SNP details
SNP: ENSRNOSNP491466
Position: Chromosome 12 at position 27041068
Allele: C to T
Consequence type: INTRONIC
Links: Transcript, Ensembl
Functional effects
SNP that creates new splice site (GeneID score)
| Transcript | Type | Allele1 score | Allele2 score |
| ENSRNOT00000001185 | donor | -1.6 | 0.85 |