View genomic variant #0000000348

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.68552419A>C
Published as -
GERP 4.970
Segregation -
DB-ID CPT1A_000009 See all 2 reported entries
MSCV MSCV_0000348
dbSNP ID rs80356783
Frequency -
Sources ; clinvar; ensembl;
Reference 20301700;15110323
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 0000000348 +/+ - 10/19 c.1027T>G p.(Phe343Val) possibly_damaging(0.711) missense_variant - deleterious(0.02)
CPT1A 00000662 NM_001876.3 0000000348 +/+ - 10/19 c.1027T>G p.(Phe343Val) possibly_damaging(0.711) missense_variant - deleterious(0.02)
CPT1A 00000664 XM_005273762.1 0000000348 +/+ - 10/19 c.1123T>G p.(Phe375Val) - missense_variant - -
CPT1A 00000661 XM_005273763.1 0000000348 +/+ - 10/19 c.1123T>G p.(Phe375Val) - missense_variant - -
CPT1A 00000663 XM_005273764.1 0000000348 +/+ - 10/19 c.1027T>G p.(Phe343Val) possibly_damaging(0.711) missense_variant - deleterious(0.02)
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000055852;
Chromosome 11:68552419..68552419
ClinVar Allele ID 76547
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.68552419A>C
ClinVar review status criteria provided, conflicting interpretations
Clinical Significance Conflicting interpretations of pathogenicity
Conflicting clinical significance Likely pathogenic(1)|Uncertain significance(1)
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA344958|UniProtKB:P50416#VAR 046768
Gene symbol:Gene id. CPT1A:1374
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 80356783
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