Variant #0001047185 (NC_000001.10:g.193117124A>T, NC_000001.10(NM_024529.4):c.828+29A>T (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.193117124A>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID CDC73_000009
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs138541554
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.01465 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2025-08-06 16:07:01 +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     
CDC73 NM_024529.4 -/. - c.828+29A>T r.(?) p.(?)


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