Variant #0000930601 (NC_000016.9:g.3708137C>T, NM_016292.2:c.2108G>A (TRAP1))

Chromosome 16
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.3708137C>T
DNA change (hg38) -
Published as DNASE1(NM_001387140.1):c.*21+269C>T, TRAP1(NM_016292.3):c.2108G>A (p.R703Q)
ISCN -
DB-ID DNASE1_000058 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) 0.00028 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-07-07 10:10:56 +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.*183C>T r.(=) p.(=)
TRAP1 NM_016292.2 -?/. - c.2108G>A r.(?) p.(Arg703Gln)


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