Variant #0000656326 (NC_000009.11:g.21385151C>A, NM_000605.3:c.178G>T (IFNA2))

Chromosome 9
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.21385151C>A
DNA change (hg38) g.21385152C>A
Published as IFNA2(NM_000605.3):c.178G>T (p.(Gly60Ter))
ISCN -
DB-ID IFNA2_000001
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2020-03-23 16:13:27 +01:00 (CET)
Date last edited 2020-06-25 12:45:04 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IFNA2 NM_000605.3 ?/. - c.178G>T r.(?) p.(Gly60Ter)


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