Variant #0000355120 (NC_000001.10:g.201328373G>A, NM_001001430.2:c.832C>T (TNNT2))
| Chromosome |
1 |
| 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.201328373G>A |
| DNA change (hg38) |
g.201359245G>A |
| Published as |
Arg278Cys |
| ISCN |
- |
| DB-ID |
TNNT2_000007 See all 33 reported entries |
| Variant remarks |
expression cloning no Ca2+–sensitizing effect |
| Reference |
{PMID10085122:Yanaga 1999} |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
In vitro (cloned) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.00036 View details |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2011-07-02 22:11:33 +02:00 (CEST) |
| Date last edited |
2020-07-14 21:50:58 +02:00 (CEST) |

Variant on transcripts
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|