Variant #0000094930 (NC_000002.11:g.179391925_179391935delinsTTTTTCTTTCA, NM_001267550.1:c.107780_107790delinsTGAAAGAAAAA (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.179391925_179391935delinsTTTTTCTTTCA |
| DNA change (hg38) |
g.178527198_178527208delinsTTTTTCTTTCA |
| Published as |
E37V (37EVTW>VKEK) |
| ISCN |
- |
| DB-ID |
TTN_000004 See all 12 reported entries |
| Variant remarks |
expression cloning in E.coli, biophysical in vitro characterization shows severe misfolding and no binding to obscurin Ig1-domain |
| 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 12:00:25 +02:00 (CEST) |
| Date last edited |
2020-07-14 21:50:58 +02:00 (CEST) |

Variant on transcripts
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