View genomic variant #0000022518

Chromosome 8
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.103231090_103231091insCTT
Published as -
GERP -
Segregation -
DB-ID RRM2B_000027
MSCV MSCV_0022518
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 0000022518 ./. - - c.851_852insAAG p.(Gly284_Leu285insSer) - - - -
RRM2B 00000284 NM_001172478.1 0000022518 ./. - - c.479_480insAAG p.(Gly160_Leu161insSer) - - - -
RRM2B 00000285 NM_015713.4 0000022518 ./. - - c.635_636insAAG p.(Gly212_Leu213insSer) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000198969;
Chromosome 8:103231090..103231091
ClinVar Allele ID 213577
Disease database name and identifier MONDO:MONDO:0012792, MedGen:C2749861, OMIM:612075, Orphanet:255235
ClinVar preferred disease name Mitochondrial DNA depletion syndrome 8a
HGVS variant names NC 000008.10:g.103231091 103231092insTTC
ClinVar review status criteria provided, single submitter
Clinical Significance Likely pathogenic
Variant type Insertion
Sequence Ontology for variant type SO:0000667
Variant clinical sources reported ClinGen:CA279000
Gene symbol:Gene id. RRM2B:50484
Molecular consequence SO:0001821|inframe insertion
Allele origin germline
dbSNP ID 863224914
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