| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs346609268 | snp | C/T | | | synonymous-codon | APG7 | TAIR10 | 5:18617391 | TTGTAAACGCCTTAG[C/T]GAGTTGATTGAATCT | 834630 |
| rs346720475 | snp | C/T | | | synonymous-codon | APG7 | TAIR10 | 5:18615405 | CTCTTTGAAACTCGA[C/T]AAACTCGGAATCGAT | 834630 |
| rs346930417 | snp | A/G | | | intron-variant | APG7 | TAIR10 | 5:18615470 | TCATCGAATTAAAAA[A/G]TCATCCAATGCATCG | 834630 |
| rs346984544 | snp | C/T | | | intron-variant | APG7 | TAIR10 | 5:18615602 | TTCTGGGCAAGTTGT[C/T]ATGATCCGTTTAGGT | 834630 |
| rs347004672 | snp | C/T | | | intron-variant | APG7 | TAIR10 | 5:18617822 | CCCACTCTTTTCTTG[C/T]ATTTGCAGTCAATGA | 834630 |
| rs347009361 | snp | A/G | | | synonymous-codon | APG7 | TAIR10 | 5:18617325 | TGTTATGGCTATACC[A/G]ATGCCCGGACATCCG | 834630 |
| rs347158831 | snp | C/T | | | missense | APG7 | TAIR10 | 5:18616070 | GACCCTTCTGTGTTA[C/T]CAAGATTCCTCGTTA | 834630 |
| rs347260337 | snp | A/G | | | intron-variant | APG7 | TAIR10 | 5:18616887 | CTGATTAGACAAACG[A/G]AATCACGTTCTTTCG | 834630 |
| rs347277080 | snp | A/G | | | synonymous-codon | APG7 | TAIR10 | 5:18617457 | AAGCAGGTGGTTACC[A/G]TCTCTTCTTTGTGCT | 834630 |
| rs347296510 | snp | G/T | | | intron-variant | APG7 | TAIR10 | 5:18615600 | TTTTCTGGGCAAGTT[G/T]TTATGATCCGTTTAG | 834630 |
| rs347354762 | snp | A/G | | | intron-variant | APG7 | TAIR10 | 5:18617806 | GTCCTGATTCGTCGT[A/G]CCCACTCTTTTCTTG | 834630 |
| rs347375874 | snp | G/T | | | synonymous-codon | APG7 | TAIR10 | 5:18617878 | CACTGTTACACGCCC[G/T]GGTCTAGCTCCTATT | 834630 |