Variant #0000487433 (NC_000017.10:g.78078931G>T, NM_000152.3:c.546G>T (GAA))
| Chromosome |
17 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
NA |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.78078931G>T |
| DNA change (hg38) |
g.80105132G>T |
| Published as |
- |
| ISCN |
- |
| DB-ID |
GAA_000466 See all 8 reported entries |
| Variant remarks |
functional analysis using expression cloning in minigene splicing assay; complete skipping of exon 2 |
| Reference |
Dardis 2019, submitted |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
In vitro (cloned) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Andrea Elena Dardis |
| Database submission license |
No license selected |
| Created by |
Andrea Elena Dardis |
| Date created |
2019-06-14 14:34:52 +02:00 (CEST) |
| Date last edited |
2019-07-08 15:36:28 +02:00 (CEST) |

Variant on transcripts
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