View genomic variant #0000022540

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.103251055C>T
Published as -
GERP -
Segregation -
DB-ID RRM2B_000007 See all 2 reported entries
MSCV MSCV_0001276
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.
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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 0000022540 ./. - - c.-5G>A p.(=) - - - -
RRM2B 00000284 NM_001172478.1 0000022540 ./. - - c.48G>A p.(=) - - - -
RRM2B 00000285 NM_015713.4 0000022540 ./. - - c.48G>A p.(=) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000118982; RCV000508788; RCV001089491; RCV001379488; RCV002498540;
Chromosome 8:103251055..103251055
ClinVar Allele ID 136325
Disease database name and identifier MONDO:MONDO:0013117, MedGen:C2751319, OMIM:613077|MONDO:MONDO:0010000, MedGen:C1849333, OMIM:268315|MONDO:MONDO:0012792, MedGen:C2749861, OMIM:612075, Orphanet:255235|MedGen:CN187502|MedGen:C3661900|MONDO:MONDO:0044970, MeSH:D028361, MedGen:C0751651, Orphanet:68380
ClinVar preferred disease name Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 5|Rod-cone dystrophy, sensorineural deafness, and Fanconi-type renal dysfunction|Mitochondrial DNA depletion syndrome 8a|RRM2B-related mitochondrial disease|not provided|Mitochondrial disease
HGVS variant names NC 000008.10:g.103251055C>T
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Pathogenic/Likely pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA345542
Gene symbol:Gene id. RRM2B:50484|LOC130000896:130000896
Molecular consequence SO:0001623|5 prime UTR variant, SO:0001819|synonymous variant
Allele origin
dbSNP ID 515726180
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