Variant #0001031245 (NC_000001.10:g.151262329C>G, NM_020832.1:c.2810C>G (ZNF687))

Chromosome 1
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.151262329C>G
DNA change (hg38) -
Published as ZNF687(NM_020832.3):c.2810C>G (p.(Pro937Arg))
ISCN -
DB-ID ZNF687_000001 See all 21 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) 0.0002 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
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PI4KB NM_002651.2 +?/. - c.*2999G>C r.(=) p.(=)
ZNF687 NM_020832.1 +?/. - c.2810C>G r.(?) p.(Pro937Arg)


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