Variant #0001003367 (NC_000017.10:g.47247031C>T, NM_153446.2:c.1642C>T (B4GALNT2))

Chromosome 17
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.47247031C>T
DNA change (hg38) -
Published as B4GALNT2(NM_001159387.1):c.1462C>T (p.(Arg488Trp))
ISCN -
DB-ID B4GALNT2_000005
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) 0.00028 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 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
B4GALNT2 NM_153446.2 ?/. - c.1642C>T r.(?) p.(Arg548Trp)


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