View genomic variant #0000022523

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.103231146C>T
Published as -
GERP -
Segregation -
DB-ID RRM2B_000016 See all 2 reported entries
MSCV MSCV_0001268
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 0000022523 ./. - - c.796G>A p.(Glu266Lys) - - - -
RRM2B 00000284 NM_001172478.1 0000022523 ./. - - c.424G>A p.(Glu142Lys) - - - -
RRM2B 00000285 NM_015713.4 0000022523 ./. - - c.580G>A p.(Glu194Lys) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV002631033;
Chromosome 8:103231146..103231146
ClinVar Allele ID 1987345
Disease database name and identifier MedGen:CN517202
ClinVar preferred disease name not provided
HGVS variant names NC 000008.10:g.103231146C>G
ClinVar review status criteria provided, single submitter
Clinical Significance Uncertain significance
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Gene symbol:Gene id. RRM2B:50484
Molecular consequence SO:0001583|missense variant
Allele origin germline
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR

RCVaccession RCV000005719; RCV000118999;
Chromosome 8:103231146..103231146
ClinVar Allele ID 20427
Disease database name and identifier MedGen:CN187502|MONDO:MONDO:0012792, MedGen:C2749861, OMIM:612075, Orphanet:255235
ClinVar preferred disease name RRM2B-related mitochondrial disease|Mitochondrial DNA depletion syndrome 8a
HGVS variant names NC 000008.10:g.103231146C>T
ClinVar review status no assertion criteria provided
Clinical Significance Pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA117479|OMIM:604712.0003|UniProtKB:Q7LG56#VAR 046220
Gene symbol:Gene id. RRM2B:50484
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 121918308
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