Variant #0000046845 (NC_000014.8:g.89338702A>G, NM_144596.2:c.1253A>G (TTC8))
| Chromosome |
14 |
| Allele |
Both (homozygous) |
| Affects function (as reported) |
Probably affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
likely pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.89338702A>G |
| DNA change (hg38) |
g.88872358A>G |
| Published as |
- |
| ISCN |
- |
| DB-ID |
TTC8_000029 See all 8 reported entries |
| Variant remarks |
- |
| Reference |
Journal: Lim et al. (2014) |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Germline |
| Segregation |
yes |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.00296 View details |
| Owner |
Marianne Vos (LOVD-team) |
| Database submission license |
No license selected |
| Created by |
Marianne Vos (LOVD-team) |
| Date created |
2014-11-13 12:07:54 +01:00 (CET) |
| Date last edited |
2016-03-11 11:30:15 +01:00 (CET) |

Variant on transcripts
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