Variant #0000624082 (NC_000019.9:g.54651931C>T, NM_014516.3:c.943C>T (CNOT3))

Chromosome 19
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.54651931C>T
DNA change (hg38) g.54148196C>T
Published as CNOT3(NM_014516.4):c.943C>T (p.Q315*)
ISCN -
DB-ID CNOT3_000012
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-06 12:43:26 +01:00 (CET)
Date last edited 2020-07-16 13:29:14 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CNOT3 NM_014516.3 +/. - c.943C>T r.(?) p.(Gln315Ter)
LENG1 NM_024316.1 +/. - c.*7528G>A r.(=) p.(=)


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