SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6373542 | snp | A/G | 0.5 | 0 | intron-variant | Senp6 | Mm_Celera | 9:80114782 | cagttctgggtactt[A/G]caagggtttgccaac | 215351 |
rs6373896 | snp | G/T | 0.5 | 0 | intron-variant | Senp6 | Mm_Celera | 9:80108222 | tgttttgttttgttt[G/T]gGGGGTGGGGGGAtt | 215351 |
rs6373956 | snp | A/G | 0.5 | 0 | intron-variant | Senp6 | Mm_Celera | 9:80108254 | agacagggtttctct[A/G]tgtagcacngactgt | 215351 |
rs6373967 | snp | C/T | 0.5 | 0 | intron-variant | Senp6 | Mm_Celera | 9:80108263 | ttctctntgtagcac[C/T]gactgtcctggaact | 215351 |
rs6374502 | snp | A/T | 0.5 | 0 | intron-variant | Senp6 | Mm_Celera | 9:80108343 | cccaagtgctggtat[A/T]aaaggcttgtgccac | 215351 |
rs6375057 | snp | G/T | 0.5 | 0 | intron-variant | Senp6 | GRCm38.p3 | 9:80108448 | AAAAAGGAAAATTTC[G/T]TCTGTCAAAATTAGA | 215351 |
rs6375200 | snp | G/T | 0.375 | 0.216506 | intron-variant | Senp6 | Mm_Celera | 9:80115089 | GCTTTGAAAATCATA[G/T]CAGGCCAGTATTTGT | 215351 |
rs6376139 | snp | A/G | 0.5 | 0 | intron-variant | Senp6 | Mm_Celera | 9:80108646 | TTACAGGTGACAGGC[A/G]TTTGCAAATTCTAGT | 215351 |
rs6393727 | snp | A/T | 0.5 | 0 | intron-variant | Senp6 | Mm_Celera | 9:80076343 | GTTTTTTTATTTTTT[A/T]AATTTTAGTTGCTGA | 215351 |
rs6395826 | snp | C/T | 0.415225 | 0.187619 | intron-variant | Senp6 | Mm_Celera | 9:80076698 | AGTTATAGGCATTGT[C/T]CATTGATAAGGCAGT | 215351 |
rs13461453 | snp | C/G | 0.32 | 0.24 | missense | Senp6 | Mm_Celera | 9:80130844 | GAGGAGAAATCCTGA[C/G]ACAACTAATCTGTCG | 215351 |
rs29633357 | snp | A/C | 0.444444 | 0.157135 | missense | Senp6 | Mm_Celera | 9:80116600 | GAGAGCACGTCCCCG[A/C]AGCCTGCCGACTCAG | 215351 |
rs29640577 | snp | C/G | 0.32 | 0.24 | intron-variant | Senp6 | Mm_Celera | 9:80087121 | TGTTAACACACAAGG[C/G]CTCATTTTGTTTTTC | 215351 |
rs29688963 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Senp6 | Mm_Celera | 9:80120695 | CTCTCCCTGAGAATG[A/G]AGGGATTGCATTTGG | 215351 |
rs29692277 | snp | C/T | 0.32 | 0.24 | intron-variant | Senp6 | Mm_Celera | 9:80130939 | CAAGACATTCATGTC[C/T]TGTGGGTGAAATGCT | 215351 |
rs29692305 | snp | C/T | 0.5 | 0 | intron-variant | Senp6 | Mm_Celera | 9:80084646 | CAGTCACAGTCCGGG[C/T]GGGTTTGCTTGGACA | 215351 |
rs29695203 | snp | A/G | 0.375 | 0.216506 | intron-variant | Senp6 | Mm_Celera | 9:80087273 | CCCTCCCCCATTTTT[A/G]TTTTAGCAACTTAAG | 215351 |
rs29696457 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Senp6 | Mm_Celera | 9:80122942 | TGATCCTTTTGGAAT[A/G]GTGGTTCTCAACCTT | 215351 |
rs29702074 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Senp6 | Mm_Celera | 9:80130451 | AGCATTTCTGCTAAT[C/T]TTTTTACAGTTTTGA | 215351 |
rs29733787 | snp | C/T | 0.375 | 0.216506 | intron-variant | Senp6 | Mm_Celera | 9:80112724 | CATACCAGAAGAGGG[C/T]GTCAGATCTCATTAT | 215351 |
rs29739362 | snp | C/T | 0.375 | 0.216506 | intron-variant | Senp6 | Mm_Celera | 9:80132305 | ATATTTTACTTGATC[C/T]CTTCCTTTCAGCAAT | 215351 |
rs29741852 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Senp6 | GRCm38.p3 | 9:80139918 | TTGTGGGAGTCAGAG[C/T]ACAACTGCTGGAAGC | 215351 |
rs29747058 | snp | C/T | 0.375 | 0.216506 | intron-variant | Senp6 | Mm_Celera | 9:80086232 | TTTTACAAAAATGAT[C/T]TCAGGCTGGAGAGAT | 215351 |
rs29786202 | snp | C/T | 0.444444 | 0.157135 | utr-variant-3-prime | Senp6 | Mm_Celera | 9:80144736 | TGTTTTGATAAAGTA[C/T]CAGGCTTTTTGCTTG | 215351 |
rs29790637 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Senp6 | Mm_Celera | 9:80091095 | TAGTTGCTGTTCTTG[C/T]GGAGGACCTGAGTTC | 215351 |
rs29793471 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Senp6 | Mm_Celera | 9:80137781 | CTGATTTCCCATCTC[G/T]GAGAGAATGACAGAC | 215351 |
rs29795250 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Senp6 | Mm_Celera | 9:80125078 | GACTGTGAGCATCCA[C/T]TTCTGTATTTGCCAG | 215351 |
rs29837673 | snp | C/T | 0.375 | 0.216506 | intron-variant | Senp6 | Mm_Celera | 9:80104264 | CACTGTGTATTCCAG[C/T]ATAACTGGCCCTTGA | 215351 |
rs29838871 | snp | A/G | 0.375 | 0.216506 | missense | Senp6 | Mm_Celera | 9:80143686 | CTCCCTATGAATTTG[A/G]TGAACTGGTTTCCTC | 215351 |
rs29839337 | snp | A/G | 0.32 | 0.24 | intron-variant | Senp6 | Mm_Celera | 9:80070676 | CAAACAATGGTGAGA[A/G]CAGTAGAAGCTCTGT | 215351 |
rs29843826 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Senp6 | Mm_Celera | 9:80125315 | TCATCCGCCTACTTC[C/T]TACCCCACTTGAAGG | 215351 |
rs29878380 | snp | A/G | 0.32 | 0.24 | intron-variant | Senp6 | GRCm38.p3 | 9:80077829 | AAAACCAGGCAAAGT[A/G]CGTGAACAGTAACTG | 215351 |
rs29883128 | snp | C/T | 0.375 | 0.216506 | intron-variant | Senp6 | GRCm38.p3 | 9:80104095 | TTAATGCACAAATAA[C/T]ATGTATCAAATGTAT | 215351 |
rs29888667 | snp | C/T | 0.5 | 0 | upstream-variant-2KB | Senp6 | Mm_Celera | 9:80065768 | CTAAAGGCCTAGAAT[C/T]TTTTGTTTTTTATGT | 215351 |
rs29932543 | snp | A/G | 0.375 | 0.216506 | intron-variant | Senp6 | Mm_Celera | 9:80073748 | CTATTAAGTGCTAGC[A/G]GCAGTGCCTTCCTGG | 215351 |
rs29943391 | snp | C/T | 0.32 | 0.24 | synonymous-codon | Senp6 | Mm_Celera | 9:80142359 | CTTCAGTGACTGTGG[C/T]GTATATGTGCTGCAG | 215351 |
rs29981633 | snp | A/C | 0.32 | 0.24 | synonymous-codon | Senp6 | Mm_Celera | 9:80142362 | CAGTGACTGTGGCGT[A/C]TATGTGCTGCAGTAT | 215351 |
rs29991473 | snp | A/T | 0.429688 | 0.173817 | intron-variant | Senp6 | Mm_Celera | 9:80124273 | TCTCTGCAGACTGCA[A/T]TCACTGCTCACTCAG | 215351 |
rs29995809 | snp | A/G | 0.375 | 0.216506 | intron-variant | Senp6 | Mm_Celera | 9:80098810 | TTTGCCTTGTTAACT[A/G]CAATAATTACAACTG | 215351 |
rs30026215 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Senp6 | Mm_Celera | 9:80125126 | TACAAGACAGATATA[A/C]CAGGGTCCCTTCAGC | 215351 |
rs30029238 | snp | C/T | 0.32 | 0.24 | intron-variant | Senp6 | Mm_Celera | 9:80113631 | GATTAAAGGTGTGTG[C/T]CACCACTGCTGGGCA | 215351 |
rs30036740 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Senp6 | Mm_Celera | 9:80111768 | TCTCCCCAGCCATTC[A/G]CATTGTCTTTACTGC | 215351 |
rs30042285 | snp | A/T | 0.375 | 0.216506 | intron-variant | Senp6 | Mm_Celera | 9:80074711 | GTTAGTCATACTTTT[A/T]TATATGAATTTAGTT | 215351 |
rs30091821 | snp | A/G | 0.387812 | 0.208586 | intron-variant | Senp6 | Mm_Celera | 9:80104187 | ATGGAATTGGATGCA[A/G]TGGGCTCTGTGTGGT | 215351 |
rs30093445 | snp | G/T | 0.375 | 0.216506 | intron-variant | Senp6 | Mm_Celera | 9:80102837 | TTTTGTTTTTTTGTT[G/T]TTTTTTCCTCAAAAT | 215351 |
rs30137332 | snp | C/T | 0.375 | 0.216506 | intron-variant | Senp6 | Mm_Celera | 9:80090030 | TGGAGGGAGGCTTGC[C/T]ACAAGTTCAAGGCCA | 215351 |
rs30179065 | snp | C/T | 0.5 | 0 | intron-variant | Senp6 | Mm_Celera | 9:80109997 | TCCTGCCTCTACCTC[C/T]TGGCACTGGGATTAA | 215351 |
rs30179816 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Senp6 | Mm_Celera | 9:80124298 | ACTCAGATTGCTGCC[C/T]TGAGTAGGGCTGAAG | 215351 |
rs30182435 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Senp6 | Mm_Celera | 9:80121691 | GCTACACAGAGAAAC[A/C]CTGTCTTGAAAAACA | 215351 |
rs30226727 | snp | G/T | 0.375 | 0.216506 | intron-variant | Senp6 | GRCm38.p3 | 9:80102834 | TTTTTTTGTTTTTTT[G/T]TTTTTTTTTCCTCAA | 215351 |
rs30229685 | snp | C/T | 0.444444 | 0.157135 | upstream-variant-2KB | Senp6 | Mm_Celera | 9:80064887 | CTCCGGTCCTTATGG[C/T]CCGAGAGGACAGCTG | 215351 |
rs30233007 | snp | A/T | 0.375 | 0.216506 | intron-variant | Senp6 | Mm_Celera | 9:80112803 | TTGGGAAGAGCAGTC[A/T]GTGCTCTTACCTGCT | 215351 |
rs30233592 | snp | C/T | 0.375 | 0.216506 | intron-variant | Senp6 | Mm_Celera | 9:80088971 | TTAAATTTGGTATTA[C/T]ATAGTTTTGAAAATG | 215351 |
rs30241468 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Senp6 | Mm_Celera | 9:80125121 | CCTCATACAAGACAG[A/C]TATAACAGGGTCCCT | 215351 |
rs30242811 | snp | A/C | 0.5 | 0 | intron-variant | Senp6 | Mm_Celera | 9:80078325 | TGTGTGTAGTCCTGC[A/C]TGGCAAGATACTTTG | 215351 |
rs30258496 | snp | A/T | 0.375 | 0.216506 | intron-variant | Senp6 | GRCm38.p3 | 9:80112663 | ATACTGATTTTTTTT[A/T]AATTTATTTATTATT | 215351 |
rs30264252 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Senp6 | Mm_Celera | 9:80072562 | GCACTGATTGCTCTT[C/T]CAGAGGTCCTGAGTT | 215351 |
rs30325250 | snp | A/G | 0.5 | 0 | intron-variant | Senp6 | Mm_Celera | 9:80141382 | GAAATTGGCAGTTCC[A/G]CTGTTTCATAGCTCC | 215351 |
rs30332702 | snp | C/T | 0.387812 | 0.208586 | intron-variant | Senp6 | Mm_Celera | 9:80103584 | CATCAATTTTTAACA[C/T]GACAAACTATGGTTT | 215351 |
rs30339031 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Senp6 | Mm_Celera | 9:80089317 | TGTTACTGTAGTAGC[A/C]GCAGTGTGGTGGCTG | 215351 |
rs30367370 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Senp6 | Mm_Celera | 9:80068692 | TTGAGTTCGAGGTCA[A/G]CCTGGTCTACAGAGT | 215351 |
rs30430915 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Senp6 | Mm_Celera | 9:80073256 | CTATCCTGCATAGTT[G/T]CTACCTGCCCATAGA | 215351 |
rs30466696 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Senp6 | Mm_Celera | 9:80137802 | AATGACAGACTGGTC[A/T]TATGAAAGATTATGA | 215351 |
rs30475169 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Senp6 | GRCm38.p3 | 9:80069841 | AGTAGGTTTTGTTTT[G/T]GTTTTTTTGTTTGTT | 215351 |
rs30475910 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Senp6 | Mm_Celera | 9:80090231 | TCCCTTCAGTATAAA[A/C]CATAGCTAAATAAGC | 215351 |
rs30480573 | snp | A/G | 0.387812 | 0.208586 | intron-variant | Senp6 | Mm_Celera | 9:80143077 | GTTCGAAGTCACTCC[A/G]TTCCTTATTGTGCCA | 215351 |
rs30485586 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Senp6 | Mm_Celera | 9:80130534 | AGTTTGTTTTTAAAA[C/T]ATATCTTTCAAGTCA | 215351 |
rs30519726 | snp | A/G | 0.375 | 0.216506 | intron-variant | Senp6 | Mm_Celera | 9:80140675 | GGAGTAACAGGCTGA[A/G]TTGTCCAGGTCACCT | 215351 |
rs30523831 | snp | G/T | 0.408163 | 0.193609 | intron-variant | Senp6 | Mm_Celera | 9:80129864 | TGTATTTCTGTGTAA[G/T]ATTTCACAAGACTTT | 215351 |
rs33623705 | snp | A/G | 0.5 | 0 | intron-variant | Senp6 | Mm_Celera | 9:80110362 | AGAGTCAAGACTGGC[A/G]TATCCAGGGCCCACA | 215351 |
rs33624683 | snp | G/T | 0.375 | 0.216506 | intron-variant | Senp6 | Mm_Celera | 9:80129994 | CCCTTGCAATATAAG[G/T]GATCATGGATGTTTG | 215351 |
rs33635015 | snp | C/G | 0.5 | 0 | intron-variant | Senp6 | GRCm38.p3 | 9:80087678 | TTATTTCTCAGTCTT[C/G]AAAATGTATGTATGT | 215351 |
rs33636814 | snp | C/T | 0.375 | 0.216506 | intron-variant | Senp6 | Mm_Celera | 9:80141037 | GGCAGATTTCTGAGT[C/T]TGAGGCCAGCCTGGT | 215351 |
rs33639071 | snp | A/C | 0.32 | 0.24 | intron-variant | Senp6 | Mm_Celera | 9:80068776 | AAAACTAAAAAAACC[A/C]AAAAAAAAAAAAAAA | 215351 |
rs33645093 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Senp6 | Mm_Celera | 9:80085437 | TTTCTGTGTCTCCCA[A/G]GTGCTGGGATGACTG | 215351 |
rs33694770 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Senp6 | Mm_Celera | 9:80076003 | TATATATACACACAC[A/G]CACACGTAAAACAAA | 215351 |
rs33772446 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Senp6 | Mm_Celera | 9:80137449 | GCATTGGAGCAGAGC[C/T]TAGGGCTTTATGTGC | 215351 |
rs33773560 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Senp6 | Mm_Celera | 9:80090608 | CACATACTTTACAAT[C/T]CTAGACTAGATCCCA | 215351 |
rs33774350 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Senp6 | Mm_Celera | 9:80089400 | GCAGCAACATCGTGC[A/G]CTCAGTTTTCCTTAG | 215351 |
rs36241057 | snp | A/G | 0.297521 | 0.245442 | intron-variant | Senp6 | Mm_Celera | 9:80129790 | TAAAACTTGAGATTC[A/G]AAATTATCAAATGGT | 215351 |
rs36248259 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Senp6 | Mm_Celera | 9:80102256 | TGTTCACATGTTCCT[A/G]ATACTGTTCTAGTCA | 215351 |
rs36260574 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Senp6 | Mm_Celera | 9:80143342 | AAGTAAATACTTGTG[C/T]TTTCGGCTGTGGAGA | 215351 |
rs36262688 | snp | C/T | 0.396694 | 0.202437 | intron-variant | Senp6 | Mm_Celera | 9:80099705 | GCTTGACAAACTGAG[C/T]TTGACCTCTGGGGTG | 215351 |
rs36266041 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Senp6 | Mm_Celera | 9:80076608 | GTCCTCCTGTGCATT[A/G]TTCCGTATTTTCCCT | 215351 |
rs36266360 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Senp6 | Mm_Celera | 9:80099756 | TTAAGCTTGAGGAAT[A/G]TTTTTATGCCTGCTT | 215351 |
rs36272429 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Senp6 | Mm_Celera | 9:80114939 | TGTCAAAGTGCACAT[C/G]CGATTTAAAAGTTAA | 215351 |
rs36274096 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Senp6 | Mm_Celera | 9:80140450 | TTTATAAGATTAAGT[G/T]GAAAGGAAAAACATA | 215351 |
rs36281315 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Senp6 | Mm_Celera | 9:80091900 | TACATTAGTGGCAGT[C/T]ATCTTGACTTTACTT | 215351 |
rs36286739 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Senp6 | Mm_Celera | 9:80094541 | GGCTCCTTGGCCAGC[A/G]TGGGGCTCTAACATA | 215351 |
rs36289177 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Senp6 | Mm_Celera | 9:80129534 | GCCCCTGAGCTGCCT[C/T]CGTATAAGAATTCTT | 215351 |
rs36289810 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Senp6 | Mm_Celera | 9:80116884 | AAATACTGTTACAAG[A/G]TTGTTCTAGACCATT | 215351 |
rs36295704 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Senp6 | Mm_Celera | 9:80142038 | AATTTTCTTATGCAC[A/C]TGTAACATAATTCAC | 215351 |
rs36296296 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Senp6 | Mm_Celera | 9:80143162 | AGGTTTGCCGTAAAC[A/G]TCAGACCTGTGGGGT | 215351 |
rs36298274 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Senp6 | Mm_Celera | 9:80107013 | AATTATAAGCATTTT[C/T]GGGAGAGGTGTTTAA | 215351 |
rs36299099 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Senp6 | Mm_Celera | 9:80109673 | GATTTTAAAAATGTT[C/T]TCTATGTTCTTTTAT | 215351 |
rs36299129 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Senp6 | Mm_Celera | 9:80143441 | CTTTATTGCAAAAAC[A/G]GGGTATGGGCAGAAC | 215351 |
rs36299520 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Senp6 | Mm_Celera | 9:80076741 | CAGAAGGGGAGGCTA[A/C]GCTTTGGAAGGACCC | 215351 |
rs36302763 | snp | C/G | 0.336735 | 0.234472 | intron-variant | Senp6 | Mm_Celera | 9:80093256 | TTCAATTTAGTAGCA[C/G]AATTAAAGTTTTAGA | 215351 |
rs36309600 | snp | A/C | 0.152778 | 0.230321 | intron-variant | Senp6 | Mm_Celera | 9:80142612 | ACCTCACCTTGCTTC[A/C]TGCTGCTTCATCGTA | 215351 |
rs36315469 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Senp6 | Mm_Celera | 9:80115948 | TTTCAAGCCATAAAT[A/G]TTTTGTAACTCAAAA | 215351 |