Variant #0000289564 (NC_000009.11:g.34660952_34660954del, NC_000009.11(NM_001142784.2):c.1252+19_1252+21del (IL11RA))

Chromosome 9
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.34660952_34660954del
DNA change (hg38) g.34660955_34660957del
Published as IL11RA(NM_001142784.2):c.1252+19_1252+21delAGA
ISCN -
DB-ID IL11RA_000005
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_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 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IL11RA NM_001142784.2 -?/. - c.1252+19_1252+21del r.(=) p.(=)
CCL27 NM_006664.2 -?/. - c.*990_*992del r.(=) p.(=)


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