View genomic variant #0000019213

Chromosome 2
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.74154174A>G
Published as -
GERP -
Segregation -
DB-ID DGUOK_000031
MSCV MSCV_0019213
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     
DGUOK 00000092 NM_080916.1 0000019213 ./. - - c.137A>G p.(Asn46Ser) - - - -
DGUOK 00003342 NM_080916.2 0000019213 ./. - - c.137A>G p.(Asn46Ser) - - - -
DGUOK 00000093 NM_080918.1 0000019213 ./. - - c.137A>G p.(Asn46Ser) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000239535; RCV000239586; RCV001550857; RCV001799645; RCV001824706;
Chromosome 2:74154174..74154174
Allele frequencies from ExAC 0.00002
ClinVar Allele ID 247473
Disease database name and identifier MedGen:C3661900|MONDO:MONDO:0009636, MedGen:C5191055, OMIM:251880, Orphanet:279934|MONDO:MONDO:8000013, MedGen:CN305369, OMIM:617068|MONDO:MONDO:0014899, MedGen:C4310733, OMIM:617070, Orphanet:329314|MONDO:MONDO:0024193, MedGen:C4310735, OMIM:PS617068
ClinVar preferred disease name not provided|Mitochondrial DNA depletion syndrome 3 (hepatocerebral type)|Portal hypertension, noncirrhotic, 1|Adult-onset multiple mitochondrial DNA deletion syndrome due to DGUOK deficiency|Portal hypertension, noncirrhotic
HGVS variant names NC 000002.11:g.74154174A>G
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Pathogenic/Likely pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA1718151|OMIM:601465.0008|UniProtKB:Q16854#VAR 076980
Gene symbol:Gene id. DGUOK:1716|LOC129934096:129934096
Molecular consequence SO:0001583|missense variant, SO:0001619|non-coding transcript variant, SO:0001623|5 prime UTR variant
Allele origin germline
dbSNP ID 763615602
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