Variant #0001053357 (NC_000009.11:g.131295851C>T, NM_001003722.1:c.1372C>T (GLE1))

Chromosome 9
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.131295851C>T
DNA change (hg38) -
Published as GLE1(NM_001003722.2):c.1372C>T (p.(Gln458*))
ISCN -
DB-ID GLE1_000030
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Function/GVS     
GLE1 NM_001003722.1 +?/. - c.1372C>T r.(?) p.(Gln458*) -


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