Variant #0000254020 (NC_000021.8:g.34799244A>C, NM_005534.3:c.466A>C (IFNGR2))

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.34799244A>C
DNA change (hg38) g.33426937A>C
Published as IFNGR2(NM_001329128.1):c.523A>C (p.I175L), IFNGR2(NM_005534.3):c.466A>C (p.I156L)
ISCN -
DB-ID IFNGR2_000016 See all 3 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) 0.00226 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 2019-12-04 15:24:38 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IFNGR2 NM_005534.3 -?/. - c.466A>C r.(?) p.(Ile156Leu)


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