SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs346439866 | snp | C/G | | | missense | HOS1 | TAIR10 | 2:16616952 | TTTTTCTCCAAAGTG[C/G]TAACAATGCCAGAGC | 818568 |
rs346459096 | snp | A/G | | | synonymous-codon | HOS1 | TAIR10 | 2:16614093 | AACAAAAGAGATGCA[A/G]GCGTGGTTAGATAAA | 818568 |
rs346467670 | snp | A/C | | | intron-variant | HOS1 | TAIR10 | 2:16613070 | TTTCTCCACTGAATT[A/C]GTTTAGCTCAGGTCT | 818568 |
rs346485856 | snp | A/C | | | missense | HOS1 | TAIR10 | 2:16616987 | GAGCCAGTGGCTAAT[A/C]ATGGCAGTCCTTTTC | 818568 |
rs346538553 | snp | A/G | | | synonymous-codon | HOS1 | TAIR10 | 2:16617022 | TGGTCATATGATAGG[A/G]AACGCGTCCCATGAT | 818568 |
rs346541202 | snp | G/T | | | intron-variant | HOS1 | TAIR10 | 2:16617452 | TTAGCCATTTGTTCC[G/T]TTCTGAATCGTGCCA | 818568 |
rs346623759 | snp | A/G | | | synonymous-codon | HOS1 | TAIR10 | 2:16617769 | TTCCATGCCGGTGAA[A/G]GGAAGGAGGAGACGT | 818568 |
rs346651051 | snp | A/T | | | intron-variant | HOS1 | TAIR10 | 2:16614036 | ATATTTGTGCACCGT[A/T]AGGTCTGTCTATCTT | 818568 |
rs346678167 | snp | C/T | | | intron-variant | HOS1 | TAIR10 | 2:16617550 | CCAGTTTGGTTTCAG[C/T]CTAAGGAACTTTGTT | 818568 |
rs346712257 | snp | C/T | | | utr-variant-5-prime | HOS1 | TAIR10 | 2:16612863 | CAACGGAGCCCTAGA[C/T]TGGTTTTATCACTCT | 818568 |
rs346719552 | snp | A/G | | | synonymous-codon | HOS1 | TAIR10 | 2:16615586 | GCAAGTCCTGTTAGA[A/G]AGGGATAACCCTGAA | 818568 |
rs346753048 | snp | A/G | | | missense | HOS1 | TAIR10 | 2:16617209 | GAATCCTCTCCAGAA[A/G]TAAATGTTGATAGAT | 818568 |
rs346755620 | snp | A/G | | | synonymous-codon | HOS1 | TAIR10 | 2:16614213 | TCAAGATGTGCAGAC[A/G]CTGAGAGAGAACATT | 818568 |
rs346759776 | snp | A/G | | | synonymous-codon | HOS1 | TAIR10 | 2:16617316 | CAACCATCTCAATGG[A/G]TCTTCACAGAAACCG | 818568 |
rs346773318 | snp | A/G | | | missense | HOS1 | TAIR10 | 2:16617398 | GATTTGGATGATCCA[A/G]TGGACATGTCTTCGA | 818568 |
rs346994695 | snp | A/T | | | missense | HOS1 | TAIR10 | 2:16617299 | ACAGTGAAATCTAGC[A/T]GCAACCATCTCAATG | 818568 |
rs347105573 | snp | C/T | | | intron-variant | HOS1 | TAIR10 | 2:16613662 | ATTCGTATGCTTGTG[C/T]TATTAGGAACTGTGT | 818568 |
rs347269192 | snp | C/G | | | intron-variant | HOS1 | TAIR10 | 2:16616660 | TTAGTGCTTAATAAC[C/G]TGTTGATGCTTGCAG | 818568 |
rs347315279 | snp | C/G | | | intron-variant | HOS1 | TAIR10 | 2:16616630 | TGTTAAAGGCTACAT[C/G]CTCACATTTGCGTTT | 818568 |
rs347385731 | snp | C/T | | | intron-variant | HOS1 | TAIR10 | 2:16614492 | CATCATCAGCTTGGA[C/T]CTGATTTTCTATCCC | 818568 |
rs347397960 | snp | A/G | | | intron-variant | HOS1 | TAIR10 | 2:16616336 | GGAAACTGCATCACT[A/G]TAGACCATGCTTATT | 818568 |
rs347428291 | snp | A/T | | | intron-variant | HOS1 | TAIR10 | 2:16616187 | CAATGATGGCTCTGT[A/T]TAGAATTAGCTCATT | 818568 |