SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs346500381 | snp | A/T | | | missense | ? | TAIR10 | 3:14930444 | TACAAATTGCGCAGT[A/T]ATCAACAACGATATC | 823327 |
rs346556352 | snp | G/T | | | intron-variant | ? | TAIR10 | 3:14930046 | TAAAAGATGACAATA[G/T]TATGGGCTTAAAACG | 823327 |
rs346599981 | snp | A/C | | | synonymous-codon | ? | TAIR10 | 3:14930272 | CTTACCCCAAGCAAC[A/C]GTGCATTCCTCACTA | 823327 |
rs346620513 | snp | C/G | | | missense | ? | TAIR10 | 3:14929854 | TACCTAGTGGACACA[C/G]TTGACGAGTTTTGAG | 823327 |
rs346628134 | snp | A/T | | | missense | ? | TAIR10 | 3:14930644 | GAGATGGAGGAGGAT[A/T]CACCCATGATAACGT | 823327 |
rs346667100 | snp | A/G | | | synonymous-codon | ? | TAIR10 | 3:14930571 | AGCCCAGAGAGCGAC[A/G]GCACTCCACTTCTTT | 823327 |
rs346759187 | snp | C/T | | | missense | ? | TAIR10 | 3:14930438 | GATTCCTACAAATTG[C/T]GCAGTTATCAACAAC | 823327 |
rs346778959 | snp | A/G | | | missense | ? | TAIR10 | 3:14930638 | GGTACGGAGATGGAG[A/G]AGGATTCACCCATGA | 823327 |
rs346801354 | snp | A/G | | | intron-variant | ? | TAIR10 | 3:14930027 | TAGAGATACTAATAA[A/G]AAGTAAAAGATGACA | 823327 |
rs346894295 | snp | A/T | | | intron-variant | ? | TAIR10 | 3:14930125 | CGTATCAGATTACTC[A/T]AAGTGCTTGTGGTAA | 823327 |
rs347018299 | snp | A/T | | | missense | ? | TAIR10 | 3:14930302 | AGTGGCACTAGCTTG[A/T]TTAGCTAGACATTCA | 823327 |
rs347099696 | snp | C/T | | | synonymous-codon | ? | TAIR10 | 3:14929864 | ACACACTTGACGAGT[C/T]TTGAGCCATCTGCTG | 823327 |
rs347113187 | snp | A/T | | | intron-variant | ? | TAIR10 | 3:14930468 | CGATATCTGAAAAAA[A/T]CAAACAAGAGTGAAT | 823327 |
rs347121892 | snp | A/C | | | intron-variant | ? | TAIR10 | 3:14930080 | AACTAGTGTTAAGGC[A/C]CACTAAGGCCTTATA | 823327 |
rs347151467 | snp | G/T | | | synonymous-codon | ? | TAIR10 | 3:14930667 | GATAACGTCGGAGTT[G/T]AGAGAAGCCATTGAT | 823327 |
rs347182692 | snp | A/G | | | intron-variant | ? | TAIR10 | 3:14929808 | AAACATTGATGAGTA[A/G]GAGAGCATGTAAGAT | 823327 |
rs347208606 | snp | C/T | | | intron-variant | ? | TAIR10 | 3:14929926 | CCCCTACAAGTCAAA[C/T]AATGGCACGTTTCTT | 823327 |
rs347461072 | snp | A/G | | | intron-variant | ? | TAIR10 | 3:14930078 | TTAACTAGTGTTAAG[A/G]CCCACTAAGGCCTTA | 823327 |
rs347483268 | snp | C/T | | | missense | ? | TAIR10 | 3:14930647 | ATGGAGGAGGATTCA[C/T]CCATGATAACGTCGG | 823327 |