View genomic variant #0000019474

Chromosome 2
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Probably does not affect function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.211070470G>A
Published as -
GERP -
Segregation -
DB-ID ACADL_000005
MSCV MSCV_0019474
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 0.01069 View details
Owner LOVD




Variant on transcripts

2 entries on 1 page. Showing entries 1 - 2.
Legend  

Gene     

Transcript ID     

AscendingTranscript     

Variant ID     

Affects function     

Location     

Exon     

DNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
ACADL 00000382 NM_001608.3 0000019474 ./. - - c.654C>T p.(=) - - - -
ACADL 00000381 XM_005246517.1 0000019474 ./. - - c.591C>T p.(=) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000956031;
Chromosome 2:211070470..211070470
Allele frequencies from ESP 0.01069
Allele frequencies from ExAC 0.00350
Allele frequencies from TGP 0.01298
ClinVar Allele ID 287603
Disease database name and identifier MedGen:C3661900
ClinVar preferred disease name not provided
HGVS variant names NC 000002.11:g.211070470G>A
ClinVar review status criteria provided, single submitter
Clinical Significance Benign
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA2084949
Gene symbol:Gene id. ACADL:33
Molecular consequence SO:0001819|synonymous variant
Allele origin germline
dbSNP ID 77160779
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