View genomic variant #0000025653

Chromosome 2
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.26417491T>C
Published as -
GERP -
Segregation -
DB-ID HADHA_000097
MSCV -
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 8.0E-5 View details
Owner Lishuang Shen




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 0000025653 ./. - - c.1637A>G p.(Tyr546Cys) - - - -
HADHA 00000787 XM_005264275.1 0000025653 ./. - - c.1499A>G p.(Tyr500Cys) - - - -
HADHA 00000788 XM_005264276.1 0000025653 ./. - - c.1376A>G p.(Tyr459Cys) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000494150; RCV000668659; RCV003230520; RCV002527077;
Chromosome 2:26417491..26417491
Allele frequencies from ESP 0.00008
Allele frequencies from ExAC 0.00005
ClinVar Allele ID 421379
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|MedGen:CN169374
ClinVar preferred disease name Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency|Mitochondrial trifunctional protein deficiency|not provided|not specified
HGVS variant names NC 000002.11:g.26417491T>C
ClinVar review status criteria provided, conflicting interpretations
Clinical Significance Conflicting interpretations of pathogenicity
Conflicting clinical significance Likely pathogenic(1)|Uncertain significance(3)
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA1559505
Gene symbol:Gene id. HADHA:3030|GAREM2:150946
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 370170143
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