Variant #0000866616 (NC_000021.8:g.34799220G>A, IFNGR2(NM_005534.3):c.442G>A)

Chromosome 21
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.34799220G>A
DNA change (hg38) -
Published as IFNGR2(NM_001329128.1):c.499G>A (p.V167M), IFNGR2(NM_001329128.2):c.499G>A (p.V167M)
ISCN -
DB-ID IFNGR2_000045 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) 1.0E-5 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 2022-05-09 16:01:56 +02:00 (CEST)
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.442G>A r.(?) p.(Val148Met)