View genomic variant #0000018959

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.26455041C>G
Published as -
GERP -
Segregation -
DB-ID HADHA_000025
MSCV MSCV_0018959
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 8.0E-5 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 0000018959 ./. - - c.560G>C p.(Arg187Thr) - - - -
HADHA 00000787 XM_005264275.1 0000018959 ./. - - c.473+87G>C p.(=) - - - -
HADHA 00000788 XM_005264276.1 0000018959 ./. - - c.299G>C p.(Arg100Thr) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000297574; RCV000394004; RCV001246947; RCV002261072;
Chromosome 2:26455041..26455041
Allele frequencies from ESP 0.00008
ClinVar Allele ID 289090
Disease database name and identifier MONDO:MONDO:0012173, MedGen:C3711645, OMIM:609016, Orphanet:5|MONDO:MONDO:0012172, MedGen:C1969443, OMIM:609015, Orphanet:746|MedGen:CN517202
ClinVar preferred disease name Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency|Mitochondrial trifunctional protein deficiency|not provided
HGVS variant names NC 000002.11:g.26455041C>G
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:CA1559863
Gene symbol:Gene id. HADHA:3030
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 146667859
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR

RCVaccession RCV003090175;
Chromosome 2:26455041..26455041
ClinVar Allele ID 1902356
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.26455041C>T
ClinVar review status criteria provided, single submitter
Clinical Significance Uncertain significance
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Gene symbol:Gene id. HADHA:3030
Molecular consequence SO:0001583|missense variant
Allele origin germline
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