Variant #0000951515 (NC_000021.8:g.45750380G>A, NC_000021.8(NM_004928.2):c.643-171C>T (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.45750380G>A
DNA change (hg38) -
Published as C21orf2(NM_001271441.1):c.965C>T (p.(Ala322Val))
ISCN -
DB-ID C21orf2_000092
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) 0.00413 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
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     
PFKL NM_002626.4 -?/. - c.*3635G>A r.(=) p.(=)
C21orf2 NM_004928.2 -?/. - c.643-171C>T r.(=) p.(=)


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