Variant #0000003391 (NC_000018.9:-, DSG2(NM_001943.3):c.1423+1G>T)
| Chromosome |
18 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Type |
Mutation 1423+1G>T affected the splice donor
site of intron 10, which may cause inclusion of
int |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
- |
| Reference |
GenBank |
| DB-ID |
DSG2_00064 |
| Frequency |
- |
| Variant remarks |
- |
| ClassClinical |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Qi Ming |
| Database submission license |
No license selected |
| Created by |
Qi Ming |

Variant on transcripts
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