View genomic variant #0000018931

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.26417473G>A
Published as -
GERP -
Segregation -
DB-ID HADHA_000077
MSCV MSCV_0018931
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 0.00023 View details
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 0000018931 ./. - - c.1655C>T p.(Ala552Val) - - - -
HADHA 00000787 XM_005264275.1 0000018931 ./. - - c.1517C>T p.(Ala506Val) - - - -
HADHA 00000788 XM_005264276.1 0000018931 ./. - - c.1394C>T p.(Ala465Val) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000366235; RCV001824740; RCV001861149;
Chromosome 2:26417473..26417473
Allele frequencies from ESP 0.00023
ClinVar Allele ID 286351
Disease database name and identifier MONDO:MONDO:0012173, MedGen:C3711645, OMIM:609016, Orphanet:5|MONDO:MONDO:0012172, MedGen:C1969443, OMIM:609015, Orphanet:746
ClinVar preferred disease name Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency|Mitochondrial trifunctional protein deficiency
HGVS variant names NC 000002.11:g.26417473G>A
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:CA1559501
Gene symbol:Gene id. HADHA:3030|GAREM2:150946
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 369588406
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR

RCVaccession RCV001905867;
Chromosome 2:26417473..26417474
ClinVar Allele ID 1357919
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.26417474dup
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|GAREM2:150946
Molecular consequence SO:0001589|frameshift variant
Allele origin germline
dbSNP ID 2147753069
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