Variant #0000570798 (NC_000021.8:g.45750687_45750696dup, NC_000021.8(NM_004928.2):c.642+17_642+26dup (C21orf2))

Chromosome 21
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.45750687_45750696dup
DNA change (hg38) g.44330804_44330813dup
Published as CFAP410(NM_001271441.2):c.656_665dup (p.(Ala223ArgfsTer38)), CFAP410(NM_001271441.2):c.656_665dupTAGGGGCCGC (p.A223Rfs*38)
ISCN -
DB-ID C21orf2_000029 See all 2 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) Retrieve
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PFKL NM_002626.4 +/. - c.*3942_*3951dup r.(=) p.(=)
C21orf2 NM_004928.2 +/. - c.642+17_642+26dup r.(=) p.(=)


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