Variant #0000246787 (NC_000009.11:g.131285955A>G, NM_001003722.1:c.727A>G (GLE1))

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.131285955A>G
DNA change (hg38) g.128523676A>G
Published as GLE1(NM_001003722.1):c.727A>G (p.I243V), GLE1(NM_001003722.2):c.727A>G (p.I243V)
ISCN -
DB-ID GLE1_000011 See all 3 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) 0.26595 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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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.727A>G r.(?) p.(Ile243Val) -


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