Variant #0000344624 (NC_000009.11:g.34648167A>G, NM_001142784.2:c.-4064A>G (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.34648167A>G
DNA change (hg38) g.34648170A>G
Published as GALT(NM_000155.3):c.563A>G (p.Q188R, p.(Gln188Arg)), GALT(NM_000155.4):c.563A>G (p.Q188R)
ISCN -
DB-ID GALT_000002 See all 10 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) 0.00143 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GALT NM_000155.3 +/. - c.563A>G r.(?) p.(Gln188Arg)
IL11RA NM_001142784.2 +/. - c.-4064A>G r.(?) p.(=)
CCL27 NM_006664.2 +/. - c.*13774T>C r.(=) p.(=)


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