Variant #0000016951 (NC_000002.11:g.179391825G>A, NM_001267550.1:c.107890C>T (TTN))
| Chromosome |
2 |
| Allele |
Parent #1 |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Probably affects function |
| Classification method |
- |
| Clinical classification |
pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.179391825G>A |
| DNA change (hg38) |
g.178527098G>A |
| Published as |
AJ277892.2:g.293379C>T (Q33396X) |
| ISCN |
- |
| DB-ID |
TTN_000043 See all 2 reported entries |
| Variant remarks |
French TMD family (het) |
| Reference |
PubMed: Hackman 2008 |
| ClinVar ID |
- |
| dbSNP ID |
rs281864929 |
| 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 13:34:38 +01:00 (CET) |
| Date last edited |
2017-05-05 19:04:32 +02:00 (CEST) |

Variant on transcripts
|