SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs346489614 | snp | A/C | | | missense | UBP2 | TAIR10 | 1:1370752 | AGCTGTAATGACATT[A/C]TCAATACCATCTTCT | 839397 |
rs346546397 | snp | C/T | | | synonymous-codon | UBP2 | TAIR10 | 1:1370167 | CCTCTCTACAGACAC[C/T]GGTAAATCCGAATCA | 839397 |
rs346930083 | snp | A/G | | | synonymous-codon | UBP2 | TAIR10 | 1:1370095 | CTTTGAACAGTTCTC[A/G]CAGTTCCAAGCATTG | 839397 |
rs347022564 | snp | A/G | | | missense | UBP2 | TAIR10 | 1:1370930 | CCATTATCAAGGGGT[A/G]CTAAACTGGAACAGG | 839397 |
rs347074560 | snp | A/G | | | synonymous-codon | UBP2 | TAIR10 | 1:1369906 | TTTTCTTCCATCAGA[A/G]CTATGATCCTTGACA | 839397 |
rs347107903 | snp | A/G | | | synonymous-codon | UBP2 | TAIR10 | 1:1371220 | AATGCTCGACGTTTC[A/G]CCTCCAAATACAGAT | 839397 |
rs347183818 | snp | A/G | | | missense | UBP2 | TAIR10 | 1:1371005 | TTCAGTTCCGAAAGA[A/G]CCATACCTGGGAGAA | 839397 |
rs347220645 | snp | A/T | | | synonymous-codon | UBP2 | TAIR10 | 1:1370836 | CCAGGAGCCATCGAA[A/T]CCAGTATCACTTTGT | 839397 |
rs347266586 | snp | A/C | | | intron-variant | UBP2 | TAIR10 | 1:1372618 | CAAATCAGTATTCTA[A/C]GAAGTACCCTACAGA | 839397 |
rs347359596 | snp | G/T | | | intron-variant | UBP2 | TAIR10 | 1:1372650 | AAATTATCCGACTTT[G/T]TAATGACTAGTACTC | 839397 |
rs347376610 | snp | A/G | | | synonymous-codon | UBP2 | TAIR10 | 1:1370275 | AAAAACAGGTCCCTC[A/G]GTAGTCTCAGGCTCA | 839397 |
rs347397404 | snp | A/G | | | synonymous-codon | UBP2 | TAIR10 | 1:1371328 | CGAATCTAGCAAACA[A/G]CGTAGCAACTCGTGG | 839397 |
rs347475296 | snp | C/G | | | synonymous-codon | UBP2 | TAIR10 | 1:1371403 | GAAAGACCCAAAAAA[C/G]GCTCTAGGATTTATC | 839397 |