Variant #0000289592 (NC_000016.9:g.27460454G>A, NM_181078.2:c.1467G>A (IL21R))

Chromosome 16
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.27460454G>A
DNA change (hg38) g.27449133G>A
Published as IL21R(NM_181079.4):c.1533G>A (p.T511=)
ISCN -
DB-ID IL21R_000005
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) 0.00102 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IL21R NM_181078.2 -?/. - c.1467G>A r.(?) p.(Thr489=)
IL21R-AS1 NR_037158.1 -?/. - n.1151C>T r.(?) -


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