Variant #0000724552 (NC_000013.10:g.48878107C>T, NM_000321.2:c.59C>T (RB1))

Chromosome 13
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.48878107C>T
DNA change (hg38) -
Published as RB1(NM_000321.2):c.59C>T (p.P20L, p.(Pro20Leu))
ISCN -
DB-ID RB1_000493 See all 3 reported entries
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) 0.00013 View details
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 2024-08-28 13:16:32 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RB1 NM_000321.2 ?/. - c.59C>T r.(?) p.(Pro20Leu)
LPAR6 NM_005767.5 ?/. - c.*107418G>A r.(=) p.(=)


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