Variant #0000923963 (NC_000003.11:g.48508253C>T, NM_016381.4:c.364C>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.48508253C>T
DNA change (hg38) -
Published as TREX1(NM_033629.6):c.199C>T (p.L67F)
ISCN -
DB-ID ATRIP_000072
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-04-16 21:50:28 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TREX1 NM_016381.4 ?/. - c.364C>T r.(?) p.(Leu122Phe)
TREX1 NM_033629.3 ?/. - c.199C>T r.(?) p.(Leu67Phe)
ATRIP NM_130384.2 ?/. - c.*1300C>T r.(=) p.(=)


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