View genomic variant #0000000792

Chromosome 2
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Type subst
DNA change (genomic) (Relative to hg19 / GRCh37) g.26427019G>A
Published as -
GERP 5.000
Segregation -
DB-ID HADHA_000003 See all 2 reported entries
MSCV MSCV_0000792
dbSNP ID rs137852770
Frequency -
Sources ; clinVar; Ensembl;
Reference 7846063
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) Variant not found in online data sets
Owner LOVD




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 0000000792 +/+ - 12/20 c.1132C>T p.(Gln378*) - stop_gained - -
HADHA 00000787 XM_005264275.1 0000000792 +/+ - 12/20 c.994C>T p.(Gln332*) - stop_gained - -
HADHA 00000788 XM_005264276.1 0000000792 +/+ - 11/19 c.871C>T p.(Gln291*) - stop_gained - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000665238; RCV001851758; RCV000009268;
Chromosome 2:26427019..26427019
ClinVar Allele ID 23768
Disease database name and identifier MONDO:MONDO:0012173, MedGen:C3711645, OMIM:609016, Orphanet:5|MONDO:MONDO:0012172, MedGen:C1969443, OMIM:609015, Orphanet:746
ClinVar preferred disease name Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency|Mitochondrial trifunctional protein deficiency
HGVS variant names NC 000002.11:g.26427019G>A
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Pathogenic/Likely pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA340815|OMIM:600890.0002
Gene symbol:Gene id. HADHA:3030|GAREM2:150946
Molecular consequence SO:0001587|nonsense
Allele origin germline
dbSNP ID 137852770
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