Variant #0000691735 (NC_000014.8:g.92477364A>G, NM_004239.3:c.1280T>C (TRIP11))
| Chromosome |
14 |
| Allele |
Unknown |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
VUS |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.92477364A>G |
| DNA change (hg38) |
- |
| Published as |
TRIP11(NM_001321851.1):c.1277T>C (p.(Leu426Ser)), TRIP11(NM_004239.4):c.1280T>C (p.L427S) |
| ISCN |
- |
| DB-ID |
TRIP11_000023 See all 2 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) |
0.00105 View details |
| Owner |
VKGL-NL_Rotterdam |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Rotterdam |
| Date created |
2020-09-15 15:50:26 +02:00 (CEST) |
| Date last edited |
2023-04-16 21:50:28 +02:00 (CEST) |

Variant on transcripts
|