Variant #0000982193 (NC_000016.9:g.88925164C>T, NM_000512.4:c.-1879G>A (GALNS))

Chromosome 16
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.88925164C>T
DNA change (hg38) -
Published as TRAPPC2L(NM_001318526.2):c.53C>T (p.(Thr18Ile))
ISCN -
DB-ID GALNS_000082
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) 7.0E-5 View details
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
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GALNS NM_000512.4 -?/. - c.-1879G>A r.(?) p.(=)
PABPN1L NM_001080487.2 -?/. - c.*5000G>A r.(=) p.(=)
TRAPPC2L NM_001318525.1 -?/. - c.171C>T r.(?) p.(=)
TRAPPC2L NM_016209.3 -?/. - c.171C>T r.(?) p.(=)


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