Variant #0001050380 (NC_000001.10:g.193150540G>A, NC_000001.10(NM_024529.4):c.973-22385G>A (CDC73))

Chromosome 1
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.193150540G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID B3GALT2_000014
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) 0.00025 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
B3GALT2 NM_003783.3 -?/. - c.153C>T r.(?) p.(Gly51=)
CDC73 NM_024529.4 -?/. - c.973-22385G>A r.(=) p.(=)


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