Variant #0000288204 (NC_000009.11:g.34649029G>T, NM_001142784.2:c.-3202G>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.34649029G>T
DNA change (hg38) g.34649032G>T
Published as GALT(NM_000155.3):c.855G>T (p.K285N), GALT(NM_000155.4):c.855G>T (p.(Lys285Asn), p.K285N)
ISCN -
DB-ID GALT_000003 See all 5 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) 0.00014 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-04-19 20:27:30 +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.855G>T r.(?) p.(Lys285Asn)
IL11RA NM_001142784.2 +/. - c.-3202G>T r.(?) p.(=)
CCL27 NM_006664.2 +/. - c.*12912C>A r.(=) p.(=)


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