Variant #0000000221 (NC_000016.9:g.88908305C>T, GALNS(NM_000512.4):c.319G>A)

Individual ID 00000015
Chromosome 16
Allele Both (homozygous)
Affects function (as reported) Not classified
Affects function (by curator) Affects function
DNA change (genomic) (Relative to hg19 / GRCh37) g.88908305C>T
Reference -
DB-ID GALNS_000003 See all 4 reported entries
Average frequency (gnomAD v.2.1.1) 2.0E-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.319G>A r.(?) p.(Ala107Thr) pathogenic
GALNS XM_005256301.1 ./+ - c.319G>A r.(?) p.(Ala107Thr) pathogenic
GALNS XM_005256302.1 ./+ - c.337G>A r.(?) p.(Ala113Thr) pathogenic
GALNS XM_005256303.1 ./+ - c.-237G>A r.(=) p.(=) pathogenic



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000017 DNA SEQ-NG GALNS 1 Variome.ir