SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs346425017 | snp | G/T | | | missense | ? | TAIR10 | 1:3963653 | TTCTTGGAGCTCTTC[G/T]TGGTAAAGACTAAAG | 837718 |
rs346460674 | snp | A/G | | | intron-variant | ? | TAIR10 | 1:3964448 | GCCAAATTTAAATCC[A/G]AATAACAACAACACA | 837718 |
rs346623787 | snp | A/G | | | intron-variant | ? | TAIR10 | 1:3964424 | TTGTTCCTCAACAAT[A/G]TGTATTTTGCCAAAT | 837718 |
rs346628382 | snp | C/T | | | intron-variant | ? | TAIR10 | 1:3965351 | AACCAAACCAAACCA[C/T]ATAAATTTGATAACC | 837718 |
rs346684110 | snp | A/G | | | intron-variant | ? | TAIR10 | 1:3964241 | GGACTTGTAGCCCCT[A/G]AACTGTGGTTAATAG | 837718 |
rs346709024 | snp | A/G | | | synonymous-codon | ? | TAIR10 | 1:3965082 | GTGCACGTCATGTTG[A/G]TCTTCCATTGCAGCT | 837718 |
rs346871946 | snp | C/T | | | missense | ? | TAIR10 | 1:3965108 | CAGCTAATAGATGTT[C/T]TGGACTTGAGAGCGG | 837718 |
rs346896918 | snp | C/G | | | missense | ? | TAIR10 | 1:3966041 | ACAAGCTAGATTGAC[C/G]ACAAAAGCCAGCTAT | 837718 |
rs347217775 | snp | A/G | | | intron-variant | ? | TAIR10 | 1:3964301 | GATTAATTATTCATG[A/G]GTGACGAGTACTTTG | 837718 |
rs347440119 | snp | C/T | | | synonymous-codon | ? | TAIR10 | 1:3965022 | AGAAGGCGTTGAAAA[C/T]GATGGACGTGAACTT | 837718 |
rs347450469 | snp | A/G | | | intron-variant | ? | TAIR10 | 1:3965532 | TTAAAATAAATTTGA[A/G]TAATGTCCAAGAATG | 837718 |
rs347454021 | snp | G/T | | | missense | ? | TAIR10 | 1:3965875 | CGCAAACCCTGCTCT[G/T]TTCCGACTTTTCTTG | 837718 |