Variant #0000008277 (NC_000001.10:-, LMNA(NM_170707.2):c.29C>T)
| 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_00113 See all 6 reported entries |
| Frequency |
- |
| Variant remarks |
APS patients have a few overlapping but some distinct clinical features as compared
with HGPS and mandibuloacral dysplasia. The pathogenesis of clinical manifestations in APS pa-
tients seems not to be related to accumulation of mutant farnesylated prelamin A. |
| 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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