Variant #0000608488 (NC_000003.11:g.3189683_3189690del, NM_182916.2:c.1150_1157del (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.3189683_3189690del
DNA change (hg38) g.3147999_3148006del
Published as TRNT1(NM_182916.3):c.1150_1157delCCTCCATT (p.P384Sfs*6)
ISCN -
DB-ID CRBN_000011
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-04 14:54:23 +01:00 (CET)
Date last edited 2020-06-12 10:59:42 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CRBN NM_016302.3 +/. - c.*2865_*2872del r.(=) p.(=)
TRNT1 NM_182916.2 +/. - c.1150_1157del r.(?) p.(Pro384SerfsTer6)


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