Variant #0000847835 (NC_000023.10:g.32662432T>C, NC_000023.10(NM_004006.2):c.1150-2A>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.32662432T>C |
DNA change (hg38) |
g.32644315T>C |
Published as |
- |
ISCN |
- |
DB-ID |
DMD_003919 See all 8 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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