SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6160465 | snp | A/G | 0.304688 | 0.243945 | intron-variant | Uba6 | Mm_Celera | 5:86147209 | TATATTCAAAATATA[A/G]TACAATGTGTTTTAA | 231380 |
rs6300712 | snp | A/G | 0.5 | 0 | intron-variant | Uba6 | Mm_Celera | 5:86134468 | TTCTATTTTCAGTCA[A/G]AATTTTTAATTGCTT | 231380 |
rs29502941 | snp | C/T | 0.5 | 0 | intron-variant | Uba6 | Mm_Celera | 5:86118775 | CAACAAAAATAATTT[C/T]AAGGCTAGGGGTCAC | 231380 |
rs29509863 | snp | A/C | 0.375 | 0.216506 | upstream-variant-2KB | Uba6 | Mm_Celera | 5:86173175 | TTTAAATTGTTTTGA[A/C]CATCTATTACTGATC | 231380 |
rs29511247 | snp | A/G | 0.498615 | 0.0262793 | synonymous-codon | Uba6 | Mm_Celera | 5:86124414 | CTTCCTTGCAGTTTC[A/G]TCTGTTTGAACAACC | 231380 |
rs29513092 | snp | C/T | 0.5 | 0 | intron-variant | Uba6 | Mm_Celera | 5:86162197 | AAGTAAAATATAATA[C/T]AGGGCAAATGGACTG | 231380 |
rs29516634 | snp | C/T | 0.492188 | 0.0620098 | intron-variant | Uba6 | Mm_Celera | 5:86114552 | AATGTGCCAGTTTCT[C/T]TGAGTAGACTATTTG | 231380 |
rs29517417 | snp | A/G | 0.498615 | 0.0262793 | synonymous-codon | Uba6 | GRCm38.p3 | 5:86142422 | TGGGAGAAACTCTTC[A/G]TGCCCAGGATTGCCT | 231380 |
rs29522704 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Uba6 | Mm_Celera | 5:86116685 | CTTATCCAGAACAGT[A/G]AGATAAGAAAAAGAA | 231380 |
rs29527361 | snp | A/C | 0.49827 | 0.0293608 | missense | Uba6 | Mm_Celera | 5:86122319 | CCAAGCCAGAAACTG[A/C]AGCAGTAGATGTTGC | 231380 |
rs29528609 | snp | C/T | 0.487535 | 0.077957 | intron-variant | Uba6 | Mm_Celera | 5:86152413 | CTTGTAGTATTACCA[C/T]GGTTCAGTATGTCCT | 231380 |
rs29544004 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Uba6 | Mm_Celera | 5:86163309 | CACTAACACCCCATA[C/T]TTCTGAAAGTTAGGC | 231380 |
rs29547378 | snp | A/G | 0.375 | 0.216506 | intron-variant | Uba6 | Mm_Celera | 5:86151449 | TCAAACATCAAATTA[A/G]AAAGCGTTTGCATAC | 231380 |
rs29552405 | snp | A/T | 0.5 | 0 | intron-variant | Uba6 | Mm_Celera | 5:86123590 | GCCACCTAGCCTGGT[A/T]CACACAACAGCAAAC | 231380 |
rs29560302 | snp | C/G/T | 0.444444 | 0.157135 | intron-variant | Uba6 | GRCm38.p3 | 5:86168466 | CACTGGATCTTTGTC[C/G/T]GGCATCTGCTGCACA | 231380 |
rs29563182 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Uba6 | GRCm38.p3 | 5:86115297 | ATATCCTGTGAAAGC[C/T]AGTTTGTAGTGAGAG | 231380 |
rs29566627 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Uba6 | Mm_Celera | 5:86171150 | TGGCGCACGCCTTTA[A/G]TCCCAGCACTCGGGA | 231380 |
rs29570678 | snp | C/G | 0.444444 | 0.157135 | downstream-variant-500B | Uba6 | Mm_Celera | 5:86110604 | GTATAATTAAATTCT[C/G]TGCGATGAACCACGG | 231380 |
rs29577495 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Uba6 | Mm_Celera | 5:86168534 | GAACTACATAGTTAG[A/T]CTCTCTCTTGTTGGC | 231380 |
rs29579543 | snp | A/G | 0.475309 | 0.108333 | intron-variant | Uba6 | Mm_Celera | 5:86144725 | TGCTTTTCTAACTGT[A/G]GTCTAGATTGCTATT | 231380 |
rs29579710 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Uba6 | Mm_Celera | 5:86113014 | AAAATCCCAAAGAGT[A/G]ATGCAGTGATTCTTC | 231380 |
rs29580791 | snp | C/G | 0.49827 | 0.0293608 | intron-variant | Uba6 | Mm_Celera | 5:86132166 | TTTTTGCTATTTTAT[C/G]ATTATTATTACACCC | 231380 |
rs29582242 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Uba6 | Mm_Celera | 5:86118832 | GTTGCAGCATTAGGA[A/C]GGTTGAGAATCACTG | 231380 |
rs29620105 | snp | G/T | 0.611111 | 0.124226 | intron-variant | Uba6 | Mm_Celera | 5:86148258 | CCAAATCCAAAACCA[G/T]AACCACTCCAGAAAA | 231380 |
rs29630735 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Uba6 | Mm_Celera | 5:86136982 | CTGCTGCCACATCCT[C/T]TGTAGTTATGCGAGA | 231380 |
rs29631049 | snp | A/G | 0.5 | 0 | intron-variant | Uba6 | Mm_Celera | 5:86162954 | TTTTGTTGGAGATAG[A/G]CCTTGCTATGTAGCC | 231380 |
rs29674103 | snp | A/G | 0.484429 | 0.0868505 | intron-variant | Uba6 | Mm_Celera | 5:86123436 | TAGGCAAAAGAACTT[A/G]TTCCATAGCATTAGA | 231380 |
rs29675373 | snp | C/T | 0.492188 | 0.0620098 | intron-variant | Uba6 | Mm_Celera | 5:86114792 | GTCTTTATAAAAAGT[C/T]TTAATCCATTGATCT | 231380 |
rs29679008 | snp | C/T | 0.497041 | 0.0383476 | intron-variant | Uba6 | Mm_Celera | 5:86123725 | CCACATGGTCACCTA[C/T]ATATATTTATTCTCA | 231380 |
rs29720897 | snp | A/G | 0.5 | 0 | intron-variant | Uba6 | Mm_Celera | 5:86134885 | GCTAAAGTCAAGATT[A/G]ATAAAGCTAAGTCAA | 231380 |
rs29728442 | snp | A/G | 0.5 | 0 | intron-variant | Uba6 | Mm_Celera | 5:86156808 | TCAGTGCTCTTGACC[A/G]CTGAGCCATCTCTCC | 231380 |
rs29731814 | snp | A/T | 0.484429 | 0.0868505 | intron-variant | Uba6 | Mm_Celera | 5:86129150 | TCATTACAATAAATT[A/T]AAAAAAAATACAAAT | 231380 |
rs29732560 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Uba6 | Mm_Celera | 5:86154627 | AACCAAAATAAAAAT[A/T]TAGAAAGAGCATATG | 231380 |
rs29732968 | snp | C/T | 0.5 | 0 | intron-variant | Uba6 | Mm_Celera | 5:86130734 | CGTTAGTGCTCTTAC[C/T]GCGCTGAGCCATCTC | 231380 |
rs29735172 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Uba6 | Mm_Celera | 5:86113161 | ATTGATTTGTGCCAG[G/T]GATGGGGGGTAGGAG | 231380 |
rs29735236 | snp | A/C | 0.5 | 0 | intron-variant | Uba6 | Mm_Celera | 5:86122020 | CTCCAGGTCCTGTAT[A/C]TCAGCTGGCTATTGG | 231380 |
rs29769541 | snp | A/G | 0.487535 | 0.077957 | utr-variant-3-prime | Uba6 | Mm_Celera | 5:86110916 | AATGGTTGTGGATTT[A/G]ATTAGAAACAAACCA | 231380 |
rs29777499 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Uba6 | Mm_Celera | 5:86158503 | TGGAAATTTTTTCAG[C/T]CAAAACTTCTGACAT | 231380 |
rs29779148 | snp | A/G | 0.5 | 0 | intron-variant | Uba6 | Mm_Celera | 5:86119030 | TTCCAGAATAGCCAG[A/G]GCTACACAGAGAAAC | 231380 |
rs29780261 | snp | C/T | 0.5 | 0 | intron-variant | Uba6 | Mm_Celera | 5:86123498 | AAAACTGGACAGACA[C/T]AGTGAGTGGATCTGC | 231380 |
rs29807959 | snp | A/G | 0.444444 | 0.157135 | downstream-variant-500B | Uba6 | Mm_Celera | 5:86110393 | AAAGAACTGACTTTA[A/G]AAACCTCAAACTAAG | 231380 |
rs29818965 | snp | G/T | 0.487535 | 0.077957 | intron-variant | Uba6 | Mm_Celera | 5:86145183 | GCTTTCTTTGTATCC[G/T]TTCTCTATCACCTCT | 231380 |
rs29821141 | snp | C/T | 0.484429 | 0.0868505 | intron-variant | Uba6 | Mm_Celera | 5:86139927 | ATGATAATAAAAGTT[C/T]CTTTCAAATTTAATA | 231380 |
rs29822642 | snp | C/T | 0.415225 | 0.187619 | intron-variant | Uba6 | Mm_Celera | 5:86124211 | TTATGATGATTCAAT[C/T]AGCTATTATGATTAA | 231380 |
rs29823427 | snp | C/T | 0.5 | 0 | intron-variant | Uba6 | Mm_Celera | 5:86122911 | TACACAGAGAAACCC[C/T]GTCTCGAAAAACCAA | 231380 |
rs29825088 | snp | A/G | 0.5 | 0 | intron-variant | Uba6 | Mm_Celera | 5:86169541 | ATGGCTTCTGCATCA[A/G]CTCCTGCTTCCTGAC | 231380 |
rs31651524 | snp | A/G | 0.486111 | 0.0821678 | intron-variant | Uba6 | Mm_Celera | 5:86121265 | GAATTTGAAAATGTT[A/G]GAGAAAGTAATTATT | 231380 |
rs31651525 | snp | C/T | 0.486111 | 0.0821678 | intron-variant | Uba6 | Mm_Celera | 5:86121317 | TAGCTTTGCAAGTGG[C/T]TTTTGAAAGCATTTT | 231380 |
rs31651526 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Uba6 | Mm_Celera | 5:86121456 | AAAAAAGCAACAAAT[A/G]ATTTTTTTTACACAT | 231380 |
rs31651527 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Uba6 | Mm_Celera | 5:86121484 | CATTCTATAATTCTC[C/T]ATTAGATCGGCATTT | 231380 |
rs31651528 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Uba6 | Mm_Celera | 5:86121545 | TAGATTCAATATGTC[C/T]AGCCTATTCCATATA | 231380 |
rs31651529 | snp | A/G/T | 0.152778 | 0.230321 | intron-variant | Uba6 | GRCm38.p3 | 5:86121725 | TCATAATGATGATTC[A/G/T]CAATTACTTACAATA | 231380 |
rs31651530 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Uba6 | Mm_Celera | 5:86121917 | TCTGAGTGTTCAAAA[G/T]CAAGTACTCTTCCGT | 231380 |
rs31651531 | snp | A/G | 0.492188 | 0.0620098 | intron-variant | Uba6 | Mm_Celera | 5:86122073 | CCCAAACCCAGGAGG[A/G]AAAGAAACGTTATTG | 231380 |
rs31651532 | snp | G/T | 0.5 | 0 | missense | Uba6 | Mm_Celera | 5:86122454 | CTATGTGTCCATTAC[G/T]GTCATCATCTTTTTC | 231380 |
rs31651533 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Uba6 | Mm_Celera | 5:86122523 | GCAACCAGACAAAGT[G/T]CTCTAGTTAGTGGTA | 231380 |
rs31652314 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Uba6 | Mm_Celera | 5:86122563 | TGAGGTAAAAAGCAA[G/T]GTACAAAGTGTATAT | 231380 |
rs31652315 | snp | A/C | 0.497041 | 0.0383476 | intron-variant | Uba6 | Mm_Celera | 5:86122622 | AAATAAGGAAATATA[A/C]AAGTTACCAAGCTGA | 231380 |
rs31652316 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Uba6 | Mm_Celera | 5:86123161 | TTTATGTATCTTTTT[A/T]AATACTTCTACATTA | 231380 |
rs31652317 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Uba6 | Mm_Celera | 5:86123305 | GATGGTAAACATACA[C/T]AAGCAGATGAACAAT | 231380 |
rs31652318 | snp | C/G | 0.492188 | 0.0620098 | intron-variant | Uba6 | Mm_Celera | 5:86123326 | GATGAACAATTAACT[C/G]TGCTTTTAAAGAATT | 231380 |
rs31652319 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Uba6 | Mm_Celera | 5:86123523 | ATCTGCAACCCTAGC[A/G]CTTCTATGGAGAGAT | 231380 |
rs31652320 | snp | C/T | 0.492188 | 0.0620098 | intron-variant | Uba6 | Mm_Celera | 5:86123593 | ACCTAGCCTGGTACA[C/T]ACAACAGCAAACCAA | 231380 |
rs31652321 | snp | A/C | 0.475309 | 0.108333 | intron-variant | Uba6 | Mm_Celera | 5:86124258 | CTTATCAATATGGCT[A/C]TTTGGGAAAGTCGGT | 231380 |
rs31652322 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Uba6 | Mm_Celera | 5:86125542 | TTATGTAAAAATCCA[A/C]TGGCTACAAAGATCC | 231380 |
rs31652323 | snp | C/T | 0.497041 | 0.0383476 | intron-variant | Uba6 | Mm_Celera | 5:86125656 | TAAAAGAATAGCATA[C/T]AGTATGTCTATAAAA | 231380 |
rs31653814 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Uba6 | Mm_Celera | 5:86125708 | TAAAAATTTTTTTCT[C/T]CAAACTTTCCTATTT | 231380 |
rs31653815 | snp | A/G | 0.5 | 0 | intron-variant | Uba6 | Mm_Celera | 5:86125911 | ATATGAATCCTCAGT[A/G]ATGTCTTGCAATTCT | 231380 |
rs31653816 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Uba6 | Mm_Celera | 5:86125991 | TGTTCAGTTTCCTAC[C/T]TTCATCCCACACTGT | 231380 |
rs31653817 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Uba6 | Mm_Celera | 5:86126196 | TTCTTGAAATACCTA[A/T]CAGGGCTGCTACTCT | 231380 |
rs31653818 | snp | A/C | 0.492188 | 0.0620098 | intron-variant | Uba6 | Mm_Celera | 5:86126334 | ATTTCTTCCTATAGC[A/C]CATCTCTACTCTTTG | 231380 |
rs31653819 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Uba6 | Mm_Celera | 5:86126341 | CCTATAGCACATCTC[C/T]ACTCTTTGGAATAAA | 231380 |
rs31653820 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Uba6 | Mm_Celera | 5:86127069 | AGCTCTCTCTAAACG[A/G]TTTGAGTCACGCACT | 231380 |
rs31653821 | snp | C/T | 0.497041 | 0.0383476 | intron-variant | Uba6 | GRCm38.p3 | 5:86127344 | AAGTATGATTGCTTT[C/T]ACAAATATTTCAACA | 231380 |
rs31653822 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Uba6 | Mm_Celera | 5:86128155 | ACTAAAAACAAAAAT[A/G]GGCATGTCATACTAG | 231380 |
rs31653823 | snp | A/G | 0.49827 | 0.0293608 | intron-variant | Uba6 | Mm_Celera | 5:86128196 | TAGTTGAATTCTGAA[A/G]GAAGTAATAGCTGAG | 231380 |
rs31654704 | snp | C/T | 0.456747 | 0.140554 | intron-variant | Uba6 | Mm_Celera | 5:86128262 | TAAGTGAAGGGAGGC[C/T]AAGTGTTCGATGAGA | 231380 |
rs31654705 | snp | A/T | 0.260355 | 0.249785 | intron-variant | Uba6 | Mm_Celera | 5:86128437 | GTAAGAACACATATT[A/T]TCATTTTTATTTTCT | 231380 |
rs31654706 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Uba6 | Mm_Celera | 5:86128580 | GACTAGAATGACTTG[C/T]TAACTTTTGGATTAA | 231380 |
rs31654707 | snp | A/C | 0.5 | 0 | intron-variant | Uba6 | Mm_Celera | 5:86128897 | AAAAGAGGAAGAAAA[A/C]ATGAAAAAAAATCCC | 231380 |
rs31654708 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Uba6 | Mm_Celera | 5:86129675 | AGTTTAGAGGCTAGG[C/T]CCTGCTCTGCAGACA | 231380 |
rs31654709 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Uba6 | Mm_Celera | 5:86129762 | CCTATGGAAGCCTGC[C/T]GCCTACTCAGTTCTC | 231380 |
rs31654710 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Uba6 | Mm_Celera | 5:86129763 | CTATGGAAGCCTGCC[A/G]CCTACTCAGTTCTCT | 231380 |
rs31654711 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Uba6 | Mm_Celera | 5:86130346 | TGTGACTGTAAGAAT[A/C]ACAGTGTGAATGAAT | 231380 |
rs31654712 | snp | C/T | 0.5 | 0 | intron-variant | Uba6 | Mm_Celera | 5:86131142 | AACAAATATTTTAAG[C/T]CTGGGAAATTAGTAA | 231380 |
rs31654713 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Uba6 | Mm_Celera | 5:86131377 | AGAAAAATAAAACAC[C/T]TGATCACAAGCACAA | 231380 |
rs31655514 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Uba6 | Mm_Celera | 5:86132053 | GTTGTGTATGATTAA[A/G]TGTAAACTACTATCT | 231380 |
rs31655515 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Uba6 | Mm_Celera | 5:86132075 | CTACTATCTTTGAAG[G/T]TGGCCTTATTGTAGT | 231380 |
rs31655516 | snp | A/G | 0.49827 | 0.0293608 | intron-variant | Uba6 | Mm_Celera | 5:86132324 | GATTCCCAGTAGAAC[A/G]TTTCACTGTGATCAA | 231380 |
rs31655517 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Uba6 | Mm_Celera | 5:86132847 | TGGCCATTTAACCTG[C/T]TGAAAGTCATGTGAA | 231380 |
rs31655518 | snp | C/T | 0.497041 | 0.0383476 | intron-variant | Uba6 | Mm_Celera | 5:86132857 | ACCTGTTGAAAGTCA[C/T]GTGAAAACACAAATC | 231380 |
rs31655519 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Uba6 | Mm_Celera | 5:86132904 | TTGTGTACTTGTGCG[A/G]TGTGGCAGAAAGTCC | 231380 |
rs31655520 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Uba6 | Mm_Celera | 5:86133314 | ATTCAATGAGGAGCA[C/T]TGTAGGAATATTAAA | 231380 |
rs31655521 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Uba6 | Mm_Celera | 5:86133548 | TAAGAAAACAGTGAA[C/T]GCTAAGAATTTAAAA | 231380 |
rs31655522 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Uba6 | Mm_Celera | 5:86134143 | CTTAATGAGGACAAA[C/T]ATTTAAGATGTACCT | 231380 |
rs31655523 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Uba6 | GRCm38.p3 | 5:86134429 | CATCAGAAAATGGAT[C/T]TGATTCCAAGTCTCT | 231380 |
rs31656624 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Uba6 | Mm_Celera | 5:86134449 | TCCAAGTCTCTGGTG[A/G]CAGTTCTATTTTCAG | 231380 |
rs31656625 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Uba6 | Mm_Celera | 5:86134876 | CCTGTCAGAGCTAAA[A/G]TCAAGATTGATAAAG | 231380 |
rs31656626 | snp | A/G | 0.492188 | 0.0620098 | intron-variant | Uba6 | Mm_Celera | 5:86134905 | AGCTAAGTCAAATTT[A/G]TTGATTCTTTCATGA | 231380 |
rs31656627 | snp | A/G | 0.459184 | 0.136902 | synonymous-codon | Uba6 | GRCm38.p3 | 5:86134974 | AATATACTGACTTAC[A/G]TGACTATTATAAGAT | 231380 |