Variant #0000885883 (NC_000003.11:g.48508128C>T, NM_016381.4:c.239C>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.48508128C>T
DNA change (hg38) -
Published as TREX1(NM_033629.6):c.74C>T (p.P25L)
ISCN -
DB-ID ATRIP_000068
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) 1.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2022-11-01 13:01:21 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TREX1 NM_016381.4 ?/. - c.239C>T r.(?) p.(Pro80Leu)
TREX1 NM_033629.3 ?/. - c.74C>T r.(?) p.(Pro25Leu)
ATRIP NM_130384.2 ?/. - c.*1175C>T r.(=) p.(=)


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