SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3681439 | snp | A/C | 0.5 | 0 | intron-variant | Rhobtb3 | Mm_Celera | 13:75930949 | GGCGGCATCTCTCCA[A/C]TCCCATATTTCCACT | 73296 |
rs3681946 | snp | A/G | 0.359862 | 0.224567 | intron-variant | Rhobtb3 | Mm_Celera | 13:75930978 | CTTTTAAAATCTCAA[A/G]ATGGCAAGCTAAGCC | 73296 |
rs3701340 | snp | C/T | 0.5 | 0 | intron-variant | Rhobtb3 | Mm_Celera | 13:75877257 | AACTGTAGCCTCATT[C/T]AGCCAAACTTTTGAA | 73296 |
rs3701352 | snp | A/C | 0.5 | 0 | intron-variant | Rhobtb3 | Mm_Celera | 13:75877265 | CCTCATTCAGCCAAA[A/C]TTTTGAATGAATACT | 73296 |
rs3701356 | snp | G/T | 0.5 | 0 | intron-variant | Rhobtb3 | Mm_Celera | 13:75877270 | TTCAGCCAAACTTTT[G/T]AATGAATACTAGTCT | 73296 |
rs3701916 | snp | A/T | 0.5 | 0 | intron-variant | Rhobtb3 | Mm_Celera | 13:75877339 | TCTGTGTATTTTAAA[A/T]CAAAAGAGCCCCACC | 73296 |
rs3702968 | snp | C/G | 0.484429 | 0.0868505 | utr-variant-3-prime | Rhobtb3 | Mm_Celera | 13:75870950 | CAGACACCATCGTCT[C/G]TACATCTAGGATATC | 73296 |
rs3703582 | snp | A/G | 0.375 | 0.216506 | utr-variant-3-prime | Rhobtb3 | Mm_Celera | 13:75871062 | CAATTCAAGCCATTG[A/G]CATCATATTCTTAAC | 73296 |
rs3704844 | snp | C/T | 0.444444 | 0.157135 | utr-variant-3-prime | Rhobtb3 | Mm_Celera | 13:75871267 | AACTGGGGGAGTGTT[C/T]CAAAACCAACAAAAA | 73296 |
rs3705339 | snp | C/G | 0.387812 | 0.208586 | utr-variant-3-prime | Rhobtb3 | Mm_Celera | 13:75871309 | TTTCTTACTGCCAGG[C/G]AATGTCTTTGTAGAG | 73296 |
rs3705368 | snp | A/G | 0.48 | 0.0979796 | utr-variant-3-prime | Rhobtb3 | Mm_Celera | 13:75871321 | AGGGAATGTCTTTGT[A/G]GAGGCGCTTGAGCAT | 73296 |
rs3717315 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Rhobtb3 | Mm_Celera | 13:75877571 | TGAGAGAAGATGTAC[A/G]GTTAGACTACTGCTC | 73296 |
rs3717885 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Rhobtb3 | Mm_Celera | 13:75877633 | TGTGTACTTCTATTT[G/T]TTACATCTATTACAT | 73296 |
rs3720315 | snp | A/G | 0.375 | 0.216506 | utr-variant-3-prime | Rhobtb3 | Mm_Celera | 13:75871450 | TTTGAGTGAGAAAAA[A/G]ACTTAAGCCAGGCAT | 73296 |
rs4135504 | snp | A/G | 0.5 | 0 | intron-variant | Rhobtb3 | Mm_Celera | 13:75877693 | GTTATTATTTCGGCA[A/G]TACTTAATATAAACA | 73296 |
rs6222990 | snp | A/T | 0.5 | 0 | upstream-variant-2KB | Rhobtb3 | Mm_Celera | 13:75945699 | CTGATCTAGAACCCT[A/T]GGGCTTACTAAGCAG | 73296 |
rs6223508 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | Rhobtb3 | Mm_Celera | 13:75945775 | AATGAGTTATGAACT[A/G]GCTTTTGTAAATGAA | 73296 |
rs6223616 | snp | C/G | 0.5 | 0 | upstream-variant-2KB | Rhobtb3 | Mm_Celera | 13:75945830 | ATGGATGATCCTTAA[C/G]GATGTGGTGCTATGT | 73296 |
rs6315111 | snp | C/T | 0.444444 | 0.157135 | upstream-variant-2KB | Rhobtb3 | Mm_Celera | 13:75944624 | GAGTTCTTGTTTATC[C/T]TTTTGGTTATTTGCT | 73296 |
rs6376275 | snp | A/C | 0.5 | 0 | intron-variant | Rhobtb3 | Mm_Celera | 13:75913310 | TCTCTAAGATCTGTG[A/C]CTTGTAAGAAANGTG | 73296 |
rs6376298 | snp | C/T | 0.5 | 0 | intron-variant | Rhobtb3 | Mm_Celera | 13:75913322 | GTGNCTTGTAAGAAA[C/T]GTGTTTTAATGCCGC | 73296 |
rs6389833 | snp | C/T | 0.5 | 0 | intron-variant | Rhobtb3 | Mm_Celera | 13:75913514 | TGTGTTCCAAACCTC[C/T]CCTGCAAATGTTCCN | 73296 |
rs6389856 | snp | A/G | 0.5 | 0 | intron-variant | Rhobtb3 | Mm_Celera | 13:75913529 | NCCTGCAAATGTTCC[A/G]ATGTTAGCACCAATA | 73296 |
rs6390864 | snp | A/T | 0.5 | 0 | intron-variant | Rhobtb3 | Mm_Celera | 13:75913694 | AGATACACTTGCTTA[A/T]GAAAAAAAAATATTT | 73296 |
rs13475470 | snp | A/G | | | intron-variant | Rhobtb3 | Mm_Celera | 13:75929998 | TGTGGGAGCTAGATG[A/G]GAACGAGACACTTAT | 73296 |
rs13481885 | snp | A/G | 0.46401 | 0.129228 | intron-variant | Rhobtb3 | Mm_Celera | 13:75915941 | AAAGATCTCACACTT[A/G]AGGTAGAGTTGTTTT | 73296 |
rs29222501 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rhobtb3 | Mm_Celera | 13:75901020 | AAAAGGACCCTGATA[C/T]AGCTGTCTCCTGAGA | 73296 |
rs29224027 | snp | C/T | 0.5 | 0 | intron-variant | Rhobtb3 | Mm_Celera | 13:75878740 | CCGAGAGCAATCTAC[C/T]AAAACGAGTAAGAAG | 73296 |
rs29225081 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rhobtb3 | Mm_Celera | 13:75938425 | TACAGAGGATGTTAC[A/G]CTTAAGTAAACACAT | 73296 |
rs29225447 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Rhobtb3 | Mm_Celera | 13:75907738 | AATTAAAGAACGATT[A/G]GTAAGAAGCTCAGAG | 73296 |
rs29225523 | snp | A/C | 0.375 | 0.216506 | intron-variant | Rhobtb3 | Mm_Celera | 13:75908633 | TCAGGGGCATGGATG[A/C]GGGTACAGGGAACCC | 73296 |
rs29225751 | snp | C/T | 0.49827 | 0.0293608 | intron-variant | Rhobtb3 | Mm_Celera | 13:75878652 | AATGCAATGTTCTCC[C/T]TATCTCAACTCCAAA | 73296 |
rs29227092 | snp | A/T | 0.375 | 0.216506 | intron-variant | Rhobtb3 | Mm_Celera | 13:75943103 | AACACAAAAACAAAC[A/T]AAAAAAACTCTCCAG | 73296 |
rs29229483 | snp | G/T | 0.375 | 0.216506 | intron-variant | Rhobtb3 | Mm_Celera | 13:75942985 | TTGAAACACAGTAAC[G/T]GCTCTATATTGCCCT | 73296 |
rs29229606 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rhobtb3 | Mm_Celera | 13:75894018 | AAAGGAAAGCCCACT[C/T]CAGCATGAACTCCAC | 73296 |
rs29231173 | snp | A/G | 0.359862 | 0.224567 | intron-variant | Rhobtb3 | Mm_Celera | 13:75928414 | GTCTCCAAGAGAATT[A/G]TCCAGCTCACTGAAA | 73296 |
rs29231739 | snp | A/T | 0.375 | 0.216506 | intron-variant | Rhobtb3 | Mm_Celera | 13:75911870 | TAATCTAAGTGAGTG[A/T]GTTTAATTTCAGCAG | 73296 |
rs29232779 | snp | A/G | 0.5 | 0 | intron-variant | Rhobtb3 | Mm_Celera | 13:75882636 | GTCCCTATTTATAGG[A/G]GAGAAGATTACAGTG | 73296 |
rs29234760 | snp | A/C | 0.375 | 0.216506 | intron-variant | Rhobtb3 | Mm_Celera | 13:75942691 | ATTAGCACTATTAAA[A/C]ACTAGTCTTTTCAGA | 73296 |
rs29235202 | snp | C/T | 0.5 | 0 | intron-variant | Rhobtb3 | Mm_Celera | 13:75894105 | GCACCACAGCACCCA[C/T]TGGGGCAACGGGCAT | 73296 |
rs29236936 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rhobtb3 | Mm_Celera | 13:75919272 | ACAGCCAGATTTATA[A/G]AAGCGTTTTCTCAGT | 73296 |
rs29237034 | snp | A/T | 0.492188 | 0.0620098 | intron-variant | Rhobtb3 | Mm_Celera | 13:75929833 | GTACCCTGTCCTGCA[A/T]GAGCTCGGTATGAAT | 73296 |
rs29237464 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rhobtb3 | Mm_Celera | 13:75908661 | CCCTTTCTTTTCTTT[C/T]CCCTTTGTCCAATGG | 73296 |
rs29239444 | snp | C/T | 0.5 | 0 | intron-variant | Rhobtb3 | Mm_Celera | 13:75874102 | TTCTAAAGCTGAAAA[C/T]GAACAGTCCCACCCA | 73296 |
rs29239681 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rhobtb3 | Mm_Celera | 13:75883038 | CATTATCATTCTCAT[A/G]TTACTTCCTAAAGCT | 73296 |
rs29240266 | snp | C/G | 0.426035 | 0.177515 | intron-variant | Rhobtb3 | Mm_Celera | 13:75928748 | GAAACACTTTTAAGT[C/G]GTCCATCATCCCTAA | 73296 |
rs29241088 | snp | A/G | 0.32 | 0.24 | intron-variant | Rhobtb3 | Mm_Celera | 13:75919277 | CAGATTTATAAAAGC[A/G]TTTTCTCAGTAGAGG | 73296 |
rs29241709 | snp | C/T | 0.46875 | 0.121031 | intron-variant | Rhobtb3 | Mm_Celera | 13:75911879 | TGAGTGAGTTTAATT[C/T]CAGCAGCAACAGAAA | 73296 |
rs29241772 | snp | C/T | 0.444444 | 0.157135 | utr-variant-3-prime | Rhobtb3 | Mm_Celera | 13:75870852 | CAATAAATAGTAATA[C/T]GTTTCTTCCATGCCT | 73296 |
rs29242076 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Rhobtb3 | Mm_Celera | 13:75879524 | CCATGCCATCTTCCC[A/T]CTGCTGCAACACAAG | 73296 |
rs29244532 | snp | A/G | 0.5 | 0 | intron-variant | Rhobtb3 | Mm_Celera | 13:75927931 | CAGATTTGTCCTTCA[A/G]AGCTATTTGTACTAT | 73296 |
rs29244780 | snp | G/T | 0.375 | 0.216506 | intron-variant | Rhobtb3 | Mm_Celera | 13:75901052 | GCCCTGCCAGTGCCT[G/T]AGTAGTACAGAAGTG | 73296 |
rs29244855 | snp | A/T | 0.375 | 0.216506 | intron-variant | Rhobtb3 | Mm_Celera | 13:75897514 | TGAAACTAACAGAAG[A/T]TATGAAACGAATGGA | 73296 |
rs29244936 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rhobtb3 | Mm_Celera | 13:75941529 | GTTGTCCAAAGCGCT[A/G]TTTGATATTCCGACT | 73296 |
rs29246048 | snp | C/T | 0.32 | 0.24 | intron-variant | Rhobtb3 | Mm_Celera | 13:75902076 | ACGGAAACATATACA[C/T]AGGGAAAACATTTAT | 73296 |
rs29246120 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Rhobtb3 | Mm_Celera | 13:75901939 | CTCCAATGGGGTGTT[C/T]TGAAGACAGAATTCA | 73296 |
rs29246589 | snp | G/T | 0.5 | 0 | intron-variant | Rhobtb3 | Mm_Celera | 13:75908601 | GAGGGAATTCAGAAA[G/T]TTGTCCCAAGTAACT | 73296 |
rs29246932 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Rhobtb3 | Mm_Celera | 13:75928686 | TTAGGTGGGAAAAAT[G/T]ACAGATTTTTCTCTG | 73296 |
rs29250196 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Rhobtb3 | GRCm38.p3 | 13:75902111 | ATGAATTATTTAACT[C/T]TGCTAGTGACTCAAT | 73296 |
rs29250451 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Rhobtb3 | Mm_Celera | 13:75874313 | CTTCTCTGATGCCAT[A/G]GTTCATAATTACAGA | 73296 |
rs29250482 | snp | A/C/T | 0.5 | 0 | intron-variant | Rhobtb3 | GRCm38.p3 | 13:75897172 | CAAATACAGACACTA[A/C/T]CTCAGAGTAAAAGGC | 73296 |
rs29250813 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Rhobtb3 | Mm_Celera | 13:75910374 | TAATTCTACTCCGTC[A/G]TATACTTAAAGATGG | 73296 |
rs29492553 | snp | A/G | 0.5 | 0 | intron-variant | Rhobtb3 | Mm_Celera | 13:75914403 | AGTAATCTGAGTCAC[A/G]TGTCTGAGAGCCTCG | 73296 |
rs29492617 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rhobtb3 | Mm_Celera | 13:75939161 | TGGGGAATGTAGCCT[C/T]GCCCATGGAATGGAC | 73296 |
rs29493046 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rhobtb3 | Mm_Celera | 13:75937795 | CAACGTGAAAGTTTA[C/T]GTCTAGGTAGAGAGC | 73296 |
rs29493986 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rhobtb3 | Mm_Celera | 13:75874397 | GAATCATACCATAGG[C/T]ACTAAAGATGTGACC | 73296 |
rs29495065 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rhobtb3 | GRCm38.p3 | 13:75923500 | TAATAGTGGGAGAGA[A/G]ACTTCAACACACCAC | 73296 |
rs29513482 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rhobtb3 | Mm_Celera | 13:75938689 | GGTGAGCCAATATGT[A/G]GCACTCCTCAATGGC | 73296 |
rs29516661 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rhobtb3 | Mm_Celera | 13:75937650 | GTACAGAGAGGCAGA[A/G]GGAATTTAGTAGGCA | 73296 |
rs29516765 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rhobtb3 | Mm_Celera | 13:75942910 | GCCAGTGGAACTTCG[C/T]GACCCTGTTTGGGGT | 73296 |
rs29527655 | snp | A/C | 0.265928 | 0.249492 | intron-variant | Rhobtb3 | Mm_Celera | 13:75919414 | TCAGCAACAAGGCAG[A/C]CGTACCTGAGACCAC | 73296 |
rs29531766 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rhobtb3 | Mm_Celera | 13:75942690 | CATTAGCACTATTAA[A/G]AACTAGTCTTTTCAG | 73296 |
rs29533897 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Rhobtb3 | Mm_Celera | 13:75927912 | CTGCATCCTAGAAAC[C/G]TTACAGATTTGTCCT | 73296 |
rs29533955 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rhobtb3 | Mm_Celera | 13:75911436 | GATGTCAAGGGCCAC[A/G]GTTCAATGACAGTGA | 73296 |
rs29548097 | snp | G/T | 0.493827 | 0.0552116 | intron-variant | Rhobtb3 | Mm_Celera | 13:75909021 | TTCTAAGTTTAAACA[G/T]TAAAACCTGTAGAAC | 73296 |
rs29548421 | snp | C/T | 0.5 | 0 | intron-variant | Rhobtb3 | Mm_Celera | 13:75897113 | GACTGGTAAGGTAAA[C/T]AGAACCCAACATTTT | 73296 |
rs29550526 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rhobtb3 | Mm_Celera | 13:75929233 | TTACAGAGGAAGTTT[C/T]TTCCTCCGAGTCACT | 73296 |
rs29550590 | snp | A/G | 0.33241 | 0.236027 | intron-variant | Rhobtb3 | Mm_Celera | 13:75880926 | AGCTTAAACAAACTG[A/G]ATGGTCTACCATTTG | 73296 |
rs29553073 | snp | A/G | 0.5 | 0 | intron-variant | Rhobtb3 | Mm_Celera | 13:75899971 | GAACACCAATGGCTT[A/G]TGCGTTCAAGAATCG | 73296 |
rs29566029 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rhobtb3 | Mm_Celera | 13:75907511 | AAAATTAAAGGACTT[A/G]TCTATCTAAAGTACT | 73296 |
rs29569379 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rhobtb3 | Mm_Celera | 13:75939024 | TCTGAGACGGACTGA[A/G]TCATCGGAACCTGCC | 73296 |
rs29582060 | snp | G/T | 0.375 | 0.216506 | intron-variant | Rhobtb3 | Mm_Celera | 13:75929151 | TTGCTTTGGGAAAGC[G/T]GAAGAATAATTTTCT | 73296 |
rs29583747 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Rhobtb3 | Mm_Celera | 13:75929626 | ACAAGGGAGACAGAT[C/T]CATTCTCGTCACCAA | 73296 |
rs29585619 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rhobtb3 | Mm_Celera | 13:75938811 | CTTCCTTTGCGCCTT[A/G]TCACAGCAACAGAAA | 73296 |
rs29588282 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rhobtb3 | Mm_Celera | 13:75938506 | AGTTTTATGTCAACT[C/T]GATAGCAGCCAGAGT | 73296 |
rs29590938 | snp | A/G | 0.456747 | 0.140554 | utr-variant-3-prime | Rhobtb3 | Mm_Celera | 13:75870129 | TAAAGATTTAAAATC[A/G]CCTATTACTTCTAGT | 73296 |
rs29610280 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rhobtb3 | Mm_Celera | 13:75911897 | GCAGCAACAGAAATC[C/T]TTTATTCTAAACAAA | 73296 |
rs29618085 | snp | C/T | 0.5 | 0 | utr-variant-3-prime | Rhobtb3 | Mm_Celera | 13:75870555 | CTAATAGTTGATTCA[C/T]TCAAGTGATTAAAAT | 73296 |
rs29630515 | snp | C/T | 0.32 | 0.24 | intron-variant | Rhobtb3 | Mm_Celera | 13:75910306 | ATGACACAAATGATA[C/T]GATTAATAAACCCTG | 73296 |
rs29634655 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rhobtb3 | Mm_Celera | 13:75908648 | CGGGTACAGGGAACC[C/T]TTTCTTTTCTTTTCC | 73296 |
rs29639820 | snp | A/C | 0.375 | 0.216506 | intron-variant | Rhobtb3 | Mm_Celera | 13:75883106 | AGCTCATAAACACGA[A/C]TTTTTCAGAATATTC | 73296 |
rs29657826 | snp | A/G | 0.33241 | 0.236027 | intron-variant, splice-donor-variant | Rhobtb3 | Mm_Celera | 13:75919537 | GGCAAAGAAGCTCCT[A/G]CCTGTGGAGAGAAAT | 73296 |
rs29661418 | snp | A/G | 0.49827 | 0.0293608 | intron-variant | Rhobtb3 | Mm_Celera | 13:75893917 | GAGCTAGTGGTGCCT[A/G]GTTGTCTACCGGGGC | 73296 |
rs29663035 | snp | A/G | 0.32 | 0.24 | intron-variant | Rhobtb3 | Mm_Celera | 13:75910261 | TTTAATTTTCTAATA[A/G]CTGTCATATTGTTTC | 73296 |
rs29663480 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Rhobtb3 | Mm_Celera | 13:75914419 | TGTCTGAGAGCCTCG[C/T]TATAGCTCTGTCTAA | 73296 |
rs29674184 | snp | A/C | 0.495868 | 0.0452663 | intron-variant | Rhobtb3 | Mm_Celera | 13:75929101 | ACATGGGAAGCATTA[A/C]AATCCTCTGGTCACT | 73296 |
rs29675844 | snp | A/T | 0.429688 | 0.173817 | intron-variant | Rhobtb3 | Mm_Celera | 13:75882388 | TACTTTCCAAGATGA[A/T]TTTTTTGAACAAGTT | 73296 |
rs29682570 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rhobtb3 | Mm_Celera | 13:75939145 | TGCACACATCTCTGC[A/G]TGGGGAATGTAGCCT | 73296 |
rs29684988 | snp | C/T | | | intron-variant | Rhobtb3 | GRCm38.p3 | 13:75878739 | ACCGAGAGCAATCTA[C/T]CAAAACGAGTAAGAA | 73296 |
rs29685188 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rhobtb3 | Mm_Celera | 13:75897231 | CAAGTAATAAGCCAT[C/T]CCAATATTGAATAAA | 73296 |