Variant #0000371899 (NC_000012.11:g.102164851dup, NM_024312.4:c.857dup (GNPTAB))
Chromosome |
12 |
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.102164851dup |
DNA change (hg38) |
g.101771073dup |
Published as |
- |
ISCN |
- |
DB-ID |
GNPTAB_000103 |
Variant remarks |
- |
Reference |
Journal: Tappino 2009 |
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 |
2018-07-09 16:10:32 +02:00 (CEST) |
Date last edited |
2020-07-02 17:53:40 +02:00 (CEST) |

Variant on transcripts
|