Variant #0000981926 (NC_000016.9:g.49671919A>G, NM_015069.3:c.1144T>C (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.49671919A>G
DNA change (hg38) -
Published as ZNF423(NM_001271620.2):c.964T>C (p.S322P), ZNF423(NM_001379286.1):c.1168T>C (p.(Ser390Pro))
ISCN -
DB-ID ZNF423_000018 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) 0.0008 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 2024-04-19 20:27:30 +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.1144T>C r.(?) p.(Ser382Pro)


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