Variant #0000855982 (NC_000021.8:g.45751839_45751840del, NM_004928.2:c.433_434del (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.45751839_45751840del
DNA change (hg38) -
Published as CFAP410(NM_001271441.1):c.433_434delCC (p.P145Rfs*24)
ISCN -
DB-ID C21orf2_000086
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:47:41 +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     
PFKL NM_002626.4 +/. - c.*5094_*5095del r.(=) p.(=)
C21orf2 NM_004928.2 +/. - c.433_434del r.(?) p.(Pro145Argfs*24)


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