Variant #0000559744 (NC_000016.9:g.88923592G>A, NM_000512.4:c.-307C>T (GALNS))

Chromosome 16
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.88923592G>A
DNA change (hg38) g.88857184G>A
Published as TRAPPC2L(NM_016209.5):c.33+1G>A
ISCN -
DB-ID GALNS_000036
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-11-27 17:27:23 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GALNS NM_000512.4 +/. - c.-307C>T r.(?) p.(=)
TRAPPC2L NM_001318525.1 +/. - c.33+1G>A r.spl? p.?
TRAPPC2L NM_016209.3 +/. - c.33+1G>A r.spl? p.?


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