SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3708027 | snp | A/C | 0.375 | 0.216506 | intron-variant | Dtl | Mm_Celera | 1:191548758 | TTAAAGCAAGACACA[A/C]CGACTATGACCAAAA | 76843 |
rs6232496 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Dtl | Mm_Celera | 1:191563404 | CCAATCTAGTAGGTA[A/G]GCACTAATCTTCCTA | 76843 |
rs13476307 | snp | C/T | 0.490978 | 0.0665555 | intron-variant, upstream-variant-2KB | Dtl, Ints7 | Mm_Celera | 1:191574250 | TACGGCTATAATCAT[C/T]TAAGGCCCAGCAACA | 76843 |
rs30468042 | snp | C/T | 0.495 | 0.0497494 | intron-variant | Dtl | Mm_Celera | 1:191543820 | TAACAGGAATGCAGG[C/T]TATTAGTGGTAGCTT | 76843 |
rs30494005 | snp | A/G | 0.345679 | 0.230967 | intron-variant, upstream-variant-2KB | Dtl | Mm_Celera | 1:191566844 | GGAATCAAAACTCAC[A/G]ACATATATTAACTTT | 76843 |
rs30567131 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Dtl | Mm_Celera | 1:191549851 | CTGTGCAGTCCTGGC[A/C]TTGAACTCAGAAATC | 76843 |
rs30672382 | snp | C/T | 0.484429 | 0.0868505 | intron-variant | Dtl | Mm_Celera | 1:191570971 | AGGACATTTGGGTTA[C/T]ACTATAAATAGGTTT | 76843 |
rs30719847 | snp | C/T | 0.32 | 0.24 | intron-variant | Dtl | Mm_Celera | 1:191557946 | TAAACTTCTTCCCAG[C/T]TCCATCACCCACTGT | 76843 |
rs31041774 | snp | A/G | 0.375 | 0.216506 | downstream-variant-500B | Dtl | Mm_Celera | 1:191536905 | TGTGTGTGTGTGTGT[A/G]TATACACAGAGAGAG | 76843 |
rs31061876 | snp | C/T | 0.487535 | 0.077957 | intron-variant | Dtl | Mm_Celera | 1:191545094 | ATGTCTAGCAACATA[C/T]CAAGTTCCAATAAGG | 76843 |
rs31124667 | snp | A/T | 0.444444 | 0.157135 | utr-variant-3-prime | Dtl | Mm_Celera | 1:191538662 | ATAGAAATCTGGTTT[A/T]AAAAAAAAGAAAAGA | 76843 |
rs31188422 | snp | A/G | 0.375 | 0.216506 | intron-variant | Dtl | Mm_Celera | 1:191563360 | GCTCACGCTCTACAC[A/G]GTTCTCACACATTAC | 76843 |
rs31254391 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Dtl | Mm_Celera | 1:191549416 | TCTATTTGTGATGAT[C/T]CTAGTCCATTAGGTT | 76843 |
rs31375629 | snp | A/C | 0.33241 | 0.236027 | intron-variant | Dtl | Mm_Celera | 1:191549154 | TACAGCTAAGATAAC[A/C]GATACTGGTCTATAA | 76843 |
rs31431855 | snp | A/T | 0.475309 | 0.108333 | upstream-variant-2KB, intron-variant | Dtl, Ints7 | Mm_Celera | 1:191576626 | CTTTGACAGATAGCT[A/T]TCCATAAAGAAGTCC | 76843 |
rs31473007 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Dtl | Mm_Celera | 1:191563519 | ATAGAACACAGAATT[C/T]CCACTTATTTGTACT | 76843 |
rs31499300 | snp | A/G | 0.498615 | 0.0262793 | utr-variant-3-prime | Dtl | GRCm38.p3 | 1:191538974 | TCTCCACTGTCCACA[A/G]AAGCACTCCTTGATT | 76843 |
rs31518283 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Dtl | Mm_Celera | 1:191558337 | CAGACAAGCCAACGT[A/G]GAAGAGGGAACCTCC | 76843 |
rs31550445 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Dtl | Mm_Celera | 1:191544959 | TCTGGCTTTGATTAC[A/G]GTAACTATGGCAGGA | 76843 |
rs31567086 | snp | G/T | | | intron-variant, upstream-variant-2KB | Dtl | GRCm38.p3 | 1:191567232 | GTGTGTGTGTGTGTG[G/T]GGGGGGAGGGGGGGG | 76843 |
rs31593632 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Dtl | Mm_Celera | 1:191562361 | GGCGGTGGTGGCGCA[C/T]GCCTTTAATCCCAGC | 76843 |
rs31630110 | snp | C/T | 0.32 | 0.24 | intron-variant | Dtl | Mm_Celera | 1:191548070 | AAATTTCAACTCCTA[C/T]TTAAGAAAAGAAGAG | 76843 |
rs31658674 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Dtl | Mm_Celera | 1:191569601 | CTGTCCATCATCCTT[A/G]TATTAAAACAATAAT | 76843 |
rs31670776 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Dtl | Mm_Celera | 1:191549852 | TGTGCAGTCCTGGCC[C/T]TGAACTCAGAAATCC | 76843 |
rs31701446 | snp | G/T | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Dtl | GRCm38.p3 | 1:191567234 | GTGTGTGTGTGTGTG[G/T]GTGTGGGGGGGGGGG | 76843 |
rs31702592 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Dtl | Mm_Celera | 1:191555300 | AGAGTACACACTTAA[C/T]AATGCACCAGGGTTA | 76843 |
rs31710055 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Dtl | Mm_Celera | 1:191553765 | ACATGCCGAAGTTGT[C/T]TATTATTATTATTGG | 76843 |
rs31721662 | snp | A/G | 0.5 | 0 | upstream-variant-2KB, intron-variant | Dtl, Ints7 | Mm_Celera | 1:191576742 | ACCTGTAGAGAACGG[A/G]ACTGGAAACCAAGGA | 76843 |
rs31738088 | snp | G/T | 0.33241 | 0.236027 | intron-variant | Dtl | Mm_Celera | 1:191547052 | TCTCTAACTTTTTAT[G/T]TAATGTTATGTAACT | 76843 |
rs31817727 | snp | A/G | 0.375 | 0.216506 | intron-variant | Dtl | Mm_Celera | 1:191553323 | GTGGTTAAGAGCGCC[A/G]ACTGCTCTTCCAAAG | 76843 |
rs31830348 | snp | A/G | 0.5 | 0 | intron-variant | Dtl | Mm_Celera | 1:191546314 | ATAAATCTTGAAGGG[A/G]AAAAAAAAGCCAAAA | 76843 |
rs31857495 | snp | C/G | 0.375 | 0.216506 | intron-variant | Dtl | Mm_Celera | 1:191545753 | TCCTGCTGTCCCTCA[C/G]TGCTTTAGTGCTAAG | 76843 |
rs32076590 | snp | A/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | Dtl, Ints7 | GRCm38.p3 | 1:191577282 | AATAAGGTTTACATT[A/T]AAAAAAAAAAAAAGA | 76843 |
rs32104211 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Dtl | Mm_Celera | 1:191563773 | ACTGAATAAAAACAC[A/C]TAATTTTGTAGGAGT | 76843 |
rs32122290 | snp | G/T | 0.375 | 0.216506 | intron-variant | Dtl | Mm_Celera | 1:191553331 | GAGCGCCGACTGCTC[G/T]TCCAAAGGTCCCGAG | 76843 |
rs32150291 | snp | C/T | 0.375 | 0.216506 | downstream-variant-500B | Dtl | Mm_Celera | 1:191536910 | GTGTGTGTGTATATA[C/T]ACAGAGAGAGAGAGA | 76843 |
rs32168724 | snp | A/T | 0.32 | 0.24 | intron-variant | Dtl | Mm_Celera | 1:191563731 | TTGAACAAAGTCCCA[A/T]AACAACTACTTGAGA | 76843 |
rs32189039 | snp | A/G | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Dtl | Mm_Celera | 1:191566902 | AACAGAATAAACTTT[A/G]TGACCTGGAGATGGT | 76843 |
rs32194274 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Dtl | Mm_Celera | 1:191561664 | AAACCGAAAAACCCC[A/G]AAGAGACTCAGTAGA | 76843 |
rs32319881 | snp | A/G/T | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Dtl | Mm_Celera | 1:191567239 | TGTGTGTGTGTGTGG[A/G/T]GGGGGGGGGTTAGTC | 76843 |
rs32326148 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Dtl | Mm_Celera | 1:191551601 | GAGTTTAGAAAAATA[A/T]ATGCAGTAAGACAGT | 76843 |
rs32356200 | snp | A/C | 0.5 | 0 | upstream-variant-2KB, intron-variant | Dtl, Ints7 | Mm_Celera | 1:191577428 | GGGTCTGTTATACAC[A/C]CATCTCTCCCTCCCC | 76843 |
rs32478629 | snp | C/T | 0.484429 | 0.0868505 | intron-variant | Dtl | Mm_Celera | 1:191556153 | GGCTAGCTCTGGCCA[C/T]AAGCCCCAGGAGTCT | 76843 |
rs32501244 | snp | C/T | 0.375 | 0.216506 | downstream-variant-500B | Dtl | Mm_Celera | 1:191537026 | GTTTTTTGCTGGCTT[C/T]CTAAGAGTTAATTAA | 76843 |
rs32536177 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Dtl | Mm_Celera | 1:191553811 | TGTGTAGCCCTGGAT[A/G]TCCTGGAACTCAGAG | 76843 |
rs32537475 | snp | C/T | 0.375 | 0.216506 | intron-variant | Dtl | Mm_Celera | 1:191543268 | TATAACCTGCAGTGA[C/T]TACGTGAGTGCAGGG | 76843 |
rs32570651 | snp | C/T | 0.375 | 0.216506 | intron-variant | Dtl | Mm_Celera | 1:191560449 | CTTTAATACAGTTCT[C/T]CACACGTCGTGGAAA | 76843 |
rs32642061 | snp | A/G | 0.5 | 0 | downstream-variant-500B | Dtl | Mm_Celera | 1:191536983 | ACCCGCTTAGTGTGT[A/G]TATTCAGGATTTCCC | 76843 |
rs32652812 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Dtl | Mm_Celera | 1:191559551 | TAATGTCATCTGGTC[C/T]CCACACACAGAGTAT | 76843 |
rs32708083 | snp | C/T | 0.487535 | 0.077957 | intron-variant | Dtl | Mm_Celera | 1:191555153 | ACCTGAGTGCTAGGA[C/T]TAAGCATGTGTCAAC | 76843 |
rs32709555 | snp | G/T | 0.484429 | 0.0868505 | upstream-variant-2KB, intron-variant | Dtl, Ints7 | Mm_Celera | 1:191576740 | TAACCTGTAGAGAAC[G/T]GGACTGGAAACCAAG | 76843 |
rs32725321 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Dtl | GRCm38.p3 | 1:191573235 | CACACACACACAAAA[C/T]CCCAAATAGAAAACT | 76843 |
rs32740291 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Dtl | Mm_Celera | 1:191552259 | TTTGTGTGGTGTTTT[C/T]CTTCATGTGGCAACT | 76843 |
rs32792192 | snp | A/G | 0.375 | 0.216506 | intron-variant | Dtl | Mm_Celera | 1:191546242 | GACTCAAAACCATGT[A/G]TAATGGGATCTGGTG | 76843 |
rs32805574 | snp | A/G | 0.32 | 0.24 | intron-variant | Dtl | Mm_Celera | 1:191562349 | GCTCCACTGCCAGGC[A/G]GTGGTGGCGCATGCC | 76843 |
rs32806806 | snp | G/T | 0.493827 | 0.0552116 | intron-variant, upstream-variant-2KB | Dtl, Ints7 | Mm_Celera | 1:191574991 | ACAACGAACTTGCAG[G/T]GATCGCTAAGGTTCT | 76843 |
rs33834774 | snp | A/G | 0.32 | 0.24 | intron-variant | Dtl | Mm_Celera | 1:191552501 | TTTTAAGAAGCATAT[A/G]TTCACTTACTAAACA | 76843 |
rs33834775 | snp | C/T | 0.32 | 0.24 | intron-variant | Dtl | Mm_Celera | 1:191552317 | GTGGCAAAGTGTGGG[C/T]TTGCAAGAAGCACAC | 76843 |
rs33834776 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Dtl | Mm_Celera | 1:191551864 | TTGGGCAGATTGGCA[A/T]CTCTATCTTGTGACT | 76843 |
rs33834777 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Dtl | Mm_Celera | 1:191551807 | TCATTACAACTCCAA[A/T]AGCAAAGATTCACGT | 76843 |
rs33834778 | snp | C/T | 0.32 | 0.24 | intron-variant | Dtl | Mm_Celera | 1:191551692 | AAGCATTTGTATTAG[C/T]AAATAAGTAGACAGT | 76843 |
rs33834779 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Dtl | Mm_Celera | 1:191551547 | AGAAACCTCAAATGA[C/T]AGATGTGTAGAATGA | 76843 |
rs33834780 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Dtl | Mm_Celera | 1:191551472 | TTATGTATGGAATTG[A/G]CCATTTTATTATGTT | 76843 |
rs33834781 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Dtl | Mm_Celera | 1:191550937 | TGAGATCATTGACAC[A/G]TCCTAAAGTGTCAGC | 76843 |
rs33834782 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Dtl | Mm_Celera | 1:191550855 | AAAAATCCATCAGCA[C/T]TTTTCCTCAAAAAAA | 76843 |
rs33834783 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Dtl | Mm_Celera | 1:191550739 | TAGAATGTTAAAGAC[A/G]CAAGAAATCACAGAG | 76843 |
rs33834844 | snp | A/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Dtl, Ints7 | Mm_Celera | 1:191574468 | TTGTGCAGGGCGGCC[A/T]TTCCTAACACAGGGC | 76843 |
rs33834845 | snp | C/T | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Dtl, Ints7 | Mm_Celera | 1:191573919 | ATGGAATAGAGAAAA[C/T]GGAAGACTCAGTTTG | 76843 |
rs33834846 | snp | A/T | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Dtl, Ints7 | Mm_Celera | 1:191573836 | AATATCGGTAGAGAA[A/T]GGAAACTAAAGGCAC | 76843 |
rs33834847 | snp | A/G | 0.32 | 0.24 | intron-variant | Dtl | Mm_Celera | 1:191573298 | CACAAGGCACCAGAT[A/G]CCTAAATCCATTTCT | 76843 |
rs33834848 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Dtl | Mm_Celera | 1:191572707 | AAAGAAATATACAAG[A/G]CTTTGCATTTTCAGA | 76843 |
rs33834849 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Dtl | Mm_Celera | 1:191572606 | TTATTATGCTATGAA[C/T]ATGAACCTGTAGTGT | 76843 |
rs33834850 | snp | C/T | 0.32 | 0.24 | intron-variant | Dtl | Mm_Celera | 1:191572563 | AGTTCATTATTTCTG[C/T]ATCTCCCCATAATAT | 76843 |
rs33834851 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Dtl | Mm_Celera | 1:191572003 | ACAGAAATATCACTC[A/G]ATCTAGTTTGAGAAG | 76843 |
rs33834852 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Dtl | Mm_Celera | 1:191571997 | AGCCTAACAGAAATA[C/T]CACTCAATCTAGTTT | 76843 |
rs33834853 | snp | C/T | 0.32 | 0.24 | intron-variant | Dtl | Mm_Celera | 1:191571976 | CTCAAACAGAGAAGA[C/T]ATTTCAGCCTAACAG | 76843 |
rs33835574 | snp | G/T | 0.32 | 0.24 | intron-variant | Dtl | Mm_Celera | 1:191549790 | AAAAAAATGTGTAAT[G/T]AAGTATCACATGACC | 76843 |
rs33835575 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Dtl | Mm_Celera | 1:191549701 | ATTAATAGCAGTAAA[C/G]TTAGCATTTATTCAC | 76843 |
rs33835576 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Dtl | Mm_Celera | 1:191549693 | GAACCAGCATTAATA[A/G]CAGTAAAGTTAGCAT | 76843 |
rs33835577 | snp | C/T | 0.32 | 0.24 | intron-variant | Dtl | Mm_Celera | 1:191549528 | CATTCTAGGACCCTG[C/T]TCAGTCCTTAGTGTC | 76843 |
rs33835578 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Dtl | Mm_Celera | 1:191549430 | TTCTAGTCCATTAGG[C/T]TTCTCTTTACCCAAG | 76843 |
rs33835579 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Dtl | Mm_Celera | 1:191548798 | TCATCCTTTCATTTG[G/T]ATGAACGTCCAATCT | 76843 |
rs33835580 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Dtl | Mm_Celera | 1:191548725 | TTTAGGATAAGAAGA[A/G]AGGTTTAATTTTTCT | 76843 |
rs33835581 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Dtl | Mm_Celera | 1:191548562 | TGTCCCTCAGCCACT[C/G]AGCACTGAAGTTCAG | 76843 |
rs33835582 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Dtl | Mm_Celera | 1:191548444 | CATAGAGGCCAGAGC[C/T]TCCCTGACTCCATCT | 76843 |
rs33835583 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Dtl | Mm_Celera | 1:191548100 | GCTCAGTGGATTAGA[A/G]ACCCAGCACATAGTG | 76843 |
rs33835844 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Dtl | Mm_Celera | 1:191571805 | TTCATGTCTTAGGGC[A/G]CTACCAATTCTCAGT | 76843 |
rs33835845 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Dtl | Mm_Celera | 1:191571794 | CAAATGTTAAATTCA[C/T]GTCTTAGGGCACTAC | 76843 |
rs33835846 | snp | C/T | 0.32 | 0.24 | intron-variant | Dtl | Mm_Celera | 1:191571728 | TTTTTAAAGAAGTAA[C/T]TGCTGATCAAGGATC | 76843 |
rs33835847 | snp | A/G | 0.32 | 0.24 | intron-variant | Dtl | Mm_Celera | 1:191571664 | ATACCAGCACTCAAA[A/G]CCTTCAGATTTTTTA | 76843 |
rs33835848 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Dtl | Mm_Celera | 1:191571504 | TAAATACTAAGTCAT[C/T]ATCTAAAATCTGATT | 76843 |
rs33835849 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Dtl | Mm_Celera | 1:191571481 | CTTTCTAATGTACAT[C/G]CCGGTTCTAAATACT | 76843 |
rs33835850 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Dtl | Mm_Celera | 1:191571459 | TTCATTTCAGAAAGA[A/T]AGCCAACTTTCTAAT | 76843 |
rs33835851 | snp | A/G | 0.32 | 0.24 | intron-variant | Dtl | Mm_Celera | 1:191571413 | GTCTCTGCCCCTAAG[A/G]AATGCAGCTTTAGAG | 76843 |
rs33835852 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Dtl | Mm_Celera | 1:191571300 | TACTGTATTGACTAG[C/T]AATTTAACTCCTTTT | 76843 |
rs33835853 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Dtl | Mm_Celera | 1:191571298 | GTTACTGTATTGACT[A/G]GCAATTTAACTCCTT | 76843 |
rs33836544 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Dtl | Mm_Celera | 1:191547260 | TGCTCTTTCAGATAG[A/G]TAAAGGAGCAATCTG | 76843 |
rs33836545 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Dtl | Mm_Celera | 1:191547135 | CTTCTAAATTCTGCA[C/T]GCTTAATCTTATGGC | 76843 |
rs33836546 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Dtl | Mm_Celera | 1:191546947 | CAACAACAGCAGAGG[A/G]CGCTCTCTCCAGCAT | 76843 |
rs33836547 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Dtl | Mm_Celera | 1:191546837 | TTTCTTGCATGGACA[A/C]GTATAGCAACGGAGA | 76843 |