View genomic variant #0000018969

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.26461801C>T
Published as -
GERP -
Segregation -
DB-ID HADHA_000066
MSCV MSCV_0018969
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 0000018969 ./. - - c.180+1G>A p.? - - - -
HADHA 00000787 XM_005264275.1 0000018969 ./. - - c.180+1G>A p.? - - - -
HADHA 00000788 XM_005264276.1 0000018969 ./. - - c.53+1G>A p.? - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000009269; RCV000665265; RCV001382535;
Chromosome 2:26461801..26461801
ClinVar Allele ID 23769
Disease database name and identifier MONDO:MONDO:0012172, MedGen:C1969443, OMIM:609015, Orphanet:746|MONDO:MONDO:0012173, MedGen:C3711645, OMIM:609016, Orphanet:5
ClinVar preferred disease name Mitochondrial trifunctional protein deficiency|Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency
HGVS variant names NC 000002.11:g.26461801C>T
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:CA340817|OMIM:600890.0003
Gene symbol:Gene id. HADHA:3030
Molecular consequence SO:0001575|splice donor variant
Allele origin germline
dbSNP ID 786205088
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