Variant #0000342056 (NC_000003.11:g.48508395G>A, NM_016381.4:c.506G>A (TREX1))

Chromosome 3
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.48508395G>A
DNA change (hg38) g.48466996G>A
Published as TREX1(NM_007248.2):c.311G>A (p.(Arg104His)), TREX1(NM_007248.4):c.311G>A (p.R104H), TREX1(NM_007248.5):c.311G>A (p.R104H), TREX1(NM_033629.6):c.341...
ISCN -
DB-ID TREX1_000006 See all 18 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) 0.00019 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2025-02-07 18:57:27 +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.506G>A r.(?) p.(Arg169His)
SHISA5 NM_016479.3 +?/. - c.*2111C>T r.(=) p.(=)
TREX1 NM_033629.3 +?/. - c.341G>A r.(?) p.(Arg114His)
ATRIP NM_130384.2 +?/. - c.*1442G>A r.(=) p.(=)


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