Variant #0000859157 (NC_000003.11:g.9962283C>T, NM_032732.5:c.574C>T (IL17RC))

Chromosome 3
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.9962283C>T
DNA change (hg38) -
Published as IL17RC(NM_153461.3):c.787C>T (p.P263S)
ISCN -
DB-ID IL17RC_000045
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) 4.0E-5 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 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IL17RC NM_032732.5 ?/. - c.574C>T r.(?) p.(Pro192Ser)
IL17RE NM_153480.1 ?/. - c.*4792C>T r.(=) p.(=)


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