Variant #0000854674 (NC_000016.9:g.88495912C>T, NM_001367624.2:c.2034C>T (ZNF469))

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.88495912C>T
DNA change (hg38) g.88429504C>T
Published as ZNF469(NM_001367624.1):c.2034C>T (p.A678=)
ISCN -
DB-ID ZNF469_000280
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) 0.00264 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2022-05-09 15:47:41 +02:00 (CEST)
Date last edited 2023-10-19 09:32:57 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ZNF469 NM_001367624.2 -/. - c.2034C>T r.(?) p.(Ala678=)


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