SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs4136736 | snp | C/T | 0.5 | 0 | intron-variant | Gnb1 | Mm_Celera | 4:155503823 | CTCCCTTCCCTTCCC[C/T]CTCCTCTTCCTCTTC | 14688 |
rs4224992 | snp | A/T | 0.21875 | 0.248039 | downstream-variant-500B | Gnb1 | Mm_Celera | 4:155559316 | TCAGCAGTTGGGGCA[A/T]ACCCCCACACACTGA | 14688 |
rs6201741 | snp | A/C/T | 0.362812 | 0.2231 | intron-variant | Gnb1 | GRCm38.p3 | 4:155513202 | AGTGGTGTTTTTGCC[A/C/T]GTCTGTCTACCTGCC | 14688 |
rs6201771 | snp | A/G | 0.32 | 0.24 | intron-variant | Gnb1 | Mm_Celera | 4:155513223 | TCTACCTGCCTGCCT[A/G]CATGGCTTTATGGAT | 14688 |
rs6202809 | snp | C/T | 0.375 | 0.216506 | intron-variant | Gnb1 | Mm_Celera | 4:155513393 | ATTGGGTATTGGATT[C/T]GATTTTATTAAATTC | 14688 |
rs6203988 | snp | A/G | 0.375 | 0.216506 | intron-variant | Gnb1 | Mm_Celera | 4:155513625 | GTCCGGTGAGGAGTA[A/G]CATGGCCACAAGATT | 14688 |
rs6356815 | snp | A/G | 0.375 | 0.216506 | intron-variant | Gnb1 | Mm_Celera | 4:155527730 | GAACGTCTTCCTCCC[A/G]GGGAACTAGGTTTTG | 14688 |
rs6357161 | snp | G/T | 0.359862 | 0.224567 | intron-variant | Gnb1 | Mm_Celera | 4:155527743 | CCNGGGAACTAGGTT[G/T]TGGACCCTCTGTGTG | 14688 |
rs6357847 | snp | A/G | 0.290657 | 0.246672 | intron-variant | Gnb1 | Mm_Celera | 4:155527928 | CAGGAAGACCATTGG[A/G]ATGTATGTAACAGCT | 14688 |
rs6358226 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Gnb1 | Mm_Celera | 4:155527956 | GCTCTTAGGCCACCA[C/T]AGAGAGCAGACTTGT | 14688 |
rs6358255 | snp | A/G | 0.359862 | 0.224567 | intron-variant | Gnb1 | Mm_Celera | 4:155527979 | AGACTTGTCTACCTG[A/G]GTACAAAACTAAATG | 14688 |
rs6359224 | snp | C/T | 0.5 | 0 | intron-variant | Gnb1 | Mm_Celera | 4:155528151 | gttcttactatgtaa[C/T]tttgtcctgaaactc | 14688 |
rs6359288 | snp | A/G | 0.5 | 0 | intron-variant | Gnb1 | Mm_Celera | 4:155528188 | gaccagactggcctt[A/G]aatgcaACATTATAC | 14688 |
rs6359317 | snp | A/G | 0.5 | 0 | intron-variant | Gnb1 | Mm_Celera | 4:155528205 | atgcaACATTATACA[A/G]AGATAAGTATGTGGG | 14688 |
rs6359888 | snp | A/C | 0.375 | 0.216506 | intron-variant | Gnb1 | Mm_Celera | 4:155528317 | AAAATCCCAGTTTTT[A/C]GTTTGTGTAAGGATT | 14688 |
rs6360283 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Gnb1 | Mm_Celera | 4:155528352 | TATTTGAAATAGCTT[C/T]CTCTGATTTTCATGT | 14688 |
rs6360382 | snp | C/T | 0.32 | 0.24 | intron-variant | Gnb1 | Mm_Celera | 4:155528403 | CTGTCTGTCCTTGAG[C/T]GTCTCACTAAGCCTT | 14688 |
rs13464618 | snp | A/G | | | intron-variant | Gnb1 | Mm_Celera | 4:155502598 | GATGGTGGCCACACA[A/G]CAAGAGATGATGGAT | 14688 |
rs13474192 | snp | G/T | | | utr-variant-3-prime | Gnb1 | Mm_Celera | 4:155557572 | GTGGACACCCACACC[G/T]CCCCTCAGAACTTCA | 14688 |
rs13478069 | snp | C/G | 0.424016 | 0.179495 | intron-variant | Gnb1 | Mm_Celera | 4:155502576 | GTCGCTGCAGTGTCA[C/G]CTGGGCATCCATTAT | 14688 |
rs31762186 | snp | G/T | 0.375 | 0.216506 | intron-variant | Gnb1 | Mm_Celera | 4:155541010 | TGGATTTGATTCCCA[G/T]AACCAGAAAAGATAA | 14688 |
rs31768546 | snp | C/T | 0.375 | 0.216506 | intron-variant | Gnb1 | Mm_Celera | 4:155507897 | GTGAGTACACTGTTG[C/T]TCTCTTCAGACATAC | 14688 |
rs31770441 | snp | C/T | 0.375 | 0.216506 | intron-variant | Gnb1 | Mm_Celera | 4:155500044 | GAGATCTGCTTCTGC[C/T]TCCTGAGTGCTGGAA | 14688 |
rs31799306 | snp | C/T | 0.32 | 0.24 | intron-variant | Gnb1 | Mm_Celera | 4:155519145 | AAGTGAGTTCCAGGA[C/T]AGCCAGGGCTATCAG | 14688 |
rs31804954 | snp | C/T | 0.375 | 0.216506 | intron-variant | Gnb1 | Mm_Celera | 4:155548488 | TCCCATCTTGCTGGC[C/T]CTTGACCTTTATTCC | 14688 |
rs31815597 | snp | C/G | 0.375 | 0.216506 | intron-variant | Gnb1 | Mm_Celera | 4:155541016 | TGATTCCCATAACCA[C/G]AAAAGATAAAAAACC | 14688 |
rs31844863 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Gnb1 | Mm_Celera | 4:155521096 | TGGGTTTGGCTTTAT[A/G]GAGTTGGTCTAATCT | 14688 |
rs31855288 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Gnb1 | Mm_Celera | 4:155538612 | TTGGAAATACTAGGT[C/T]GTAGTTGAGTTCCCT | 14688 |
rs31870184 | snp | C/G | 0.345679 | 0.230967 | intron-variant | Gnb1 | Mm_Celera | 4:155533530 | GTTTAGGTGTTGTGA[C/G]TTGTGTCTGTTTTGG | 14688 |
rs31870343 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Gnb1 | Mm_Celera | 4:155495000 | TTTAGAAGTACACTA[C/T]CTGCAGTTACTAGTT | 14688 |
rs31877045 | snp | A/G | 0.415225 | 0.187619 | intron-variant | Gnb1 | Mm_Celera | 4:155493057 | CAGGTAATTTGTAGT[A/G]TTGGTTTGGTAGTAA | 14688 |
rs31880958 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Gnb1 | Mm_Celera | 4:155504738 | TAGTGCTTTATCCCA[C/T]GCGTCACATTTCCTT | 14688 |
rs31889532 | snp | A/G | 0.375 | 0.216506 | intron-variant | Gnb1 | Mm_Celera | 4:155499698 | GGTAACATACTATAG[A/G]AACTCTCAGGGTTTT | 14688 |
rs31913045 | snp | A/T | 0.456747 | 0.140554 | intron-variant | Gnb1 | Mm_Celera | 4:155514633 | GAGGGTTCTTCAGGC[A/T]TGTACTTACGGGACC | 14688 |
rs31914189 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Gnb1 | Mm_Celera | 4:155512729 | AGAAGCAACTAACAC[C/T]GAAGGGCATAGGGTC | 14688 |
rs31919925 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Gnb1 | Mm_Celera | 4:155493123 | AGCAATCAAGCCTTT[C/T]TCTGTGTGTGGTTAA | 14688 |
rs31972017 | snp | A/G | 0.456747 | 0.140554 | intron-variant | Gnb1 | Mm_Celera | 4:155542338 | CTAACTGTGTTACCA[A/G]TGTGCAGTTAGGTTA | 14688 |
rs31973404 | snp | A/C | 0.375 | 0.216506 | intron-variant | Gnb1 | GRCm38.p3 | 4:155497484 | ACATACATAAAATAA[A/C]TCTTAAGGAAAAAAA | 14688 |
rs31974636 | snp | C/T | 0.375 | 0.216506 | intron-variant | Gnb1 | Mm_Celera | 4:155524899 | TTATTATTATTATTA[C/T]AAAATTTGTGTGTGC | 14688 |
rs31985405 | snp | A/G/T | 0.32 | 0.24 | intron-variant | Gnb1 | GRCm38.p3 | 4:155525949 | ACTGGTGCATAGGTC[A/G/T]GGCTGGCCTTGAGTT | 14688 |
rs31993260 | snp | G/T | 0.375 | 0.216506 | intron-variant | Gnb1 | Mm_Celera | 4:155493433 | TTGCAAAAGGAAAAT[G/T]TCTTCCACTGGGTGT | 14688 |
rs32011072 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Gnb1 | Mm_Celera | 4:155493442 | GAAAATGTCTTCCAC[C/T]GGGTGTTTGGCCAGG | 14688 |
rs32016938 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Gnb1 | Mm_Celera | 4:155541284 | TTGAGAATGTAAGCA[A/G]GAGCCTCAAGCATTA | 14688 |
rs32042073 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Gnb1 | Mm_Celera | 4:155528514 | TTTTAGCCAACTTTT[A/G]CTTGAATTTAAGAAA | 14688 |
rs32059492 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Gnb1 | Mm_Celera | 4:155540718 | TGTTGCTGACCCATT[A/G]AGCTTGGCACACAGT | 14688 |
rs32060814 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Gnb1 | Mm_Celera | 4:155533480 | TTTCTCCCGGGCCTG[C/T]CCAGAGTTCTATGGG | 14688 |
rs32079220 | snp | C/G | 0.32 | 0.24 | intron-variant | Gnb1 | Mm_Celera | 4:155518713 | ACTTCAGTCAGTGTG[C/G]GGGAGGGAAGGAAAT | 14688 |
rs32117964 | snp | A/T | 0.375 | 0.216506 | intron-variant | Gnb1 | Mm_Celera | 4:155548042 | TATAGTAGTAGTAGT[A/T]GTTGTTGTTGTTGTT | 14688 |
rs32130340 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Gnb1 | Mm_Celera | 4:155499331 | TCTCTGAGTTTGAGG[G/T]AAGCATGGTCTGCAT | 14688 |
rs32173611 | snp | A/C | 0.32 | 0.24 | intron-variant | Gnb1 | Mm_Celera | 4:155504462 | CCTGTTAGGTGTATA[A/C]TGCTTTGCCATTGAG | 14688 |
rs32202623 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Gnb1 | Mm_Celera | 4:155506350 | TGTTTTTTGTTTTTT[G/T]TTTTCCTTCTCTTCA | 14688 |
rs32208543 | snp | A/G | 0.401235 | 0.199068 | intron-variant | Gnb1 | Mm_Celera | 4:155508158 | CATCTCCCATCCCTA[A/G]TTCTGCTTACCCTAG | 14688 |
rs32242014 | snp | G/T | 0.375 | 0.216506 | intron-variant | Gnb1 | Mm_Celera | 4:155536894 | AATAAACCAGGGGCT[G/T]GTGAGATGGCTCAGT | 14688 |
rs32245927 | snp | C/T | 0.32 | 0.24 | intron-variant | Gnb1 | Mm_Celera | 4:155544635 | GTCCTCTGTTAGTCT[C/T]TGGATAGGCATACAC | 14688 |
rs32259888 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Gnb1 | Mm_Celera | 4:155500750 | ATTGACACAGTATCC[A/G]GTATTTTAATGGATG | 14688 |
rs32261157 | snp | C/T | 0.375 | 0.216506 | intron-variant | Gnb1 | Mm_Celera | 4:155529953 | TCAAGAAGAGGGCAT[C/T]AGATTTTTGTTACAG | 14688 |
rs32270948 | snp | A/G | 0.375 | 0.216506 | intron-variant | Gnb1 | Mm_Celera | 4:155494790 | GTGGTGGCGCACTCT[A/G]GAGGCAGAGGCAGAG | 14688 |
rs32271213 | snp | A/G | 0.375 | 0.216506 | intron-variant | Gnb1 | Mm_Celera | 4:155506565 | GAAAAAGAAAGAAAG[A/G]AAGAAGGAAAAGTAC | 14688 |
rs32279030 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Gnb1 | Mm_Celera | 4:155540688 | GATGACCTCGGAGGG[C/T]GATAGAAGAGCTTGT | 14688 |
rs32299874 | snp | A/G | 0.456747 | 0.140554 | intron-variant | Gnb1 | Mm_Celera | 4:155495612 | CGGCGCGGAACAAGT[A/G]CTCTTGACATCTGAG | 14688 |
rs32305389 | snp | C/T | 0.375 | 0.216506 | intron-variant | Gnb1 | Mm_Celera | 4:155516619 | ATCTGAACTCAGGAG[C/T]TCACGCTTGTGTATT | 14688 |
rs32317921 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Gnb1 | Mm_Celera | 4:155529981 | CAGATGGTTGTGAGT[C/T]ACCATGTGGTTGCTG | 14688 |
rs32323078 | snp | A/C | 0.32 | 0.24 | intron-variant | Gnb1 | Mm_Celera | 4:155520801 | TTTATTTATTATTAT[A/C]CATAAGTACACTGTA | 14688 |
rs32338887 | snp | A/G | 0.32 | 0.24 | intron-variant | Gnb1 | Mm_Celera | 4:155504650 | ATTATACCTGAAAGA[A/G]ACCTCTTTCCAAATA | 14688 |
rs32350906 | snp | A/G | 0.375 | 0.216506 | intron-variant | Gnb1 | Mm_Celera | 4:155555950 | TTTGGAGGAGGGAGG[A/G]AGGGTTGTGACCATG | 14688 |
rs32355733 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Gnb1 | Mm_Celera | 4:155499383 | GGCTTTAAAAAAACC[A/G]TTAGTCCAGGCTGCA | 14688 |
rs32358985 | snp | A/G | 0.375 | 0.216506 | intron-variant | Gnb1 | Mm_Celera | 4:155516575 | ATATAGGCAGTCACT[A/G]TCATGCCCAGTTTTC | 14688 |
rs32365498 | snp | A/C | 0.375 | 0.216506 | intron-variant | Gnb1 | Mm_Celera | 4:155536733 | AAAATAAAGATCATA[A/C]AAAAAAAACCTAAGC | 14688 |
rs32372413 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Gnb1 | Mm_Celera | 4:155537580 | CTAGAACAGGGAAAC[A/C]GTCTGCTTCCTTTGA | 14688 |
rs32383946 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Gnb1 | Mm_Celera | 4:155533783 | AATGCGCAGTCTGCC[A/G]CGGGCTTGTATCATG | 14688 |
rs32393296 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Gnb1 | Mm_Celera | 4:155505484 | AATGTTTAGCTGAAA[C/T]ATACTTTACAATACT | 14688 |
rs32427136 | snp | A/T | 0.359862 | 0.224567 | intron-variant | Gnb1 | Mm_Celera | 4:155542363 | AGGTTATTGCATGTG[A/T]GTGTCAGAGAGAATG | 14688 |
rs32441407 | snp | C/T | 0.375 | 0.216506 | intron-variant | Gnb1 | Mm_Celera | 4:155517445 | CGTTCTGTCTGCATG[C/T]ATCCTGCAGGGCAGA | 14688 |
rs32445206 | snp | A/T | 0.49827 | 0.0293608 | intron-variant | Gnb1 | Mm_Celera | 4:155519556 | TGTACCGGAACAAAA[A/T]GATGCTGGCACAGCA | 14688 |
rs32513883 | snp | A/G | 0.32 | 0.24 | intron-variant | Gnb1 | Mm_Celera | 4:155492832 | TTGCTGTTTTGCCTG[A/G]ATGTGTCTGTGTCTG | 14688 |
rs32538240 | snp | G/T | 0.32 | 0.24 | intron-variant | Gnb1 | Mm_Celera | 4:155504414 | CAGGGTGCAGGCAGG[G/T]GTATGCTGCAACTGC | 14688 |
rs32578127 | snp | A/T | 0.375 | 0.216506 | intron-variant | Gnb1 | Mm_Celera | 4:155536732 | AAAAATAAAGATCAT[A/T]AAAAAAAAACCTAAG | 14688 |
rs32602118 | snp | A/G | 0.32 | 0.24 | intron-variant | Gnb1 | Mm_Celera | 4:155519123 | TTTGCGGCCAGCCTG[A/G]TCTACAAAGTGAGTT | 14688 |
rs32629396 | snp | C/T | 0.375 | 0.216506 | intron-variant | Gnb1 | Mm_Celera | 4:155499704 | ATACTATAGGAACTC[C/T]CAGGGTTTTATTTTA | 14688 |
rs32631267 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Gnb1 | Mm_Celera | 4:155535216 | AGGGCTTCTGCATGC[C/T]AAAAATATTCTCTCA | 14688 |
rs32665084 | snp | C/T | | | intron-variant | Gnb1 | GRCm38.p3 | 4:155529980 | ACAGATGGTTGTGAG[C/T]TACCATGTGGTTGCT | 14688 |
rs32691659 | snp | A/T | 0.375 | 0.216506 | intron-variant | Gnb1 | Mm_Celera | 4:155521489 | TACAGTGAGACCCTG[A/T]CTCAAAAAACCAAAG | 14688 |
rs32698867 | snp | C/T | 0.375 | 0.216506 | intron-variant | Gnb1 | Mm_Celera | 4:155514608 | AGACCCTGCTTCAGA[C/T]GAAGGCTTTGAGGGT | 14688 |
rs32715640 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Gnb1 | Mm_Celera | 4:155520095 | TTTCCCTTCTAAAAA[C/T]GTATATACAGCTGAA | 14688 |
rs32730534 | snp | A/G | 0.375 | 0.216506 | intron-variant | Gnb1 | Mm_Celera | 4:155493440 | AGGAAAATGTCTTCC[A/G]CTGGGTGTTTGGCCA | 14688 |
rs32737246 | snp | A/C | 0.375 | 0.216506 | intron-variant | Gnb1 | Mm_Celera | 4:155494562 | CTGGGCTGGAGGTTC[A/C]GGTACTTGGTGCCAA | 14688 |
rs32747859 | snp | A/G | 0.32 | 0.24 | intron-variant | Gnb1 | Mm_Celera | 4:155525825 | AGTTCAGGCAGGCAC[A/G]CAGGCATTTCTATGT | 14688 |
rs32751006 | snp | C/T | 0.375 | 0.216506 | intron-variant | Gnb1 | Mm_Celera | 4:155550318 | TCTGATGTAACATGG[C/T]GTTGCCATTTAGTAT | 14688 |
rs32773463 | snp | C/G | 0.32 | 0.24 | intron-variant | Gnb1 | Mm_Celera | 4:155544394 | AAGAAGCATGGTATA[C/G]TTCTCAAGTATATGA | 14688 |
rs32777887 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Gnb1 | Mm_Celera | 4:155515505 | TAGATGCTTTAATGA[A/G]TAAAGCAGTTTGTTG | 14688 |
rs32780233 | snp | C/T | 0.375 | 0.216506 | intron-variant | Gnb1 | Mm_Celera | 4:155506636 | CTGTTTACGCTATGG[C/T]AAAGTCCCCTGACTG | 14688 |
rs32786951 | snp | A/G | 0.375 | 0.216506 | intron-variant | Gnb1 | Mm_Celera | 4:155494577 | CGGTACTTGGTGCCA[A/G]CCAAGCCTGAGCACC | 14688 |
rs32793628 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Gnb1 | Mm_Celera | 4:155493630 | GGGTTCTGACTGCAC[G/T]TATTTCACTTCTACA | 14688 |
rs32796590 | snp | A/C | 0.375 | 0.216506 | intron-variant | Gnb1 | Mm_Celera | 4:155506628 | AAGAATTCCTGTTTA[A/C]GCTATGGTAAAGTCC | 14688 |
rs32813953 | snp | A/G | 0.5 | 0 | intron-variant | Gnb1 | Mm_Celera | 4:155533971 | TTTAAAACATGTACC[A/G]GGCTGATGAGATGAC | 14688 |
rs32817495 | snp | A/G | 0.375 | 0.216506 | intron-variant | Gnb1 | Mm_Celera | 4:155548640 | CAGCGAAGCCAGAGT[A/G]AGGGTACTGGGTTTC | 14688 |
rs32830167 | snp | C/T | 0.32 | 0.24 | intron-variant | Gnb1 | Mm_Celera | 4:155519096 | GGAGGCAGAGGCAGG[C/T]GGATTTCAGAGTTTG | 14688 |
rs32860598 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Gnb1 | Mm_Celera | 4:155532424 | AATGATTGATTAAAT[A/G]GATCAGTCTACATGA | 14688 |
rs32869707 | snp | C/T | 0.32 | 0.24 | intron-variant | Gnb1 | Mm_Celera | 4:155519110 | GTGGATTTCAGAGTT[C/T]GCGGCCAGCCTGATC | 14688 |
rs32878949 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Gnb1 | Mm_Celera | 4:155537530 | TGAGCTTCCGGTTCA[G/T]TGTGAGACTGCTTGA | 14688 |