Variant #0000519000 (NC_000003.11:g.3189141_3189142insAAACTT, NM_182916.2:c.810_811insAAACTT (TRNT1))

Chromosome 3
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification 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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-08-06 14:59:34 +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.*3408_*3409insAGTTTA r.(=) p.(=)
TRNT1 NM_182916.2 -/. - c.810_811insAAACTT r.(?) p.(Pro270_Ala271insLysLeu)


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