View genomic variant #0000000800

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.26508381G>A
Published as -
GERP 5.670
Segregation -
DB-ID HADHB_000004 See all 2 reported entries
MSCV MSCV_0000800
dbSNP ID rs121913134
Frequency -
Sources ; clinVar; Ensembl;
Reference 19699128;9259266
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 0000000800 +/+ - 15/16 c.1331G>A p.(Arg444Lys) probably_damaging(0.999) missense_variant - tolerated(0.08)
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ClinVar @ MSeqDR

RCVaccession RCV003156217;
Chromosome 2:26508381..26508381
ClinVar Allele ID 29886
Disease database name and identifier MedGen:C5830374, OMIM:620300
ClinVar preferred disease name Mitochondrial trifunctional protein deficiency 2
HGVS variant names NC 000002.11:g.26508381G>A
ClinVar review status no assertion criteria provided
Clinical Significance Pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA341341|OMIM:143450.0004|UniProtKB:P55084#VAR 017409
Gene symbol:Gene id. HADHB:3032
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 121913134
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