Variant #0001031648 (NC_000001.10:g.214819839G>A, NM_016343.3:c.6926G>A (CENPF))

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.214819839G>A
DNA change (hg38) -
Published as CENPF(NM_016343.3):c.6926G>A (p.R2309H), CENPF(NM_016343.4):c.6926G>A (p.R2309H)
ISCN -
DB-ID CENPF_000006 See all 3 reported entries
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) 0.00088 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2025-05-05 21:14:00 +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     
CENPF NM_016343.3 -?/. - c.6926G>A r.(?) p.(Arg2309His)


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