Variant #0000606178 (NC_000002.11:g.163174756C>A, NM_022168.3:c.62G>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.163174756C>A
DNA change (hg38) g.162318246C>A
Published as IFIH1(NM_022168.4):c.62G>T (p.R21M)
ISCN -
DB-ID GCA_000006
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 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 2019-12-04 14:54:23 +01:00 (CET)
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.-26003C>A r.(?) p.(=)
IFIH1 NM_022168.3 ?/. - c.62G>T r.(?) p.(Arg21Met)


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