Variant #0000923965 (NC_000003.11:g.48508966G>A, NM_016381.4:c.1077G>A (TREX1))

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.48508966G>A
DNA change (hg38) -
Published as TREX1(NM_007248.2):c.882G>A (p.(Leu294=)), TREX1(NM_007248.4):c.882G>A (p.L294=), TREX1(NM_007248.5):c.882G>A (p.L294=)
ISCN -
DB-ID ATRIP_000025 See all 3 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) 0.00924 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2023-04-16 21:50:28 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TREX1 NM_016381.4 -/. - c.1077G>A r.(?) p.(Leu359=)
SHISA5 NM_016479.3 -/. - c.*1540C>T r.(=) p.(=)
TREX1 NM_033629.3 -/. - c.912G>A r.(?) p.(Leu304=)
ATRIP NM_130384.2 -/. - c.*2013G>A r.(=) p.(=)


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