Variant #0000008336 (NC_000001.10:-, LMNA(NM_170707.2):c.1868C>G)
| Chromosome |
1 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Type |
Substitution |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
- |
| Reference |
GenBank |
| DB-ID |
LMNA_00204 See all 3 reported entries |
| Frequency |
- |
| Variant remarks |
The LMNA c.1868C>G (p.T623S) mutation either
leads to the substitution of a serine to a threonine or activates a cryptic splice site, producing a protein
product that truncates 35 amino acids |
| 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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