Variant #0000984012 (NC_000021.8:g.45750612_45750644del, NC_000021.8(NM_004928.2):c.642+95_642+127del (C21orf2))

Chromosome 21
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.45750612_45750644del
DNA change (hg38) -
Published as CFAP410(NM_001271441.2):c.734_766del (p.(Pro245_Gly255del))
ISCN -
DB-ID C21orf2_000096
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 2024-04-19 20:27:30 +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.*3867_*3899del r.(=) p.(=)
C21orf2 NM_004928.2 -?/. - c.642+95_642+127del r.(=) p.(=)


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