SNP details
SNP: ENSRNOSNP2834478
Position: Chromosome 12 at position 26867604
Allele: T to C
Consequence type: INTRONIC
Links: Transcript, Ensembl
Functional effects
SNP that creates new splice site (GeneID score)
Transcript | Type | Allele1 score | Allele2 score |
ENSRNOT00000001185 | acceptor | -0.18 | 0.57 |