View genomic variant #0000026648

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.103231055A>C
Published as -
GERP -
Segregation -
DB-ID RRM2B_000107
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 0000026648 ./. - - c.887T>G p.(Ile296Ser) - - - -
RRM2B 00000284 NM_001172478.1 0000026648 ./. - - c.515T>G p.(Ile172Ser) - - - -
RRM2B 00000285 NM_015713.4 0000026648 ./. - - c.671T>G p.(Ile224Ser) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000119006; RCV000199478; RCV000659254; RCV002483200;
Chromosome 8:103231055..103231055
Allele frequencies from ExAC 0.00001
ClinVar Allele ID 136344
Disease database name and identifier MONDO:MONDO:0013117, MedGen:C2751319, OMIM:613077|MONDO:MONDO:0012792, MedGen:C2749861, OMIM:612075, Orphanet:255235|MONDO:MONDO:0010000, MedGen:C1849333, OMIM:268315|MedGen:CN187502|MedGen:C3661900
ClinVar preferred disease name Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 5|Mitochondrial DNA depletion syndrome 8a|Rod-cone dystrophy, sensorineural deafness, and Fanconi-type renal dysfunction|RRM2B-related mitochondrial disease|not provided
HGVS variant names NC 000008.10:g.103231055A>C
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:CA324021|UniProtKB:Q7LG56#VAR 046221
Gene symbol:Gene id. RRM2B:50484
Molecular consequence SO:0001583|missense variant
Allele origin
dbSNP ID 515726196
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