Variant #0000008133 (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 |
These patients extend the spectrum of abnormal
phenotypes caused by LMNA mutations, which may
complicate the clinical diagnosis of some patients with
laminopathies, but suggest that LMNA is a good
candidate for evaluation in patients with other atypical
progeria phenotypes |
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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