Variant #0000538035 (NC_000009.11:g.34648114C>A, NM_001142784.2:c.-4117C>A (IL11RA))

Chromosome 9
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.34648114C>A
DNA change (hg38) g.34648117C>A
Published as GALT(NM_000155.3):c.510C>A (p.I170=), GALT(NM_000155.4):c.510C>A (p.I170=)
ISCN -
DB-ID CCL27_000002 See all 2 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) 0.00302 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +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.510C>A r.(?) p.(Ile170=)
IL11RA NM_001142784.2 -/. - c.-4117C>A r.(?) p.(=)
CCL27 NM_006664.2 -/. - c.*13827G>T r.(=) p.(=)


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