Variant #0000848994 (NC_000002.11:g.163134090C>A, NM_022168.3:c.1879G>T (IFIH1))

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.163134090C>A
DNA change (hg38) -
Published as IFIH1(NM_022168.3):c.1879G>T (p.(Glu627Ter)), IFIH1(NM_022168.4):c.1879G>T (p.E627*)
ISCN -
DB-ID IFIH1_000003 See all 9 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) 0.0032 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2022-05-09 15:40:45 +02:00 (CEST)
Date last edited 2024-08-28 13:07:21 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IFIH1 NM_022168.3 ?/. - c.1879G>T r.(?) p.(Glu627Ter)


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