View genomic variant #0000019483

Chromosome 2
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.211085510C>T
Published as -
GERP -
Segregation -
DB-ID ACADL_000014
MSCV MSCV_0019483
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) Variant not found in online data sets
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 0000019483 ./. - - c.94G>A p.(Gly32Arg) - - - -
ACADL 00000381 XM_005246517.1 0000019483 ./. - - c.31G>A p.(Gly11Arg) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV003173294;
Chromosome 2:211085510..211085510
Allele frequencies from ExAC 0.00019
ClinVar Allele ID 284495
Disease database name and identifier MeSH:D030342, MedGen:C0950123
ClinVar preferred disease name Inborn genetic diseases
HGVS variant names NC 000002.11:g.211085510C>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. ACADL:33
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 767313935
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