Variant #0000949277 (NC_000009.11:g.34658593A>G, NM_001142784.2:c.723A>G (IL11RA))

Chromosome 9
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.34658593A>G
DNA change (hg38) -
Published as IL11RA(NM_001142784.2):c.723A>G (p.T241=, p.(Thr241=))
ISCN -
DB-ID IL11RA_000006 See all 2 reported entries
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) 0.00395 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 2023-11-27 17:35:39 +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.723A>G r.(?) p.(Thr241=)
CCL27 NM_006664.2 -/. - c.*3348T>C r.(=) p.(=)


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