SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs346458192 | snp | C/T | | | intron-variant | ? | TAIR10 | 4:16816479 | AAACTGTTTCCATGC[C/T]CTTTCAAGCTAGCAT | 829690 |
rs346502721 | snp | C/T | | | missense | ? | TAIR10 | 4:16815153 | ATGACGATAGTTGCA[C/T]TTTCATGGATCCCAA | 829690 |
rs346569752 | snp | G/T | | | intron-variant | ? | TAIR10 | 4:16816911 | TTTTCTTCTTCCATC[G/T]TAGGTGAGTCTCAAA | 829690 |
rs346610505 | snp | C/T | | | intron-variant | ? | TAIR10 | 4:16817222 | ATGCTGTAAGAGCCA[C/T]GAATAAGAACTTTTG | 829690 |
rs346993816 | snp | C/T | | | synonymous-codon | ? | TAIR10 | 4:16817175 | GGATCTTTCAAACAA[C/T]CAACCATCATGGATT | 829690 |
rs347245275 | snp | A/T | | | intron-variant | ? | TAIR10 | 4:16816481 | ACTGTTTCCATGCTC[A/T]TTCAAGCTAGCATCT | 829690 |
rs347409713 | snp | C/T | | | synonymous-codon | ? | TAIR10 | 4:16815745 | CGAGGTTTATGTATA[C/T]GAGGAATCCGAAAAC | 829690 |
rs347439056 | snp | C/G | | | missense | ? | TAIR10 | 4:16815509 | AGCTCTGGGCAGGGA[C/G]ACCTTTATTATCCAA | 829690 |