SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs346427356 | snp | A/G | | | synonymous-codon | AGB1 | TAIR10 | 4:16478554 | CGTTGAGCTAAGGCT[A/G]AAGATAGAACATACA | 829597 |
rs346474382 | snp | C/T | | | synonymous-codon | AGB1 | TAIR10 | 4:16478515 | GAGCATTCTTGAAAC[C/T]GGTACAGTTCCATCC | 829597 |
rs346539733 | snp | C/T | | | missense, stop-gained | AGB1 | TAIR10 | 4:16477625 | GCTGTAATCCCAAAT[C/T]CAATACAACCTGCAA | 829597 |
rs346542790 | snp | C/T | | | synonymous-codon, missense | AGB1 | TAIR10 | 4:16477608 | ATTCCTGTGTGAATC[C/T]TGCTGTAATCCCAAA | 829597 |
rs346571783 | snp | A/C | | | missense | AGB1 | TAIR10 | 4:16477824 | ATGGAGGTGACAGGT[A/C]CGTTCTCACCATCAC | 829597 |
rs346592321 | snp | A/G | | | intron-variant | AGB1 | TAIR10 | 4:16478106 | TGGGGAATAATCACC[A/G]AGTAAGAGGGCGAGT | 829597 |
rs346613377 | snp | C/G | | | utr-variant-3-prime | AGB1 | TAIR10 | 4:16477338 | CTTACTTCCCGACTA[C/G]AGAATATATTAACCA | 829597 |
rs346707605 | snp | C/G | | | intron-variant, utr-variant-5-prime | AGB1 | TAIR10 | 4:16478979 | TGAAGGATAAAGATG[C/G]AAACTTTGAGTCACC | 829597 |
rs346718995 | snp | A/G | | | synonymous-codon | AGB1 | TAIR10 | 4:16477736 | TACCTCTCCCAAGAG[A/G]GTATCCCAAACGTAG | 829597 |
rs346797641 | snp | C/G | | | utr-variant-5-prime | AGB1 | TAIR10 | 4:16479283 | CCGGGATCAGACTTA[C/G]GCTTCTCCGTCGCCG | 829597 |
rs346812605 | snp | C/G | | | synonymous-codon | AGB1 | TAIR10 | 4:16478539 | TCCATCCTTGTCCGC[C/G]GTTGAGCTAAGGCTA | 829597 |
rs346837183 | snp | C/G | | | intron-variant | AGB1 | TAIR10 | 4:16478220 | ATGTTGATTCCAACA[C/G]TCGATCCAAATGGTA | 829597 |
rs347131294 | snp | A/C | | | intron-variant | AGB1 | TAIR10 | 4:16479153 | GAGACGAAAAGGAAT[A/C]CACAAACCATCGGTA | 829597 |
rs347194269 | snp | G/T | | | synonymous-codon | AGB1 | TAIR10 | 4:16478036 | TGCTGTGGAATCGCA[G/T]GAACCAGATATAAAC | 829597 |
rs347478321 | snp | G/T | | | missense | AGB1 | TAIR10 | 4:16477770 | GTGTTGTTGCTCGCA[G/T]AGCCAGCGAAAAGAA | 829597 |