| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs346542193 | snp | A/C | | | missense, utr-variant-5-prime | ? | TAIR10 | 3:1918143 | TCATTGAAGTCCACT[A/C]CTTCATTCAAAAGTG | 819807 |
| rs346689088 | snp | G/T | | | synonymous-codon | ? | TAIR10 | 3:1919264 | AGCACCATTTTCACT[G/T]ACGTTAGGCCTCTTA | 819807 |
| rs346725611 | snp | A/G | | | intron-variant | ? | TAIR10 | 3:1919162 | TGATACAAAATATGT[A/G]TTTTGGTTGATACTT | 819807 |
| rs346789417 | snp | C/T | | | missense, utr-variant-5-prime | ? | TAIR10 | 3:1918048 | CTACTGAAGATGTGC[C/T]GAGCTGCTCTCACTT | 819807 |
| rs346813704 | snp | C/G | | | intron-variant | ? | TAIR10 | 3:1917748 | TCCATATGGAATCTG[C/G]ATTTTGATCAAACCT | 819807 |
| rs346875993 | snp | C/T | | | intron-variant, utr-variant-3-prime | ? | TAIR10 | 3:1919379 | CAAAATTTGAAAACG[C/T]TTTTTTGCTATAATC | 819807 |
| rs346979679 | snp | A/T | | | missense | ? | TAIR10 | 3:1919289 | CTCTTAGCATCCATT[A/T]TTGCCATTGTTCTCG | 819807 |
| rs347025706 | snp | A/G | | | intron-variant | ? | TAIR10 | 3:1918659 | GTCTTTCTTATGTTT[A/G]TTGGTTCCTCCATCT | 819807 |
| rs347113209 | snp | C/T | | | intron-variant | ? | TAIR10 | 3:1919205 | CATTGACAAATGTTT[C/T]TTTGGTAGATTCGTG | 819807 |
| rs347117523 | snp | A/C | | | intron-variant | ? | TAIR10 | 3:1917527 | ATCTGAAATCTTTAC[A/C]TCATTAGCATGTGTC | 819807 |
| rs347137266 | snp | C/T | | | intron-variant, utr-variant-5-prime | ? | TAIR10 | 3:1917476 | TTGTCTCCTAATTCG[C/T]TTTTTCCGGGGTTGT | 819807 |
| rs347369668 | snp | C/T | | | intron-variant | ? | TAIR10 | 3:1918660 | TCTTTCTTATGTTTA[C/T]TGGTTCCTCCATCTT | 819807 |
| rs347415766 | snp | A/T | | | intron-variant | ? | TAIR10 | 3:1919528 | GTTTCCTCATTCCAT[A/T]ACTGATAAAGGGAAA | 819807 |
| rs347446349 | snp | A/G | | | intron-variant | ? | TAIR10 | 3:1917675 | AAATTACCTGTGAAA[A/G]TTCTAGGGTTTATAT | 819807 |