SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6228201 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Mid1 | Mm_Celera | X:169952974 | CCAATGGTACTTTTT[A/T]AAAAGCAACATTTAT | 17318 |
rs6228238 | snp | A/T | 0.5 | 0 | intron-variant | Mid1 | Mm_Celera | X:169953000 | TTTATTCTTTGACTT[A/T]GCCTCATTAACAAAA | 17318 |
rs6235276 | snp | A/C | 0.5 | 0 | intron-variant | Mid1 | Mm_Celera | X:169749209 | tccaggtaactgcca[A/C]acccaagatcttgag | 17318 |
rs6235772 | snp | G/T | 0.5 | 0 | intron-variant | Mid1 | Mm_Celera | X:169749281 | gctttaactactgag[G/T]catttccacagcccT | 17318 |
rs6243046 | snp | G/T | 0.21875 | 0.248039 | intron-variant | Mid1 | Mm_Celera | X:169953395 | TAGAAGCTGAAATTT[G/T]TCTCCTAAATCTTCA | 17318 |
rs6243051 | snp | A/C | 0.290657 | 0.246672 | intron-variant | Mid1 | Mm_Celera | X:169761556 | AAAATATTCCTTTAG[A/C]ATCCATGTTGCTTCT | 17318 |
rs6244136 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Mid1 | Mm_Celera | X:169761756 | AACCATCCTGGCCTG[C/T]CTTTATTCCTGTGAG | 17318 |
rs6248022 | snp | A/G | 0.359862 | 0.224567 | intron-variant | Mid1 | Mm_Celera | X:169920949 | GGTGGTGAAAGAAGC[A/G]CTGTAGGAGACACCT | 17318 |
rs6262366 | snp | A/G | 0.207612 | 0.24638 | intron-variant | Mid1 | Mm_Celera | X:169921410 | TTTGAGAAGAGCCCA[A/G]GCATCTAAGGATACA | 17318 |
rs6262797 | snp | A/T | 0.207612 | 0.24638 | intron-variant | Mid1 | Mm_Celera | X:169921431 | TAAGGATACAAGGTT[A/T]CAGTGAACTCTATCG | 17318 |
rs6283733 | snp | G/T | 0.5 | 0 | intron-variant | Mid1 | Mm_Celera | X:169731016 | tgagagttctgcatc[G/T]tgattggaaggtacc | 17318 |
rs6283828 | snp | C/G | 0.5 | 0 | intron-variant | Mid1 | Mm_Celera | X:169731076 | aggagggtctctacc[C/G]naatgggtatagcct | 17318 |
rs6283829 | snp | A/C | 0.5 | 0 | intron-variant | Mid1 | Mm_Celera | X:169731077 | ggagggtctctaccn[A/C]aatgggtatagcctg | 17318 |
rs6284282 | snp | C/T | 0.5 | 0 | intron-variant | Mid1 | Mm_Celera | X:169731121 | tccaaaacccactcc[C/T]acagtgacacacctt | 17318 |
rs6284804 | snp | A/T | 0.5 | 0 | intron-variant | Mid1 | Mm_Celera | X:169731230 | acacccacaggctag[A/T]tcaaacacatgagtc | 17318 |
rs6284867 | snp | C/T | 0.5 | 0 | intron-variant | Mid1 | Mm_Celera | X:169731265 | ggagccatacctagc[C/T]gtagcataatgtaaa | 17318 |
rs6284908 | snp | A/G | 0.5 | 0 | intron-variant | Mid1 | Mm_Celera | X:169731290 | tgtaaaatacatata[A/G]tccaacttcaaaaaa | 17318 |
rs6285337 | snp | C/T | 0.5 | 0 | intron-variant | Mid1 | Mm_Celera | X:169731338 | agcaatatttaaatg[C/T]ctaacgtttaaagtc | 17318 |
rs6298774 | snp | A/T | 0.5 | 0 | intron-variant | Mid1 | Mm_Celera | X:169731444 | atcacaggatataTG[A/T]GAGACAAAAatggtg | 17318 |
rs6298842 | snp | A/G | 0.5 | 0 | intron-variant | Mid1 | Mm_Celera | X:169731491 | agctagggctgctgg[A/G]cgaggtgaatgtggg | 17318 |
rs6304254 | snp | C/T | 0.5 | 0 | intron-variant | Mid1 | Mm_Celera | X:169917859 | CAATTCTATTAAAAT[C/T]TAACCTTTCTGAAAC | 17318 |
rs6304762 | snp | G/T | 0.5 | 0 | intron-variant | Mid1 | Mm_Celera | X:169917956 | ttacaattcataaca[G/T]tagcaaaactagtta | 17318 |
rs6316955 | snp | G/T | 0.5 | 0 | intron-variant | Mid1 | Mm_Celera | X:169957918 | TTTGTATGCAGATTG[G/T]GTTTTATTAGGTTTT | 17318 |
rs6353597 | snp | A/T | 0.5 | 0 | intron-variant | Mid1 | Mm_Celera | X:169861275 | GAAAACTTCAGAGCC[A/T]GTTCTTTCTCTACAA | 17318 |
rs6367387 | snp | C/T | 0.5 | 0 | intron-variant | Mid1 | Mm_Celera | X:169861503 | CACATTTCTGGAATT[C/T]TTCTTCGGAACGGGT | 17318 |
rs6382407 | snp | A/C | 0.5 | 0 | intron-variant | Mid1 | Mm_Celera | X:169901919 | GTTGCCATTTTAGAA[A/C]GTTGACCTGCTGTAG | 17318 |
rs6382480 | snp | C/T | 0.207612 | 0.24638 | intron-variant | Mid1 | Mm_Celera | X:169901958 | ATCTGTTGCTTTGCA[C/T]CTTTATGTACAATTC | 17318 |
rs6383591 | snp | A/C | 0.5 | 0 | intron-variant | Mid1 | Mm_Celera | X:169902172 | gtttacattcataac[A/C]gtagcaaacttatga | 17318 |
rs30532758 | snp | A/G | 0.5 | 0 | intron-variant | Mid1 | GRCm38.p3 | X:169981127 | AAGCAAGACAGAATC[A/G]GGAACTAGAATGGAG | 17318 |
rs30563752 | snp | C/T | 0.5 | 0 | intron-variant | Mid1 | GRCm38.p3 | X:169980946 | CTTGGAATTTTAATT[C/T]TAACTTGGCTCCTGG | 17318 |
rs30568408 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Mid1 | GRCm38.p3 | X:169981022 | GTCAAGCGGCTTCCC[C/T]TGGACTTCTCTTGAC | 17318 |
rs30628840 | snp | C/T | 0 | 0 | intron-variant, upstream-variant-2KB | Mid1, G530011O06Rik | GRCm38.p3 | X:169980690 | TCCTTCCTTTTTTTT[C/T]CTCCAAGATTAAAGT | 17318 |
rs30871001 | snp | C/T | 0 | 0 | intron-variant, upstream-variant-2KB | Mid1, G530011O06Rik | GRCm38.p3 | X:169980688 | CTTCCTTCCTTTTTT[C/T]TTCTCCAAGATTAAA | 17318 |
rs31068549 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Mid1 | Mm_Celera | X:169787461 | CCGGCCATTTTTTTT[C/T]TTAACTCTTGCAAAA | 17318 |
rs31792697 | snp | C/T | 0.231111 | 0.249285 | upstream-variant-2KB | Mid1 | Mm_Celera | X:169683263 | ATACATTCTAAATTT[C/T]CTGCATAAACATTAC | 17318 |
rs31792700 | snp | A/T | 0.231111 | 0.249285 | upstream-variant-2KB | Mid1 | Mm_Celera | X:169684344 | AACTATATTTCAAAC[A/T]TGAGTTAGGCCTTCT | 17318 |
rs31792703 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Mid1 | Mm_Celera | X:169685585 | CTGAGGCAATAATCC[G/T]AGCACCTTAGGCATT | 17318 |
rs31793734 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Mid1 | Mm_Celera | X:169685705 | TTTCCAGATCATCGT[A/G]AAGAGCAAACTTTCT | 17318 |
rs31793737 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Mid1 | Mm_Celera | X:169686056 | CCTGTTTATATATAA[A/G]GTGCAAGTGATAAAT | 17318 |
rs31793740 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Mid1 | Mm_Celera | X:169686789 | CAACCATGTTTAGTA[A/G]CACAATTTAAGTGCT | 17318 |
rs31793743 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Mid1 | Mm_Celera | X:169687132 | TTGTGAGTTGATGTG[C/T]ACTTTGTTATTACAT | 17318 |
rs31794526 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Mid1 | Mm_Celera | X:169687348 | AATCTCATTTACGGG[C/T]AACAATACTGATTAT | 17318 |
rs31794529 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Mid1 | Mm_Celera | X:169687678 | ACTTCCTGAAGTGTG[A/G]TATGCACCCTATAAA | 17318 |
rs31794532 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Mid1 | Mm_Celera | X:169688449 | CTGTGTAAAGAGAGA[G/T]TTCATAATGTGAATG | 17318 |
rs31795325 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Mid1 | Mm_Celera | X:169688857 | TCCCAGCACAGAAAA[G/T]GAAAACCTGAACTGT | 17318 |
rs31795327 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Mid1 | Mm_Celera | X:169689104 | GATGCATAGTCTACC[A/G]CCTCATTTTTAGAAC | 17318 |
rs31795330 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Mid1 | Mm_Celera | X:169690340 | GTAGGAAGGTTTAGC[C/T]GATCAGGGTGACATT | 17318 |
rs31795333 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Mid1 | Mm_Celera | X:169691630 | TGCATGAAATCCCAA[A/C]TCCAAGTCACTGGCA | 17318 |
rs31796145 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Mid1 | Mm_Celera | X:169691709 | TTTTTTAGGGCAAGT[C/G]TGCATATTATAGTGT | 17318 |
rs31796148 | snp | A/T | 0.32 | 0.24 | intron-variant | Mid1 | Mm_Celera | X:169692254 | CACATCAGCACAGCA[A/T]GTTAAAAGAAACTGC | 17318 |
rs31796150 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Mid1 | Mm_Celera | X:169692376 | AAGGCTTTGCTATCG[A/C]CTTCTTTACGTATTT | 17318 |
rs31796152 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Mid1 | Mm_Celera | X:169692463 | CCAGTACAGATAAGT[C/T]TAGTGGCAGCCAGCT | 17318 |
rs31797075 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Mid1 | Mm_Celera | X:169692648 | AAATCTGAGCAAGGA[C/T]TGATCTTAGGTGTAA | 17318 |
rs31797077 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Mid1 | Mm_Celera | X:169692971 | GTGCAGAGAGAATAT[A/T]GGTGGCTATGTGAGG | 17318 |
rs31797079 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Mid1 | Mm_Celera | X:169692992 | CTATGTGAGGTTGCA[A/G]TGATTTCTTTCCCCA | 17318 |
rs31797081 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Mid1 | Mm_Celera | X:169693580 | ATTCCAGTCAGAGGA[A/G]AGTGTAAGAAAGTAA | 17318 |
rs31798154 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Mid1 | Mm_Celera | X:169693951 | AAGCAGGCAAAATAT[A/C]CCACCTCTAGGATAG | 17318 |
rs31798157 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Mid1 | Mm_Celera | X:169693989 | CCATTGAACTTGTTA[A/G]TAGGCCTTTTACTCT | 17318 |
rs31798160 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Mid1 | Mm_Celera | X:169694110 | TGATGATAAATAGAA[A/G]CAATGACTACTAAAG | 17318 |
rs31798163 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Mid1 | Mm_Celera | X:169694370 | TCTGTAAAAAAAAAA[A/T]ATATGCTTGAACAAA | 17318 |
rs31798664 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Mid1 | Mm_Celera | X:169695815 | ATAGAGACCAGGCAC[A/G]GTGGCCTAGGCTGAG | 17318 |
rs31798667 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Mid1 | Mm_Celera | X:169695947 | ATATCTGAAACAAGA[A/G]TTCTGATAAACGCTT | 17318 |
rs31798670 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Mid1 | Mm_Celera | X:169696315 | AACTTCTGGGTGATT[A/G]AAAACAGTGCTGTAT | 17318 |
rs31798673 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Mid1 | Mm_Celera | X:169696348 | TAACAAATTTCAGAC[G/T]CTCCAAGTGAGAATT | 17318 |
rs31798936 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Mid1 | Mm_Celera | X:169694784 | TTTAGTGTGTAAATC[A/G]TGGACAAATGATTGT | 17318 |
rs31798939 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Mid1 | Mm_Celera | X:169694804 | CAAATGATTGTTTGA[C/T]TGATTTTGTTCAAAG | 17318 |
rs31798942 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Mid1 | Mm_Celera | X:169694869 | TAAGACTACTGAAAA[A/C]CACATCAGTTACCAT | 17318 |
rs31799054 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Mid1 | Mm_Celera | X:169702628 | CTAACTCCTTTTTAA[C/G]TAACCCCAGAGCATC | 17318 |
rs31799057 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Mid1 | Mm_Celera | X:169702657 | TCATTCACCAAAACA[C/T]GTCTCAGAAACAAGG | 17318 |
rs31799060 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Mid1 | Mm_Celera | X:169704064 | TCAATGATGGTTAAA[A/G]AATTCAGATGAGAAA | 17318 |
rs31799063 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Mid1 | Mm_Celera | X:169704602 | GAAAGTAGAATTGCC[C/T]GAACTGCACTGGGGT | 17318 |
rs31799396 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Mid1 | Mm_Celera | X:169696536 | ACACTGTTGCAACAC[C/T]TCCCATGTATGAAGA | 17318 |
rs31799398 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Mid1 | Mm_Celera | X:169696670 | CTAACTTTTCTGGTG[A/G]GATTAAGATCAGGAA | 17318 |
rs31799400 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Mid1 | Mm_Celera | X:169696947 | GTGACAAGAACAGAG[C/T]TCATAAAATCCCCAA | 17318 |
rs31799402 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Mid1 | Mm_Celera | X:169698341 | ACTAATTAATTTCAA[C/T]GGCTCCTCTACTTTT | 17318 |
rs31799774 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Mid1 | Mm_Celera | X:169695041 | AATACTGAAAGATCA[A/G]CATCAATGGATTATG | 17318 |
rs31799777 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Mid1 | Mm_Celera | X:169695078 | TTTGATTTATCTAGT[A/T]AGGTCACATAATTTG | 17318 |
rs31799780 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Mid1 | Mm_Celera | X:169695197 | TAAGCTGAGGCCTAT[A/C]ACCTCACTTGGGTGG | 17318 |
rs31799905 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Mid1 | Mm_Celera | X:169747966 | AACATGGGCAAAGAA[A/G]TTCTGTCTTGCAAAT | 17318 |
rs31799908 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Mid1 | Mm_Celera | X:169748094 | TAAAAGTAATTCCAG[A/G]GAAACTAGTGTAGAT | 17318 |
rs31799911 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Mid1 | Mm_Celera | X:169748180 | GTCTTATAGCTTGTG[C/G]TTTTCTCAGATACCT | 17318 |
rs31799986 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Mid1 | Mm_Celera | X:169704774 | TCTAAAACCTAGCCA[A/T]CCATTACTGGATATG | 17318 |
rs31799989 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Mid1 | Mm_Celera | X:169711777 | GGCTGGAGCAACTCA[C/T]TCACAAAACCATGAG | 17318 |
rs31799992 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Mid1 | Mm_Celera | X:169727298 | TTTGATGTCTTTTAG[C/T]CTTCTTAGGAATATT | 17318 |
rs31800364 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Mid1 | Mm_Celera | X:169698876 | AGAAAATGTTACTGC[C/T]TGAATCAATACCAGG | 17318 |
rs31800366 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Mid1 | Mm_Celera | X:169699002 | TATGTTTCTTATGAG[C/T]AGCACAAGAAAAATG | 17318 |
rs31800367 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Mid1 | Mm_Celera | X:169699060 | CAGGTTCATCACTCC[A/G]GCATTTCCCAGCTAT | 17318 |
rs31800369 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Mid1 | Mm_Celera | X:169699082 | CCCAGCTATATAACA[C/T]GGGCAAGTCCCTCGC | 17318 |
rs31800371 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Mid1 | Mm_Celera | X:169699130 | GAGTCAAGGTAAATA[C/T]GCTTCCTTCTCTGGA | 17318 |
rs31800373 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Mid1 | Mm_Celera | X:169699160 | AGTCTGAGAGGATAC[A/G]GTGAACCTGTACAGC | 17318 |
rs31800614 | snp | C/T | 0.375 | 0.216506 | intron-variant | Mid1 | GRCm38.p3 | X:169748315 | CAGAGACCTTATGAA[C/T]AAAAAAAAAGCAGAA | 17318 |
rs31800617 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Mid1 | Mm_Celera | X:169748633 | ACAACATTAAAGTTA[C/T]GTTTAGAGCAATATA | 17318 |
rs31800620 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Mid1 | Mm_Celera | X:169748934 | CATGGTTTATCAACC[A/G]TTTCCTAATTTTCTA | 17318 |
rs31800623 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Mid1 | Mm_Celera | X:169761126 | AATAGATATCAGAGA[A/G]CTCATTTGATACCAA | 17318 |
rs31800654 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Mid1 | Mm_Celera | X:169782027 | CACCTACCTTATGGT[G/T]AGAAGTATGAAGGTC | 17318 |
rs31800657 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Mid1 | Mm_Celera | X:169782033 | CCTTATGGTTAGAAG[A/T]ATGAAGGTCAAGCTC | 17318 |
rs31800659 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Mid1 | Mm_Celera | X:169782885 | CTGCCCTTTTGTGTT[G/T]GTTGCCTCTTGAACT | 17318 |
rs31800662 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Mid1 | Mm_Celera | X:169783463 | CCCCATGAAGTCTAC[A/T]CTTTTCTTCCCCTGT | 17318 |
rs31800795 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Mid1 | Mm_Celera | X:169727783 | TTACCTAGGGCTAGG[A/C]TATACCATACAGGTG | 17318 |
rs31800798 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Mid1 | Mm_Celera | X:169729988 | TTCAAAAGTTGAGGC[A/T]TTTTTCTCTATTATC | 17318 |