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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