View genomic variant #0000025660

Chromosome 2
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.26432752C>T
Published as -
GERP -
Segregation -
DB-ID HADHA_000104
MSCV -
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 Lishuang Shen




Variant on transcripts

3 entries on 1 page. Showing entries 1 - 3.
Legend  

Gene     

Transcript ID     

AscendingTranscript     

Variant ID     

Affects function     

Location     

Exon     

DNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
HADHA 00000786 NM_000182.4 0000025660 ./. - - c.982G>A p.(Gly328Arg) - - - -
HADHA 00000787 XM_005264275.1 0000025660 ./. - - c.844G>A p.(Gly282Arg) - - - -
HADHA 00000788 XM_005264276.1 0000025660 ./. - - c.721G>A p.(Gly241Arg) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000185932; RCV000674081;
Chromosome 2:26432752..26432752
ClinVar Allele ID 199999
Disease database name and identifier MedGen:CN169374|MONDO:MONDO:0012173, MedGen:C3711645, OMIM:609016, Orphanet:5
ClinVar preferred disease name not specified|Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency
HGVS variant names NC 000002.11:g.26432752C>T
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Uncertain significance
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA312581
Gene symbol:Gene id. HADHA:3030
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 796051970
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