Variant #0000513431 (NC_000002.11:g.179641277T>C, NM_001267550.1:c.5314A>G (TTN))
| Chromosome |
2 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
likely benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.179641277T>C |
| DNA change (hg38) |
g.178776550T>C |
| Published as |
TTN(NM_001267550.1):c.5314A>G (p.S1772G), TTN(NM_001267550.2):c.5314A>G (p.S1772G, p.(Ser1772Gly)), TTN(NM_133432.3):c.5176A>G (p.S1726G) |
| ISCN |
- |
| DB-ID |
TTN_000190 See all 7 reported entries |
| Variant remarks |
VKGL data sharing initiative Nederland |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
CLASSIFICATION record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.00011 View details |
| Owner |
VKGL-NL_Utrecht |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Utrecht |
| Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
| Date last edited |
2025-05-05 21:14:00 +02:00 (CEST) |

Variant on transcripts
|