Full data view for gene IL2

Information The variants shown are described using the NM_000586.3 transcript reference sequence.

5 entries on 1 page. Showing entries 1 - 5.
Legend  

Effect     

Exon     

AscendingDNA change (cDNA)     

ClassClinical     

RNA change     

Protein     

Allele     

DNA change (genomic) (hg19)     

DNA change (hg38)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Template     

Technique     

Tissue     

Remarks     

Disease     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age/Death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
?/? 1 c.114G>T - r.(=) p.(=) Unknown g.123377482C>A g.122456327C>A - - IL2_000001 - dbSNP - - Unknown - - - - - - - - - - - - - - - - - - - - - - -
?/? 1 c.114G>T - r.(=) p.(=) Unknown g.123377482C>A g.122456327C>A - - IL2_000001 - - - - Unknown - 74/166 - - - DNA ? - - Healthy/Control - - association study - - - - - - - - 166 Mads V Hollegaard
?/? 1 c.114G>T - r.(=) p.(=) Both (homozygous) g.123377482C>A g.122456327C>A - - IL2_000001 - - - - Unknown - 26/166 - - - DNA ? - - Healthy/Control - - association study - - - - - - - - 166 Mads V Hollegaard
?/? 1 c.114G>T - r.(=) p.(=) Unknown g.123377482C>A g.122456327C>A - - IL2_000001 - - - - Unknown - 90/202 - - - DNA ? - - SCP - - association study - - - - - - - - 202 Mads V Hollegaard
?/? 1 c.114G>T - r.(=) p.(=) Both (homozygous) g.123377482C>A g.122456327C>A - - IL2_000001 - - - - Unknown - 30/202 - - - DNA ? - - SCP - - association study - - - - - - - - 202 Mads V Hollegaard
Legend