View genomic variant #0000022504

Chromosome 8
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.103220438G>A
Published as -
GERP -
Segregation -
DB-ID RRM2B_000009 See all 2 reported entries
MSCV MSCV_0001261
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     
RRM2B 00000286 NM_001172477.1 0000022504 ./. - - c.1195C>T p.(Arg399*) - - - -
RRM2B 00000284 NM_001172478.1 0000022504 ./. - - c.823C>T p.(Arg275*) - - - -
RRM2B 00000285 NM_015713.4 0000022504 ./. - - c.979C>T p.(Arg327*) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000005722; RCV000119016; RCV000197531;
Chromosome 8:103220438..103220438
ClinVar Allele ID 20430
Disease database name and identifier MedGen:CN187502|MedGen:C3661900|MONDO:MONDO:0013117, MedGen:C2751319, OMIM:613077
ClinVar preferred disease name RRM2B-related mitochondrial disease|not provided|Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 5
HGVS variant names NC 000008.10:g.103220438G>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:CA117487|OMIM:604712.0006
Gene symbol:Gene id. RRM2B:50484
Molecular consequence SO:0001587|nonsense
Allele origin germline
dbSNP ID 121918310
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