View genomic variant #0000018974

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.26467464T>C
Published as -
GERP -
Segregation -
DB-ID HADHA_000071
MSCV MSCV_0018974
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
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 0000018974 ./. - - c.1A>G p.? - - - -
HADHA 00000787 XM_005264275.1 0000018974 ./. - - c.1A>G p.? - - - -
HADHA 00000788 XM_005264276.1 0000018974 ./. - - c.-127A>G p.(=) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000410119;
Chromosome 2:26467464..26467464
ClinVar Allele ID 357264
Disease database name and identifier MONDO:MONDO:0012173, MedGen:C3711645, OMIM:609016, Orphanet:5
ClinVar preferred disease name Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency
HGVS variant names NC 000002.11:g.26467464T>C
ClinVar review status criteria provided, single submitter
Clinical Significance Likely pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA16040883
Gene symbol:Gene id. HADHA:3030
Molecular consequence SO:0001582|initiator codon variant, SO:0001583|missense variant
Allele origin unknown
dbSNP ID 1057517430
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