View genomic variant #0000001267

Chromosome 8
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Type subst
DNA change (genomic) (Relative to hg19 / GRCh37) g.103231119C>T
Published as -
GERP 5.370
Segregation -
DB-ID RRM2B_000015
MSCV MSCV_0001267
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 0000001267 ?/? - 6/9 c.823G>A p.(Ala275Thr) - missense_variant - -
RRM2B 00000284 NM_001172478.1 0000001267 ?/? - 5/8 c.451G>A p.(Ala151Thr) probably_damaging(0.991) missense_variant - deleterious(0.01)
RRM2B 00000285 NM_015713.4 0000001267 ?/? - 6/9 c.607G>A p.(Ala203Thr) probably_damaging(0.993) missense_variant - deleterious(0)
Legend  


MSeqDR View Variant at Gbrowse

Mitomap Mitochondrial Variant Phenotype Information:

None

Ensembl Variant Phenotype Information:

None