Variant #0001054930 (NC_000014.8:g.89307769G>A, NM_144596.2:c.490G>A (TTC8))
| 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.89307769G>A |
| DNA change (hg38) |
- |
| Published as |
TTC8(NM_001288781.1):c.460G>A (p.A154T), TTC8(NM_144596.3):c.490G>A (p.A164T), TTC8(NM_144596.4):c.490G>A (p.(Ala164Thr)) |
| ISCN |
- |
| DB-ID |
TTC8_000057 See all 3 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) |
1.0E-5 View details |
| Owner |
VKGL-NL_Leiden |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Leiden |
| Date created |
2025-11-01 13:22:20 +01:00 (CET) |
| Date last edited |
N/A |

Variant on transcripts
|