Variant #0000722502 (NC_000009.11:g.34658652G>A, NM_001142784.2:c.782G>A (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.34658652G>A
DNA change (hg38) -
Published as IL11RA(NM_001142784.2):c.782G>A (p.(Arg261His))
ISCN -
DB-ID CCL27_000023
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) 0.00192 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IL11RA NM_001142784.2 -?/. - c.782G>A r.(?) p.(Arg261His)
CCL27 NM_006664.2 -?/. - c.*3289C>T r.(=) p.(=)


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