Variant #0000445529 (NC_000011.9:g.47354270_47354294del, NC_000011.9(NM_000256.3):c.3491-41_3491-17del (MYBPC3))
| Chromosome |
11 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
NA |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.47354270_47354294del |
| DNA change (hg38) |
g.47332719_47332743del |
| Published as |
- |
| ISCN |
- |
| DB-ID |
MYBPC3_000297 See all 5 reported entries |
| Variant remarks |
- |
| Reference |
PubMed: Waldmuller 2003 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
In vitro (cloned) |
| 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 |
2013-12-31 16:29:42 +01:00 (CET) |
| Date last edited |
2020-07-14 21:57:48 +02:00 (CEST) |

Variant on transcripts
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