Variant #0000850232 (NC_000003.11:g.3186395G>T, NC_000003.11(NM_182916.2):c.608+1G>T (TRNT1))

Chromosome 3
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.3186395G>T
DNA change (hg38) -
Published as TRNT1(NM_001367321.1):c.608+1G>T
ISCN -
DB-ID CRBN_000018 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) 9.0E-5 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 2022-05-09 15:40:45 +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     
CRBN NM_016302.3 +?/. - c.*6154C>A r.(=) p.(=)
TRNT1 NM_182916.2 +?/. - c.608+1G>T r.spl? p.?


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