View genomic variant #0000000353

Chromosome 11
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Type subst
DNA change (genomic) (Relative to hg19 / GRCh37) g.68562328C>T
Published as -
GERP 0.172
Segregation -
DB-ID CPT1A_000014 See all 2 reported entries
MSCV MSCV_0000353
dbSNP ID rs2229738
Frequency -
Sources ; clinvar; ensembl;
Reference 11441142;20301700
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 0.05574 View details
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 0000000353 +/+ - 8/19 c.823G>A p.(Ala275Thr) benign(0.006) missense_variant - tolerated(0.38)
CPT1A 00000662 NM_001876.3 0000000353 +/+ - 8/19 c.823G>A p.(Ala275Thr) benign(0.006) missense_variant - tolerated(0.38)
CPT1A 00000664 XM_005273762.1 0000000353 +/+ - 8/19 c.919G>A p.(Ala307Thr) - missense_variant - -
CPT1A 00000661 XM_005273763.1 0000000353 +/+ - 8/19 c.919G>A p.(Ala307Thr) - missense_variant - -
CPT1A 00000663 XM_005273764.1 0000000353 +/+ - 8/19 c.823G>A p.(Ala275Thr) benign(0.006) missense_variant - tolerated(0.38)
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000055868; RCV000180224;
Chromosome 11:68562328..68562328
Allele frequencies from ESP 0.05574
Allele frequencies from ExAC 0.06470
Allele frequencies from TGP 0.02376
ClinVar Allele ID 76563
Disease database name and identifier MedGen:CN169374|MONDO:MONDO:0009705, MedGen:C1829703, OMIM:255120, Orphanet:156
ClinVar preferred disease name not specified|Carnitine palmitoyl transferase 1A deficiency
HGVS variant names NC 000011.9:g.68562328C>T
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Benign/Likely benign
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA303058|UniProtKB:P50416#VAR 020547
Gene symbol:Gene id. CPT1A:1374
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 2229738
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