Variant #0000847834 (NC_000023.10:g.32662433G>C, NC_000023.10(NM_004006.2):c.1150-3C>G (DMD))
| Chromosome |
X |
| 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.32662433G>C |
| DNA change (hg38) |
g.32644316G>C |
| Published as |
- |
| ISCN |
- |
| DB-ID |
DMD_003206 See all 3 reported entries |
| Variant remarks |
expression in 293T cells in vitro mini-gene splicing assay |
| Reference |
PubMed: Zhang 2022 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
In vitro (cloned) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2022-05-06 09:13:56 +02:00 (CEST) |
| Date last edited |
N/A |

Variant on transcripts
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