Variant #0000008380 (NC_000001.10:-, LMNA(NM_170707.2):c.103C>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_00102 See all 3 reported entries |
| Frequency |
- |
| Variant remarks |
The fact that the p.L35P change leads to an
L-CMD phenotype, whereas the p.L35V mutation
leads to an EDMD phenotype, further demonstrates
the challenge in predicting phenotype/
genotype correlations in laminopathies |
| 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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