Variant #0000016946 (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) |
Affects function |
| Classification method |
- |
| Clinical classification |
pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.179391925_179391935delinsTTTTTCTTTCA |
| DNA change (hg38) |
g.178527198_178527208delinsTTTTTCTTTCA |
| Published as |
AJ277892: 293268-293280 AAGTAACATGG>TGAAAGAAAAA |
| ISCN |
- |
| DB-ID |
TTN_000004 See all 12 reported entries |
| Variant remarks |
Finnish major/founder TMD mutation, 12 Finnish TMD families; not in 216 controls (Finnish) |
| Reference |
PubMed: Hackman 2002 |
| ClinVar ID |
- |
| dbSNP ID |
rs281864927 |
| Origin |
SUMMARY record |
| Segregation |
yes |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Anne Polvi |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Anne Polvi |
| Date created |
2012-12-17 12:40:55 +01:00 (CET) |
| Date last edited |
2017-05-05 19:04:32 +02:00 (CEST) |

Variant on transcripts
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