Variant #0000314166 (NC_000012.11:g.56740682C>G, NM_005419.3:c.1782G>C (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.56740682C>G
DNA change (hg38) g.56346898C>G
Published as STAT2(NM_005419.3):c.1782G>C (p.(Met594Ile)), STAT2(NM_005419.4):c.1782G>C (p.M594I)
ISCN -
DB-ID STAT2_000002 See all 4 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) 0.04917 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.1782G>C r.(?) p.(Met594Ile)


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