SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs346474045 | snp | C/T | | | synonymous-codon | UBC25 | TAIR10 | 3:5185789 | CTTTTTTGATATCTT[C/T]TTCCCGGATACATAC | 820772 |
rs346482469 | snp | A/G | | | intron-variant | UBC25 | TAIR10 | 3:5184056 | GATTTTGGGGATTGT[A/G]TGATTGTGTGATCAT | 820772 |
rs346520311 | snp | C/T | | | utr-variant-3-prime | UBC25 | TAIR10 | 3:5186756 | CTCCCTTCTTACAAT[C/T]ATGGATCCTCTTTTT | 820772 |
rs346529652 | snp | A/G | | | synonymous-codon | UBC25 | TAIR10 | 3:5185819 | CCCTTCTACGCCACC[A/G]GTAAGTCAACTGAAC | 820772 |
rs346558522 | snp | A/G | | | synonymous-codon | UBC25 | TAIR10 | 3:5184992 | CAAGAAAGCAACAAA[A/G]GCAAGTGGAATCCAT | 820772 |
rs346578749 | snp | G/T | | | intron-variant | UBC25 | TAIR10 | 3:5185613 | GTTGGTATACACGCT[G/T]TCTTATACAACAATC | 820772 |
rs346694373 | snp | A/T | | | intron-variant | UBC25 | TAIR10 | 3:5186292 | AGCGTAAACCTTTTC[A/T]CTAAAACTTGAGATT | 820772 |
rs346726768 | snp | A/G | | | intron-variant | UBC25 | TAIR10 | 3:5184607 | AGTATGCTGTGGTAA[A/G]TGTTTGAATTTTCGT | 820772 |
rs346731837 | snp | C/T | | | missense | UBC25 | TAIR10 | 3:5186452 | TGGTGAAGGGGGCTC[C/T]AGATGTGGAAGAGAA | 820772 |
rs346743988 | snp | C/T | | | synonymous-codon | UBC25 | TAIR10 | 3:5186071 | TGTCTCGATCCAAGG[C/T]CTAATCTTAAATCAA | 820772 |
rs346752561 | snp | A/G | | | missense | UBC25 | TAIR10 | 3:5186394 | GCTCACGACGTGTTG[A/G]AGGCGTGTAATGCTT | 820772 |
rs347095396 | snp | A/T | | | intron-variant | UBC25 | TAIR10 | 3:5184300 | GTTATAGACTTGTTT[A/T]TGTTATGTAATGTGA | 820772 |
rs347174394 | snp | C/G | | | intron-variant | UBC25 | TAIR10 | 3:5184218 | TCTTTGAAGGATCGT[C/G]ATTCGTTTCGGCGAT | 820772 |
rs347446737 | snp | A/G | | | intron-variant | UBC25 | TAIR10 | 3:5184653 | AATGAGTCTACTTAC[A/G]TTGTCACAACTAAAA | 820772 |
rs347461014 | snp | C/T | | | intron-variant | UBC25 | TAIR10 | 3:5184233 | CATTCGTTTCGGCGA[C/T]CACTTTCTAACGTTT | 820772 |