Variant #0000314167 (NC_000012.11:g.56737256C>A, NM_005419.3:c.2473G>T (STAT2))

Chromosome 12
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.56737256C>A
DNA change (hg38) g.56343472C>A
Published as STAT2(NM_005419.4):c.2473G>T (p.G825C)
ISCN -
DB-ID STAT2_000001
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) 0.0166 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
STAT2 NM_005419.3 -/. - c.2473G>T r.(?) p.(Gly825Cys)
IL23A NM_016584.2 -/. - c.*3368C>A r.(=) p.(=)


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