SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs346746492 | snp | A/T | | | missense | EMB2766 | TAIR10 | 2:18565461 | TCTGCAACCAACACC[A/T]CTCCGGCTAGCTCCG | 819108 |
rs346800868 | snp | C/T | | | synonymous-codon | EMB2766 | TAIR10 | 2:18564377 | ATTCGGAGCTTCCTC[C/T]ACTCCTTCCTTCGGA | 819108 |
rs346812323 | snp | A/T | | | synonymous-codon | EMB2766 | TAIR10 | 2:18564443 | CGGATTCGGATCTTC[A/T]GCCTCCGTGACTCCT | 819108 |
rs346884918 | snp | A/G | | | missense | EMB2766 | TAIR10 | 2:18567212 | TCTGAGCTAGTAGAA[A/G]GAGAACTGGAGCATA | 819108 |
rs346921260 | snp | A/T | | | missense | EMB2766 | TAIR10 | 2:18564318 | TTCGGTTTCGGATCC[A/T]CCGTATCATCAACTC | 819108 |
rs346933985 | snp | C/T | | | intron-variant | EMB2766 | TAIR10 | 2:18566073 | GTTCTACATTCACCT[C/T]GATTATGTTGTTGCT | 819108 |
rs347085800 | snp | C/G | | | intron-variant | EMB2766 | TAIR10 | 2:18566531 | ATACAGGCCTCTACT[C/G]TATAATTAGCTCATT | 819108 |
rs347127695 | snp | C/T | | | intron-variant | EMB2766 | TAIR10 | 2:18566062 | CGGCTGTACATGTTC[C/T]ACATTCACCTTGATT | 819108 |
rs347174211 | snp | A/G | | | intron-variant | EMB2766 | TAIR10 | 2:18566557 | TCATTCTTTTTGTGT[A/G]CTTGACCAACAAACA | 819108 |
rs347201926 | snp | A/T | | | synonymous-codon | EMB2766 | TAIR10 | 2:18564212 | ATTCTCATTCGGATC[A/T]TCTTCTGCAACTAAT | 819108 |
rs347242848 | snp | A/G | | | synonymous-codon | EMB2766 | TAIR10 | 2:18566333 | CACAGGGAGATTCCG[A/G]AAACAGGCAAATGCA | 819108 |
rs347350072 | snp | A/T | | | intron-variant | EMB2766 | TAIR10 | 2:18566794 | CAGTCGCACTCTTTT[A/T]TTATCTGACATGGAG | 819108 |