Variant #0000292311 (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_Rotterdam |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Rotterdam |
Date created |
2018-01-15 20:58:59 +01:00 (CET) |
Date last edited |
2022-05-09 15:24:52 +02:00 (CEST) |

Variant on transcripts
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