Variant #0000656801 (NC_000011.9:g.47359111_47359113del, NM_000256.3:c.2441_2443del (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.47359111_47359113del |
| DNA change (hg38) |
g.47337560_47337562del |
| Published as |
MYBPC3(NM_000256.3):c.2441_2443delAGA (p.K814del) |
| ISCN |
- |
| DB-ID |
MYBPC3_000151 See all 10 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_Utrecht |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Utrecht |
| Date created |
2020-03-23 16:13:27 +01:00 (CET) |
| Date last edited |
2022-05-09 15:24:52 +02:00 (CEST) |

Variant on transcripts
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