View genomic variant #0000022474

Chromosome 8
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.103218033T>A
Published as -
GERP -
Segregation -
DB-ID RRM2B_000071
MSCV MSCV_0022474
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 0000022474 ./. - - c.*2328A>T p.(=) - - - -
RRM2B 00000284 NM_001172478.1 0000022474 ./. - - c.*2328A>T p.(=) - - - -
RRM2B 00000285 NM_015713.4 0000022474 ./. - - c.*2328A>T p.(=) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000270614; RCV000365149;
Chromosome 8:103218033..103218033
ClinVar Allele ID 303737
Disease database name and identifier MONDO:MONDO:0000090, MedGen:CN294859, OMIM:PS157640|MONDO:MONDO:0018158, MedGen:C0342782, OMIM:PS603041, Orphanet:35698
ClinVar preferred disease name Progressive external ophthalmoplegia with mitochondrial DNA deletions|Mitochondrial DNA depletion syndrome
HGVS variant names NC 000008.10:g.103218033T>A
ClinVar review status criteria provided, single submitter
Clinical Significance Uncertain significance
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA10624465
Gene symbol:Gene id. RRM2B:50484
Molecular consequence SO:0001624|3 prime UTR variant
Allele origin germline
dbSNP ID 886062565
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