Variant #0000016950 (NC_000002.11:g.179391828del, NM_001267550.1:c.107889del (TTN))
| Chromosome |
2 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably affects function |
| Affects function (by curator) |
Probably affects function |
| Classification method |
- |
| Clinical classification |
likely pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.179391828del |
| DNA change (hg38) |
g.178527101del |
| Published as |
AJ277892.2:g.293378delA (K33395NfsX9) |
| ISCN |
- |
| DB-ID |
TTN_000042 See all 13 reported entries |
| Variant remarks |
2 Spanish TMD families (het) |
| Reference |
PubMed: Hackman 2008 |
| ClinVar ID |
- |
| dbSNP ID |
rs281864930 |
| 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 13:32:12 +01:00 (CET) |
| Date last edited |
2020-06-10 09:18:15 +02:00 (CEST) |

Variant on transcripts
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