SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs346477297 | snp | A/G | | | missense | UBC12 | TAIR10 | 3:2643515 | TCAAGGGAACTGAGG[A/G]ATATGCAGAGACATC | 820017 |
rs346713489 | snp | C/T | | | missense | UBC12 | TAIR10 | 3:2643985 | CTGAGGAGGACATAT[C/T]CCATTGGCAAGCAAC | 820017 |
rs347042223 | snp | C/G | | | intron-variant | UBC12 | TAIR10 | 3:2643777 | GAAAACTCGTTAAAC[C/G]TTTGCCTGGTACGAT | 820017 |
rs347063815 | snp | A/G | | | intron-variant | UBC12 | TAIR10 | 3:2643927 | TGTCTTTTTCGATGA[A/G]TAAATGGGTCTGATT | 820017 |
rs347218645 | snp | C/T | | | intron-variant | UBC12 | TAIR10 | 3:2643811 | GAATATCCAGAGGTT[C/T]AGCTTGCTTTTATTT | 820017 |
rs347293412 | snp | A/G | | | synonymous-codon | UBC12 | TAIR10 | 3:2644091 | TTTCAAGCCACCAAA[A/G]GTGTTGTGTTTTTTC | 820017 |
rs347325435 | snp | A/C | | | synonymous-codon | UBC12 | TAIR10 | 3:2644494 | CAAGGTAGATAAATC[A/C]AAATACGAGTCAACT | 820017 |
rs347399923 | snp | C/T | | | missense | UBC12 | TAIR10 | 3:2644274 | AATGGAGTCCTGCTC[C/T]TACCACATCCAAGGT | 820017 |
rs347406443 | snp | G/T | | | intron-variant | UBC12 | TAIR10 | 3:2643900 | AGTATCACTTGATCA[G/T]GCAGGTTTTATTGTC | 820017 |
rs347439496 | snp | A/G | | | intron-variant | UBC12 | TAIR10 | 3:2644169 | GGCTTATTAGCGAGT[A/G]TACGATTTTGCAGGT | 820017 |
rs347440790 | snp | C/G | | | missense | UBC12 | TAIR10 | 3:2643527 | AGGGATATGCAGAGA[C/G]ATCCTCCAGCAAACT | 820017 |