Variant #0000978680 (NC_000009.11:g.34648157C>T, NM_001142784.2:c.-4074C>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.34648157C>T
DNA change (hg38) -
Published as GALT(NM_000155.4):c.553C>T (p.(Pro185Ser))
ISCN -
DB-ID CCL27_000032
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GALT NM_000155.3 +/. - c.553C>T r.(?) p.(Pro185Ser)
IL11RA NM_001142784.2 +/. - c.-4074C>T r.(?) p.(=)
CCL27 NM_006664.2 +/. - c.*13784G>A r.(=) p.(=)


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