Variant #0000485488 (NC_000013.10:g.48878093_48878094insN[23], NM_000321.2:c.45_46insN[23] (RB1))

Chromosome 13
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.48878093_48878094insN[23]
DNA change (hg38) -
Published as 45_46ins23
ISCN -
DB-ID RB1_000864
Variant remarks -
Reference data copied from the RB1-LSDB
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Dietmar Lohmann
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2019-06-08 19:09:47 +02:00 (CEST)
Date last edited 2021-12-15 17:25:19 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RB1 NM_000321.2 ?/? - c.45_46insN[23] r.(?) p.?


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