Variant #0001052108 (NC_000005.9:g.137665336T>G, NM_016605.2:c.-8813T>G (FAM53C))

Chromosome 5
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.137665336T>G
DNA change (hg38) -
Published as CDC25C(NM_001790.5):c.195A>C (p.(Gly65=))
ISCN -
DB-ID CDC25C_000001
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
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     
CDC25C NM_001790.3 -?/. - c.195A>C r.(?) p.(=)
FAM53C NM_016605.2 -?/. - c.-8813T>G r.(?) p.(=)


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