Variant #0000848432 (NC_000001.10:g.193111246_193111247del, NC_000001.10(NM_024529.4):c.729+50_729+51del (CDC73))

Chromosome 1
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.193111246_193111247del
DNA change (hg38) -
Published as CDC73(NM_024529.4):c.729+50_729+51delAG
ISCN -
DB-ID B3GALT2_000004
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_NKI
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_NKI
Date created 2022-05-09 15:40:45 +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     
B3GALT2 NM_003783.3 -/. - c.*38194_*38195del r.(=) p.(=)
CDC73 NM_024529.4 -/. - c.729+50_729+51del r.(=) p.(=)


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