SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3712747 | snp | C/T | 0.5 | 0 | intron-variant | Cul9 | Mm_Celera | 17:46534823 | GCGCAGCTGCGTCTG[C/T]AGCCAGAGCTCACCG | 78309 |
rs6183669 | snp | C/T | 0.5 | 0 | intron-variant | Cul9 | Mm_Celera | 17:46524185 | TCTCCTGGCTGCTCC[C/T]CTGCNGCCATGACGC | 78309 |
rs6183674 | snp | C/T | 0.5 | 0 | intron-variant | Cul9 | Mm_Celera | 17:46524190 | TGGCTGCTCCNCTGC[C/T]GCCATGACGCCCCTT | 78309 |
rs29499329 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Cul9 | Mm_Celera | 17:46522784 | GTTTTTTTTTTTTTG[G/T]TTTTTTTTGTTTTTT | 78309 |
rs29500286 | snp | A/G | 0.375 | 0.216506 | intron-variant | Cul9 | Mm_Celera | 17:46538080 | GACATAGTCAAGCTC[A/G]TGGAGAGACACATGG | 78309 |
rs29501284 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Cul9 | Mm_Celera | 17:46541189 | TTGTGTGTGTGTGGT[A/G]TATATATGTGGTACC | 78309 |
rs29506189 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Cul9 | Mm_Celera | 17:46513135 | ATGCCTACAGTGCCA[G/T]CATACAGAAGATAGA | 78309 |
rs29509752 | snp | A/C | 0.375 | 0.216506 | intron-variant | Cul9 | Mm_Celera | 17:46501443 | CCTGGCCCCATACCC[A/C]CCCCCCCCCCAATTT | 78309 |
rs29513576 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Cul9 | Mm_Celera | 17:46513412 | TTCGAGAATGACTAG[C/G]CTCATTTTGAAATAT | 78309 |
rs29515367 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Cul9 | Mm_Celera | 17:46529762 | CCTCTGGAAGAGCAG[A/T]CAGTGCTCTTAACCA | 78309 |
rs29519258 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Cul9 | Mm_Celera | 17:46502980 | AGGCCTCACAGCTCC[A/T]GTCTATCCCCTCTGA | 78309 |
rs29520531 | snp | G/T | 0.375 | 0.216506 | missense, nc-transcript-variant | Cul9 | Mm_Celera | 17:46519795 | TCGCAGAGCTCCGCC[G/T]GTAGGTGCTTTCTGG | 78309 |
rs29522025 | snp | A/T | 0.375 | 0.216506 | intron-variant | Cul9 | Mm_Celera | 17:46509311 | ACTTGTGTCTCTGGG[A/T]CTCCTGCCTAAAGAG | 78309 |
rs29534964 | snp | A/G | 0.5 | 0 | intron-variant | Cul9 | Mm_Celera | 17:46540985 | GGCCTGTGGAGGCTA[A/G]AAAGGGCAATTAGAT | 78309 |
rs33053881 | snp | C/T | 0.375 | 0.216506 | intron-variant | Cul9 | Mm_Celera | 17:46519492 | ATTTGGAAAGATGTC[C/T]CCATGACTGGAAACG | 78309 |
rs33054782 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Cul9 | Mm_Celera | 17:46524976 | ACAGAGTTTACAAAG[A/G]GCATTGTGGGACGGT | 78309 |
rs33056682 | snp | C/G | 0.375 | 0.216506 | intron-variant | Cul9 | Mm_Celera | 17:46509332 | GCCTAAAGAGCATGG[C/G]TCTTGCCTTGATTGG | 78309 |
rs33064498 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Cul9 | Mm_Celera | 17:46525547 | GCTCAACCCTTCTCA[C/T]CAAGTCCTGATGGGA | 78309 |
rs33076495 | snp | C/T | 0.375 | 0.216506 | intron-variant | Cul9 | Mm_Celera | 17:46518982 | CCTGGGCACCAGGCA[C/T]GCATCCTATATACAG | 78309 |
rs33107607 | snp | A/G | 0.375 | 0.216506 | intron-variant | Cul9 | Mm_Celera | 17:46524372 | CCTTCTCTGACCCTC[A/G]TTGGCCCCGGAACCC | 78309 |
rs33121025 | snp | A/G | 0.375 | 0.216506 | intron-variant | Cul9 | Mm_Celera | 17:46535387 | CTATAAGAAAGAGCC[A/G]GGCGTGGTGGTGCAT | 78309 |
rs33124415 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Cul9 | Mm_Celera | 17:46537943 | CACTACTGTAGTTCA[A/G]CATTTATAGCTTCAT | 78309 |
rs33160277 | snp | A/G | 0.375 | 0.216506 | intron-variant | Cul9 | Mm_Celera | 17:46518859 | TGGCTCTGCAGTTAA[A/G]ACCAATGGCCTCTCT | 78309 |
rs33190685 | snp | A/C | 0.475309 | 0.108333 | missense, nc-transcript-variant | Cul9 | GRCm38.p3 | 17:46525758 | TGCTGCAGAGCTGCG[A/C]GTACTTCTCACACTC | 78309 |
rs33192393 | snp | A/T | 0.375 | 0.216506 | intron-variant | Cul9 | Mm_Celera | 17:46519670 | GTGCACACTCCTGCC[A/T]GGTGGCCTCTCCTTT | 78309 |
rs33201735 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Cul9 | Mm_Celera | 17:46506711 | CCTACCCTCACTTTA[C/T]CTACACTGGCTTTTA | 78309 |
rs33214872 | snp | C/T | 0.375 | 0.216506 | intron-variant | Cul9 | Mm_Celera | 17:46501708 | TTGGGCCCCTCGCTG[C/T]GTTTCCCTCTGGACT | 78309 |
rs33219671 | snp | A/G | 0.375 | 0.216506 | intron-variant | Cul9 | Mm_Celera | 17:46519457 | TAAAATGATGGGGAT[A/G]AATAGCCTTCAATAT | 78309 |
rs33221465 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Cul9 | Mm_Celera | 17:46513389 | TGAAAATAAATAAAA[A/C]AAAATGCTTCGAGAA | 78309 |
rs33244603 | snp | G/T | 0.375 | 0.216506 | intron-variant | Cul9 | Mm_Celera | 17:46518698 | ACTTGACCATGTCCA[G/T]GACTCTAGTCCTAGA | 78309 |
rs33246854 | snp | C/T | 0.375 | 0.216506 | intron-variant | Cul9 | Mm_Celera | 17:46509312 | CTTGTGTCTCTGGGT[C/T]TCCTGCCTAAAGAGC | 78309 |
rs33259313 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Cul9 | Mm_Celera | 17:46530712 | GGAGACAGGAGAACT[G/T]TCCAGAACTGTCTTA | 78309 |
rs33270573 | snp | A/G | 0.5 | 0 | intron-variant | Cul9 | Mm_Celera | 17:46526527 | CGCTAGCAGTCGCTC[A/G]GTCCCTGTGCACGGA | 78309 |
rs33271544 | snp | A/G | 0.432133 | 0.171253 | intron-variant | Cul9 | Mm_Celera | 17:46502819 | TTGGCCTTCCTTTAC[A/G]TGGTGATGCCAGGGT | 78309 |
rs33286135 | snp | A/G | 0.375 | 0.216506 | intron-variant | Cul9 | Mm_Celera | 17:46503690 | CCCACATCTGTTGGG[A/G]CTGGGGAAGACAGAC | 78309 |
rs33297288 | snp | A/G | 0.375 | 0.216506 | intron-variant | Cul9 | Mm_Celera | 17:46531763 | AGAACAGTGTATGGA[A/G]ATGGTTAAGAGATGG | 78309 |
rs33351405 | snp | A/G | 0.5 | 0 | intron-variant | Cul9 | Mm_Celera | 17:46528670 | GCCTGCAAGAAAGAA[A/G]CAGGGGCGGAGTTAG | 78309 |
rs33366559 | snp | C/T | 0.32 | 0.24 | intron-variant | Cul9 | Mm_Celera | 17:46531949 | TTCCTTCCTTCCTTC[C/T]TTCTTTCTTTCTCTC | 78309 |
rs33369129 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Cul9 | Mm_Celera | 17:46512811 | GTATCTTTGTCTGCG[A/T]GTCTGTCTGTGCACC | 78309 |
rs33374709 | snp | A/G | 0.5 | 0 | intron-variant | Cul9 | Mm_Celera | 17:46518341 | GGTCTCTGTGTGCTA[A/G]GTAGGCATGGCTGTA | 78309 |
rs33383536 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Cul9 | Mm_Celera | 17:46529075 | CCTGGGCTCCCTAAA[C/T]CCACCGTCCCCCAGT | 78309 |
rs33387335 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Cul9 | Mm_Celera | 17:46522495 | CGCTAGGGAGAGCCC[G/T]TGCTTCCTCCTGGCC | 78309 |
rs33405663 | snp | A/G | 0.444444 | 0.157135 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | Cul9 | GRCm38.p3 | 17:46538571 | GAGAACCTGTAGTAC[A/G]CCCTCAGCCATCTCT | 78309 |
rs33408137 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Cul9 | Mm_Celera | 17:46540810 | TTTCACCCCCAGCCC[C/T]CAGCATCTTCCTCTA | 78309 |
rs33408717 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Cul9 | Mm_Celera | 17:46537939 | TATTCACTACTGTAG[C/T]TCAGCATTTATAGCT | 78309 |
rs33432370 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Cul9 | GRCm38.p3 | 17:46533646 | TTCTATGTGTAAAAA[A/T]ATATATATATATACT | 78309 |
rs33438409 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Cul9 | Mm_Celera | 17:46506630 | CTGGAGCTCACGGAT[A/C]CTGACTGGTCTGCCC | 78309 |
rs33439616 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Cul9 | Mm_Celera | 17:46530835 | CCCGTCATGCTCTTG[C/T]GCTCAGATACGTCAT | 78309 |
rs33444369 | snp | A/G | 0.188366 | 0.242283 | synonymous-codon, nc-transcript-variant | Cul9 | Mm_Celera | 17:46522287 | CCGAACCCGAGTGTC[A/G]ATACCACCCTGCAGG | 78309 |
rs33448858 | snp | C/T | 0.5 | 0 | synonymous-codon, nc-transcript-variant | Cul9 | GRCm38.p3 | 17:46540443 | AGTGACGATGGTGGG[C/T]AGCAGCAGAGGCGGA | 78309 |
rs33456822 | snp | A/G | 0.5 | 0 | intron-variant | Cul9 | GRCm38.p3 | 17:46530333 | CCCCCACACACACAC[A/G]CGCACACACCGTTTC | 78309 |
rs33470098 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Cul9 | Mm_Celera | 17:46506215 | GGCTAGTTGACTTTG[C/T]CATAAAATATCTAGC | 78309 |
rs33472197 | snp | C/T | 0.375 | 0.216506 | intron-variant | Cul9 | Mm_Celera | 17:46537288 | CTAGGGCTAAAGGAC[C/T]TAGGCTTGCAGCCTG | 78309 |
rs33479929 | snp | C/T | 0.5 | 0 | intron-variant | Cul9 | Mm_Celera | 17:46540967 | TACCACATATGTGTC[C/T]GGGGCCTGTGGAGGC | 78309 |
rs33483056 | snp | A/T | 0.375 | 0.216506 | intron-variant | Cul9 | Mm_Celera | 17:46509313 | TTGTGTCTCTGGGTC[A/T]CCTGCCTAAAGAGCA | 78309 |
rs33492583 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Cul9 | Mm_Celera | 17:46540907 | ATTATCTTTTTTTTT[A/T]AATTATGTGCACGGG | 78309 |
rs33499017 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Cul9 | Mm_Celera | 17:46506546 | CCAAAGCTTCTGGGG[A/G]CTTCCACATCAGTTC | 78309 |
rs33513856 | snp | A/G | 0.375 | 0.216506 | intron-variant | Cul9 | Mm_Celera | 17:46531771 | GTATGGAGATGGTTA[A/G]GAGATGGCTCCTAAC | 78309 |
rs33516366 | snp | A/T | 0.375 | 0.216506 | intron-variant | Cul9 | Mm_Celera | 17:46509595 | GAGCTAGCTCAGTGG[A/T]TAAAAGCACTGCTCT | 78309 |
rs33541139 | snp | A/G | 0.487535 | 0.077957 | intron-variant, missense | Cul9 | Mm_Celera | 17:46502707 | TGAAGACACATGGAG[A/G]GATGGCTGTGTACAT | 78309 |
rs33597213 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Cul9 | Mm_Celera | 17:46522920 | CTGCCTCTGCCTCCC[A/G]AGTGCTGGGATTAAA | 78309 |
rs33611956 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Cul9 | Mm_Celera | 17:46544913 | CAGAGTGAGTTCCAG[A/G]ACAGCCAGGGCTACA | 78309 |
rs33620856 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Cul9 | Mm_Celera | 17:46512916 | TGTGAGCAGCTGTGT[G/T]GGGGCTGGGAATTGA | 78309 |
rs33628991 | snp | C/T | 0.375 | 0.216506 | intron-variant | Cul9 | Mm_Celera | 17:46538156 | TTCCCCTCCACTCTA[C/T]CCACTTCTACTGGAC | 78309 |
rs33649095 | snp | C/G | 0.375 | 0.216506 | intron-variant | Cul9 | Mm_Celera | 17:46520714 | GGGAAGGAGGGGAAA[C/G]GGAAGGGGAGGAGAT | 78309 |
rs33651535 | snp | C/T | 0.375 | 0.216506 | intron-variant | Cul9 | Mm_Celera | 17:46535330 | ATGCAAACAAAATGT[C/T]TTAAACACAGATAAC | 78309 |
rs33658344 | snp | C/G/T | 0.375 | 0.216506 | intron-variant | Cul9 | GRCm38.p3 | 17:46538157 | TCCCCTCCACTCTAC[C/G/T]CACTTCTACTGGACC | 78309 |
rs33668001 | snp | A/G | 0.375 | 0.216506 | intron-variant | Cul9 | Mm_Celera | 17:46509648 | CCCAGCAACCACATG[A/G]TGGCTAACCACTATC | 78309 |
rs33678445 | snp | A/C | 0.5 | 0 | intron-variant | Cul9 | Mm_Celera | 17:46518312 | GTTTGTGTGATGCTG[A/C]GGTTTGCATCCTGGG | 78309 |
rs33687392 | snp | G/T | 0.375 | 0.216506 | intron-variant | Cul9 | Mm_Celera | 17:46512730 | TATGCTGGAGTTTAT[G/T]CTGTTTGTATATATT | 78309 |
rs33689481 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Cul9 | Mm_Celera | 17:46522793 | TTTTTGGTTTTTTTT[G/T]TTTTTTTTGGTTTTT | 78309 |
rs33699221 | snp | C/T | 0.375 | 0.216506 | intron-variant | Cul9 | Mm_Celera | 17:46541611 | TTCCTCAGATGTTAA[C/T]CCGCAGCCCTGAATC | 78309 |
rs33700576 | snp | A/G | 0.375 | 0.216506 | intron-variant | Cul9 | Mm_Celera | 17:46535200 | CATAGAGACATGCCT[A/G]GCTTTGCCCTGAGTG | 78309 |
rs33720943 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Cul9 | Mm_Celera | 17:46531962 | TCTTTCTTTCTTTCT[C/T]TCTTTCTTTCTTTCT | 78309 |
rs33721532 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Cul9 | Mm_Celera | 17:46521031 | CCTGCCAGGGCTTGC[A/G]TCTGCCTACCTGTCC | 78309 |
rs45694080 | snp | A/G | 0.42 | 0.183303 | intron-variant, downstream-variant-500B | Cul9 | Mm_Celera | 17:46503059 | TGTCTGTATTGACTG[A/G]CCAGGCCTCTGCTGT | 78309 |
rs45798213 | snp | C/T | 0.486111 | 0.0821678 | intron-variant | Cul9 | Mm_Celera | 17:46529848 | CGACTTCACTACCCA[C/T]TGCTTGGTCTGAATC | 78309 |
rs45829958 | snp | C/G | 0.486111 | 0.0821678 | intron-variant | Cul9 | Mm_Celera | 17:46507409 | AGGGGGACAGTAAAG[C/G]CCGCTACTCTTCAAA | 78309 |
rs46000200 | snp | A/C | 0.408163 | 0.193609 | intron-variant | Cul9 | Mm_Celera | 17:46506489 | CAAACCACACCTTCA[A/C]CCTCACACAATACCC | 78309 |
rs46023864 | snp | C/T | 0.32 | 0.24 | synonymous-codon, nc-transcript-variant | Cul9 | GRCm38.p3 | 17:46525161 | GTTGCGGTCCGTCAG[C/T]TTGCTGGCCCGGTGT | 78309 |
rs46122303 | snp | A/G | | | intron-variant | Cul9 | Mm_Celera | 17:46507660 | TCTAGGAGCAGAGAT[A/G]GGGGGGGGGCGGGCA | 78309 |
rs46123040 | snp | C/T | | | intron-variant | Cul9 | Mm_Celera | 17:46508860 | GGCACTGGAAGCCAG[C/T]GGGGTAGGTCACAGT | 78309 |
rs46137263 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Cul9 | Mm_Celera | 17:46505505 | TCAAAGCACAGGGAC[C/G]CCAGTTGACAGTGCC | 78309 |
rs46189134 | snp | C/T | 0.408163 | 0.193609 | synonymous-codon, nc-transcript-variant | Cul9 | GRCm38.p3 | 17:46521349 | ACGGGGCTGCGAGGA[C/T]GGCTCAGGAGAAGGC | 78309 |
rs46214530 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Cul9 | Mm_Celera | 17:46543996 | AAGAACGGTGTGAAC[G/T]GAGCAAAGAGATGCG | 78309 |
rs46293347 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cul9 | Mm_Celera | 17:46521006 | GCCTGCTTGTGTTCC[A/G]TTCTGCCTGCCTGCC | 78309 |
rs46341096 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Cul9 | Mm_Celera | 17:46508800 | CCTTCACAGATGAGA[C/T]TTGGGAGTAAATGTG | 78309 |
rs46345106 | snp | C/T | 0.132653 | 0.220748 | downstream-variant-500B | Cul9 | Mm_Celera | 17:46500265 | TGGGTGGGTTGCATT[C/T]TTTTCACCTCTGAAC | 78309 |
rs46384929 | snp | A/G | | | intron-variant | Cul9 | GRCm38.p3 | 17:46514575 | ACTCCTCCATTGTTG[A/G]TGGGATTGCAAACTT | 78309 |
rs46436079 | snp | A/G | | | intron-variant | Cul9 | Mm_Celera | 17:46507687 | GGCACAGAGCCACAC[A/G]TCACCCACCCCTGGG | 78309 |
rs46514811 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon, nc-transcript-variant | Cul9 | Mm_Celera | 17:46521948 | AGGGAGAAAGCGATC[A/G]GCAAAATTCTGTTCA | 78309 |
rs46568560 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Cul9 | Mm_Celera | 17:46522323 | CAGACTTGTTATCTA[C/T]GTCACCTCTCCGGAG | 78309 |
rs46573016 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Cul9 | Mm_Celera | 17:46507846 | CACTCTGGGTCCCGG[A/C]ACCTCTGCCCTCTCC | 78309 |
rs46604777 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon, nc-transcript-variant | Cul9 | Mm_Celera | 17:46525182 | GGCCCGGTGTGGGTT[C/T]GAGGACACCTCCACT | 78309 |
rs46698940 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Cul9 | Mm_Celera | 17:46537837 | TTAGTGAGGGAAAGT[C/T]GGTCGCTCAAACAGT | 78309 |
rs46704556 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Cul9 | Mm_Celera | 17:46504706 | TAGAAACAATGGCGA[C/T]AACTAGCTGCAGACT | 78309 |
rs46706267 | snp | A/G | 0.391111 | 0.206368 | synonymous-codon | Cul9 | Mm_Celera | 17:46502400 | CTTTCGAGCCTGCTC[A/G]AGGGCCCGGCAGGCA | 78309 |
rs46707818 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Cul9 | Mm_Celera | 17:46509054 | ACACGGAGGCGTGAG[A/G]AAAGTCAGAGAACTC | 78309 |
rs46727165 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Cul9 | Mm_Celera | 17:46506095 | ATCAGTTACATTTTG[C/T]AGGCCCCCTGTCTCT | 78309 |
rs46762135 | snp | C/T | 0.124444 | 0.216185 | missense, nc-transcript-variant | Cul9 | Mm_Celera | 17:46523276 | TAAGTTCTGTGCTGA[C/T]GCAGCCAACATTGTC | 78309 |