Variant #0000246202 (NC_000003.11:g.48508968A>G, NM_016381.4:c.1079A>G (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.48508968A>G
DNA change (hg38) g.48467569A>G
Published as TREX1(NM_007248.5):c.884A>G (p.Y295C)
ISCN -
DB-ID TREX1_000012 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) 0.00012 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2018-01-15 20:58:59 +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.1079A>G r.(?) p.(Tyr360Cys)
SHISA5 NM_016479.3 ?/. - c.*1538T>C r.(=) p.(=)
TREX1 NM_033629.3 ?/. - c.914A>G r.(?) p.(Tyr305Cys)
ATRIP NM_130384.2 ?/. - c.*2015A>G r.(=) p.(=)


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