| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs346487259 | snp | C/T | | | intron-variant | RGLG1 | TAIR10 | 3:244425 | ATTTTTCTAACATGT[C/T]TGCTCTGTTTCTAGT | 819911 |
| rs346576379 | snp | A/T | | | synonymous-codon | RGLG1 | TAIR10 | 3:242871 | TCCCGCTCCATCTCC[A/T]GCTCCTGCTCCTGCT | 819911 |
| rs346631916 | snp | A/G | | | intron-variant | RGLG1 | TAIR10 | 3:242353 | CGGCTCAAAGTCGGT[A/G]ATTGGAGGTAACGTG | 819911 |
| rs346758724 | snp | A/C | | | intron-variant | RGLG1 | TAIR10 | 3:242186 | TCATCTTAATTAGGA[A/C]AAATCTCTCTAATTA | 819911 |
| rs346770669 | snp | C/G | | | intron-variant | RGLG1 | TAIR10 | 3:243763 | GCAGGTTTATTTCCT[C/G]CTCTGACCTGCACTG | 819911 |
| rs346831867 | snp | G/T | | | intron-variant | RGLG1 | TAIR10 | 3:242597 | ATTGCATGTTGAATC[G/T]GTTACGTTCTTCTTG | 819911 |
| rs346877911 | snp | C/G | | | utr-variant-5-prime | RGLG1 | TAIR10 | 3:242013 | CAACACCACCTCTGT[C/G]TTATTGCTCTCTTTT | 819911 |
| rs347002108 | snp | C/T | | | intron-variant | RGLG1 | TAIR10 | 3:242498 | CTTCTTTCAAAGTCG[C/T]AATTGCTCTCTCTCA | 819911 |
| rs347083739 | snp | C/G | | | intron-variant | RGLG1 | TAIR10 | 3:242225 | CAGATTTTGTCTTCA[C/G]TTGTTTTGTTTTAAA | 819911 |
| rs347303100 | snp | G/T | | | missense | RGLG1 | TAIR10 | 3:242872 | CCCGCTCCATCTCCT[G/T]CTCCTGCTCCTGCTC | 819911 |
| rs347330862 | snp | C/T | | | intron-variant | RGLG1 | TAIR10 | 3:242223 | CTCAGATTTTGTCTT[C/T]AGTTGTTTTGTTTTA | 819911 |
| rs347443355 | snp | A/G | | | intron-variant | RGLG1 | TAIR10 | 3:242374 | AGGTAACGTGATTGA[A/G]TCTTCTTCATCAATC | 819911 |
| rs347458724 | snp | C/T | | | missense | RGLG1 | TAIR10 | 3:243461 | ACTTGAGCAATACCC[C/T]GAATCCATACGAGCA | 819911 |