Variant #0000538039 (NC_000009.11:g.34648992C>T, NM_001142784.2:c.-3239C>T (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.34648992C>T
DNA change (hg38) g.34648995C>T
Published as GALT(NM_000155.3):c.821-3C>T (p.?)
ISCN -
DB-ID CCL27_000004
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-25 13:17:46 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GALT NM_000155.3 -?/. - c.821-3C>T r.spl? p.?
IL11RA NM_001142784.2 -?/. - c.-3239C>T r.(?) p.(=)
CCL27 NM_006664.2 -?/. - c.*12949G>A r.(=) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.