Variant #0000285253 (NC_000003.11:g.9959640T>C, NM_032732.5:c.161T>C (IL17RC))

Chromosome 3
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.9959640T>C
DNA change (hg38) g.9917956T>C
Published as IL17RC(NM_153460.3):c.161T>C (p.(Val54Ala)), IL17RC(NM_153461.3):c.374T>C (p.V125A), IL17RC(NM_153461.4):c.374T>C (p.V125A)
ISCN -
DB-ID IL17RC_000002 See all 3 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) 0.00185 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 13:16:32 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IL17RC NM_032732.5 -?/. - c.161T>C r.(?) p.(Val54Ala)
IL17RE NM_153480.1 -?/. - c.*2149T>C r.(=) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.