Variant #0000978418 (NC_000009.11:g.131262512G>A, NM_001003722.1:c.-4573G>A (GLE1))

Chromosome 9
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.131262512G>A
DNA change (hg38) -
Published as ODF2(NM_001351578.2):c.2717G>A (p.(Arg906His))
ISCN -
DB-ID GLE1_000029
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) 0.00596 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +02:00 (CEST)
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.-4573G>A r.(?) p.(=) -
ODF2 NM_001242352.1 -?/. - c.2453G>A r.(?) p.(Arg818His) -


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