| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs346479723 | snp | C/G | | | intron-variant | ? | TAIR10 | 3:2777013 | CAAGATTTCTATTGG[C/G]AACCTAAAACATGTC | 820061 |
| rs346512001 | snp | C/T | | | missense | ? | TAIR10 | 3:2780314 | TTGAACCTGACATTT[C/T]ATTGCAAGCCATTCG | 820061 |
| rs346512335 | snp | C/T | | | missense | ? | TAIR10 | 3:2780788 | TCAATTTGTTCGTCA[C/T]TTCCACTAGAGTTCA | 820061 |
| rs346624286 | snp | C/G | | | missense | ? | TAIR10 | 3:2777438 | CGGTTCTTGAACCTT[C/G]CTTGGGAGTTTGGTA | 820061 |
| rs346652922 | snp | A/C | | | intron-variant | ? | TAIR10 | 3:2781717 | TTTGGTGAGCAAGTG[A/C]ATTGATATAATGATA | 820061 |
| rs346658038 | snp | C/T | | | intron-variant | ? | TAIR10 | 3:2781001 | GTCACAGAAGTTATC[C/T]CAGAGCAATTAGAAC | 820061 |
| rs346672281 | snp | C/G/T | | | intron-variant | ? | TAIR10 | 3:2776659 | GAGATTTTATGCATC[C/G/T]ATGAGTGATTTTAAG | 820061 |
| rs346733319 | snp | C/T | | | missense | ? | TAIR10 | 3:2780412 | TAACATGAAAAATTA[C/T]TGATGTCTGTGGACC | 820061 |
| rs346772297 | snp | G/T | | | intron-variant | ? | TAIR10 | 3:2779481 | TTAAAATATTGAGTG[G/T]ACGAGTTGAAAACAA | 820061 |
| rs346926500 | snp | C/G | | | intron-variant | ? | TAIR10 | 3:2780937 | AACAGTCCAGAACTT[C/G]AAGTGCTTATTCCCG | 820061 |
| rs346933435 | snp | C/T | | | intron-variant | ? | TAIR10 | 3:2778401 | AGATCATATTGTCAG[C/T]ACTAGAACATCAAAC | 820061 |
| rs346935526 | snp | G/T | | | intron-variant | ? | TAIR10 | 3:2777046 | AGCAAATAGGGAAGA[G/T]AGATCTTACATTGTC | 820061 |
| rs346949111 | snp | C/G | | | intron-variant | ? | TAIR10 | 3:2780949 | CTTCAAGTGCTTATT[C/G]CCGGAAGTAACAATG | 820061 |
| rs347010057 | snp | A/G | | | intron-variant | ? | TAIR10 | 3:2780922 | CCTCTGAAAAGAACC[A/G]ACAGTCCAGAACTTC | 820061 |
| rs347025508 | snp | G/T | | | missense | ? | TAIR10 | 3:2777222 | ATAGTGTTCCAACGG[G/T]TTTTTTCTTTCCTAT | 820061 |
| rs347028324 | snp | A/C | | | missense | ? | TAIR10 | 3:2780391 | GTATCTGAATGTTCC[A/C]CAAGCTAACATGAAA | 820061 |
| rs347064688 | snp | A/G | | | intron-variant | ? | TAIR10 | 3:2780430 | ATGTCTGTGGACCTA[A/G]AGTCAACGCATACAA | 820061 |
| rs347095514 | snp | A/C | | | missense | ? | TAIR10 | 3:2778701 | CCTGATGTTGGATCT[A/C]CAGCCACATCATAGA | 820061 |
| rs347170162 | snp | C/T | | | synonymous-codon | ? | TAIR10 | 3:2778718 | AGCCACATCATAGAT[C/T]GTTCCATGAGAGAGA | 820061 |
| rs347172731 | snp | A/G | | | missense | ? | TAIR10 | 3:2780279 | ATCAATCGACTGGAT[A/G]CAGATAGAGCAAAAC | 820061 |
| rs347228814 | snp | C/G | | | missense | ? | TAIR10 | 3:2779423 | TTTGCTACCACATGT[C/G]TCAACGAGATCACGT | 820061 |
| rs347273219 | snp | A/C | | | intron-variant | ? | TAIR10 | 3:2777323 | AATTGCAGTAATGAC[A/C]AGAAACAAGCTAGAG | 820061 |
| rs347330254 | snp | A/G | | | synonymous-codon | ? | TAIR10 | 3:2780901 | TCCTACTTTACTTGA[A/G]CGTGTCCTCTGAAAA | 820061 |
| rs347341193 | snp | A/G | | | intron-variant | ? | TAIR10 | 3:2778612 | ATTAATTGACTCAAT[A/G]TGCTCGAGATAAGGT | 820061 |
| rs347396505 | snp | A/T | | | intron-variant | ? | TAIR10 | 3:2779021 | TGTATGGCCTTGCCA[A/T]GGAAATCAAAAGACC | 820061 |
| rs347419011 | snp | G/T | | | missense | ? | TAIR10 | 3:2780175 | TTTCAGTGTTGCTGC[G/T]TTTAGCATCTGAAAA | 820061 |