SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs4169765 | snp | A/G | 0.444444 | 0.157135 | downstream-variant-500B | Senp5 | Mm_Celera | 16:31959353 | GCAGGAGGGTCTAAG[A/G]CTCCAAGGCCACCAG | 320213 |
rs4169766 | snp | C/G/T | 0.493827 | 0.0552116 | utr-variant-3-prime | Senp5 | GRCm38.p3 | 16:31960092 | AAGGGACAAGTCACA[C/G/T]TAGACAAGTACTGGC | 320213 |
rs4169767 | snp | C/T | 0.493827 | 0.0552116 | utr-variant-3-prime | Senp5 | GRCm38.p3 | 16:31960128 | CCCTAGTTAGCTCTG[C/T]ACTGGTATATTCCAA | 320213 |
rs4169768 | snp | C/G | 0.489796 | 0.070696 | utr-variant-3-prime | Senp5 | GRCm38.p3 | 16:31960582 | GTTTACATGTAATTA[C/G]AAGAAGAAAAAGAAC | 320213 |
rs4169769 | snp | C/T | 0.498866 | 0.0237825 | utr-variant-3-prime | Senp5 | GRCm38.p3 | 16:31961735 | CTCCACCTCGGTCAG[C/T]GCAAGGACTGCTGAC | 320213 |
rs4169770 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Senp5 | Mm_Celera | 16:31969112 | GGTCTTTCAAGAAAG[A/G]GTTTCTCAGCCGGGC | 320213 |
rs4169771 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Senp5 | GRCm38.p3 | 16:31970966 | AATGCTGGGATCACA[C/G]GGATGTGCTATGAGG | 320213 |
rs4169772 | snp | G/T | 0.46281 | 0.131194 | intron-variant | Senp5 | GRCm38.p3 | 16:31971653 | CAATGCATGTCATAG[G/T]ATGTGTTGTCAAAGG | 320213 |
rs4169773 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Senp5 | GRCm38.p3 | 16:31972239 | GATGGAAGGCACATA[C/T]CATGACACCAGCTTT | 320213 |
rs4169774 | snp | A/C/T | 0.375 | 0.216506 | intron-variant | Senp5 | GRCm38.p3 | 16:31974119 | TGCCTCAAAAACAAA[A/C/T]AAACAAACAAACAAA | 320213 |
rs4169775 | snp | C/T | 0.396694 | 0.202437 | intron-variant | Senp5 | Mm_Celera | 16:31974471 | CTAAAAACAGAACAA[C/T]GAGCTCCTTCCTGGT | 320213 |
rs4169776 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Senp5 | Mm_Celera | 16:31974505 | GTTTTTTTTTTTTTT[G/T]TTTTTTTTGTTTTTG | 320213 |
rs4169777 | snp | A/T | 0.415225 | 0.187619 | intron-variant | Senp5 | GRCm38.p3 | 16:31977793 | AGTCAGCCAGGTTAC[A/T]ACACGCAGCACCCAG | 320213 |
rs4169778 | snp | A/T | 0.375 | 0.216506 | intron-variant | Senp5 | GRCm38.p3 | 16:31977796 | CAGCCAGGTTACAAC[A/T]CGCAGCACCCAGATT | 320213 |
rs4169779 | snp | A/C | 0.5 | 0 | intron-variant | Senp5 | GRCm38.p3 | 16:31978894 | GAAAAAAACAAAAAA[A/C]AAAAAACAAAAAACA | 320213 |
rs4169780 | snp | A/G | 0.5 | 0 | intron-variant | Senp5 | GRCm38.p3 | 16:31980187 | AATCAAAACAAAGAA[A/G]CATTCTGCTATTATT | 320213 |
rs4169781 | snp | C/T | 0.5 | 0 | intron-variant | Senp5 | GRCm38.p3 | 16:31982066 | CCTTGTTAAACATAT[C/T]TTTTTTTTTTTTTTT | 320213 |
rs4169782 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Senp5 | GRCm38.p3 | 16:31982355 | ACTGACTGCTCTTCC[A/G]GAGGTCCTGAGTTCA | 320213 |
rs4169783 | snp | C/T | 0.5 | 0 | intron-variant | Senp5 | Mm_Celera | 16:31982433 | AGGCAAGTGGCACAG[C/T]ACTCATACATTAAAT | 320213 |
rs4169784 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Senp5 | Mm_Celera | 16:31982822 | AGACCAGGCTGGCCT[C/T]GAACTCAGAAATCCG | 320213 |
rs4169785 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Senp5 | GRCm38.p3 | 16:31982841 | CTCAGAAATCCGCCT[A/G]CCTCTTCCTCCCAAG | 320213 |
rs4169786 | snp | G/T | 0.5 | 0 | intron-variant | Senp5 | Mm_Celera | 16:31982847 | AATCCGCCTGCCTCT[G/T]CCTCCCAAGTGCTGG | 320213 |
rs4169787 | snp | A/C | 0.5 | 0 | intron-variant | Senp5 | Mm_Celera | 16:31983208 | CACAGAAAACCTAAC[A/C]ACCACCTTATTTTGA | 320213 |
rs4169788 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Senp5 | GRCm38.p3 | 16:31983667 | AAAAGTTAAAATGAA[A/G]TGCACTTTATTCGAT | 320213 |
rs4169789 | snp | A/C | 0.408163 | 0.193609 | intron-variant | Senp5 | Mm_Celera | 16:31984622 | ATATAATAAATAAAT[A/C]TTTAAAAAAAAAAAA | 320213 |
rs4169790 | snp | A/T | 0.408163 | 0.193609 | intron-variant | Senp5 | Mm_Celera | 16:31984623 | TATAATAAATAAATC[A/T]TTAAAAAAAAAAAAA | 320213 |
rs4169791 | snp | A/T | 0.408163 | 0.193609 | intron-variant | Senp5 | Mm_Celera | 16:31984625 | TAATAAATAAATCTT[A/T]AAAAAAAAAAAAAAG | 320213 |
rs4169792 | snp | A/G | 0.5 | 0 | intron-variant | Senp5 | Mm_Celera | 16:31985356 | GTGTGTGGGGGGGGG[A/G]GATAAGCGTTAATCA | 320213 |
rs4169793 | snp | A/G | 0.5 | 0 | intron-variant | Senp5 | GRCm38.p3 | 16:31986254 | ATCTGCATTTGAGCT[A/G]TATCTGCATTTGAGC | 320213 |
rs4169794 | snp | A/T | 0.491493 | 0.0646602 | intron-variant | Senp5, Gm15694 | GRCm38.p3 | 16:31986623 | AGGAACCTCATAACC[A/T]GCTCCTTCTGTGGCT | 320213 |
rs4169795 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | Senp5, Gm15694 | Mm_Celera | 16:31988286 | AATAATAGTTCAAAT[C/T]CCAGCAACCACATGG | 320213 |
rs4169796 | snp | C/G | 0.375 | 0.216506 | intron-variant | Senp5 | GRCm38.p3 | 16:31992282 | TAGCTGTGAACTACT[C/G]TGTGGGTGCTGGAAA | 320213 |
rs4169797 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Senp5 | GRCm38.p3 | 16:31992654 | TATAAGGAACACAAA[C/T]AAACACGAGCACGCA | 320213 |
rs4169798 | snp | C/G | 0.459184 | 0.136902 | intron-variant | Senp5 | GRCm38.p3 | 16:31993492 | TCAATGAGTAACACA[C/G]TTAACAGGTCAAAAA | 320213 |
rs4169799 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Senp5 | GRCm38.p3 | 16:31996161 | TACTGTTATGAACCA[A/T]AAGCAAATATCTATG | 320213 |
rs4169800 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Senp5 | GRCm38.p3 | 16:31998088 | AACAAACCTAACAAA[A/C]AAAAAAGACAAAAAG | 320213 |
rs4169801 | snp | A/C | 0.499055 | 0.0217186 | intron-variant | Senp5 | GRCm38.p3 | 16:31999224 | GTTCTACTGCTGAAT[A/C]TCTCTTAGTCCCTGA | 320213 |
rs4169802 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Senp5 | Mm_Celera | 16:32000196 | GTGTGCGTGGGGGGG[A/G]GGGGAGTGGGGGAAG | 320213 |
rs4169803 | snp | C/T | 0.5 | 0 | intron-variant | Senp5 | Mm_Celera | 16:32000687 | TGCAGCCAGGTGTAA[C/T]CACAATTCTGAAATC | 320213 |
rs4169804 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Senp5 | GRCm38.p3 | 16:32001454 | CCAGGCAGTGGTGGC[A/G]CATGACTTTAATCCC | 320213 |
rs4169805 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Senp5 | GRCm38.p3 | 16:32001459 | CAGTGGTGGCACATG[A/C]CTTTAATCCCAGCAC | 320213 |
rs4169806 | snp | C/G/T | 0.444444 | 0.157135 | intron-variant | Senp5 | GRCm38.p3 | 16:32001591 | GGAAAAAAAAAAAAG[C/G/T]GGGCATGCTCCAGAT | 320213 |
rs4169807 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Senp5 | GRCm38.p3 | 16:32001612 | TGCTCCAGATGGTTA[A/G]GAGCACCTGCTCTCT | 320213 |
rs4169808 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Senp5 | GRCm38.p3 | 16:32001759 | TGCATGCACCTTTTT[C/T]CCCCCTAAAAGAAAA | 320213 |
rs4169809 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Senp5 | GRCm38.p3 | 16:32001786 | AAAATGGAGGAGGGT[A/G]GCAAAAGAAGTGAGA | 320213 |
rs4169810 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Senp5 | GRCm38.p3 | 16:32001867 | GGCCAAGACAAGGGG[A/G]TCACTGCAGGTTCAA | 320213 |
rs4169811 | snp | C/T | 0.495 | 0.0497494 | intron-variant | Senp5 | GRCm38.p3 | 16:32001943 | GAAATGGTTTAGAAG[C/T]AAAGTACGGGATTCT | 320213 |
rs4169812 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Senp5 | GRCm38.p3 | 16:32002305 | GGACAAAAGGCAAAA[A/G]CATAATTAGTAATGC | 320213 |
rs4169813 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Senp5 | GRCm38.p3 | 16:32002556 | GGCCCCCACAGTGGG[C/T]TAATTAACCTCATCG | 320213 |
rs4169814 | snp | A/G | 0.471655 | 0.115624 | intron-variant | Senp5 | GRCm38.p3 | 16:32002600 | TACCCAGCACGGACA[A/G]AATAAAAAAAAGTAG | 320213 |
rs4169815 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Senp5 | GRCm38.p3 | 16:32002741 | CTCCGCAGGAGCTGA[A/G]AGCCTGACAGCGATC | 320213 |
rs4169816 | snp | C/T | 0.444444 | 0.157135 | utr-variant-5-prime, intron-variant, nc-transcript-variant | Senp5 | GRCm38.p3 | 16:32003198 | GCGTCACCTCCTTCC[C/T]TGCCCTTCCGCCAGA | 320213 |
rs4169817 | snp | A/G | 0.489796 | 0.070696 | upstream-variant-2KB, intron-variant | Senp5 | GRCm38.p3 | 16:32004941 | CACTCAGGAGGCAGA[A/G]GCAATCTTGAGGCCA | 320213 |
rs4169818 | snp | A/G | 0.489796 | 0.070696 | upstream-variant-2KB, intron-variant | Senp5 | Mm_Celera | 16:32005360 | GAAGACAGCAACAGT[A/G]TACTTACACCTTACA | 320213 |
rs4169819 | snp | C/T | 0.48 | 0.0979796 | upstream-variant-2KB, intron-variant | Senp5 | GRCm38.p3 | 16:32005472 | CTGTATAGGAGAGAA[C/T]CACAAGAGAAGTAAG | 320213 |
rs4169820 | snp | C/T | 0.48 | 0.0979796 | upstream-variant-2KB, intron-variant | Senp5 | GRCm38.p3 | 16:32005568 | AGGCCCATCCCCCAC[C/T]ACGCCAGGCTTCTTG | 320213 |
rs4169821 | snp | C/T | 0.48 | 0.0979796 | upstream-variant-2KB, intron-variant | Senp5 | GRCm38.p3 | 16:32005585 | CGCCAGGCTTCTTGA[C/T]GCTTTGTTGCTAAGT | 320213 |
rs4169822 | snp | A/T | 0.471655 | 0.115624 | intron-variant | Senp5 | Mm_Celera | 16:32006336 | GGGTAAGACTTCAAA[A/T]TTTCAAATCCAGACA | 320213 |
rs4169823 | snp | A/C/T | 0.444444 | 0.157135 | intron-variant | Senp5 | GRCm38.p3 | 16:32006709 | TGTCGCTGTTGCTGC[A/C/T]GCTGCCGCCGCCGCC | 320213 |
rs4169824 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Senp5 | Mm_Celera | 16:32006718 | TGCTGCCGCTGCCGC[C/T]GCCGCCGCCGCCGCC | 320213 |
rs4169825 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Senp5 | Mm_Celera | 16:32006727 | TGCCGCCGCCGCCGC[C/T]GCCGCCTCCTCCTCC | 320213 |
rs4169826 | snp | C/G | 0.375 | 0.216506 | upstream-variant-2KB | Senp5 | GRCm38.p3 | 16:32011735 | ACTAACCAGAGCTAC[C/G]GTCCAAGATGAGGCA | 320213 |
rs6274897 | snp | A/C | 0.5 | 0 | upstream-variant-2KB | Senp5 | Mm_Celera | 16:32012036 | CTTCTCCCTCCCTCT[A/C]AGATCACTTGTATCC | 320213 |
rs6274931 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | Senp5 | Mm_Celera | 16:32012059 | TTGTATCCCAGGCTA[A/G]TCTCAGTCTATGTAG | 320213 |
rs6293036 | snp | G/T | 0.5 | 0 | intron-variant | Senp5 | Mm_Celera | 16:31979591 | AGTCTCACAGAGCAG[G/T]CCCTCTAACTTCAGG | 320213 |
rs6360485 | snp | C/T | 0.5 | 0 | utr-variant-3-prime | Senp5 | Mm_Celera | 16:31962750 | aataaCCCCTCCCCC[C/T]GCCTTTTTAAAAATC | 320213 |
rs6361547 | snp | A/G | 0.5 | 0 | utr-variant-3-prime | Senp5 | GRCm38.p3 | 16:31962921 | GAGACTCAGCTGAGG[A/G]ACATCAGCAAANGGG | 320213 |
rs6361563 | snp | C/T | 0.5 | 0 | utr-variant-3-prime | Senp5 | GRCm38.p3 | 16:31962933 | AGGNACATCAGCAAA[C/T]GGGACTGCTGGTGTA | 320213 |
rs13474115 | snp | A/G | | | intron-variant, nc-transcript-variant | Senp5, Gm15694 | Mm_Celera | 16:31987257 | GCCGCCGAGAGTTCT[A/G]CAATGGCAGCCACTG | 320213 |
rs32542065 | snp | C/T | 0.231111 | 0.249285 | utr-variant-3-prime | Senp5 | GRCm38.p3 | 16:31961897 | TACTCAGCCATTTTG[C/T]CTTTTTTGTTTTTCA | 320213 |
rs32542067 | snp | A/G | 0.231111 | 0.249285 | utr-variant-3-prime | Senp5 | GRCm38.p3 | 16:31963399 | CTGCTCCATCATGGC[A/G]CCTTCTGGAGTCCCT | 320213 |
rs32542069 | snp | C/T | 0.231111 | 0.249285 | synonymous-codon | Senp5 | GRCm38.p3 | 16:31963433 | GAGTGAGTCTCAGTC[C/T]AGGAGCCGGCACTCA | 320213 |
rs32542071 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Senp5 | Mm_Celera | 16:31963903 | CCCAAGGGCGACTTG[C/T]TAGCCTGCACTTAGA | 320213 |
rs32542073 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Senp5 | Mm_Celera | 16:31964165 | ATCCCAACAACAAAG[A/G]GAAAGTGCTGTATTC | 320213 |
rs32542415 | snp | C/T | 0.48 | 0.0979796 | upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant | Senp5 | GRCm38.p3 | 16:32003375 | TTTCCGACTTCCGGT[C/T]ATCAGCTGTCCTCAA | 320213 |
rs32542417 | snp | A/G/T | 0.497778 | 0.0332592 | upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant | Senp5 | GRCm38.p3 | 16:32003575 | GCCTTCATCTGGACC[A/G/T]TAACTGACCTACCGG | 320213 |
rs32542419 | snp | A/G | 0.231111 | 0.249285 | upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant | Senp5 | Mm_Celera | 16:32003601 | ACCGGAACTCAGGAA[A/G]TCTTCTCTTTCTGGT | 320213 |
rs32542421 | snp | C/T | 0.124444 | 0.216185 | upstream-variant-2KB, intron-variant | Senp5 | Mm_Celera | 16:32005850 | ACCAGTCCTGAGATA[C/T]TGAAAGTGTTTGGAC | 320213 |
rs32542805 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Senp5 | GRCm38.p3 | 16:31964410 | TAAATGACCAAGAGA[C/T]GAGAAACTCTTCTGT | 320213 |
rs32542807 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Senp5 | Mm_Celera | 16:31964956 | AGAGGATAAATCGGC[C/T]GATCAATGAAACCTG | 320213 |
rs32542809 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Senp5 | Mm_Celera | 16:31965255 | GCCTGACACAGGCTG[A/T]AAAGGTCAAATGAGA | 320213 |
rs32542813 | snp | A/G | 0.375 | 0.216506 | intron-variant | Senp5 | Mm_Celera | 16:31976474 | TATCTCTCTTCTCAG[A/G]TTTGTAGATAAAAAA | 320213 |
rs32543224 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Senp5 | Mm_Celera | 16:32006361 | CAGACACAAAGGTAA[C/T]TTGCTAAGTCCAGGA | 320213 |
rs32543226 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Senp5 | Mm_Celera | 16:32006386 | CCAGGAAGAAGAGAC[A/G]GTGCTGGTTTGGGTT | 320213 |
rs32543228 | snp | A/T | 0.473373 | 0.11227 | intron-variant | Senp5 | GRCm38.p3 | 16:32007509 | CAAATGTACCTCCTC[A/T]GAGCAATACTCAGGG | 320213 |
rs32543230 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Senp5 | GRCm38.p3 | 16:32008071 | CTGAGGAAGGCATCC[A/G]AGGAACCAGGAAAGG | 320213 |
rs32543232 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Senp5 | Mm_Celera | 16:32009063 | AGGTTGAGAACCAGT[A/G]ATCTCAGAGGTCAGC | 320213 |
rs32543627 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Senp5 | Mm_Celera | 16:31983936 | TGTTTTCATAACACA[G/T]ATTCACACCTATTAC | 320213 |
rs32543628 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Senp5 | Mm_Celera | 16:31983941 | TCATAACACATATTC[A/T]CACCTATTACAGAGA | 320213 |
rs32543630 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Senp5 | Mm_Celera | 16:31983981 | CATAACCCGTAAAAA[C/T]GGTTACATCATTAAG | 320213 |
rs32543631 | snp | C/T | 0.32 | 0.24 | intron-variant | Senp5 | Mm_Celera | 16:31984231 | CCTCCTACACTCTGG[C/T]GTTACAGGTGTGTGC | 320213 |
rs32543632 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Senp5 | Mm_Celera | 16:31985873 | CCATGCTGCCTAAGC[C/T]GGCCTGAGATTCTCC | 320213 |
rs32543994 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Senp5 | Mm_Celera | 16:32009329 | TTTTCACCACTCCAT[A/G]TCTCTGTAATTGGTG | 320213 |
rs32544634 | snp | A/G | 0.32 | 0.24 | intron-variant | Senp5, Gm15694 | Mm_Celera | 16:31986551 | ACATGACTTTGAGAC[A/G]ATGCTGTAAAGGAGG | 320213 |
rs32544637 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Senp5, Gm15694 | Mm_Celera | 16:31986648 | GTGGCTCTCACGCAA[C/T]GGTTTCTGCCAGGCC | 320213 |
rs32544638 | snp | C/T | 0.375 | 0.216506 | intron-variant, nc-transcript-variant | Senp5, Gm15694 | Mm_Celera | 16:31987166 | CAAGGTAACCTAGGG[C/T]AGGGTCACAGGTATG | 320213 |
rs32544640 | snp | C/T | 0.124444 | 0.216185 | intron-variant, nc-transcript-variant | Senp5, Gm15694 | Mm_Celera | 16:31987428 | CCAGATGCCCAGTTC[C/T]GCTGCTTTTAGATAG | 320213 |
rs32544641 | snp | A/G | 0.244898 | 0.249948 | intron-variant, nc-transcript-variant | Senp5, Gm15694 | Mm_Celera | 16:31987521 | GAAATCATTCTCTCT[A/G]ATTCTCCACCCAAGT | 320213 |
rs32544643 | snp | C/T | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Senp5, Gm15694 | Mm_Celera | 16:31988843 | AAAGGTATCACAACA[C/T]CTAGGTTTAAAGGCA | 320213 |
rs32545525 | snp | C/T | 0.124444 | 0.216185 | missense, upstream-variant-2KB, nc-transcript-variant | Senp5, Gm15694 | Mm_Celera | 16:31989420 | GCTGGTCAGGGAATG[C/T]GTCATCTAAACCATG | 320213 |