Variant #0001051189 (NC_000003.11:g.3189785dup, NM_182916.2:c.1252dup (TRNT1))

Chromosome 3
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.3189785dup
DNA change (hg38) -
Published as TRNT1(NM_001367321.1):c.1252dupA (p.S418Kfs*9), TRNT1(NM_182916.3):c.1252dup (p.(Ser418Lysfs*9))
ISCN -
DB-ID CRBN_000015 See all 6 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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CRBN NM_016302.3 +/. - c.*2770dup r.(?) p.(=)
TRNT1 NM_182916.2 +/. - c.1252dup r.(?) p.(Ser418Lysfs*9)


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