Variant #0000000392 (NC_000016.9:g.88898452C>G, NM_000512.4:c.956G>C (GALNS))

Individual ID 00000172
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.88898452C>G
Reference -
DB-ID GALNS_000053 See all 2 reported entries
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Variome.ir
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Variome.ir
Date created 2020-12-26 08:08:21 +00:00 (UTC)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Clinical classification     
GALNS NM_000512.4 ./. - c.956G>C r.(?) p.(Arg319Thr) likely pathogenic



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000176 DNA SEQ-NG GALNS 1 Variome.ir