Variant #0000895458 (NC_000021.8:g.34793888C>T, IFNGR2(NM_005534.3):c.308C>T)

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.34793888C>T
DNA change (hg38) -
Published as IFNGR2(NM_001329128.1):c.365C>T (p.A122V), IFNGR2(NM_005534.3):c.308C>T (p.A103V)
ISCN -
DB-ID IFNGR2_000040 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) 0.00024 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-11-01 13:41:49 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IFNGR2 NM_005534.3 -?/. - c.308C>T r.(?) p.(Ala103Val)