Variant #0000008272 (NC_000001.10:-, LMNA(NM_170707.2):c.406G>C)
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_00185 See all 2 reported entries |
Frequency |
- |
Variant remarks |
APS patients have a few overlapping but some distinct clinical features as comparedrnwith HGPS and mandibuloacral dysplasia. The pathogenesis of clinical manifestations in APS pa-rntients 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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