Variant #0000544211 (NC_000011.9:g.47359281dup, NM_000256.3:c.2373dup (MYBPC3))
| Chromosome |
11 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.47359281dup |
| DNA change (hg38) |
g.47337730dup |
| Published as |
MYBPC3(NM_000256.3):c.2372delAinsAG (p.W792Vfs*41), MYBPC3(NM_000256.3):c.2373dupG (p.(Trp792Valfs*41)), MYBPC3(NM_000256.3):c.2373dupG (p.W792Vfs*41) |
| ISCN |
- |
| DB-ID |
MYBPC3_000149 See all 23 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) |
Retrieve |
| Owner |
VKGL-NL_Rotterdam |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Rotterdam |
| Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
| Date last edited |
2024-08-28 13:16:32 +02:00 (CEST) |

Variant on transcripts
|