Variant #0000800375 (NC_000002.11:g.219505465G>A, NM_001105537.1:c.4516C>T (ZNF142))

Chromosome 2
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.219505465G>A
DNA change (hg38) -
Published as ZNF142(NM_001105537.1):c.4516C>T (p.(Arg1506Trp)), ZNF142(NM_001105537.4):c.4516C>T (p.R1506W)
ISCN -
DB-ID PLCD4_000008 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) 0.00195 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ZNF142 NM_001105537.1 -?/. - c.4516C>T r.(?) p.(Arg1506Trp)
PLCD4 NM_032726.3 -?/. - c.*4165G>A r.(=) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.