Variant #0000538048 (NC_000009.11:g.34659861_34659869dup, NM_001142784.2:c.916_924dup (IL11RA))

Chromosome 9
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.34659861_34659869dup
DNA change (hg38) g.34659864_34659872dup
Published as IL11RA(NM_001142784.2):c.916_924dupACCTGGAGC (p.T306_S308dup)
ISCN -
DB-ID CCL27_000013
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 2019-07-18 18:22:55 +02:00 (CEST)
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.916_924dup r.(?) p.(Thr306_Ser308dup)
CCL27 NM_006664.2 +/. - c.*2083_*2091dup r.(=) p.(=)


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