Variant #0000682198 (NC_000023.10:g.152710750C>T, NM_001711.4:c.-49833C>T (BGN))

Chromosome X
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.152710750C>T
DNA change (hg38) -
Published as TREX2(NM_080701.3):c.139G>A (p.E47K)
ISCN -
DB-ID BGN_000057
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-08-06 14:59:34 +02:00 (CEST)
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     
BGN NM_001711.4 -?/. - c.-49833C>T r.(?) p.(=)
HAUS7 NM_017518.6 -?/. - c.*2586G>A r.(=) p.(=)
TREX2 NM_080701.3 -?/. - c.139G>A r.(?) p.(Glu47Lys)


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