Variant #0000013686 (NC_000011.9:-, SCN4B(NM_174934.3):c.628A>C)
| Chromosome |
11 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Type |
unknown |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
- |
| Reference |
GenBank |
| DB-ID |
SCN4B_00003 |
| Frequency |
- |
| Variant remarks |
Exon |
| 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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