Variant #0000485201 (NC_000013.10:g.49033829C>T, NM_000321.2:c.1966C>T (RB1))

Chromosome 13
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Probably does not affect function
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.49033829C>T
DNA change (hg38) g.48459693C>T
Published as -
ISCN -
DB-ID RB1_000403 See all 3 reported entries
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) 0.00066 View details
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 -?/-? - c.1966C>T r.(?) p.(Arg656Trp)


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