SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs346496378 | snp | C/T | | | intron-variant | TAF5 | TAIR10 | 5:8677865 | AGGTACTTGTCAATA[C/T]AGCAAATTAGATGTA | 832586 |
rs346547627 | snp | A/G | | | missense | TAF5 | TAIR10 | 5:8679845 | AGTGATCAAAGCATA[A/G]GACCAAATGGCAGAA | 832586 |
rs346607497 | snp | C/G | | | intron-variant | TAF5 | TAIR10 | 5:8681199 | TTAAAGGGTAGTTCA[C/G]GGTTATGATATAGAG | 832586 |
rs346656729 | snp | C/G | | | intron-variant | TAF5 | TAIR10 | 5:8677530 | ATGACATCTCAGTGG[C/G]AAGAAATTAGGTTTT | 832586 |
rs346710304 | snp | A/G | | | synonymous-codon | TAF5 | TAIR10 | 5:8679904 | AGGGCCAGTTTACTC[A/G]GCCACTTTCAGTCCC | 832586 |
rs346748205 | snp | A/C | | | missense | TAF5 | TAIR10 | 5:8679813 | TTCCAGGTGCTTTGC[A/C]GGCTGAAAATGATTC | 832586 |
rs346759242 | snp | A/G | | | missense | TAF5 | TAIR10 | 5:8677220 | ATCACCAGAACAATA[A/G]TGGTAGCTCCTTCAC | 832586 |
rs346864171 | snp | A/G | | | missense | TAF5 | TAIR10 | 5:8677973 | TGTATTCCAGCTAGA[A/G]CCTTCTTTAACAGCT | 832586 |
rs346879162 | snp | A/G | | | synonymous-codon | TAF5 | TAIR10 | 5:8679003 | GAAGAAGGACAAAGC[A/G]GGTAATGCAACAGCA | 832586 |
rs346882687 | snp | A/C | | | intron-variant | TAF5 | TAIR10 | 5:8681591 | GGAAAAGTGAGTTTG[A/C]TCTTTCAAGTTGTAT | 832586 |
rs346941393 | snp | C/T | | | intron-variant | TAF5 | TAIR10 | 5:8679390 | ACTCATAACGGGTAA[C/T]GTCCACCTCTCCTCC | 832586 |
rs346995568 | snp | A/C | | | missense | TAF5 | TAIR10 | 5:8678024 | GTACACTTACGGGAT[A/C]TTCAGAAGCTTGAAG | 832586 |
rs347158534 | snp | C/T | | | intron-variant | TAF5 | TAIR10 | 5:8680359 | TGTCTCCCTCATCTT[C/T]ATTGTTTGGGTTTAA | 832586 |
rs347165327 | snp | A/G | | | intron-variant | TAF5 | TAIR10 | 5:8679165 | CATGTGATATCTATG[A/G]GTGATGCATGATTGT | 832586 |
rs347359144 | snp | A/G | | | intron-variant | TAF5 | TAIR10 | 5:8678482 | AGTTTTTTGAGTAGA[A/G]AATTGAATCAATTGG | 832586 |
rs347443204 | snp | A/G | | | intron-variant | TAF5 | TAIR10 | 5:8681330 | TTCTTGTCATGGGTT[A/G]TGGAATGTTGTATAG | 832586 |
rs347467139 | snp | G/T | | | intron-variant | TAF5 | TAIR10 | 5:8678470 | ATAGCTTGTAGCAGT[G/T]TTTTGAGTAGAAAAT | 832586 |