View genomic variant #0000022507

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.103220467del
Published as -
GERP -
Segregation -
DB-ID RRM2B_000078
MSCV MSCV_0022507
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 0000022507 ./. - - c.1166del p.(Leu389*) - - - -
RRM2B 00000284 NM_001172478.1 0000022507 ./. - - c.794del p.(Leu265*) - - - -
RRM2B 00000285 NM_015713.4 0000022507 ./. - - c.950del p.(Leu317*) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000023385; RCV000119013; RCV000508947;
Chromosome 8:103220467..103220467
ClinVar Allele ID 39389
Disease database name and identifier MedGen:CN187502|MONDO:MONDO:0044970, MeSH:D028361, MedGen:C0751651, Orphanet:68380|MONDO:MONDO:0013117, MedGen:C2751319, OMIM:613077
ClinVar preferred disease name RRM2B-related mitochondrial disease|Mitochondrial disease|Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 5
HGVS variant names NC 000008.10:g.103220469del
ClinVar review status no assertion criteria provided
Clinical Significance Pathogenic
Variant type Deletion
Sequence Ontology for variant type SO:0000159
Variant clinical sources reported ClinGen:CA213025|OMIM:604712.0010
Gene symbol:Gene id. RRM2B:50484
Molecular consequence SO:0001587|nonsense
Allele origin germline
dbSNP ID 515726199
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR

RCVaccession RCV000119012;
Chromosome 8:103220468..103220468
ClinVar Allele ID 136347
Disease database name and identifier MedGen:CN187502
ClinVar preferred disease name RRM2B-related mitochondrial disease
HGVS variant names NC 000008.10:g.103220468A>C
ClinVar review status no assertion provided
Clinical Significance not provided
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA345618|UniProtKB:Q7LG56#VAR 046224
Gene symbol:Gene id. RRM2B:50484
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 515726198
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