Variant #0000570541 (NC_000021.8:g.34805196dup, IFNGR2(NM_005534.3):c.879+18dup)

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.34805196dup
DNA change (hg38) g.33432889dup
Published as IFNGR2(NM_005534.3):c.879+18dupT
ISCN -
DB-ID IFNGR2_000043
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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     
IFNGR2 NM_005534.3 -?/. - c.879+18dup r.(=) p.(=)
TMEM50B NR_040016.1 -?/. - n.2811-87dup r.(?) -