Variant #0000452201 (NC_000001.10:g.156084714A>G, NM_170707.3:c.5A>G (LMNA))
| Chromosome |
1 |
| Allele |
Unknown |
| Affects function (as reported) |
Does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.156084714A>G |
| DNA change (hg38) |
g.156114923A>G |
| Published as |
- |
| ISCN |
- |
| DB-ID |
LMNA_000136 |
| Variant remarks |
- |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
rs11549669 |
| Origin |
Germline |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2005-02-11 12:15:19 +01:00 (CET) |
| Date last edited |
2019-01-20 16:58:51 +01:00 (CET) |

Variant on transcripts
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