Variant #0000570811 (NC_000021.8:g.45759060C>T, NM_004928.2:c.18G>A (C21orf2))

Chromosome 21
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.45759060C>T
DNA change (hg38) g.44339177C>T
Published as C21orf2(NM_001271441.1):c.18G>A (p.K6=), CFAP410(NM_001271441.2):c.18G>A (p.K6=)
ISCN -
DB-ID C21orf2_000016 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) 0.00026 View details
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 2020-07-16 22:42:51 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C21orf2 NM_004928.2 -/. - c.18G>A r.(?) p.(Lys6=)


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