Variant #0000264570 (NC_000002.11:g.182423344G>A, NM_001030311.2:c.847C>T (CERKL))

Chromosome 2
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.182423344G>A
DNA change (hg38) g.181558617G>A
Published as CERKL(NM_001030311.2):c.847C>T (p.R283*), CERKL(NM_001030311.3):c.847C>T (p.R283*)
ISCN -
DB-ID CERKL_000003 See all 120 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) 0.00035 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-11-27 17:27:23 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ITGA4 NM_000885.4 +/. - c.*23090G>A r.(=) p.(=)
CERKL NM_001030311.2 +/. - c.847C>T r.(?) p.(Arg283Ter)
CERKL NM_201548.4 +/. - c.769C>T r.(?) p.(Arg257Ter)


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