View genomic variant #0000000836

Chromosome 2
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Type subst
DNA change (genomic) (Relative to hg19 / GRCh37) g.74184339G>A
Published as -
GERP 5.010
Segregation -
DB-ID DGUOK_000004 See all 2 reported entries
MSCV MSCV_0000836
dbSNP ID rs104893632
Frequency -
Sources ; clinVar; Ensembl;
Reference 12205643
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 0000000836 +/+ - 5/7 c.679G>A p.(Glu227Lys) probably_damaging(0.994) missense_variant - deleterious(0)
DGUOK 00003342 NM_080916.2 0000000836 +/+ - 5/7 c.679G>A p.(Glu227Lys) probably_damaging(0.994) missense_variant - deleterious(0)
DGUOK 00000093 NM_080918.1 0000000836 +/+ - - c.444-934G>A p.(=) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000008636; RCV001568974; RCV002512917;
Chromosome 2:74184339..74184339
ClinVar Allele ID 23197
Disease database name and identifier MeSH:D030342, MedGen:C0950123|MedGen:CN517202|MONDO:MONDO:0009636, MedGen:C5191055, OMIM:251880, Orphanet:279934
ClinVar preferred disease name Inborn genetic diseases|not provided|Mitochondrial DNA depletion syndrome 3 (hepatocerebral type)
HGVS variant names NC 000002.11:g.74184339G>A
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA254329|OMIM:601465.0006|UniProtKB:Q16854#VAR 019418
Gene symbol:Gene id. DGUOK:1716
Molecular consequence SO:0001583|missense variant, SO:0001619|non-coding transcript variant, SO:0001627|intron variant
Allele origin germline
dbSNP ID 104893632
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