Variant #0000075165 (NC_000016.9:g.4385061T>C, NM_032575.2:c.523T>C (GLIS2))

Chromosome 16
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.4385061T>C
DNA change (hg38) g.4335060T>C
Published as -
ISCN -
DB-ID GLIS2_000002 See all 2 reported entries
Variant remarks characterization of GLIS2 c.523T>C (p.C175R) by Halbritter shows C175R interferes with GLIS2 nuclear localization
Reference -
ClinVar ID -
dbSNP ID rs587777353
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Gerd Walz
Database submission license No license selected
Created by Gerd Walz
Date created 2015-07-21 19:38:43 +02:00 (CEST)
Date last edited 2019-12-04 12:41:11 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GLIS2 NM_032575.2 +?/. 4 c.523T>C r.(spl?) p.(Cys175Arg)



Screenings

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