Variant #0000615972 (NC_000016.9:g.3705873_3705928dup, NM_016292.2:c.*2202_*2257dup (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.3705873_3705928dup
DNA change (hg38) g.3655872_3655927dup
Published as -
ISCN -
DB-ID DNASE1_000025
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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-07-09 11:21:58 +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.171_226dup r.(?) p.(Asn76ThrfsTer11)
TRAP1 NM_016292.2 +?/. - c.*2202_*2257dup r.(=) p.(=)


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