Variant #0001002386 (NC_000016.9:g.49670556G>A, NM_015069.3:c.2507C>T (ZNF423))

Chromosome 16
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.49670556G>A
DNA change (hg38) -
Published as ZNF423(NM_001271620.2):c.2327C>T (p.A776V), ZNF423(NM_001379286.1):c.2531C>T (p.A844V, p.(Ala844Val))
ISCN -
DB-ID ZNF423_000060 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) 0.00035 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 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ZNF423 NM_015069.3 -?/. - c.2507C>T r.(?) p.(Ala836Val)


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