View genomic variant #0000019230

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.74177836A>T
Published as -
GERP -
Segregation -
DB-ID DGUOK_000014
MSCV MSCV_0019230
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 0000019230 ./. - - c.568A>T p.(Ile190Phe) - - - -
DGUOK 00003342 NM_080916.2 0000019230 ./. - - c.568A>T p.(Ile190Phe) - - - -
DGUOK 00000093 NM_080918.1 0000019230 ./. - - c.443+3803A>T p.(=) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000285612;
Chromosome 2:74177836..74177836
ClinVar Allele ID 290528
Disease database name and identifier MONDO:MONDO:0009636, MedGen:C5191055, OMIM:251880, Orphanet:279934
ClinVar preferred disease name Mitochondrial DNA depletion syndrome 3 (hepatocerebral type)
HGVS variant names NC 000002.11:g.74177836A>T
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 ClinGen:CA10615970
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 757043357
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