View genomic variant #0000025675

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.26467440_26467441insGCCAATCGCCCGGCAGGCC
Published as -
GERP -
Segregation -
DB-ID HADHA_000113
MSCV -
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 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 0000025675 ./. - - c.24_25insGGCCTGCCGGGCGATTGGC p.(Ile9Glyfs*40) - - - -
HADHA 00000787 XM_005264275.1 0000025675 ./. - - c.24_25insGGCCTGCCGGGCGATTGGC p.(Ile9Glyfs*40) - - - -
HADHA 00000788 XM_005264276.1 0000025675 ./. - - c.-104_-103insGGCCTGCCGGGCGATTGGC p.(=) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000703162;
Chromosome 2:26467440..26467441
ClinVar Allele ID 561248
Disease database name and identifier MONDO:MONDO:0012172, MedGen:C1969443, OMIM:609015, Orphanet:746|MONDO:MONDO:0012173, MedGen:C3711645, OMIM:609016, Orphanet:5
ClinVar preferred disease name Mitochondrial trifunctional protein deficiency|Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency
HGVS variant names NC 000002.11:g.26467441 26467459dup
ClinVar review status criteria provided, single submitter
Clinical Significance Pathogenic
Variant type Duplication
Sequence Ontology for variant type SO:1000035
Gene symbol:Gene id. HADHA:3030
Molecular consequence SO:0001589|frameshift variant
Allele origin germline
dbSNP ID 1456890163
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR

RCVaccession RCV001451235;
Chromosome 2:26467441..26467441
ClinVar Allele ID 763143
Disease database name and identifier MONDO:MONDO:0012172, MedGen:C1969443, OMIM:609015, Orphanet:746|MONDO:MONDO:0012173, MedGen:C3711645, OMIM:609016, Orphanet:5
ClinVar preferred disease name Mitochondrial trifunctional protein deficiency|Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency
HGVS variant names NC 000002.11:g.26467441G>T
ClinVar review status criteria provided, single submitter
Clinical Significance Likely benign
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Gene symbol:Gene id. HADHA:3030
Molecular consequence SO:0001819|synonymous variant
Allele origin germline
dbSNP ID 942208244
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