Variant #0000255847 (NC_000022.10:g.17601501A>G, NM_014339.5:c.*10791A>G (IL17RA))

Chromosome 22
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.17601501A>G
DNA change (hg38) g.17120611A>G
Published as CECR6(NM_031890.3):c.517T>C (p.C173R)
ISCN -
DB-ID CECR6_000001
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) 0.00029 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IL17RA NM_014339.5 ?/. - c.*10791A>G r.(=) p.(=)
CECR6 NM_031890.3 ?/. - c.517T>C r.(?) p.(Cys173Arg)


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