View genomic variant #0000019216

Chromosome 2
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Probably does not affect function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.74166053G>A
Published as -
GERP -
Segregation -
DB-ID DGUOK_000034
MSCV MSCV_0019216
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 0.01991 View details
Owner LOVD




Variant on transcripts

3 entries on 1 page. Showing entries 1 - 3.
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Gene     

Transcript ID     

AscendingTranscript     

Variant ID     

Affects function     

Location     

Exon     

DNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
DGUOK 00000092 NM_080916.1 0000019216 ./. - - c.159G>A p.(=) - - - -
DGUOK 00003342 NM_080916.2 0000019216 ./. - - c.159G>A p.(=) - - - -
DGUOK 00000093 NM_080918.1 0000019216 ./. - - c.159G>A p.(=) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000124675; RCV000384705; RCV000677026;
Chromosome 2:74166053..74166053
Allele frequencies from ESP 0.01991
Allele frequencies from ExAC 0.02035
Allele frequencies from TGP 0.00699
ClinVar Allele ID 140783
Disease database name and identifier MedGen:CN169374|MedGen:C3661900|MONDO:MONDO:0009636, MedGen:C5191055, OMIM:251880, Orphanet:279934
ClinVar preferred disease name not specified|not provided|Mitochondrial DNA depletion syndrome 3 (hepatocerebral type)
HGVS variant names NC 000002.11:g.74166053G>A
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:CA290582
Gene symbol:Gene id. DGUOK:1716
Molecular consequence SO:0001627|intron variant, SO:0001819|synonymous variant
Allele origin germline
dbSNP ID 62641680
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