SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs193924526 | snp | A/T | | | missense | ? | TAIR10 | 3:7113719 | CTTGCGTGATCTTCA[A/T]AATGTCAAGAACGAT | 5008015 |
rs193927458 | snp | C/T | | | intron-variant | ? | TAIR10 | 3:7113607 | ATGCTGTTTGTTCCC[C/T]TTTTTTTTTTTGAAT | 5008015 |
rs346689903 | snp | C/G | | | intron-variant | ? | TAIR10 | 3:7112707 | TCATATTTTTGTCAC[C/G]AAACTATTGTTACCA | 5008015 |
rs346849761 | snp | G/T | | | synonymous-codon | ? | TAIR10 | 3:7112119 | CATATGAAATGTGTG[G/T]CCACATCTTGCTAGC | 5008015 |
rs347074608 | snp | A/T | | | intron-variant | ? | TAIR10 | 3:7113268 | TAAATTCAATTAAGG[A/T]ATGCATAGACAACAA | 5008015 |
rs347171180 | snp | C/G | | | missense | ? | TAIR10 | 3:7112129 | GTGTGGCCACATCTT[C/G]CTAGCTTTCTTCCTA | 5008015 |
rs347263126 | snp | A/C | | | synonymous-codon | ? | TAIR10 | 3:7112912 | ATCACTATGTAGCAC[A/C]GGTCCAAAGAGTTGG | 5008015 |
rs347266322 | snp | C/T | | | missense | ? | TAIR10 | 3:7112953 | TAACTCCAGCCACCA[C/T]TCCAAGCACACTACC | 5008015 |
rs347283110 | snp | C/T | | | intron-variant | ? | TAIR10 | 3:7113541 | AAACCAATGAGATGG[C/T]GTCTCAAGTTTCATC | 5008015 |