View genomic variant #0000018978

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.26467665G>A
Published as -
GERP -
Segregation -
DB-ID HADHA_000031
MSCV MSCV_0018978
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

4 entries on 1 page. Showing entries 1 - 4.
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 0000018978 ./. - - c.-201C>T p.(=) - - - -
HADHB 00000789 NM_000183.2 0000018978 ./. - - c.-202G>A p.(=) - - - -
HADHA 00000787 XM_005264275.1 0000018978 ./. - - c.-201C>T p.(=) - - - -
HADHA 00000788 XM_005264276.1 0000018978 ./. - - c.-328C>T p.(=) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000335438;
Chromosome 2:26467665..26467665
ClinVar Allele ID 285654
Disease database name and identifier MONDO:MONDO:0012172, MedGen:C1969443, OMIM:609015, Orphanet:ORPHA746, SNOMED CT:237999008
ClinVar preferred disease name Mitochondrial trifunctional protein deficiency
HGVS variant names NC 000002.11:g.26467665G>A
ClinVar review status criteria provided, single submitter
Clinical Significance Uncertain significance
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported Illumina Clinical Services Laboratory, Illumina:699161
Gene symbol:Gene id. HADHB:3032
Allele origin germline
dbSNP ID 886055865
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