Variant #0001026707 (NC_000016.9:g.3716055dup, NM_016292.2:c.1300dup (TRAP1))

Chromosome 16
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.3716055dup
DNA change (hg38) -
Published as TRAP1(NM_016292.3):c.1300dupG (p.A434Gfs*2)
ISCN -
DB-ID DNASE1_000090
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2025-02-07 18:57:27 +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     
DNASE1 NM_005223.3 +?/. - c.*8101dup r.(?) p.(=)
TRAP1 NM_016292.2 +?/. - c.1300dup r.(?) p.(Ala434Glyfs*2)


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