Variant #0000371894 (NC_000012.11:g.102173930C>T, NM_024312.4:c.771G>A (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.102173930C>T |
| DNA change (hg38) |
g.101780152C>T |
| Published as |
- |
| ISCN |
- |
| DB-ID |
GNPTAB_000098 See all 2 reported entries |
| Variant remarks |
Splicing defect, exon 7 skipped. |
| Reference |
Journal: Steet 2005 |
| 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 15:38:30 +02:00 (CEST) |
| Date last edited |
2019-01-25 14:59:05 +01:00 (CET) |

Variant on transcripts
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