Variant #0000008251 (NC_000001.10:-, LMNA(NM_170707.2):c.178C>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_00009 See all 4 reported entries |
| Frequency |
- |
| Variant remarks |
The findings demonstrate that the exon 1 c.178 C/G, p.Arg 60 Gly LMNA
gene mutation is associated with a novel phenotype featuring cardiac
involvement followed by late lipodystrophy, diabetes, and peripheral axonal
neuropathy. |
| 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
|
|