View genomic variant #0000022510

Chromosome 8
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Probably does not affect function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.103220504C>A
Published as -
GERP -
Segregation -
DB-ID RRM2B_000081
MSCV MSCV_0022510
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 0000022510 ./. - - c.1129G>T p.(Ala377Ser) - - - -
RRM2B 00000284 NM_001172478.1 0000022510 ./. - - c.757G>T p.(Ala253Ser) - - - -
RRM2B 00000285 NM_015713.4 0000022510 ./. - - c.913G>T p.(Ala305Ser) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000303281; RCV000392494;
Chromosome 8:103220504..103220504
Allele frequencies from ExAC 0.00003
Allele frequencies from TGP 0.00020
ClinVar Allele ID 312098
Disease database name and identifier MONDO:MONDO:0013117, MedGen:C2751319, OMIM:613077|MONDO:MONDO:0012792, MedGen:C2749861, OMIM:612075, Orphanet:255235
ClinVar preferred disease name Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 5|Mitochondrial DNA depletion syndrome 8a
HGVS variant names NC 000008.10:g.103220504C>A
ClinVar review status criteria provided, conflicting interpretations
Clinical Significance Conflicting interpretations of pathogenicity
Conflicting clinical significance Uncertain significance(1)|Benign(1)
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA4830963
Gene symbol:Gene id. RRM2B:50484
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 201440849
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