Variant #0001041156 (NC_000016.9:g.49670325G>A, NM_015069.3:c.2738C>T (ZNF423))

Chromosome 16
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.49670325G>A
DNA change (hg38) -
Published as ZNF423(NM_001271620.2):c.2558C>T (p.P853L), ZNF423(NM_001379286.1):c.2762C>T (p.(Pro921Leu))
ISCN -
DB-ID ZNF423_000034 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) 0.00016 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 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ZNF423 NM_015069.3 ?/. - c.2738C>T r.(?) p.(Pro913Leu)


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