| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs193927927 | snp | A/G | | | intron-variant | APG12B | TAIR10 | 3:4614391 | TCTAATCATATCCTT[A/G]ACAGTGTTCTATATC | 820611 |
| rs346436926 | snp | G/T | | | intron-variant | APG12B | TAIR10 | 3:4613845 | GATCAAACAAGCCAT[G/T]CTTGACGATGTATAT | 820611 |
| rs346469716 | snp | A/C | | | intron-variant | APG12B | TAIR10 | 3:4614577 | GAACAACAACTGCGA[A/C]GAAATTAAGGAAAAG | 820611 |
| rs346475350 | snp | A/C | | | utr-variant-3-prime | APG12B | TAIR10 | 3:4613590 | AATGAAGGATGTACA[A/C]CAAGTTTCTTCTACA | 820611 |
| rs346641910 | snp | A/T | | | intron-variant | APG12B | TAIR10 | 3:4614293 | CAAAGAAGAACAAAC[A/T]GGTGGATTTCTCGTA | 820611 |
| rs346936171 | snp | A/G | | | synonymous-codon | APG12B | TAIR10 | 3:4614071 | CAATGAGTCAGAGTG[A/G]AGCTGCCGTCTTAGA | 820611 |
| rs347174584 | snp | A/C | | | intron-variant | APG12B | TAIR10 | 3:4614726 | AAATGCAAGAGATTC[A/C]ATGGAAGAAGAAAGT | 820611 |