Variant #0000571242 (NC_000022.10:g.17600904C>A, NM_014339.5:c.*10194C>A (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.17600904C>A
DNA change (hg38) g.17120014C>A
Published as CECR6(NM_031890.3):c.1114G>T (p.(Glu372Ter))
ISCN -
DB-ID CECR6_000003
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2022-11-01 13:01:21 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IL17RA NM_014339.5 ?/. - c.*10194C>A r.(=) p.(=)
CECR6 NM_031890.3 ?/. - c.1114G>T r.(?) p.(Glu372Ter)


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