View genomic variant #0000026649

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.103231064T>C
Published as -
GERP -
Segregation -
DB-ID RRM2B_000108
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 0000026649 ./. - - c.878A>G p.(Asn293Ser) - - - -
RRM2B 00000284 NM_001172478.1 0000026649 ./. - - c.506A>G p.(Asn169Ser) - - - -
RRM2B 00000285 NM_015713.4 0000026649 ./. - - c.662A>G p.(Asn221Ser) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000196496; RCV000714482; RCV000680084;
Chromosome 8:103231064..103231064
ClinVar Allele ID 211320
Disease database name and identifier MedGen:CN517202|MONDO:MONDO:0012792, MedGen:C2749861, OMIM:612075, Orphanet:255235|Human Phenotype Ontology:HP:0004900, MedGen:C1839436
ClinVar preferred disease name not provided|Mitochondrial DNA depletion syndrome 8a|Severe lactic acidosis
HGVS variant names NC 000008.10:g.103231064T>C
ClinVar review status criteria provided, conflicting interpretations
Clinical Significance Conflicting interpretations of pathogenicity
Conflicting clinical significance Likely pathogenic(2)|Uncertain significance(1)
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA320911|OMIM:604712.0015
Gene symbol:Gene id. RRM2B:50484
Molecular consequence SO:0001583|missense variant
Allele origin
dbSNP ID 863224193
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