SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs13481137 | snp | C/T | 0.484429 | 0.0868505 | synonymous-codon | Rnft1 | GRCm38.p3 | 11:86489141 | CCTCTTATATTACAC[C/T]TTTCATTCTCAGTCA | 76892 |
rs27027067 | snp | C/T | 0.132653 | 0.220748 | utr-variant-3-prime, downstream-variant-500B | Rps6kb1, Rnft1 | GRCm38.p3 | 11:86499499 | TCTCATGAGAATAAT[C/T]TTAGATCTAGCCCTT | 76892 |
rs27027068 | snp | G/T | 0.231111 | 0.249285 | downstream-variant-500B, utr-variant-3-prime | Rps6kb1, Rnft1 | Mm_Celera | 11:86498711 | TTATGTGAAACTAGA[G/T]TCCACATAGCTTGTT | 76892 |
rs27027069 | snp | A/G | 0.231111 | 0.249285 | downstream-variant-500B, utr-variant-3-prime | Rps6kb1, Rnft1 | Mm_Celera | 11:86498514 | AACCACTATTATGTG[A/G]GTACTAGAAACCAAA | 76892 |
rs27027070 | snp | A/G | 0.415225 | 0.187619 | utr-variant-3-prime | Rnft1 | GRCm38.p3 | 11:86497863 | AAACCAGAAAATGTA[A/G]TAAGGTTGTGGTACT | 76892 |
rs27027071 | snp | A/G | 0.475309 | 0.108333 | utr-variant-3-prime | Rnft1 | GRCm38.p3 | 11:86497274 | CTCAACCAGATAAAC[A/G]CCACATCACTTTTTG | 76892 |
rs27027072 | snp | C/T | 0.231111 | 0.249285 | utr-variant-3-prime | Rnft1 | Mm_Celera | 11:86496954 | TCTTCGCATTTATCA[C/T]CAGTAACAAGGAGAA | 76892 |
rs27027073 | snp | A/C | 0.124444 | 0.216185 | utr-variant-3-prime | Rnft1 | Mm_Celera | 11:86496851 | TTCTGCAAGAAGAAA[A/C]GGTAATGGCGCACTT | 76892 |
rs27027074 | snp | A/G | 0.124444 | 0.216185 | utr-variant-3-prime | Rnft1 | Mm_Celera | 11:86496768 | GCTGAATTCCACATC[A/G]AGGAGAAAGGGAGAA | 76892 |
rs27027075 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime | Rnft1 | Mm_Celera | 11:86496739 | AGTGCCTGCTTAGTG[C/T]GCACTGTGTCCTGGC | 76892 |
rs27027076 | snp | C/T | 0.231111 | 0.249285 | utr-variant-3-prime | Rnft1 | Mm_Celera | 11:86496709 | TATGAAAGCTTGCAC[C/T]CAAGGCTGTGGTGGA | 76892 |
rs27027077 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime | Rnft1 | Mm_Celera | 11:86496684 | GTTTTACAATCACCA[C/T]CTGTTGAGATATGAA | 76892 |
rs27027078 | snp | A/G | 0.231111 | 0.249285 | utr-variant-3-prime | Rnft1 | Mm_Celera | 11:86496568 | GTGGACCTGTTATGT[A/G]CTCCTTGCCACTAGC | 76892 |
rs27027079 | snp | A/C | 0.124444 | 0.216185 | utr-variant-3-prime | Rnft1 | Mm_Celera | 11:86496273 | AAAGGGGTTCAGGTA[A/C]TGTTTCCTGACAGGT | 76892 |
rs27027080 | snp | A/G | 0.124444 | 0.216185 | utr-variant-3-prime | Rnft1 | Mm_Celera | 11:86496070 | GGTATCACGAGACAT[A/G]TTTATAGTTCAGTTT | 76892 |
rs27027081 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Rnft1 | GRCm38.p3 | 11:86495671 | TAAAAAGCAGCACCC[A/G]GGAAAATAGTTAAGT | 76892 |
rs27027082 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnft1 | Mm_Celera | 11:86495663 | GCAGGTTTTAAAAAG[C/T]AGCACCCGGGAAAAT | 76892 |
rs27027083 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Rnft1 | Mm_Celera | 11:86493302 | TAGTGTTACAAATAG[A/G]CATTCATAAGCTCTT | 76892 |
rs27027084 | snp | C/G | 0.493827 | 0.0552116 | intron-variant | Rnft1 | GRCm38.p3 | 11:86493301 | GTAGTGTTACAAATA[C/G]ACATTCATAAGCTCT | 76892 |
rs27027085 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Rnft1 | Mm_Celera | 11:86493105 | AATTTTACCTTTGGT[A/C]TTTAGGTTTAGCATA | 76892 |
rs27027086 | snp | A/T | 0.489796 | 0.070696 | intron-variant | Rnft1 | GRCm38.p3 | 11:86493035 | TAAGCTTGAAATAAA[A/T]TCATAATGGACGACT | 76892 |
rs29386491 | snp | A/C | 0.444444 | 0.157135 | upstream-variant-2KB | Rnft1 | Mm_Celera | 11:86483617 | AGAAGCAGAAGCAAA[A/C]GAGCATTGGGATTTT | 76892 |
rs29389015 | snp | C/G | 0.5 | 0 | intron-variant | Rnft1 | GRCm38.p3 | 11:86491062 | TTTATTATTTTGTGT[C/G]TACCTCTCCACCACA | 76892 |
rs29409567 | snp | A/T | 0.5 | 0 | upstream-variant-2KB | Rnft1 | GRCm38.p3 | 11:86483635 | GCATTGGGATTTTTT[A/T]AAGTGCTTTTTGACT | 76892 |
rs29413222 | snp | G/T | 0.444444 | 0.157135 | upstream-variant-2KB | Rnft1 | GRCm38.p3 | 11:86484188 | GTCACACAACCTCTC[G/T]GCCCAGGCAGCCCAG | 76892 |
rs29420449 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rnft1 | Mm_Celera | 11:86487598 | AATTTCACCAGAAGA[A/G]GGGTTGTATCTGGGA | 76892 |
rs29421481 | snp | C/T | 0.5 | 0 | upstream-variant-2KB | Rnft1 | GRCm38.p3 | 11:86483815 | CAAAATTACTGGACA[C/T]GTAACTCAGAAGTGT | 76892 |
rs29442099 | snp | C/T | 0.444444 | 0.157135 | upstream-variant-2KB | Rnft1 | Mm_Celera | 11:86484365 | CGCAAGACGTGACAG[C/T]CACGCAGACTTAATT | 76892 |
rs29447630 | snp | C/G | 0.444444 | 0.157135 | upstream-variant-2KB | Rnft1 | Mm_Celera | 11:86483612 | CAGAGAGAAGCAGAA[C/G]CAAACGAGCATTGGG | 76892 |
rs29449465 | snp | A/G | 0.5 | 0 | intron-variant | Rnft1 | Mm_Celera | 11:86488989 | ATACATTGATCATCA[A/G]ATGAAAATGCTATTT | 76892 |
rs29452194 | snp | A/G | 0.5 | 0 | intron-variant | Rnft1 | Mm_Celera | 11:86486967 | GGAACTCACTTTGTA[A/G]ACCAGGCTGGCCTCG | 76892 |
rs29452462 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnft1 | GRCm38.p3 | 11:86491977 | TAGAAATGTAGAAAT[A/G]TACCTGTATATTTCT | 76892 |
rs29462549 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnft1 | Mm_Celera | 11:86486590 | TTTTAAAAATTATAT[C/T]AGTATATATAATCTT | 76892 |
rs29471277 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Rnft1 | GRCm38.p3 | 11:86489887 | CCAGGTCCAGGGGTC[G/T]GATGCCCTCTGCTGA | 76892 |
rs29473087 | snp | A/C/T | 0.444444 | 0.157135 | intron-variant | Rnft1 | GRCm38.p3 | 11:86486557 | TATTAATAATTTTAA[A/C/T]ATATTTTGGTTGCTA | 76892 |
rs29474236 | snp | A/T | 0.444444 | 0.157135 | upstream-variant-2KB | Rnft1 | Mm_Celera | 11:86483611 | ACAGAGAGAAGCAGA[A/T]GCAAACGAGCATTGG | 76892 |
rs29483839 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnft1 | Mm_Celera | 11:86486756 | GACAAGCAACTAAAT[C/T]ATTAACTCTTTCTCT | 76892 |
rs29484138 | snp | C/T | 0.5 | 0 | synonymous-codon | Rnft1 | Mm_Celera | 11:86486381 | ACCTGATGACTTTGC[C/T]ACAGAGTCTGGGGAA | 76892 |
rs29486208 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Rnft1 | GRCm38.p3 | 11:86490174 | AGGTGACATCTCTGA[C/T]TTAAAGCTATTGTAG | 76892 |
rs46651706 | snp | G/T | | | upstream-variant-2KB | Rnft1 | GRCm38.p3 | 11:86484410 | CCACTACGCCACTCG[G/T]ATAACATCACCAACA | 76892 |
rs46905919 | snp | C/T | | | upstream-variant-2KB | Rnft1 | Mm_Celera | 11:86483051 | TGTTATTTTTTGAGA[C/T]TTAGAGTTTTACTCT | 76892 |
rs47273026 | snp | C/T | | | upstream-variant-2KB | Rnft1 | Mm_Celera | 11:86483180 | TGTAACAAGATCTGA[C/T]GCCCTCTTCTGGAGT | 76892 |
rs47295568 | snp | A/G | | | upstream-variant-2KB | Rnft1 | GRCm38.p3 | 11:86482777 | GGCTGCTCTTCCAGA[A/G]GTCCTGAGTTCAATT | 76892 |
rs48581912 | snp | C/T | | | intron-variant | Rnft1 | Mm_Celera | 11:86490053 | CCCAGTGAGGTCAGC[C/T]TAGGTGAAAGAACAT | 76892 |
rs48686418 | snp | A/C | | | upstream-variant-2KB | Rnft1 | Mm_Celera | 11:86483131 | AAGGTCCAGAGTTCA[A/C]ATCCCAGCAACCACG | 76892 |
rs48725512 | snp | A/G | | | upstream-variant-2KB | Rnft1 | GRCm38.p3 | 11:86482979 | TGTTGTTCTGCTGTC[A/G]TTGGGGCGTGATTAT | 76892 |
rs49251775 | snp | G/T | | | upstream-variant-2KB | Rnft1 | Mm_Celera | 11:86483089 | GTGAGATGGCTCAGT[G/T]GGTAAGAGCACCCGA | 76892 |
rs50578753 | snp | A/C | | | upstream-variant-2KB | Rnft1 | GRCm38.p3 | 11:86482947 | ATTTGAACATTAGGT[A/C]TATTAAGTTTACAAA | 76892 |
rs50929817 | snp | A/G | | | upstream-variant-2KB | Rnft1 | Mm_Celera | 11:86483146 | AATCCCAGCAACCAC[A/G]TGGTGGCTCACAACC | 76892 |
rs51135995 | snp | A/T | | | upstream-variant-2KB | Rnft1 | Mm_Celera | 11:86483053 | TTATTTTTTGAGATT[A/T]AGAGTTTTACTCTGG | 76892 |
rs52279374 | snp | C/T | | | upstream-variant-2KB | Rnft1 | GRCm38.p3 | 11:86482877 | TATATACAGGGAGAA[C/T]GTTGTATACATACTA | 76892 |
rs52426435 | snp | C/T | | | intron-variant | Rnft1 | Mm_Celera | 11:86488577 | TTTAAATTTCTGTTT[C/T]GTGGAAGAGAAAAAA | 76892 |
rs108515818 | snp | A/G | | | intron-variant | Rnft1 | GRCm38.p3 | 11:86485594 | TCAGAGGACTTGTGG[A/G]AGTCAGTTCATTGCT | 76892 |
rs212022317 | snp | G/T | | | utr-variant-3-prime | Rnft1 | Mm_Celera | 11:86497578 | TCTCCAGGCAACTTG[G/T]TTTTTTAATATGATT | 76892 |
rs212031946 | snp | A/C | | | downstream-variant-500B, utr-variant-3-prime | Rps6kb1, Rnft1 | Mm_Celera | 11:86498654 | TGAGGTGTACTTAGG[A/C]AAATTGTTGATTATT | 76892 |
rs212039365 | snp | G/T | | | intron-variant | Rnft1 | Mm_Celera | 11:86485563 | AAAAATCTATTGTAT[G/T]TATTTAGTGTGTGTG | 76892 |
rs212050991 | in-del | -/AA | | | intron-variant | Rnft1 | GRCm38.p3 | 11:86494734 | TACCTAACACACAAG[-/AA]AAAAAAAAAAACTAA | 76892 |
rs212052180 | snp | C/T | | | upstream-variant-2KB | Rnft1 | Mm_Celera | 11:86484225 | TGGCGTAGCTAGCAA[C/T]ACGCAGCCGGAAGCC | 76892 |
rs212200235 | snp | C/T | | | intron-variant | Rnft1 | GRCm38.p3 | 11:86488255 | GTCCTGAGTTCAAAT[C/T]CCAGCCACCACATGG | 76892 |
rs212371796 | in-del | -/GCGTGCGCCACCAT | | | intron-variant | Rnft1 | Mm_Celera | 11:86492910 | GTGCTGGGATTAAAG[-/GCGTGCGCCACCAT]GCCCGGTGCAGCCAG | 76892 |
rs213703405 | snp | C/G | | | intron-variant | Rnft1 | Mm_Celera | 11:86494902 | CCCTCGGGTGTTTCT[C/G]ACCACCTCCCCCTTC | 76892 |
rs213710403 | snp | A/G | | | intron-variant | Rnft1 | Mm_Celera | 11:86493239 | CCGGTAAGTACTTTT[A/G]TCAGTTAAGGGAAAT | 76892 |
rs213781617 | snp | A/G | | | intron-variant | Rnft1 | Mm_Celera | 11:86495783 | AGTATGTGACCTAGA[A/G]TGCACTGTGTAAGAT | 76892 |
rs213794480 | snp | C/T | | | downstream-variant-500B, utr-variant-3-prime | Rps6kb1, Rnft1 | Mm_Celera | 11:86498795 | CTGTAACACTTAATA[C/T]ATAAAATGACCACTA | 76892 |
rs213942209 | snp | C/T | | | upstream-variant-2KB | Rnft1 | Mm_Celera | 11:86483274 | AAGAGTTTTACTCTG[C/T]ATCATAGATTGGCCT | 76892 |
rs214038130 | in-del | -/ACCACC | | | utr-variant-3-prime | Rnft1 | Mm_Celera | 11:86497102 | TTAAAGTCGTGTGCT[-/ACCACC]ACCACCACCACCACC | 76892 |
rs214436437 | snp | C/T | | | intron-variant | Rnft1 | Mm_Celera | 11:86490247 | ATAGTTCAATGCTAG[C/T]GCTCTGAACGCTCAT | 76892 |
rs214566250 | snp | G/T | | | intron-variant | Rnft1 | Mm_Celera | 11:86491358 | ACCTGTAGAAGCAAC[G/T]AACAGTTGCTTGGTT | 76892 |
rs214738650 | snp | A/G | | | intron-variant | Rnft1 | Mm_Celera | 11:86487060 | TGCGCTACCACACCC[A/G]GCTTAAGTTCCCTGT | 76892 |
rs214802806 | in-del | -/CCTGCTG | | | upstream-variant-2KB | Rnft1 | GRCm38.p3 | 11:86483013 | ACATTTCATGATTTT[-/CCTGCTG]CCTAAATTTGCATTT | 76892 |
rs214950407 | snp | C/T | | | intron-variant | Rnft1 | Mm_Celera | 11:86485660 | AAAGGTCTTGACTTA[C/T]CCAGCCATCTCACCC | 76892 |
rs215418267 | snp | A/T | | | intron-variant | Rnft1 | Mm_Celera | 11:86494629 | GAATTTAGTAAGGCT[A/T]GTGCTGAAATAGCCT | 76892 |
rs215607485 | snp | C/T | | | intron-variant | Rnft1 | GRCm38.p3 | 11:86488305 | ATGAGATTTGACTCC[C/T]TCTTCTGGTGTGTCT | 76892 |
rs215635020 | snp | C/T | | | upstream-variant-2KB | Rnft1 | Mm_Celera | 11:86484032 | TAGAAGTCGAGTTCC[C/T]TGCTCGCCAACACGG | 76892 |
rs215716260 | snp | A/G | | | intron-variant | Rnft1 | Mm_Celera | 11:86485474 | TCAGCATAAAATGAA[A/G]TGTTTATTATCTTTG | 76892 |
rs215881576 | snp | C/T | | | utr-variant-3-prime | Rnft1 | Mm_Celera | 11:86497318 | TTCACTCTATATTTG[C/T]GTATATTGTATGTGT | 76892 |
rs215891873 | snp | C/T | | | synonymous-codon | Rnft1 | Mm_Celera | 11:86495943 | CACTTCATCTCACCT[C/T]CAGATGTACTAAGTT | 76892 |
rs216089233 | snp | A/C | | | intron-variant | Rnft1 | Mm_Celera | 11:86487083 | TTCCCTGTCCTAATG[A/C]GTAACTAAGCAATTT | 76892 |
rs216560430 | in-del | -/CA | | | intron-variant | Rnft1 | Mm_Celera | 11:86485803 | GCTGATGTCTTTTGG[-/CA]CATTTGAAAAATCAA | 76892 |
rs216591521 | snp | A/G | | | intron-variant | Rnft1 | GRCm38.p3 | 11:86488162 | CCAGTGTTTTGACTT[A/G]GTGGTGAAGTCATGT | 76892 |
rs217010330 | snp | A/C | | | intron-variant | Rnft1 | Mm_Celera | 11:86491541 | GTCAGATTTGTGTTA[A/C]TCATAGTTCTGAAAT | 76892 |
rs217021481 | snp | C/T | | | intron-variant | Rnft1 | Mm_Celera | 11:86490326 | ATGTTTCTGTGTTGC[C/T]TTAATAAATGCTTAT | 76892 |
rs217055283 | in-del | -/A | | | intron-variant | Rnft1 | Mm_Celera | 11:86494549 | AAAAATTAGAAAAAG[-/A]AAAAAAAAATTCAGA | 76892 |
rs217163164 | snp | C/T | | | upstream-variant-2KB | Rnft1 | Mm_Celera | 11:86482693 | GTATGTACTGATATG[C/T]CTTCAGTGTGTTATA | 76892 |
rs217264619 | in-del | -/AAAG | | | upstream-variant-2KB | Rnft1 | Mm_Celera | 11:86483258 | TTTAAAAAAAAAAAA[-/AAAG]AGTTTTACTCTGTAT | 76892 |
rs218010474 | snp | G/T | | | upstream-variant-2KB | Rnft1 | Mm_Celera | 11:86483400 | AAAACTACTCACATA[G/T]GATCTCTGCTGTGCA | 76892 |
rs218820793 | snp | G/T | | | intron-variant | Rnft1 | Mm_Celera | 11:86494777 | GAGTGCATATACATA[G/T]ATCTGTCAACCCTAT | 76892 |
rs219314656 | in-del | -/AA | | | upstream-variant-2KB | Rnft1 | GRCm38.p3 | 11:86483246 | AATAAATAAATCTTT[-/AA]AAAAAAAAAAAAAGA | 76892 |
rs219362568 | in-del | -/TTTTT | | | intron-variant | Rnft1 | Mm_Celera | 11:86486894 | ATAAGTACCCTGTCC[-/TTTTT]TTTTTTTTTTTTTTG | 76892 |
rs219550589 | snp | A/T | | | utr-variant-3-prime | Rnft1 | Mm_Celera | 11:86497660 | GGCTATCACTTAAAA[A/T]TAGGAAAAGGGAAGT | 76892 |
rs219881671 | in-del | -/GAGCAA | | | intron-variant | Rnft1 | Mm_Celera | 11:86494089 | ATGGGTTGAGAGGGG[-/GAGCAA]GAGCAAGAGAAGAAG | 76892 |
rs220160833 | snp | C/T | | | intron-variant | Rnft1 | Mm_Celera | 11:86487541 | GTAATGTGAAAAGTT[C/T]TAATCATCTGAATCA | 76892 |
rs220378211 | snp | A/G | | | utr-variant-3-prime | Rnft1 | Mm_Celera | 11:86498020 | TGCTGCTAGGGCATA[A/G]AGCAATGGCTCAGCA | 76892 |
rs220433717 | snp | A/G | | | intron-variant | Rnft1 | Mm_Celera | 11:86491142 | CACTGTAACTTGCTG[A/G]TAGTAAGTTGCCACT | 76892 |
rs220561654 | snp | G/T | | | intron-variant | Rnft1 | Mm_Celera | 11:86492224 | AGGAGTAGCAAAGAT[G/T]AACATACACGTGCTA | 76892 |
rs220772590 | snp | C/T | | | intron-variant | Rnft1 | Mm_Celera | 11:86490859 | AGTCTTCACATCATA[C/T]ATCAGACAATTCTAA | 76892 |
rs220887736 | snp | G/T | | | synonymous-codon | Rnft1 | Mm_Celera | 11:86486135 | CAGCTGTAACCAACT[G/T]CATGATCCTCCGGGC | 76892 |
rs220978853 | snp | A/C | | | utr-variant-3-prime, downstream-variant-500B | Rps6kb1, Rnft1 | Mm_Celera | 11:86499356 | CAAATATTGTCACAA[A/C]TGTTTGTCCAGCTAG | 76892 |
rs221153158 | snp | C/T | | | intron-variant | Rnft1 | Mm_Celera | 11:86494243 | GCAGATAGATCTCTG[C/T]GAGTTAAGGCCAGCC | 76892 |
rs221408779 | in-del | -/TT | | | intron-variant | Rnft1 | Mm_Celera | 11:86494311 | AAAAAAAAAAAAAAA[-/TT]TCCTGTTAAAACAAA | 76892 |