Variant #0000249671 (NC_000013.10:g.48951169A>G, NM_000321.2:c.1331A>G (RB1))

Chromosome 13
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.48951169A>G
DNA change (hg38) g.48377033A>G
Published as RB1(NM_000321.3):c.1331A>G (p.Q444R)
ISCN -
DB-ID RB1_000280 See all 2 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) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RB1 NM_000321.2 +/. - c.1331A>G r.(?) p.(Gln444Arg)
LPAR6 NM_005767.5 +/. - c.*34356T>C r.(=) p.(=)


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