Variant #0000983132 (NC_000019.9:g.10475421C>T, NM_003331.4:c.1236G>A (TYK2))

Chromosome 19
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.10475421C>T
DNA change (hg38) -
Published as TYK2(NM_003331.4):c.1236G>A (p.A412=), TYK2(NM_003331.5):c.1236G>A (p.(Ala412=))
ISCN -
DB-ID TYK2_000039 See all 2 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) 0.00013 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TYK2 NM_003331.4 ?/. - c.1236G>A r.(?) p.(Ala412=)


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