Variant #0000371892 (NC_000012.11:g.102173950_102173951insT, NM_024312.4:c.750_751insA (GNPTAB))
| Chromosome |
12 |
| Allele |
Maternal (confirmed) |
| 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.102173950_102173951insT |
| DNA change (hg38) |
g.101780172_101780173insT |
| Published as |
- |
| ISCN |
- |
| DB-ID |
GNPTAB_000096 |
| Variant remarks |
- |
| Reference |
Journal: Cathey 2010 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Germline |
| 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 15:33:36 +02:00 (CEST) |
| Date last edited |
2018-07-31 16:16:12 +02:00 (CEST) |

Variant on transcripts
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