Variant #0000329383 (NC_000003.11:g.48506237G>A, NM_016381.4:c.-1653G>A (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.48506237G>A
DNA change (hg38) g.48464838G>A
Published as ATRIP(NM_001271022.1):c.1682G>A (p.(Arg561Lys))
ISCN -
DB-ID ATRIP_000006
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2022-11-01 13:01:21 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TREX1 NM_016381.4 ?/. - c.-1653G>A r.(?) p.(=)
SHISA5 NM_016479.3 ?/. - c.*4269C>T r.(=) p.(=)
TREX1 NM_033629.3 ?/. - c.-1498G>A r.(?) p.(=)
ATRIP NM_130384.2 ?/. - c.2063G>A r.(?) p.(Arg688Lys)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.