SNP details
SNP:
Position: Chromosome 14 at position 1901166
Allele: T to C
Consequence type:
Links: Transcript, Ensembl
Functional effects
SNP in rat gene orthologous of human disease or cancer gene
| Rat gene stable | Human gene stable | Description |
| ENSRNOT00000000077 | ENSG00000133256 | Night_blindness,_congenital_stationary,_type_3,_163500_(3) |
SNP that creates new splice site (GeneID score)
| Transcript | Type | Allele1 score | Allele2 score |
| donor | 0 | 1.61 |