View genomic variant #0000018921

Chromosome 2
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.26415267T>C
Published as -
GERP -
Segregation -
DB-ID HADHA_000053
MSCV MSCV_0018921
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 0000018921 ./. - - c.1912A>G p.(Ile638Val) - - - -
HADHA 00000787 XM_005264275.1 0000018921 ./. - - c.1774A>G p.(Ile592Val) - - - -
HADHA 00000788 XM_005264276.1 0000018921 ./. - - c.1651A>G p.(Ile551Val) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000351798; RCV000371597; RCV002480192;
Chromosome 2:26415267..26415267
Allele frequencies from ExAC 0.00002
Allele frequencies from TGP 0.00020
ClinVar Allele ID 285639
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.26415267T>C
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Uncertain significance
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA1559418
Gene symbol:Gene id. HADHA:3030|GAREM2:150946
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 545660610
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