SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs4222683 | snp | C/T | 0.21875 | 0.248039 | utr-variant-3-prime | Ivns1abp | GRCm38.p3 | 1:151364117 | TTGAATTACTGTTAC[C/T]ATTCAGCAACTCCAT | 117198 |
rs13462535 | snp | G/T | | | missense | Ivns1abp | Mm_Celera | 1:151363303 | GAGTTTCTGAATACT[G/T]TGGAAGTCTACAACC | 117198 |
rs13462536 | snp | C/T | 0.33241 | 0.236027 | missense | Ivns1abp | Mm_Celera | 1:151361590 | TGGACTTTAATTGCA[C/T]CCATGAATGTGGCGA | 117198 |
rs13462537 | snp | A/G | | | utr-variant-5-prime | Ivns1abp | Mm_Celera | 1:151344648 | CCACTGGTCTTCCTC[A/G]GCCCGCAGCCTCCCG | 117198 |
rs13462539 | snp | A/T | | | utr-variant-3-prime | Ivns1abp | Mm_Celera | 1:151364112 | TTTGGATGGAGTTGC[A/T]GAATGGTAACAGTAA | 117198 |
rs13462540 | snp | C/T | | | utr-variant-5-prime | Ivns1abp | Mm_Celera | 1:151349433 | CTTTTAAGGACTTGA[C/T]TACATCATTTTCAAG | 117198 |
rs13462541 | snp | C/G | 0.244898 | 0.249948 | utr-variant-3-prime | Ivns1abp | GRCm38.p3 | 1:151364038 | AGAACGCAGACTTCA[C/G]CATTTGCCGCAGCTG | 117198 |
rs30475835 | snp | C/T | 0.255 | 0.24995 | intron-variant | Ivns1abp | GRCm38.p3 | 1:151358586 | GTTAATGCCAGTAGT[C/T]TTTAGTGCTGGAGTG | 117198 |
rs30525806 | snp | A/G/T | 0.32 | 0.24 | intron-variant | Ivns1abp | GRCm38.p3 | 1:151354409 | CGTTTCTGGCCCCAC[A/G/T]TGCTGCTTGTTACTG | 117198 |
rs30754789 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Ivns1abp | Mm_Celera | 1:151363062 | TTTTTTTTTTTTTTT[A/T]AATTTGTTTTCTGAG | 117198 |
rs30770515 | snp | A/T | 0.345679 | 0.230967 | intron-variant | Ivns1abp | Mm_Celera | 1:151357478 | AGTGGTAGGCTGTGA[A/T]GCTCGACGTGAAGAC | 117198 |
rs31113346 | snp | A/G | 0.375 | 0.216506 | upstream-variant-2KB | Ivns1abp | GRCm38.p3 | 1:151343171 | CTCTCACTGCCAGAA[A/G]GAGCTCAGTAATCCA | 117198 |
rs31152925 | snp | A/G | 0.32 | 0.24 | intron-variant | Ivns1abp | GRCm38.p3 | 1:151346938 | AACCAAAACAGCCAC[A/G]GTTTCTGGACTCTGT | 117198 |
rs31197549 | snp | C/T | 0.484429 | 0.0868505 | intron-variant | Ivns1abp | GRCm38.p3 | 1:151354619 | GATATTTGTTTTATT[C/T]ATATACAATTCTAGT | 117198 |
rs31323814 | snp | C/G | 0.32 | 0.24 | intron-variant | Ivns1abp | GRCm38.p3 | 1:151350824 | GTCCTTGACTTTACT[C/G]TCTTGTGTATGACCA | 117198 |
rs31351080 | snp | G/T | 0.345679 | 0.230967 | intron-variant | Ivns1abp | GRCm38.p3 | 1:151353416 | TCACATTCCAGCTTC[G/T]TCCTAATACAGATAC | 117198 |
rs31374575 | snp | A/G | 0.32 | 0.24 | upstream-variant-2KB | Ivns1abp | GRCm38.p3 | 1:151343696 | ACATTTGACCTAAAC[A/G]ACTGCCTGCCTCCTA | 117198 |
rs31413825 | snp | C/T | 0.255 | 0.24995 | downstream-variant-500B, intron-variant | Ivns1abp | GRCm38.p3 | 1:151356839 | ACACGCACTTAAATT[C/T]ATACACATTTTTAAC | 117198 |
rs31804702 | snp | A/T | 0.375 | 0.216506 | intron-variant | Ivns1abp | Mm_Celera | 1:151348412 | ACAGTCGGGTGCTCT[A/T]ACCCACTGAGCCATC | 117198 |
rs31824889 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ivns1abp | Mm_Celera | 1:151345578 | GTAAGGAAATCTGTA[C/T]ACACACACACACAAA | 117198 |
rs31865627 | snp | A/C | 0.265928 | 0.249492 | downstream-variant-500B, intron-variant | Ivns1abp | GRCm38.p3 | 1:151357084 | GGAGCCTTTCTCTTC[A/C]ATCACCGCTCTACAC | 117198 |
rs31953623 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | Ivns1abp | Mm_Celera | 1:151344282 | TAAGTAACAGGAGGA[A/G]CGGTCCCCGCCGCCC | 117198 |
rs31985645 | snp | A/G | 0.32 | 0.24 | intron-variant | Ivns1abp | GRCm38.p3 | 1:151358518 | AGGTGATCTAAAGAG[A/G]GGAGTAGTTGTGTTT | 117198 |
rs32030693 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ivns1abp | GRCm38.p3 | 1:151350728 | TAAATGTTTTGGTGT[A/G]TTGGTAGGATAGAAT | 117198 |
rs32133670 | snp | A/G | 0.375 | 0.216506 | upstream-variant-2KB | Ivns1abp | GRCm38.p3 | 1:151343246 | AGAGAAAAGCTGGAC[A/G]GCAAATGCCAGTTTC | 117198 |
rs32188205 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ivns1abp | Mm_Celera | 1:151347245 | AATATTTGTGGTTTA[C/T]CTTAGCAATGTTTGA | 117198 |
rs32239780 | snp | C/T | 0.345679 | 0.230967 | downstream-variant-500B | Ivns1abp | Mm_Celera | 1:151364799 | ACCATAAGTGGCTGA[C/T]TTGGGATGTAAATGT | 117198 |
rs32289984 | snp | C/T | 0.32 | 0.24 | intron-variant | Ivns1abp | GRCm38.p3 | 1:151351187 | TGTGCCCCCACCCCC[C/T]AAACAGGCAATTAAT | 117198 |
rs32313886 | snp | A/G | 0.375 | 0.216506 | upstream-variant-2KB | Ivns1abp | GRCm38.p3 | 1:151343569 | AACTCGATTATGTGT[A/G]TACTTTATAGACCTT | 117198 |
rs32399315 | snp | A/G | 0.444444 | 0.157135 | downstream-variant-500B | Ivns1abp | Mm_Celera | 1:151364809 | GCTGATTTGGGATGT[A/G]AATGTATTTTCTTCA | 117198 |
rs32512928 | snp | A/T | 0.32 | 0.24 | intron-variant | Ivns1abp | Mm_Celera | 1:151350843 | TGTGTATGACCAGGC[A/T]GGCCTCAAACTCAGG | 117198 |
rs32545483 | snp | C/T | 0.59375 | 0.121031 | intron-variant | Ivns1abp | Mm_Celera | 1:151358718 | GTGATACTTGGGACC[C/T]CTTTCCACAGATTGA | 117198 |
rs32559301 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ivns1abp | Mm_Celera | 1:151354968 | TTCTTTTTTTTTTTT[C/T]TTTTTTTTCCTTTTT | 117198 |
rs32564170 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ivns1abp | Mm_Celera | 1:151348074 | TCTCAAAATTGAAAG[C/T]AGTATTGTAGTGTAC | 117198 |
rs32576761 | snp | G/T | 0.375 | 0.216506 | intron-variant | Ivns1abp | GRCm38.p3 | 1:151349267 | ATGTAATGTGAATAT[G/T]TTTTGCCTTTTACCT | 117198 |
rs32648157 | snp | A/G | 0.32 | 0.24 | upstream-variant-2KB | Ivns1abp | GRCm38.p3 | 1:151343724 | CTAGGGGCAAGGTGG[A/G]TGGATGACTGGGCTT | 117198 |
rs32719544 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ivns1abp | Mm_Celera | 1:151354969 | TCTTTTTTTTTTTTT[C/T]TTTTTTTCCTTTTTT | 117198 |
rs32747463 | snp | A/C/T | 0.375 | 0.216506 | upstream-variant-2KB | Ivns1abp | GRCm38.p3 | 1:151343387 | TAATGAAGACCCCCC[A/C/T]CCCCCAATTTCTATT | 117198 |
rs45673640 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Ivns1abp | Mm_Celera | 1:151360928 | CTTATCACTTTTGAT[A/T]TAGGGACAGCTCTAT | 117198 |
rs45723934 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Ivns1abp | Mm_Celera | 1:151352397 | GTGGTGTATTGACAG[C/T]GTCTGATACAACAGA | 117198 |
rs45912269 | snp | A/G | 0.124444 | 0.216185 | utr-variant-3-prime, intron-variant | Ivns1abp | Mm_Celera | 1:151356072 | TTGTGAAATCTTCGT[A/G]CTAGCGAGTAGCCAT | 117198 |
rs45974026 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon | Ivns1abp | Mm_Celera | 1:151360743 | CAGAGAGGAATGTCT[C/T]CGAACAGTTGAATGC | 117198 |
rs45974445 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Ivns1abp | Mm_Celera | 1:151357514 | GTGTGTAGCTTCTAT[A/T]ACAGGACCCTACCAA | 117198 |
rs46033182 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ivns1abp | Mm_Celera | 1:151362833 | TTCTTGTCCATTTTA[C/T]TCATCTCTATGGTTT | 117198 |
rs46163457 | snp | C/G | | | upstream-variant-2KB | Ivns1abp | GRCm38.p3 | 1:151342983 | GTAAAATTATGCCAG[C/G]ATTCATAGAGCAGGA | 117198 |
rs46220932 | snp | C/T | 0.231111 | 0.249285 | downstream-variant-500B, intron-variant | Ivns1abp | Mm_Celera | 1:151357111 | ACACCTTCCAAAAAC[C/T]GATTGTCCTAGCTTG | 117198 |
rs46285560 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Ivns1abp | Mm_Celera | 1:151358097 | CACAGGGTAGATTAA[A/C]GCTTGTGAGAGCAGT | 117198 |
rs46316234 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ivns1abp | Mm_Celera | 1:151358278 | AGTTTGGGAATGAGA[A/G]GAAGATCATGGGAGT | 117198 |
rs46340172 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ivns1abp | Mm_Celera | 1:151358834 | CAATACAGGTTTTTA[C/T]TAGAAACTACTTGTT | 117198 |
rs46358145 | snp | A/T | 0.336735 | 0.234472 | intron-variant | Ivns1abp | Mm_Celera | 1:151362157 | AGTTTTCTTTTGTAG[A/T]CAGTGTCCTTTCACA | 117198 |
rs46375426 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Ivns1abp | Mm_Celera | 1:151359908 | ACCACCCTAAGTGTT[A/G]ATATTAATAGTTCCA | 117198 |
rs46377753 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Ivns1abp | GRCm38.p3 | 1:151354442 | GGCTATGGGACAATC[C/T]ACTGAGCCCTAGTGG | 117198 |
rs46398379 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ivns1abp | Mm_Celera | 1:151352074 | ACAAGGAAGGAAAAC[C/T]TGTCCTCTTGACTGA | 117198 |
rs46489061 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ivns1abp | Mm_Celera | 1:151351983 | GAAATTATCACAAAA[C/T]ATCTAATTAGGCCCA | 117198 |
rs46491932 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ivns1abp | Mm_Celera | 1:151354399 | TCCTCTCAACCGTTT[C/T]TGGCCCCACATGCTG | 117198 |
rs46687205 | snp | C/G | 0.124444 | 0.216185 | utr-variant-3-prime, intron-variant | Ivns1abp | Mm_Celera | 1:151356734 | GTTGATCATGTGTTA[C/G]AGTGTGGTCTGGATG | 117198 |
rs46743558 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Ivns1abp | Mm_Celera | 1:151354117 | TAGGCCACATAGGTC[A/C]TACAGGTCGAGTAAT | 117198 |
rs46802459 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Ivns1abp | Mm_Celera | 1:151359363 | TTGACCTGTGGTGTG[G/T]TTTTTGAATTGTTCA | 117198 |
rs46853442 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ivns1abp | Mm_Celera | 1:151353902 | TAAATGTTGGCACTT[C/T]TGTATTTCTTTTCTA | 117198 |
rs46999224 | snp | A/T | 0.260355 | 0.249785 | intron-variant | Ivns1abp | Mm_Celera | 1:151354329 | ATTCTTGAGAATTTT[A/T]AAAAAGTGTACAGTG | 117198 |
rs47188319 | snp | C/G | 0.391111 | 0.206368 | utr-variant-3-prime | Ivns1abp | Mm_Celera | 1:151363713 | ACTCTTCCCTCAATT[C/G]TGTCTTAAGAGGCAA | 117198 |
rs47202851 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ivns1abp | Mm_Celera | 1:151353793 | CTGATGTCACCATTT[A/G]TCCATGTGCTGTCCC | 117198 |
rs47629356 | snp | A/G | 0.444444 | 0.157135 | utr-variant-3-prime, intron-variant | Ivns1abp | Mm_Celera | 1:151355359 | AGCTTTGTGTTTTCA[A/G]TGGTGTTGCTCTTAC | 117198 |
rs47735623 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Ivns1abp | Mm_Celera | 1:151354305 | GGAATACAACTTTTT[A/T]AATACAATATTCTTG | 117198 |
rs47860111 | snp | G/T | | | upstream-variant-2KB | Ivns1abp | Mm_Celera | 1:151342536 | TGGACACAGACATCT[G/T]TCTCTTAAAACAGTC | 117198 |
rs47963094 | snp | C/T | | | upstream-variant-2KB | Ivns1abp | Mm_Celera | 1:151342781 | TGTGTGTTTACAGTG[C/T]TAGAGATGAAACCCA | 117198 |
rs48022242 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Ivns1abp | Mm_Celera | 1:151361063 | TTGTAATGCAGGTAA[A/T]AACACTCTTCTAACC | 117198 |
rs48102765 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Ivns1abp | Mm_Celera | 1:151361357 | AAACTGTCTGGCCTT[G/T]AACTTGTAGTTCTTT | 117198 |
rs48248273 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ivns1abp | Mm_Celera | 1:151357996 | TCTCTGGGCTGACTA[C/T]GTGATGATCTTAACA | 117198 |
rs48253300 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ivns1abp | Mm_Celera | 1:151352292 | ACTACACAGAACTGT[C/T]GCTTGGCCTTGACAT | 117198 |
rs48463403 | snp | A/G | 0.444444 | 0.157135 | utr-variant-3-prime | Ivns1abp | Mm_Celera | 1:151363745 | AGGGGTAGGGTTTAC[A/G]CGTAGGCAGTTGGGT | 117198 |
rs48591545 | snp | A/G | 0.444444 | 0.157135 | utr-variant-3-prime, intron-variant | Ivns1abp | Mm_Celera | 1:151356701 | TAATAACTTTATACA[A/G]TGTTGAACTCAGAAA | 117198 |
rs48641568 | snp | A/G | 0.32 | 0.24 | intron-variant | Ivns1abp | Mm_Celera | 1:151358122 | AGCAGTTTGTACACC[A/G]TTTCAGGTAATAGTT | 117198 |
rs48793622 | snp | C/T | 0.391111 | 0.206368 | synonymous-codon, utr-variant-5-prime | Ivns1abp | Mm_Celera | 1:151351709 | AGTCTTGCTGAATTA[C/T]GCATACACGGCTCAG | 117198 |
rs48810452 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Ivns1abp | Mm_Celera | 1:151357966 | TAATCATAGGAAATG[A/G]CTAATTGTTGGGTGT | 117198 |
rs48850116 | snp | A/C | 0.408163 | 0.193609 | intron-variant | Ivns1abp | Mm_Celera | 1:151358187 | CTAAGGATATGGAGA[A/C]GGACCAATTCCACTC | 117198 |
rs48893536 | snp | A/G | 0.444444 | 0.157135 | downstream-variant-500B | Ivns1abp | Mm_Celera | 1:151364811 | TGACTTGGGATGTGA[A/G]TGTATTTTCTTCAGA | 117198 |
rs48935996 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Ivns1abp | Mm_Celera | 1:151361439 | GCTGTAATAATAATC[C/T]TGGTTTGCCTTAACT | 117198 |
rs48968105 | snp | A/C | 0.32 | 0.24 | utr-variant-3-prime | Ivns1abp | Mm_Celera | 1:151364294 | TGTTCAGCTTTCTTA[A/C]CTGGATTAATACTGG | 117198 |
rs49048354 | snp | G/T | 0.124444 | 0.216185 | utr-variant-3-prime | Ivns1abp | Mm_Celera | 1:151363641 | AATTGATTGGGAACA[G/T]CATTTCAAGAAGTCC | 117198 |
rs49254635 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Ivns1abp | Mm_Celera | 1:151354451 | ACAATCCACTGAGCC[C/G]TAGTGGCCTGCCAGG | 117198 |
rs49367628 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ivns1abp | Mm_Celera | 1:151362260 | GACTTTGTGGCTCAA[C/T]CAGTGAGCATGTAAG | 117198 |
rs49373239 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Ivns1abp | Mm_Celera | 1:151351933 | ACATTGTGAAAGTAG[A/T]ATACTGGCAAGGTGT | 117198 |
rs49419018 | snp | C/T | 0.391111 | 0.206368 | downstream-variant-500B | Ivns1abp | Mm_Celera | 1:151364858 | TGCCACCTCATTTCT[C/T]TGGTGTACAACCACC | 117198 |
rs49445136 | snp | C/T | 0.32 | 0.24 | utr-variant-3-prime, intron-variant | Ivns1abp | Mm_Celera | 1:151356523 | AATATGTTAGGGTTT[C/T]GTTAATTTGGTTAGA | 117198 |
rs49482624 | snp | A/G | | | utr-variant-5-prime | Ivns1abp | Mm_Celera | 1:151344537 | GCGCGCGCGGCGGCG[A/G]CGGCGGTGGCAGTGT | 117198 |
rs49505835 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Ivns1abp | Mm_Celera | 1:151362056 | TTCCCTCTGTGAGAT[A/G]TATCCATTATTCAGT | 117198 |
rs49791801 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Ivns1abp | Mm_Celera | 1:151357752 | GCAAGAAGAATTTTT[G/T]TAAAAATTTTGTGTG | 117198 |
rs49982199 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ivns1abp | Mm_Celera | 1:151361642 | TGCTTGATGGTGAGT[A/G]TCCAGGTTTAGAGAG | 117198 |
rs50016959 | snp | C/T | | | upstream-variant-2KB | Ivns1abp | Mm_Celera | 1:151342539 | ACACAGACATCTTTC[C/T]CTTAAAACAGTCTGT | 117198 |
rs50459958 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ivns1abp | Mm_Celera | 1:151354815 | TTATTTTTGCTATAA[C/T]ATGAAGGATTCCCTT | 117198 |
rs50544740 | snp | A/G | 0.345679 | 0.230967 | utr-variant-3-prime | Ivns1abp | Mm_Celera | 1:151364031 | AATGCTCAGAACGCA[A/G]ACTTCACCATTTGCC | 117198 |
rs50570077 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ivns1abp | Mm_Celera | 1:151352711 | ATAAAGACCAGCTAT[A/G]TGTATTCTATATATA | 117198 |
rs50583573 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Ivns1abp | Mm_Celera | 1:151359048 | AATTCTCGAAGAATC[C/T]GGCATTACTGTTCCT | 117198 |
rs50621176 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ivns1abp | Mm_Celera | 1:151360233 | TGATTGACTTGCAGC[A/G]AGAGGACTCAACATG | 117198 |
rs50644175 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Ivns1abp | Mm_Celera | 1:151359921 | TTAATATTAATAGTT[C/T]CATGGTAAACACAGA | 117198 |
rs50854265 | snp | A/T | 0.297521 | 0.245442 | intron-variant | Ivns1abp | Mm_Celera | 1:151361919 | TAGGAATCATTTTTT[A/T]AAAATTCAGATTATT | 117198 |
rs50972182 | snp | A/G | 0.32 | 0.24 | intron-variant | Ivns1abp | Mm_Celera | 1:151351736 | TCAGTGAGTGCCTTC[A/G]AATGAACCAGAACAT | 117198 |
rs51036447 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ivns1abp | Mm_Celera | 1:151357627 | GGCGTGGGATTTAGT[A/G]GATTAGTCTTAGATG | 117198 |
rs51041927 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Ivns1abp | Mm_Celera | 1:151360642 | GATATAGTAAGATGC[A/C]CACTGCCACTAGGGG | 117198 |