Variant #0000924017 (NC_000003.11:g.9959227_9959228insCTTTCTGGT, NC_000003.11(NM_032732.5):c.105+123_105+124insCTTTCTGGT (IL17RC))

Chromosome 3
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.9959227_9959228insCTTTCTGGT
DNA change (hg38) -
Published as IL17RC(NM_153461.4):c.228_229insCTTTCTGGT (p.L74_G76dup)
ISCN -
DB-ID IL17RC_000055
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-04-16 21:50:28 +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.105+123_105+124insCTTTCTGGT r.(=) p.(=)
IL17RE NM_153480.1 -/. - c.*1736_*1737insCTTTCTGGT r.(=) p.(=)


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