Variant #0000722497 (NC_000009.11:g.34648350T>C, NM_001142784.2:c.-3881T>C (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.34648350T>C
DNA change (hg38) -
Published as GALT(NM_000155.3):c.584T>C (p.(Leu195Pro)), GALT(NM_000155.4):c.584T>C (p.L195P)
ISCN -
DB-ID CCL27_000003 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) 7.0E-5 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2024-08-28 13:16:32 +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.584T>C r.(?) p.(Leu195Pro)
IL11RA NM_001142784.2 +/. - c.-3881T>C r.(?) p.(=)
CCL27 NM_006664.2 +/. - c.*13591A>G r.(=) p.(=)


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