Variant #0000801153 (NC_000003.11:g.3188202A>G, NM_182916.2:c.697A>G (TRNT1))

Chromosome 3
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.3188202A>G
DNA change (hg38) -
Published as TRNT1(NM_001302946.2):c.697A>G (p.I233V)
ISCN -
DB-ID CRBN_000016
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) 3.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +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.*4347T>C r.(=) p.(=)
TRNT1 NM_182916.2 ?/. - c.697A>G r.(?) p.(Ile233Val)


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