SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3655658 | snp | A/G | 0.375 | 0.216506 | intron-variant | Usp14 | Mm_Celera | 18:10007732 | TACACAAAGTGGCAT[A/G]ATGAAAATCTCTAAT | 59025 |
rs3714553 | snp | A/C | 0.426035 | 0.177515 | intron-variant | Usp14 | Mm_Celera | 18:10007705 | TCAGGGATAAGCTTA[A/C]ATTTGTTATACTACA | 59025 |
rs13467634 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB | Usp14 | GRCm38.p3 | 18:10029986 | GAGTTGCTTCGTATT[C/T]CTCGGCTGCCCTTGT | 59025 |
rs29542928 | snp | A/C | 0.345679 | 0.230967 | intron-variant | Usp14 | Mm_Celera | 18:10025736 | CACAAGCCTGATGAC[A/C]AGAACTCAATCCCCA | 59025 |
rs29625268 | snp | A/G | 0.32 | 0.24 | intron-variant | Usp14 | Mm_Celera | 18:10013760 | AAATTTAACTACATT[A/G]AAATGTTCTTTAAAT | 59025 |
rs29635259 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Usp14 | Mm_Celera | 18:10004370 | AGCATTCAATTCTAA[C/T]GCAATAACATTAACA | 59025 |
rs29672884 | snp | C/G | 0.375 | 0.216506 | intron-variant | Usp14 | Mm_Celera | 18:10011978 | CGCCACATTGTTGTT[C/G]TTCTTCTTTTTTGTT | 59025 |
rs29676827 | snp | A/G | 0.401235 | 0.199068 | intron-variant | Usp14 | Mm_Celera | 18:10004531 | CTATCTATCGAGGAC[A/G]CCCTGAGCCATGAAC | 59025 |
rs29727317 | snp | A/T | 0.415225 | 0.187619 | intron-variant | Usp14 | Mm_Celera | 18:10001148 | GCAGGACAGTGATTC[A/T]GAAGTAATATGTGAG | 59025 |
rs29812985 | snp | G/T | 0.426035 | 0.177515 | intron-variant | Usp14 | Mm_Celera | 18:10000938 | GAAGTAATAGTGCTA[G/T]AAGACTGAGAGAAAA | 59025 |
rs29815791 | snp | A/G | 0.5 | 0 | intron-variant | Usp14 | Mm_Celera | 18:10004423 | ATTGAATTCAGTAAT[A/G]TATAAAACTATGTTA | 59025 |
rs29957364 | snp | G/T | 0.387812 | 0.208586 | intron-variant | Usp14 | Mm_Celera | 18:10013833 | TTAAAGGGCTTTCAG[G/T]CATTCATTCTCTCCT | 59025 |
rs30052121 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Usp14 | Mm_Celera | 18:10011282 | AAATAGAAATGGCTC[C/T]AGATGAGTAACACCT | 59025 |
rs30076825 | snp | G/T | 0.32 | 0.24 | intron-variant | Usp14 | Mm_Celera | 18:10011640 | GGCCTTGTAATCTCC[G/T]GCCTCTGTCTCCTAA | 59025 |
rs30126048 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Usp14 | Mm_Celera | 18:10004591 | TGGACACTTCTGGCC[A/G]CGTTTCCATCAACCA | 59025 |
rs30163702 | snp | C/T | 0.32 | 0.24 | intron-variant | Usp14 | Mm_Celera | 18:10025789 | GCCAACCCCCGAAAG[C/T]TGTCTTGTACCTGCA | 59025 |
rs30256321 | snp | C/G | 0.290657 | 0.246672 | intron-variant | Usp14 | Mm_Celera | 18:10011183 | TACTCCAAAACTAGG[C/G]TGGTGGCAATAGGCG | 59025 |
rs30309871 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Usp14 | Mm_Celera | 18:10013603 | GAGACAGATGAATTT[C/T]TATAAATTCAATACC | 59025 |
rs30978654 | snp | A/T | 0.35503 | 0.226867 | intron-variant | Usp14 | Mm_Celera | 18:10015866 | CCAGCATTTCTCATG[A/T]TAAAGAGTGGACACA | 59025 |
rs30978656 | snp | A/G | 0.396694 | 0.202437 | intron-variant | Usp14 | Mm_Celera | 18:10015415 | ATCTATCATAAGGAT[A/G]AATTCTAGTCACTGA | 59025 |
rs30978658 | snp | C/G | 0.197531 | 0.244432 | intron-variant | Usp14 | Mm_Celera | 18:10014360 | AATCAAAGTCAGACT[C/G]TAACAAGTACTGAAC | 59025 |
rs30978660 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Usp14 | Mm_Celera | 18:10014283 | AAGATGCTCATCATC[A/G]TTAGACATTAGAAAC | 59025 |
rs30978662 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Usp14 | Mm_Celera | 18:10014270 | ATAGTCAAGTGAAAA[A/G]ATGCTCATCATCATT | 59025 |
rs30979255 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Usp14 | Mm_Celera | 18:10011691 | TACTACCATGCCTGG[C/T]TCCACTTCATTAGTT | 59025 |
rs30979257 | snp | A/T | 0.375 | 0.216506 | intron-variant | Usp14 | Mm_Celera | 18:10011358 | ACACAAAAATATACC[A/T]GCAAGAACACACACA | 59025 |
rs30979260 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Usp14 | Mm_Celera | 18:10011199 | TGGTGGCAATAGGCG[C/T]ATCCCTGGGTTCGAT | 59025 |
rs30979261 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Usp14 | Mm_Celera | 18:10011095 | TCAATCAAGTGGTTA[C/T]CAGAAAGCACAGGAG | 59025 |
rs30979263 | snp | C/T | 0.375 | 0.216506 | intron-variant | Usp14 | Mm_Celera | 18:10010963 | TTATAACAATCACAT[C/T]AATACTAAGTCTTAT | 59025 |
rs30979996 | snp | A/T | 0.336735 | 0.234472 | upstream-variant-2KB | Usp14 | Mm_Celera | 18:10032114 | TAATATAGACTAGTA[A/T]CTGTCAAGGCCATGA | 59025 |
rs30979997 | snp | C/T | 0.142012 | 0.225474 | upstream-variant-2KB | Usp14 | Mm_Celera | 18:10031294 | TAAAGCACTTAATCA[C/T]CTATCCTTAGTGAGT | 59025 |
rs30979999 | snp | C/T | 0.124444 | 0.216185 | upstream-variant-2KB | Usp14 | Mm_Celera | 18:10030532 | AAATGCATGATTCTG[C/T]AACAACAACAACAAA | 59025 |
rs30980001 | snp | A/G | 0.124444 | 0.216185 | upstream-variant-2KB | Usp14 | Mm_Celera | 18:10030395 | TAGATCATCCTCACT[A/G]CTGTGCTTTCATTAA | 59025 |
rs30980003 | snp | A/G | 0.132653 | 0.220748 | utr-variant-5-prime, upstream-variant-2KB | Usp14 | Mm_Celera | 18:10029977 | CTGGGTCTGACAAGG[A/G]CAGCCGAGGAATACG | 59025 |
rs30980625 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Usp14 | Mm_Celera | 18:10010870 | ATCGCTAGGTTCAAT[C/T]CTTAGCACCACAAAA | 59025 |
rs30980627 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Usp14 | Mm_Celera | 18:10010720 | GGATCTAAAACCCTC[A/G]CACCAATGCATTAAA | 59025 |
rs30980629 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Usp14 | Mm_Celera | 18:10010627 | CTGCAGAGATGGCTC[A/G]GTGGTTCCAGAAGAC | 59025 |
rs30980631 | snp | C/T | 0.32 | 0.24 | intron-variant | Usp14 | Mm_Celera | 18:10010551 | ACTTGGACTACATGG[C/T]AACATCCTGTCTCAG | 59025 |
rs30980633 | snp | A/G | 0.32 | 0.24 | intron-variant | Usp14 | Mm_Celera | 18:10010464 | GGCTCATTTTTAGTC[A/G]GGCATGGTGGTAGGC | 59025 |
rs30980945 | snp | A/C | 0.152778 | 0.230321 | utr-variant-5-prime, upstream-variant-2KB | Usp14 | Mm_Celera | 18:10029953 | GGAAGGAAGAAAAGG[A/C]GCGGGAGGCTGGGTC | 59025 |
rs30980947 | snp | C/G | 0.165289 | 0.235211 | intron-variant | Usp14 | Mm_Celera | 18:10028923 | GTGCACATCTTTAAT[C/G]CCAGCAATTGGTAGG | 59025 |
rs30980948 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Usp14 | Mm_Celera | 18:10028490 | AAATAGATTCAAATC[A/G]GTACAAACTGCAATC | 59025 |
rs30980950 | snp | A/G | 0.297521 | 0.245442 | intron-variant | Usp14 | Mm_Celera | 18:10027840 | AAGATCTTGAGTAAG[A/G]AAGTATTCCTATTTG | 59025 |
rs30980952 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Usp14 | Mm_Celera | 18:10027765 | GCCTTGAACTCACAG[A/G]AGGACTCTGCCTCTC | 59025 |
rs30981425 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Usp14 | Mm_Celera | 18:10010102 | AAAAGAAAACAAACA[C/T]TGGTTAAGAAAAACA | 59025 |
rs30981427 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Usp14 | Mm_Celera | 18:10009939 | CAAGATGAGAGACAC[C/T]CGTCCCTTTTACCTG | 59025 |
rs30981429 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Usp14 | Mm_Celera | 18:10009781 | CAGCCAGCCTGGAGG[A/G]CACAGTGGAAAAACA | 59025 |
rs30981431 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Usp14 | Mm_Celera | 18:10009716 | ACCTGCAGCTTAAGC[A/C]TTTGTAATCGCAGTG | 59025 |
rs30981433 | snp | C/G | 0.426035 | 0.177515 | intron-variant | Usp14 | Mm_Celera | 18:10009522 | CATCAAGATGACCAG[C/G]TAAGATTATACACAA | 59025 |
rs30981854 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Usp14 | Mm_Celera | 18:10027664 | AGGACATAGTAGTGA[C/T]AATGCTTACCATAAA | 59025 |
rs30981856 | snp | A/T | 0.152778 | 0.230321 | intron-variant | Usp14 | Mm_Celera | 18:10027626 | TCATAGCAACCAAGC[A/T]AATACAGCCTAATAA | 59025 |
rs30981858 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Usp14 | Mm_Celera | 18:10027478 | AACAGTTCATTGAGT[A/G]TGTTAAAGCCTGATT | 59025 |
rs30981860 | snp | C/G | 0.152778 | 0.230321 | intron-variant | Usp14 | Mm_Celera | 18:10026196 | GGTCAGAGGAGAGTT[C/G]CTATGAGCTGGTTCT | 59025 |
rs30981861 | snp | A/T | 0.35503 | 0.226867 | intron-variant | Usp14 | Mm_Celera | 18:10026167 | GGAGGTGCCCATGCC[A/T]CTGCAATCGCTGTGG | 59025 |
rs30981863 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Usp14 | Mm_Celera | 18:10025831 | ACGTGCACCACACCA[G/T]TTTTTGAAAAAAAAT | 59025 |
rs30982115 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Usp14 | Mm_Celera | 18:10009127 | GTGCCCGAGGAAAGC[C/T]CAACAGCACGTTTTC | 59025 |
rs30982117 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Usp14 | Mm_Celera | 18:10008999 | CAAACAGATTTAGAC[C/T]GAGGCAGCAAATCAC | 59025 |
rs30982119 | snp | C/T | 0.375 | 0.216506 | intron-variant | Usp14 | Mm_Celera | 18:10008299 | TCCTTGAAATCCACA[C/T]GATAGAAAGGGAAAA | 59025 |
rs30982786 | snp | C/G | 0.35503 | 0.226867 | intron-variant | Usp14 | Mm_Celera | 18:10025372 | TAAAGGGTCAAGACC[C/G]ACAGGTTAAAAAATC | 59025 |
rs30982788 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Usp14 | Mm_Celera | 18:10024918 | AGTATAAATGCAATG[A/G]ATCCAAAGCAAAACT | 59025 |
rs30982790 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Usp14 | Mm_Celera | 18:10024750 | AATTTAGAAAATCAT[C/T]AGGGCATAACCTTTT | 59025 |
rs30982792 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Usp14 | Mm_Celera | 18:10024491 | CTAGTCTCTAGCATT[C/T]GTCCTGTTAAGCAGC | 59025 |
rs30983145 | snp | C/G | 0.42 | 0.183303 | intron-variant | Usp14 | Mm_Celera | 18:10006895 | GGAAGCTACGCTCTT[C/G]TGCTTCCTATATACT | 59025 |
rs30983147 | snp | A/G/T | 0.345679 | 0.230967 | intron-variant | Usp14 | GRCm38.p3 | 18:10005595 | CTTAAAAATTATAAA[A/G/T]ACCATCTATACAAAG | 59025 |
rs30983149 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Usp14 | Mm_Celera | 18:10004876 | AACCCACAAATGAGG[C/T]TCAACCATGACTTCC | 59025 |
rs30983153 | snp | C/G | 0.35503 | 0.226867 | intron-variant | Usp14 | Mm_Celera | 18:10003314 | AACTTGTTAATCTAA[C/G]GCAGCAGTCCTCAAC | 59025 |
rs30983644 | snp | A/T | 0.165289 | 0.235211 | intron-variant | Usp14 | Mm_Celera | 18:10024032 | ACTTAAATTATAGAC[A/T]GTCGTGGGTCCCCAG | 59025 |
rs30983645 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Usp14 | Mm_Celera | 18:10023966 | TTGCATTTTTATTCT[C/T]CTATAGCTCATGTGC | 59025 |
rs30983647 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Usp14 | Mm_Celera | 18:10023870 | CAGGGCTCTGATGAA[A/G]ATGTTAAACTAAATT | 59025 |
rs30983649 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Usp14 | Mm_Celera | 18:10023349 | CTTATGTGGTATGAA[G/T]AACAATAAGAGGAAA | 59025 |
rs30983651 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Usp14 | Mm_Celera | 18:10023231 | ACAAGTTTTCATCAA[C/T]ATCTCTATCTATACC | 59025 |
rs30983653 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Usp14 | Mm_Celera | 18:10022987 | TTTTACATCTCACAT[C/T]TTATGTTCCCTTAGC | 59025 |
rs30984325 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Usp14 | Mm_Celera | 18:10003111 | TGTTGCTCTAAGTCA[A/G]GAAGGTATGCTATAG | 59025 |
rs30984327 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Usp14 | Mm_Celera | 18:10002840 | TTTTGCCTACTTTGG[A/G]ACCTTTTTCTTCCTA | 59025 |
rs30984329 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Usp14 | Mm_Celera | 18:10002711 | CACAGAGACTGACGC[A/G]ACAATCAAAAAGCCT | 59025 |
rs30984331 | snp | A/C/T | 0.260355 | 0.249785 | intron-variant | Usp14 | GRCm38.p3 | 18:10002708 | GCTCACAGAGACTGA[A/C/T]GCAACAATCAAAAAG | 59025 |
rs30984333 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Usp14 | Mm_Celera | 18:10001986 | AGGAGCACATAAAAA[C/T]AAAGATTAGACAAGA | 59025 |
rs30984625 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Usp14 | Mm_Celera | 18:10022265 | TAGCAATTATATCTC[A/C]ATAAAAGTCACAATA | 59025 |
rs30984626 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Usp14 | Mm_Celera | 18:10020518 | TGACACAGGCCTCTA[A/G]TCCTAGCACCAGGAG | 59025 |
rs30984627 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Usp14 | Mm_Celera | 18:10020253 | TCCCTTTCTTTAAAA[C/T]ACCCTCATTGAAAAC | 59025 |
rs30984628 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Usp14 | Mm_Celera | 18:10020178 | ACACAGCAGCAAAGA[A/G]GCCCTATCTCAAACA | 59025 |
rs30984629 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Usp14 | Mm_Celera | 18:10020106 | AGTGCTCCTAGACAA[A/G]AAAGGAACCACATAC | 59025 |
rs30984630 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Usp14 | Mm_Celera | 18:10019097 | AAGGAGTGGATCTGC[A/G]GAAGAAGGGAAGTAG | 59025 |
rs30984631 | snp | A/G | 0.396694 | 0.202437 | intron-variant | Usp14 | Mm_Celera | 18:10019004 | CCTCAACTAGCCTTA[A/G]TATCAGGGTATGTGG | 59025 |
rs30984633 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Usp14 | Mm_Celera | 18:10018674 | TGCAGAGTTGAGCAG[A/G]TACAGAGACCCACAG | 59025 |
rs30985215 | snp | A/G/T | 0.152778 | 0.230321 | intron-variant | Usp14 | GRCm38.p3 | 18:10001905 | TTTAATCTATGCCAT[A/G/T]TAAGGGTTTTCTGTT | 59025 |
rs30985217 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Usp14 | Mm_Celera | 18:10001454 | AATGTGCTTACTGCA[G/T]CTGTCCTCATTTCCA | 59025 |
rs30985221 | snp | C/T | 0.336735 | 0.234472 | synonymous-codon | Usp14 | Mm_Celera | 18:10000540 | TTCTAGATCCTTGAA[C/T]TTTGACCGAAAAGAG | 59025 |
rs30985885 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Usp14 | Mm_Celera | 18:10018457 | ACAAACCAATGACTG[A/G]CCAACTTGAGGCCAC | 59025 |
rs30985887 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Usp14 | Mm_Celera | 18:10016381 | CAGCCATGCCACTCA[C/T]CCAAAAGTCAACCAC | 59025 |
rs30985889 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Usp14 | Mm_Celera | 18:10016000 | AAAGAATAAATCCAA[C/T]TGGAAGACCACATAT | 59025 |
rs45707954 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Usp14 | Mm_Celera | 18:10000417 | CTGATATGCAGGCTG[A/G]TCACTCATAACAGTA | 59025 |
rs46057624 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Usp14 | Mm_Celera | 18:9998214 | ACACTAAAAGTAGTA[C/T]GAGCCGGGCGTGGTG | 59025 |
rs46229359 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Usp14 | Mm_Celera | 18:9996734 | TAACTGCTGATGTTG[C/T]AAGTTTCGGTAGAAA | 59025 |
rs46753676 | snp | A/G | 0.32 | 0.24 | intron-variant | Usp14 | Mm_Celera | 18:9997884 | AAATCAATGAATCAC[A/G]GACAACATAATAGTC | 59025 |
rs46791327 | snp | A/G | 0.32 | 0.24 | intron-variant | Usp14 | Mm_Celera | 18:9998105 | CCTGCAGGAGCAAAG[A/G]CTACCTCAAAACAAA | 59025 |
rs47205959 | snp | A/T | | | intron-variant | Usp14 | Mm_Celera | 18:10004332 | TACAAAATTAAAAAA[A/T]CTGCCTGCAGAATCC | 59025 |
rs47339836 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Usp14 | Mm_Celera | 18:9999039 | AGATCAGCACCAACA[A/G]AGCAAGTGATGCCAC | 59025 |
rs47799875 | snp | G/T | 0.32 | 0.24 | intron-variant | Usp14 | Mm_Celera | 18:9996742 | GATGTTGTAAGTTTC[G/T]GTAGAAAAGATAAGC | 59025 |
rs48279084 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Usp14 | Mm_Celera | 18:9999536 | CTTTCTTCTCTGCCA[C/T]AAGGAGCATGAAGAG | 59025 |
rs48770949 | snp | A/G | | | intron-variant | Usp14 | Mm_Celera | 18:10002659 | AGGACACAAGAACAC[A/G]GCCCACAGAACTAAC | 59025 |