Variant #0000008124 (NC_000001.10:-, LMNA(NM_170707.2):c.98A>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_00109 See all 2 reported entries |
Frequency |
- |
Variant remarks |
To our knowledge, this is the first LMNA mutation to bernfound in an autosomal dominant form of CMT2, andrnimplies that LMNA is responsible for both autosomalrndominant and recessive forms of axonal Charcot-rnMarie-Tooth disease. |
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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