Variant #0000947672 (NC_000002.11:g.191937906T>A, NM_003151.3:c.383A>T (STAT4))

Chromosome 2
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.191937906T>A
DNA change (hg38) -
Published as STAT4(NM_003151.3):c.383A>T (p.E128V, p.(Glu128Val)), STAT4(NM_003151.4):c.383A>T (p.E128V)
ISCN -
DB-ID STAT4_000001 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) 0.00099 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-11-27 17:35:39 +01:00 (CET)
Date last edited 2024-08-28 13:07:21 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
STAT4 NM_003151.3 ?/. - c.383A>T r.(?) p.(Glu128Val)


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