Variant #0000000269 (NC_000016.9:g.88902169G>T, GALNS(NM_000512.4):c.722C>A)

Individual ID 00000057
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.88902169G>T
Reference -
DB-ID GALNS_000020
Average frequency (gnomAD v.2.1.1) Variant not found in online data sets
Owner Variome.ir
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Variome.ir
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Clinical classification     
GALNS NM_000512.4 ./. - c.722C>A r.(?) p.(Ala241Asp) likely pathogenic
GALNS XM_005256302.1 ./. - c.740C>A r.(?) p.(Ala247Asp) likely pathogenic
GALNS XM_005256303.1 ./. - c.167C>A r.(?) p.(Ala56Asp) likely pathogenic



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000060 DNA SEQ-NG GALNS, HOGA1 2 Variome.ir