Variant #0000007970 (NC_000001.10:-, LMNA(NM_170707.2):c.148C>A)
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_00013 See all 3 reported entries |
Frequency |
- |
Variant remarks |
The C148A mutation creates an additional AluI restriction endonuclease site within the exon 1 amplimer, allowing the rapid detection of this mutation in his daughter, who presented at age 24 with isolated quadricep weakness, and at age 28 with atrial and ventricular extrasystoles with no AV block. |
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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