Variant #0000975748 (NC_000003.11:g.3188173T>C, NM_182916.2:c.668T>C (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.3188173T>C
DNA change (hg38) -
Published as TRNT1(NM_182916.3):c.668T>C (p.(Ile223Thr))
ISCN -
DB-ID TRNT1_000029 See all 4 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) 4.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +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.*4376A>G r.(=) p.(=)
TRNT1 NM_182916.2 +/. - c.668T>C r.(?) p.(Ile223Thr)


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