SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs346429610 | snp | G/T | | | missense | HOS15 | TAIR10 | 5:26858949 | GAAGGATCATTCAAA[G/T]CTGTGCATACTGGTC | 836867 |
rs346438664 | snp | C/G | | | intron-variant | HOS15 | TAIR10 | 5:26860681 | TGGACACAGGTAAAA[C/G]TTAAACCTCAATGTA | 836867 |
rs346471716 | snp | C/G | | | intron-variant | HOS15 | TAIR10 | 5:26860737 | GTTGGTTATAAGTTT[C/G]GTTGTTGTGATATGA | 836867 |
rs346568386 | snp | A/G | | | utr-variant-5-prime | HOS15 | TAIR10 | 5:26857253 | GTGATTTAAAGTTAG[A/G]ATTTGGCTGTGGAGA | 836867 |
rs346659580 | snp | A/T | | | intron-variant | HOS15 | TAIR10 | 5:26859130 | AAAGCCATAGGATAT[A/T]TGAAGCATTTCTGGA | 836867 |
rs346682594 | snp | A/G | | | intron-variant | HOS15 | TAIR10 | 5:26860115 | ATGGCTTCCATAATG[A/G]CAGGGTGAGGTCAAC | 836867 |
rs346700589 | snp | A/G | | | missense | HOS15 | TAIR10 | 5:26858622 | CAAGTCACATTCCTA[A/G]TTCTGATGTGAGGAT | 836867 |
rs346710886 | snp | C/G | | | intron-variant | HOS15 | TAIR10 | 5:26859096 | TATTCCTGGTCACTG[C/G]TAATTACTGCTAATT | 836867 |
rs346761771 | snp | A/T | | | intron-variant | HOS15 | TAIR10 | 5:26859281 | GTATGTCCACGTTGA[A/T]TTTTTGGTTTCACTC | 836867 |
rs346795901 | snp | A/C | | | synonymous-codon | HOS15 | TAIR10 | 5:26858566 | TTTTATTTGAACAGG[A/C]GCAGAACCTATGGAT | 836867 |
rs346865306 | snp | C/T | | | missense | HOS15 | TAIR10 | 5:26858194 | AAGGAAAAGGATAGG[C/T]ACGAGAAGCAGAAGG | 836867 |
rs346919807 | snp | C/G | | | intron-variant | HOS15 | TAIR10 | 5:26860504 | ACTCTTGCAAGGTTA[C/G]AACACGCTTTAAACA | 836867 |
rs346931256 | snp | C/G | | | intron-variant | HOS15 | TAIR10 | 5:26857606 | CGTACTGCTACTCGC[C/G]AATCTAGGTTTTGAT | 836867 |
rs347295744 | snp | C/T | | | utr-variant-3-prime | HOS15 | TAIR10 | 5:26861112 | TTATTTTATCTATCA[C/T]TGCAACTTTTGGGTT | 836867 |
rs347394746 | snp | C/T | | | intron-variant | HOS15 | TAIR10 | 5:26859382 | ATCAATGAATATGCT[C/T]AGTTATTTATGCCTA | 836867 |