SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs346513269 | snp | A/C | | | intron-variant | ? | TAIR10 | 2:12850994 | TCAATGTTTTTCGAC[A/C]AGCTAAACCAAAGGA | 10723124 |
rs346666331 | snp | A/T | | | synonymous-codon | ? | TAIR10 | 2:12851669 | GCTCTCAACTTTAGG[A/T]CTCCACAACACAGAG | 10723124 |
rs347230437 | snp | G/T | | | missense | ? | TAIR10 | 2:12849857 | CGAAGATCCAACAAT[G/T]GCAGATTCCACGATT | 10723124 |
rs347243604 | snp | C/T | | | missense | ? | TAIR10 | 2:12850347 | TTAAGGAAGCTAGTA[C/T]AAGGCCAATCTCTAG | 10723124 |
rs347283946 | snp | A/G | | | intron-variant | ? | TAIR10 | 2:12850540 | ACATAAGGACAAGCC[A/G]TTACTACCTTCTCAT | 10723124 |
rs347289206 | snp | A/T | | | missense | ? | TAIR10 | 2:12851430 | AGTATCGGAAACTGT[A/T]CATTCCTCATGGAGG | 10723124 |
rs347444443 | snp | A/G | | | intron-variant | ? | TAIR10 | 2:12850570 | TAACTGCTTATTTGT[A/G]AGTAGCTAGATTGTT | 10723124 |
rs347470653 | snp | C/T | | | missense | ? | TAIR10 | 2:12849978 | ATCACCAACGTTCTT[C/T]CTCGTGGCCAGAAGC | 10723124 |