View genomic variant #0000026652

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.103238212_103238214del
Published as -
GERP -
Segregation -
DB-ID RRM2B_000104
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 0000026652 ./. - - c.469_471del p.(Glu157del) - - - -
RRM2B 00000284 NM_001172478.1 0000026652 ./. - - c.97_99del p.(Glu33del) - - - -
RRM2B 00000285 NM_015713.4 0000026652 ./. - - c.253_255del p.(Glu85del) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000005720; RCV000118988; RCV000186558; RCV000413797; RCV002483199;
Chromosome 8:103238212..103238214
Allele frequencies from ExAC 0.00001
ClinVar Allele ID 136331
Disease database name and identifier MONDO:MONDO:0013117, MedGen:C2751319, OMIM:613077|MONDO:MONDO:0012792, MedGen:C2749861, OMIM:612075, Orphanet:255235|MONDO:MONDO:0010000, MedGen:C1849333, OMIM:268315|Human Phenotype Ontology:HP:0100595, MONDO:MONDO:0015271, MedGen:C0264162, Orphanet:1320|MedGen:CN187502|MedGen:C3661900
ClinVar preferred disease name Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 5|Mitochondrial DNA depletion syndrome 8a|Rod-cone dystrophy, sensorineural deafness, and Fanconi-type renal dysfunction|Idiopathic camptocormia|RRM2B-related mitochondrial disease|not provided
HGVS variant names NC 000008.10:g.103238212 103238214del
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Likely pathogenic
Variant type Deletion
Sequence Ontology for variant type SO:0000159
Variant clinical sources reported ClinGen:CA204014|OMIM:604712.0004
Gene symbol:Gene id. RRM2B:50484
Molecular consequence SO:0001822|inframe deletion
Allele origin germline
dbSNP ID 515726184
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR

RCVaccession RCV003019380;
Chromosome 8:103238213..103238214
ClinVar Allele ID 2169089
Disease database name and identifier MedGen:CN517202
ClinVar preferred disease name not provided
HGVS variant names NC 000008.10:g.103238213 103238214delinsAT
ClinVar review status criteria provided, single submitter
Clinical Significance Uncertain significance
Variant type Indel
Sequence Ontology for variant type SO:1000032
Gene symbol:Gene id. RRM2B:50484
Molecular consequence SO:0001583|missense variant
Allele origin germline
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