Variant #0000314911 (NC_000014.8:g.89310195G>A, NC_000014.8(NM_144596.2):c.624+1G>A (TTC8))
| Chromosome |
14 |
| 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.89310195G>A |
| DNA change (hg38) |
g.88843851G>A |
| Published as |
TTC8(NM_001288781.1):c.594+1G>A, TTC8(NM_144596.3):c.624+1G>A |
| ISCN |
- |
| DB-ID |
TTC8_000034 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) |
Retrieve |
| Owner |
VKGL-NL_Utrecht |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Utrecht |
| Date created |
2018-01-15 20:58:59 +01:00 (CET) |
| Date last edited |
2020-07-05 16:30:04 +02:00 (CEST) |

Variant on transcripts
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