Variant #0000369825 (NC_000016.9:g.1412294dup, NM_032520.4:c.499dup (GNPTG))
Chromosome |
16 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Affects function |
Classification method |
- |
Clinical classification |
pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.1412294dup |
DNA change (hg38) |
g.1362293dup |
Published as |
- |
ISCN |
- |
DB-ID |
GNPTG_000026 See all 5 reported entries |
Variant remarks |
- |
Reference |
Journal: Raas-Rothschild 2000 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
Germline/De novo (untested) |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Renata Voltolini Velho |
Database submission license |
No license selected |
Created by |
Renata Voltolini Velho |
Date created |
2018-06-26 16:24:15 +02:00 (CEST) |
Date last edited |
N/A |

Variant on transcripts
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