Variant #0000001917 (NC_000001.10:g.156105059C>T, LMNA(NM_170707.3):c.892C>T)
Individual ID |
00001917 |
Chromosome |
1 |
Allele |
Unknown |
Affects function (as reported) |
Not classified |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.156105059C>T |
Reference |
De Sandre-Giovannoli A1, Chaouch M, Kozlov S, Vallat JM, Tazir M, Kassouri N, Szepetowski P, Hammadouche T, Vandenberghe A, Stewart CL, Grid D, Lévy N.(2002) |
DB-ID |
LMNA_000003 |
Frequency |
- |
Average frequency (gnomAD v.2.1.1) |
3.0E-5 View details |
Owner |
Y Yang |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Y Yang |
Variant on transcripts
Screenings
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