Variant #0000000277 (NC_000006.11:g.31828287C>T, NEU1(NM_000434.3):c.727G>A)

Individual ID 00000064
Chromosome 6
Allele Both (homozygous)
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.31828287C>T
Reference -
DB-ID NEU1_000001
Average frequency (gnomAD v.2.1.1) 1.0E-5 View details
Owner Variome.ir
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Variome.ir
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Clinical classification     
NEU1 NM_000434.3 ./. - c.727G>A r.(?) p.(Gly243Arg) pathogenic



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000067 DNA SEQ-NG NEU1 1 Variome.ir