Variant #0000285275 (NC_000002.11:g.113820124C>T, NM_173170.1:c.338C>T (IL36RN))

Chromosome 2
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.113820124C>T
DNA change (hg38) g.113062547C>T
Published as IL36RN(NM_012275.2):c.338C>T (p.S113L), IL36RN(NM_012275.3):c.338C>T (p.S113L), IL36RN(NM_173170.1):c.338C>T (p.S113L)
ISCN -
DB-ID IL36RN_000008 See all 6 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) 0.0029 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-08-28 13:07:21 +02:00 (CEST)
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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)


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