SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs193923314 | snp | C/G | | | intron-variant, splice-acceptor-variant | BOP1 | TAIR10 | 3:21148551 | GGAAAGAAAGTTGCA[C/G]TACGTGCAATGCAAG | 824880 |
rs193927485 | snp | C/T | | | intron-variant | BOP1 | TAIR10 | 3:21148489 | AGAAAATAACAACTC[C/T]TATCTATATATCCAC | 824880 |
rs193927767 | snp | A/G | | | intron-variant | BOP1 | TAIR10 | 3:21148884 | GACAATTCTCA[A/G] | 824880 |
rs346423873 | snp | C/T | | | synonymous-codon | BOP1 | TAIR10 | 3:21147972 | CCGTTGCATCCTCGC[C/T]GCTCGTAGCCTCTTC | 824880 |
rs346549010 | snp | C/T | | | synonymous-codon | BOP1 | TAIR10 | 3:21148269 | TTTAGCCGCCGCTCG[C/T]TACTTTGGCGTCGAG | 824880 |
rs346583084 | snp | G/T | | | synonymous-codon | BOP1 | TAIR10 | 3:21149580 | CGCTCTTCACATTGC[G/T]GCTGAAATGGTGTCT | 824880 |
rs346711802 | snp | A/G | | | synonymous-codon | BOP1 | TAIR10 | 3:21147873 | ACTCAAATCTATGTC[A/G]TTGGATTACCTAAAC | 824880 |
rs346960119 | snp | A/G | | | intron-variant | BOP1 | TAIR10 | 3:21149032 | GGAAGTGGTGGATAT[A/G]TAGTGTCTCTAACTT | 824880 |
rs346999487 | snp | A/G | | | synonymous-codon | BOP1 | TAIR10 | 3:21148140 | TCTACTTCAATTCTT[A/G]TACAGTGGTCAAGTC | 824880 |
rs347043566 | snp | C/T | | | synonymous-codon | BOP1 | TAIR10 | 3:21148209 | TGGAGATAGAGGATG[C/T]TGGCACACGCATTGC | 824880 |
rs347224168 | snp | C/G | | | intron-variant | BOP1 | TAIR10 | 3:21149090 | TGTGTTTTTTTCCCT[C/G]ACAGAAACATTTGAC | 824880 |
rs347313785 | snp | A/T | | | synonymous-codon | BOP1 | TAIR10 | 3:21149637 | CCACCACGCCGACCC[A/T]AACGTCCAGACAGTG | 824880 |
rs347388944 | snp | C/T | | | utr-variant-5-prime | BOP1 | TAIR10 | 3:21147834 | AATCAACAAAGGAGC[C/T]ATGAGCAATACTTTC | 824880 |
rs347427959 | snp | A/G | | | intron-variant | BOP1 | TAIR10 | 3:21148958 | ATATAATAATCTCTT[A/G]AACCATAGTCGCGTG | 824880 |
rs347464247 | snp | G/T | | | missense | BOP1 | TAIR10 | 3:21149263 | CTCCCAATCGAACTT[G/T]TAGCCAAGATTGAGG | 824880 |