Variant #0000335985 (NC_000023.10:g.152710348G>A, NM_001711.4:c.-50235G>A (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.152710348G>A
DNA change (hg38) g.153444890G>A
Published as TREX2(NM_080701.3):c.541C>T (p.(Arg181Trp))
ISCN -
DB-ID TREX2_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) 0.00057 View details
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)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BGN NM_001711.4 -?/. - c.-50235G>A r.(?) p.(=)
HAUS7 NM_017518.6 -?/. - c.*2988C>T r.(=) p.(=)
TREX2 NM_080701.3 -?/. - c.541C>T r.(?) p.(Arg181Trp)


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