Variant #0000275409 (NC_000016.9:g.3706687C>T, NM_016292.2:c.*1443G>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.3706687C>T |
DNA change (hg38) |
g.3656686C>T |
Published as |
DNASE1(NM_005223.3):c.369C>T (p.C123=) |
ISCN |
- |
DB-ID |
DNASE1_000001 |
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) |
0.00011 View details |
Owner |
VKGL-NL_Rotterdam |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Rotterdam |
Date created |
2018-01-15 20:58:59 +01:00 (CET) |
Date last edited |
2020-07-09 11:22:18 +02:00 (CEST) |

Variant on transcripts
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