View genomic variant #0000001263

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.103225061C>G
Published as -
GERP 5.640
Segregation -
DB-ID RRM2B_000011 See all 2 reported entries
MSCV MSCV_0001263
dbSNP ID rs182614164
Frequency -
Sources ; ensembl;
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 0000001263 +?/+? - 8/9 c.1062G>C p.(Met354Ile) - missense_variant - -
RRM2B 00000284 NM_001172478.1 0000001263 +?/+? - 7/8 c.690G>C p.(Met230Ile) probably_damaging(0.913) missense_variant - tolerated(0.08)
RRM2B 00000285 NM_015713.4 0000001263 +?/+? - 8/9 c.846G>C p.(Met282Ile) possibly_damaging(0.901) missense_variant - tolerated(0.08)
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000119009; RCV001091699;
Chromosome 8:103225061..103225061
Allele frequencies from ExAC 0.00001
Allele frequencies from TGP 0.00020
ClinVar Allele ID 136345
Disease database name and identifier MedGen:CN187502|MedGen:C3661900
ClinVar preferred disease name RRM2B-related mitochondrial disease|not provided
HGVS variant names NC 000008.10:g.103225061C>G
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:CA345612|UniProtKB:Q7LG56#VAR 046223
Gene symbol:Gene id. RRM2B:50484
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 182614164
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