Variant #0000485164 (NC_000013.10:g.48878102_48878127del, NM_000321.2:c.54_79del (RB1))

Chromosome 13
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.48878102_48878127del
DNA change (hg38) g.48303966_48303991del
Published as -
ISCN -
DB-ID RB1_000360
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 N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RB1 NM_000321.2 +/+ 1 c.54_79del r.(?) p.(Glu19Profs*3)


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