SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3667154 | snp | C/T | 0.444444 | 0.157135 | synonymous-codon | Mycbp2 | GRCm38.p3 | 14:103122596 | TCGCCGACAGCACTG[C/T]AAGTGGAACACATGA | 105689 |
rs3667169 | snp | C/T | 0.444444 | 0.157135 | synonymous-codon | Mycbp2 | GRCm38.p3 | 14:103122605 | GCACTGTAAGTGGAA[C/T]ACATGACTGCAGTCC | 105689 |
rs3667203 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Mycbp2 | Mm_Celera | 14:103122625 | GACTGCAGTCCAACT[G/T]AAAGAGAGAAACACG | 105689 |
rs3667228 | snp | A/C | 0.5 | 0 | intron-variant | Mycbp2 | Mm_Celera | 14:103122639 | TGAAAGAGAGAAACA[A/C]GGACGAGAGTGAGCG | 105689 |
rs3667230 | snp | C/T | 0.5 | 0 | intron-variant | Mycbp2 | Mm_Celera | 14:103122643 | AGAGAGAAACACGGA[C/T]GAGAGTGAGCGAATG | 105689 |
rs3667249 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Mycbp2 | Mm_Celera | 14:103122654 | CGGACGAGAGTGAGC[A/G]AATGCAGCCATGGCC | 105689 |
rs3667690 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Mycbp2 | Mm_Celera | 14:103122674 | CAGCCATGGCCACAC[G/T]GAAGGAATGGGGAGA | 105689 |
rs3668465 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Mycbp2 | Mm_Celera | 14:103122827 | GTCATGTATTGATGC[C/T]ACTTATATAACAACT | 105689 |
rs3681573 | snp | A/G | 0.5 | 0 | intron-variant | Mycbp2 | Mm_Celera | 14:103119811 | GAAATGTAGCTGTTC[A/G]GTATGTTATTGGAGG | 105689 |
rs4137223 | snp | C/T | 0.5 | 0 | intron-variant | Mycbp2 | Mm_Celera | 14:103119998 | AAACAGACAGACACA[C/T]ATTACACACTGGAAA | 105689 |
rs4187282 | snp | G/T | 0.375 | 0.216506 | intron-variant | Mycbp2 | Mm_Celera | 14:103311466 | ATCTCAGGTGCAGAA[G/T]ATTCCATAGAAACCA | 105689 |
rs4230522 | snp | C/T | 0.183257 | 0.240926 | utr-variant-3-prime | Mycbp2 | Mm_Celera | 14:103113972 | CAAGAATTATGTACA[C/T]GGTATTTGGCATCAT | 105689 |
rs4230523 | snp | A/T | 0.244898 | 0.249948 | utr-variant-3-prime | Mycbp2 | Mm_Celera | 14:103114031 | TGTAAAATGGTCCCG[A/T]TCTTATCCTGAGCAG | 105689 |
rs4230524 | snp | G/T | 0.244898 | 0.249948 | synonymous-codon | Mycbp2 | GRCm38.p3 | 14:103114147 | AGCATTTCTGCACAC[G/T]CCGCACCCGAGAGCA | 105689 |
rs4230525 | snp | C/T | 0.244898 | 0.249948 | synonymous-codon | Mycbp2 | Mm_Celera | 14:103114180 | CTCTTCCCCCGTGGG[C/T]GGATGAACAACGTGG | 105689 |
rs4230526 | snp | C/T | 0.244898 | 0.249948 | synonymous-codon | Mycbp2 | Mm_Celera | 14:103114204 | AACGTGGAGTGGACA[C/T]TCAGTTCCTTCTAGC | 105689 |
rs4230527 | snp | C/T | 0.426035 | 0.177515 | missense | Mycbp2 | Mm_Celera | 14:103156668 | TTAAACCCGACGGGC[C/T]TGTGAGCCGGACTCC | 105689 |
rs4230528 | snp | A/C | 0.244898 | 0.249948 | synonymous-codon | Mycbp2 | Mm_Celera | 14:103156457 | CCCAGGACCAGGCTC[A/C]AGGTCATCCTCCCCT | 105689 |
rs4230529 | snp | A/C | 0.287335 | 0.247197 | synonymous-codon | Mycbp2 | Mm_Celera | 14:103156424 | GCCCAAGCCTCTGCC[A/C]ACTCCCAGGTCTAGC | 105689 |
rs4230530 | snp | C/G | 0.21875 | 0.248039 | missense | Mycbp2 | Mm_Celera | 14:103156408 | ACTCCCAGGTCTAGC[C/G]CATCTGGTGCAAGCT | 105689 |
rs4230531 | snp | A/C | 0.21875 | 0.248039 | missense | Mycbp2 | Mm_Celera | 14:103156383 | CAAGCTCTCCACGCT[A/C]CTCCTCACCACAGGA | 105689 |
rs6176572 | snp | A/G | 0.5 | 0 | intron-variant | Mycbp2 | Mm_Celera | 14:103266539 | CCACTATACTCTTCA[A/G]CACTCTNTCAAggtt | 105689 |
rs6176576 | snp | G/T | 0.456747 | 0.140554 | intron-variant | Mycbp2 | Mm_Celera | 14:103266546 | ACTCTTCANCACTCT[G/T]TCAAggtttgccttt | 105689 |
rs6178165 | snp | C/T | 0.5 | 0 | intron-variant | Mycbp2 | Mm_Celera | 14:103266867 | ggcggtggtggagca[C/T]gcctttaatcccagg | 105689 |
rs6178233 | snp | G/T | 0.5 | 0 | intron-variant | Mycbp2 | Mm_Celera | 14:103266915 | tcgaggccagcctgg[G/T]ctacaaagtgagttc | 105689 |
rs6186774 | snp | C/G | 0.304688 | 0.243945 | intron-variant | Mycbp2 | Mm_Celera | 14:103182564 | GAGGTCTGAGAATGA[C/G]CAGAGCAGGAAAAGA | 105689 |
rs6220123 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Mycbp2 | Mm_Celera | 14:103124623 | GCCCTAATTAGTAAT[C/T]ACCAAAGGGATAAAA | 105689 |
rs6221130 | snp | A/T | 0.489796 | 0.070696 | intron-variant | Mycbp2 | Mm_Celera | 14:103124789 | ATAAGTATTATAATT[A/T]AAAAAATAAAGAACA | 105689 |
rs6316882 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Mycbp2 | Mm_Celera | 14:103124377 | CTTCCTGGGATGGCC[C/T]AACCTCTGAGTAGAT | 105689 |
rs6317409 | snp | C/G | 0.46281 | 0.131194 | intron-variant | Mycbp2 | Mm_Celera | 14:103124506 | TGGTGGGTTTGCCTA[C/G]GTTCAAGAAGAAGAA | 105689 |
rs6319223 | snp | A/T | 0.290657 | 0.246672 | intron-variant | Mycbp2 | Mm_Celera | 14:103280799 | TTAATTGGCTAAGTG[A/T]TAGCAATGAAAATTG | 105689 |
rs6319688 | snp | A/G | 0.290657 | 0.246672 | intron-variant | Mycbp2 | Mm_Celera | 14:103280868 | TTAGTAGGACACAGA[A/G]AATTCAAAAGTATGT | 105689 |
rs6333606 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Mycbp2 | Mm_Celera | 14:103281065 | aaataaGTTAGGTCA[C/T]TAAAGTAGAAAATGG | 105689 |
rs6333652 | snp | C/T | 0.35124 | 0.228584 | intron-variant | Mycbp2 | Mm_Celera | 14:103281096 | TATCCAACAAAGCAC[C/T]ACAGAATAAAAATTA | 105689 |
rs6361531 | snp | G/T | 0.290657 | 0.246672 | intron-variant | Mycbp2 | Mm_Celera | 14:103210467 | tctggcctcCATTAA[G/T]ACTAACTCTTAAGAC | 105689 |
rs6362042 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Mycbp2 | Mm_Celera | 14:103210546 | ATGAAGACTAACGCA[C/T]AATCAGTTTAAATAC | 105689 |
rs6362510 | snp | G/T | 0.290657 | 0.246672 | intron-variant | Mycbp2 | Mm_Celera | 14:103210608 | ATTACTTAAACAGTA[G/T]AACACTACAGTATTG | 105689 |
rs6363160 | snp | G/T | 0.5 | 0 | intron-variant | Mycbp2 | Mm_Celera | 14:103210764 | TTTCTACTTATATTG[G/T]ACAGCNTTTTAAAAA | 105689 |
rs6363163 | snp | C/T | 0.5 | 0 | intron-variant | Mycbp2 | Mm_Celera | 14:103210770 | CTTATATTGNACAGC[C/T]TTTTAAAAAGCTAAA | 105689 |
rs6363702 | snp | C/G | 0.290657 | 0.246672 | intron-variant | Mycbp2 | Mm_Celera | 14:103210868 | TTTGATACATGTAAA[C/G]ACCAGAGCATAATAT | 105689 |
rs6373118 | snp | A/G | 0.5 | 0 | intron-variant | Mycbp2 | Mm_Celera | 14:103295780 | gaaggattagtaggc[A/G]tagccttgttggagg | 105689 |
rs6377127 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Mycbp2 | Mm_Celera | 14:103210999 | tttattgttaattag[C/T]atgcatgcatatcta | 105689 |
rs6387298 | snp | C/T | 0.5 | 0 | intron-variant | Mycbp2 | Mm_Celera | 14:103296092 | gcaactgaacagtaa[C/T]gaagacaAACTAACA | 105689 |
rs6388299 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Mycbp2 | Mm_Celera | 14:103296254 | ACTTTGTCTCAAAGA[C/T]AAAATTACAACAAAA | 105689 |
rs6397336 | snp | A/G | 0.5 | 0 | intron-variant | Mycbp2 | Mm_Celera | 14:103147066 | TAGTAATCTCCATAG[A/G]TAGTATACAATTAGC | 105689 |
rs13482346 | snp | A/G | 0.235537 | 0.249581 | synonymous-codon | Mycbp2 | Mm_Celera | 14:103127931 | TTGCTTCTGTTGCCC[A/G]TCCTTTCCCATCCAT | 105689 |
rs30105998 | snp | A/G | 0.375 | 0.216506 | intron-variant | Mycbp2 | Mm_Celera | 14:103145332 | CCTGATAAGGTGCAC[A/G]CCCTGTTTTTCTGGG | 105689 |
rs30109943 | snp | A/G | 0.375 | 0.216506 | intron-variant | Mycbp2 | Mm_Celera | 14:103334690 | TATCCCATAGATGCA[A/G]ATAGGAAAGCTCAGT | 105689 |
rs30121831 | snp | A/G | 0.401235 | 0.199068 | intron-variant | Mycbp2 | Mm_Celera | 14:103249488 | ATGCAGCTAAGCCTC[A/G]CCCCTAGGAAGAGAA | 105689 |
rs30125194 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Mycbp2 | Mm_Celera | 14:103151785 | AGACAACAAGAAGCT[A/G]CAGTTCATGATCGGT | 105689 |
rs30139002 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Mycbp2 | Mm_Celera | 14:103231399 | TATCAGTTCTGGTTT[A/G]CAGGCCCCTCTCTCC | 105689 |
rs30144238 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Mycbp2 | Mm_Celera | 14:103218210 | TATTTCTTTCCCTGG[A/C]ATTCATTAATAACTA | 105689 |
rs30144997 | snp | A/C | 0.375 | 0.216506 | intron-variant | Mycbp2 | Mm_Celera | 14:103126339 | AAGGACAACATGTAA[A/C]TGGGGCTGGCTTACA | 105689 |
rs30161935 | snp | C/T | 0.265928 | 0.249492 | intron-variant | Mycbp2 | Mm_Celera | 14:103187592 | GGACAAGCATCTGGG[C/T]GGCAGCAGTGCTTGG | 105689 |
rs30165390 | snp | G/T | 0.429688 | 0.173817 | intron-variant | Mycbp2 | Mm_Celera | 14:103296243 | AGGAAACCTGGACTT[G/T]GTCTCAAAGACAAAA | 105689 |
rs30172898 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Mycbp2 | Mm_Celera | 14:103165115 | CAAGTATGCATAAAA[C/T]CCACACACATATAAA | 105689 |
rs30174833 | snp | C/T | 0.375 | 0.216506 | synonymous-codon | Mycbp2 | Mm_Celera | 14:103145975 | GGGAGAAGGCGTCAG[C/T]GCAGCCACAAAGTGC | 105689 |
rs30187225 | snp | A/G | 0.5 | 0 | intron-variant | Mycbp2 | Mm_Celera | 14:103144676 | AATTTATATTCAAAC[A/G]TAAATATATTTTATG | 105689 |
rs30188082 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Mycbp2 | Mm_Celera | 14:103316695 | AATGGTCCCAAGAAA[A/C]AAGCTGGAGAAGCCA | 105689 |
rs30191283 | snp | A/G | 0.5 | 0 | intron-variant | Mycbp2 | Mm_Celera | 14:103324183 | TTGTTCCTCCTATAG[A/G]GTTGCAGACCCCTTT | 105689 |
rs30194082 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Mycbp2 | Mm_Celera | 14:103129369 | CACACACACACACAC[A/T]CTCACCACTTGCATG | 105689 |
rs30194580 | snp | A/C | 0.5 | 0 | intron-variant | Mycbp2 | Mm_Celera | 14:103228677 | GGAAGGAAGGAAGGT[A/C]GGTCGGTCCCCGTCT | 105689 |
rs30200119 | snp | A/G | 0.46875 | 0.121031 | synonymous-codon | Mycbp2 | GRCm38.p3 | 14:103314464 | GAAGGCAGAGGGATT[A/G]CTATGTAGTTTGATA | 105689 |
rs30202001 | snp | C/G | 0.375 | 0.216506 | intron-variant | Mycbp2 | Mm_Celera | 14:103246288 | GCTGATATGAGGCCC[C/G]CAACACACATACAGT | 105689 |
rs30205030 | snp | A/C/T | 0.48 | 0.0979796 | intron-variant | Mycbp2 | GRCm38.p3 | 14:103254859 | TGGTGTCTATATAGA[A/C/T]ATGGTATCTGTCTAT | 105689 |
rs30207658 | snp | A/C | 0.375 | 0.216506 | intron-variant | Mycbp2 | Mm_Celera | 14:103246285 | CCAGCTGATATGAGG[A/C]CCGCAACACACATAC | 105689 |
rs30210291 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Mycbp2 | Mm_Celera | 14:103130611 | TATACCCTGAACCTT[A/G]ATCCTTACGAGCAGC | 105689 |
rs30224986 | snp | A/G | 0.455 | 0.143091 | intron-variant | Mycbp2 | Mm_Celera | 14:103274442 | CTATGAAATTACTGG[A/G]TTTTGTAGGTCAATT | 105689 |
rs30236237 | snp | A/G | 0.387812 | 0.208586 | intron-variant | Mycbp2 | Mm_Celera | 14:103241693 | AAGACAGATCCCTCC[A/G]TCATCTCACTTCATC | 105689 |
rs30243218 | snp | A/G | 0.359862 | 0.224567 | missense | Mycbp2 | Mm_Celera | 14:103136638 | TCAGCATCAGATGTC[A/G]CCTTCACACAGAAAA | 105689 |
rs30246222 | snp | G/T | 0.5 | 0 | intron-variant | Mycbp2 | Mm_Celera | 14:103163938 | ATTCTAAAAACATGT[G/T]GTTTGGGTCTGAATG | 105689 |
rs30249086 | snp | A/G | 0.375 | 0.216506 | intron-variant | Mycbp2 | Mm_Celera | 14:103124994 | TGCGCCACCACACCC[A/G]GCTGTTTTTGAATAT | 105689 |
rs30250814 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Mycbp2 | Mm_Celera | 14:103148440 | TCTCTCTCTCTCTCT[C/T]TCTCTCTCTCTCTTT | 105689 |
rs30252103 | snp | A/G | 0.207612 | 0.24638 | intron-variant | Mycbp2 | Mm_Celera | 14:103165425 | TAGAAGTTTTAAAAC[A/G]TTCATTAAAGAATAG | 105689 |
rs30256821 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Mycbp2 | Mm_Celera | 14:103176369 | ATTGCTACTTCTCAA[C/T]AGTAAACTTCAGTAA | 105689 |
rs30261763 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Mycbp2 | Mm_Celera | 14:103254992 | GTGTCTATATAGATA[A/T]GGTGTCTATATAGAT | 105689 |
rs30274081 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Mycbp2 | Mm_Celera | 14:103340922 | CTTTCTGAAGTGGTG[A/G]AAATAGTCTAAGATT | 105689 |
rs30284016 | snp | G/T | 0.375 | 0.216506 | intron-variant | Mycbp2 | Mm_Celera | 14:103273728 | AGAGATATGAAAATA[G/T]CACTTAAAAGAAAAT | 105689 |
rs30287381 | snp | C/T | 0.42 | 0.183303 | intron-variant | Mycbp2 | Mm_Celera | 14:103146635 | AAAATAAAGATTTGG[C/T]ATACTTAAATGTACA | 105689 |
rs30293028 | snp | A/C/G | 0.214533 | 0.265333 | intron-variant | Mycbp2 | GRCm38.p3 | 14:103226620 | TCACAAAGTGCTTTC[A/C/G]GGCCAGAGAGAGAAC | 105689 |
rs30303833 | snp | G/T | 0.375 | 0.216506 | intron-variant | Mycbp2 | GRCm38.p3 | 14:103331059 | TTAAAAAGAATGAAT[G/T]TATGAAATTCCTAGG | 105689 |
rs30303894 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Mycbp2 | Mm_Celera | 14:103165248 | AGTACTAAAAATAAA[A/G]CCAAGAGAAATGTTA | 105689 |
rs30311895 | snp | C/T | 0.375 | 0.216506 | intron-variant | Mycbp2 | Mm_Celera | 14:103246903 | CACCAGCCCGGCAAT[C/T]TCACTTGTTCTTTTA | 105689 |
rs30311957 | snp | G/T | 0.375 | 0.216506 | intron-variant | Mycbp2 | Mm_Celera | 14:103335193 | AGCCCCAAGTTGTTG[G/T]TTTTTTTTAAATAAA | 105689 |
rs30332465 | snp | G/T | 0.432133 | 0.171253 | intron-variant | Mycbp2 | Mm_Celera | 14:103121354 | AGAGAGAAAGTAATG[G/T]GGAAGACAGTGATAC | 105689 |
rs30340456 | snp | A/T | 0.375 | 0.216506 | intron-variant | Mycbp2 | GRCm38.p3 | 14:103234731 | TGAATGAGTGGCAGC[A/T]TCAGGAGGTGAGAAG | 105689 |
rs30353644 | snp | A/G | 0.375 | 0.216506 | intron-variant | Mycbp2 | Mm_Celera | 14:103234632 | ATATCAGAAATTTAC[A/G]TTCGATTCATAACTA | 105689 |
rs30354703 | snp | A/G | 0.375 | 0.216506 | intron-variant | Mycbp2 | Mm_Celera | 14:103272759 | TAAACTGCAACGTAC[A/G]CAGCACATTTATGCA | 105689 |
rs30357230 | snp | C/T | 0.375 | 0.216506 | intron-variant | Mycbp2 | Mm_Celera | 14:103312866 | TTATCCTTTTTTTTT[C/T]CCCCCAACTTTCCTA | 105689 |
rs30362060 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Mycbp2 | Mm_Celera | 14:103217107 | GTAATTAAAATAATC[A/C]ATTTTTAATTAAAAC | 105689 |
rs30363989 | snp | A/G | 0.375 | 0.216506 | intron-variant | Mycbp2 | Mm_Celera | 14:103124959 | CTGCCTCTGCCTCCC[A/G]AGTGCTGGGATTAAA | 105689 |
rs30369629 | snp | C/T | 0.375 | 0.216506 | intron-variant | Mycbp2 | Mm_Celera | 14:103286688 | CACCTTACATGTAAA[C/T]GTTCAATTTCTATCA | 105689 |
rs30373501 | snp | A/G | 0.375 | 0.216506 | intron-variant | Mycbp2 | Mm_Celera | 14:103272336 | CTCTGTAGGTAAAGT[A/G]CTCACCATGTAAGCG | 105689 |
rs30401042 | snp | A/G | 0.456747 | 0.140554 | intron-variant | Mycbp2 | Mm_Celera | 14:103339937 | AAGGTTCCTAAGACC[A/G]TTCCTGGTAGCAAGT | 105689 |
rs30403548 | snp | A/G | 0.5 | 0 | intron-variant | Mycbp2 | Mm_Celera | 14:103186159 | GATAATAATAATGAT[A/G]ATAATAATAATAATA | 105689 |
rs30410897 | snp | A/G | 0.375 | 0.216506 | intron-variant | Mycbp2 | Mm_Celera | 14:103234384 | ATGAGGAAGTGAGAC[A/G]TGCAGGAAGAGTTGT | 105689 |
rs30411155 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Mycbp2 | Mm_Celera | 14:103291169 | ATCCTAAAAAATTTT[A/T]AAAATTAAGAATTAA | 105689 |
rs30422213 | snp | C/G | 0.455 | 0.143091 | intron-variant | Mycbp2 | Mm_Celera | 14:103127713 | CTAGAAATTTTGCTG[C/G]TATAAGCATGAACCA | 105689 |
rs30430441 | snp | A/G | 0.375 | 0.216506 | intron-variant | Mycbp2 | Mm_Celera | 14:103126355 | TGGGGCTGGCTTACA[A/G]GTTCCAAGGTTCAGT | 105689 |
rs30432734 | snp | A/G | 0.375 | 0.216506 | intron-variant | Mycbp2 | Mm_Celera | 14:103312198 | TAAAGATGAAGGCCC[A/G]AAGGGACCCTGTCCG | 105689 |