View genomic variant #0000018961

Chromosome 2
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Does not affect function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.26455127G>A
Published as -
GERP -
Segregation -
DB-ID HADHA_000027
MSCV MSCV_0018961
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 0.16139 View details
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 0000018961 ./. - - c.474C>T p.(=) - - - -
HADHA 00000787 XM_005264275.1 0000018961 ./. - - c.473+1C>T p.? - - - -
HADHA 00000788 XM_005264276.1 0000018961 ./. - - c.213C>T p.(=) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000078336; RCV000276323; RCV000370977; RCV001519830;
Chromosome 2:26455127..26455127
Allele frequencies from ESP 0.16139
Allele frequencies from ExAC 0.20391
Allele frequencies from TGP 0.14237
ClinVar Allele ID 98504
Disease database name and identifier MONDO:MONDO:0012173, MedGen:C3711645, OMIM:609016, Orphanet:5|MONDO:MONDO:0012172, MedGen:C1969443, OMIM:609015, Orphanet:746|MedGen:CN169374
ClinVar preferred disease name Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency|Mitochondrial trifunctional protein deficiency|not specified
HGVS variant names NC 000002.11:g.26455127G>A
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Benign
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA285332
Gene symbol:Gene id. HADHA:3030
Molecular consequence SO:0001819|synonymous variant
Allele origin germline
dbSNP ID 11552518
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR

RCVaccession RCV001263589;
Chromosome 2:26455127..26455127
ClinVar Allele ID 971800
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.26455127G>T
ClinVar review status criteria provided, single submitter
Clinical Significance Likely pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Gene symbol:Gene id. HADHA:3030
Molecular consequence SO:0001587|nonsense
Allele origin unknown
dbSNP ID 11552518
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