Variant #0000000294 (NC_000016.9:g.88907476C>T, GALNS(NM_000512.4):c.346G>A)

Individual ID 00000080
Chromosome 16
Allele Both (homozygous)
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.88907476C>T
Reference -
DB-ID GALNS_000026 See all 3 reported entries
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     
GALNS NM_000512.4 ./. - c.346G>A r.(?) p.(Gly116Ser) pathogenic
GALNS XM_005256302.1 ./. - c.364G>A r.(?) p.(Gly122Ser) pathogenic



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000083 DNA SEQ GALNS 1 Variome.ir