Variant #0000000296 (NC_000002.11:g.113820124C>T, NM_173170.1:c.338C>T (IL36RN))

Chromosome 2
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
DNA change (genomic) (Relative to hg19 / GRCh37) g.113820124C>T
Reference -
DB-ID IL36RN_000001
Frequency -
Average frequency (gnomAD v.2.1.1) 0.0029 View details
Owner Florian Bayersdorfer
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Florian Bayersdorfer
Date created 2023-06-29 13:32:08 +00:00 (UTC)
Date last edited 2023-06-29 13:33:11 +00:00 (UTC)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IL36RN NM_173170.1 +?/+? - c.338C>T r.(?) p.(Ser113Leu)