Variant #0000008369 (NC_000001.10:-, LMNA(NM_170707.2):c.73C>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_00101 See all 4 reported entries |
| Frequency |
- |
| Variant remarks |
The mutation R25G in exon 1 of LMNA gene we reported here in a Chinese family had a phenotype of
malignant arrhythmia and mild LGMD, suggesting that patients with familial DCM, conduction system defects and skeletal
muscle dystrophy should be screened by genetic testing for the LMNA gene |
| 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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