SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs346451751 | snp | A/G | | | intron-variant | EOL2 | TAIR10 | 5:23666494 | ATGTAGCTTCCGTCA[A/G]CTCCTGAAGAATTCA | 835968 |
rs346614770 | snp | G/T | | | utr-variant-3-prime, intron-variant | EOL2 | TAIR10 | 5:23665365 | CTTTACAGCATCCAT[G/T]TATAGAAGAAGAAAA | 835968 |
rs346664145 | snp | C/T | | | missense | EOL2 | TAIR10 | 5:23666832 | TCACCAGTGGCTAAA[C/T]ACAGCCAAGCCCTCA | 835968 |
rs346852991 | snp | C/T | | | missense | EOL2 | TAIR10 | 5:23667804 | GAAAGCGCTGCGATT[C/T]TCGACCTAACACACT | 835968 |
rs346920172 | snp | C/G | | | missense | EOL2 | TAIR10 | 5:23666977 | ACAGTGTCGGGTCAA[C/G]TTCAGTGGCGGTTGC | 835968 |
rs347093576 | snp | C/G | | | synonymous-codon | EOL2 | TAIR10 | 5:23665778 | GAAGAGTTAGTTACC[C/G]GCAGCTCGGTATCTG | 835968 |
rs347150604 | snp | A/C | | | synonymous-codon | EOL2 | TAIR10 | 5:23666822 | ACTCTCCCGGTCACC[A/C]GTGGCTAAATACAGC | 835968 |
rs347151881 | snp | A/C | | | missense | EOL2 | TAIR10 | 5:23667632 | TAATTGAAGCAGCTC[A/C]AATACAGTTTCCACA | 835968 |
rs347346716 | snp | C/G | | | missense | EOL2 | TAIR10 | 5:23668082 | TCTCAACCAAGCAGA[C/G]AAAACAACCTTACAA | 835968 |
rs347357072 | snp | A/T | | | intron-variant | EOL2 | TAIR10 | 5:23665709 | CATCAGCACTGCCAC[A/T]CATACGATCACTTCT | 835968 |
rs347446318 | snp | C/T | | | synonymous-codon | EOL2 | TAIR10 | 5:23667095 | GTTCATGAGCCTGTA[C/T]GCCGAATACCTCTTC | 835968 |