Variant #0000982192 (NC_000016.9:g.88923593T>G, NM_000512.4:c.-308A>C (GALNS))

Chromosome 16
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.88923593T>G
DNA change (hg38) -
Published as TRAPPC2L(NM_001318525.2):c.33+2T>G
ISCN -
DB-ID GALNS_000081
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GALNS NM_000512.4 +?/. - c.-308A>C r.(?) p.(=)
TRAPPC2L NM_001318525.1 +?/. - c.33+2T>G r.spl? p.?
TRAPPC2L NM_016209.3 +?/. - c.33+2T>G r.spl? p.?


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.