Variant #0000608759 (NC_000003.11:g.48508970G>A, NM_016381.4:c.1081G>A (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.48508970G>A
DNA change (hg38) g.48467571G>A
Published as TREX1(NM_033629.6):c.916G>A (p.G306R)
ISCN -
DB-ID ATRIP_000044
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 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.1081G>A r.(?) p.(Gly361Arg)
SHISA5 NM_016479.3 ?/. - c.*1536C>T r.(=) p.(=)
TREX1 NM_033629.3 ?/. - c.916G>A r.(?) p.(Gly306Arg)
ATRIP NM_130384.2 ?/. - c.*2017G>A r.(=) p.(=)


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