Variant #0000355100 (NC_000019.9:g.55663260C>T, NM_000363.4:c.575G>A (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.55663260C>T |
DNA change (hg38) |
g.55151892C>T |
Published as |
- |
ISCN |
- |
DB-ID |
TNNI3_000024 See all 4 reported entries |
Variant remarks |
- |
Reference |
{PMID15961398:Gomes 2005} |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
In vitro (cloned) |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Johan den Dunnen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Johan den Dunnen |
Date created |
2011-08-02 10:19:14 +02:00 (CEST) |
Date last edited |
2020-07-16 13:56:46 +02:00 (CEST) |

Variant on transcripts
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