Variant #0000929596 (NC_000009.11:g.34649520G>T, NM_001142784.2:c.-2711G>T (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.34649520G>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID CCL27_000030
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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2023-07-07 10:10:56 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GALT NM_000155.3 +/. - c.1018G>T r.(?) p.(Glu340*)
IL11RA NM_001142784.2 +/. - c.-2711G>T r.(?) p.(=)
CCL27 NM_006664.2 +/. - c.*12421C>A r.(=) p.(=)


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