Variant #0000509781 (NC_000002.11:g.163174560G>C, NM_022168.3:c.258C>G (IFIH1))

Chromosome 2
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.163174560G>C
DNA change (hg38) g.162318050G>C
Published as IFIH1(NM_022168.4):c.258C>G (p.T86=)
ISCN -
DB-ID GCA_000005
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) 0.00116 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GCA NM_012198.3 -/. - c.-26199G>C r.(?) p.(=)
IFIH1 NM_022168.3 -/. - c.258C>G r.(?) p.(Thr86=)


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