Variant #0000680728 (NC_000016.9:g.88923239A>C, NM_000512.4:c.47T>G (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.88923239A>C
DNA change (hg38) -
Published as GALNS(NM_000512.4):c.47T>G (p.V16G)
ISCN -
DB-ID GALNS_000051
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2023-11-27 17:27:23 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GALNS NM_000512.4 ?/. - c.47T>G r.(?) p.(Val16Gly)
TRAPPC2L NM_001318525.1 ?/. - c.-320A>C r.(?) p.(=)
TRAPPC2L NM_016209.3 ?/. - c.-320A>C r.(?) p.(=)


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