Variant #0000520070 (NC_000003.11:g.48507959C>G, NM_016381.4:c.70C>G (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.48507959C>G
DNA change (hg38) g.48466560C>G
Published as ATRIP(NM_130384.3):c.*1006C>G, TREX1(NM_016381.4):c.70C>G (p.(Pro24Ala))
ISCN -
DB-ID ATRIP_000031 See all 2 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) 0.00015 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TREX1 NM_016381.4 ?/. - c.70C>G r.(?) p.(Pro24Ala)
SHISA5 NM_016479.3 ?/. - c.*2547G>C r.(=) p.(=)
TREX1 NM_033629.3 ?/. - c.-26-70C>G r.(=) p.(=)
ATRIP NM_130384.2 ?/. - c.*1006C>G r.(=) p.(=)


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