Variant #0000690546 (NC_000009.11:g.36217445C>T, NM_001128227.2:c.2179G>A (GNE))

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.36217445C>T
DNA change (hg38) -
Published as GNE(NM_001128227.2):c.2179G>A (p.V727M), GNE(NM_001128227.3):c.2179G>A (p.V727M), GNE(NM_005476.7):c.2086G>A (p.(Val696Met))
ISCN -
DB-ID GNE_000007 See all 99 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) 0.00173 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GNE NM_001128227.2 +/. - c.2179G>A r.(?) p.(Val727Met)


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