Variant #0000003683 (NC_000023.10:-, EMD(NM_000117.2):c.619delC)
| Chromosome |
X |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Type |
Hydrophobicity plots showed that the mutant emerin lacked a C-terminal hydrophobic domain that is pr |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
- |
| Reference |
GenBank |
| DB-ID |
EMD_00054 |
| Frequency |
- |
| Variant remarks |
deletion of 1 bp (C at nucleotide 672 or 673) |
| 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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