SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6166406 | snp | C/G | 0.5 | 0 | upstream-variant-2KB, utr-variant-5-prime | Usp32, 1700125H20Rik | Mm_Celera | 11:85140322 | TCTTCCCGCCCCCCA[C/G]GTTCTGGCGTTCGAC | 237898 |
rs6167941 | snp | A/C | 0.408163 | 0.193609 | upstream-variant-2KB, intron-variant | Usp32, 1700125H20Rik | Mm_Celera | 11:85140564 | CTAGAGATGGAGCCT[A/C]AGGACAGGGCAGTGG | 237898 |
rs6168529 | snp | A/G | 0.408163 | 0.193609 | upstream-variant-2KB, intron-variant | Usp32, 1700125H20Rik | Mm_Celera | 11:85140667 | GGCCCAAGCCACTAT[A/G]TTGGTCCATTTTTCC | 237898 |
rs6229332 | snp | C/T | 0.5 | 0 | intron-variant | Usp32 | Mm_Celera | 11:85071598 | gcctctactaataca[C/T]cagagttacagatct | 237898 |
rs6239802 | snp | C/T | 0.5 | 0 | intron-variant | Usp32 | Mm_Celera | 11:85012466 | tcttaatcagtaagc[C/T]atctctctagttccC | 237898 |
rs6240362 | snp | A/T | 0.5 | 0 | intron-variant | Usp32 | Mm_Celera | 11:85012587 | tggtgttgaagttac[A/T]ggcttgtgagccatc | 237898 |
rs6259735 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Usp32 | Mm_Celera | 11:85013921 | TATGAGTCCTTCACA[C/T]ACACCCTGCCAAATT | 237898 |
rs6359327 | snp | C/T | 0.5 | 0 | intron-variant | Usp32 | Mm_Celera | 11:85097045 | tagttcaaggtcacg[C/T]cttgctatatagtaa | 237898 |
rs6359796 | snp | A/G | 0.5 | 0 | intron-variant | Usp32 | Mm_Celera | 11:85097097 | aactaaaaGCTAGCc[A/G]accacaactactacc | 237898 |
rs6359867 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Usp32 | Mm_Celera | 11:85097135 | CCACCACCACCACCA[C/G]CAGCAGCACCAAAAT | 237898 |
rs26965086 | snp | A/G | 0.415225 | 0.187619 | intron-variant | Usp32 | Mm_Celera | 11:85021530 | TATAAGCAGTCTTAG[A/G]TAATTCCCTTCTCTC | 237898 |
rs26965087 | snp | A/G | 0.415225 | 0.187619 | intron-variant | Usp32 | Mm_Celera | 11:85020264 | CAACTATCTAAACTG[A/G]AAACCCTGGCCCCTG | 237898 |
rs26965088 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Usp32 | Mm_Celera | 11:85020238 | GTGCCTGGAAGTTTT[A/G]CCTTTTGTCTCAACT | 237898 |
rs26965089 | snp | C/T | 0.46281 | 0.131194 | intron-variant | Usp32 | Mm_Celera | 11:85018233 | GATAAAAATGTATTC[C/T]CTTAGTGAGTAGGGT | 237898 |
rs26965090 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Usp32 | Mm_Celera | 11:85017587 | GCATTTCACCAATGA[G/T]GGCTGACATGACCAA | 237898 |
rs26965091 | snp | A/G | 0.46281 | 0.131194 | intron-variant | Usp32 | Mm_Celera | 11:85017545 | TGAGAGTATGTTCAA[A/G]AAACACTTGAAAGCA | 237898 |
rs26965092 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Usp32 | Mm_Celera | 11:85014718 | CTCTCCACAAAGCTC[A/C]TTTCCCTTTCCTTTC | 237898 |
rs26965093 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Usp32 | Mm_Celera | 11:85013879 | GTAAATTCAATCTTA[A/C]TGGCAAAGAGTTTTT | 237898 |
rs26965094 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Usp32 | Mm_Celera | 11:85013723 | TATTCTATTTCCACT[A/T]TTGTTTTCTATATAG | 237898 |
rs26965095 | snp | G/T | 0.375 | 0.216506 | intron-variant | Usp32 | Mm_Celera | 11:85012292 | TACACATGCATGCAT[G/T]CGTGCGTGCATTTGT | 237898 |
rs26965096 | snp | C/T | 0.401235 | 0.199068 | intron-variant | Usp32 | Mm_Celera | 11:85011898 | ATACACAAGAATGCA[C/T]ACAAATGAGGGAGCC | 237898 |
rs26965097 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Usp32 | Mm_Celera | 11:85010857 | GAAGACTTCCTAGTG[C/T]ACACCCAAGTGTACT | 237898 |
rs26965098 | snp | C/T | 0.387812 | 0.208586 | intron-variant | Usp32 | Mm_Celera | 11:85009609 | ATTACAGAAGCTAAG[C/T]TTTCATTGCCACAAT | 237898 |
rs26965099 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Usp32 | Mm_Celera | 11:85009116 | GATTCCTGCCCCTTT[A/G]TGAGCTCATTTCACA | 237898 |
rs26965100 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Usp32 | Mm_Celera | 11:85008563 | GGTTGGTGGTCTTTA[C/T]TCTTGTTTTGTGGGA | 237898 |
rs26965101 | snp | C/T | 0.387812 | 0.208586 | intron-variant | Usp32 | Mm_Celera | 11:85008481 | ATGCCACAGGAGAAT[C/T]CCATCTTAGAGAGAT | 237898 |
rs26965102 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon | Usp32 | Mm_Celera | 11:85005895 | AATGAAAGCTCTGTC[C/T]TCTCCACAATCGATT | 237898 |
rs26965103 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Usp32 | Mm_Celera | 11:85003897 | ATTTGTGATGACAGA[A/G]ACTTGTAAATCTGTC | 237898 |
rs26965104 | snp | C/T | 0.415225 | 0.187619 | intron-variant | Usp32 | Mm_Celera | 11:85003874 | TGTCGGGATAATGTC[C/T]TGTTATAATTTGTGA | 237898 |
rs26965105 | snp | C/G | 0.387812 | 0.208586 | intron-variant | Usp32 | Mm_Celera | 11:85003740 | GGGTGAGAGTGACAG[C/G]TTGCATGTAGGCGCT | 237898 |
rs26965106 | snp | A/G | 0.375 | 0.216506 | intron-variant | Usp32 | Mm_Celera | 11:85003350 | CTGGTATCTTGTTTC[A/G]TAGTAAAAAATCAAT | 237898 |
rs26965107 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Usp32 | Mm_Celera | 11:85001621 | ATAAAAATTTACTTT[A/G]CCTCTTGGGCTCCGT | 237898 |
rs26965108 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Usp32 | Mm_Celera | 11:85001385 | TAAGTGTACAAAATA[C/T]CTGTGATGTCTCTCT | 237898 |
rs26965109 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Usp32 | Mm_Celera | 11:85000465 | ACTCCAGGTCTTCAG[A/G]TGAGACTTTTTCCCT | 237898 |
rs26965110 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Usp32 | Mm_Celera | 11:85000445 | ATAAATTGGCCATTT[A/C]ATTTACTCCAGGTCT | 237898 |
rs26965111 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Usp32 | Mm_Celera | 11:85000396 | TTCCTGTTAGCTTTC[C/T]CTAAACTCTTGGGAA | 237898 |
rs26965112 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Usp32 | Mm_Celera | 11:85000118 | AGCAGTCAAGGGTTC[C/T]CTCCCCAATCTCATA | 237898 |
rs26981503 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Usp32 | Mm_Celera | 11:85130529 | CTGGAGTTTCAAGAA[A/G]AAACTGCATTACAGC | 237898 |
rs26981504 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Usp32 | Mm_Celera | 11:85129274 | GGAAAAGATGTAAGA[A/G]TATCTGACAATCTCT | 237898 |
rs26981505 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Usp32 | Mm_Celera | 11:85128907 | GAAACAGAAACTTCT[A/G]GGAGAGATATACAGC | 237898 |
rs26981506 | snp | C/G | 0.387812 | 0.208586 | intron-variant | Usp32 | Mm_Celera | 11:85128788 | ATAAAGCCACTCAAA[C/G]TTCAAAATGTGTGCA | 237898 |
rs26981507 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Usp32 | Mm_Celera | 11:85126081 | ACCTGAAAAAAAATG[C/T]TAGCCTTACAAAAAC | 237898 |
rs26981508 | snp | C/T | 0.387812 | 0.208586 | intron-variant | Usp32 | Mm_Celera | 11:85123498 | TCTGTTACATAAAAG[C/T]CAAAGCATGTAAACA | 237898 |
rs26981509 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Usp32 | Mm_Celera | 11:85116709 | TCAAAAGGAGCCACG[C/T]CACCCTTACAGAGCA | 237898 |
rs26981510 | snp | A/C/T | 0.391111 | 0.206368 | intron-variant | Usp32 | GRCm38.p3 | 11:85116678 | TCTTCACCTCTCAGA[A/C/T]CACAAGTATCTGTAA | 237898 |
rs26981511 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Usp32 | Mm_Celera | 11:85114155 | AGCAGGGATTGCAAC[C/T]TATTTTTTCATCAAA | 237898 |
rs26981512 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Usp32 | Mm_Celera | 11:85111769 | GAAGGAAGCTGCAGA[A/G]CAAGATGTTGAAAAG | 237898 |
rs26981513 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Usp32 | Mm_Celera | 11:85111619 | GCTGATAGGACCCGT[A/G]ATGCCCATCCGGAAT | 237898 |
rs26981514 | snp | A/G | 0.387812 | 0.208586 | intron-variant | Usp32 | Mm_Celera | 11:85111617 | CAGCTGATAGGACCC[A/G]TAATGCCCATCCGGA | 237898 |
rs26981515 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Usp32 | Mm_Celera | 11:85111464 | TGGACCCCAGGAGGC[A/G]AAACAAGTCCACGGA | 237898 |
rs26981516 | snp | C/T | 0.401235 | 0.199068 | intron-variant | Usp32 | Mm_Celera | 11:85111312 | CCCTCGGCCCGCGTC[C/T]GGTCCCATCAGGCCG | 237898 |
rs26981517 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Usp32 | Mm_Celera | 11:85111243 | AGGCGCAAGGCCCGG[C/T]GCGCAAGATCCACAG | 237898 |
rs26981518 | snp | C/T | 0.401235 | 0.199068 | intron-variant | Usp32 | Mm_Celera | 11:85110173 | ATAATCTGAGTCTTG[C/T]TCCAAGTCAGTTACT | 237898 |
rs26981519 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Usp32 | Mm_Celera | 11:85107786 | CTAACAAATGAAGTT[A/G]CTTCTGATCTAGTGG | 237898 |
rs26981520 | snp | A/C | 0.277778 | 0.248452 | intron-variant | Usp32 | Mm_Celera | 11:85106877 | AGGAGAAAAGAAGAT[A/C]GGGAGATGAAGTCTA | 237898 |
rs26981521 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Usp32 | Mm_Celera | 11:85105929 | AAGATGTGGGGCACA[A/G]GATACATGCCAACAC | 237898 |
rs26981522 | snp | G/T | 0.408163 | 0.193609 | intron-variant | Usp32 | Mm_Celera | 11:85103519 | TGTAGAGGATTTCCA[G/T]TCAACCTTCAAGAAT | 237898 |
rs26981523 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Usp32 | Mm_Celera | 11:85103481 | TTATCAGACGCAAAC[A/G]CACCAAAAAGCAAAA | 237898 |
rs26981524 | snp | A/G | 0.375 | 0.216506 | intron-variant | Usp32 | Mm_Celera | 11:85100499 | ATAATATTAAAATGG[A/G]AGGTTCAGCAGATGA | 237898 |
rs26981525 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Usp32 | Mm_Celera | 11:85100465 | CACTATTAATCCTTT[C/T]AGTACTGCCAACTAC | 237898 |
rs26981526 | snp | C/T | 0.18 | 0.24 | intron-variant | Usp32 | Mm_Celera | 11:85097761 | TCACAAGGGCAACTA[C/T]AATGTTTCACCCATC | 237898 |
rs26981527 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Usp32 | Mm_Celera | 11:85095246 | TTGACCACAGATGAC[A/G]ACAGATGAAAGACTC | 237898 |
rs26981528 | snp | C/T | 0.18 | 0.24 | intron-variant | Usp32 | Mm_Celera | 11:85089302 | GGCTTTCCCTGCTTA[C/T]CAGAGGAAGCCTGTG | 237898 |
rs26981529 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Usp32 | Mm_Celera | 11:85087450 | TATTGACAATAGCAC[G/T]AATGCAGAAAGGCTG | 237898 |
rs26981530 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Usp32 | Mm_Celera | 11:85086145 | AAACTCAGATTCCAC[G/T]GCAGAGGCCTCAGAG | 237898 |
rs26981531 | snp | C/T | 0.42 | 0.183303 | intron-variant | Usp32 | Mm_Celera | 11:85086095 | GAAAGGGATCCCACC[C/T]TGTGCTTTTTAGAGC | 237898 |
rs26981532 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Usp32 | Mm_Celera | 11:85086025 | AAGAAAGATGGCTCA[A/G]GCAGTACATGAGGAT | 237898 |
rs26981533 | snp | A/G | 0.401235 | 0.199068 | intron-variant | Usp32 | Mm_Celera | 11:85083445 | TATCAATCCAGATAG[A/G]CCCTGAGTTTAATTC | 237898 |
rs26981534 | snp | A/C | 0.408163 | 0.193609 | intron-variant | Usp32 | Mm_Celera | 11:85083348 | AGTAAAGTATTTTTA[A/C]GGCTTCTCTATGTTT | 237898 |
rs26981535 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Usp32 | Mm_Celera | 11:85082934 | ACCACAGAAAGGGGA[A/T]AGCAAAACATAAACC | 237898 |
rs26981536 | snp | G/T | 0.408163 | 0.193609 | intron-variant | Usp32 | Mm_Celera | 11:85081374 | TCTTCAATGACCTCT[G/T]CCTCCTCCTGAGATG | 237898 |
rs26981537 | snp | A/C | 0.42 | 0.183303 | intron-variant | Usp32 | Mm_Celera | 11:85081330 | AATTCATTGCACATC[A/C]TGAGTACACTTTGTT | 237898 |
rs26981538 | snp | C/T | 0.42 | 0.183303 | intron-variant | Usp32 | Mm_Celera | 11:85081283 | AATTAATCTTCACAT[C/T]AAGTACAGTTCAGTT | 237898 |
rs26981539 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Usp32 | Mm_Celera | 11:85080445 | AACACATGGGAACAC[G/T]AAATAGATCTAATGT | 237898 |
rs26981540 | snp | A/G | 0.359862 | 0.224567 | intron-variant | Usp32 | Mm_Celera | 11:85080079 | CTCTCATTCTATTTA[A/G]CTTCCTTATAGCACT | 237898 |
rs26981541 | snp | C/G/T | 0.124444 | 0.216185 | intron-variant | Usp32 | Mm_Celera | 11:85078692 | AAAAGTGTGCTGACA[C/G/T]TGCTCTCTAATCAAG | 237898 |
rs26981542 | snp | C/T | 0.415225 | 0.187619 | intron-variant | Usp32 | Mm_Celera | 11:85078035 | TTTTCACTTATCCCT[C/T]ATCTTGAATACTCTG | 237898 |
rs26981543 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Usp32 | Mm_Celera | 11:85076956 | CTTTGGATTCCTGAC[A/G]GCAGGGAGAAGGATG | 237898 |
rs26981544 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Usp32 | Mm_Celera | 11:85074616 | TGCTCTCAGGAGCAA[A/C]GGCCTTCTGAGATTA | 237898 |
rs26981545 | snp | C/T | 0.32 | 0.24 | intron-variant | Usp32 | Mm_Celera | 11:85074605 | AGGAGACAACCTGCT[C/T]TCAGGAGCAACGGCC | 237898 |
rs26981546 | snp | A/G | 0.401235 | 0.199068 | intron-variant | Usp32 | Mm_Celera | 11:85073275 | CTATGATGAGGTATG[A/G]TGATTATAAAAAAGA | 237898 |
rs26981547 | snp | A/C | 0.401235 | 0.199068 | intron-variant | Usp32 | Mm_Celera | 11:85073216 | TGATATCTAAATGAG[A/C]TGTCACTTCTCTCCT | 237898 |
rs26981548 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Usp32 | Mm_Celera | 11:85072999 | TACAAAAACTAACCC[C/T]GGATCTTACTGTTAA | 237898 |
rs26981549 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Usp32 | Mm_Celera | 11:85072864 | AGTCCTCGGAAGGGC[C/T]GAGAGGTGTACCAAC | 237898 |
rs26981550 | snp | A/G | 0.32 | 0.24 | intron-variant | Usp32 | Mm_Celera | 11:85072752 | GTGCACTGTGGGTGA[A/G]TAGCAGGGCCCTGAG | 237898 |
rs26981551 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Usp32 | Mm_Celera | 11:85072714 | TCACAGATGATGTGC[A/G]GATTCTGAAAGTACC | 237898 |
rs26981552 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Usp32 | Mm_Celera | 11:85072663 | TCTGTCCCTGTCCCG[C/G]ATGATCCAAAAGATG | 237898 |
rs26981553 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Usp32 | Mm_Celera | 11:85072581 | GGTTTTTGGCCAGAC[A/G]GACCAACTCCACCTT | 237898 |
rs26981554 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Usp32 | Mm_Celera | 11:85072552 | CTACCTGAGGCTGCT[A/T]GTCAAGCTGTACAGG | 237898 |
rs26981555 | snp | A/G | 0.32 | 0.24 | intron-variant | Usp32 | Mm_Celera | 11:85072525 | GCGCAAGGAGCCCAA[A/G]AGCCAGGACATCTAC | 237898 |
rs26981556 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Usp32 | Mm_Celera | 11:85072511 | GACCGAAAGGTTCAG[C/T]GCAAGGAGCCCAAGA | 237898 |
rs26981557 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Usp32 | Mm_Celera | 11:85072470 | CAGGAGGCGCCATCA[C/T]GGGTGTTGACATTCG | 237898 |
rs26981558 | snp | A/T | 0.359862 | 0.224567 | intron-variant | Usp32 | Mm_Celera | 11:85072142 | TACTGTAAAAGTCAT[A/T]GGAAAGGAAACTAGT | 237898 |
rs26981559 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Usp32 | Mm_Celera | 11:85071316 | GAGTCACAGGACTTG[A/G]GAAGGAGTAGCAAAA | 237898 |
rs26981560 | snp | A/C | 0.465374 | 0.126941 | intron-variant | Usp32 | Mm_Celera | 11:85059536 | ATAAGAAGAGCAGGG[A/C]CCAGATTTAATTCAC | 237898 |
rs26981561 | snp | A/T | 0.277778 | 0.248452 | intron-variant | Usp32 | Mm_Celera | 11:85059493 | TAAATTTTGTATGCA[A/T]ATCTTCTCTCCTGGT | 237898 |
rs26981562 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Usp32 | Mm_Celera | 11:85059301 | AAACTCAAAATGCCC[C/T]TTTGGCCCGTTAGTT | 237898 |
rs26981563 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Usp32 | Mm_Celera | 11:85059264 | TGACTCTTCCACTAA[A/G]AATCAAATCAAACAA | 237898 |
rs26981564 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon | Usp32 | Mm_Celera | 11:85059236 | AATACCGTTTCTCCA[A/G]ATCGATGATGTCTGA | 237898 |
rs26981565 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Usp32 | Mm_Celera | 11:85058750 | CACCTGAGGAGACCT[A/G]GAGCTCGCCCGCCCT | 237898 |