View genomic variant #0000026647

Chromosome 8
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.103225090C>T
Published as -
GERP -
Segregation -
DB-ID RRM2B_000012 See all 2 reported entries
MSCV -
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 Lishuang Shen




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 0000026647 ./. - - c.1033G>A p.(Gly345Ser) - - - -
RRM2B 00000284 NM_001172478.1 0000026647 ./. - - c.661G>A p.(Gly221Ser) - - - -
RRM2B 00000285 NM_015713.4 0000026647 ./. - - c.817G>A p.(Gly273Ser) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000023388; RCV000119008; RCV001582496;
Chromosome 8:103225090..103225090
Allele frequencies from ExAC 0.00002
ClinVar Allele ID 39392
Disease database name and identifier MedGen:CN187502|MedGen:C3661900|Human Phenotype Ontology:HP:0000562, Human Phenotype Ontology:HP:0000590, MONDO:MONDO:0005181, MedGen:C0162674, Orphanet:520820
ClinVar preferred disease name RRM2B-related mitochondrial disease|not provided|Progressive external ophthalmoplegia
HGVS variant names NC 000008.10:g.103225090C>T
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Uncertain significance
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA278600|OMIM:604712.0013
Gene symbol:Gene id. RRM2B:50484
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 387906891
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