| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs346487370 | snp | C/G | | | intron-variant | ? | TAIR10 | 4:16267372 | ACAAATCAAAAACCA[C/G]CAATGAAGGGTTAAA | 829539 |
| rs346492864 | snp | A/T | | | intron-variant | ? | TAIR10 | 4:16267150 | ATATCTCTACCCACT[A/T]ATTCTTGTTGTCATT | 829539 |
| rs346542691 | snp | C/T | | | intron-variant | ? | TAIR10 | 4:16266615 | TTGTTTGCAATGTCA[C/T]AAAAAGATCTGAAAG | 829539 |
| rs346686363 | snp | A/G | | | intron-variant | ? | TAIR10 | 4:16266504 | TTTGGGTTGGAATTG[A/G]TTTAGGGTTCCTTTT | 829539 |
| rs346690668 | snp | C/G | | | synonymous-codon | ? | TAIR10 | 4:16267507 | GATTGCTATGATCCT[C/G]ATTCTACGCTTAGTA | 829539 |
| rs346957758 | snp | A/G | | | missense | ? | TAIR10 | 4:16267487 | ACAGTTTTTGACTAC[A/G]CTGCGATTGCTATGA | 829539 |
| rs347030496 | snp | A/G | | | intron-variant | ? | TAIR10 | 4:16266469 | TATTTCTGTTCGTCA[A/G]AGGTAAATTTGGAGA | 829539 |
| rs347262367 | snp | C/T | | | missense | ? | TAIR10 | 4:16266176 | ACGCCGCCGCTGTGA[C/T]GGAAAATCTTGATCG | 829539 |
| rs347307059 | snp | A/G | | | intron-variant | ? | TAIR10 | 4:16267188 | TGTACTAATGGCCAA[A/G]CAAGACAATCTTTGT | 829539 |
| rs347437259 | snp | C/T | | | utr-variant-3-prime | ? | TAIR10 | 4:16267636 | TGAATCTATTAAGTC[C/T]TGTGCAGTTTGATCC | 829539 |