Variant #0000801264 (NC_000003.11:g.48506317C>T, NM_016381.4:c.-1573C>T (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.48506317C>T
DNA change (hg38) -
Published as ATRIP(NM_130384.3):c.2143C>T (p.R715W)
ISCN -
DB-ID ATRIP_000054
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) 2.0E-5 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 2021-09-17 14:40:49 +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.-1573C>T r.(?) p.(=)
SHISA5 NM_016479.3 ?/. - c.*4189G>A r.(=) p.(=)
TREX1 NM_033629.3 ?/. - c.-1418C>T r.(?) p.(=)
ATRIP NM_130384.2 ?/. - c.2143C>T r.(?) p.(Arg715Trp)


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