Variant #0000355099 (NC_000019.9:g.55665463G>A, NM_000363.4:c.484C>T (TNNI3))
| Chromosome |
19 |
| Allele |
Unknown |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
NA |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.55665463G>A |
| DNA change (hg38) |
g.55154095G>A |
| Published as |
- |
| ISCN |
- |
| DB-ID |
TNNI3_000013 See all 9 reported entries |
| Variant remarks |
- |
| Reference |
{PMID10806205:Elliott 2000} |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
In vitro (cloned) |
| Segregation |
- |
| Frequency |
- |
| 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 |
2011-08-01 11:40:36 +02:00 (CEST) |
| Date last edited |
2020-07-16 13:59:33 +02:00 (CEST) |

Variant on transcripts
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