SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs346466602 | snp | A/T | | | intron-variant | SAY1 | TAIR10 | 4:7073465 | TTCTCTGTAACGCTT[A/T]GCTACTGTGTTATCT | 826779 |
rs346476144 | snp | A/T | | | synonymous-codon | SAY1 | TAIR10 | 4:7071978 | ACCGAATCAGGAAGC[A/T]ATCGACACTTTCATC | 826779 |
rs346489195 | snp | G/T | | | intron-variant | SAY1 | TAIR10 | 4:7072110 | TTGATTTCGAAGTTT[G/T]TTTAGAATCGGTAAA | 826779 |
rs346504560 | snp | A/T | | | synonymous-codon | SAY1 | TAIR10 | 4:7074651 | TAAGGAGCCTCAAGC[A/T]GATGAAGAGAATGCC | 826779 |
rs346517157 | snp | G/T | | | synonymous-codon | SAY1 | TAIR10 | 4:7074190 | GTATGTTGCGTCCCT[G/T]CAAGCTGACCGAGAT | 826779 |
rs346530408 | snp | C/T | | | synonymous-codon | SAY1 | TAIR10 | 4:7073643 | TGATGAGCAACCTCT[C/T]GTTAGACACAGGCCA | 826779 |
rs346535873 | snp | A/C | | | intron-variant | SAY1 | TAIR10 | 4:7075027 | GGCCATACTGGCTAG[A/C]CAGCGGTTAACTACC | 826779 |
rs346548008 | snp | C/T | | | intron-variant | SAY1 | TAIR10 | 4:7073549 | GTGTTTGTCAAAAAT[C/T]GATGTCTAACTAATC | 826779 |
rs346550890 | snp | C/T | | | missense | SAY1 | TAIR10 | 4:7072891 | ATGTTCAGGGTCCAG[C/T]AACTACCCAAGGAAC | 826779 |
rs346551797 | snp | A/T | | | missense | SAY1 | TAIR10 | 4:7072990 | GACCTGCTGGTTCTG[A/T]AGCCAATAATAATAA | 826779 |
rs346552962 | snp | A/C | | | missense | SAY1 | TAIR10 | 4:7072480 | AGCGAAGGAGATCGA[A/C]ATGTGTATGACATCT | 826779 |
rs346581397 | snp | A/G | | | synonymous-codon | SAY1 | TAIR10 | 4:7074277 | GAGAAAGGCTTTTCT[A/G]GAGGAAGAAAAGAAA | 826779 |
rs346591525 | snp | C/G | | | intron-variant | SAY1 | TAIR10 | 4:7073503 | TAATATCTGCAGTTG[C/G]AAAAACATCTGTCAA | 826779 |
rs346616221 | snp | C/G | | | intron-variant | SAY1 | TAIR10 | 4:7073460 | GGTTCTTCTCTGTAA[C/G]GCTTTGCTACTGTGT | 826779 |
rs346616495 | snp | A/G | | | missense | SAY1 | TAIR10 | 4:7073227 | TGATGACATAGCAAT[A/G]GCTGTTACAATGTCA | 826779 |
rs346629352 | snp | G/T | | | intron-variant | SAY1 | TAIR10 | 4:7072281 | TTTCTAGAAGGATTT[G/T]TGTTCTTACATTGCT | 826779 |
rs346640373 | snp | C/G | | | intron-variant | SAY1 | TAIR10 | 4:7072186 | ATGCTTTTTCCCTTA[C/G]TCGTTTTGATATTTG | 826779 |
rs346651522 | snp | A/C | | | intron-variant | SAY1 | TAIR10 | 4:7072132 | ATCGGTAAAGTGAAA[A/C]TGAAAGTTCGATGAG | 826779 |
rs346689081 | snp | A/G | | | intron-variant | SAY1 | TAIR10 | 4:7072084 | TTCGCGATTCCTTAT[A/G]ATTCAGATGTTTGAT | 826779 |
rs346706289 | snp | C/T | | | intron-variant | SAY1 | TAIR10 | 4:7072302 | TTACATTGCTTTTTT[C/T]GCTCAAACGATATCT | 826779 |
rs346710606 | snp | A/G | | | synonymous-codon | SAY1 | TAIR10 | 4:7073751 | AAGTATTAATCCAGC[A/G]GAGCGTGGCAGTGGG | 826779 |
rs346723878 | snp | C/G | | | intron-variant | SAY1 | TAIR10 | 4:7075038 | CTAGCCAGCGGTTAA[C/G]TACCATAATGTATAG | 826779 |
rs346725730 | snp | A/G | | | intron-variant | SAY1 | TAIR10 | 4:7074445 | TAGTGGATAGAGAAA[A/G]ATCAGCCAAAACACC | 826779 |
rs346726242 | snp | C/G | | | intron-variant | SAY1 | TAIR10 | 4:7075102 | CGGACGGTTTAAAAT[C/G]ATTAGAAAATTTTCA | 826779 |
rs346739782 | snp | C/G | | | synonymous-codon | SAY1 | TAIR10 | 4:7075199 | GGAAAGTGAGTCGAC[C/G]TTAAACGATCTTGGA | 826779 |
rs346761336 | snp | A/G | | | synonymous-codon | SAY1 | TAIR10 | 4:7073423 | ACCTCAGGATACCCA[A/G]GCCCTGAACGGAAGG | 826779 |
rs346768968 | snp | A/G | | | intron-variant | SAY1 | TAIR10 | 4:7074553 | GTAGGCGTTCTCTTC[A/G]TTACTGATTTAAGTT | 826779 |
rs346792136 | snp | G/T | | | intron-variant | SAY1 | TAIR10 | 4:7074771 | TTCATTTCACTTAGT[G/T]TTGCATTACTCAAAA | 826779 |
rs346794334 | snp | A/T | | | intron-variant | SAY1 | TAIR10 | 4:7073533 | AGCAGTTTGTCTATT[A/T]GTGTTTGTCAAAAAT | 826779 |
rs346826975 | snp | A/C | | | missense | SAY1 | TAIR10 | 4:7074239 | AGAGATGCTGAGGCA[A/C]GTCAGCTAGAGGAAG | 826779 |
rs346834155 | snp | A/G | | | missense | SAY1 | TAIR10 | 4:7073376 | GCCTCAACCTCGGAA[A/G]TAGGAGCTTCTGCAG | 826779 |
rs346857109 | snp | G/T | | | intron-variant | SAY1 | TAIR10 | 4:7072197 | CTTACTCGTTTTGAT[G/T]TTTGATGTTTTGGGG | 826779 |
rs346873440 | snp | A/T | | | intron-variant | SAY1 | TAIR10 | 4:7075098 | ATACCGGACGGTTTA[A/T]AATCATTAGAAAATT | 826779 |
rs346878993 | snp | A/C | | | intron-variant | SAY1 | TAIR10 | 4:7074965 | TGAGTGCCGGTTCCG[A/C]ATCAGGTCAATGACT | 826779 |
rs346890712 | snp | A/G | | | intron-variant | SAY1 | TAIR10 | 4:7074422 | CGGATTGTTTTGGAG[A/G]CTTCTGCTAGTGGAT | 826779 |
rs346916222 | snp | A/G | | | synonymous-codon | SAY1 | TAIR10 | 4:7074039 | TCCACCCTCACCTTC[A/G]CTGACAGCTCAGAGG | 826779 |
rs346925810 | snp | A/G | | | missense | SAY1 | TAIR10 | 4:7072984 | AAGACAGACCTGCTG[A/G]TTCTGTAGCCAATAA | 826779 |
rs346949161 | snp | G/T | | | synonymous-codon | SAY1 | TAIR10 | 4:7074241 | AGATGCTGAGGCACG[G/T]CAGCTAGAGGAAGAA | 826779 |
rs346963368 | snp | C/T | | | synonymous-codon | SAY1 | TAIR10 | 4:7072461 | AGCAGTGAATGCATA[C/T]TTCAGCGAAGGAGAT | 826779 |
rs346984478 | snp | A/G | | | missense | SAY1 | TAIR10 | 4:7073702 | CACCTAACGCTGATC[A/G]TTCCCGGAGTGGGAG | 826779 |
rs346996087 | snp | C/T | | | intron-variant | SAY1 | TAIR10 | 4:7072156 | CGATGAGACGACGAT[C/T]GTTTGATTATTCTGA | 826779 |
rs347059956 | snp | A/T | | | intron-variant | SAY1 | TAIR10 | 4:7074411 | TATGTTGACTGCGGA[A/T]TGTTTTGGAGGCTTC | 826779 |
rs347089990 | snp | C/G | | | intron-variant | SAY1 | TAIR10 | 4:7072068 | TTGATTCATGTCCTT[C/G]TTCGCGATTCCTTAT | 826779 |
rs347102018 | snp | G/T | | | intron-variant | SAY1 | TAIR10 | 4:7073846 | GTATTACTTATTGGT[G/T]AGAGTAGCTAGTCCT | 826779 |
rs347108742 | snp | A/T | | | synonymous-codon | SAY1 | TAIR10 | 4:7072458 | TCAAGCAGTGAATGC[A/T]TATTTCAGCGAAGGA | 826779 |
rs347131580 | snp | A/T | | | intron-variant | SAY1 | TAIR10 | 4:7074370 | ATCTCTCTTTGTAAA[A/T]CCGCGTTCAAACAAG | 826779 |
rs347148780 | snp | A/T | | | missense | SAY1 | TAIR10 | 4:7074212 | GACCGAGATAAAGAA[A/T]TGAAGTCCATTAGAG | 826779 |
rs347186697 | snp | A/C | | | synonymous-codon | SAY1 | TAIR10 | 4:7074851 | CTTTATAGACATTGC[A/C]AGAGTGGTGAAACCC | 826779 |
rs347188029 | snp | A/T | | | intron-variant | SAY1 | TAIR10 | 4:7073147 | ATTTATGAGGTTTTT[A/T]ATATTTTCTTATAGG | 826779 |
rs347209170 | snp | A/C | | | synonymous-codon | SAY1 | TAIR10 | 4:7074015 | TCCTCAGCCGAGGGC[A/C]CAACCACGTCCACCC | 826779 |
rs347228065 | snp | C/T | | | intron-variant | SAY1 | TAIR10 | 4:7072574 | GTTATGCTCTTTGTG[C/T]AGAGTACGTGAAGCG | 826779 |
rs347229965 | snp | C/T | | | synonymous-codon | SAY1 | TAIR10 | 4:7073673 | AAGACGTGCAGCATC[C/T]GGATCTCTGGCTCCA | 826779 |
rs347239204 | snp | A/G | | | missense | SAY1 | TAIR10 | 4:7073400 | TCTGCAGTGACTGCT[A/G]CTCAAGGACCTCAGG | 826779 |
rs347239805 | snp | A/C | | | intron-variant | SAY1 | TAIR10 | 4:7075081 | TTGACCGGTTTGGTC[A/C]TATACCGGACGGTTT | 826779 |
rs347270839 | snp | G/T | | | intron-variant | SAY1 | TAIR10 | 4:7072560 | AATTTTTTTACGTTG[G/T]TATGCTCTTTGTGTA | 826779 |
rs347293011 | snp | A/T | | | synonymous-codon | SAY1 | TAIR10 | 4:7072796 | GGTTAGGCAGATACC[A/T]ATAGAGGTTAAGGAT | 826779 |
rs347314255 | snp | C/T | | | synonymous-codon | SAY1 | TAIR10 | 4:7072811 | TATAGAGGTTAAGGA[C/T]AGCAGTGGGCCATCT | 826779 |
rs347319461 | snp | G/T | | | synonymous-codon | SAY1 | TAIR10 | 4:7075172 | ATATCCGAGGCATGC[G/T]TTTGGAGATGGGGAA | 826779 |
rs347327091 | snp | C/T | | | intron-variant | SAY1 | TAIR10 | 4:7074532 | TAATCTGGTTTGAGT[C/T]CCTATGTAGGCGTTC | 826779 |
rs347331035 | snp | A/G | | | synonymous-codon | SAY1 | TAIR10 | 4:7072425 | TTGATTACTGCAGGA[A/G]CATCGTGGTGATCTT | 826779 |
rs347339497 | snp | C/T | | | utr-variant-3-prime | SAY1 | TAIR10 | 4:7075495 | TATCACATCTTCAAA[C/T]TTGCTCTTTCAGCTT | 826779 |
rs347369249 | snp | A/G | | | intron-variant | SAY1 | TAIR10 | 4:7072150 | AAAGTTCGATGAGAC[A/G]ACGATCGTTTGATTA | 826779 |
rs347390011 | snp | G/T | | | intron-variant | SAY1 | TAIR10 | 4:7075010 | CTCCCGGCCAGCCCT[G/T]TGGCCATACTGGCTA | 826779 |
rs347423701 | snp | A/G | | | intron-variant | SAY1 | TAIR10 | 4:7073863 | GAGTAGCTAGTCCTT[A/G]CCTTTGCTAATACTC | 826779 |
rs347425198 | snp | C/T | | | missense | SAY1 | TAIR10 | 4:7072484 | AAGGAGATCGAAATG[C/T]GTATGACATCTCTAT | 826779 |
rs347469994 | snp | A/G | | | intron-variant | SAY1 | TAIR10 | 4:7074434 | GAGGCTTCTGCTAGT[A/G]GATAGAGAAAGATCA | 826779 |