Variant #0000654873 (NC_000003.11:g.3189141_3189142insAAACTT, NM_182916.2:c.810_811insAAACTT (TRNT1))

Chromosome 3
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.3189141_3189142insAAACTT
DNA change (hg38) g.3147457_3147458insAAACTT
Published as TRNT1(NM_182916.3):c.810_811insAAACTT (p.P270_A271insKL)
ISCN -
DB-ID TRNT1_000011 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) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2020-03-23 16:13:27 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CRBN NM_016302.3 -?/. - c.*3408_*3409insAGTTTA r.(=) p.(=)
TRNT1 NM_182916.2 -?/. - c.810_811insAAACTT r.(?) p.(Pro270_Ala271insLysLeu)


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