Variant #0000249490 (NC_000001.10:g.193091327dup, NM_024529.4:c.-4dup (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.193091327dup
DNA change (hg38) g.193122197dup
Published as CDC73(NM_024529.5):c.-3delAinsGA
ISCN -
DB-ID CDC73_000006
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
B3GALT2 NM_003783.3 -?/. - c.*58104dup r.(?) p.(=)
CDC73 NM_024529.4 -?/. - c.-4dup r.(?) p.(=)


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