Variant #0000311457 (NC_000016.9:g.49672775G>A, NM_015069.3:c.288C>T (ZNF423))

Chromosome 16
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.49672775G>A
DNA change (hg38) g.49638864G>A
Published as ZNF423(NM_001271620.2):c.108C>T (p.D36=), ZNF423(NM_015069.4):c.288C>T (p.D96=)
ISCN -
DB-ID ZNF423_000023 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) 0.00386 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-02-08 18:36:18 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ZNF423 NM_015069.3 -/. - c.288C>T r.(?) p.(Asp96=)


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