Variant #0000445524 (NC_000011.9:g.47354175C>T, NM_000256.3:c.3569G>A (MYBPC3))
| Chromosome |
11 |
| Allele |
Unknown |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
VUS |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.47354175C>T |
| DNA change (hg38) |
g.47332624C>T |
| Published as |
- |
| ISCN |
- |
| DB-ID |
MYBPC3_000409 See all 4 reported entries |
| Variant remarks |
- |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
rs117354682 |
| Origin |
Germline |
| Segregation |
- |
| Frequency |
T=0.003/1 |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
4.0E-5 View details |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2011-11-01 13:37:12 +01:00 (CET) |
| Date last edited |
2019-01-06 17:31:14 +01:00 (CET) |

Variant on transcripts
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