View genomic variant #0000018939

Chromosome 2
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.26426939C>G
Published as -
GERP -
Segregation -
DB-ID HADHA_000010
MSCV MSCV_0018939
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 0.00077 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 0000018939 ./. - - c.1212G>C p.(=) - - - -
HADHA 00000787 XM_005264275.1 0000018939 ./. - - c.1074G>C p.(=) - - - -
HADHA 00000788 XM_005264276.1 0000018939 ./. - - c.951G>C p.(=) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000281388; RCV000373682; RCV000728811; RCV001079829;
Chromosome 2:26426939..26426939
Allele frequencies from ESP 0.00077
Allele frequencies from ExAC 0.00035
Allele frequencies from TGP 0.00020
ClinVar Allele ID 289076
Disease database name and identifier MONDO:MONDO:0012173, MedGen:C3711645, OMIM:609016, Orphanet:5|MONDO:MONDO:0012172, MedGen:C1969443, OMIM:609015, Orphanet:746|MedGen:C3661900
ClinVar preferred disease name Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency|Mitochondrial trifunctional protein deficiency|not provided
HGVS variant names NC 000002.11:g.26426939C>G
ClinVar review status criteria provided, conflicting interpretations
Clinical Significance Conflicting interpretations of pathogenicity
Conflicting clinical significance Uncertain significance(3)|Likely benign(3)
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA1559642
Gene symbol:Gene id. HADHA:3030|GAREM2:150946
Molecular consequence SO:0001819|synonymous variant
Allele origin germline
dbSNP ID 116396996
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