Variant #0000000258 (NC_000016.9:g.88898474T>C, NM_000512.4:c.934A>G (GALNS))

Individual ID 00000047
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.88898474T>C
Reference -
DB-ID GALNS_000017
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 2020-12-20 01:02:09 +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.934A>G r.(?) p.(Thr312Ala) likely pathogenic



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000050 DNA SEQ-NG GALNS 1 Variome.ir