Variant #0000251707 (NC_000009.11:g.34649442A>G, NM_001142784.2:c.-2789A>G (IL11RA))

Chromosome 9
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.34649442A>G
DNA change (hg38) g.34649445A>G
Published as GALT(NM_000155.4):c.940A>G (p.N314D)
ISCN -
DB-ID GALT_000004 See all 4 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) 0.0924 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-07-07 10:10:56 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GALT NM_000155.3 ?/. - c.940A>G r.(?) p.(Asn314Asp)
IL11RA NM_001142784.2 ?/. - c.-2789A>G r.(?) p.(=)
CCL27 NM_006664.2 ?/. - c.*12499T>C r.(=) p.(=)


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