Variant #0000692068 (NC_000016.9:g.3714412_3714414dup, NM_016292.2:c.1430_1432dup (TRAP1))

Chromosome 16
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.3714412_3714414dup
DNA change (hg38) -
Published as TRAP1(NM_016292.3):c.1430_1432dupCCG (p.S477_G478insA)
ISCN -
DB-ID DNASE1_000040
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 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DNASE1 NM_005223.3 -/. - c.*6458_*6460dup r.(=) p.(=)
TRAP1 NM_016292.2 -/. - c.1430_1432dup r.(?) p.(Ser477_Gly478insAla)


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