View genomic variant #0000001266

Chromosome 8
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Type subst
DNA change (genomic) (Relative to hg19 / GRCh37) g.103226385C>A
Published as -
GERP 5.480
Segregation -
DB-ID RRM2B_000014 See all 2 reported entries
MSCV MSCV_0001266
dbSNP ID rs121918311
Frequency -
Sources ; clinVar; Ensembl;
Reference 19138848
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 0000001266 +/+ - 7/9 c.902G>T p.(Gly301Val) - missense_variant,splice_region_variant - -
RRM2B 00000284 NM_001172478.1 0000001266 +/+ - 6/8 c.530G>T p.(Gly177Val) probably_damaging(0.999) missense_variant,splice_region_variant - deleterious(0)
RRM2B 00000285 NM_015713.4 0000001266 +/+ - 7/9 c.686G>T p.(Gly229Val) probably_damaging(0.998) missense_variant,splice_region_variant - deleterious(0)
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000005723; RCV000119005; RCV001818139;
Chromosome 8:103226385..103226385
Allele frequencies from ExAC 0.00002
ClinVar Allele ID 20431
Disease database name and identifier MedGen:CN187502|MedGen:C3661900|MONDO:MONDO:0012792, MedGen:C2749861, OMIM:612075, Orphanet:255235
ClinVar preferred disease name RRM2B-related mitochondrial disease|not provided|Mitochondrial DNA depletion syndrome 8a
HGVS variant names NC 000008.10:g.103226385C>A
ClinVar review status criteria provided, conflicting interpretations
Clinical Significance Conflicting interpretations of pathogenicity
Conflicting clinical significance Pathogenic(1)|Uncertain significance(1)
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA117492|OMIM:604712.0007
Gene symbol:Gene id. RRM2B:50484
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 121918311
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