SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3023354 | snp | A/G | 0.32 | 0.24 | utr-variant-3-prime | Psen1 | Mm_Celera | 12:83734262 | ACTGTGGAAGGAAGC[A/G]TCTACAGAGAACGGT | 19164 |
rs3023355 | snp | A/G | 0.32 | 0.24 | utr-variant-3-prime | Psen1 | Mm_Celera | 12:83734292 | TTTCCAACATCCATC[A/G]CTGCAGCAGACGGTG | 19164 |
rs6244915 | snp | A/G | 0.5 | 0 | intron-variant | Psen1 | Mm_Celera | 12:83717388 | AGCAAAGTAAAAACA[A/G]CTGAGCCGGGGTCTG | 19164 |
rs6244953 | snp | A/G | 0.5 | 0 | intron-variant | Psen1 | Mm_Celera | 12:83717410 | cggggtctgacgagc[A/G]agccagtgaggcaaa | 19164 |
rs6245460 | snp | A/G | 0.5 | 0 | intron-variant | Psen1 | Mm_Celera | 12:83717478 | acagggtttctctgt[A/G]tagccctggctgtcc | 19164 |
rs6246011 | snp | C/T | 0.5 | 0 | intron-variant | Psen1 | Mm_Celera | 12:83717555 | cctgcctctgcctcc[C/T]gagtgctgagattaa | 19164 |
rs6246043 | snp | C/T | 0.5 | 0 | intron-variant | Psen1 | Mm_Celera | 12:83717581 | attaaaggcgtgcgc[C/T]ancactgnctggcAA | 19164 |
rs6246045 | snp | A/C | 0.5 | 0 | intron-variant | Psen1 | Mm_Celera | 12:83717583 | taaaggcgtgcgcna[A/C]cactgnctggcAAGG | 19164 |
rs6246061 | snp | C/T | 0.5 | 0 | intron-variant | Psen1 | Mm_Celera | 12:83717589 | cgtgcgcnancactg[C/T]ctggcAAGGATATAC | 19164 |
rs6386037 | snp | G/T | 0.5 | 0 | intron-variant | Psen1 | Mm_Celera | 12:83731655 | GAAAGAATGACAAAC[G/T]TATTCTTTCTTTTTT | 19164 |
rs6386715 | snp | G/T | 0.290657 | 0.246672 | intron-variant | Psen1 | Mm_Celera | 12:83731843 | GATTCTGCATACCTT[G/T]ATGGTAATTTTCTTT | 19164 |
rs6400792 | snp | A/G | 0.5 | 0 | intron-variant | Psen1 | Mm_Celera | 12:83732064 | taggacactaggatt[A/G]cnggtgggcgcccac | 19164 |
rs6400794 | snp | A/G | 0.5 | 0 | intron-variant | Psen1 | Mm_Celera | 12:83732066 | ggacactaggattnc[A/G]ggtgggcgcccacca | 19164 |
rs6401275 | snp | C/T | 0.5 | 0 | intron-variant | Psen1 | Mm_Celera | 12:83732146 | tgggtggcaagtgct[C/T]nttacctgccgggcc | 19164 |
rs6401276 | snp | G/T | 0.5 | 0 | intron-variant | Psen1 | Mm_Celera | 12:83732147 | gggtggcaagtgctn[G/T]ttacctgccgggcca | 19164 |
rs6401404 | snp | A/T | 0.290657 | 0.246672 | intron-variant | Psen1 | Mm_Celera | 12:83732228 | TTATAACGCTTTTTT[A/T]AAATGGATAATCAGA | 19164 |
rs6401827 | snp | A/G | 0.5 | 0 | intron-variant | Psen1 | Mm_Celera | 12:83732256 | AGAGCCTGCCTGAGT[A/G]TCTCTCCACTCTGGC | 19164 |
rs13464996 | snp | G/T | 0.32 | 0.24 | missense | Psen1 | Mm_Celera | 12:83712330 | AGAACGGCAGCAGCA[G/T]CATGACAGGCAGAGA | 19164 |
rs29132325 | snp | C/T | 0.375 | 0.216506 | upstream-variant-2KB, utr-variant-5-prime | Psen1 | Mm_Celera | 12:83688255 | AGCTGAGGCGGAAAC[C/T]TAGGCTGCGAGCCGG | 19164 |
rs29179121 | snp | C/T | 0.444444 | 0.157135 | upstream-variant-2KB, utr-variant-5-prime | Psen1 | Mm_Celera | 12:83688186 | CCTCTAGGGCGGGGC[C/T]TAGGACGACCTGCTC | 19164 |
rs36240551 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Psen1 | Mm_Celera | 12:83701282 | CAGCTTGAGAACCAC[C/T]GATCTAGAGTGTAGC | 19164 |
rs36244517 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon | Psen1 | Mm_Celera | 12:83730606 | CAGTGAGGAGTGGGA[A/G]GCCCAAAGAGACAGT | 19164 |
rs36248110 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Psen1 | Mm_Celera | 12:83732324 | TGTCTTTTCTGCGGA[A/G]TGTATTGCTGAGGAT | 19164 |
rs36248749 | snp | C/T | 0.32 | 0.24 | upstream-variant-2KB | Psen1 | Mm_Celera | 12:83687664 | TAGAAGCTTGCCATC[C/T]GGGAAGACTTTCAGA | 19164 |
rs36249051 | snp | A/G | 0.124444 | 0.216185 | downstream-variant-500B, utr-variant-3-prime | Psen1 | Mm_Celera | 12:83735203 | CCAATGCTGGGAGTT[A/G]GTCAGTTCAGAACCA | 19164 |
rs36250572 | snp | A/C | 0.32 | 0.24 | intron-variant | Psen1 | Mm_Celera | 12:83732858 | CTGTGGCTTTCAAAC[A/C]TGACTTAGAGCACTG | 19164 |
rs36260773 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Psen1 | Mm_Celera | 12:83694878 | CATTGTCTTGGGTAA[A/G]TGTATAGATTGGCCC | 19164 |
rs36262685 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Psen1 | Mm_Celera | 12:83702561 | AGCTTCCCAATGCTG[G/T]CGTGATGATCGACTG | 19164 |
rs36271017 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Psen1 | Mm_Celera | 12:83699485 | CGTAGCCACCTCAAA[C/G]CATAAAGTCTTGTTT | 19164 |
rs36275273 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Psen1 | Mm_Celera | 12:83719076 | CTTTGAAGAGTTTAT[A/T]AGAGTCATTTTGCAT | 19164 |
rs36281553 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Psen1 | Mm_Celera | 12:83719284 | AAGATTAGTGTCTTC[G/T]AGAAAGGAACAGGGC | 19164 |
rs36282543 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Psen1 | Mm_Celera | 12:83713375 | GCCTCAGTTTTCATT[C/T]GACAGCAGGAGGGAG | 19164 |
rs36291975 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Psen1 | Mm_Celera | 12:83729164 | GTATGTCCAGAATAA[C/G]TGAAAACATTAGGTG | 19164 |
rs36292441 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Psen1 | Mm_Celera | 12:83726257 | ATGAAAGCCAAAAAG[A/G]AGTCTGTTGTCAGGG | 19164 |
rs36293673 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Psen1 | Mm_Celera | 12:83717810 | GTATGTTGTTGCCGA[C/G]TGGGCCGCAGGAATC | 19164 |
rs36294388 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Psen1 | Mm_Celera | 12:83700656 | AATGTAAGACTTTGC[A/G]TTTTAAAACTGTTAT | 19164 |
rs36297653 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Psen1 | Mm_Celera | 12:83720265 | CATTTACACCTAAGA[A/T]TTGGAACATATGTGT | 19164 |
rs36323586 | snp | A/G | 0.35503 | 0.226867 | utr-variant-3-prime | Psen1 | Mm_Celera | 12:83734746 | GAGAGTTGTAACCTC[A/G]ACTTCCAAAGTTTAT | 19164 |
rs36328433 | snp | A/G | 0.231111 | 0.249285 | utr-variant-3-prime | Psen1 | Mm_Celera | 12:83737244 | AAGGCCAGGCTTCTA[A/G]TGGGAGTCTCTGTCT | 19164 |
rs36333981 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Psen1 | Mm_Celera | 12:83717750 | AGCTACCTTTCTGCA[C/T]TTGGGCTGCTAGAAT | 19164 |
rs36334117 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Psen1 | Mm_Celera | 12:83711016 | AGGAAAGTGGGATTT[A/T]AAAAAAGATTATAAA | 19164 |
rs36334325 | snp | A/G | 0.32 | 0.24 | intron-variant | Psen1 | Mm_Celera | 12:83690829 | GTTATAACACACATG[A/G]TCACTTTATGGAATC | 19164 |
rs36338836 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Psen1 | Mm_Celera | 12:83708173 | TTTAAAATAAGTTGT[A/G]CCTTCTAAAAGTTGA | 19164 |
rs36345526 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Psen1 | Mm_Celera | 12:83698900 | CTATTCTCACGTGGC[A/T]GGGGCCTCAACTCCT | 19164 |
rs36346521 | snp | A/G | 0.231111 | 0.249285 | utr-variant-3-prime | Psen1 | Mm_Celera | 12:83738375 | CTTTCAAACTCTTGG[A/G]AAGCTATAATTTTGA | 19164 |
rs36352197 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Psen1 | Mm_Celera | 12:83692099 | AGAGGATATTTACTG[A/G]ATAATAATTGTCTCT | 19164 |
rs36371862 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Psen1 | Mm_Celera | 12:83705060 | TCATAACCAGTTTTT[A/G]ACTCATAGTTTAATA | 19164 |
rs36380506 | snp | A/G | 0.231111 | 0.249285 | utr-variant-3-prime | Psen1 | Mm_Celera | 12:83736545 | ACGAGAGCCAGCTTC[A/G]CCATCAGAGGCTGGA | 19164 |
rs36382704 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Psen1 | Mm_Celera | 12:83694076 | TTTTAGAAGTTTTGG[C/T]GTTGAGAGGAGGTTT | 19164 |
rs36389060 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Psen1 | Mm_Celera | 12:83732709 | GGCTGTCATAGTCCA[C/T]GGGCTGAGTCAGTGA | 19164 |
rs36397422 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Psen1 | Mm_Celera | 12:83702119 | ATTTCTCTTAAAATA[A/G]CACTATGTCTAAACC | 19164 |
rs36403282 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Psen1 | Mm_Celera | 12:83705129 | GCCCTGCCATCTGCA[C/T]GATGAGTTATCTTTT | 19164 |
rs36414836 | snp | A/G | 0.231111 | 0.249285 | synonymous-codon | Psen1 | Mm_Celera | 12:83712408 | AAGACAGGTGGTGGA[A/G]CAAGATGAGGAGGAA | 19164 |
rs36437685 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Psen1 | Mm_Celera | 12:83706976 | CGGCTTGGCTTTCTG[A/G]TGTCTTTGCGGTAAT | 19164 |
rs36443048 | snp | G/T | 0.124444 | 0.216185 | utr-variant-3-prime | Psen1 | Mm_Celera | 12:83738226 | ATTCCAATCCATACT[G/T]GTTGAAGGGCACTGC | 19164 |
rs36450707 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Psen1 | Mm_Celera | 12:83711060 | TCCATCTAGCATTTA[C/T]GTTCTTTCTCAGGCT | 19164 |
rs36459261 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Psen1 | Mm_Celera | 12:83708975 | GTAGAAGTCTCCTGA[C/T]TACTTGTGGGACCGT | 19164 |
rs36478343 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Psen1 | Mm_Celera | 12:83724910 | CAGCCTGAGAGTGAG[A/G]GTTTGTAGTTCCTTG | 19164 |
rs36480411 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Psen1 | Mm_Celera | 12:83732679 | TGAGAGTCCAGCTGT[A/G]TAGGGCTCAACAAAG | 19164 |
rs36480692 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Psen1 | Mm_Celera | 12:83726660 | GGCACAATAAATAAT[A/G]TAATTTACAATCCCG | 19164 |
rs36497670 | snp | A/C/G | 0.124444 | 0.216185 | intron-variant | Psen1 | GRCm38.p3 | 12:83726497 | TTTTGTCAGTCGCTG[A/C/G]GAGTAGGAGTACCAT | 19164 |
rs36503592 | snp | C/T | 0.32 | 0.24 | utr-variant-3-prime | Psen1 | Mm_Celera | 12:83734238 | CTCCCTAGCCACCCG[C/T]ACTACTGGACTGTGG | 19164 |
rs36506154 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Psen1 | Mm_Celera | 12:83721065 | GCCTTGCATGGAAGT[A/G]AGCAGAAAGGAAGGG | 19164 |
rs36512936 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Psen1 | Mm_Celera | 12:83695063 | AGAGAGGAGCTAGAT[A/G]TCAGGAAGGTGTTGC | 19164 |
rs36515475 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Psen1 | Mm_Celera | 12:83698620 | CCAATTTGGATAAAG[C/T]TTTCAATTTTAGATG | 19164 |
rs36519065 | snp | A/G | 0.408163 | 0.193609 | upstream-variant-2KB | Psen1 | Mm_Celera | 12:83687984 | TCACTTGTAGACTGG[A/G]AGAACGCTAGACGCG | 19164 |
rs36541690 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Psen1 | Mm_Celera | 12:83728692 | CAGCTTTGTCTTTCT[C/T]AACAGCAACAATGGT | 19164 |
rs36541798 | snp | C/T | 0.231111 | 0.249285 | downstream-variant-500B, utr-variant-3-prime | Psen1 | Mm_Celera | 12:83735599 | CTCAAGCAAGGCTGC[C/T]GGCTTTCTTTCCCAG | 19164 |
rs36545550 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Psen1 | Mm_Celera | 12:83718818 | CCTTGCATCTTCTAC[A/G]GTTTGTTAATACTGT | 19164 |
rs36556449 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Psen1 | Mm_Celera | 12:83692931 | AGATGAGGGAGTAAA[A/C]CAAGAAAAGCTGGGT | 19164 |
rs36561147 | snp | A/G | 0.486111 | 0.0821678 | intron-variant | Psen1 | Mm_Celera | 12:83710075 | TTAGCTTAATCAGGT[A/G]CTGTTTACCAACAGT | 19164 |
rs36567676 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Psen1 | Mm_Celera | 12:83716616 | AATTTGGCCTTGATT[A/G]ACTGACAGGCATTAT | 19164 |
rs36569200 | snp | C/T | 0.124444 | 0.216185 | downstream-variant-500B, utr-variant-3-prime | Psen1 | Mm_Celera | 12:83735557 | CAGCCAGAAGACCAA[C/T]TGAAAAGACTTGAGA | 19164 |
rs36575140 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Psen1 | Mm_Celera | 12:83694055 | TTAAACATTGCTCCT[G/T]AGATGTTTTAGAAGT | 19164 |
rs36582471 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Psen1 | Mm_Celera | 12:83717842 | TGTGAGGTTCTGTTC[C/T]CTCAGCTATGTGGCC | 19164 |
rs36582747 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Psen1 | Mm_Celera | 12:83716418 | GTTTTTCCTGCACTG[A/G]TCTGTTGATGACAAT | 19164 |
rs36586874 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Psen1 | Mm_Celera | 12:83718897 | TCTGTTTTAAAGATG[C/T]TAGATCATTTTGGGT | 19164 |
rs36589901 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Psen1 | Mm_Celera | 12:83722038 | CCAAAAATTTAAAGT[A/G]GAAGATAGCTGTTCA | 19164 |
rs36591385 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Psen1 | Mm_Celera | 12:83694726 | TCTAGTAAAGAAAAT[A/G]CATTGTGGGCAGAAA | 19164 |
rs36595460 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Psen1 | Mm_Celera | 12:83716244 | ATTTTTCAAAGTTGC[C/T]TGTGTACTACATACA | 19164 |
rs36606490 | snp | G/T | 0.32 | 0.24 | intron-variant | Psen1 | Mm_Celera | 12:83713310 | TTCACAAAGCATGTG[G/T]GCTCCTCTCTTCAGC | 19164 |
rs36606605 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Psen1 | Mm_Celera | 12:83726817 | AGTTACTCTCTCCAC[A/G]ACCTTCAGCCTCTGC | 19164 |
rs36619318 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Psen1 | Mm_Celera | 12:83713283 | AGTCCAGATTGGTAT[A/C]CGGGTCTTTTATTCA | 19164 |
rs36620982 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Psen1 | Mm_Celera | 12:83693357 | ATAGCCATTTATGTA[G/T]AGCAAAAAAATAATT | 19164 |
rs36624319 | snp | C/G | 0.152778 | 0.230321 | intron-variant | Psen1 | Mm_Celera | 12:83717969 | AAGTGCCTTCACCAA[C/G]AAAGCTATCTTGCTG | 19164 |
rs36625874 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Psen1 | Mm_Celera | 12:83698407 | ATCTTTCTGGCAGCG[G/T]GTGATTTAAGTAGCA | 19164 |
rs36628477 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Psen1 | Mm_Celera | 12:83692176 | AGCCACCCTCAACCG[A/G]CTGCATCACTGCCCT | 19164 |
rs36635830 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Psen1 | Mm_Celera | 12:83706924 | ACAGAGTTCGTAGCT[C/G]TACTGCTCAGTGGGA | 19164 |
rs36639915 | snp | A/T | 0.277778 | 0.248452 | upstream-variant-2KB | Psen1 | Mm_Celera | 12:83687431 | GATTTCAGATACAAC[A/T]CCATCCCGATGTATT | 19164 |
rs36646824 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Psen1 | Mm_Celera | 12:83691389 | AAATAAGTTGCAGCA[A/G]TAAGTCTCCATAGCA | 19164 |
rs36647470 | snp | A/G | 0.32 | 0.24 | intron-variant | Psen1 | Mm_Celera | 12:83733859 | GAGTATTCCCTGAGC[A/G]TGGTGCTGATGCTGC | 19164 |
rs36649296 | snp | A/G | 0.444444 | 0.157135 | synonymous-codon | Psen1 | Mm_Celera | 12:83724550 | TACAGTAGCACTCCT[A/G]ATCTGGAATTTTGGT | 19164 |
rs36652468 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Psen1 | Mm_Celera | 12:83717749 | CAGCTACCTTTCTGC[A/T]TTTGGGCTGCTAGAA | 19164 |
rs36657311 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Psen1 | Mm_Celera | 12:83710210 | CTCTGTTACTGTTCT[G/T]TTTATTCATTTTACC | 19164 |
rs36663084 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Psen1 | Mm_Celera | 12:83720707 | AATACCTTTTTAAAA[C/T]AGAACAAGAGTCACG | 19164 |
rs36664433 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Psen1 | Mm_Celera | 12:83720870 | AAGCTGGGAAGTCAG[A/G]GAGCTACACAAGACT | 19164 |
rs36670216 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Psen1 | Mm_Celera | 12:83722154 | AAATTATTTTAAAAG[C/T]CTGTCATATAACAGA | 19164 |
rs36674025 | snp | A/G | 0.231111 | 0.249285 | utr-variant-3-prime | Psen1 | Mm_Celera | 12:83737641 | CTGTTAAGAGACCTC[A/G]TTCCTTCAGAAGCCC | 19164 |
rs36674210 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Psen1 | Mm_Celera | 12:83727248 | CGTCAGCTGTCAAGT[C/T]TCCCATTCCTGTTTT | 19164 |
rs36675665 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime | Psen1 | Mm_Celera | 12:83736531 | GATGCCTACAGGATA[C/T]GAGAGCCAGCTTCGC | 19164 |