Variant #0001049311 (NC_000001.10:g.193119670A>G, NC_000001.10(NM_024529.4):c.907+158A>G (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.193119670A>G
DNA change (hg38) -
Published as -
ISCN -
DB-ID CDC73_000015
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs150244719
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2025-10-13 13:36:01 +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.907+158A>G r.(?) p.(?)


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