Variant #0000947116 (NC_000001.10:g.214813455_214813458del, NM_016343.3:c.1774_1777del (CENPF))

Chromosome 1
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.214813455_214813458del
DNA change (hg38) -
Published as CENPF(NM_016343.4):c.1774_1777delGAGA (p.E592Kfs*7)
ISCN -
DB-ID CENPF_000062
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-11-27 17:35:39 +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     
CENPF NM_016343.3 +/. - c.1774_1777del r.(?) p.(Glu592Lysfs*7)


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