View genomic variant #0000000793

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.26432709A>G
Published as -
GERP 6.060
Segregation -
DB-ID HADHA_000004 See all 2 reported entries
MSCV MSCV_0000793
dbSNP ID rs137852772
Frequency -
Sources ; clinVar; Ensembl;
Reference 9266371
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) Variant not found in online data sets
Owner LOVD




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 0000000793 +/+ - 11/20 c.1025T>C p.(Leu342Pro) probably_damaging(1) missense_variant - deleterious(0)
HADHA 00000787 XM_005264275.1 0000000793 +/+ - 11/20 c.887T>C p.(Leu296Pro) - missense_variant - -
HADHA 00000788 XM_005264276.1 0000000793 +/+ - 10/19 c.764T>C p.(Leu255Pro) - missense_variant - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000009273;
Chromosome 2:26432709..26432709
ClinVar Allele ID 23773
Disease database name and identifier MONDO:MONDO:0012172, MedGen:C1969443, OMIM:609015, Orphanet:746
ClinVar preferred disease name Mitochondrial trifunctional protein deficiency
HGVS variant names NC 000002.11:g.26432709A>G
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:CA340820|OMIM:600890.0007|UniProtKB:P40939#VAR 021127
Gene symbol:Gene id. HADHA:3030
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 137852772
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