View genomic variant #0000000355

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.68575021G>A
Published as -
GERP 3.980
Segregation -
DB-ID CPT1A_000016 See all 2 reported entries
MSCV MSCV_0000355
dbSNP ID rs80356775
Frequency -
Sources ; clinvar; ensembl;
Reference 11441142;23757202;20301700
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 0000000355 +/+ - 4/4 c.367C>T p.(Arg123Cys) possibly_damaging(0.692) missense_variant - deleterious(0)
CPT1A 00000662 NM_001876.3 0000000355 +/+ - 4/4 c.367C>T p.(Arg123Cys) possibly_damaging(0.692) missense_variant - deleterious(0)
CPT1A 00000664 XM_005273762.1 0000000355 +/+ - 4/19 c.463C>T p.(Arg155Cys) - missense_variant - -
CPT1A 00000661 XM_005273763.1 0000000355 +/+ - 4/19 c.463C>T p.(Arg155Cys) - missense_variant - -
CPT1A 00000663 XM_005273764.1 0000000355 +/+ - 4/4 c.367C>T p.(Arg123Cys) possibly_damaging(0.692) missense_variant - deleterious(0)
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000055866; RCV000079915;
Chromosome 11:68575021..68575021
Allele frequencies from ExAC 0.00001
ClinVar Allele ID 76561
Disease database name and identifier MONDO:MONDO:0009705, MedGen:C1829703, OMIM:255120, Orphanet:156|MedGen:C3661900
ClinVar preferred disease name Carnitine palmitoyl transferase 1A deficiency|not provided
HGVS variant names NC 000011.9:g.68575021G>A
ClinVar review status criteria provided, single submitter
Clinical Significance Uncertain significance
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA221862|UniProtKB:P50416#VAR 020546
Gene symbol:Gene id. CPT1A:1374
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 80356775
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