Variant #0000608914 (NC_000003.11:g.9959671G>A, NM_032732.5:c.192G>A (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.9959671G>A
DNA change (hg38) g.9917987G>A
Published as IL17RC(NM_153461.3):c.405G>A (p.T135=)
ISCN -
DB-ID IL17RC_000027
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) 0.00022 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 2019-12-04 14:54:23 +01:00 (CET)
Date last edited 2020-06-12 11:22:35 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IL17RC NM_032732.5 -?/. - c.192G>A r.(?) p.(Thr64=)
IL17RE NM_153480.1 -?/. - c.*2180G>A r.(=) p.(=)


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