SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs346449685 | snp | C/T | | | synonymous-codon | ? | TAIR10 | 2:15749235 | CTTCGTGATCCCAGT[C/T]GAGCTAAGATGCTTA | 818328 |
rs346506066 | snp | A/T | | | missense | ? | TAIR10 | 2:15749105 | CATTAGATGGGTAGC[A/T]CAAAGAAACAATCTT | 818328 |
rs346565605 | snp | A/G | | | intron-variant | ? | TAIR10 | 2:15747054 | CGTCGTCCCTGAACC[A/G]AAGTTCCATATGCTC | 818328 |
rs346611185 | snp | C/G | | | intron-variant | ? | TAIR10 | 2:15746763 | TAGATTCCACATCAT[C/G]CACAGTAATCAAAAT | 818328 |
rs346672260 | snp | A/G | | | intron-variant | ? | TAIR10 | 2:15747720 | TTTGTCTGCAATAAC[A/G]AACCTGCGTTTTCAC | 818328 |
rs346709106 | snp | A/G | | | intron-variant | ? | TAIR10 | 2:15748035 | ATAATTGTCCATAAG[A/G]ACCATAAGTAATACT | 818328 |
rs346753283 | snp | A/G | | | missense | ? | TAIR10 | 2:15747956 | TTCTTATGGCAACCC[A/G]TACCAGATACATGAG | 818328 |
rs347095049 | snp | A/T | | | intron-variant | ? | TAIR10 | 2:15747083 | TCTATGGTTGAGGAA[A/T]CCATTATGGATCTGT | 818328 |
rs347209643 | snp | A/C | | | missense | ? | TAIR10 | 2:15748597 | CCAAGCTCGTAAGCC[A/C]TCCTCATTCAGAGCA | 818328 |
rs347223984 | snp | A/C | | | stop-gained | ? | TAIR10 | 2:15748201 | TAAGGCTCTGACTCT[A/C]ATCAAGACCAGGACC | 818328 |
rs347361513 | snp | C/T | | | missense | ? | TAIR10 | 2:15748200 | GTAAGGCTCTGACTC[C/T]CATCAAGACCAGGAC | 818328 |
rs347409227 | snp | G/T | | | missense | ? | TAIR10 | 2:15745556 | TGGTACTCTCGGCTT[G/T]TGGCCACTATAGGAA | 818328 |
rs347472880 | snp | A/T | | | missense | ? | TAIR10 | 2:15748649 | ACTTCCTCGAGAACA[A/T]CACGAGGAGCAGTCT | 818328 |
rs347477611 | snp | C/T | | | missense | ? | TAIR10 | 2:15748698 | TATAAACCGCCCTTC[C/T]ATTCTCCAAAAATAT | 818328 |