SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs8169503 | snp | A/G | | | intron-variant, downstream-variant-500B | Fbxo3 | Rn_Celera | 3:93998095 | AAGGTTTTTTATTGA[A/G]CTCCAAAGACACATT | 690634 |
rs8172182 | snp | A/C | | | intron-variant, utr-variant-3-prime | Fbxo3 | Rn_Celera | 3:93995967 | CCCATACTTTACATC[A/C]ACTGAAACAAATATT | 690634 |
rs105001286 | snp | A/G | 0.375 | 0.216506 | intron-variant | Fbxo3 | Rn_Celera | 3:93973294 | TCATGAGCCTTTAGA[A/G]AATAAAATGTAAACT | 690634 |
rs105098892 | snp | A/G | 0 | 0 | intron-variant | Fbxo3 | Rn_Celera | 3:93972909 | GTTTAGATACGATAC[A/G]AAGGAAAGGATAAAT | 690634 |
rs105579673 | snp | A/G | 0 | 0 | intron-variant | Fbxo3 | Rn_Celera | 3:93987043 | AACATGCGAACATGA[A/G]ACCTTTTCAGATACT | 690634 |
rs106505538 | snp | G/T | 0.375 | 0.216506 | intron-variant | Fbxo3 | Rn_Celera | 3:93973063 | AACCTGAAGCGAGCT[G/T]CGGTGACCAGGTGAA | 690634 |
rs106887728 | snp | A/T | 0.375 | 0.216506 | intron-variant | Fbxo3 | Rn_Celera | 3:93973259 | GGAGGACAAGCAACC[A/T]TAGAAGGTACTTGAA | 690634 |
rs106895216 | snp | G/T | 0.5 | 0 | intron-variant | Fbxo3 | Rn_Celera | 3:93971699 | AAATAACTTTATGGT[G/T]GGGGTTCACAACATG | 690634 |
rs107184523 | snp | G/T | 0.5 | 0 | intron-variant | Fbxo3 | Rn_Celera | 3:93984705 | AATTCACTCGGTTAA[G/T]AAGAAAAATTCTGAT | 690634 |
rs197019075 | snp | C/T | 0 | 0 | intron-variant | Fbxo3 | Rn_Celera | 3:93988160 | CGAGCCCATGGTGGG[C/T]AAAAGCTACACCAAG | 690634 |
rs197071681 | snp | A/C | 0 | 0 | intron-variant | Fbxo3 | Rn_Celera | 3:93979160 | CTTGGTGAGCGACTT[A/C]AGAACCCTGCCCAGT | 690634 |
rs197126386 | snp | A/T | 0 | 0 | intron-variant | Fbxo3 | Rn_Celera | 3:93991611 | GGCAGACTTGTTTTG[A/T]TTGTCTGTTTAAGTA | 690634 |
rs197133979 | snp | A/G | 0 | 0 | intron-variant | Fbxo3 | Rn_Celera | 3:93981943 | AAATCTAATACATGC[A/G]TACTTTGTTTGAAAA | 690634 |
rs197171387 | snp | C/T | 0 | 0 | synonymous-codon | Fbxo3 | Rn_Celera | 3:93985091 | CATGCTTCCCAGCAA[C/T]CTGAGGATACAGACG | 690634 |
rs197180410 | snp | C/G | 0 | 0 | intron-variant | Fbxo3 | Rn_Celera | 3:93975768 | TCTGTCTCTGTCTCT[C/G]TCTCTCTCACACACA | 690634 |
rs197289229 | snp | C/T | 0 | 0 | utr-variant-3-prime | Fbxo3 | Rn_Celera | 3:94000446 | TTTCAAATTTCCTAA[C/T]GATTATTCACTTTAG | 690634 |
rs197289711 | snp | A/C | 0 | 0 | intron-variant | Fbxo3 | Rn_Celera | 3:93974061 | ATCTTTTTTCTTTTC[A/C]TTTGTCTTTTGAGTT | 690634 |
rs197356679 | snp | A/T | 0 | 0 | intron-variant, upstream-variant-2KB | Fbxo3, LOC108350426 | Rn_Celera | 3:93970475 | TCAAAAAAAAAAAAA[A/T]AAAACAAACCTGAAC | 690634 |
rs197577193 | snp | C/T | 0 | 0 | intron-variant | Fbxo3 | Rn_Celera | 3:93979347 | GGGCCATTCAAGATA[C/T]TTTTCTTTTTAATTA | 690634 |
rs197740712 | snp | C/T | 0 | 0 | intron-variant | Fbxo3 | Rn_Celera | 3:93992827 | CAAATAAAAGTGTCA[C/T]AGACACTTTGAGACA | 690634 |
rs197822167 | snp | A/T | 0 | 0 | intron-variant | Fbxo3 | Rn_Celera | 3:93973840 | TTTAACTTACTTTTT[A/T]GCTACAAAGAGAACG | 690634 |
rs197823822 | snp | A/T | 0 | 0 | intron-variant | Fbxo3 | Rn_Celera | 3:93986029 | GGTCTCCACCTACAC[A/T]GCTATGGGGAAGTCC | 690634 |
rs197977730 | snp | C/T | 0 | 0 | intron-variant | Fbxo3 | Rn_Celera | 3:93970849 | TGATCTCACCAGCCA[C/T]ACTCCATGCAGCTGC | 690634 |
rs198019313 | snp | A/G | 0 | 0 | intron-variant | Fbxo3 | Rn_Celera | 3:93975377 | CCACCTAGTGAGCAA[A/G]TCTGGAAAACTTCAG | 690634 |
rs198028288 | snp | C/T | 0 | 0 | intron-variant | Fbxo3 | Rn_Celera | 3:93973069 | GGCAATAACCTGAAG[C/T]GAGCTTCGGTGACCA | 690634 |
rs198064084 | snp | A/G | 0 | 0 | intron-variant | Fbxo3 | Rn_Celera | 3:93988407 | CAAGTTTCTTTTCCC[A/G]ATTCTAATTCTAATT | 690634 |
rs198146092 | snp | A/G | 0 | 0 | intron-variant | Fbxo3 | Rn_Celera | 3:93980409 | TCCATCTTAATGTAG[A/G]CACAGAGAGAAAAAC | 690634 |
rs198200354 | snp | A/G | 0 | 0 | intron-variant | Fbxo3 | Rn_Celera | 3:93986043 | GAAGACCAGGGCAGG[A/G]TCTCCACCTACACAG | 690634 |
rs198212047 | snp | C/T | 0 | 0 | intron-variant | Fbxo3 | Rn_Celera | 3:93981678 | TGCACACTTGAAACA[C/T]GGCCTGCATTCTAGC | 690634 |
rs198305785 | snp | C/T | 0 | 0 | intron-variant | Fbxo3 | Rn_Celera | 3:93977429 | ATTTGAAAACATAGA[C/T]GTAGTAGGCAATTTC | 690634 |
rs198501054 | snp | C/T | 0 | 0 | intron-variant | Fbxo3 | Rn_Celera | 3:93989768 | GATTCAGATATAAAA[C/T]GGTCCCCAAATGCTC | 690634 |
rs198649599 | snp | A/G | 0 | 0 | upstream-variant-2KB, intron-variant | Fbxo3, LOC108350426 | Rn_Celera | 3:93967618 | TGGCTCAGCTCTTTG[A/G]AATGTGGAAGGGTCA | 690634 |
rs198720908 | snp | A/T | 0 | 0 | intron-variant | Fbxo3 | Rn_Celera | 3:93975761 | CTGTCTCTGTCTCTC[A/T]CACACACACACACAC | 690634 |
rs198894243 | snp | C/T | 0 | 0 | intron-variant | Fbxo3 | Rn_Celera | 3:93986777 | CACTTCAACCTCCCG[C/T]GTGAGCTCTGTCTTG | 690634 |
rs198934335 | snp | A/G | 0 | 0 | intron-variant | Fbxo3 | Rn_Celera | 3:93981428 | GAAAAAGGAAAAACA[A/G]AAACAAAACAATCAA | 690634 |
rs198988112 | snp | A/C | 0 | 0 | intron-variant | Fbxo3 | Rnor_6.0 | 3:93983192 | TCAATCTCAATCTCT[A/C]TCTCTCTCTCTCTCT | 690634 |
rs199005694 | snp | A/C | 0 | 0 | intron-variant | Fbxo3 | Rn_Celera | 3:93992957 | TGAGCTAAATCCCCA[A/C]CCCTCAACATTTTTT | 690634 |
rs199018621 | snp | G/T | 0 | 0 | intron-variant | Fbxo3 | Rn_Celera | 3:93977503 | CACATAATGAACTCA[G/T]AAATGGAAAAGGTTG | 690634 |
rs199134300 | snp | A/T | 0 | 0 | intron-variant | Fbxo3 | Rn_Celera | 3:93987858 | TACATCTAGGAAAAA[A/T]GCATTAAGACAAATT | 690634 |
rs199221604 | snp | C/T | 0 | 0 | intron-variant | Fbxo3 | Rn_Celera | 3:93981816 | CGCTTCCTAGGTAAG[C/T]GCTCTACCACTGAGC | 690634 |
rs199311310 | snp | A/G | 0 | 0 | utr-variant-3-prime | Fbxo3 | Rn_Celera | 3:93998937 | AACATCTGTTCTTCA[A/G]CTATAGAATTGCTCT | 690634 |
rs199397843 | snp | A/G | 0 | 0 | upstream-variant-2KB, intron-variant | Fbxo3, LOC108350426 | Rn_Celera | 3:93968058 | TAAGCATAAGTTTGT[A/G]TTATCTAGACACAAT | 690634 |