View genomic variant #0000025667

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.26438045C>T
Published as -
GERP -
Segregation -
DB-ID HADHA_000105
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 0000025667 ./. - - c.677-1G>A p.? - - - -
HADHA 00000787 XM_005264275.1 0000025667 ./. - - c.539-1G>A p.? - - - -
HADHA 00000788 XM_005264276.1 0000025667 ./. - - c.416-1G>A p.? - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000674355; RCV002261169;
Chromosome 2:26438045..26438045
ClinVar Allele ID 542089
Disease database name and identifier MedGen:CN517202|MONDO:MONDO:0012173, MedGen:C3711645, OMIM:609016, Orphanet:5
ClinVar preferred disease name not provided|Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency
HGVS variant names NC 000002.11:g.26438045C>T
ClinVar review status criteria provided, single submitter
Clinical Significance Likely pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Gene symbol:Gene id. HADHA:3030
Molecular consequence SO:0001574|splice acceptor variant
Allele origin somatic
dbSNP ID 1553314070
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