Variant #0001037497 (NC_000009.11:g.34648453G>T, NM_001142784.2:c.-3778G>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.34648453G>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID CCL27_000039
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 2025-05-05 21:14:00 +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.687G>T r.(?) p.(Lys229Asn)
IL11RA NM_001142784.2 +/. - c.-3778G>T r.(?) p.(=)
CCL27 NM_006664.2 +/. - c.*13488C>A r.(=) p.(=)


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