Variant #0000094929 (NC_000002.11:g.179391878T>G, NM_001267550.1:c.107837A>C (TTN))
| Chromosome |
2 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
NA |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.179391878T>G |
| DNA change (hg38) |
g.178527151T>G |
| Published as |
H56P (H66P) |
| ISCN |
- |
| DB-ID |
TTN_000567 See all 4 reported entries |
| Variant remarks |
expression cloning in E.coli, biophysical in vitro characterization shows normal folding room T but unfolding at 37oC rendering it binding incompetent |
| Reference |
PubMed: Rudloff 2015, Journal: Rudloff 2015 |
| 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 |
2016-04-19 10:57:28 +02:00 (CEST) |
| Date last edited |
2020-07-14 21:50:58 +02:00 (CEST) |

Variant on transcripts
|