View genomic variant #0000000801

Chromosome 2
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Type subst
DNA change (genomic) (Relative to hg19 / GRCh37) g.26508414T>A
Published as -
GERP 5.670
Segregation -
DB-ID HADHB_000005
MSCV MSCV_0000801
dbSNP ID NA
Frequency -
Sources ;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) Variant not found in online data sets
Owner LOVD




Variant on transcripts

1 entry on 1 page. Showing entry 1.
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Gene     

Transcript ID     

AscendingTranscript     

Variant ID     

Affects function     

Location     

Exon     

DNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
HADHB 00000789 NM_000183.2 0000000801 ./. - 15/16 c.1364T>A p.(Val455Glu) probably_damaging(0.932) missense_variant - deleterious(0)
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ClinVar @ MSeqDR

RCVaccession RCV000015974; RCV003125832;
Chromosome 2:26508414..26508414
ClinVar Allele ID 29888
Disease database name and identifier MedGen:CN517202|MONDO:MONDO:0012172, MedGen:C1969443, OMIM:609015, Orphanet:746
ClinVar preferred disease name not provided|Mitochondrial trifunctional protein deficiency
HGVS variant names NC 000002.11:g.26508414T>G
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA341344|OMIM:143450.0006|OMIM:143450.0009
Gene symbol:Gene id. HADHB:3032
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 267606859
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