Variant #0000394424 (NC_000012.11:g.102179805_102179806ins[U14569.1:g.1_288], NM_024312.4:c.555_556ins[U14569.1:g.1_288] (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.102179805_102179806ins[U14569.1:g.1_288] |
| DNA change (hg38) |
- |
| Published as |
Alu insertion mutation |
| ISCN |
- |
| DB-ID |
GNPTAB_000284 |
| Variant remarks |
- |
| Reference |
Journal: Tappino 2008 |
| 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 |
2018-07-30 15:48:04 +02:00 (CEST) |
| Date last edited |
2024-08-16 12:27:59 +02:00 (CEST) |

Variant on transcripts
|