View genomic variant #0000018950

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.26437372C>T
Published as -
GERP -
Segregation -
DB-ID HADHA_000017
MSCV MSCV_0018950
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 0000018950 ./. - - c.858G>A p.(=) - - - -
HADHA 00000787 XM_005264275.1 0000018950 ./. - - c.720G>A p.(=) - - - -
HADHA 00000788 XM_005264276.1 0000018950 ./. - - c.597G>A p.(=) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000288747; RCV000404527; RCV000877582;
Chromosome 2:26437372..26437372
Allele frequencies from ExAC 0.00003
ClinVar Allele ID 289078
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.26437372C>T
ClinVar review status criteria provided, conflicting interpretations
Clinical Significance Conflicting interpretations of pathogenicity
Conflicting clinical significance Uncertain significance(2)|Likely benign(1)
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA1559764
Gene symbol:Gene id. HADHA:3030
Molecular consequence SO:0001819|synonymous variant
Allele origin germline
dbSNP ID 373864418
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