Variant #0000677021 (NC_000003.11:g.48508097_48508099dup, NM_016381.4:c.208_210dup (TREX1))

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.48508097_48508099dup
DNA change (hg38) -
Published as TREX1(NM_007248.4):c.13_15dupATC (p.I5dup)
ISCN -
DB-ID ATRIP_000049
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 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TREX1 NM_016381.4 ?/. - c.208_210dup r.(?) p.(Ile70dup)
SHISA5 NM_016479.3 ?/. - c.*2409_*2411dup r.(=) p.(=)
TREX1 NM_033629.3 ?/. - c.43_45dup r.(?) p.(Ile15dup)
ATRIP NM_130384.2 ?/. - c.*1144_*1146dup r.(=) p.(=)


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