Variant #0000727879 (NC_000021.8:g.34635572G>A, IFNAR2(NM_000874.3):c.*551G>A)

Chromosome 21
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.34635572G>A
DNA change (hg38) -
Published as IFNAR2(NM_001289125.1):c.1315G>A (p.D439N), IFNAR2(NM_207585.2):c.1315G>A (p.D439N)
ISCN -
DB-ID IFNAR2_000011 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) 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
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IL10RB NM_000628.4 -?/. - c.-3199G>A r.(?) p.(=)
IFNAR2 NM_000874.3 -?/. - c.*551G>A r.(=) p.(=)