View genomic variant #0000022505

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.103220451_103220452insT
Published as -
GERP -
Segregation -
DB-ID RRM2B_000076
MSCV MSCV_0022505
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 0000022505 ./. - - c.1181_1182insA p.(Asn394Lysfs*4) - - - -
RRM2B 00000284 NM_001172478.1 0000022505 ./. - - c.809_810insA p.(Asn270Lysfs*4) - - - -
RRM2B 00000285 NM_015713.4 0000022505 ./. - - c.965_966insA p.(Asn322Lysfs*4) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000023386; RCV000119015;
Chromosome 8:103220451..103220452
ClinVar Allele ID 39390
Disease database name and identifier MedGen:CN187502|MONDO:MONDO:0013117, MedGen:C2751319, OMIM:613077
ClinVar preferred disease name RRM2B-related mitochondrial disease|Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 5
HGVS variant names NC 000008.10:g.103220454dup
ClinVar review status no assertion criteria provided
Clinical Significance Pathogenic
Variant type Duplication
Sequence Ontology for variant type SO:1000035
Variant clinical sources reported ClinGen:CA213027|OMIM:604712.0011
Gene symbol:Gene id. RRM2B:50484
Molecular consequence SO:0001589|frameshift variant
Allele origin germline
dbSNP ID 515726201
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