Variant #0001041463 (NC_000016.9:g.88925169G>A, NM_000512.4:c.-1884C>T (GALNS))

Chromosome 16
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.88925169G>A
DNA change (hg38) -
Published as TRAPPC2L(NM_001318525.2):c.176G>A (p.(Gly59Asp))
ISCN -
DB-ID GALNS_000105
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 2025-05-05 21:14:00 +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.-1884C>T r.(?) p.(=)
PABPN1L NM_001080487.2 ?/. - c.*4995C>T r.(=) p.(=)
TRAPPC2L NM_001318525.1 ?/. - c.176G>A r.(?) p.(Gly59Asp)
TRAPPC2L NM_016209.3 ?/. - c.176G>A r.(?) p.(Gly59Asp)


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