View genomic variant #0000018918

Chromosome 2
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.26415212del
Published as -
GERP -
Segregation -
DB-ID HADHA_000050
MSCV MSCV_0018918
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

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 0000018918 ./. - - c.1967del p.(Leu656*) - - - -
HADHA 00000787 XM_005264275.1 0000018918 ./. - - c.1829del p.(Leu610*) - - - -
HADHA 00000788 XM_005264276.1 0000018918 ./. - - c.1706del p.(Leu569*) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000169001; RCV000255407; RCV001239627;
Chromosome 2:26415212..26415212
ClinVar Allele ID 186665
Disease database name and identifier MONDO:MONDO:0012172, MedGen:C1969443, OMIM:609015, Orphanet:746|MONDO:MONDO:0012173, MedGen:C3711645, OMIM:609016, Orphanet:5|MedGen:C3661900
ClinVar preferred disease name Mitochondrial trifunctional protein deficiency|Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency|not provided
HGVS variant names NC 000002.11:g.26415215del
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Pathogenic/Likely pathogenic
Variant type Deletion
Sequence Ontology for variant type SO:0000159
Variant clinical sources reported ClinGen:CA199043
Gene symbol:Gene id. HADHA:3030|GAREM2:150946
Molecular consequence SO:0001587|nonsense
Allele origin germline
dbSNP ID 779113356
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