Variant #0000520069 (NC_000003.11:g.48507934G>T, NM_016381.4:c.45G>T (TREX1))

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.48507934G>T
DNA change (hg38) g.48466535G>T
Published as ATRIP(NM_130384.3):c.*981G>T
ISCN -
DB-ID ATRIP_000030
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) 0.00044 View details
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 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.45G>T r.(?) p.(Arg15Ser)
SHISA5 NM_016479.3 -?/. - c.*2572C>A r.(=) p.(=)
TREX1 NM_033629.3 -?/. - c.-26-95G>T r.(=) p.(=)
ATRIP NM_130384.2 -?/. - c.*981G>T r.(=) p.(=)


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