View genomic variant #0000022538

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.103244459C>G
Published as -
GERP -
Segregation -
DB-ID RRM2B_000004 See all 2 reported entries
MSCV MSCV_0001273
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 0000022538 ./. - - c.338G>C p.(Arg113Pro) - - - -
RRM2B 00000284 NM_001172478.1 0000022538 ./. - - c.49-6197G>C p.(=) - - - -
RRM2B 00000285 NM_015713.4 0000022538 ./. - - c.122G>C p.(Arg41Pro) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000118985; RCV003324724;
Chromosome 8:103244459..103244459
ClinVar Allele ID 136328
Disease database name and identifier MedGen:CN187502|MedGen:C3661900
ClinVar preferred disease name RRM2B-related mitochondrial disease|not provided
HGVS variant names NC 000008.10:g.103244459C>G
ClinVar review status criteria provided, single submitter
Clinical Significance Likely pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA345556
Gene symbol:Gene id. RRM2B:50484
Molecular consequence SO:0001583|missense variant, SO:0001627|intron variant
Allele origin germline
dbSNP ID 200273673
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR

RCVaccession RCV000118984; RCV001854572;
Chromosome 8:103244459..103244459
ClinVar Allele ID 136327
Disease database name and identifier MedGen:CN187502|MedGen:C3661900
ClinVar preferred disease name RRM2B-related mitochondrial disease|not provided
HGVS variant names NC 000008.10:g.103244459C>T
ClinVar review status criteria provided, conflicting interpretations
Clinical Significance Conflicting interpretations of pathogenicity
Conflicting clinical significance Likely pathogenic(1)|Uncertain significance(1)
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA345551
Gene symbol:Gene id. RRM2B:50484
Molecular consequence SO:0001583|missense variant, SO:0001627|intron variant
Allele origin germline
dbSNP ID 200273673
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