View genomic variant #0000018992

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.26496536C>T
Published as -
GERP -
Segregation -
DB-ID HADHB_000009
MSCV MSCV_0018992
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 0.00031 View details
Owner LOVD




Variant on transcripts

1 entry on 1 page. Showing entry 1.
Legend  

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 0000018992 ./. - - c.272C>T p.(Thr91Ile) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000376635; RCV001507553;
Chromosome 2:26496536..26496536
Allele frequencies from ESP 0.00031
Allele frequencies from ExAC 0.00005
ClinVar Allele ID 289112
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.26496536C>T
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:CA1560167
Gene symbol:Gene id. HADHB:3032
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 145712438
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