Variant #0000272267 (NC_000021.8:g.45753117C>A, NM_004928.2:c.172G>T (C21orf2))

Chromosome 21
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.45753117C>A
DNA change (hg38) g.44333234C>A
Published as C21orf2(NM_001271440.1):c.172G>T (p.(Val58Leu)), C21orf2(NM_001271441.1):c.172G>T (p.V58L)
ISCN -
DB-ID C21orf2_000013 See all 3 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) 0.00803 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2019-12-04 15:24:38 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C21orf2 NM_004928.2 ?/. - c.172G>T r.(?) p.(Val58Leu)


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