View genomic variant #0000022513

Chromosome 8
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Does not affect function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.103225125G>T
Published as -
GERP -
Segregation -
DB-ID RRM2B_000024
MSCV MSCV_0022513
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 8.0E-5 View details
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 0000022513 ./. - - c.1006-8C>A p.(=) - - - -
RRM2B 00000284 NM_001172478.1 0000022513 ./. - - c.634-8C>A p.(=) - - - -
RRM2B 00000285 NM_015713.4 0000022513 ./. - - c.790-8C>A p.(=) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000127808; RCV000339380; RCV000392490; RCV000973700; RCV002492486;
Chromosome 8:103225125..103225125
Allele frequencies from ESP 0.00008
Allele frequencies from TGP 0.01458
ClinVar Allele ID 142633
Disease database name and identifier MedGen:C3661900|MONDO:MONDO:0012792, MedGen:C2749861, OMIM:612075, Orphanet:255235|MONDO:MONDO:0010000, MedGen:C1849333, OMIM:268315|MONDO:MONDO:0013117, MedGen:C2751319, OMIM:613077|MedGen:CN169374
ClinVar preferred disease name not provided|Mitochondrial DNA depletion syndrome 8a|Rod-cone dystrophy, sensorineural deafness, and Fanconi-type renal dysfunction|Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 5|not specified
HGVS variant names NC 000008.10:g.103225125G>T
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Benign/Likely benign
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA293110
Gene symbol:Gene id. RRM2B:50484
Molecular consequence SO:0001627|intron variant
Allele origin germline
dbSNP ID 376542259
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