SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3657198 | snp | A/T | 0.5 | 0 | intron-variant | Herc6 | Mm_Celera | 6:57649330 | ACCCTGTCTGGAAAT[A/T]AAAAAAAAAATCCAA | 67138 |
rs3657277 | snp | C/G | 0.484429 | 0.0868505 | intron-variant | Herc6 | Mm_Celera | 6:57649377 | GCAGTTGTTATAAAT[C/G]CAAACAACACTGACC | 67138 |
rs3657756 | snp | A/G | 0.429688 | 0.173817 | intron-variant | Herc6 | Mm_Celera | 6:57649390 | ATGCAAACAACACTG[A/G]CCATCTGTATAAAAC | 67138 |
rs3657885 | snp | C/T | 0.456747 | 0.140554 | intron-variant | Herc6 | Mm_Celera | 6:57649455 | CCATTTGACACAAAG[C/T]ATTTCCTTTTTATAC | 67138 |
rs4136061 | snp | A/G | 0.484429 | 0.0868505 | intron-variant | Herc6 | Mm_Celera | 6:57649576 | AATATCATTCCAAAG[A/G]TAGACTTATCACTCT | 67138 |
rs6209205 | snp | A/G | 0.5 | 0 | intron-variant | Herc6 | Mm_Celera | 6:57635036 | tgaactttattaaag[A/G]gtcatagcacnaggg | 67138 |
rs6209595 | snp | G/T | 0.5 | 0 | intron-variant | Herc6 | Mm_Celera | 6:57635047 | aaagngtcatagcac[G/T]agggaggttgagaac | 67138 |
rs6209656 | snp | C/T | 0.5 | 0 | intron-variant | Herc6 | Mm_Celera | 6:57635091 | caagcagtggtatag[C/T]tgggttatttggtgg | 67138 |
rs6209719 | snp | C/T | 0.5 | 0 | intron-variant | Herc6 | Mm_Celera | 6:57635134 | ctttttgaggattct[C/T]cacactgatttccag | 67138 |
rs6210678 | snp | C/T | 0.5 | 0 | intron-variant | Herc6 | Mm_Celera | 6:57635263 | gccatgtgactagag[C/T]aaaatgaaatctcaa | 67138 |
rs6283086 | snp | A/G | 0.5 | 0 | intron-variant | Herc6 | Mm_Celera | 6:57610092 | tgtgtgtgtgtgtgt[A/G]tatgagtgtAGTgtc | 67138 |
rs6283716 | snp | C/T | 0.5 | 0 | intron-variant | Herc6 | Mm_Celera | 6:57610219 | ttgcattcataatgc[C/T]attaagtatcatcac | 67138 |
rs6284178 | snp | C/T | 0.5 | 0 | intron-variant | Herc6 | Mm_Celera | 6:57610271 | atcgcaagcagacac[C/T]tgatatctattaaat | 67138 |
rs6285209 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Herc6 | Mm_Celera | 6:57610471 | CAATGCTGAGTAATA[C/T]TTCACTGCATATTAT | 67138 |
rs6298602 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Herc6 | Mm_Celera | 6:57610574 | GATTTATAAGCACCT[A/T]TCTGTCTCTATTTTT | 67138 |
rs6299256 | snp | A/C | 0.475309 | 0.108333 | intron-variant | Herc6 | Mm_Celera | 6:57610710 | ACCTATGCAAGAGGA[A/C]AGGCCTTGCCTGTGC | 67138 |
rs6372711 | snp | A/G | 0.5 | 0 | intron-variant | Herc6 | Mm_Celera | 6:57588467 | tggagaatcatttgg[A/G]tatgtgcccaggagt | 67138 |
rs6373659 | snp | C/T | 0.5 | 0 | intron-variant | Herc6 | Mm_Celera | 6:57588620 | acatccttgccagca[C/T]ctgctgtcacctgaa | 67138 |
rs6373722 | snp | A/T | 0.5 | 0 | intron-variant | Herc6 | Mm_Celera | 6:57588659 | cttagtcattctgac[A/T]ggtgcgaggtggaat | 67138 |
rs6387268 | snp | C/G | 0.5 | 0 | intron-variant | Herc6 | Mm_Celera | 6:57588801 | acccattttaaaatt[C/G]ttttaggttttcttt | 67138 |
rs29831365 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Herc6 | Mm_Celera | 6:57597221 | AGGGTCCTGCAGGTG[A/G]GTTACCTGTGTCTTC | 67138 |
rs29833606 | snp | G/T | 0.432133 | 0.171253 | intron-variant | Herc6 | Mm_Celera | 6:57607857 | CCCTAAATTTCAGAG[G/T]ATTGTTTGAGACAGT | 67138 |
rs29871069 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Herc6 | Mm_Celera | 6:57656242 | CTGGCGGTTCCTCAG[A/G]AAATTGGACATAGTA | 67138 |
rs29872711 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Herc6 | Mm_Celera | 6:57607779 | TTTCCTGGTGCTGGG[A/G]ACTCAAACCCAGAGC | 67138 |
rs29873868 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Herc6 | Mm_Celera | 6:57646545 | TGGTGAAGGATAGAG[A/G]ATCAGAAGTACAGGG | 67138 |
rs29874254 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Herc6 | Mm_Celera | 6:57654713 | GTCCTGGCATGTGTC[C/T]GTAATTTTTAGAGTT | 67138 |
rs29876541 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Herc6 | Mm_Celera | 6:57607626 | ACGTGGATCTCTTAA[C/T]TTTATAGACCTTGTG | 67138 |
rs29877495 | snp | A/G | 0.375 | 0.216506 | intron-variant | Herc6 | Mm_Celera | 6:57660935 | ACTTTATAAGGAAAA[A/G]AGTTTTATTTGTGTC | 67138 |
rs29917414 | snp | C/T | 0.5 | 0 | intron-variant | Herc6 | Mm_Celera | 6:57594768 | CGAAGATGGCGCCGC[C/T]TCAGAAGCTCTGTGG | 67138 |
rs29921912 | snp | C/T | 0.444444 | 0.157135 | downstream-variant-500B | Herc6 | Mm_Celera | 6:57665394 | AGTTGTGGCCTTTGC[C/T]GGAGGAAGTGTGTCA | 67138 |
rs29927556 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Herc6 | Mm_Celera | 6:57597493 | TTGAACTCTACATAG[C/T]TTTGTCAGTGGGGGG | 67138 |
rs29927567 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Herc6 | Mm_Celera | 6:57626563 | CATTGATGTAGCTTC[A/C]CTTTCACTTCTAGGA | 67138 |
rs29966366 | snp | A/C | 0.465374 | 0.126941 | intron-variant | Herc6 | Mm_Celera | 6:57654792 | GTAAAGATAGCTGTT[A/C]ATTCTGAGATATTGG | 67138 |
rs29968006 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Herc6 | Mm_Celera | 6:57587640 | CCAAGGGCCTTCCCC[C/T]CACCCCCCATTGATG | 67138 |
rs29972216 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Herc6 | Mm_Celera | 6:57601201 | CTGACTGCTGCTCTT[C/T]CAGAAGTCCCGAGCT | 67138 |
rs30018762 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Herc6 | Mm_Celera | 6:57585327 | CTACTATCTCTAGGA[C/T]TTTTATTCTGACAGT | 67138 |
rs30020621 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Herc6 | Mm_Celera | 6:57626757 | GTTCTCCATTTGTTA[C/T]AAAGAGAAGCATGTT | 67138 |
rs30022458 | snp | C/T | 0.375 | 0.216506 | intron-variant | Herc6 | Mm_Celera | 6:57640641 | CACATTTCCTTCCTT[C/T]CATTCTTAGGTTAGG | 67138 |
rs30023158 | snp | A/C/G/T | 0.722222 | 0.0785674 | intron-variant | Herc6 | Mm_Celera | 6:57583884 | ATCCTTACCTACATA[A/C/G/T]AGACATCAGAGACCA | 67138 |
rs30032917 | snp | G/T | 0.375 | 0.216506 | intron-variant | Herc6 | Mm_Celera | 6:57655336 | CCTGGGCTGCTGTTT[G/T]GGCCTGGAAAGTTTT | 67138 |
rs30033285 | snp | G/T | 0.290657 | 0.246672 | intron-variant | Herc6 | Mm_Celera | 6:57602928 | GAAATGCCCAAATAA[G/T]TAAAGCAGCCAACCC | 67138 |
rs30067691 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Herc6 | Mm_Celera | 6:57599136 | ATGTCAACTGGTCAG[C/T]GTTTTAAAATTCGAC | 67138 |
rs30068175 | snp | C/G | 0.375 | 0.216506 | synonymous-codon | Herc6 | Mm_Celera | 6:57598625 | GAGCAACAGATCTGG[C/G]CAGTTGGCTCTCAGC | 67138 |
rs30070171 | snp | C/G | 0.432133 | 0.171253 | missense | Herc6 | Mm_Celera | 6:57654392 | TTCTTTCTTCAGGTT[C/G]GATTTATTAATGAAA | 67138 |
rs30079744 | snp | A/C | 0.375 | 0.216506 | intron-variant | Herc6 | Mm_Celera | 6:57594932 | CCCTGTGCTCTCACC[A/C]GGAAGGTGGCGGTTG | 67138 |
rs30116239 | snp | A/G | 0.5 | 0 | intron-variant | Herc6 | Mm_Celera | 6:57585294 | TAATTATTAATTTGC[A/G]TTACATTCCCTCTAG | 67138 |
rs30116569 | snp | G/T | 0.387812 | 0.208586 | intron-variant | Herc6 | Mm_Celera | 6:57610647 | GCAAAATGGCACAAG[G/T]TAGGAAACAGAATGT | 67138 |
rs30120442 | snp | A/G | 0.429688 | 0.173817 | intron-variant | Herc6 | Mm_Celera | 6:57658308 | TGACTTGCAGTAAAT[A/G]GAGTAAGCCTTCAGA | 67138 |
rs30131914 | snp | C/T | 0.375 | 0.216506 | missense | Herc6 | Mm_Celera | 6:57598588 | TTGCTCTGTCTCTCA[C/T]GGGGACATCATTTGG | 67138 |
rs30169258 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Herc6 | Mm_Celera | 6:57583644 | TTTTAAACTACAAAC[C/T]ATCAAGATACCAAGG | 67138 |
rs30171935 | snp | G/T | 0.375 | 0.216506 | intron-variant | Herc6 | Mm_Celera | 6:57655995 | AAGCTCAGGTGCTTC[G/T]CAGCCATTCGGTATT | 67138 |
rs30209255 | snp | C/T | 0.375 | 0.216506 | intron-variant | Herc6 | Mm_Celera | 6:57639832 | AATTGTGATTTGGGT[C/T]AGTCTAAGAAAGCTA | 67138 |
rs30210765 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Herc6 | Mm_Celera | 6:57594833 | TTCTACACTGTCACC[C/T]GTGCAGCCTGCCCTC | 67138 |
rs30214301 | snp | A/G | 0.444444 | 0.157135 | upstream-variant-2KB | Herc6 | Mm_Celera | 6:57579330 | AGGTTCTGGTGGGAA[A/G]GAAGAGAGGAAATGG | 67138 |
rs30219031 | snp | G/T | 0.375 | 0.216506 | intron-variant | Herc6 | Mm_Celera | 6:57640676 | CCTTAATATAAGCAG[G/T]CTGGTTTAGTTCAGC | 67138 |
rs30223756 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Herc6 | Mm_Celera | 6:57646535 | CTTTATACTTTGGTG[A/G]AGGATAGAGAATCAG | 67138 |
rs30224640 | snp | A/G | 0.46875 | 0.121031 | intron-variant | Herc6 | Mm_Celera | 6:57655616 | CCAGAGTGACAATAC[A/G]GCCTCATGAGCACCA | 67138 |
rs30259389 | snp | G/T | 0.46875 | 0.121031 | intron-variant | Herc6 | Mm_Celera | 6:57612923 | TTTGCTATGCAACTT[G/T]TATTTCATTTTATTT | 67138 |
rs30264496 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Herc6 | Mm_Celera | 6:57596872 | TAAGACACTTATTCT[A/C]CAAGTTCACTAAATA | 67138 |
rs30264508 | snp | A/G | 0.375 | 0.216506 | intron-variant | Herc6 | Mm_Celera | 6:57586034 | GTTTATTCCTAGATC[A/G]TTTATTTTCCCCGAG | 67138 |
rs30264602 | snp | C/T | 0.375 | 0.216506 | intron-variant | Herc6 | Mm_Celera | 6:57627141 | ACTATAAAAACTGGA[C/T]ACCAGGGAGGGGTCT | 67138 |
rs30267419 | snp | A/C | 0.5 | 0 | intron-variant | Herc6 | Mm_Celera | 6:57596752 | ATTCCATTTTCATTT[A/C]AGCTTGGGTTCTCTT | 67138 |
rs30267677 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Herc6 | Mm_Celera | 6:57607514 | AATTAATTCTTATGC[C/T]ATTTGTAGTCAGAAT | 67138 |
rs30269804 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Herc6 | Mm_Celera | 6:57598123 | TAGTTGGTCTCAGCA[C/T]ACTCTAGAGCTACAG | 67138 |
rs30274374 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Herc6 | Mm_Celera | 6:57619172 | GCCTTAGTTTCAAAC[C/T]GACTATTCACTGTGT | 67138 |
rs30274376 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Herc6 | Mm_Celera | 6:57619368 | ATGGAAGAAAACCTG[C/T]AGCTACAACTTGTAT | 67138 |
rs30274378 | snp | A/G | 0.444444 | 0.157135 | missense | Herc6 | Mm_Celera | 6:57619448 | TTTTGACCACAGATA[A/G]CCACGTGTCTTGAGG | 67138 |
rs30274379 | snp | G/T | 0.444444 | 0.157135 | missense | Herc6 | Mm_Celera | 6:57619466 | ACGTGTCTTGAGGAG[G/T]ATCTGCTCAGAGATC | 67138 |
rs30274380 | snp | G/T | 0.475309 | 0.108333 | synonymous-codon | Herc6 | Mm_Celera | 6:57619516 | CCAAGAAGCTCTACT[G/T]GTTTTTCTTTTGCTC | 67138 |
rs30274382 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Herc6 | Mm_Celera | 6:57619686 | AATCACTTTTGATGT[A/C]GAAATCATAGCATAC | 67138 |
rs30274756 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Herc6 | Mm_Celera | 6:57626763 | CATTTGTTACAAAGA[A/G]AAGCATGTTTGATGA | 67138 |
rs30275594 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Herc6 | GRCm38.p3 | 6:57619763 | TTTTGTAAAGATCAA[C/T]CCAAAACTATTATAC | 67138 |
rs30275596 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Herc6 | Mm_Celera | 6:57619787 | ATTATACCTGCCACA[C/T]TTCTTACCATACAAA | 67138 |
rs30275597 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Herc6 | Mm_Celera | 6:57619831 | TTAGACTTTGTTAGC[C/T]ATAACTGCCAGTCAA | 67138 |
rs30275599 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Herc6 | Mm_Celera | 6:57624602 | CAGGCCTGGAGGAAC[A/G]AACTCTAGCTGTTCC | 67138 |
rs30275601 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Herc6 | Mm_Celera | 6:57624761 | TGCCCATGCATCATT[A/G]TTAATGGAATGAGCA | 67138 |
rs30275603 | snp | A/T | 0.18 | 0.24 | intron-variant | Herc6 | Mm_Celera | 6:57625235 | AAATTAAAAAAAAAA[A/T]TCCCATGTCCCTACC | 67138 |
rs30276764 | snp | A/G/T | 0.444444 | 0.157135 | intron-variant | Herc6 | Mm_Celera | 6:57625329 | CTACCTAAAATAAGT[A/G/T]TATATCCATATGTGA | 67138 |
rs30276766 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Herc6 | Mm_Celera | 6:57625370 | TGTAATCTGAAAATA[A/G]GCATTACTTAATTTT | 67138 |
rs30276768 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Herc6 | Mm_Celera | 6:57625828 | GTCTTAAACATCCCA[A/G]AAGAAACTGAGGAAA | 67138 |
rs30276770 | snp | A/C | 0.444444 | 0.157135 | missense | Herc6 | Mm_Celera | 6:57625899 | TCACACCCTCAGGAA[A/C]GTGTTGGGCATCTTT | 67138 |
rs30276772 | snp | A/G | 0.444444 | 0.157135 | missense | Herc6 | Mm_Celera | 6:57625964 | CTAAAGAAAGCCATC[A/G]TCTCTCAAATACAGT | 67138 |
rs30277664 | snp | A/G | 0.444444 | 0.157135 | missense | Herc6 | Mm_Celera | 6:57625994 | TATGGAGTTGCAACG[A/G]AGCAGTATATTACTA | 67138 |
rs30277666 | snp | A/C/T | 0.444444 | 0.157135 | missense | Herc6 | GRCm38.p3 | 6:57626022 | CTAATATTAAAGTTC[A/C/T]TTTAGAAGTGATAAA | 67138 |
rs30277668 | snp | A/G | 0.35503 | 0.226867 | synonymous-codon | Herc6 | Mm_Celera | 6:57626044 | AGTGATAAAAGAAGT[A/G]CATAAGGTAAAATCT | 67138 |
rs30277669 | snp | A/T | 0.426035 | 0.177515 | intron-variant | Herc6 | Mm_Celera | 6:57626148 | TGTCAATTACATTTT[A/T]AAAAATACTTGAAAT | 67138 |
rs30277672 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Herc6 | Mm_Celera | 6:57634598 | GTCCTTTCGGCATAT[A/G]CCAGCAGTTCTCAAC | 67138 |
rs30278834 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Herc6 | Mm_Celera | 6:57634904 | TTTCCATATTGGTAG[C/T]GTTGGATTTTCCTGG | 67138 |
rs30278835 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Herc6 | Mm_Celera | 6:57634942 | TAAAGATACTTGGAG[A/G]TTAATAAAGAAGTTA | 67138 |
rs30278837 | snp | C/T | 0.486111 | 0.0821678 | intron-variant | Herc6 | Mm_Celera | 6:57637045 | TGATGGCGTATAGAA[C/T]GTATAAGCATTACAT | 67138 |
rs30278839 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Herc6 | Mm_Celera | 6:57637075 | TCTCTGAGGGGAAAG[A/G]AATCCTGGCAGTTGG | 67138 |
rs30278841 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Herc6 | Mm_Celera | 6:57637589 | GAGCTGCAAGGGTAG[C/T]GCCTATAACAGGAGT | 67138 |
rs30278843 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Herc6 | Mm_Celera | 6:57637625 | CATTTGGTCTGGAAA[A/G]TCACCCTGCTGCCTG | 67138 |
rs30279875 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Herc6 | Mm_Celera | 6:57637832 | GCCTGATCTTGGGCC[A/G]TTTTACTCCATAGGG | 67138 |
rs30279877 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Herc6 | Mm_Celera | 6:57637865 | GTGTGTGGCCACTTC[C/T]GATTTGAGGGGCTGG | 67138 |
rs30279879 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Herc6 | Mm_Celera | 6:57637934 | AACCTGGTGAGTTTC[C/T]GGGTCCTGGGGGTTG | 67138 |
rs30279881 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Herc6 | Mm_Celera | 6:57637967 | CCGTGCTACTCCTGT[A/G]CCTCCAAGGCTTATA | 67138 |
rs30279883 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Herc6 | Mm_Celera | 6:57641280 | TGCATGTTATTGCTC[C/T]CAGGTAACTTCATTA | 67138 |
rs30280784 | snp | A/C/G | 0.375 | 0.216506 | intron-variant | Herc6 | GRCm38.p3 | 6:57644188 | GCTACTTTCTGATTA[A/C/G]TTACAAGTGGGCAAC | 67138 |
rs30280786 | snp | C/G | 0.459184 | 0.136902 | intron-variant | Herc6 | Mm_Celera | 6:57644199 | ATTAGTTACAAGTGG[C/G]CAACCCATATCTTGT | 67138 |