SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6171888 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Nebl | Mm_Celera | 2:17392641 | ACTATTGAAGAAAGT[A/G]TACAATGAAGTTAAA | 74103 |
rs6179408 | snp | G/T | 0.408163 | 0.193609 | intron-variant | Nebl | Mm_Celera | 2:17697123 | CAATTGACTTTAGAC[G/T]ATGATTGAATAAAAC | 74103 |
rs6181565 | snp | A/G | 0.5 | 0 | intron-variant | Nebl | Mm_Celera | 2:17697504 | GTAAAATAAGGGCAT[A/G]TGATAAAAATAAATC | 74103 |
rs6182187 | snp | A/G | 0.5 | 0 | intron-variant | Nebl | Mm_Celera | 2:17697642 | ggagacaaatataaa[A/G]ttataatccttctac | 74103 |
rs6182727 | snp | A/T | 0.5 | 0 | intron-variant | Nebl | Mm_Celera | 2:17360021 | GTTTTCTATTGAAAA[A/T]TATTTTTATCTCTGA | 74103 |
rs6314026 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | Nebl, Mir6419 | Mm_Celera | 2:17562576 | GCCAATCCCAAGCCC[C/T]TAACTCCTCGGTTAA | 74103 |
rs6314088 | snp | A/C/T | 0.415225 | 0.187619 | intron-variant, upstream-variant-2KB | Nebl, Mir6419 | GRCm38.p3 | 2:17562616 | GCCACACAGACACCG[A/C/T]GTCCCAGTGAAAGCC | 74103 |
rs6315052 | snp | A/T | 0.207612 | 0.24638 | intron-variant, upstream-variant-2KB | Nebl, Mir6419 | Mm_Celera | 2:17562773 | AGATTTTCTGTATAG[A/T]CACTACCCCATAGAT | 74103 |
rs6315117 | snp | C/T | 0.290657 | 0.246672 | intron-variant, upstream-variant-2KB | Nebl, Mir6419 | Mm_Celera | 2:17562821 | TACCACATCCCAGTT[C/T]CTGCCATAGTTTCCT | 74103 |
rs6316116 | snp | A/G | 0.304688 | 0.243945 | intron-variant, upstream-variant-2KB | Nebl, Mir6419 | Mm_Celera | 2:17562988 | ATTTGTACCAGCATC[A/G]TTCAGAATGCAAGTG | 74103 |
rs6316587 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | Nebl, Mir6419 | Mm_Celera | 2:17563071 | CTTACAGCTGCACCT[C/T]TAGTGCTAGTGNGTC | 74103 |
rs6316601 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | Nebl, Mir6419 | Mm_Celera | 2:17563083 | CCTNTAGTGCTAGTG[A/G]GTCTTACTGACCNCA | 74103 |
rs6316617 | snp | A/G/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | Nebl, Mir6419 | GRCm38.p3 | 2:17563096 | TGNGTCTTACTGACC[A/G/T]CACTCACTGGGTAAG | 74103 |
rs6335717 | snp | A/T | 0.375 | 0.216506 | intron-variant | Nebl | Mm_Celera | 2:17392852 | AATGTTGTCAATCAA[A/T]ACTCTGGAAGCAGGC | 74103 |
rs6364844 | snp | A/G | 0.5 | 0 | intron-variant | Nebl | Mm_Celera | 2:17499550 | ATTGAGAAAGATCAG[A/G]AAAGAACTTTTTTGT | 74103 |
rs6364964 | snp | A/G | 0.359862 | 0.224567 | intron-variant | Nebl | Mm_Celera | 2:17499614 | TCCTGTATGCCATAT[A/G]AAAATACCAGTATCT | 74103 |
rs6365920 | snp | A/G | 0.359862 | 0.224567 | intron-variant | Nebl | Mm_Celera | 2:17499735 | GCAAGATTGATACAG[A/G]CTTACCCTGAAATTA | 74103 |
rs6365951 | snp | A/T | 0.5 | 0 | intron-variant | Nebl | Mm_Celera | 2:17499760 | AAATTATAGCCAGCT[A/T]GGGGGCAGAGCTGAA | 74103 |
rs6366027 | snp | C/T | 0.5 | 0 | intron-variant | Nebl | Mm_Celera | 2:17499807 | TGTGGGAATACAGAA[C/T]TNTAGCCACTACAGT | 74103 |
rs6366029 | snp | A/C | 0.5 | 0 | intron-variant | Nebl | Mm_Celera | 2:17499809 | TGGGAATACAGAANT[A/C]TAGCCACTACAGTGC | 74103 |
rs6366255 | snp | C/T | 0.5 | 0 | intron-variant | Nebl | Mm_Celera | 2:17726155 | AAATGTAGCTTTCCA[C/T]GGACAGACAGAAAAT | 74103 |
rs6366489 | snp | A/G | 0.5 | 0 | intron-variant | Nebl | Mm_Celera | 2:17499851 | ATCTGTAATCCTCTA[A/G]GGAANTTGATTAATT | 74103 |
rs6366503 | snp | C/T | 0.5 | 0 | intron-variant | Nebl | Mm_Celera | 2:17499856 | TAATCCTCTANGGAA[C/T]TTGATTAATTTTTTA | 74103 |
rs6367650 | snp | A/G | 0.5 | 0 | intron-variant | Nebl | Mm_Celera | 2:17500060 | AGGCAATATAGTATC[A/G]CATATTATATTCTAA | 74103 |
rs6369454 | snp | A/C | 0.5 | 0 | intron-variant | Nebl | Mm_Celera | 2:17726691 | ATACTTCATTTAGAG[A/C]TATNTAAAATTATTA | 74103 |
rs6369470 | snp | C/G | 0.5 | 0 | intron-variant | Nebl | Mm_Celera | 2:17726695 | TTCATTTAGAGNTAT[C/G]TAAAATTATTAAAAA | 74103 |
rs6369513 | snp | C/T | 0.5 | 0 | intron-variant | Nebl | Mm_Celera | 2:17726723 | AAACTAATACTCAAG[C/T]TTGTGAATCTATACA | 74103 |
rs6388342 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Nebl | Mm_Celera | 2:17727892 | TACCTGGGAACACTA[A/G]ACTAGACCCAAAAGA | 74103 |
rs6402129 | snp | A/C | 0.5 | 0 | intron-variant | Nebl | Mm_Celera | 2:17728150 | gcACTGATGCTTATG[A/C]CACAAGCGCTCTTTT | 74103 |
rs6402657 | snp | A/C | 0.5 | 0 | intron-variant | Nebl | Mm_Celera | 2:17728225 | CACCAGAGGTCTGAG[A/C]ACATTGTCTATCAAG | 74103 |
rs6402709 | snp | A/C | 0.5 | 0 | intron-variant | Nebl | Mm_Celera | 2:17728258 | CCTGCTGACTATGAT[A/C]TACTCTCTGTACAGG | 74103 |
rs6403218 | snp | A/T | 0.5 | 0 | intron-variant | Nebl | Mm_Celera | 2:17728323 | CTGTGCAGCTGCTTC[A/T]GACATGCTGGGGAGG | 74103 |
rs27125568 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Nebl | Mm_Celera | 2:17611257 | CACTCAACAAAGAGC[A/G]TCTGCGTGTCAAGAG | 74103 |
rs27125569 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Nebl | Mm_Celera | 2:17611011 | GTGCCTTCTTAACCC[A/C]TATGTCCCTCTTCTC | 74103 |
rs27125570 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Nebl | Mm_Celera | 2:17610816 | GAGCGTGTTTTAACT[C/T]CATTCTCCTTTGTCC | 74103 |
rs27125571 | snp | A/G | 0.5 | 0 | intron-variant | Nebl | Mm_Celera | 2:17610338 | CTCATCAGGATTAAG[A/G]GGATTAGAATGCTGT | 74103 |
rs27125572 | snp | A/G | 0.5 | 0 | intron-variant | Nebl | Mm_Celera | 2:17608029 | TTAGAAAGGGTCTGA[A/G]CAATACCCATTCGTC | 74103 |
rs27125573 | snp | A/G | 0.5 | 0 | intron-variant | Nebl | Mm_Celera | 2:17606621 | TGAAGTAAAAGTTAC[A/G]CATTAAAGGATTCTG | 74103 |
rs27125574 | snp | A/G | 0.5 | 0 | intron-variant | Nebl | Mm_Celera | 2:17604419 | GGAGTGACCTCTGTG[A/G]ATTGAGACTAGCAGT | 74103 |
rs27125575 | snp | A/G | 0.5 | 0 | intron-variant | Nebl | Mm_Celera | 2:17604014 | CTTTCTCTACAATAA[A/G]CACTCTGCAGAGGTC | 74103 |
rs27125576 | snp | C/G | 0.5 | 0 | intron-variant | Nebl | Mm_Celera | 2:17603909 | GAGAGAAGTTCAATG[C/G]TAAATGACTGTATGG | 74103 |
rs27125577 | snp | A/G | 0.5 | 0 | intron-variant | Nebl | Mm_Celera | 2:17603880 | AAATCTCAATATGTG[A/G]GCTCTCCTTTTGTGA | 74103 |
rs27125578 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Nebl | Mm_Celera | 2:17603837 | GTCCTGCCACACTGG[G/T]AGAGAAAACAAACAA | 74103 |
rs27125579 | snp | A/G | 0.5 | 0 | intron-variant | Nebl | Mm_Celera | 2:17603748 | TTTTGGTTTTATAAT[A/G]CAAAGAAGGGAGTGT | 74103 |
rs27125580 | snp | G/T | 0.5 | 0 | intron-variant | Nebl | Mm_Celera | 2:17603718 | CCTCTGAATGTAAAA[G/T]AGCTCTCATCTGCCT | 74103 |
rs27125581 | snp | A/G | 0.5 | 0 | intron-variant | Nebl | Mm_Celera | 2:17603650 | CTAATCAAGTTCCCA[A/G]TTGTGCCCTTTAAAC | 74103 |
rs27125582 | snp | G/T | 0.5 | 0 | intron-variant | Nebl | Mm_Celera | 2:17603288 | AACTGTAGTTTTCAG[G/T]GTGAGGTAGAAGAAA | 74103 |
rs27125583 | snp | A/G | 0.5 | 0 | intron-variant | Nebl | Mm_Celera | 2:17603073 | ACTTTTTTTCTAGGC[A/G]CAGGTTTGCATGTGG | 74103 |
rs27125584 | snp | C/G | 0.5 | 0 | intron-variant | Nebl | Mm_Celera | 2:17602882 | GAGTATTTTACATTT[C/G]ATCATGATCACAGTG | 74103 |
rs27125585 | snp | A/T | 0.5 | 0 | intron-variant | Nebl | Mm_Celera | 2:17602454 | GAAGCACAGAGATGT[A/T]GGTAGGATAGCATAA | 74103 |
rs27125586 | snp | C/T | 0.5 | 0 | intron-variant | Nebl | Mm_Celera | 2:17602332 | CCTCTGAGACAGAAA[C/T]GGATCCTGGACACTT | 74103 |
rs27125587 | snp | A/G | 0.5 | 0 | intron-variant | Nebl | Mm_Celera | 2:17602246 | TCCTAGAACACAAGG[A/G]TTCTACTTGCTGAGG | 74103 |
rs27125588 | snp | A/G | 0.5 | 0 | intron-variant | Nebl | Mm_Celera | 2:17601961 | CATAGGATCAGATTG[A/G]ATCAGCTTGACAGAA | 74103 |
rs27125589 | snp | A/G | 0.5 | 0 | intron-variant | Nebl | Mm_Celera | 2:17601139 | GGGTAAGTAAACTGA[A/G]GGAAGGAAGGAGGGA | 74103 |
rs27125590 | snp | A/G | 0.5 | 0 | intron-variant | Nebl | Mm_Celera | 2:17601076 | AATATGCTTCAATTT[A/G]TCAGCTTCTAATTTT | 74103 |
rs27125591 | snp | A/G | 0.5 | 0 | intron-variant | Nebl | Mm_Celera | 2:17600842 | TCCAGAGTCCACAAA[A/G]GACCCAACACAGTGA | 74103 |
rs27125592 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nebl | Mm_Celera | 2:17600208 | ATTAGAACCTGTCAC[C/T]AGATTTTGAATTATG | 74103 |
rs27125593 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nebl | Mm_Celera | 2:17600168 | AGCAAACCTGACCCA[C/T]CACACTAGGAAATGC | 74103 |
rs27125594 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nebl | Mm_Celera | 2:17600118 | TAACTCCCCTCGAGT[A/G]TTCAGAAAGAAAGGT | 74103 |
rs27125595 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nebl | Mm_Celera | 2:17600011 | CTGAAAGGAGGTAGA[A/G]AACACAAGCCCTCGC | 74103 |
rs27125596 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nebl | Mm_Celera | 2:17599655 | AAGGTATACAATTCT[A/G]ACCGCAATGTTTGCC | 74103 |
rs27125597 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nebl | Mm_Celera | 2:17598801 | AGGGAAACCCCAGAA[A/G]TTCCCAAGTCAGCTC | 74103 |
rs27125598 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nebl | Mm_Celera | 2:17598608 | AATGTCATTATTTGA[A/G]AGACTGAGAAAACTC | 74103 |
rs27125599 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Nebl | Mm_Celera | 2:17598552 | GGATGAGCACATTCC[C/G]TGCACCCAAAGACTT | 74103 |
rs27125600 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Nebl | Mm_Celera | 2:17598498 | GTCAGAGCATATTTG[C/G]ATGCACGTCTATCTG | 74103 |
rs27125601 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nebl | Mm_Celera | 2:17598456 | CCTCAAAGGCAAGCC[C/T]GTGTCTTCCTCCACT | 74103 |
rs27125602 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Nebl | Mm_Celera | 2:17598390 | CCTCTGAGCAGAATG[A/C]TCACCTACCATGCTG | 74103 |
rs27125603 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nebl | Mm_Celera | 2:17598301 | ATGCCTAGAAGAGCT[A/G]AATGCAAGCCAGCTC | 74103 |
rs27125604 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nebl | Mm_Celera | 2:17598111 | AAGCACCTGCAGAGC[C/T]ATGGCGGCTGACCAG | 74103 |
rs27125605 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Nebl | Mm_Celera | 2:17597998 | AATCCCATGCTGACC[A/C]TGAAAAGAGCAGCTG | 74103 |
rs27125606 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nebl | Mm_Celera | 2:17597894 | TGGTGTGAACCTAGA[A/G]CAAAGCATAGAAGAA | 74103 |
rs27125607 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nebl | Mm_Celera | 2:17597849 | TGTCTGAATGTGCCT[C/T]GCTCAGGATGTCTGT | 74103 |
rs27125608 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nebl | Mm_Celera | 2:17597827 | ATGCTGGCTTCTCAC[A/G]GGATTCTGTCTGAAT | 74103 |
rs27125609 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nebl | Mm_Celera | 2:17597810 | CTAGTCTCTCTGTCA[C/T]GATGCTGGCTTCTCA | 74103 |
rs27125610 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nebl | Mm_Celera | 2:17597797 | GATGAAAGGAGCACT[A/G]GTCTCTCTGTCACGA | 74103 |
rs27125611 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nebl | Mm_Celera | 2:17597764 | TGGTACCAGTGTGCC[C/T]TGTGGGTTGGAAGAA | 74103 |
rs27125612 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Nebl | Mm_Celera | 2:17597707 | AATATGTAACAGTAG[A/C]CATTGTCCTGCTTCC | 74103 |
rs27125613 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nebl | Mm_Celera | 2:17597678 | CTGGCTTATCAGAGC[A/G]GGAGTGACTATCCAA | 74103 |
rs27125614 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nebl | Mm_Celera | 2:17597662 | CAATCAAAAAGGGTG[C/T]CTGGCTTATCAGAGC | 74103 |
rs27125615 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Nebl | Mm_Celera | 2:17597615 | CACAAAAGGAAAGGG[A/T]CTATGCAAACCTAAC | 74103 |
rs27125616 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nebl | Mm_Celera | 2:17597579 | TAGCATAGGAGAAAC[C/T]CTGAGTTTGAACCCC | 74103 |
rs27125617 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nebl | Mm_Celera | 2:17597517 | CAATCCCTGGCATGT[A/G]GCATTCAAAATATGA | 74103 |
rs27125618 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nebl | Mm_Celera | 2:17597502 | TACAGAACTCATCAT[C/T]AATCCCTGGCATGTA | 74103 |
rs27125619 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Nebl | Mm_Celera | 2:17597372 | AGAATGTAAAATTAA[C/T]AAGGCAAGGGAATTG | 74103 |
rs27125620 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nebl | Mm_Celera | 2:17597249 | TTATTGTGCAGGTAC[C/T]GGTGATAAAGGCTGA | 74103 |
rs27125621 | snp | A/G | 0.18 | 0.24 | intron-variant | Nebl | Mm_Celera | 2:17596955 | AATTATCCTATAAAA[A/G]TTCAAATATCATGAA | 74103 |
rs27125622 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nebl | Mm_Celera | 2:17596791 | ACCATCTGAGAATTT[C/T]TGAAGACAAATCTAA | 74103 |
rs27125623 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Nebl | Mm_Celera | 2:17596689 | CCACCTATACACAGA[A/G]GCATACAGTATGCTC | 74103 |
rs27125624 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nebl | Mm_Celera | 2:17596176 | TCAAGGGATGGTAGG[A/G]TTTACATGTAATTTG | 74103 |
rs27125625 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nebl | Mm_Celera | 2:17596093 | ACTAGACCATCTTTC[A/G]TACACTGAGTGACTC | 74103 |
rs27125626 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nebl | Mm_Celera | 2:17595307 | ATAAGACTTTCATCA[C/T]TGACAAACACTGGTG | 74103 |
rs27125627 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nebl | Mm_Celera | 2:17595231 | CCAGATCCTCAGTAA[A/G]AGACCTAGGCACAGA | 74103 |
rs27125628 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nebl | Mm_Celera | 2:17594991 | ACCTGTGCTTTAATG[C/T]GATGCTTCTCAACCA | 74103 |
rs27125629 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Nebl | Mm_Celera | 2:17594882 | TAGAATCACATAGCA[A/G]AGATTTAGAAATTGA | 74103 |
rs27125630 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nebl | Mm_Celera | 2:17594688 | CAGCAATCATGCAAA[A/G]CAGTTCAGATAATGT | 74103 |
rs27125631 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nebl | Mm_Celera | 2:17593964 | AGCTGGGAGCCTGGC[A/G]GTGCTTGATGAGAGT | 74103 |
rs27125632 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Nebl | Mm_Celera | 2:17593935 | CAAAAGAAAAGAGAG[A/C]CAGGCATGAAATAAG | 74103 |
rs27125633 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nebl | Mm_Celera | 2:17593808 | GGAAATGCTGTCAAA[C/T]GCTGGGTTTCTCAAG | 74103 |
rs27125634 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nebl | Mm_Celera | 2:17593571 | GTAATAACACAAATG[A/G]AAATCTGTGGATTTG | 74103 |
rs27125635 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Nebl | Mm_Celera | 2:17593485 | AGTCCTCTTGTTTAG[C/T]CTTATAACCAAACTA | 74103 |