Variant #0000279384 (NC_000005.9:g.126161690C>T, NM_005573.3:c.1502C>T (LMNB1))
| Chromosome |
5 |
| 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.126161690C>T |
| DNA change (hg38) |
g.126825998C>T |
| Published as |
LMNB1(NM_001198557.1):c.872C>T (p.(Ala291Val)), LMNB1(NM_005573.4):c.1502C>T (p.A501V) |
| ISCN |
- |
| DB-ID |
LMNB1_000006 See all 5 reported entries |
| Variant remarks |
VKGL data sharing initiative Nederland |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
CLASSIFICATION record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.01973 View details |
| Owner |
VKGL-NL_AMC |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_AMC |
| Date created |
2018-01-15 20:58:59 +01:00 (CET) |
| Date last edited |
2023-01-11 15:44:22 +01:00 (CET) |

Variant on transcripts
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