Variant #0000310564 (NC_000002.11:g.179456704C>T, NC_000002.11(NM_001267550.1):c.59926+1G>A (TTN))
| Chromosome |
2 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.179456704C>T |
| DNA change (hg38) |
g.178591977C>T |
| Published as |
TTN(NM_001267550.1):c.59926+1G>A, TTN(NM_001267550.2):c.59926+1G>A, TTN(NM_133432.3):c.33106+1G>A, TTN-AS1(NR_038272.1):n.3364+663C>T |
| ISCN |
- |
| DB-ID |
TTN_000081 See all 6 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 View details |
| Owner |
VKGL-NL_AMC |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_AMC |
| Date created |
2018-01-15 20:58:59 +01:00 (CET) |
| Date last edited |
2024-10-29 20:49:11 +01:00 (CET) |

Variant on transcripts
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