Variant #0001013902 (NC_000003.11:g.48508793G>C, NM_016381.4:c.904G>C (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.48508793G>C
DNA change (hg38) -
Published as TREX1(NM_007248.4):c.709G>C (p.A237P), TREX1(NM_007248.5):c.709G>C (p.A237P), TREX1(NM_033629.6):c.739G>C (p.(Ala247Pro), p.A247P)
ISCN -
DB-ID TREX1_000056 See all 6 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) 0.00011 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2024-10-29 20:49:11 +01:00 (CET)
Date last edited 2025-11-01 13:22:20 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TREX1 NM_016381.4 ?/. - c.904G>C r.(?) p.(Ala302Pro)
SHISA5 NM_016479.3 ?/. - c.*1713C>G r.(=) p.(=)
TREX1 NM_033629.3 ?/. - c.739G>C r.(?) p.(Ala247Pro)
ATRIP NM_130384.2 ?/. - c.*1840G>C r.(=) p.(=)


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