View genomic variant #0000018927

Chromosome 2
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.26416647C>T
Published as -
GERP -
Segregation -
DB-ID HADHA_000074
MSCV MSCV_0018927
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 0.00408 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 0000018927 ./. - - c.1690-6G>A p.(=) - - - -
HADHA 00000787 XM_005264275.1 0000018927 ./. - - c.1552-6G>A p.(=) - - - -
HADHA 00000788 XM_005264276.1 0000018927 ./. - - c.1429-6G>A p.(=) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000185926; RCV000340887; RCV000395377; RCV000870997; RCV003456373;
Chromosome 2:26416647..26416647
Allele frequencies from ESP 0.00408
Allele frequencies from ExAC 0.00114
Allele frequencies from TGP 0.00379
ClinVar Allele ID 199996
Disease database name and identifier MONDO:MONDO:0012172, MedGen:C1969443, OMIM:609015, Orphanet:746|MONDO:MONDO:0012173, MedGen:C3711645, OMIM:609016, Orphanet:5|MedGen:CN169374|MedGen:C3661900
ClinVar preferred disease name Mitochondrial trifunctional protein deficiency|Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency|not specified|not provided
HGVS variant names NC 000002.11:g.26416647C>T
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Benign
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA312574
Gene symbol:Gene id. HADHA:3030|GAREM2:150946
Molecular consequence SO:0001627|intron variant
Allele origin germline
dbSNP ID 111662358
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