| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs346673568 | snp | A/G | | | synonymous-codon | BT1 | TAIR10 | 5:25334528 | ACAGAGGTCAGGTGC[A/G]TCGCAGAGACGAGCC | 836437 |
| rs346873100 | snp | A/C/G | | | intron-variant | BT1 | TAIR10 | 5:25334352 | AGAACCAAAAAAAAA[A/C/G]AAAACAAAAAAGTGT | 836437 |
| rs346954069 | snp | C/T | | | synonymous-codon | BT1 | TAIR10 | 5:25335138 | AATCTTCCTCGGCTT[C/T]TCGATGATGTTCGTC | 836437 |
| rs346998148 | snp | A/G | | | missense | BT1 | TAIR10 | 5:25333990 | GATTGGTCACAAATC[A/G]AAGAATGGAGTCTAA | 836437 |
| rs347089228 | snp | A/T | | | utr-variant-3-prime | BT1 | TAIR10 | 5:25333443 | AATGGCTTCTAACAA[A/T]CGCTCACTATATAAT | 836437 |
| rs347160952 | snp | A/T | | | synonymous-codon | BT1 | TAIR10 | 5:25334390 | GTTAATTACCGATTC[A/T]GCATCGTCGATGAAT | 836437 |
| rs347287736 | snp | G/T | | | missense | BT1 | TAIR10 | 5:25335294 | AGTGTGCCGGAATAC[G/T]ACGACGACCGGAGGT | 836437 |
| rs347326024 | snp | A/C | | | intron-variant | BT1 | TAIR10 | 5:25334346 | TCTTGAAGAACCAAA[A/C]AAAAAGAAAACAAAA | 836437 |
| rs347353601 | snp | C/G | | | missense | BT1 | TAIR10 | 5:25333512 | GTTCCGGATTCTGAT[C/G]AAATCTTCTGCTTCT | 836437 |