SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs346649405 | snp | A/G | | | synonymous-codon | PRT1 | TAIR10 | 3:9057330 | TCTCAAAGAAGGCCC[A/G]TCCTTATCAAACGAC | 822078 |
rs346666215 | snp | C/T | | | missense | PRT1 | TAIR10 | 3:9056972 | GTGAAGGATGTGTAG[C/T]AGATATGGCTGAAGA | 822078 |
rs346681510 | snp | A/T | | | missense | PRT1 | TAIR10 | 3:9056551 | GAGATTCTCTCAATG[A/T]CTCTGGTGAGAGTTC | 822078 |
rs346707414 | snp | G/T | | | intron-variant | PRT1 | TAIR10 | 3:9055936 | CTTAATCTCTGTGTG[G/T]AATCGTAATCGTAAT | 822078 |
rs346735301 | snp | A/T | | | intron-variant | PRT1 | TAIR10 | 3:9057232 | AAGCTTAGTTCTTGT[A/T]GTTACACAAAATATG | 822078 |
rs346753392 | snp | C/T | | | intron-variant | PRT1 | TAIR10 | 3:9055848 | CGAAAAATCTCATGA[C/T]GCAATTGTTTCCATT | 822078 |
rs346782708 | snp | C/T | | | intron-variant | PRT1 | TAIR10 | 3:9057487 | TGAATCGTAATTTGA[C/T]ACTGGTGCGGTTTGC | 822078 |
rs346789486 | snp | C/T | | | missense | PRT1 | TAIR10 | 3:9056317 | TCTGTGTGCCAGAAG[C/T]TTTATTTTCTGTTAA | 822078 |
rs346808959 | snp | C/T | | | synonymous-codon | PRT1 | TAIR10 | 3:9056696 | ATCAAGTAGAGGTGA[C/T]ATTCCATGTATCCCC | 822078 |
rs346816275 | snp | A/C | | | missense | PRT1 | TAIR10 | 3:9057676 | TCTCCTCAGGTTCTG[A/C]TCAATTTCAATTCTA | 822078 |
rs346982093 | snp | A/G | | | intron-variant | PRT1 | TAIR10 | 3:9055835 | GTTTAGCTAATTTCG[A/G]AAAATCTCATGATGC | 822078 |
rs347076011 | snp | C/T | | | synonymous-codon | PRT1 | TAIR10 | 3:9056705 | AGGTGACATTCCATG[C/T]ATCCCCAAAAATCAA | 822078 |
rs347143062 | snp | A/G | | | missense | PRT1 | TAIR10 | 3:9056739 | CCCACAGATGCAAAA[A/G]CTCTTAATGTTCATG | 822078 |
rs347340301 | snp | A/C | | | missense | PRT1 | TAIR10 | 3:9057744 | CATGGATACAGATGA[A/C]GGCGAGGAAGGGCCT | 822078 |
rs347385541 | snp | C/G | | | missense | PRT1 | TAIR10 | 3:9056281 | TGTCCGATATGTAGA[C/G]ACCCGTATGTTCACT | 822078 |
rs347410174 | snp | C/G | | | intron-variant | PRT1 | TAIR10 | 3:9056191 | CTTTTGTATGGAATT[C/G]GCAATGAAGCTTGTG | 822078 |