View genomic variant #0000018956

Chromosome 2
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Probably does not affect function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.26453147C>A
Published as -
GERP -
Segregation -
DB-ID HADHA_000022
MSCV MSCV_0018956
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 0.00115 View details
Owner LOVD




Variant on transcripts

3 entries on 1 page. Showing entries 1 - 3.
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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 0000018956 ./. - - c.589G>T p.(Ala197Ser) - - - -
HADHA 00000787 XM_005264275.1 0000018956 ./. - - c.474-23G>T p.(=) - - - -
HADHA 00000788 XM_005264276.1 0000018956 ./. - - c.328G>T p.(Ala110Ser) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV001080057; RCV000757349;
Chromosome 2:26453147..26453147
Allele frequencies from ESP 0.00115
Allele frequencies from TGP 0.00319
ClinVar Allele ID 518053
Disease database name and identifier MedGen:C3661900|MONDO:MONDO:0012172, MedGen:C1969443, OMIM:609015, Orphanet:746|MONDO:MONDO:0012173, MedGen:C3711645, OMIM:609016, Orphanet:5
ClinVar preferred disease name not provided|Mitochondrial trifunctional protein deficiency|Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency
HGVS variant names NC 000002.11:g.26453147C>A
ClinVar review status criteria provided, conflicting interpretations
Clinical Significance Conflicting interpretations of pathogenicity
Conflicting clinical significance Uncertain significance(1)|Likely benign(2)
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA1559835
Gene symbol:Gene id. HADHA:3030
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 116320983
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