Variant #0000864791 (NC_000016.9:g.3712006G>A, NM_016292.2:c.1922C>T (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.3712006G>A
DNA change (hg38) -
Published as TRAP1(NM_001272049.1):c.1763C>T (p.(Thr588Met)), TRAP1(NM_016292.3):c.1922C>T (p.T641M)
ISCN -
DB-ID DNASE1_000004 See all 2 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) 0.00151 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 2022-05-09 16:01:56 +02:00 (CEST)
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.*4052G>A r.(=) p.(=)
TRAP1 NM_016292.2 -/. - c.1922C>T r.(?) p.(Thr641Met)


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