Variant #0000892965 (NC_000016.9:g.3707257C>T, NM_016292.2:c.*873G>A (TRAP1))

Chromosome 16
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.3707257C>T
DNA change (hg38) -
Published as DNASE1(NM_005223.3):c.619C>T (p.R207C), DNASE1(NM_005223.4):c.619C>T (p.(Arg207Cys))
ISCN -
DB-ID DNASE1_000022 See all 4 reported entries
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) 0.00122 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-11-01 13:41:49 +01:00 (CET)
Date last edited 2024-04-19 20:27:30 +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.619C>T r.(?) p.(Arg207Cys)
TRAP1 NM_016292.2 ?/. - c.*873G>A r.(=) p.(=)


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