Variant #0000721743 (NC_000008.10:g.103251007G>C, NM_015902.5:c.*15523C>G (UBR5))

Chromosome 8
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.103251007G>C
DNA change (hg38) -
Published as RRM2B(NM_001172477.1):c.44C>G (p.P15R)
ISCN -
DB-ID RRM2B_000021
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RRM2B NM_015713.4 ?/. - c.48+48C>G r.(=) p.(=)
UBR5 NM_015902.5 ?/. - c.*15523C>G r.(=) p.(=)


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