
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Gene symbol:Gene id. CPT1A:1374
Molecular consequence SO:0001583|missense variant
Allele origin germline
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR

RCVaccession RCV003067028;
Chromosome 11:68527728..68527728
ClinVar Allele ID 1876852
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.68527728G>T
ClinVar review status criteria provided, single submitter
Clinical Significance Uncertain significance
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Gene symbol:Gene id. CPT1A:1374
Molecular consequence SO:0001583|missense variant
Allele origin germline
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