View genomic variant #0000003378

Chromosome 8
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
Type ins
DNA change (genomic) (Relative to hg19 / GRCh37) g.103220235_103220236insTT
Published as -
GERP -
Segregation -
DB-ID RRM2B_000021
MSCV MSCV_0003378
dbSNP ID -
Frequency -
Sources ;
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 0000003378 ./. - - c.*125_*126insAA p.(=) - - - -
RRM2B 00000284 NM_001172478.1 0000003378 ./. - - c.*125_*126insAA p.(=) - - - -
RRM2B 00000285 NM_015713.4 0000003378 ./. - - c.*125_*126insAA p.(=) - - - -
Legend  


MSeqDR View Variant at Gbrowse

Mitomap Mitochondrial Variant Phenotype Information:

None

Ensembl Variant Phenotype Information:

None