SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6190365 | snp | C/T | 0.5 | 0 | intron-variant | Mid2 | Mm_Celera | X:140730788 | atgtagctagctgtc[C/T]ccaggtntatctgct | 23947 |
rs6190369 | snp | C/T | 0.5 | 0 | intron-variant | Mid2 | Mm_Celera | X:140730795 | tagctgtcnccaggt[C/T]tatctgctgtcatcc | 23947 |
rs6190447 | snp | G/T | 0.5 | 0 | intron-variant | Mid2 | Mm_Celera | X:140730836 | atgtacactggaact[G/T]tgagccaaagcaagc | 23947 |
rs6192000 | snp | A/G | 0.359862 | 0.224567 | intron-variant | Mid2 | GRCm38.p3 | X:140731100 | AAAGGAGCTGTTGAA[A/G]GGTAAACAGTTGACA | 23947 |
rs6285993 | snp | A/G | 0.5 | 0 | intron-variant | Mid2 | Mm_Celera | X:140670432 | TTTAAAAACAAAACA[A/G]AACAAAGAGAAACTA | 23947 |
rs6301063 | snp | A/C | 0.5 | 0 | intron-variant | Mid2 | Mm_Celera | X:140670838 | GAAAACTTTAAGAAC[A/C]CTTTAGTAAAAGAAT | 23947 |
rs6346537 | snp | C/T | 0.5 | 0 | intron-variant | Mid2 | Mm_Celera | X:140718788 | ATCCATTTTCAATTT[C/T]AATGGAATTTTGTTA | 23947 |
rs13484034 | snp | A/G | 0.457278 | 0.13977 | synonymous-codon | Mid2 | GRCm38.p3 | X:140678432 | TGAGCAGGACCCTCC[A/G]AGAGATGCTGTAAAG | 23947 |
rs29253584 | snp | C/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Mid2 | Mm_Celera | X:140734189 | TGAAATAGCAAGCAG[C/T]ATTACTGAATTATAT | 23947 |
rs29253585 | snp | C/T | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Mid2 | Mm_Celera | X:140734087 | TCTAGGATGCATCGT[C/T]CACTATTCTGGAGAT | 23947 |
rs29253586 | snp | C/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Mid2 | Mm_Celera | X:140734059 | GTTCACTCCAACAGA[C/T]ACTGACATAATGTCT | 23947 |
rs29253587 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Mid2 | Mm_Celera | X:140733987 | ATACTAACACAGAGA[A/G]CCATTTGCACATATT | 23947 |
rs29253588 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Mid2 | Mm_Celera | X:140733388 | TTGGGACTATTGAGA[A/G]TTTACATGGACTATT | 23947 |
rs29253589 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Mid2 | Mm_Celera | X:140733341 | TTACTAGAGGAACTT[C/T]AGGGAGATCCAAATG | 23947 |
rs29253590 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Mid2 | Mm_Celera | X:140733003 | CGTGACTCAGTTGGT[A/T]CTTATGCTACCTTGA | 23947 |
rs29253591 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Mid2 | Mm_Celera | X:140732570 | TTCATTAAAAAAAAA[A/G]GTCAACTGAGGACTT | 23947 |
rs29253592 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Mid2 | Mm_Celera | X:140731855 | CTTGATTTGGAGTTT[C/T]GCCTCTTCAGCCAAC | 23947 |
rs29253593 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Mid2 | Mm_Celera | X:140731256 | GGAAAACAATATGCA[A/G]GTCAAGTTCTTGCTG | 23947 |
rs29253724 | snp | A/G | 0.32 | 0.24 | intron-variant | Mid2 | Mm_Celera | X:140763318 | TAGGAGATGGGAAGT[A/G]CTGCATCACTCTAGT | 23947 |
rs29253725 | snp | G/T | 0.32 | 0.24 | intron-variant | Mid2 | Mm_Celera | X:140763298 | TTTTGGAAAATATAC[G/T]GGGCTAGGAGATGGG | 23947 |
rs29253726 | snp | A/C | 0.32 | 0.24 | intron-variant | Mid2 | Mm_Celera | X:140763201 | AATTGAACAGCTAAA[A/C]AAAAATACTAGGAAG | 23947 |
rs29253727 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Mid2 | Mm_Celera | X:140762537 | TCAATGATGGATGGA[G/T]GATGGAGGATGAGAG | 23947 |
rs29253728 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Mid2 | Mm_Celera | X:140762522 | AGAAGGTGAAGCTCC[C/T]CAATGATGGATGGAG | 23947 |
rs29253729 | snp | A/C | 0.32 | 0.24 | intron-variant | Mid2 | Mm_Celera | X:140762300 | TGCACTCCGATTTCA[A/C]GAAAGCAAACGTCTC | 23947 |
rs29253730 | snp | C/G/T | 0.142012 | 0.225474 | intron-variant | Mid2 | Mm_Celera | X:140762271 | CCACTCTAACAAAGT[C/G/T]ACCTAATTATATGTG | 23947 |
rs29253731 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Mid2 | Mm_Celera | X:140762220 | GAGTCTCTGAACTGA[A/C]GCACATGCTATCTTT | 23947 |
rs29253732 | snp | A/G | 0.32 | 0.24 | intron-variant | Mid2 | Mm_Celera | X:140762206 | TCGCATGGTTATAAG[A/G]GTCTCTGAACTGAAG | 23947 |
rs29253733 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Mid2 | Mm_Celera | X:140762116 | ATAAACACACAGTGT[C/T]TATCACAGAGGCATA | 23947 |
rs29253974 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Mid2 | Mm_Celera | X:140730479 | CAGAGAGAAGGCAGA[C/T]GCACTTTAAACACAG | 23947 |
rs29253975 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Mid2 | Mm_Celera | X:140730178 | TGCAGAAACAAAAAG[G/T]TCTCCATGTGATCTT | 23947 |
rs29253976 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Mid2 | Mm_Celera | X:140730036 | ATTGTATAACTTGAG[C/T]GTTCTTTAAATTCTA | 23947 |
rs29253977 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Mid2 | Mm_Celera | X:140729917 | TGTTTAACCCCACTT[C/T]TTCATGCCCAACTGT | 23947 |
rs29253978 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Mid2 | Mm_Celera | X:140729384 | TTCACTCTGTTGCCC[A/G]GGCAATCTGATCTGC | 23947 |
rs29253979 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Mid2 | Mm_Celera | X:140728390 | TTGGGTCCTGTGCCT[A/G]TTTTCTCTCCCTACA | 23947 |
rs29253980 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Mid2 | Mm_Celera | X:140728312 | TATGGAGTGTGAGAC[A/G]AAGGAGCAAAACAGT | 23947 |
rs29253981 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Mid2 | Mm_Celera | X:140728277 | GAATGACTTCCAACT[C/T]AGGCTCTTTTGTCTG | 23947 |
rs29253982 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Mid2 | Mm_Celera | X:140728275 | GTGAATGACTTCCAA[C/T]TTAGGCTCTTTTGTC | 23947 |
rs29253983 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Mid2 | Mm_Celera | X:140728258 | ACAGAAAGCAACTGA[A/C]TGTGAATGACTTCCA | 23947 |
rs29254004 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Mid2 | Mm_Celera | X:140762036 | CTTCCTATTAACTAT[C/T]CCTAGCAGCAAGGGT | 23947 |
rs29254005 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Mid2 | Mm_Celera | X:140761771 | GTTTGTCTTTTTTTT[A/T]AACTTCCTGTCACAC | 23947 |
rs29254006 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Mid2 | Mm_Celera | X:140761699 | GCTCTTGAGCAAAAC[C/T]GACAAGAGTCCTAGC | 23947 |
rs29254007 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Mid2 | Mm_Celera | X:140761672 | CCACAGAGAAGCCAT[A/T]GTTTTAGGAGTGCTC | 23947 |
rs29254008 | snp | A/G | 0.231111 | 0.249285 | synonymous-codon | Mid2 | Mm_Celera | X:140761261 | AGTTCATGGACTCCA[A/G]AGTGGGACACGCTAC | 23947 |
rs29254009 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Mid2 | Mm_Celera | X:140761174 | TACTTTTGTCTTTCC[C/T]TACTTCACAGGCCTG | 23947 |
rs29254010 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Mid2 | Mm_Celera | X:140761083 | AAGAAAATGAATTCA[C/T]GTAGGTGGTTTATAA | 23947 |
rs29254011 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Mid2 | Mm_Celera | X:140761053 | GTTCATCTCATTATA[G/T]CTTTCAAGGCTCAAA | 23947 |
rs29254012 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Mid2 | Mm_Celera | X:140760910 | ATAACTGTGAGGATT[C/T]TACTATTTGTGTTCT | 23947 |
rs29254013 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Mid2 | Mm_Celera | X:140760137 | GCCAAAGAGAAAAAA[A/G]GAAGAACCCATCAGA | 23947 |
rs29254374 | snp | A/T | 0.375 | 0.216506 | intron-variant | Mid2 | Mm_Celera | X:140727585 | TTCAACAACTATTTC[A/T]CATCCATATCCTAAT | 23947 |
rs29254375 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Mid2 | Mm_Celera | X:140727504 | TCAATATCTGTCTGG[C/T]GCTCAACTCATTAGC | 23947 |
rs29254376 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Mid2 | Mm_Celera | X:140718426 | CCTGGTCCGGGATGT[C/T]CCACAAAACAAAGCA | 23947 |
rs29254377 | snp | A/G | 0.415225 | 0.187619 | intron-variant | Mid2 | GRCm38.p3 | X:140704679 | AATATGGAAAGGAAG[A/G]GGAAACAAAACAAGG | 23947 |
rs29254378 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Mid2 | GRCm38.p3 | X:140704588 | TTAGTAGGAAAGCAT[C/T]AGGCCAGGGACATTC | 23947 |
rs29254379 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Mid2 | Mm_Celera | X:140704550 | GGAATGGGGCAGCAG[A/G]CATCTGAATGCCCAA | 23947 |
rs29254380 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Mid2 | Mm_Celera | X:140704448 | CCTCAAAGAGCCATT[A/G]TACCAATTGGAGTCC | 23947 |
rs29254381 | snp | C/T | 0.49827 | 0.0293608 | intron-variant | Mid2 | GRCm38.p3 | X:140704428 | TTTAAGCCTATAAGA[C/T]TTTTCCTCAAAGAGC | 23947 |
rs29254382 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Mid2 | Mm_Celera | X:140704398 | ATCAAAGGCCCCAAA[C/T]GGTTTTGGAATAGTT | 23947 |
rs29254383 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Mid2 | Mm_Celera | X:140704373 | CCCTGTTCACCTTCT[C/T]CTCACTAAAATCAAA | 23947 |
rs29254484 | snp | A/G | 0.32 | 0.24 | intron-variant | Mid2 | Mm_Celera | X:140760098 | ATGTTAAACCAACTG[A/G]GAAACGGATAACAGA | 23947 |
rs29254485 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Mid2 | Mm_Celera | X:140760042 | GTCCTCATTTTCCAT[G/T]CCCTTTCCTTTCCAT | 23947 |
rs29254486 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Mid2 | Mm_Celera | X:140760001 | CTCAATTCTTCATTC[A/G]AACTCTATAACAATG | 23947 |
rs29254487 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Mid2 | Mm_Celera | X:140759695 | TTTCTGTAGTACATC[C/T]TTTTGTTCCCTCATT | 23947 |
rs29254488 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Mid2 | Mm_Celera | X:140759662 | CTCCAGCCTCCTCTC[A/C]ATCAATGCTTTGTCC | 23947 |
rs29254489 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Mid2 | Mm_Celera | X:140759638 | GTTATGGGAATTAAA[C/G]AGCCATCTCTCCAGC | 23947 |
rs29254490 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Mid2 | Mm_Celera | X:140759548 | TCTCAATCAATTCTT[C/T]TTTAATTTACTTACT | 23947 |
rs29254491 | snp | A/T | 0.32 | 0.24 | intron-variant | Mid2 | Mm_Celera | X:140754927 | CCAAGTCTTATTGAT[A/T]CCCACAGAATCATAT | 23947 |
rs29254492 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Mid2 | Mm_Celera | X:140754888 | TATTTTTTTTTACAT[A/T]ATTCATGTGCTGGTC | 23947 |
rs29254493 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Mid2 | Mm_Celera | X:140754850 | ATTTCCATATTTTGA[A/C]ATTTTTTGTTGACTA | 23947 |
rs29254764 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Mid2 | Mm_Celera | X:140704281 | ATGGCCTTTGTTTAT[C/T]CTAGTTTAAAGTATT | 23947 |
rs29254765 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Mid2 | Mm_Celera | X:140704266 | ACAACACTGGGAAAC[A/G]TGGCCTTTGTTTATT | 23947 |
rs29254766 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Mid2 | Mm_Celera | X:140704208 | GCTTTTCCCATGGTG[A/G]TCAATTCCTTAGCGT | 23947 |
rs29254767 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Mid2 | Mm_Celera | X:140704112 | ATGACCATTGACTGG[A/G]CATGTTAGCTACTTG | 23947 |
rs29254768 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Mid2 | Mm_Celera | X:140704047 | AGAGAATGAAAATGG[A/G]TGGTGGTGGTGAATT | 23947 |
rs29254769 | snp | A/G | 0.415225 | 0.187619 | intron-variant | Mid2 | Mm_Celera | X:140703938 | TCTGCAAGAGTGAAT[A/G]CATGTGTGCATGTGT | 23947 |
rs29254770 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Mid2 | Mm_Celera | X:140703640 | GACCATGAAAGTACA[G/T]AAAAATAAAGTAGTC | 23947 |
rs29254771 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Mid2 | Mm_Celera | X:140703473 | ACTTGGCATTCCTTA[A/G]TCTAAGCCTCATAGA | 23947 |
rs29254772 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Mid2 | Mm_Celera | X:140703401 | CAGCTCTGGAGAGCC[C/T]ACTTTTCCCTCCGCT | 23947 |
rs29254773 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Mid2 | Mm_Celera | X:140703367 | ATCTGTTCACTGGCC[G/T]CTGATTCATAAAAGG | 23947 |
rs29254914 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Mid2 | Mm_Celera | X:140754796 | TATCTTTTCAGTAAT[A/T]CATTTGTCTCCATCA | 23947 |
rs29254915 | snp | C/T | 0.32 | 0.24 | intron-variant | Mid2 | Mm_Celera | X:140754571 | AGGCAGTCTGTAGCA[C/T]ATTGCCACAAAGATA | 23947 |
rs29254916 | snp | A/G | 0.32 | 0.24 | intron-variant | Mid2 | Mm_Celera | X:140754548 | TTAGACAGAAAGTTT[A/G]TCTAGTCAGGCAGTC | 23947 |
rs29254917 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Mid2 | Mm_Celera | X:140754404 | CCCCTGGATTCTGAG[C/T]GTTCCTATCATCTCT | 23947 |
rs29254918 | snp | A/G | 0.32 | 0.24 | intron-variant | Mid2 | Mm_Celera | X:140753905 | GGTCTGCCGAGGATG[A/G]CCGAGCACCAGCACT | 23947 |
rs29254919 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Mid2 | Mm_Celera | X:140753880 | AAGTCCTGGTCTCCC[C/T]AGCTGGTCAGGTCTG | 23947 |
rs29254920 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Mid2 | Mm_Celera | X:140753865 | AAGAAATATCATTCC[A/G]AGTCCTGGTCTCCCC | 23947 |
rs29254921 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Mid2 | Mm_Celera | X:140753597 | TTTTCCTTACATTTG[C/T]TTTCCCTCTCAGCCT | 23947 |
rs29254922 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Mid2 | Mm_Celera | X:140753497 | GCTCAAACTCAGCAC[C/T]TTTGACTTTCTGCTT | 23947 |
rs29254923 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Mid2 | Mm_Celera | X:140753459 | CTGAGATTCCCATGT[A/G]TGATAAGTTCTGTCT | 23947 |
rs29255184 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Mid2 | Mm_Celera | X:140703051 | TCGAGACATCCTTTT[A/T]AAAAAATCTGTCTTT | 23947 |
rs29255185 | snp | C/T | 0.5 | 0 | intron-variant | Mid2 | GRCm38.p3 | X:140703037 | TGCACACACAGCTGT[C/T]GAGACATCCTTTTAA | 23947 |
rs29255186 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Mid2 | Mm_Celera | X:140702846 | AAGTCTTCACACTTT[G/T]CCCGAATTCTCCATT | 23947 |
rs29255187 | snp | C/T | 0.415225 | 0.187619 | intron-variant | Mid2 | GRCm38.p3 | X:140702416 | TGTTCCCTATTTGTT[C/T]ACTGTCTTAGAGTTT | 23947 |
rs29255188 | snp | C/G | 0.391111 | 0.206368 | intron-variant | Mid2 | GRCm38.p3 | X:140701750 | GTTTCAAAGGACAGG[C/G]AGTTATTTAGGATTT | 23947 |
rs29255189 | snp | C/G | 0.32 | 0.24 | intron-variant | Mid2 | Mm_Celera | X:140701610 | CAAGAATAGCTAAGG[C/G]ATTCTTTCCATTGGC | 23947 |
rs29255190 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Mid2 | Mm_Celera | X:140701522 | CTAATGTTTTATGAT[C/T]AGTGAGCTGGCACTT | 23947 |
rs29255191 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Mid2 | Mm_Celera | X:140700907 | TACAACTCGCTTCTC[C/T]GAGACATGCTCTGTA | 23947 |
rs29255192 | snp | A/T | 0.498615 | 0.0262793 | intron-variant | Mid2 | GRCm38.p3 | X:140700817 | TGCCTCCAATCATGC[A/T]AGCTCAACCTCCCCT | 23947 |
rs29255193 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Mid2 | GRCm38.p3 | X:140700605 | AGATTGAGAGAGGTC[C/T]AGGAGAAAGCAAGCT | 23947 |
rs29255314 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Mid2 | Mm_Celera | X:140753384 | TGGGTTATATTTCTT[A/G]TACTGTACCTTTTTT | 23947 |
rs29255315 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Mid2 | Mm_Celera | X:140753082 | CTTTTAAAACATGCA[G/T]CCATCGTGTCAAAAG | 23947 |