Variant #0000511566 (NC_000002.11:g.179449579C>T, NM_001267550.1:c.64789G>A (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.179449579C>T |
| DNA change (hg38) |
g.178584852C>T |
| Published as |
TTN(NM_001256850.1):c.59866G>A (p.(Val19956Met)), TTN(NM_001267550.1):c.64789G>A (p.V21597M), TTN(NM_001267550.2):c.64789G>A (p.V21597M) |
| ISCN |
- |
| DB-ID |
TTN_000251 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) |
0.0037 View details |
| Owner |
VKGL-NL_Leiden |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Leiden |
| Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
| Date last edited |
2023-01-11 15:44:22 +01:00 (CET) |

Variant on transcripts
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