SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3686926 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Tep1 | Mm_Celera | 14:50833350 | CAGCAAGCGTTAGCA[C/T]GACCATCATTAATAG | 21745 |
rs3704151 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Tep1 | Mm_Celera | 14:50831054 | TGCCCAGAGACAGCA[C/T]ACCTTACTTATGTAT | 21745 |
rs3708364 | snp | A/G | 0.5 | 0 | missense | Tep1 | Mm_Celera | 14:50837148 | AGTTGAGAGACTTTG[A/G]ATGGGTGTACTGAAA | 21745 |
rs3723288 | snp | C/T | 0.5 | 0 | synonymous-codon | Tep1 | Mm_Celera | 14:50837176 | AAAAGCCAGCTGTCC[C/T]CGGACTGTGTCCCAC | 21745 |
rs3723400 | snp | A/G | 0.5 | 0 | intron-variant | Tep1 | Mm_Celera | 14:50837225 | AGGAGAAACCAGGGT[A/G]GGTGCTGGACACAAA | 21745 |
rs3723963 | snp | C/T | 0.5 | 0 | intron-variant | Tep1 | Mm_Celera | 14:50837291 | TATCTAGTCCCCTGA[C/T]TCAGCAAGGCTTCCC | 21745 |
rs3724067 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Tep1 | Mm_Celera | 14:50837349 | CAACAAAATCAGTTT[C/T]GGCTCATGGTTGAGG | 21745 |
rs3724654 | snp | A/G | 0.5 | 0 | missense | Tep1 | Mm_Celera | 14:50837421 | TGGCCAGCAGGCGGC[A/G]GTCTGGGCTCAGGCA | 21745 |
rs4138218 | snp | A/T | 0.408163 | 0.193609 | intron-variant | Tep1 | Mm_Celera | 14:50837497 | GCCCCAGGAAGACCA[A/T]GTCAGGGTTCTGGGG | 21745 |
rs4139133 | snp | A/C | 0.444444 | 0.157135 | intron-variant, downstream-variant-500B | Tep1 | Mm_Celera | 14:50831528 | TGGAGTTGAGTGGCT[A/C]GGAAACTTTGCCAGA | 21745 |
rs6332574 | snp | A/G | 0.408163 | 0.193609 | synonymous-codon | Tep1 | Mm_Celera | 14:50847000 | AATGAAAAGCCGGAT[A/G]TTGCACCATCTGGGG | 21745 |
rs6332587 | snp | A/G | 0.408163 | 0.193609 | missense | Tep1 | Mm_Celera | 14:50847005 | AAAGCCGGATGTTGC[A/G]CCATCTGGGGGCAAG | 21745 |
rs6334652 | snp | C/T | 0.5 | 0 | intron-variant | Tep1 | Mm_Celera | 14:50847386 | TATATCGATGTGGAG[C/T]CTNCTCTCCTCCCTA | 21745 |
rs6334654 | snp | G/T | 0.5 | 0 | intron-variant | Tep1 | Mm_Celera | 14:50847389 | ATCGATGTGGAGNCT[G/T]CTCTCCTCCCTANAT | 21745 |
rs6334670 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Tep1 | Mm_Celera | 14:50847402 | CTGCTCTCCTCCCTA[C/T]ATACAGACATTTTTT | 21745 |
rs30114581 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Tep1 | Mm_Celera | 14:50865565 | GCTTTTGTTTAGAGT[A/G]ACTTACTGCAGGCAC | 21745 |
rs30140774 | snp | C/T | 0.375 | 0.216506 | intron-variant | Tep1 | Mm_Celera | 14:50865361 | CATAGTCTTATTAGA[C/T]TAAATAAGAGTAAAA | 21745 |
rs30147712 | snp | A/G | 0.375 | 0.216506 | intron-variant | Tep1 | Mm_Celera | 14:50864650 | TAAATATATATATAT[A/G]TATGTATATGTATAT | 21745 |
rs30150550 | snp | C/T | 0.375 | 0.216506 | intron-variant | Tep1 | Mm_Celera | 14:50858079 | CATGGTGGCTCACAA[C/T]CCTCAGTAACTCCAG | 21745 |
rs30152229 | snp | C/T | 0.375 | 0.216506 | intron-variant | Tep1 | Mm_Celera | 14:50859369 | GAGTTTCAAAGCCCA[C/T]CCCCACAGTGACACA | 21745 |
rs30159566 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Tep1 | Mm_Celera | 14:50865557 | CCTAAGTGGCTTTTG[G/T]TTAGAGTGACTTACT | 21745 |
rs30159626 | snp | C/T | 0.375 | 0.216506 | intron-variant | Tep1 | Mm_Celera | 14:50864987 | ACATCCCTCCATGGC[C/T]CCTGCATCAGCTCCT | 21745 |
rs30172052 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Tep1 | Mm_Celera | 14:50842232 | TAGGCTGCTGGCCAT[G/T]CCTTGGGGAGTTATC | 21745 |
rs30203158 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Tep1 | Mm_Celera | 14:50832443 | CCCCAGAAGAGGGCA[A/T]CAGATCTCATTACAG | 21745 |
rs30204975 | snp | A/G | 0.32 | 0.24 | intron-variant | Tep1 | Mm_Celera | 14:50858661 | AGAAATTAACCATGG[A/G]GAATTTAGTCTCAAA | 21745 |
rs30227862 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Tep1 | Mm_Celera | 14:50842242 | GCCATGCCTTGGGGA[A/G]TTATCTTGAGGAAAG | 21745 |
rs30242262 | snp | C/T | 0.32 | 0.24 | intron-variant | Tep1 | Mm_Celera | 14:50850161 | GGGTAGTGGCTTACA[C/T]CTGCAATCCCAGCAC | 21745 |
rs30246037 | snp | A/G | 0.375 | 0.216506 | intron-variant | Tep1 | Mm_Celera | 14:50854636 | GAGCAGAGGAGGAAG[A/G]AGGATGAGGAGCCAT | 21745 |
rs30252469 | snp | A/G | 0.375 | 0.216506 | intron-variant | Tep1 | Mm_Celera | 14:50866951 | AAAGTATCTCTTAGA[A/G]ATATGAAAGGTCCAA | 21745 |
rs30259462 | snp | C/T | 0.260355 | 0.249785 | upstream-variant-2KB, intron-variant | Tep1, Gm26782 | Mm_Celera | 14:50872262 | AAACCATCCCTAGAA[C/T]GCAATACCATCCATA | 21745 |
rs30267621 | snp | C/G | 0.375 | 0.216506 | intron-variant | Tep1 | Mm_Celera | 14:50864894 | GGCCCATTGTGGGTG[C/G]TGCCATCCCTGGGCT | 21745 |
rs30302957 | snp | C/T | 0.387812 | 0.208586 | intron-variant | Tep1 | Mm_Celera | 14:50866901 | TATAAAATTGCACCA[C/T]GAATGCATGCACAGC | 21745 |
rs30305719 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Tep1 | Mm_Celera | 14:50857407 | AAATCATGTAATTTT[A/G]ATTTCAAAAAGTAAA | 21745 |
rs30309297 | snp | C/T | 0.32 | 0.24 | synonymous-codon | Tep1 | Mm_Celera | 14:50837703 | ACTCACCAGAGCCTT[C/T]TCCTCCTGAAACGGC | 21745 |
rs30314601 | snp | C/T | 0.401235 | 0.199068 | intron-variant | Tep1 | Mm_Celera | 14:50843323 | TAGGGAAGCCTACCA[C/T]AGCTGGGTCTGTGAC | 21745 |
rs30373494 | snp | C/T | 0.188366 | 0.242283 | synonymous-codon | Tep1 | Mm_Celera | 14:50841920 | GACATCATGGCCATG[C/T]TCTTGCTCCAAGGTG | 21745 |
rs30420251 | snp | A/G | 0.32 | 0.24 | intron-variant | Tep1 | Mm_Celera | 14:50847477 | TCCCAGGAAGCCCCT[A/G]CCTGGGGAGGAGAAC | 21745 |
rs30425371 | snp | C/T | 0.32 | 0.24 | intron-variant | Tep1 | Mm_Celera | 14:50843504 | AATTCTACTCATCCT[C/T]CCTAGGGAGATAGAT | 21745 |
rs30456593 | snp | A/T | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Tep1, Gm26782 | Mm_Celera | 14:50870028 | TGTGTATACACTAGT[A/T]TGTATGTATACCTGC | 21745 |
rs30481502 | snp | C/T | 0.375 | 0.216506 | intron-variant | Tep1 | Mm_Celera | 14:50842032 | ACACTTTGTCTGGGG[C/T]GGGAGGAGGCAGACA | 21745 |
rs30490120 | snp | A/G | 0.401235 | 0.199068 | missense | Tep1 | Mm_Celera | 14:50862904 | ACCGATGTTTCCGTG[A/G]GTTGTACTTAGCTAG | 21745 |
rs30507435 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Tep1 | Mm_Celera | 14:50863859 | AGGCCTGGCCTTGTC[A/G]GGAAGAGTCTTCATT | 21745 |
rs30525815 | snp | A/G | 0.375 | 0.216506 | intron-variant | Tep1 | Mm_Celera | 14:50854771 | CCATGGGGCTACAGG[A/G]AGGATGAGGAGCCAT | 21745 |
rs30543913 | snp | A/C | 0.375 | 0.216506 | synonymous-codon | Tep1 | Mm_Celera | 14:50836703 | GCCATCTTCTCCAGC[A/C]GTCAGGAACCGGTCT | 21745 |
rs30551770 | snp | G/T | 0.375 | 0.216506 | intron-variant | Tep1 | Mm_Celera | 14:50853797 | ACAAAATGTACTGCT[G/T]TAATACTAAATCCTC | 21745 |
rs30567398 | snp | A/C | 0.375 | 0.216506 | intron-variant | Tep1 | Mm_Celera | 14:50857869 | CAAAAAGGGAGATAA[A/C]GAGAGAGGAAGAAAA | 21745 |
rs30572808 | snp | A/C | 0.32 | 0.24 | intron-variant | Tep1 | Mm_Celera | 14:50837565 | TCAGGGCTTCTCACT[A/C]AGTCATGGGAGGTCT | 21745 |
rs30604270 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Tep1 | Mm_Celera | 14:50863024 | CCAGGCTCTGTAGAA[A/G]AAAACAAAACAAACA | 21745 |
rs30618487 | snp | C/T | 0.207612 | 0.24638 | intron-variant | Tep1 | Mm_Celera | 14:50863390 | TATCCTCTCTGGGCA[C/T]TTGGATGCAGGAAAA | 21745 |
rs30629225 | snp | A/G | 0.375 | 0.216506 | intron-variant | Tep1 | Mm_Celera | 14:50858965 | GAAAGGCTGACAGAT[A/G]ATGGGGAATTTAATT | 21745 |
rs30629294 | snp | C/T | 0.207612 | 0.24638 | intron-variant | Tep1 | Mm_Celera | 14:50860230 | AGATCTAATCCCACT[C/T]GGTTACAATATATTC | 21745 |
rs30633820 | snp | C/G | 0.5 | 0 | synonymous-codon | Tep1 | Mm_Celera | 14:50826831 | TATAGAAAGTAATCC[C/G]GAGTCCCCCTGCTGC | 21745 |
rs30634549 | snp | C/T | 0.5 | 0 | intron-variant | Tep1 | Mm_Celera | 14:50862331 | ATCCGCCTGCCTCTG[C/T]CTCCCAAGTGCTGGG | 21745 |
rs30637815 | snp | C/T | 0.387812 | 0.208586 | synonymous-codon | Tep1 | Mm_Celera | 14:50866809 | ACTGTACAAAGGCAT[C/T]GGGACTTCTGTGCTT | 21745 |
rs30682067 | snp | A/G | 0.359862 | 0.224567 | intron-variant | Tep1 | Mm_Celera | 14:50862694 | CTTCTGGCCCTGAGC[A/G]CTACACAGGTTATCT | 21745 |
rs30682659 | snp | A/G | 0.444444 | 0.157135 | downstream-variant-500B | Tep1 | Mm_Celera | 14:50823593 | TTGAGGGAGAAATAG[A/G]TTTGTGATCTCTGTA | 21745 |
rs30697623 | snp | C/T | 0.207612 | 0.24638 | intron-variant | Tep1 | Mm_Celera | 14:50857766 | CACTCTGGGTGACCA[C/T]ACGCGGAAGCATGAT | 21745 |
rs30702718 | snp | A/C | 0.375 | 0.216506 | intron-variant | Tep1 | Mm_Celera | 14:50829609 | GTTACCCTGGCATTC[A/C]TTGCTCCACTCATCT | 21745 |
rs30717258 | snp | C/T | 0.265928 | 0.249492 | intron-variant | Tep1 | Mm_Celera | 14:50857819 | CATAAGGACTGGGAT[C/T]TGAGACTAGGCTGGA | 21745 |
rs30721394 | snp | A/G | 0.375 | 0.216506 | intron-variant | Tep1 | Mm_Celera | 14:50865640 | ATTCTTTATCTGTCT[A/G]CTTCACACATATCTG | 21745 |
rs30725470 | snp | A/C | 0.32 | 0.24 | intron-variant | Tep1 | Mm_Celera | 14:50847586 | TGGCAACCCTTCCAG[A/C]TCACCAAGTCCCACA | 21745 |
rs30745844 | snp | A/G | 0.46875 | 0.121031 | intron-variant | Tep1 | Mm_Celera | 14:50850771 | GGCTAAAATAGACAT[A/G]GATGAGCTCAGAGCG | 21745 |
rs30767865 | snp | A/G | 0.375 | 0.216506 | intron-variant | Tep1 | Mm_Celera | 14:50842015 | GGCAGTGAAAGAAGA[A/G]AACACTTTGTCTGGG | 21745 |
rs30791091 | snp | A/G | 0.188366 | 0.242283 | intron-variant | Tep1 | Mm_Celera | 14:50860525 | GAAGGGAGAAGTCAG[A/G]AAAGGAACTGCCGAT | 21745 |
rs30794152 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Tep1 | Mm_Celera | 14:50864484 | GGCAACATTATTTAT[A/G]ATGGCCTAGAAGTAC | 21745 |
rs30828160 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Tep1 | Mm_Celera | 14:50829506 | ATAAATACATACATA[A/C]ATAAATAAATAAATA | 21745 |
rs30842992 | snp | A/T | 0.207612 | 0.24638 | intron-variant | Tep1 | Mm_Celera | 14:50863885 | TCATTCCAACATCTA[A/T]CAAGAACTCACTGAT | 21745 |
rs30852738 | snp | C/T | 0.375 | 0.216506 | intron-variant | Tep1 | Mm_Celera | 14:50860554 | ATCGAATCGATCGAT[C/T]GATCACCGATCAACG | 21745 |
rs30869315 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Tep1 | Mm_Celera | 14:50843124 | CAACTAAGACAGGCT[A/G]GGATGAGGGATGGAA | 21745 |
rs30876523 | snp | A/G | 0.5 | 0 | intron-variant | Tep1 | Mm_Celera | 14:50845955 | TTGAAGATTGGATTC[A/G]GAACCATACTTGTAG | 21745 |
rs30877310 | snp | C/T | 0.375 | 0.216506 | intron-variant | Tep1 | Mm_Celera | 14:50849695 | GAGTTCAATTCCTTG[C/T]AACCACATGGTGGCT | 21745 |
rs30886305 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Tep1 | Mm_Celera | 14:50856102 | ACTGCTACCTGCTGA[A/G]AAGCACCTGAGACAT | 21745 |
rs30892230 | snp | C/T | 0.375 | 0.216506 | intron-variant | Tep1 | Mm_Celera | 14:50858594 | GGTGTCTCTTCACAG[C/T]AACAGAATTGTGACT | 21745 |
rs30897276 | snp | A/G | 0.5 | 0 | intron-variant | Tep1 | Mm_Celera | 14:50846105 | CTCAAACTCATGGAG[A/G]GCCTTCTGCCTTTCA | 21745 |
rs30940227 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Tep1 | Mm_Celera | 14:50862737 | CTTCTCTGCTTTCTG[G/T]TATCTAAACATGTCA | 21745 |
rs30943120 | snp | A/G | 0.375 | 0.216506 | upstream-variant-2KB, intron-variant | Tep1, Gm26782 | Mm_Celera | 14:50871833 | ATAAAATAAGTAAGT[A/G]AGTAAATAAATAAAT | 21745 |
rs30947804 | snp | A/G | 0.375 | 0.216506 | intron-variant | Tep1 | Mm_Celera | 14:50864951 | AGGCTGAGCAAGCCA[A/G]GGGAAGCAAGCCAGT | 21745 |
rs30972614 | snp | A/G | 0.375 | 0.216506 | upstream-variant-2KB, intron-variant | Tep1, Gm26782 | Mm_Celera | 14:50872196 | GCTAAAAATTATCCT[A/G]ATTGTGAGAAATAAA | 21745 |
rs30977487 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Tep1 | Mm_Celera | 14:50862741 | TCTGCTTTCTGGTAT[A/C]TAAACATGTCAGATA | 21745 |
rs30995072 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Tep1 | Mm_Celera | 14:50846207 | TCTGAAACAATGTCA[C/T]TTAGTTGCCCAGGCT | 21745 |
rs31010879 | snp | C/T | 0.207612 | 0.24638 | intron-variant | Tep1 | Mm_Celera | 14:50867642 | GTTATGATAATCATG[C/T]TGGATTTCTTCTTGA | 21745 |
rs31015217 | snp | A/T | 0.375 | 0.216506 | intron-variant | Tep1 | GRCm38.p3 | 14:50864635 | TAATAAATATTATAA[A/T]AAATATATATATATA | 21745 |
rs31029753 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Tep1 | Mm_Celera | 14:50855144 | GTATGCCTGGTGCTA[C/T]GGAGGACAGAAGAGA | 21745 |
rs31041633 | snp | C/T | 0.401235 | 0.199068 | intron-variant | Tep1 | Mm_Celera | 14:50859005 | TTCTTATACAGATAT[C/T]AACAGAGGCACCGGT | 21745 |
rs31063831 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Tep1 | Mm_Celera | 14:50865610 | ACATCCCTCTTCTCT[A/G]CTTCTGAAGCAGCCA | 21745 |
rs31084815 | snp | A/G | 0.207612 | 0.24638 | intron-variant | Tep1 | Mm_Celera | 14:50860797 | TTGGAAAGAGCCAAA[A/G]TCAGCCAGTCATGTT | 21745 |
rs31089592 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Tep1 | Mm_Celera | 14:50859740 | ACCAGGAGAGAGCAT[A/G]AGATATTCTAAGGCT | 21745 |
rs31091953 | snp | A/G | 0.375 | 0.216506 | intron-variant | Tep1 | Mm_Celera | 14:50841782 | TACATGACCCCACCC[A/G]GCATCTCTGGCTAAT | 21745 |
rs31117208 | snp | G/T | 0.444444 | 0.157135 | synonymous-codon | Tep1 | Mm_Celera | 14:50827163 | CAGACCTGTCAAGAC[G/T]CCCCAGTCCTCCTGC | 21745 |
rs31126458 | snp | C/T | 0.375 | 0.216506 | intron-variant | Tep1 | Mm_Celera | 14:50865903 | CTCTTCGTACCATAA[C/T]TACATTAATATCTCC | 21745 |
rs31129493 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Tep1 | Mm_Celera | 14:50830576 | TCCATCAAACATAGA[C/T]GGGTTCTATTCAGGC | 21745 |
rs31134152 | snp | A/G | 0.375 | 0.216506 | intron-variant | Tep1 | Mm_Celera | 14:50829142 | TTAAGCACACGGGTG[A/G]ACAGAATTCGTATAG | 21745 |
rs31140633 | snp | C/T | 0.375 | 0.216506 | intron-variant | Tep1 | Mm_Celera | 14:50858769 | GACTCAGCCCAACAC[C/T]ACAACATCCTTCTTT | 21745 |
rs31141096 | snp | A/C | 0.375 | 0.216506 | upstream-variant-2KB, intron-variant | Tep1, Gm26782 | Mm_Celera | 14:50871787 | AAGGATCTCAAGTTC[A/C]AGCCAGATTCCTTAG | 21745 |
rs31141807 | snp | C/T | 0.207612 | 0.24638 | missense | Tep1 | Mm_Celera | 14:50854230 | AGGGTGCACAGGTGC[C/T]TCCGACTGGCAGGCC | 21745 |
rs31150205 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Tep1 | Mm_Celera | 14:50832429 | GCTGTCTTCAGACAC[A/C]CCAGAAGAGGGCATC | 21745 |
rs31167703 | snp | A/G | 0.5 | 0 | intron-variant | Tep1 | Mm_Celera | 14:50857553 | GGCTCACAACCATCC[A/G]TAACAAGATCTGACT | 21745 |
rs31191022 | snp | A/G | 0.375 | 0.216506 | intron-variant | Tep1 | Mm_Celera | 14:50843084 | GCTGCTTGTGTCAGG[A/G]TATTTTATCTTAACA | 21745 |
rs31194411 | snp | G/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | Tep1, Gm26782 | Mm_Celera | 14:50869086 | AAAAGGAGACCATAA[G/T]AACATGGAGGCCAGC | 21745 |
rs31217337 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Tep1 | Mm_Celera | 14:50865868 | TGTTCCTTGCATTCC[C/T]ACGTGGAGCCAATAA | 21745 |
rs31256254 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Tep1 | Mm_Celera | 14:50863820 | CATCACGCCATCTCC[C/T]GGCCATCTTCTACAT | 21745 |
rs31280162 | snp | C/T | 0.375 | 0.216506 | intron-variant | Tep1 | Mm_Celera | 14:50864988 | CATCCCTCCATGGCC[C/T]CTGCATCAGCTCCTG | 21745 |
rs31281750 | snp | C/T | 0.21875 | 0.248039 | intron-variant | Tep1 | Mm_Celera | 14:50850807 | ATGCTTAAGGACTGA[C/T]GGGTTAGAATGCTGA | 21745 |
rs31286911 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Tep1 | Mm_Celera | 14:50863434 | GAGGCTACCTTGTCT[A/G]AAAATGTCCTCTATG | 21745 |
rs31310885 | snp | A/C | 0.375 | 0.216506 | intron-variant | Tep1 | Mm_Celera | 14:50859257 | CATCATGGCAGGAAG[A/C]ACAGCAGCATCCAGG | 21745 |
rs31325940 | snp | A/T | 0.33241 | 0.236027 | intron-variant | Tep1 | Mm_Celera | 14:50842077 | TACAAGAGAGGATGG[A/T]GTAGCAAGAACTACA | 21745 |
rs31331037 | snp | C/T | 0.375 | 0.216506 | intron-variant | Tep1 | Mm_Celera | 14:50860550 | GCCGATCGAATCGAT[C/T]GATCGATCACCGATC | 21745 |
rs31336905 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Tep1 | Mm_Celera | 14:50860404 | ACAGTGGTGCGGTAA[A/G]TGGCAAACTTCAAAA | 21745 |
rs31365098 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Tep1 | Mm_Celera | 14:50859934 | GTTACTAAGCTTAAC[C/T]CCTAACACCTACAGT | 21745 |
rs31382250 | snp | A/T | 0.375 | 0.216506 | intron-variant | Tep1 | Mm_Celera | 14:50849154 | AAAGCTAAAAACATA[A/T]GGAAATTAATAAAGT | 21745 |
rs31447646 | snp | A/T | 0.375 | 0.216506 | intron-variant | Tep1 | Mm_Celera | 14:50864653 | ATATATATATATATA[A/T]GTATATGTATATAAA | 21745 |
rs31462787 | snp | A/G | 0.375 | 0.216506 | intron-variant | Tep1 | Mm_Celera | 14:50856319 | CTCCCTGGTGTACCC[A/G]GTCCTTGTAAGCCGC | 21745 |
rs31475071 | snp | G/T | 0.32 | 0.24 | intron-variant | Tep1 | Mm_Celera | 14:50847496 | GGGGAGGAGAACAAA[G/T]ACCTTAGTAAACAGA | 21745 |
rs31480224 | snp | A/C | 0.32 | 0.24 | intron-variant | Tep1 | Mm_Celera | 14:50867912 | CATCAGAGGTGGAAA[A/C]TAAGGCACTGAAATC | 21745 |
rs31486246 | snp | C/T | 0.32 | 0.24 | intron-variant | Tep1 | Mm_Celera | 14:50847581 | TCTGATGGCAACCCT[C/T]CCAGCTCACCAAGTC | 21745 |
rs31493777 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Tep1 | Mm_Celera | 14:50864065 | AATAAAATACTATTC[A/G]TTAGAAAAGCAAAAC | 21745 |
rs31500928 | snp | A/G | 0.444444 | 0.157135 | upstream-variant-2KB, intron-variant | Tep1, Gm26782 | Mm_Celera | 14:50872045 | CCATCTCATAGCCCC[A/G]TGGATTTTTAATGTG | 21745 |
rs31517494 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Tep1 | Mm_Celera | 14:50830976 | GACCAAGCTGACCTC[A/G]AATTCACAGAGCTCC | 21745 |
rs31536772 | snp | C/T | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Tep1, Gm26782 | Mm_Celera | 14:50869443 | CTCAGTAGTCTATGA[C/T]TGTAATCCCAACACT | 21745 |
rs36246355 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tep1 | Mm_Celera | 14:50838478 | CCGTCAGGGTAGTAC[A/G]TGAGGGTTTTCTGAC | 21745 |
rs36248621 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tep1 | Mm_Celera | 14:50848065 | CTACAAAACACTGGG[A/G]ATGAAGGATGTCACC | 21745 |
rs36282119 | snp | C/T | 0.396694 | 0.202437 | intron-variant | Tep1 | Mm_Celera | 14:50864134 | GTCATCTTCCAAAGC[C/T]TCACAGAAAACATTT | 21745 |
rs36306332 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Tep1 | Mm_Celera | 14:50847889 | CCCTCAGGAAGACAG[C/T]CATAGAGCAGACCTG | 21745 |
rs36313378 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Tep1 | Mm_Celera | 14:50826985 | TACCCTGAGTCTGAC[A/G]CAGTCTTGGGGTAAC | 21745 |
rs36324072 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Tep1 | Mm_Celera | 14:50855427 | TGGAGGGCTGACTAA[A/G]CCCAAAGACCTGTCT | 21745 |
rs36374058 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Tep1 | Mm_Celera | 14:50863154 | TCTGTGTTCAAGACA[A/C]ATCAGCAGTCTTCTC | 21745 |
rs36456654 | snp | A/G | 0.231111 | 0.249285 | synonymous-codon | Tep1 | Mm_Celera | 14:50845068 | AGCTCACCTGCGACA[A/G]GTAACCTCTTTCTGT | 21745 |
rs36502029 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Tep1 | Mm_Celera | 14:50825474 | TATTACAAACTCCAC[A/G]TCAGTGAGATCTCTG | 21745 |
rs36509048 | snp | A/C | 0.18 | 0.24 | intron-variant | Tep1 | Mm_Celera | 14:50838836 | TGCCTCTTTCTCTGC[A/C]TCTCTGCCTGCACCC | 21745 |
rs36524731 | snp | A/G | 0.32 | 0.24 | synonymous-codon | Tep1 | GRCm38.p3 | 14:50839101 | AGGATACTGGGTAAG[A/G]AGTGAAGCCTGTTGT | 21745 |
rs36542405 | snp | C/G | 0.48 | 0.0979796 | missense | Tep1 | Mm_Celera | 14:50824784 | ATCCAGCAATCAATG[C/G]AAAAATCCAACTCTG | 21745 |
rs36543850 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Tep1 | Mm_Celera | 14:50826635 | CACAATGAAATCTTA[C/T]ATGGAAACTTAGCAT | 21745 |
rs36558100 | snp | C/G | 0.444444 | 0.157135 | downstream-variant-500B | Tep1 | GRCm38.p3 | 14:50823946 | AGGAATAGAATCTGC[C/G]TGTTAAAGATGCTCA | 21745 |
rs36583589 | snp | A/G | 0.231111 | 0.249285 | synonymous-codon | Tep1 | Mm_Celera | 14:50845116 | CAGCTCTGAGACCCG[A/G]TGTGCAGCTTCTTCT | 21745 |
rs36594597 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Tep1 | Mm_Celera | 14:50855770 | CCCCAGCAGGAAACA[C/T]AGAGCCACACAGAAG | 21745 |
rs36600824 | snp | C/T | 0.244898 | 0.249948 | synonymous-codon | Tep1 | GRCm38.p3 | 14:50825108 | CCCATTAGGATTATT[C/T]AAGTTCAGATTGAAG | 21745 |
rs36619248 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tep1 | Mm_Celera | 14:50848173 | TTTAAGACCTTCCCT[A/G]TTCTGTGCGATCAGC | 21745 |
rs36626513 | snp | C/T | 0.132653 | 0.220748 | missense | Tep1 | Mm_Celera | 14:50853017 | GCAGTCTTCAGGATG[C/T]CTTCATCGGCTGTAA | 21745 |
rs36627067 | snp | A/G | 0.132653 | 0.220748 | upstream-variant-2KB, intron-variant | Tep1, Gm26782 | Mm_Celera | 14:50870939 | CTTTCATCCACCATG[A/G]AAGTAAACAGTTTCG | 21745 |
rs36637097 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Tep1 | Mm_Celera | 14:50853282 | GACTTGGGGGAACCA[G/T]AAAGAAGTCAGAATC | 21745 |
rs36717650 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Tep1 | Mm_Celera | 14:50848044 | AAAGTGTACTGGAAA[A/T]TAAGACTACAAAACA | 21745 |
rs36717806 | snp | C/T | 0.231111 | 0.249285 | synonymous-codon | Tep1 | Mm_Celera | 14:50844062 | GTCTGAAATCAGCTG[C/T]CCATTACGATCCACC | 21745 |
rs36717876 | snp | A/G | 0.336735 | 0.234472 | upstream-variant-2KB, intron-variant | Tep1, Gm26782 | Mm_Celera | 14:50871119 | AGGCTCTGGCAGGAA[A/G]ATCAAAGAGTTAACT | 21745 |
rs36733741 | snp | G/T | 0.336735 | 0.234472 | upstream-variant-2KB, intron-variant | Tep1, Gm26782 | Mm_Celera | 14:50871086 | TGGTGGCACACACAT[G/T]TAATCCTAGTACTTA | 21745 |
rs36770495 | snp | C/T | 0.132653 | 0.220748 | intron-variant, upstream-variant-2KB | Tep1, Gm26782 | Mm_Celera | 14:50869065 | ACCTGTCTAGAATCA[C/T]AGCTGAAAAGGAGAC | 21745 |
rs36783629 | snp | G/T | 0.48 | 0.0979796 | missense | Tep1 | Mm_Celera | 14:50824758 | GCTGTGCCTTTAAAT[G/T]TGTGGGATCAATCCA | 21745 |
rs36793910 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tep1 | Mm_Celera | 14:50850562 | CTGTCTTCAGACGCC[A/G]TACAAGAACAACCAG | 21745 |
rs36797268 | snp | C/T | 0.244898 | 0.249948 | downstream-variant-500B | Tep1 | Mm_Celera | 14:50823831 | CCTTTCATGACCAAA[C/T]GAGAATTCCTCAGGT | 21745 |
rs36817866 | snp | C/T | 0.396694 | 0.202437 | intron-variant | Tep1 | Mm_Celera | 14:50825870 | GTGAGGTACCTGCAC[C/T]ATGCACCATGACAGA | 21745 |
rs36871246 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Tep1 | Mm_Celera | 14:50861318 | AAGAACTCCACAACA[A/G]ATCCAGAGAGCGCAA | 21745 |
rs36872028 | snp | A/G | 0.277778 | 0.248452 | synonymous-codon | Tep1 | Mm_Celera | 14:50837622 | AAGCTCTAGGTGCCC[A/G]TCGAAGGTAGTAAGG | 21745 |
rs36890818 | snp | A/C | 0.5 | 0 | missense | Tep1 | Mm_Celera | 14:50824780 | ATCAATCCAGCAATC[A/C]ATGGAAAAATCCAAC | 21745 |
rs36898769 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Tep1 | Mm_Celera | 14:50855519 | TGACTGCTTCAGGCA[C/T]GTGGAAGAGTCTGGC | 21745 |
rs36951408 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Tep1 | Mm_Celera | 14:50838775 | TGCCTCTTTCTCTGC[A/C]TCTCTGCCTGCACCC | 21745 |
rs36984396 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tep1 | GRCm38.p3 | 14:50838922 | CTCTGAAAGGCTTAC[C/T]ACAGCTAGGCTCAAG | 21745 |
rs37011229 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Tep1 | Mm_Celera | 14:50861351 | CAGTATGGGTAACAT[A/G]GTAGAACACGTCAAA | 21745 |
rs37018435 | snp | A/G | 0.32 | 0.24 | intron-variant | Tep1 | Mm_Celera | 14:50837724 | CTGAAACGGCCAGTC[A/G]GGAAGTGTGGCTCAG | 21745 |
rs37041046 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Tep1 | Mm_Celera | 14:50834312 | TGGCGGAACTCAGTC[A/G]AGTGTGGCTCCGTGT | 21745 |
rs37078003 | snp | G/T | 0.260355 | 0.249785 | intron-variant | Tep1 | Mm_Celera | 14:50851664 | ATCACTAAAGATTTA[G/T]GAGCACAGCCCTTTC | 21745 |
rs37100962 | snp | A/G | 0.231111 | 0.249285 | intron-variant, utr-variant-3-prime | Tep1 | Mm_Celera | 14:50841077 | AAGAACAGACATTGA[A/G]AAGGGCTTCCCACTG | 21745 |
rs37130257 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Tep1 | Mm_Celera | 14:50862156 | ACAATCACAACTGAG[A/G]ACACCCAGGTAGGAG | 21745 |
rs37148067 | snp | A/G | 0.5 | 0 | intron-variant | Tep1 | Mm_Celera | 14:50825562 | TACTTATCATGTTCT[A/G]CTTTCTGCTGTCATG | 21745 |
rs37150108 | snp | A/C | 0.32 | 0.24 | intron-variant | Tep1 | Mm_Celera | 14:50825905 | CGGTGTAGCCCTTGA[A/C]CTTAAAATGCTAATA | 21745 |
rs37157466 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Tep1 | Mm_Celera | 14:50855808 | GGGAGAATGCAATCT[A/G]CTCTACTCAAAAGAT | 21745 |
rs37162179 | snp | A/G | 0.391111 | 0.206368 | synonymous-codon | Tep1 | Mm_Celera | 14:50841571 | CCTGCGTAGACTCTG[A/G]ACAAGGTAGGCAAAT | 21745 |
rs37179640 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Tep1 | GRCm38.p3 | 14:50838900 | CTCTTTCTCTGAAGG[A/G]CCGCTGCTCTGAAAG | 21745 |
rs37198603 | snp | C/T | 0.5 | 0 | intron-variant | Tep1 | GRCm38.p3 | 14:50860798 | TGGAAAGAGCCAAAA[C/T]CAGCCAGTCATGTTC | 21745 |
rs37228247 | snp | G/T | 0.260355 | 0.249785 | intron-variant | Tep1 | Mm_Celera | 14:50852156 | CCTGTATTGATAGGT[G/T]ATGCCCAGCAAGATA | 21745 |
rs37233878 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tep1 | Mm_Celera | 14:50847875 | CAGTTCAGCGGCTCC[C/T]CTCAGGAAGACAGCC | 21745 |
rs37253682 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Tep1 | Mm_Celera | 14:50866583 | TTAGGAAGCAGGAAA[C/T]GGGATCTTTTCCCTC | 21745 |
rs37254187 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Tep1 | Mm_Celera | 14:50844234 | GACAGCAACACAGCT[A/G]GCTAATCTTGAGGTA | 21745 |
rs37270215 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Tep1 | Mm_Celera | 14:50850897 | TAGGGTGGCATCAAA[A/G]AATCAGGGACAGCAG | 21745 |
rs37276671 | snp | C/T | 0.444444 | 0.157135 | missense | Tep1 | Mm_Celera | 14:50829017 | AGATCAGGTGACTGA[C/T]GCGGCCTGGAGCCTG | 21745 |
rs37283804 | snp | A/T | 0.396694 | 0.202437 | synonymous-codon | Tep1 | Mm_Celera | 14:50845122 | TGAGACCCGATGTGC[A/T]GCTTCTTCTGACTCA | 21745 |
rs37300322 | snp | A/G | 0.124444 | 0.216185 | intron-variant, downstream-variant-500B | Tep1 | Mm_Celera | 14:50840814 | CCTGGGAAAAGAACC[A/G]GAGGGAAGACAGCAG | 21745 |
rs37323864 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Tep1 | Mm_Celera | 14:50825882 | CACCATGCACCATGA[C/G]AGAGACACGGTGTAG | 21745 |
rs37354041 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tep1 | Mm_Celera | 14:50841416 | AACACATGTGCCAAC[A/G]TTCCCATTGCAGAAT | 21745 |
rs37360419 | snp | G/T | 0.408163 | 0.193609 | intron-variant | Tep1 | Mm_Celera | 14:50825508 | TGTGGCCATGTTTGT[G/T]ACTGGCTTCCTTTGC | 21745 |
rs37412844 | snp | C/T | 0.132653 | 0.220748 | missense | Tep1 | Mm_Celera | 14:50868233 | AGAGTAGCTAGACAT[C/T]GGTTTTCCAAAGAAA | 21745 |
rs37465458 | snp | A/G | 0.152778 | 0.230321 | missense | Tep1 | Mm_Celera | 14:50860976 | TGTGGATATGTAGAT[A/G]CTCTACCAACTTCTT | 21745 |
rs37587297 | snp | A/G | 0.197531 | 0.244432 | upstream-variant-2KB, intron-variant | Tep1, Gm26782 | Mm_Celera | 14:50871067 | CTGAAAATATGATTC[A/G]GAATGGTGGCACACA | 21745 |
rs37607539 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Tep1 | Mm_Celera | 14:50863948 | AACAGGCTGACAACT[A/G]GTTCTGATCTTCCTG | 21745 |
rs37644799 | snp | C/T | 0.32 | 0.24 | intron-variant | Tep1 | Mm_Celera | 14:50843898 | TCGCTGTGACATTTG[C/T]ACGAAGGGAACAGAA | 21745 |
rs37662768 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tep1 | Mm_Celera | 14:50827517 | TGCTGTCTTTTGCTT[C/T]CATCAGTAAGTTCTG | 21745 |
rs37709078 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Tep1 | Mm_Celera | 14:50840434 | AAAGGGTTTCCTAAG[A/G]ATCATTTGCTTACAT | 21745 |
rs37788397 | snp | A/G | 0.5 | 0 | intron-variant | Tep1 | Mm_Celera | 14:50837967 | GTTTGAGTCAGAAGA[A/G]AAAGCTGTGGCTCTC | 21745 |
rs37802990 | snp | A/G | 0.46281 | 0.131194 | intron-variant | Tep1 | Mm_Celera | 14:50825793 | GAAACAAGAGACCTT[A/G]GGAATCTTGGGAATG | 21745 |
rs38059474 | snp | G/T | 0.231111 | 0.249285 | missense | Tep1 | Mm_Celera | 14:50844331 | GTCTGAGGAGGTTGA[G/T]AGCAAGACACTGGTC | 21745 |
rs38080413 | snp | C/T | 0.35503 | 0.226867 | missense | Tep1 | Mm_Celera | 14:50855613 | GGAGTCTCTGGAGAA[C/T]GAGTTCATGGTGGCG | 21745 |
rs38089709 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tep1 | Mm_Celera | 14:50840170 | ATCACTAGGAATCCC[A/G]CCTGGACTCCATTAA | 21745 |
rs38116168 | snp | C/T | 0.244898 | 0.249948 | upstream-variant-2KB, intron-variant | Tep1, Gm26782 | Mm_Celera | 14:50870887 | TGTGCCCTTGGCTGA[C/T]CTTTGAAAGTCAGGC | 21745 |
rs38117083 | snp | C/T | 0.32 | 0.24 | intron-variant | Tep1 | Mm_Celera | 14:50839822 | CACTGCCCTGCGAGA[C/T]CTTTTCTCAATGGAG | 21745 |
rs38122976 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Tep1 | Mm_Celera | 14:50824422 | ACTTTCATTTCGTTG[A/C]CACGCCTTAGCCTGC | 21745 |
rs38164677 | snp | A/G | 0.244898 | 0.249948 | synonymous-codon | Tep1 | Mm_Celera | 14:50868133 | GTTGCTAGTTTTCAG[A/G]CTATGCAGATCAGCT | 21745 |
rs38168673 | snp | C/T | 0.375 | 0.216506 | intron-variant | Tep1 | Mm_Celera | 14:50825850 | CAGTTAAGCATAAAG[C/T]ATCTGTGAGGTACCT | 21745 |
rs38206405 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Tep1 | Mm_Celera | 14:50845408 | AACCTGGTAGCAACA[A/G]GAGGTACCTAAGGAA | 21745 |
rs38238190 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Tep1 | Mm_Celera | 14:50830550 | GGAATACATTTCTTT[C/T]CCTGCTAACCTCCAT | 21745 |
rs38265020 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Tep1 | Mm_Celera | 14:50855741 | CAAGTGAGTGACACA[C/T]ACAAAGTTATAGTCC | 21745 |
rs38311897 | snp | A/C | 0.336735 | 0.234472 | intron-variant | Tep1 | Mm_Celera | 14:50861199 | TCTCTAAAACATATG[A/C]TGACAAAGAATAGAA | 21745 |
rs38369901 | snp | G/T | 0.132653 | 0.220748 | missense | Tep1 | Mm_Celera | 14:50863639 | TGTCCCGGAGGTTAA[G/T]TTGCTGCCGAGCATA | 21745 |
rs38469197 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Tep1 | Mm_Celera | 14:50825819 | GAATGAAATCTAGCT[C/T]TGACAGAATCCCAAA | 21745 |
rs38475146 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Tep1 | Mm_Celera | 14:50860385 | AAAGCAAATTCCAGG[A/G]TCTACAGTGGTGCGG | 21745 |
rs38500303 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon | Tep1 | Mm_Celera | 14:50851988 | GGGCCACTCATCATT[A/G]CCTTCTAACTCCTGA | 21745 |
rs38753083 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Tep1 | Mm_Celera | 14:50854457 | TGAAAATACCTGAGC[A/G]TTGTCTCATTTACAA | 21745 |
rs38966278 | snp | A/T | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Tep1, Gm26782 | GRCm38.p3 | 14:50869590 | ATCCGCATATGCACA[A/T]ACTCTTGCACACACA | 21745 |
rs39057684 | snp | C/T | 0.375 | 0.216506 | downstream-variant-500B | Tep1 | Mm_Celera | 14:50823838 | TGACCAAACGAGAAT[C/T]CCTCAGGTCTCTTCA | 21745 |
rs39207525 | snp | A/T | 0.5 | 0 | intron-variant | Tep1 | Mm_Celera | 14:50825509 | GTGGCCATGTTTGTG[A/T]CTGGCTTCCTTTGCA | 21745 |
rs39260164 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Tep1 | Mm_Celera | 14:50843299 | AGGATTCAGCATTAT[G/T]CAGGAGATTAGGGAA | 21745 |
rs39348169 | snp | G/T | 0.277778 | 0.248452 | intron-variant | Tep1 | Mm_Celera | 14:50852946 | GTTCTGTCACTTATA[G/T]ATTTCTGAACAGCAG | 21745 |
rs39649413 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Tep1 | Mm_Celera | 14:50851909 | AGTTTCATAGGAATC[G/T]AGTAGGACTCACGGG | 21745 |
rs39657331 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Tep1 | Mm_Celera | 14:50855585 | TCCCCAGGGATCACT[C/T]GTACCTCATGCTGGA | 21745 |
rs39717625 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Tep1 | Mm_Celera | 14:50826587 | AGTCCTCCTAGGTGT[C/T]TGACTTAAAAAAAAC | 21745 |
rs45637568 | snp | A/G | | | synonymous-codon | Tep1 | Mm_Celera | 14:50824777 | GGGATCAATCCAGCA[A/G]TCAATGGAAAAATCC | 21745 |
rs45778746 | snp | G/T | | | intron-variant | Tep1 | Mm_Celera | 14:50838375 | CCCGCTGCTGAATGA[G/T]CCTTTGACTAAGATG | 21745 |
rs45818181 | snp | C/T | | | downstream-variant-500B | Tep1 | Mm_Celera | 14:50823945 | CAGGAATAGAATCTG[C/T]GTGTTAAAGATGCTC | 21745 |
rs45835103 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50857572 | CAAGATCTGACTCCC[C/T]CTTCTGGTGTGTCTG | 21745 |
rs45881823 | snp | C/T | | | upstream-variant-2KB, intron-variant | Tep1, Gm26782 | Mm_Celera | 14:50870696 | CACAGTTTAGGGATT[C/T]ATACTTCCGGCTAGG | 21745 |
rs45973203 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50834370 | CAGCTGTGGCAGAGG[C/T]ATTTTCTCAAGGCCT | 21745 |
rs46095782 | snp | A/T | | | upstream-variant-2KB, intron-variant | Tep1, Gm26782 | Mm_Celera | 14:50871332 | TGCCCCTGCCTCCCA[A/T]CTCCTGGGATTTAAA | 21745 |
rs46328918 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50857197 | AAAGTGGAGGTTGTA[A/G]GTTTTCCTTTGAATC | 21745 |
rs46345513 | snp | G/T | | | upstream-variant-2KB, intron-variant | Tep1, Gm26782 | GRCm38.p3 | 14:50872220 | AAATAAATGTGTGTG[G/T]GGGGGGGAGAGAGAG | 21745 |
rs46347982 | snp | A/G | | | intron-variant | Tep1 | GRCm38.p3 | 14:50839396 | GGGCAGAGGCAGGTA[A/G]ATTTCTGAGTTCGAG | 21745 |
rs46388917 | snp | G/T | | | intron-variant, downstream-variant-500B | Tep1 | Mm_Celera | 14:50840888 | CGGGTGGGGTTGGTG[G/T]GAAAGGGAAGAGCAA | 21745 |
rs46399478 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50834173 | GGAGCAGAGCCCAGC[A/G]CCCACCCGAGTAAAG | 21745 |
rs46499642 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50839797 | TGCTGGGATTAAAGG[C/T]GTGCGCCACCACTGC | 21745 |
rs46665657 | snp | C/T | | | upstream-variant-2KB, intron-variant | Tep1, Gm26782 | Mm_Celera | 14:50871534 | TTTTTGCAGAAGGCC[C/T]AGGTTCAGTACCCAG | 21745 |
rs46670691 | snp | C/G | | | intron-variant | Tep1 | GRCm38.p3 | 14:50839525 | CACATGCACCTGTAA[C/G]CCCAGTGCTGGTGCC | 21745 |
rs46692889 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50838353 | TTACAAGTGTGAACT[A/G]TCATACCCCGCTGCT | 21745 |
rs46791292 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50832450 | AGAGGGCAACAGATC[C/T]CATTACAGATGGTTG | 21745 |
rs46917989 | snp | C/G | | | missense | Tep1 | Mm_Celera | 14:50837696 | CACAGCCACTCACCA[C/G]AGCCTTCTCCTCCTG | 21745 |
rs46961352 | snp | A/T | | | upstream-variant-2KB, intron-variant | Tep1, Gm26782 | Mm_Celera | 14:50870917 | CCCCTTCTCTCCCTT[A/T]TGCTTCCTTTCATCC | 21745 |
rs47045763 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50852463 | TTTCATTAGGGCAAG[A/G]AAAGACTAATATAAT | 21745 |
rs47168371 | snp | C/G | | | intron-variant | Tep1 | Mm_Celera | 14:50834277 | CACAGCATGGGAGCG[C/G]CCTGTGCCAAGCTTC | 21745 |
rs47219423 | snp | G/T | | | upstream-variant-2KB, intron-variant | Tep1, Gm26782 | Mm_Celera | 14:50872463 | GACAAAACAACTTGG[G/T]GAAGAAAAGGTTTAT | 21745 |
rs47258756 | snp | A/C | | | intron-variant | Tep1 | Mm_Celera | 14:50853207 | AGCTCTAGAGGCCAA[A/C]CGCCTGGTTTGGGGA | 21745 |
rs47270124 | snp | A/T | | | upstream-variant-2KB, intron-variant | Tep1, Gm26782 | Mm_Celera | 14:50872428 | CTATTGCTGTGGTTT[A/T]AAAAAAAAATGAACA | 21745 |
rs47353738 | snp | A/C | | | intron-variant | Tep1 | Mm_Celera | 14:50838362 | TGAACTGTCATACCC[A/C]GCTGCTGAATGAGCC | 21745 |
rs47421021 | snp | A/G | | | intron-variant | Tep1 | GRCm38.p3 | 14:50839252 | AATAGCTGAGGAGAT[A/G]ACTCAGGGAGTTGAA | 21745 |
rs47482605 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50828860 | AAAATGCTAGGCGTG[C/T]GTGGCTTGCCATGCG | 21745 |
rs47489887 | snp | G/T | | | intron-variant | Tep1 | Mm_Celera | 14:50862285 | TGTCCTGGAACTCGC[G/T]CTGTAGACCAGGCTG | 21745 |
rs47508175 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50824626 | TCGGAAAGGAGGGGA[A/G]CAACATGAGTTCTCA | 21745 |
rs47629129 | snp | A/G | | | upstream-variant-2KB, intron-variant | Tep1, Gm26782 | Mm_Celera | 14:50871637 | CTTGGCATGAAGGTG[A/G]TGCACAGACATACAT | 21745 |
rs47637222 | snp | A/T | | | intron-variant | Tep1 | Mm_Celera | 14:50848752 | GACTTTTGTTTTTTT[A/T]AAATTGTTTTAAAAA | 21745 |
rs47661654 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50837797 | AGGGGTTTAAGTCCT[C/T]GGCTGTCTACATTCC | 21745 |
rs47786665 | snp | A/C | | | intron-variant | Tep1 | Mm_Celera | 14:50828880 | CTTGCCATGCGCAGC[A/C]GCCGCCGCCGCCGCC | 21745 |
rs47839772 | snp | A/G | | | downstream-variant-500B | Tep1 | Mm_Celera | 14:50823948 | GAATAGAATCTGCGT[A/G]TTAAAGATGCTCATG | 21745 |
rs47909718 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50828200 | TCTGAGTTTGATTCC[A/G]GCCTGATCTACAGAG | 21745 |
rs48082100 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50829049 | GAACGAAGCAGGTTC[A/G]GTTGAGGACTTTTGA | 21745 |
rs48149789 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50855257 | AGAGCTGTCGGTGCC[C/T]TTACCCACCTCAAGC | 21745 |
rs48153708 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50824322 | AACGGGGGAAGTGAA[A/G]CTATAGGCCTGAGGT | 21745 |
rs48178131 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50832662 | GACCCCTTGAGGGGT[C/T]AAACAACCCTTTCAC | 21745 |
rs48203846 | snp | A/G | | | missense | Tep1 | Mm_Celera | 14:50824890 | TCCATTCTCCCTCTG[A/G]GGTACATTCAGATAA | 21745 |
rs48356288 | snp | C/G | | | intron-variant | Tep1 | Mm_Celera | 14:50824467 | ACTAGCCCTTTCTCC[C/G]CTTGTGTGCACGTGT | 21745 |
rs48361910 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50862306 | GACCAGGCTGGCCTC[A/G]AACTCAGAAATCCGC | 21745 |
rs48398606 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50866251 | TCCAGCTCCAGAGTG[C/T]GGGACAGATGCAGGG | 21745 |
rs48422772 | snp | C/T | | | upstream-variant-2KB, intron-variant | Tep1, Gm26782 | Mm_Celera | 14:50870916 | GCCCCTTCTCTCCCT[C/T]TTGCTTCCTTTCATC | 21745 |
rs48533832 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50834632 | TCTCTCCAGTTTCAA[A/G]TTTGTGTAAACATTG | 21745 |
rs48699327 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50838403 | ATGTCTAATATGATA[A/G]GAGTTGAATGAAGTT | 21745 |
rs48766532 | snp | G/T | | | intron-variant | Tep1 | Mm_Celera | 14:50825211 | AGTTCATGACACAAC[G/T]CCACTATCAAAGCTC | 21745 |
rs48816874 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50858234 | TCATATATTTGAATG[A/G]TGTTTGAAAAGATTA | 21745 |
rs48837339 | snp | A/G/T | | | intron-variant | Tep1 | GRCm38.p3 | 14:50842674 | CTATACCCGTGAACT[A/G/T]TGAGCAAGAAATGCT | 21745 |
rs48887414 | snp | A/G | | | synonymous-codon | Tep1 | Mm_Celera | 14:50836864 | GTTTGTTGAATGCCA[A/G]ACTACAGACAGAGGG | 21745 |
rs48992570 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50834109 | AAAAGGAAGCAAGTA[C/T]CTTCTAAAAGCAGAA | 21745 |
rs49053367 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50834445 | TCAGGGGACTAGTAC[C/T]GTCTTCCTCCTCCCA | 21745 |
rs49084995 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50843684 | TACCCCACATCTCCA[C/T]GAGCCCTGGTCTGGG | 21745 |
rs49150904 | snp | A/C | | | intron-variant | Tep1 | Mm_Celera | 14:50838102 | AAAGTTCTCTTGTAT[A/C]TACACAACTCTCATA | 21745 |
rs49156094 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50842645 | GCTCCTCTTGGCTTC[C/T]TCACCATGAGGAACT | 21745 |
rs49547420 | snp | A/G | | | missense | Tep1 | Mm_Celera | 14:50868273 | GATGACTAGACATAT[A/G]TCCACATAGCTTCTC | 21745 |
rs49727650 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50828400 | CACTGACTGCTCTTC[C/T]AGAGGTCCTAAGTTC | 21745 |
rs49858981 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50840359 | TGAAATTTTAACAAA[C/T]CTCCTAGATAATTTA | 21745 |
rs49885279 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50844495 | TCCCGGATCTACCTC[C/T]TTAGCCCCAAAGCTC | 21745 |
rs49886696 | snp | A/T | | | intron-variant | Tep1 | Mm_Celera | 14:50825208 | TTTAGTTCATGACAC[A/T]ACGCCACTATCAAAG | 21745 |
rs49941509 | snp | A/G | | | upstream-variant-2KB, intron-variant | Tep1, Gm26782 | Mm_Celera | 14:50871324 | GATCCGCCTGCCCCT[A/G]CCTCCCATCTCCTGG | 21745 |
rs49964384 | snp | A/T | | | intron-variant | Tep1 | Mm_Celera | 14:50828292 | ATAAATAAAAACAAT[A/T]CATTGATACCACACT | 21745 |
rs49981340 | snp | C/G | | | intron-variant | Tep1 | Mm_Celera | 14:50852462 | ATTTCATTAGGGCAA[C/G]GAAAGACTAATATAA | 21745 |
rs50006398 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50835785 | TAAAACCCCAGAGGA[A/G]CAAAGCATAGGCAAT | 21745 |
rs50087305 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50826735 | GCTCGCCTTACACTC[C/T]ATGGTGGATTCCAAG | 21745 |
rs50116580 | snp | A/G | | | intron-variant | Tep1 | GRCm38.p3 | 14:50839381 | ATTTCAGTGCTTGGG[A/G]GGCAGAGGCAGGTAA | 21745 |
rs50229514 | snp | A/G | | | synonymous-codon | Tep1 | Mm_Celera | 14:50824786 | CCAGCAATCAATGGA[A/G]AAATCCAACTCTGAG | 21745 |
rs50267514 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50852616 | TAGTCTTGACTAGAA[C/T]CCACTATGTAAGTAA | 21745 |
rs50319000 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50824479 | TCCGCTTGTGTGCAC[A/G]TGTGCACACAGAGAC | 21745 |
rs50464981 | snp | A/G | | | upstream-variant-2KB, intron-variant | Tep1, Gm26782 | Mm_Celera | 14:50871180 | TCTTTTTGTTACTGC[A/G]ACAAACTACCTGAGA | 21745 |
rs50478675 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50830820 | GGAATCAAGCTCCTC[C/T]CTCTTTCAGCCCTTA | 21745 |
rs50617145 | snp | A/G | | | upstream-variant-2KB, intron-variant | Tep1, Gm26782 | Mm_Celera | 14:50872461 | CTGACAAAACAACTT[A/G]GGGAAGAAAAGGTTT | 21745 |
rs50679219 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50839728 | GTCCTGGAACTCACT[C/T]TGTAGACCAGGCTGG | 21745 |
rs50726710 | snp | A/C | | | intron-variant | Tep1 | Mm_Celera | 14:50834286 | GGAGCGCCCTGTGCC[A/C]AGCTTCTGCATGGCG | 21745 |
rs50843569 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50838363 | GAACTGTCATACCCC[A/G]CTGCTGAATGAGCCT | 21745 |
rs51019071 | snp | C/T | | | missense | Tep1 | GRCm38.p3 | 14:50824820 | GGGGACAACTCTGTC[C/T]CCAGAGTCTGAGTTT | 21745 |
rs51145688 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50828283 | ACAAAACAAATAAAT[A/G]AAAACAATTCATTGA | 21745 |
rs51150975 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50856572 | TTTCCCCACCCACTT[A/G]ATGGAAGGAGAGAAC | 21745 |
rs51229227 | snp | C/T | | | intron-variant | Tep1 | GRCm38.p3 | 14:50839394 | GGGGGCAGAGGCAGG[C/T]AAATTTCTGAGTTCG | 21745 |
rs51250730 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50826736 | CTCGCCTTACACTCC[A/G]TGGTGGATTCCAAGG | 21745 |
rs51411668 | snp | A/T | | | synonymous-codon | Tep1 | Mm_Celera | 14:50825057 | CTTCTCCCACTAACC[A/T]GACTCAGGTTTGGCC | 21745 |
rs51432470 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50856460 | AACTCACTTTGTAGA[C/T]CAGGCTGGCCTTGAA | 21745 |
rs51466176 | snp | G/T | | | missense | Tep1 | Mm_Celera | 14:50868261 | AAAGGACGTCTGGAT[G/T]ACTAGACATATGTCC | 21745 |
rs51573713 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50857240 | ACTCAATGCCAAGTG[C/T]TCAGCCTTGAAATCA | 21745 |
rs51783603 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50861888 | TCTCAACCTCCACAT[A/G]GTGACTCACAAATGT | 21745 |
rs51815909 | snp | A/C | | | intron-variant | Tep1 | Mm_Celera | 14:50828293 | TAAATAAAAACAATT[A/C]ATTGATACCACACTG | 21745 |
rs51974639 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50856378 | CAATATACTCTTCTT[C/T]TTTTTTTTTTTTTTT | 21745 |
rs52072619 | snp | G/T | | | intron-variant | Tep1 | Mm_Celera | 14:50852623 | GACTAGAATCCACTA[G/T]GTAAGTAAAGCTGAC | 21745 |
rs52082826 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50826602 | CTGACTTAAAAAaaa[C/T]tatacaactctgttt | 21745 |
rs52087062 | snp | C/T | | | intron-variant | Tep1 | GRCm38.p3 | 14:50848508 | ctctcgctctctctc[C/T]ctctccctctccctc | 21745 |
rs52117939 | snp | A/T | | | intron-variant | Tep1 | Mm_Celera | 14:50832566 | TAAAAAAAAACTAAG[A/T]CTTTAAAAACAAAAA | 21745 |
rs52129702 | snp | A/C | | | intron-variant | Tep1 | GRCm38.p3 | 14:50861406 | AGTTCTTTGGGTCCC[A/C]AAAGAAaaagaaaga | 21745 |
rs52133731 | snp | A/T | | | intron-variant | Tep1 | Mm_Celera | 14:50832553 | AAATAATTCTTTTTA[A/T]AAAAAAACTAAGACT | 21745 |
rs52157863 | snp | G/T | | | intron-variant | Tep1 | Mm_Celera | 14:50852716 | AGTTACCATGCCCAG[G/T]TTATATGCTAGAGAA | 21745 |
rs52177888 | snp | A/T | | | intron-variant | Tep1 | Mm_Celera | 14:50832552 | CAAATAATTCTTTTT[A/T]AAAAAAAACTAAGAC | 21745 |
rs52240205 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50827880 | TGTCTCGAAGAAGAA[A/G]AAAAAAAAAAAAAAC | 21745 |
rs52262310 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50854744 | CCATGGGGCTACAGG[A/G]AGGATGAGGAGCCAT | 21745 |
rs52278936 | snp | C/G | | | intron-variant | Tep1 | Mm_Celera | 14:50827848 | TCCAGGACAGCCAGG[C/G]CTACACAGAGAAACC | 21745 |
rs52296056 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50827852 | GGACAGCCAGGCCTA[C/T]ACAGAGAAACCCTGT | 21745 |
rs52321704 | snp | C/G | | | intron-variant | Tep1 | Mm_Celera | 14:50856911 | agagagagagagaga[C/G]agaCCAGACAGACAG | 21745 |
rs52348491 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50856420 | TTCGAGACAGGGTTT[C/T]TCTGTATAGTCCTGG | 21745 |
rs52372227 | snp | A/G | | | intron-variant | Tep1 | GRCm38.p3 | 14:50861521 | AAGAAAGAAAGAAAG[A/G]AAGAAAGAAAGAAAG | 21745 |
rs52380177 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50852801 | agagacagagcgaga[A/G]CGAGAAcactttgta | 21745 |
rs52443490 | snp | C/G/T | | | intron-variant | Tep1 | GRCm38.p3 | 14:50856837 | TCTTTATTCATCTCT[C/G/T]TGTGTGTGTGTGTGT | 21745 |
rs52469836 | snp | A/G | | | intron-variant | Tep1 | GRCm38.p3 | 14:50826520 | gaaggaaggaaggaa[A/G]gagagaaaaagagag | 21745 |
rs52476101 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50842449 | ATCTAATGTCCTCTT[C/T]TGACCTCTGTGGGCA | 21745 |
rs52493688 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50861546 | AGAAAGAAAGAAAGA[A/G]AGAGAGGAGAGAGAG | 21745 |
rs52503941 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50842457 | TCCTCTTCTGACCTC[C/T]GTGGGCACCAAGCAT | 21745 |
rs52528866 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50834793 | acacagagagagaag[A/G]TGGACgaggaaggag | 21745 |
rs52533156 | snp | A/T | | | intron-variant | Tep1 | Mm_Celera | 14:50834847 | AAGAGAAGCAAGCCA[A/T]GAGGAGAGAGTGTGA | 21745 |
rs52551070 | snp | C/T | | | intron-variant | Tep1 | GRCm38.p3 | 14:50854710 | TGAGGAGCCATGGGG[C/T]TACAGGGAGGATGAG | 21745 |
rs108172806 | snp | A/T | | | intron-variant | Tep1 | Mm_Celera | 14:50826574 | ACGAAGGAGAGAAAG[A/T]CCTCCTAGGTGTCTG | 21745 |
rs211701007 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50862064 | GACATTTTAAATTCA[C/T]GGATCCAGCTGGATA | 21745 |
rs211756027 | in-del | -/C | | | intron-variant, upstream-variant-2KB | Tep1, Gm26782 | Mm_Celera | 14:50869910 | ACATGTAATTTTTTT[-/C]CCTCTCTGGAGTTTA | 21745 |
rs211787892 | snp | A/G | | | synonymous-codon | Tep1 | Mm_Celera | 14:50862905 | CCGATGTTTCCGTGG[A/G]TTGTACTTAGCTAGC | 21745 |
rs211893593 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50855933 | TATGTCACTAACTGT[C/T]GGCTCTACTTGCTGG | 21745 |
rs212027946 | in-del | -/A | | | intron-variant | Tep1 | Mm_Celera | 14:50828529 | AGTAAATAAATGTTT[-/A]AAAAAAAAAACCTTT | 21745 |
rs212061381 | snp | C/T | | | upstream-variant-2KB, intron-variant | Tep1, Gm26782 | Mm_Celera | 14:50872166 | CTCTTAAGTCCCACC[C/T]ACTAAATATTAAATG | 21745 |
rs212165421 | snp | A/C | | | intron-variant | Tep1 | Mm_Celera | 14:50828883 | GCCATGCGCAGCAGC[A/C]GCCGCCGCCGCCTCG | 21745 |
rs212264288 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50856794 | AAGCATGCACCACCA[C/T]TCCCAGGTTTTCTTC | 21745 |
rs212352722 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50837223 | AAAGGAGAAACCAGG[A/G]TAGGTGCTGGACACA | 21745 |
rs212444101 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50837723 | CCTGAAACGGCCAGT[C/T]GGGAAGTGTGGCTCA | 21745 |
rs212476214 | snp | C/G | | | intron-variant | Tep1 | Mm_Celera | 14:50828377 | AGAGATGGCTCAGAG[C/G]TTAAGAACACTGACT | 21745 |
rs212517996 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50825677 | GACTATGTATACTTC[C/T]TTCACTTAAGTACAT | 21745 |
rs212519135 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50824723 | TATGACCCCTCCCTC[C/T]AAGCTCACCTTTTTA | 21745 |
rs212553831 | snp | A/G | | | synonymous-codon | Tep1 | Mm_Celera | 14:50845475 | AGGCTGCGAGCGTTG[A/G]CCACGGTTCAGGAAT | 21745 |
rs212560791 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50832943 | GGCAGAGGGGCTTTC[C/T]TCTCAGAATGTTTCT | 21745 |
rs212589690 | in-del | -/C | | | intron-variant | Tep1 | GRCm38.p3 | 14:50847318 | AAACAATCAAGCAAG[-/C]CCCATGTGAAAAGCC | 21745 |
rs212676037 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50850501 | CAAGATACAAAACAT[C/T]AAACAAGTGAGACTT | 21745 |
rs212754556 | snp | A/T | | | intron-variant | Tep1 | Mm_Celera | 14:50840349 | TCTTAGAATCTGAAA[A/T]TTTAACAAACCTCCT | 21745 |
rs212977862 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50842852 | GTTTCAATCTGCTTG[C/T]GTCCTGGGAACTTGG | 21745 |
rs213036232 | in-del | -/GAGAGAGT | | | intron-variant | Tep1 | Mm_Celera | 14:50839226 | AGAGAGAGAGAGAGA[-/GAGAGAGT]GAGAATAGCTGAGGA | 21745 |
rs213045047 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50825830 | AGCTCTGACAGAATC[C/T]CAAACAGTTAAGCAT | 21745 |
rs213065744 | snp | C/G | | | intron-variant | Tep1 | Mm_Celera | 14:50859472 | AGGTCATACCTCCTA[C/G]TAGTGCCACTCCCTG | 21745 |
rs213068149 | snp | C/T | | | synonymous-codon | Tep1 | Mm_Celera | 14:50844026 | CCTCACACTCACCCG[C/T]GGAAGAGACTTGGGG | 21745 |
rs213103681 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | Tep1, Gm26782 | Mm_Celera | 14:50870550 | AACACCCTAGTGAGG[C/T]CAAGGGGTGAGGCTG | 21745 |
rs213104296 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50835021 | ATATAATATGAAAAT[A/G]TAGTCTCTGTCTCAC | 21745 |
rs213117811 | snp | A/T | | | intron-variant | Tep1 | Mm_Celera | 14:50851813 | TTGGGAGATGGAGGC[A/T]GGAGAAGCAGGTATG | 21745 |
rs213154195 | snp | G/T | | | intron-variant | Tep1 | Mm_Celera | 14:50860467 | AAATTCACTGCACCA[G/T]TTTGTGGAAATCTTC | 21745 |
rs213197684 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50853369 | ATTAGCTAGCTAAAC[C/T]TGAAATGTTAGTATT | 21745 |
rs213198371 | snp | A/T | | | upstream-variant-2KB, intron-variant | Tep1, Gm26782 | Mm_Celera | 14:50871306 | TGGCTTCTGACTCAC[A/T]GAGATCCGCCTGCCC | 21745 |
rs213294849 | snp | G/T | | | intron-variant | Tep1 | Mm_Celera | 14:50857665 | ACAAAAAGGGAAACA[G/T]GAATTCGGCTGTGGA | 21745 |
rs213328143 | snp | A/G | | | synonymous-codon | Tep1 | Mm_Celera | 14:50854513 | AGAAAGAATACCTTT[A/G]CTTCTGAGCTGAGCC | 21745 |
rs213435473 | snp | C/G | | | intron-variant | Tep1 | Mm_Celera | 14:50848274 | CCAAAGAAAACTTGA[C/G]GAGAGGAAACAAACA | 21745 |
rs213435521 | snp | C/G | | | intron-variant | Tep1 | Mm_Celera | 14:50838703 | GAAAGCCAGTGGGAA[C/G]CAAGTTCTGCATCTC | 21745 |
rs213680566 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50866563 | TGAGAGGCTGAACAA[A/G]TAGATTAGGAAGCAG | 21745 |
rs213686751 | snp | A/G | | | synonymous-codon | Tep1 | Mm_Celera | 14:50860953 | GGCCTGGACGTGCTG[A/G]GCAGGCTTGTGGATA | 21745 |
rs213717001 | snp | A/T | | | intron-variant | Tep1 | Mm_Celera | 14:50865144 | AACCCTGACTAAGAC[A/T]TGAGGGCTGCTTTCT | 21745 |
rs213759002 | in-del | -/AA | | | intron-variant | Tep1 | Mm_Celera | 14:50828528 | AAGTAAATAAATGTT[-/AA]TAAAAAAAAAACCTT | 21745 |
rs213759758 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50867216 | AGCTTCTTCATTCAC[C/T]ATCACCTCCCTGAGA | 21745 |
rs213968074 | snp | A/C | | | intron-variant | Tep1 | Mm_Celera | 14:50829125 | AGCCCACAGAGGTTC[A/C]ATTAAGCACACGGGT | 21745 |
rs213993101 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50858936 | CTCACTATATCTTAA[C/T]TTGTAAATTGGTGGA | 21745 |
rs214108062 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50864218 | GGAAACCTCAGGGGA[A/G]ATACTCCCTAGATCT | 21745 |
rs214156120 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50857007 | CTGGAGCTGGAGTTA[C/T]AGGTAGTTATGAGCC | 21745 |
rs214165872 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50830019 | TATAATAGAGGGCTG[A/G]CCTAGCAAGCACCAG | 21745 |
rs214347369 | snp | A/T | | | upstream-variant-2KB, intron-variant | Tep1, Gm26782 | Mm_Celera | 14:50871386 | ACGCCCAGCAACAAA[A/T]TTTTTTAAATTTTGA | 21745 |
rs214364952 | in-del | -/A | | | intron-variant | Tep1 | Mm_Celera | 14:50829588 | ATGGGATAAAGACTT[-/A]ATAAGGTTACCCTGG | 21745 |
rs214537032 | in-del | -/G | | | intron-variant | Tep1 | Mm_Celera | 14:50859087 | ATAACAAACAACAAA[-/G]GGCATTTGGGCTCAA | 21745 |
rs214663030 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50855898 | ACAATGTGTATCGGA[C/T]AGCTGCTTATATAAC | 21745 |
rs214689827 | snp | C/T | | | downstream-variant-500B | Tep1 | Mm_Celera | 14:50823702 | GGTTTCCCACTCTGG[C/T]CAGTTAGTTCTGGGG | 21745 |
rs214749363 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50845242 | CTCAGACCCTCTGTC[C/T]CCTGTCATCAGCCAG | 21745 |
rs214817148 | snp | A/T | | | upstream-variant-2KB, intron-variant | Tep1, Gm26782 | Mm_Celera | 14:50872090 | AGAATCATTCAAAGT[A/T]GTAAGCACAAGAATG | 21745 |
rs214844820 | snp | C/G | | | intron-variant | Tep1 | Mm_Celera | 14:50862024 | TAAATATTTTTAAAG[C/G]TTTATATGGAGTGGA | 21745 |
rs214881728 | in-del | -/AGAGAGAGAGAC | | | intron-variant | Tep1 | Mm_Celera | 14:50856911 | GAGAGAGAGAGAGAG[-/AGAGAGAGAGAC]AGACCAGACAGACAG | 21745 |
rs214928514 | snp | A/G | | | downstream-variant-500B | Tep1 | Mm_Celera | 14:50823898 | TTCCTTCTGACAAGA[A/G]TGGACCTTAGAACTT | 21745 |
rs214989726 | in-del | -/AAAAAAAAAAAAAAAAAAAAAA | | | intron-variant | Tep1 | GRCm38.p3 | 14:50840525 | GGTATCCCATATCTC[-/AAAAAAAAAAAAAAAAAAAAAA]AAAAAAAAAGGCTCA | 21745 |
rs215007018 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50834231 | CAGAACGGGCAGAGG[C/T]CCTGGGCAAGAGTCA | 21745 |
rs215028328 | snp | C/T | | | intron-variant | Tep1 | GRCm38.p3 | 14:50858332 | GTGGGCTTTAAGGTT[C/T]TAAAAAATCCATACC | 21745 |
rs215033427 | snp | A/C | | | intron-variant | Tep1 | Mm_Celera | 14:50862776 | TGGATAGGAGCTCCC[A/C]AGCTCAACTTGTTCC | 21745 |
rs215066934 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50858850 | CAAACTAGTCCTCCT[C/T]CTGCCTCAGTCCCCA | 21745 |
rs215068542 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50848863 | AGTGGGGATCTAAAC[A/G]GAGAAGCACAGGTAA | 21745 |
rs215133547 | in-del | -/AGG | | | intron-variant | Tep1 | Mm_Celera | 14:50857933 | TACAGTCTCAACAGA[-/AGG]AGAATAGCTGAGAAC | 21745 |
rs215148686 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50850416 | CAGTATCTAATAGCA[C/T]ACAGGGGCAAAAAGA | 21745 |
rs215217516 | in-del | -/AATAAATAAAT | | | intron-variant | Tep1 | Mm_Celera | 14:50866480 | ATACTCATAGGCATA[-/AATAAATAAAT]AATAAATAAATAGGT | 21745 |
rs215259253 | snp | A/C | | | intron-variant | Tep1 | Mm_Celera | 14:50827691 | CAAGGAACTTTGCTT[A/C]TTGCCTTGTTTGACT | 21745 |
rs215281249 | in-del | -/CAGTAAACTCCAC | | | intron-variant | Tep1 | Mm_Celera | 14:50864558 | GTAGACTTACTACAA[-/CAGTAAACTCCAC]CAGCTGTATGCAACA | 21745 |
rs215315390 | snp | A/G | | | intron-variant, downstream-variant-500B | Tep1 | Mm_Celera | 14:50831314 | CACACATGATGTTGG[A/G]AATTGATCTCAGGTC | 21745 |
rs215348545 | snp | C/G | | | missense | Tep1 | Mm_Celera | 14:50841987 | GGCAGGGTTCGAAGT[C/G]TCTCAGACACCTGGC | 21745 |
rs215350112 | snp | A/T | | | intron-variant | Tep1 | Mm_Celera | 14:50854370 | TTCCCTTAGTATGTT[A/T]AACCCCTATCCTCAG | 21745 |
rs215607772 | in-del | -/G | | | upstream-variant-2KB, intron-variant | Tep1, Gm26782 | Mm_Celera | 14:50871857 | AATAAATATAAAAAT[-/G]AAAAACCCCTAAAGA | 21745 |
rs215629285 | snp | C/G | | | intron-variant | Tep1 | Mm_Celera | 14:50856928 | GACCAGACAGACAGA[C/G]AGAGAATACCACTTG | 21745 |
rs215676032 | snp | A/G | | | synonymous-codon | Tep1 | Mm_Celera | 14:50837161 | TGGATGGGTGTACTG[A/G]AAAGCCAGCTGTCCT | 21745 |
rs215739425 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50840247 | TCTGAGGGAGTATCA[C/T]CCTCTAAACTTCACA | 21745 |
rs215779943 | snp | A/C/G | | | downstream-variant-500B | Tep1 | GRCm38.p3 | 14:50824039 | TCTAAAATCACCAGC[A/C/G]AACACAATCGGGCAT | 21745 |
rs215789952 | snp | C/T | | | intron-variant, downstream-variant-500B | Tep1 | Mm_Celera | 14:50840916 | CAATCTAAGAACGGT[C/T]CAAGCAGACCGTTTA | 21745 |
rs215833013 | snp | G/T | | | intron-variant | Tep1 | Mm_Celera | 14:50832201 | GAAATGGCTACCATT[G/T]CAAAACTGTTCTAGC | 21745 |
rs215882362 | snp | C/G | | | intron-variant | Tep1 | Mm_Celera | 14:50863162 | CAAGACAAATCAGCA[C/G]TCTTCTCTAAGTGCA | 21745 |
rs215962801 | snp | C/G | | | intron-variant | Tep1 | Mm_Celera | 14:50833342 | TACATGCCCAGCAAG[C/G]GTTAGCACGACCATC | 21745 |
rs215980112 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50867001 | CTCTCCCTTTACCCC[A/G]GCTTGGTGCTCTTTA | 21745 |
rs216111500 | snp | C/T | | | intron-variant, upstream-variant-2KB | Tep1, Gm26782 | Mm_Celera | 14:50869128 | AGCAAATTCCAGGTC[C/T]ACGTGAGCACTGACA | 21745 |
rs216214386 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50860405 | CAGTGGTGCGGTAAA[C/T]GGCAAACTTCAAAAA | 21745 |
rs216446962 | in-del | -/CTACAAG | | | intron-variant | Tep1 | GRCm38.p3 | 14:50861633 | TCTTGTGTTTCACTC[-/CTACAAG]CTACAAGACTGACCT | 21745 |
rs216530728 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50855238 | CAAATCCAAGTCTTC[C/T]AGAAGAGCTGTCGGT | 21745 |
rs216620689 | snp | A/G | | | intron-variant, upstream-variant-2KB | Tep1, Gm26782 | Mm_Celera | 14:50870363 | GCACCACGCTCGCCC[A/G]GAGGTCCTTCCGGGA | 21745 |
rs216663641 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50833153 | CTGATGCACACAAAA[A/G]TGTAACGCTGATTAG | 21745 |
rs216695676 | snp | A/T | | | intron-variant | Tep1 | Mm_Celera | 14:50825245 | GACAGGATATATATG[A/T]CACAAAATATTAGTA | 21745 |
rs216864257 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50827628 | TAGGCCAGGAAACTC[A/G]TCATGTAAACCGCAC | 21745 |
rs216893117 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50866329 | GTTGGCTTCAAACTT[C/T]CATAGATCCACCTGC | 21745 |
rs216894294 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50846453 | GTTTCTTCCCCAGCT[C/T]CACCAACCTTGTCTG | 21745 |
rs216934034 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50862013 | CATAAAAAAGATAAA[C/T]ATTTTTAAAGCTTTA | 21745 |
rs217008656 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50855523 | TGCTTCAGGCATGTG[A/G]AAGAGTCTGGCCTCT | 21745 |
rs217035688 | in-del | -/A | | | intron-variant | Tep1 | Mm_Celera | 14:50860543 | AGGAACTGCCGATCG[-/A]ATCGATTGATTGATC | 21745 |
rs217165827 | snp | C/G | | | intron-variant | Tep1 | Mm_Celera | 14:50830114 | GGAGGAAGGGGAAAG[C/G]CTGGCAGTTTGATAC | 21745 |
rs217188769 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50831198 | GGCTTCCTGGTCTCC[C/T]TGGACACACATGGTA | 21745 |
rs217206195 | in-del | -/GGCACCAACAACT | | | intron-variant | Tep1 | Mm_Celera | 14:50853420 | CTAAAACTGTCCCAG[-/GGCACCAACAACT]GGCACTTGGAAGAAA | 21745 |
rs217240464 | in-del | -/GTGTGTGTGTGTGTGTGTGTGT | | | intron-variant | Tep1 | Mm_Celera | 14:50842479 | ACCAAGCATATACAA[-/GTGTGTGTGTGTGTGTGTGTGT]GTGTGTGTGTGTGTG | 21745 |
rs217257485 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50865354 | TAGCATACATAGTCT[C/T]ATTAGACTAAATAAG | 21745 |
rs217337495 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50866228 | ATTGGTTCATGACCT[C/T]CTTTAAATCCAGCTC | 21745 |
rs217340117 | snp | A/G | | | intron-variant, upstream-variant-2KB | Tep1, Gm26782 | Mm_Celera | 14:50868998 | TCTAAGGGGACAGGG[A/G]GGAAAAGGGAAAGCA | 21745 |
rs217421711 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50839633 | CAAAAACCAGTGAGC[A/G]CCAGATTCAGTAAGA | 21745 |
rs217426665 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50860388 | GCAAATTCCAGGGTC[C/T]ACAGTGGTGCGGTAA | 21745 |
rs217572927 | snp | G/T | | | intron-variant | Tep1 | Mm_Celera | 14:50867396 | AGGGGGAATATTAGC[G/T]TTGCCTAAGGCAAAC | 21745 |
rs217628968 | snp | A/C | | | intron-variant | Tep1 | Mm_Celera | 14:50829653 | CTCCCCCTCCCTCCC[A/C]CTTACTCACCTGCTT | 21745 |
rs217790394 | snp | A/T | | | intron-variant, utr-variant-3-prime | Tep1 | Mm_Celera | 14:50841130 | TGCAGCAGACTTATC[A/T]ACCCAGTGGCCAGTG | 21745 |
rs217880696 | snp | A/G | | | upstream-variant-2KB, intron-variant | Tep1, Gm26782 | Mm_Celera | 14:50871454 | ATCTATATAACCCCA[A/G]CTGGCCTGCAGCTCA | 21745 |
rs217881919 | snp | C/T | | | missense | Tep1 | Mm_Celera | 14:50860668 | GCTTCATCCGCTGAC[C/T]AGCTCTGCTAGACTC | 21745 |
rs217922213 | snp | A/T | | | intron-variant | Tep1 | Mm_Celera | 14:50852948 | TCTGTCACTTATATA[A/T]TTCTGAACAGCAGGG | 21745 |
rs217936998 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50834622 | TTATTCCAAATCTCT[C/T]CAGTTTCAAATTTGT | 21745 |
rs217962389 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50861403 | AGTAGTTCTTTGGGT[C/T]CCCAAAGAAAAAGAA | 21745 |
rs217976208 | snp | C/T | | | synonymous-codon | Tep1 | Mm_Celera | 14:50841890 | GACCTCAAGGGCAGT[C/T]AAAGCCTGAGGAAGG | 21745 |
rs217997358 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50826186 | ATCAAACAGTAGAAG[A/G]AGAGAACCAACCTCA | 21745 |
rs218213349 | snp | A/G | | | synonymous-codon | Tep1 | Mm_Celera | 14:50836020 | CATGAGTTCCCGGGA[A/G]GCAGCCAGTCCCAGC | 21745 |
rs218271293 | snp | C/G | | | intron-variant | Tep1 | Mm_Celera | 14:50837015 | GCGTGTTCTCCTGGA[C/G]AGCCGACGCAGGACC | 21745 |
rs218330594 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50864265 | TGTCTGGGAGGAGAT[C/T]GTCTTAATTATTATT | 21745 |
rs218371482 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50836497 | TTAAAGGTACTTCTC[C/T]GCCCCGTCCCTGCCC | 21745 |
rs218392924 | in-del | -/CCTTAGCCCT | | | intron-variant | Tep1 | Mm_Celera | 14:50837746 | TGGCTCAGGTGACTC[-/CCTTAGCCCT]CCAAATCCAACCCAT | 21745 |
rs218409121 | snp | C/G | | | missense | Tep1 | Mm_Celera | 14:50827090 | ACCCAGGCTTCATCT[C/G]TAGTAATTCCACATC | 21745 |
rs218486062 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50827744 | TGACTCTACCTGGGC[A/G]TGGTGGCGCATGCCT | 21745 |
rs218599137 | snp | A/G | | | missense | Tep1 | Mm_Celera | 14:50868111 | TAGGAAGCTCAGGGA[A/G]CAGGCAGTTGCTAGT | 21745 |
rs218606391 | snp | C/T | | | missense | Tep1 | Mm_Celera | 14:50844136 | GCTGCAGCGACTGAG[C/T]GAATTTGAGGAGCAA | 21745 |
rs218676353 | snp | A/C | | | intron-variant, upstream-variant-2KB | Tep1, Gm26782 | Mm_Celera | 14:50869437 | GTAAGGCTCAGTAGT[A/C]TATGACTGTAATCCC | 21745 |
rs218727003 | snp | C/T | | | intron-variant | Tep1 | GRCm38.p3 | 14:50839605 | ACTGGAGCTTGCTGG[C/T]CATCAGCCTAACCAA | 21745 |
rs218738544 | snp | A/C | | | intron-variant | Tep1 | GRCm38.p3 | 14:50839447 | GAGTTCCAGGACAGC[A/C]AGGGATACACAGAGA | 21745 |
rs218739280 | snp | C/T | | | synonymous-codon, utr-variant-3-prime | Tep1 | Mm_Celera | 14:50833475 | GTTGTCTTTGGTCCA[C/T]GCACAGCCAGTGATC | 21745 |
rs218806669 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50840153 | GGGTCAGAAAACACA[A/G]TATCACTAGGAATCC | 21745 |
rs218994461 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50857689 | CTGTGGAGCTAAATC[A/G]GTGTGGGATTATAGG | 21745 |
rs219044497 | snp | G/T | | | missense | Tep1 | Mm_Celera | 14:50847695 | TGTGTCTTTCCTGGG[G/T]GTGGGGGGATCTTGA | 21745 |
rs219074096 | snp | C/T | | | missense | Tep1 | Mm_Celera | 14:50846509 | TCAGGAAGATCATAG[C/T]TGGGGGGAATGTAGC | 21745 |
rs219147003 | in-del | -/ACACACACACACACAT | | | intron-variant | Tep1 | Mm_Celera | 14:50826268 | CAAACACACACACAC[-/ACACACACACACACAT]ACACACACACACAAA | 21745 |
rs219328106 | in-del | -/GA | | | upstream-variant-2KB, intron-variant | Tep1, Gm26782 | GRCm38.p3 | 14:50872227 | TGTGTGTGTGGGGGG[-/GA]GAGAGAGAGAGAGTT | 21745 |
rs219341978 | snp | A/C | | | intron-variant | Tep1 | Mm_Celera | 14:50845651 | TCTTGTGTCCTTCCC[A/C]GAAACACAGACCGTA | 21745 |
rs219379726 | in-del | -/T | | | intron-variant | Tep1 | Mm_Celera | 14:50830543 | GAACAATGGAATACA[-/T]TTCTTTCCCTGCTAA | 21745 |
rs219441244 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50851877 | AAGAGCAGGCTGTGG[A/G]GGAAATGCTAGGAGG | 21745 |
rs219448851 | in-del | -/AT | | | intron-variant | Tep1 | Mm_Celera | 14:50833290 | TTAACTGTGGCGATA[-/AT]ATGATTGAGCCTTTG | 21745 |
rs219675383 | snp | A/C | | | intron-variant | Tep1 | Mm_Celera | 14:50847982 | ATCATATAATGAGAC[A/C]CATCTCAAAAAGACT | 21745 |
rs219681503 | in-del | -/AA | | | intron-variant | Tep1 | Mm_Celera | 14:50842114 | AGGAATGAAGAGGTT[-/AA]AAAAAAAAACAAAAA | 21745 |
rs219704855 | snp | C/G | | | intron-variant | Tep1 | Mm_Celera | 14:50848998 | CACCAACTGAGCTGA[C/G]CTAGTTATAGTCTCT | 21745 |
rs220018247 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50853829 | CTCTCTCTCTCCTTA[C/T]GCACTATCCCATCCT | 21745 |
rs220033580 | snp | C/G | | | synonymous-codon | Tep1 | Mm_Celera | 14:50855644 | GGCACTGATCCCAGT[C/G]CGCAGCAGGTTACAC | 21745 |
rs220049063 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50842442 | CCTGAGGATCTAATG[C/T]CCTCTTCTGACCTCT | 21745 |
rs220374374 | snp | C/T | | | upstream-variant-2KB, intron-variant | Tep1, Gm26782 | Mm_Celera | 14:50872341 | ATGAGTCTACGATTC[C/T]TACCACAAGACTGAA | 21745 |
rs220508850 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50843147 | GGATGGAACCCAAAA[A/G]GGCCACCAGCAATGG | 21745 |
rs220789444 | snp | A/T | | | intron-variant | Tep1 | Mm_Celera | 14:50852069 | CTGGATGCTGTTTGA[A/T]TGTATCCTCCACTGG | 21745 |
rs220823808 | snp | A/C | | | synonymous-codon, intron-variant | Tep1 | Mm_Celera | 14:50841334 | CTCCACTGGGCCCTC[A/C]CCTAGTAAACTGTCC | 21745 |
rs220874273 | in-del | -/T | | | upstream-variant-2KB, intron-variant | Tep1, Gm26782 | Mm_Celera | 14:50871892 | AGTAATTTTAATAGA[-/T]TTTTGTTGTAGTTCC | 21745 |
rs220909565 | in-del | -/TAACAACACTCCTA | | | intron-variant | Tep1 | Mm_Celera | 14:50861272 | AGCTAAAGGCCCCGG[-/TAACAACACTCCTA]CAGCGTCAGCAACTT | 21745 |
rs220960770 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50858591 | CATGGTGTCTCTTCA[C/T]AGTAACAGAATTGTG | 21745 |
rs221069616 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50850885 | TACACCCCAACCTAG[A/G]GTGGCATCAAAGAAT | 21745 |
rs221095425 | snp | C/T | | | downstream-variant-500B | Tep1 | Mm_Celera | 14:50823967 | AAGATGCTCATGTTC[C/T]TGCAGTTCTCCTTAG | 21745 |
rs221228694 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50859343 | AAGCAGACTATGTTC[C/T]AGGCAGCAAGGAGTT | 21745 |
rs221282699 | in-del | -/TTT/TTTT/TTTTT | | | intron-variant | Tep1 | Mm_Celera | 14:50839671 | TCTCTTTTGTTTTTG[-/TTT/TTTT/TTTTT]TTTTTTTTTCCGAGA | 21745 |
rs221318058 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50861719 | TAGAAGATCCTCATT[C/T]TCTCAGAGAAGGAAA | 21745 |
rs221325442 | in-del | -/ATAA | | | intron-variant | Tep1 | Mm_Celera | 14:50866477 | CAAATACTCATAGGC[-/ATAA]ATAAATAAATAATAA | 21745 |
rs221365989 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50859966 | AGTCTATAACTCCAG[C/T]TCCGGGGTATTCGAT | 21745 |
rs221405463 | snp | A/C | | | intron-variant | Tep1 | Mm_Celera | 14:50855746 | GAGTGACACATACAA[A/C]GTTATAGTCCCCAGC | 21745 |
rs221469874 | in-del | -/AACAAA | | | intron-variant | Tep1 | Mm_Celera | 14:50832598 | AAAAACAACAACAAC[-/AACAAA]AAAAAAAAACCCCAG | 21745 |
rs221478300 | snp | G/T | | | intron-variant | Tep1 | Mm_Celera | 14:50852212 | TGGGAGACTCTGAGG[G/T]ATCTATCTGTTCCTG | 21745 |
rs221667659 | snp | A/G | | | synonymous-codon | Tep1 | Mm_Celera | 14:50824933 | CCCATCAGAGGTGGC[A/G]CACAAAAGGGATGAT | 21745 |
rs221712481 | snp | G/T | | | intron-variant | Tep1 | Mm_Celera | 14:50827912 | CTGAACTGATTCTAT[G/T]CTTTGTATGTACCTA | 21745 |
rs221904456 | in-del | -/TT | | | intron-variant | Tep1 | GRCm38.p3 | 14:50845717 | AACAGGTACTGGGTA[-/TT]TTTTTTTTAAGATTT | 21745 |
rs221906460 | snp | A/C | | | intron-variant | Tep1 | Mm_Celera | 14:50855767 | AGTCCCCAGCAGGAA[A/C]CACAGAGCCACACAG | 21745 |
rs221913077 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50851035 | TTTTTTAAATTTTTT[C/T]GTTTTTTGTTCTTGT | 21745 |
rs221916437 | in-del | -/TTT | | | intron-variant | Tep1 | Mm_Celera | 14:50847411 | CCCTACATACAGACA[-/TTT]TTTTTTTTTTCTCTC | 21745 |
rs222024119 | snp | G/T | | | synonymous-codon | Tep1 | Mm_Celera | 14:50846925 | TCTGGCCTGCAGTGC[G/T]GGCAGAACAGATCTC | 21745 |
rs222026464 | snp | G/T | | | intron-variant | Tep1 | Mm_Celera | 14:50857771 | TGGGTGACCACACGC[G/T]GAAGCATGATTTCAG | 21745 |
rs222251369 | snp | C/T | | | intron-variant | Tep1 | GRCm38.p3 | 14:50858396 | CCACTGCCCCCCTCC[C/T]CCTTTTACTCCCCTC | 21745 |
rs222342920 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50828572 | CCATATGCTGGTAAG[A/G]TGAGCCAATTCCCTC | 21745 |
rs222350615 | snp | G/T | | | intron-variant | Tep1 | Mm_Celera | 14:50838776 | GCCTCTTTCTCTGCA[G/T]CTCTGCCTGCACCCT | 21745 |
rs222352173 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50828759 | ACGGAGATCAATAAA[C/T]GCAATTTGAAAACAA | 21745 |
rs222385112 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50860098 | AAATAGACAATCAAC[A/G]GAGAAAGAAAAGACT | 21745 |
rs222387812 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50829335 | AAGAATACATTAAGA[A/G]CTCTGCACTGATCGC | 21745 |
rs222404467 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50863308 | ATAAGACCAACTTTT[C/T]CTCAAACTTTGATCC | 21745 |
rs222513560 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50831871 | GAAGAACAAGATCAT[C/T]TACATTCCTCTCACA | 21745 |
rs222543206 | snp | A/T | | | intron-variant | Tep1 | Mm_Celera | 14:50864667 | AAGTATATGTATATA[A/T]AATTGAGAAGTGGTG | 21745 |
rs222547372 | snp | A/C | | | intron-variant | Tep1 | Mm_Celera | 14:50832457 | AACAGATCCCATTAC[A/C]GATGGTTGTGAGCCA | 21745 |
rs222608057 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50857995 | AAAATAAAAGGGGGG[A/G]GGGGTAGAGAAATGT | 21745 |
rs222665629 | in-del | -/T | | | intron-variant | Tep1 | Mm_Celera | 14:50847412 | CCCTACATACAGACA[-/T]TTTTTTTTTCTCTCT | 21745 |
rs222694674 | snp | C/T | | | synonymous-codon | Tep1 | Mm_Celera | 14:50860609 | CACAGAAGCTTTGTT[C/T]CCCCGTAAACTCAGC | 21745 |
rs222737114 | snp | C/G | | | intron-variant | Tep1 | Mm_Celera | 14:50858987 | AATTTAATTCCCAGG[C/G]ATTTCTTATACAGAT | 21745 |
rs222770910 | snp | A/C | | | intron-variant | Tep1 | Mm_Celera | 14:50859845 | TTCTTAACTGCTAGG[A/C]CAACTCTCCACCCCC | 21745 |
rs222932649 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50853747 | AGACATAGACACGGG[A/G]CTCAGCAGCTTGTCT | 21745 |
rs223028479 | snp | A/T | | | intron-variant | Tep1 | Mm_Celera | 14:50866650 | TCTCCAGCCTCACCC[A/T]TCCCTCCACCATCAA | 21745 |
rs223028583 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50858024 | GTCTGAGCAGTTAAC[A/G]ACACTGGCTGCTCTT | 21745 |
rs223068528 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50858528 | AACTATAAGCAAGTC[C/T]ACTCACATCTACAAT | 21745 |
rs223135142 | snp | A/G | | | upstream-variant-2KB, intron-variant | Tep1, Gm26782 | Mm_Celera | 14:50870881 | TGAGAGTGTGCCCTT[A/G]GCTGACCTTTGAAAG | 21745 |
rs223272830 | in-del | -/AGAGAGAGAG | | | intron-variant | Tep1 | GRCm38.p3 | 14:50852751 | GAGAGAGAGGCAGAA[-/AGAGAGAGAG]AGAGAGAGAGAGACA | 21745 |
rs223290604 | in-del | -/AAAAAAAAAA | | | intron-variant, upstream-variant-2KB | Tep1, Gm26782 | Mm_Celera | 14:50869354 | TAGGAGACTTTGTCC[-/AAAAAAAAAA]AAAAAAAAAAGGTGG | 21745 |
rs223370547 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50862446 | TAGTGCAGACAGACA[A/G]ACAGACAGACAGACA | 21745 |
rs223453896 | snp | G/T | | | intron-variant | Tep1 | Mm_Celera | 14:50834447 | AGGGGACTAGTACCG[G/T]CTTCCTCCTCCCACT | 21745 |
rs223600755 | snp | A/C | | | intron-variant | Tep1 | Mm_Celera | 14:50825930 | CTAATACTGACAGAA[A/C]CCAAAAAAAAAAAAA | 21745 |
rs223610419 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50830719 | AAGAAGATACATTGT[A/G]GTAAATGACTTATGC | 21745 |
rs223719013 | in-del | -/G | | | upstream-variant-2KB, intron-variant | Tep1, Gm26782 | Mm_Celera | 14:50870586 | GGGAGGGGCGGGGCT[-/G]GGGGCAGGGCGGGGC | 21745 |
rs223808700 | in-del | -/AAA | | | intron-variant, upstream-variant-2KB | Tep1, Gm26782 | Mm_Celera | 14:50869202 | CCCTGTACTACAAGG[-/AAA]AAAAAAAAAAAGTAG | 21745 |
rs223811526 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50836491 | AAAAGTTTAAAGGTA[C/T]TTCTCTGCCCCGTCC | 21745 |
rs223842519 | snp | A/T | | | intron-variant | Tep1 | Mm_Celera | 14:50826956 | GACTGCCTCTCTTCA[A/T]GACCCCAGTGCTTTA | 21745 |
rs223876310 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50833056 | ATAGGTACAAAGGGA[A/G]CACTGACTACTTACT | 21745 |
rs223876455 | snp | A/C | | | intron-variant | Tep1 | Mm_Celera | 14:50842572 | AAAATGAATAGATTT[A/C]ATGATATTTTTAGAG | 21745 |
rs223958894 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50833812 | GCCTGCAGCTCTGGT[A/G]GATCAAAAAGTTCAA | 21745 |
rs223998415 | snp | C/T | | | missense | Tep1 | Mm_Celera | 14:50866820 | GCATTGGGACTTCTG[C/T]GCTTTCTTCTTCTTG | 21745 |
rs224157651 | snp | A/C | | | intron-variant | Tep1 | GRCm38.p3 | 14:50839452 | CCAGGACAGCCAGGG[A/C]TACACAGAGAAACCC | 21745 |
rs224180835 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50829365 | CTTAATAGTGGTGCA[C/T]TCCTTTAATCCTAGC | 21745 |
rs224199445 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50830446 | TGTATTGAGCATACT[C/T]CCCTCTCCAAACAAC | 21745 |
rs224209343 | snp | A/T | | | intron-variant | Tep1 | Mm_Celera | 14:50841778 | ATTATACATGACCCC[A/T]CCCAGCATCTCTGGC | 21745 |
rs224243753 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50862613 | AAATGGAAGTTGCTC[A/G]TTCCAGTAGCCCTGA | 21745 |
rs224248953 | snp | A/G | | | intron-variant, downstream-variant-500B | Tep1 | Mm_Celera | 14:50840774 | TGTTCAACCATGCCT[A/G]TGCATCTAGGACTTA | 21745 |
rs224287083 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50832000 | TGGGACCTTTCTCAT[A/G]TCTTTTTAAAAACAA | 21745 |
rs224399429 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50832515 | GGAAGAAGCAGCCAG[C/T]GCTCTTAACCACTCC | 21745 |
rs224449418 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50826085 | AGACAGGACAGCAAG[A/G]GCTGCACAGAAAGCC | 21745 |
rs224470607 | snp | C/T | | | upstream-variant-2KB, intron-variant | Tep1, Gm26782 | Mm_Celera | 14:50871313 | TGACTCACAGAGATC[C/T]GCCTGCCCCTGCCTC | 21745 |
rs224474423 | in-del | -/AC | | | intron-variant | Tep1 | Mm_Celera | 14:50832607 | CAACAACAAAAAAAA[-/AC]CCCAGCATGCTCTAG | 21745 |
rs224496709 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50867844 | AACTATCCAAAAAAA[C/T]CCAAAAGGCTGATAC | 21745 |
rs224505030 | snp | C/T | | | upstream-variant-2KB, intron-variant | Tep1, Gm26782 | Mm_Celera | 14:50871780 | GAAGCAGAAGGATCT[C/T]AAGTTCAAGCCAGAT | 21745 |
rs224508139 | snp | A/C | | | intron-variant, upstream-variant-2KB | Tep1, Gm26782 | Mm_Celera | 14:50868927 | GCAGTGTTGTACAGC[A/C]ATCACTTTTAACCAT | 21745 |
rs224586173 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50861964 | GAAGGAATACATGTG[A/G]CACACAGACACACAG | 21745 |
rs224594191 | snp | C/G | | | intron-variant | Tep1 | Mm_Celera | 14:50856074 | TGCCACCTGCCACTG[C/G]CCTTTCCAAGACACT | 21745 |
rs224595108 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50859105 | CATTTGGGCTCAAAA[A/G]TTCCAAAATTGGAAG | 21745 |
rs224662527 | snp | A/T | | | intron-variant | Tep1 | Mm_Celera | 14:50866883 | CCTACGAACAGTGGC[A/T]GTTATAAAATTGCAC | 21745 |
rs224668290 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50845565 | GAGGGAAGACAGAGG[C/T]AGGGTCAGTCCCAAG | 21745 |
rs224743840 | snp | C/T | | | missense | Tep1 | Mm_Celera | 14:50844704 | CTTCTGAGATGGATG[C/T]TGGCTGCTCCAACTG | 21745 |
rs224758916 | snp | C/T | | | intron-variant, downstream-variant-500B | Tep1 | Mm_Celera | 14:50840873 | AGAGGCTAAATGACA[C/T]GGGTGGGGTTGGTGT | 21745 |
rs224798717 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50832131 | TTCACTCTCAGGCAT[C/T]CCAAAGCTACAGAGG | 21745 |
rs224882462 | in-del | -/CAGCG | | | downstream-variant-500B | Tep1 | GRCm38.p3 | 14:50824035 | TTGATCTAAAATCAC[-/CAGCG]AACACAATCGGGCAT | 21745 |
rs224952364 | in-del | -/CAACAAGGCCACACCCACTCCAATGAGGCCACACCCACTC | | | intron-variant | Tep1 | GRCm38.p3 | 14:50859392 | GTGACACAGTCCCTT[lengthTooLong]CAACAAGGCCACACC | 21745 |
rs224960170 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50865871 | TCCTTGCATTCCTAC[A/G]TGGAGCCAATAACCA | 21745 |
rs225107307 | snp | G/T | | | intron-variant | Tep1 | Mm_Celera | 14:50825538 | CAGAAGGACATGTCT[G/T]TATTTCCCTACTTAT | 21745 |
rs225110127 | snp | G/T | | | missense | Tep1 | Mm_Celera | 14:50843768 | GCTCTTCTCTCACAA[G/T]CTGAGCCCTTGAAGA | 21745 |
rs225207558 | snp | A/T | | | intron-variant | Tep1 | Mm_Celera | 14:50844972 | TTCACAGGAGTAGCT[A/T]TAGGGAAAACATAAC | 21745 |
rs225251563 | snp | C/T | | | missense | Tep1 | Mm_Celera | 14:50836824 | ACTGTCCCATCTATC[C/T]GGCCCACAGCCACAA | 21745 |
rs225352738 | in-del | -/T | | | intron-variant | Tep1 | Mm_Celera | 14:50864633 | TAATAAATATTATAA[-/T]AAAAATATATATATA | 21745 |
rs225482538 | in-del | -/C | | | intron-variant | Tep1 | GRCm38.p3 | 14:50825017 | GCCTCCCCTAAGCCA[-/C]CCCAGAAAGAGCACT | 21745 |
rs225489662 | snp | A/G | | | upstream-variant-2KB, intron-variant | Tep1, Gm26782 | Mm_Celera | 14:50870750 | TTTCCACCCAATACA[A/G]TCATGCTCTGATGCT | 21745 |
rs225533340 | in-del | -/CCAGC | | | downstream-variant-500B | Tep1 | GRCm38.p3 | 14:50824034 | GTTGATCTAAAATCA[-/CCAGC]GAACACAATCGGGCA | 21745 |
rs225642769 | in-del | -/T | | | downstream-variant-500B | Tep1 | Mm_Celera | 14:50824013 | GAATATCCAGAGCCC[-/T]TCCCCGTTGATCTAA | 21745 |
rs225714763 | in-del | -/AAAAA | | | intron-variant | Tep1 | GRCm38.p3 | 14:50847201 | TGTGCCTCTTTCTTT[-/AAAAA]AAAAAAAAAAATCAT | 21745 |
rs225729045 | snp | C/T | | | intron-variant, upstream-variant-2KB | Tep1, Gm26782 | Mm_Celera | 14:50869482 | GGCAGATTCTTACAT[C/T]AAGCTGGCCAGCCAG | 21745 |
rs225902281 | snp | A/C | | | intron-variant | Tep1 | Mm_Celera | 14:50838206 | GGGAAGCCACACAGT[A/C]ATGGTGCACAGTCAC | 21745 |
rs226167267 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50846152 | ATTAAAGCCATTAAA[A/G]CCATTAAAAGCAGGA | 21745 |
rs226179801 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50843081 | CAGGCTGCTTGTGTC[A/G]GGGTATTTTATCTTA | 21745 |
rs226190315 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50854456 | CTGAAAATACCTGAG[C/T]GTTGTCTCATTTACA | 21745 |
rs226207681 | snp | C/G | | | intron-variant, downstream-variant-500B | Tep1 | Mm_Celera | 14:50840926 | ACGGTCCAAGCAGAC[C/G]GTTTAGATTGGACTA | 21745 |
rs226209690 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50852703 | AAAGGTGTATACTAG[C/T]TACCATGCCCAGGTT | 21745 |
rs226300310 | snp | A/G | | | missense | Tep1 | Mm_Celera | 14:50841629 | TGACTGGCAGCCAGC[A/G]CTTCTTCCCAGCTCT | 21745 |
rs226511110 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50857191 | TTTAGTAAAGTGGAG[A/G]TTGTAGGTTTTCCTT | 21745 |
rs226515834 | in-del | -/GCC | | | intron-variant | Tep1 | Mm_Celera | 14:50828881 | TTGCCATGCGCAGCA[-/GCC]GCCGCCGCCGCCTCG | 21745 |
rs226559679 | snp | A/C | | | intron-variant | Tep1 | Mm_Celera | 14:50851714 | GTGAGCTGACGAGAA[A/C]ACTGCAAAGTTTGAC | 21745 |
rs226612922 | snp | A/T | | | intron-variant | Tep1 | Mm_Celera | 14:50846720 | TTTCTGTTGGTATCT[A/T]AAAGGCCCGCCCTCA | 21745 |
rs226622971 | snp | A/G | | | upstream-variant-2KB, intron-variant | Tep1, Gm26782 | Mm_Celera | 14:50871709 | AGGTCTGTTTTGTAT[A/G]TAAATTACTACTAGC | 21745 |
rs226633994 | snp | A/C | | | intron-variant | Tep1 | Mm_Celera | 14:50833613 | ACACAGACTGTAAGA[A/C]TACCAAAGCCATTTC | 21745 |
rs226653473 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50858085 | GGCTCACAACCCTCA[A/G]TAACTCCAGTCAGTC | 21745 |
rs226750591 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50849367 | CCTTTGGAGCTGGAT[A/G]CAATTACAGGTAGTT | 21745 |
rs226945335 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50845901 | ACCATCTCTCCAGCC[C/T]GGTACTGGGTATTTT | 21745 |
rs226981019 | in-del | -/G | | | intron-variant | Tep1 | GRCm38.p3 | 14:50865018 | CTTCATGACCTGCTT[-/G]AGTTCCAGTCCTGAC | 21745 |
rs227051006 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50848181 | CTTCCCTGTTCTGTG[C/T]GATCAGCTCTGTATA | 21745 |
rs227072544 | in-del | -/A | | | intron-variant | Tep1 | Mm_Celera | 14:50861832 | AGACTACTCAATTGT[-/A]AAAAAAATACTGGCT | 21745 |
rs227084473 | in-del | -/A | | | upstream-variant-2KB, intron-variant | Tep1, Gm26782 | Mm_Celera | 14:50872427 | CTATTGCTGTGGTTT[-/A]TAAAAAAAAATGAAC | 21745 |
rs227122203 | snp | A/C | | | intron-variant | Tep1 | Mm_Celera | 14:50849788 | ACTCATACACATGGA[A/C]TAAACAAATACATTT | 21745 |
rs227371228 | in-del | -/ACAG | | | intron-variant | Tep1 | GRCm38.p3 | 14:50839851 | GTAAGGTGGAGAGCA[-/ACAG]ACAATTAACAGCTCC | 21745 |
rs227394182 | in-del | -/TT | | | intron-variant | Tep1 | Mm_Celera | 14:50851008 | AAACTGTTTTTTGGG[-/TT]TTTTTTTTGGTTTTT | 21745 |
rs227407285 | snp | C/T | | | missense | Tep1 | Mm_Celera | 14:50854236 | CACAGGTGCTTCCGA[C/T]TGGCAGGCCTCCTAT | 21745 |
rs227419981 | snp | A/C | | | downstream-variant-500B | Tep1 | Mm_Celera | 14:50823564 | ATCCATCTCTCAGCT[A/C]CATGAACTTCAATTT | 21745 |
rs227488815 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50855360 | GGATCTTTCTGTAAG[C/T]TTGTGAGCTCACAAA | 21745 |
rs227625064 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50853934 | AGCAAGCAAGGCAGA[A/G]TCCGTGGCAAAGCCG | 21745 |
rs227809724 | in-del | -/AA | | | intron-variant | Tep1 | Mm_Celera | 14:50825933 | ATACTGACAGAAACC[-/AA]AAAAAAAAAAAAAAA | 21745 |
rs227830484 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50826158 | AAGCCTCACAACAGA[A/G]TTTGATCTCTAGATC | 21745 |
rs227899280 | snp | C/G | | | intron-variant | Tep1 | Mm_Celera | 14:50827246 | AAGGATACTTCTTAA[C/G]CTAACCTTTCAGACT | 21745 |
rs227900634 | in-del | -/AA | | | intron-variant | Tep1 | GRCm38.p3 | 14:50867951 | AACAGAACATATAGC[-/AA]AAAAAAAGGCTAGAG | 21745 |
rs227981018 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50860368 | TGATAGCAACACTAT[C/T]TAAAGCAAATTCCAG | 21745 |
rs228032670 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50852924 | AATTATTTGAGATGA[A/G]CCCAGCGTTCTGTCA | 21745 |
rs228107921 | snp | A/T | | | intron-variant | Tep1 | Mm_Celera | 14:50856596 | AGAGAACTGATTACT[A/T]CAAGTTGTCCTTTGA | 21745 |
rs228158462 | snp | G/T | | | intron-variant | Tep1 | Mm_Celera | 14:50846063 | TGACCTGGATGGCCT[G/T]GAACTTACTATGCAA | 21745 |
rs228221285 | in-del | -/T | | | upstream-variant-2KB, intron-variant | Tep1, Gm26782 | Mm_Celera | 14:50872221 | ATAAATGTGTGTGTG[-/T]GGGGGGAGAGAGAGA | 21745 |
rs228246008 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50862017 | AAAAAGATAAATATT[C/T]TTAAAGCTTTATATG | 21745 |
rs228295290 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50858208 | GTTTGAGTAAGAATG[A/G]CTTCATAGGCTCATA | 21745 |
rs228318829 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50855832 | AAAAGATTTTAAAGA[C/T]CCAGGAAGAAGAAGC | 21745 |
rs228341106 | snp | C/T | | | intron-variant | Tep1 | GRCm38.p3 | 14:50859415 | CCACACCCACTCCAA[C/T]GAGGCCACACCCACT | 21745 |
rs228351748 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50848306 | GAAGGTTCAAACGCA[C/T]CTGCAGCTCTTCCCA | 21745 |
rs228491441 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50866946 | GTAGGAAAGTATCTC[C/T]TAGAAATATGAAAGG | 21745 |
rs228540107 | snp | C/G | | | intron-variant | Tep1 | Mm_Celera | 14:50858845 | GATCTCAAACTAGTC[C/G]TCCTCCTGCCTCAGT | 21745 |
rs228563945 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50860398 | GGGTCTACAGTGGTG[C/T]GGTAAATGGCAAACT | 21745 |
rs228669353 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50860824 | TGTTCACACCACTGA[C/T]GACCCTCATACTGCT | 21745 |
rs228719501 | snp | C/G | | | intron-variant | Tep1 | Mm_Celera | 14:50832173 | CGTGTTAGGAACACG[C/G]GCTTTGGGGCTAGAA | 21745 |
rs228749454 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50824418 | AACAACTTTCATTTC[A/G]TTGACACGCCTTAGC | 21745 |
rs228755411 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50832647 | TTCTCTGTGGGTCAT[A/G]ACCCCTTGAGGGGTC | 21745 |
rs228884434 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50858688 | CAAACAAGATAAATG[C/T]TGCCGTTGAAATGTT | 21745 |
rs228986711 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50850125 | CAGTCACTAAGCACC[A/G]AAATCGATGCCTGGA | 21745 |
rs229037010 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50859537 | GTCTAATGTTACATA[C/T]ATTTCAACATAGAGA | 21745 |
rs229044317 | snp | A/T | | | intron-variant | Tep1 | Mm_Celera | 14:50864982 | AAGAACATCCCTCCA[A/T]TGGCTTCTGCATCAG | 21745 |
rs229045468 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50856828 | TAAAAATTATCTTTA[C/T]TCATCTCTCTGTGTG | 21745 |
rs229048570 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50829468 | AGCTAAGACTACATA[A/G]TGAGACACTGTCTCA | 21745 |
rs229089615 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50836977 | GGAATATAGCTGTCA[C/T]TCTCCACTTTCACCA | 21745 |
rs229122958 | snp | G/T | | | intron-variant | Tep1 | Mm_Celera | 14:50827573 | CCCAGATCTTAGTGG[G/T]CTCCAGACCTCAGCA | 21745 |
rs229161824 | snp | C/G | | | synonymous-codon | Tep1 | Mm_Celera | 14:50837476 | GGCCTTGGTCTGAAA[C/G]ACCCTGCCCCAGGAA | 21745 |
rs229201713 | snp | A/C | | | intron-variant | Tep1 | Mm_Celera | 14:50827994 | AAAGAAACAAAAACC[A/C]CCAAATCCACCACAG | 21745 |
rs229210083 | in-del | -/CCTCCCTCTATGACC | | | intron-variant | Tep1 | Mm_Celera | 14:50824700 | CCAGATTTAGAACCG[-/CCTCCCTCTATGACC]CCTCCCTCCAAGCTC | 21745 |
rs229261542 | snp | G/T | | | intron-variant | Tep1 | Mm_Celera | 14:50828893 | GCAGCCGCCGCCGCC[G/T]CCTCGCTTCACCTGG | 21745 |
rs229281040 | in-del | -/CAGT | | | intron-variant | Tep1 | Mm_Celera | 14:50825231 | ATCAAAGCTCTAAGA[-/CAGT]CAGGATATATATGAC | 21745 |
rs229282894 | snp | A/G | | | downstream-variant-500B | Tep1 | Mm_Celera | 14:50823806 | TACTGACTTTAACTC[A/G]CTCTTGTGTCCTTTC | 21745 |
rs229291438 | snp | A/T | | | intron-variant | Tep1 | Mm_Celera | 14:50824294 | GAACAAGCCCAGCTG[A/T]AACAGGAACAGAAAC | 21745 |
rs229296781 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50829613 | CCCTGGCATTCCTTG[C/T]TCCACTCATCTTCTT | 21745 |
rs229400797 | snp | A/C | | | intron-variant | Tep1 | Mm_Celera | 14:50827450 | CCGTCTTTCTTATCA[A/C]AACATCTTCCATCAT | 21745 |
rs229445487 | in-del | -/GA | | | intron-variant | Tep1 | Mm_Celera | 14:50863923 | GGGTGCGTTGTAAAT[-/GA]GAGAGAAATAACAGG | 21745 |
rs229544915 | in-del | -/A | | | intron-variant | Tep1 | Mm_Celera | 14:50860415 | TAAATGGCAAACTTC[-/A]AAAAATCCAGTTTTT | 21745 |
rs229751739 | in-del | -/T | | | intron-variant | Tep1 | Mm_Celera | 14:50857118 | TAGCCTCAGCTGTAA[-/T]TTTTTTTTTAAAGGA | 21745 |
rs229753040 | snp | G/T | | | upstream-variant-2KB, intron-variant | Tep1, Gm26782 | Mm_Celera | 14:50870628 | CTGCCGCGTGTAGGA[G/T]ATCGCAAATGCCGGG | 21745 |
rs229832174 | snp | C/T | | | missense, utr-variant-3-prime | Tep1 | Mm_Celera | 14:50831757 | ACGGCGCTCACGGCA[C/T]TCTGGTGGCCTGAGA | 21745 |
rs229833646 | snp | C/T | | | intron-variant, utr-variant-3-prime | Tep1 | Mm_Celera | 14:50841088 | TTGAGAAGGGCTTCC[C/T]ACTGCAGCATATCCG | 21745 |
rs229935879 | in-del | -/GAG | | | intron-variant | Tep1 | Mm_Celera | 14:50826188 | CAAACAGTAGAAGAA[-/GAG]AACCAACCTCACCAA | 21745 |
rs229948452 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50862832 | GGGGCCATGAACTCC[C/T]AGGGCTGAGGCAAAG | 21745 |
rs230117277 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50860468 | AATTCACTGCACCAT[C/T]TTGTGGAAATCTTCA | 21745 |
rs230117833 | snp | A/C | | | intron-variant | Tep1 | Mm_Celera | 14:50834981 | GGTTTAGAGTACATT[A/C]ATAACTCAGCTATGT | 21745 |
rs230132409 | snp | A/T | | | intron-variant | Tep1 | GRCm38.p3 | 14:50835210 | GCAAGCAAGCAAACA[A/T]ATATATATATATATA | 21745 |
rs230160565 | snp | A/C | | | intron-variant | Tep1 | Mm_Celera | 14:50826363 | GGAAGCAGAGGCAAG[A/C]AGATGTCAGTGAGCT | 21745 |
rs230167239 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50828874 | GTGTGGCTTGCCATG[C/T]GCAGCAGCCGCCGCC | 21745 |
rs230229585 | snp | A/C | | | intron-variant | Tep1 | Mm_Celera | 14:50825719 | GAATCACTGCTTTCT[A/C]GACAGACTTTGTACG | 21745 |
rs230331790 | snp | A/T | | | intron-variant | Tep1 | Mm_Celera | 14:50863874 | AGGAAGAGTCTTCAT[A/T]CCAACATCTAACAAG | 21745 |
rs230385079 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50856726 | TCTGCAGGTCAGGCT[A/G]GCCTTAAACTCACAG | 21745 |
rs230453906 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50838769 | CTCTTCTGCCTCTTT[C/T]TCTGCATCTCTGCCT | 21745 |
rs230529458 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50855246 | AGTCTTCCAGAAGAG[C/T]TGTCGGTGCCCTTAC | 21745 |
rs230543644 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50865210 | GTTTTGCTGAAGGGG[A/G]AAGTGACAGGGACTG | 21745 |
rs230682433 | in-del | -/AGGCCACACCCACTCCAATG | | | intron-variant | Tep1 | GRCm38.p3 | 14:50859397 | ACAGTCCCTTCAACA[-/AGGCCACACCCACTCCAATG]AGGCCACACCCACTC | 21745 |
rs230693195 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50857359 | AGACAGCAAGCAACA[C/T]GGAAGGGTTGGAGGA | 21745 |
rs230716394 | snp | C/T | | | missense | Tep1 | Mm_Celera | 14:50846519 | CATAGCTGGGGGGAA[C/T]GTAGCCATAGCGGGA | 21745 |
rs230785616 | snp | A/C | | | intron-variant | Tep1 | Mm_Celera | 14:50867229 | ACTATCACCTCCCTG[A/C]GAGGGCTGTTGAAAG | 21745 |
rs230885971 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50832864 | TGGGCTAGAGGAATG[A/G]TTAGAGGGCACAGCA | 21745 |
rs230895745 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50860231 | GATCTAATCCCACTT[A/G]GTTACAATATATTCT | 21745 |
rs230929082 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50830080 | AGGAACAGGAAATGG[A/G]AGAGGAGGAAATAAA | 21745 |
rs231008224 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50861886 | ACTCTCAACCTCCAC[A/G]TGGTGACTCACAAAT | 21745 |
rs231011366 | snp | A/G | | | intron-variant, upstream-variant-2KB | Tep1, Gm26782 | Mm_Celera | 14:50868838 | AGCATGTGTGAGGCT[A/G]GAGGACAATCCTTGG | 21745 |
rs231060230 | snp | C/T | | | intron-variant | Tep1 | GRCm38.p3 | 14:50859431 | GAGGCCACACCCACT[C/T]CAACAAGGCCACACC | 21745 |
rs231095030 | snp | A/C | | | intron-variant | Tep1 | Mm_Celera | 14:50855453 | TGTCTTTCCCAACAT[A/C]TGTAGGTTTTCACAC | 21745 |
rs231115062 | snp | C/T | | | upstream-variant-2KB, intron-variant | Tep1, Gm26782 | Mm_Celera | 14:50872113 | CAAGAATGCCCCTCA[C/T]TGTAGAAGTGCTCTG | 21745 |
rs231142814 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50833752 | CCAGGTTTCAAGCAG[A/G]AAGTTTTAAAGAAGA | 21745 |
rs231261269 | snp | A/C | | | intron-variant | Tep1 | Mm_Celera | 14:50860887 | ATGAGCCAGAATGAC[A/C]AGGTCAATGGAATGC | 21745 |
rs231359097 | snp | C/G/T | | | intron-variant | Tep1 | Mm_Celera | 14:50865016 | CTGCTTCATGACCTG[C/G/T]TTAGTTCCAGTCCTG | 21745 |
rs231433413 | snp | A/T | | | upstream-variant-2KB, intron-variant | Tep1, Gm26782 | Mm_Celera | 14:50871392 | AGCAACAAATTTTTT[A/T]AAATTTTGATTTTGG | 21745 |
rs231466733 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50825204 | TTTGTTTAGTTCATG[A/G]CACAACGCCACTATC | 21745 |
rs231788085 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50865762 | AAACCAATTCTAGTA[C/T]ACCTTCCCCCATCTC | 21745 |
rs231813707 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50867199 | ATTCCCCAGAAGCCC[C/T]AAGCTTCTTCATTCA | 21745 |
rs231935621 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50838182 | AAAGACTAAGTCACA[C/T]GACTCAAAGGGAAGC | 21745 |
rs231939187 | snp | C/T | | | intron-variant | Tep1 | GRCm38.p3 | 14:50839373 | CACCTTTAATTTCAG[C/T]GCTTGGGGGGCAGAG | 21745 |
rs231946707 | in-del | -/TGTATGTG | | | intron-variant, upstream-variant-2KB | Tep1, Gm26782 | Mm_Celera | 14:50869709 | GTATGTATGTATGTA[-/TGTATGTG]TTGAAACAAGGTCTC | 21745 |
rs231973859 | snp | A/G | | | missense | Tep1 | Mm_Celera | 14:50829743 | GCCTCTGAAGCAGCA[A/G]CTGCTGTGACTGGGC | 21745 |
rs231985562 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50828818 | TCTCACAGCCTTGCC[C/T]GAAAGCAGACACAGA | 21745 |
rs231993293 | in-del | -/AA | | | intron-variant | Tep1 | Mm_Celera | 14:50860167 | TTTACCAGTAGAGGG[-/AA]AAATGATTAAACTTT | 21745 |
rs232162148 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50845361 | TGGGGGTTGAGGACG[A/G]GATCTATCTGGCTTT | 21745 |
rs232162424 | snp | G/T | | | intron-variant | Tep1 | Mm_Celera | 14:50836492 | AAAGTTTAAAGGTAC[G/T]TCTCTGCCCCGTCCC | 21745 |
rs232182242 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50830878 | GCCCTTCACTCAGGA[A/G]GACACAGCTTTTTGC | 21745 |
rs232197664 | snp | G/T | | | intron-variant | Tep1 | Mm_Celera | 14:50853244 | AGACTGTGGGTCATC[G/T]TCAGCAATTCTCTGG | 21745 |
rs232227146 | snp | A/G | | | synonymous-codon | Tep1 | Mm_Celera | 14:50841992 | GGTTCGAAGTCTCTC[A/G]GACACCTGGCAGTGA | 21745 |
rs232288246 | snp | A/G | | | missense | Tep1 | Mm_Celera | 14:50837162 | GGATGGGTGTACTGA[A/G]AAGCCAGCTGTCCTC | 21745 |
rs232307656 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50842737 | ATCACAATAGAAAAT[A/G]AAACTAAGAAAACAT | 21745 |
rs232325449 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50843516 | CCTCCCTAGGGAGAT[A/G]GATCACCATGGAAAA | 21745 |
rs232477756 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50852134 | AAAAGAGGGGGCTCA[A/G]CTGGACCCTGTATTG | 21745 |
rs232528590 | snp | C/G | | | intron-variant | Tep1 | Mm_Celera | 14:50837532 | CTGGCAAGTAGGCTC[C/G]CTCCTCACTCATTTC | 21745 |
rs232553094 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50839787 | GCCCCCCAAGTGCTG[A/G]GATTAAAGGCGTGCG | 21745 |
rs232562612 | snp | C/G | | | intron-variant | Tep1 | Mm_Celera | 14:50856966 | GTAAGTGCCCACAGA[C/G]TCTAGAAGAGGATGC | 21745 |
rs232563785 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50845610 | TGGAAGCCTTCAGAT[A/G]CCCGAGATCACCCTT | 21745 |
rs232595581 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50846463 | CAGCTCCACCAACCT[C/T]GTCTGCCTTACCCAG | 21745 |
rs232638471 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50848912 | AGAAGAAAGGCTTCC[C/T]CAGGGATGAGCCCTC | 21745 |
rs232642842 | in-del | -/AG | | | intron-variant | Tep1 | Mm_Celera | 14:50826547 | GAGAGAAAGAATGAA[-/AG]AGAAAGGAAGAACGA | 21745 |
rs232686400 | snp | A/C | | | intron-variant | Tep1 | Mm_Celera | 14:50850469 | TTAAATTCAATAGAA[A/C]TAATAAAGCAAGAAG | 21745 |
rs232776955 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50850165 | AGTGGCTTACATCTG[C/T]AATCCCAGCACCTGC | 21745 |
rs232814853 | snp | A/G | | | upstream-variant-2KB, intron-variant | Tep1, Gm26782 | Mm_Celera | 14:50871961 | ACTCAGTCTGTAGAC[A/G]AGGCTGGCCTTTAAC | 21745 |
rs232831188 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50840270 | ACTTCACATCAGAAA[C/T]ACACCTATTCAGAAC | 21745 |
rs232853805 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50840174 | CTAGGAATCCCGCCT[A/G]GACTCCATTAACTTC | 21745 |
rs232940004 | in-del | -/CGTATATATATCCGCATATGCACATACT | | | intron-variant, upstream-variant-2KB | Tep1, Gm26782 | GRCm38.p3 | 14:50869566 | TAGTCTCCACATACC[-/CGTATATATATCCGCATATGCACATACT]CTTGCACACACAAAC | 21745 |
rs232970354 | in-del | -/AAA | | | intron-variant | Tep1 | Mm_Celera | 14:50849846 | AAAAGTGCTCTATTT[-/AAA]AAAAAAAAAAGGCAG | 21745 |
rs233133987 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50845178 | CTGGCACAGAGCTGA[C/T]CACAAAAGACACCCC | 21745 |
rs233676040 | snp | C/T | | | synonymous-codon | Tep1 | Mm_Celera | 14:50826828 | CAATATAGAAAGTAA[C/T]CCGGAGTCCCCCTGC | 21745 |
rs233711770 | snp | A/T | | | intron-variant | Tep1 | Mm_Celera | 14:50827672 | AGCCCCTAGACGCCG[A/T]GACCAAGGAACTTTG | 21745 |
rs233731927 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50851201 | TCTAGGATTAAAGGA[A/G]TGTGCCACCATGCCT | 21745 |
rs233775799 | snp | A/G | | | intron-variant, downstream-variant-500B | Tep1 | Mm_Celera | 14:50840880 | AAATGACACGGGTGG[A/G]GTTGGTGTGAAAGGG | 21745 |
rs233933347 | in-del | -/AAG | | | intron-variant | Tep1 | Mm_Celera | 14:50826183 | AGATCAAACAGTAGA[-/AAG]AGAGAACCAACCTCA | 21745 |
rs234031985 | snp | A/T | | | intron-variant | Tep1 | Mm_Celera | 14:50830363 | GCCTGGGACTGCACT[A/T]GTTTGAAGTGTGCAT | 21745 |
rs234067760 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50831201 | TTCCTGGTCTCCTTG[A/G]ACACACATGGTATTA | 21745 |
rs234163580 | snp | C/T | | | intron-variant, upstream-variant-2KB | Tep1, Gm26782 | Mm_Celera | 14:50870321 | CACCCCACCTCCCTG[C/T]CAGCCGCCCGGAAGG | 21745 |
rs234368088 | snp | C/G/T | | | intron-variant | Tep1 | Mm_Celera | 14:50825235 | AAAGCTCTAAGACAG[C/G/T]ATATATATGACACAA | 21745 |
rs234385837 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50850817 | ACTGATGGGTTAGAA[C/T]GCTGAGGGGAAAGGA | 21745 |
rs234386929 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50859809 | GAATCAAACCCAGAA[C/T]CTTTTGAAGAACAAC | 21745 |
rs234454525 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50851907 | GGAGTTTCATAGGAA[C/T]CTAGTAGGACTCACG | 21745 |
rs234503127 | snp | G/T | | | intron-variant | Tep1 | Mm_Celera | 14:50851850 | CAGCCTCAGCTACAG[G/T]TGACAACAAAAAAGA | 21745 |
rs234566264 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50861237 | GGGAAAATCTGTGGG[A/G]GCTCCCAAGGACACA | 21745 |
rs234603488 | snp | C/T | | | downstream-variant-500B | Tep1 | Mm_Celera | 14:50823877 | ACTGGCCACCAATAG[C/T]CTTCCTTCCTTCTGA | 21745 |
rs234706714 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50843011 | ACAACCCTGCAACAA[C/T]AGACTGTAAACTCCA | 21745 |
rs234732705 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50825293 | ACAAAAAACTAAAAC[C/T]CACCACACCTACAAA | 21745 |
rs234962661 | in-del | -/TG | | | intron-variant | Tep1 | Mm_Celera | 14:50842520 | GTGTGTGTGTGTGTG[-/TG]TGTGTGTGTGTGTGT | 21745 |
rs235031948 | snp | A/G | | | intron-variant | Tep1 | GRCm38.p3 | 14:50839261 | GGAGATGACTCAGGG[A/G]GTTGAAGAGCTTGCT | 21745 |
rs235040221 | in-del | -/CC | | | intron-variant, upstream-variant-2KB | Tep1, Gm26782 | GRCm38.p3 | 14:50868950 | TTAACCATCTTGCTG[-/CC]CCCCCCCCTTTTAGA | 21745 |
rs235068144 | snp | A/G | | | synonymous-codon | Tep1 | Mm_Celera | 14:50854540 | AGCCTCAAGTTTATC[A/G]ATAGAGTCATGAGCA | 21745 |
rs235071944 | snp | A/C | | | intron-variant | Tep1 | Mm_Celera | 14:50854963 | GTAAGGAAAGAAAAA[A/C]AGATCTCAAGAAGAA | 21745 |
rs235099074 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50855539 | AAGAGTCTGGCCTCT[A/G]GGTGCACAGTCTCCT | 21745 |
rs235175657 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50862110 | ACAGAGGAGAAAAAG[C/T]TCCTTCCCTTTGTTC | 21745 |
rs235239222 | in-del | -/AAAAA | | | intron-variant | Tep1 | GRCm38.p3 | 14:50864632 | TGTAATAAATATTAT[-/AAAAA]AATATATATATATGT | 21745 |
rs235347165 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50864219 | GAAACCTCAGGGGAG[A/G]TACTCCCTAGATCTG | 21745 |
rs235375669 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50857022 | TAGGTAGTTATGAGC[C/T]GCCTGATGTACATGC | 21745 |
rs235451817 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50858263 | TATAAAGATTAGGGG[A/G]TGTGGCCTTGTTGGA | 21745 |
rs235505732 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50858453 | AGCCCTCAGCTACAG[C/T]TACAGCACTAGGCAT | 21745 |
rs235575336 | in-del | -/AG | | | intron-variant | Tep1 | GRCm38.p3 | 14:50827879 | CTGTCTCGAAGAAGA[-/AG]AAAAAAAAAAAAAAC | 21745 |
rs235705580 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50848048 | TGTACTGGAAAATAA[A/G]ACTACAAAACACTGG | 21745 |
rs235839692 | snp | A/T | | | intron-variant | Tep1 | Mm_Celera | 14:50826207 | ACCAACCTCACCAAG[A/T]TGTCTTCTAACTTCC | 21745 |
rs235896105 | snp | C/T | | | missense | Tep1 | Mm_Celera | 14:50833549 | CTTGGGCTATCTTCA[C/T]GTCCCAGCAAAGGAG | 21745 |
rs235932126 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50862045 | ATGGAGTGGAAATGT[C/T]TTTGACATTTTAAAT | 21745 |
rs235986730 | snp | A/T | | | intron-variant | Tep1 | Mm_Celera | 14:50825521 | GTGACTGGCTTCCTT[A/T]GCAGAAGGACATGTC | 21745 |
rs236039799 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50834242 | GAGGCCCTGGGCAAG[A/G]GTCAGTCATGACATA | 21745 |
rs236138000 | snp | A/G | | | intron-variant, downstream-variant-500B | Tep1 | Mm_Celera | 14:50840875 | AGGCTAAATGACACG[A/G]GTGGGGTTGGTGTGA | 21745 |
rs236225480 | in-del | -/GTG | | | upstream-variant-2KB, intron-variant | Tep1, Gm26782 | GRCm38.p3 | 14:50872219 | GAAATAAATGTGTGT[-/GTG]GGGGGGAGAGAGAGA | 21745 |
rs236247250 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50827728 | TTTTAAATCTAAGAA[C/T]TGACTCTACCTGGGC | 21745 |
rs236274652 | snp | A/T | | | intron-variant | Tep1 | Mm_Celera | 14:50832554 | AATAATTCTTTTTAA[A/T]AAAAAACTAAGACTT | 21745 |
rs236352082 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50838025 | ATCACTCACAGCCAC[A/G]TACAGAACCACTCTC | 21745 |
rs236505074 | in-del | -/ACACACACAT | | | intron-variant | Tep1 | Mm_Celera | 14:50826274 | CACACACACACACAC[-/ACACACACAT]ACACACACACACAAA | 21745 |
rs236520948 | in-del | -/TATGTATGTATG | | | intron-variant, upstream-variant-2KB | Tep1, Gm26782 | GRCm38.p3 | 14:50869668 | TCAGAATTAATCCAA[-/TATGTATGTATG]TATGTATGTATGTAT | 21745 |
rs236530259 | snp | A/T | | | intron-variant | Tep1 | Mm_Celera | 14:50864435 | TATAATTGAAATGCC[A/T]GTATGAGTACACTTA | 21745 |
rs236559367 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50845031 | ACCACGCCTCTAACG[A/G]AGGGGTGCCTCGGCC | 21745 |
rs236598386 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50845679 | GTAAAATATAGTTAC[C/T]AGCTAACCATTAGCA | 21745 |
rs236624737 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50853436 | GGCACTTGGAAGAAA[C/T]CCATACCACTTCTTT | 21745 |
rs236683256 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50837367 | CTCATGGTTGAGGGT[C/T]ACTTTTTGTTACCTT | 21745 |
rs236704339 | in-del | -/GGGGGGGG | | | intron-variant | Tep1 | GRCm38.p3 | 14:50846027 | TGTGTGTGTGTGTGT[-/GGGGGGGG]GGGGGGGGGTCCTCA | 21745 |
rs236712882 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50832289 | CAGTTTCAGGGGATC[C/T]ACCATCCTCTTCTGG | 21745 |
rs236835768 | snp | A/C | | | synonymous-codon | Tep1 | Mm_Celera | 14:50847661 | GATGTTCTCCTCCAG[A/C]GGCCGGAGAGACGGT | 21745 |
rs236869865 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50858870 | CTCAGTCCCCAATCA[C/T]TATGATTACAAGTGT | 21745 |
rs236972331 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50860061 | TTAAAGAAAAAAGCA[C/T]TAAGGAGCCTTTCAT | 21745 |
rs237020915 | snp | C/G | | | intron-variant | Tep1 | Mm_Celera | 14:50830597 | CTATTCAGGCATACT[C/G]TCTACTGTGTGAGTA | 21745 |
rs237042939 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50865571 | GTTTAGAGTAACTTA[C/T]TGCAGGCACAGAATG | 21745 |
rs237129344 | in-del | -/TT | | | intron-variant | Tep1 | Mm_Celera | 14:50842112 | GAAGGAATGAAGAGG[-/TT]AAAAAAAAAAACAAA | 21745 |
rs237259487 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50857672 | GGGAAACATGAATTC[A/G]GCTGTGGAGCTAAAT | 21745 |
rs237359023 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50858950 | ACTTGTAAATTGGTG[A/G]AAAGGCTGACAGATG | 21745 |
rs237363983 | snp | G/T | | | utr-variant-5-prime, upstream-variant-2KB | Tep1, Gm26782 | GRCm38.p3 | 14:50870452 | TGCGCAATGAGAGGC[G/T]CGTTGGTTCTCCGCA | 21745 |
rs237388402 | in-del | -/T | | | upstream-variant-2KB, intron-variant | Tep1, Gm26782 | GRCm38.p3 | 14:50872220 | AAATAAATGTGTGTG[-/T]GGGGGGGAGAGAGAG | 21745 |
rs237417366 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50850526 | AGACTTTGACAGGAG[C/T]AGACGGGAAAATATG | 21745 |
rs237424007 | snp | A/C | | | intron-variant | Tep1 | Mm_Celera | 14:50860451 | ATGTAAATTAAGTTG[A/C]AAATTCACTGCACCA | 21745 |
rs237624022 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50861330 | ACAGATCCAGAGAGC[A/G]CAAGGCAGTATGGGT | 21745 |
rs237672842 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50837828 | CAGCCCAAATACAGG[C/T]CCAAGTGCACCTCAT | 21745 |
rs237825328 | snp | G/T | | | intron-variant | Tep1 | Mm_Celera | 14:50863253 | CAATTGGGATGTACA[G/T]AAATAAAATAATTAA | 21745 |
rs237852353 | snp | A/C | | | intron-variant | Tep1 | Mm_Celera | 14:50825498 | ATCTCTGTAGTGTGG[A/C]CATGTTTGTGACTGG | 21745 |
rs237942439 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50865561 | AGTGGCTTTTGTTTA[A/G]AGTAACTTACTGCAG | 21745 |
rs238115730 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50828551 | AAAACCTTTGATCCC[C/T]AGAACCCATATGCTG | 21745 |
rs238118370 | in-del | -/TTTG | | | intron-variant | Tep1 | Mm_Celera | 14:50848740 | ACACCACACTCGACT[-/TTTG]TTTGTTTTTTTAAAA | 21745 |
rs238170323 | snp | A/C | | | missense | Tep1 | GRCm38.p3 | 14:50839139 | AGGTATGGAAAACAG[A/C]AACATCTGCCGCTGG | 21745 |
rs238225893 | in-del | -/CACACA | | | intron-variant | Tep1 | Mm_Celera | 14:50863064 | CTCAGCAGAACCCAC[-/CACACA]CACACACACACATCC | 21745 |
rs238254397 | snp | G/T | | | intron-variant | Tep1 | Mm_Celera | 14:50829572 | GGCTACTGGATGGGT[G/T]GATGGGATAAAGACT | 21745 |
rs238256648 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50839631 | ACCAAAAACCAGTGA[A/G]CGCCAGATTCAGTAA | 21745 |
rs238418412 | snp | C/T | | | upstream-variant-2KB, intron-variant | Tep1, Gm26782 | Mm_Celera | 14:50871372 | CACCACCAACCACCA[C/T]GCCCAGCAACAAATT | 21745 |
rs238428863 | snp | G/T | | | intron-variant | Tep1 | Mm_Celera | 14:50855900 | AATGTGTATCGGATA[G/T]CTGCTTATATAACAA | 21745 |
rs238438924 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50841386 | GTAAGGGAGGAGAAA[C/T]AGAGCCAGTCAGTGA | 21745 |
rs238504699 | snp | C/T | | | missense | Tep1 | Mm_Celera | 14:50841897 | AGGGCAGTCAAAGCC[C/T]GAGGAAGGACATCAT | 21745 |
rs238596754 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50833265 | GTCTACTTTACAGGG[C/T]ATAGTAAAGATTAAC | 21745 |
rs238632567 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50843160 | AAAGGCCACCAGCAA[C/T]GGGAAATACAACTAA | 21745 |
rs238641065 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50849928 | TGTGAAAGAAAATAA[A/G]CCATCTTATTTTGAA | 21745 |
rs238647149 | snp | A/G | | | intron-variant, downstream-variant-500B | Tep1 | Mm_Celera | 14:50831366 | TGACCCATCTCGCCA[A/G]CCCATTCTGTGTGTG | 21745 |
rs238673083 | in-del | -/GTT | | | intron-variant | Tep1 | Mm_Celera | 14:50830382 | TGAAGTGTGCATACA[-/GTT]GTCTTGTAATAATTC | 21745 |
rs238709629 | snp | A/G | | | missense | Tep1 | Mm_Celera | 14:50836091 | GGGAGTCTCCCTTGA[A/G]CATCCAACCATGCAG | 21745 |
rs238768115 | snp | A/G | | | intron-variant, downstream-variant-500B | Tep1 | Mm_Celera | 14:50840816 | TGGGAAAAGAACCGG[A/G]GGGAAGACAGCAGGA | 21745 |
rs238771903 | in-del | -/T | | | intron-variant, upstream-variant-2KB | Tep1, Gm26782 | Mm_Celera | 14:50868960 | TGCTGCCCCCCCCCC[-/T]TTTAGATTTATCCAG | 21745 |
rs238799876 | in-del | -/TG | | | intron-variant | Tep1 | Mm_Celera | 14:50851017 | TTTGGGTTTTTTTTT[-/TG]GTTTTTTAAATTTTT | 21745 |
rs239077257 | snp | C/T | | | synonymous-codon | Tep1 | Mm_Celera | 14:50844161 | GAGCAACTTCTGCTG[C/T]AGTTCCCACACCAGG | 21745 |
rs239176289 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50855747 | AGTGACACATACAAA[A/G]TTATAGTCCCCAGCA | 21745 |
rs239177376 | snp | A/T | | | intron-variant | Tep1 | Mm_Celera | 14:50834542 | AAGATTATCCTGTGT[A/T]ATTCAAATGCTGACT | 21745 |
rs239178115 | snp | A/T | | | intron-variant | Tep1 | Mm_Celera | 14:50843562 | TGAAACATCAGCACT[A/T]TCTAATGAACAACTT | 21745 |
rs239214640 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50844744 | CTGAGGGTCACAGAG[C/T]GCTGATTATATCTCC | 21745 |
rs239282255 | snp | A/G | | | intron-variant, upstream-variant-2KB | Tep1, Gm26782 | Mm_Celera | 14:50869131 | AAATTCCAGGTCCAC[A/G]TGAGCACTGACACTC | 21745 |
rs239329823 | snp | A/G | | | upstream-variant-2KB, intron-variant | Tep1, Gm26782 | Mm_Celera | 14:50871731 | ACTACTAGCCAGGTA[A/G]TATACCCTTATAATT | 21745 |
rs239389539 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50847852 | CAGGCAGCAAAGACA[C/T]GCCTGCTCAGTTCAG | 21745 |
rs239399552 | snp | C/G | | | intron-variant | Tep1 | Mm_Celera | 14:50859887 | CTGAAGAGAGTGAAT[C/G]GGCAGTGAAGAAAGA | 21745 |
rs239478647 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50838843 | TTCTCTGCATCTCTG[C/T]CTGCACCCTCCTCTC | 21745 |
rs239647603 | in-del | -/CTCG | | | intron-variant | Tep1 | Mm_Celera | 14:50826717 | CCACCTGCCTTTCCC[-/CTCG]TCGCCTTACACTCCA | 21745 |
rs239682689 | snp | C/G | | | intron-variant | Tep1 | Mm_Celera | 14:50828452 | AATTCACGACCATCT[C/G]TCATGGGATCTGATG | 21745 |
rs239746878 | in-del | -/AGAGAGAG | | | intron-variant | Tep1 | GRCm38.p3 | 14:50852752 | GAGAGAGAGGCAGAA[-/AGAGAGAG]AGAGACAGAGAGACA | 21745 |
rs239887608 | snp | A/G | | | intron-variant, upstream-variant-2KB | Tep1, Gm26782 | Mm_Celera | 14:50869046 | CTGGCATGGCATAGC[A/G]GTGACCTGTCTAGAA | 21745 |
rs240008141 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50855934 | ATGTCACTAACTGTT[A/G]GCTCTACTTGCTGGT | 21745 |
rs240100117 | snp | G/T | | | synonymous-codon | Tep1 | Mm_Celera | 14:50845517 | CATCTCTGTCACGGA[G/T]CGCCCTGAAGGGTAC | 21745 |
rs240149100 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50866404 | CCCAGAGGGGTCTGA[C/T]GTCCTTCCTGACCTC | 21745 |
rs240199614 | snp | A/C | | | intron-variant | Tep1 | GRCm38.p3 | 14:50858334 | GGGCTTTAAGGTTTT[A/C]AAAAATCCATACCAG | 21745 |
rs240369254 | in-del | -/A | | | intron-variant | Tep1 | Mm_Celera | 14:50847777 | GGCAATGAATCTAAG[-/A]AAAAGCATGATGAAA | 21745 |
rs240462051 | in-del | -/A | | | intron-variant | Tep1 | Mm_Celera | 14:50833816 | CAGCTCTGGTAGATC[-/A]AAAAAGTTCAAGGAA | 21745 |
rs240465662 | snp | G/T | | | intron-variant | Tep1 | Mm_Celera | 14:50829349 | AGCTCTGCACTGATC[G/T]CTTAATAGTGGTGCA | 21745 |
rs240544441 | snp | A/G | | | upstream-variant-2KB, intron-variant | Tep1, Gm26782 | Mm_Celera | 14:50870771 | CTCTGATGCTATTAT[A/G]TATCCTGAAAATACC | 21745 |
rs240580437 | snp | A/C | | | intron-variant | Tep1 | Mm_Celera | 14:50857242 | TCAATGCCAAGTGCT[A/C]AGCCTTGAAATCATG | 21745 |
rs240665613 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50865685 | ATACCCACGGGTCCA[A/G]ATCCAAGTTTCATCA | 21745 |
rs240699647 | snp | C/G | | | intron-variant | Tep1 | Mm_Celera | 14:50847954 | GGGCAATCACAAGTA[C/G]AGGTGAGCCCGGATC | 21745 |
rs240793984 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50832460 | AGATCCCATTACAGA[C/T]GGTTGTGAGCCACCA | 21745 |
rs240827918 | snp | A/C | | | intron-variant | Tep1 | Mm_Celera | 14:50828761 | GGAGATCAATAAATG[A/C]AATTTGAAAACAACC | 21745 |
rs240927720 | in-del | -/T | | | intron-variant | Tep1 | GRCm38.p3 | 14:50848473 | ATAAAAGTAATATAA[-/T]TTTTTCATATCGCTC | 21745 |
rs240933131 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50856630 | TTCACACAGCTCACC[C/T]CACACACAAATATAT | 21745 |
rs240946061 | in-del | -/CTT | | | cds-indel | Tep1 | Mm_Celera | 14:50866772 | AGACCGGTGCCTCCA[-/CTT]CTTCTTCTTCCAAGC | 21745 |
rs240974223 | snp | A/T | | | intron-variant | Tep1 | Mm_Celera | 14:50860186 | ATGATTAAACTTTTC[A/T]GATCCTACATGAATT | 21745 |
rs241072122 | snp | A/G | | | synonymous-codon | Tep1 | Mm_Celera | 14:50866749 | AGAGTCTCCAGATGT[A/G]AGTTTTAAGACCGGT | 21745 |
rs241072210 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50858026 | CTGAGCAGTTAACAA[C/T]ACTGGCTGCTCTTCC | 21745 |
rs241084872 | in-del | -/GGA | | | intron-variant | Tep1 | Mm_Celera | 14:50863189 | GCATCACTGTTAAAG[-/GGA]GGAAGTCTGAGGGTA | 21745 |
rs241116341 | snp | C/T | | | downstream-variant-500B | Tep1 | GRCm38.p3 | 14:50824035 | TTGATCTAAAATCAC[C/T]AGCGAACACAATCGG | 21745 |
rs241121339 | snp | C/T | | | downstream-variant-500B | Tep1 | Mm_Celera | 14:50823977 | TGTTCCTGCAGTTCT[C/T]CTTAGATGTTAAATT | 21745 |
rs241143691 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50858538 | AAGTCCACTCACATC[C/T]ACAATTAAATGCTTT | 21745 |
rs241232434 | snp | C/T | | | synonymous-codon | Tep1 | Mm_Celera | 14:50837116 | TACCACCTGCCCCTC[C/T]GGGTGGAAGGCAACG | 21745 |
rs241277629 | snp | A/G | | | intron-variant | Tep1 | GRCm38.p3 | 14:50859416 | CACACCCACTCCAAT[A/G]AGGCCACACCCACTC | 21745 |
rs241387588 | in-del | -/GTG | | | intron-variant | Tep1 | GRCm38.p3 | 14:50846026 | TTTGTGTGTGTGTGT[-/GTG]GGGGGGGGTCCTCAC | 21745 |
rs241415497 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50860742 | GCTGGGTACCTGAGA[A/G]AGGGAAGAAAGTACC | 21745 |
rs241454085 | in-del | -/TT | | | intron-variant | Tep1 | Mm_Celera | 14:50857117 | TAGCCTCAGCTGTAA[-/TT]TTTTTTTTTTAAAGG | 21745 |
rs241503175 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50861628 | GAAAGCTCTTGTGTT[C/T]CACTCCTACAAGACT | 21745 |
rs241533219 | snp | G/T | | | intron-variant | Tep1 | Mm_Celera | 14:50852356 | CTGAGATCCTTACCA[G/T]CGTCATCCAATGCCA | 21745 |
rs241582756 | in-del | -/A | | | intron-variant | Tep1 | Mm_Celera | 14:50854603 | ACCACAGATTTCTGT[-/A]AAAACAAGAAGGACG | 21745 |
rs241585956 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50841485 | GTGTGGGGCTTTACC[A/G]AAGGACGGGTGGGAT | 21745 |
rs241594991 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50834434 | AACCTCTGCTTTCAG[A/G]GGACTAGTACCGTCT | 21745 |
rs241636045 | snp | G/T | | | intron-variant | Tep1 | GRCm38.p3 | 14:50839450 | TTCCAGGACAGCCAG[G/T]GATACACAGAGAAAC | 21745 |
rs241715825 | snp | C/T | | | intron-variant | Tep1 | GRCm38.p3 | 14:50827957 | AGACTGGAAAAAAAA[C/T]AAAAACAAAAATAAA | 21745 |
rs241766478 | snp | C/T | | | intron-variant, upstream-variant-2KB | Tep1, Gm26782 | GRCm38.p3 | 14:50869593 | CGCATATGCACATAC[C/T]CTTGcacacacaaac | 21745 |
rs241767566 | in-del | -/TCAATTCC | | | intron-variant | Tep1 | Mm_Celera | 14:50858054 | CCAGAAAACTTGGGT[-/TCAATTCC]TCAAACCCACATGGT | 21745 |
rs242073062 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50848794 | GTGTTTGTGTATATG[C/T]CTCTGTGTGGCAACC | 21745 |
rs242103645 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50830764 | TACTTAATCCAAGCC[C/T]GGGTATAACAATAGA | 21745 |
rs242108313 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50840023 | TACAAAAACACGCAC[A/G]CACACACATATACAC | 21745 |
rs242185718 | snp | A/T | | | intron-variant | Tep1 | Mm_Celera | 14:50831872 | AAGAACAAGATCATC[A/T]ACATTCCTCTCACAT | 21745 |
rs242191048 | snp | C/T | | | downstream-variant-500B | Tep1 | Mm_Celera | 14:50823562 | AGATCCATCTCTCAG[C/T]TCCATGAACTTCAAT | 21745 |
rs242288151 | in-del | -/TTTTG | | | intron-variant | Tep1 | Mm_Celera | 14:50854079 | AGCATCCAGTTGGGT[-/TTTTG]TTTTGTTTTGTTTTG | 21745 |
rs242306648 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50849046 | AAAGAAAAAGAGACT[A/G]TATATTTGAGAGCAA | 21745 |
rs242324684 | snp | C/T | | | missense, intron-variant | Tep1 | Mm_Celera | 14:50841270 | CATAGCGACGTTTAA[C/T]TGTTGTCCTCAGGGG | 21745 |
rs242398287 | snp | A/G | | | intron-variant, upstream-variant-2KB | Tep1, Gm26782 | Mm_Celera | 14:50868978 | TAGATTTATCCAGGC[A/G]TAATTCTAAGGGGAC | 21745 |
rs242433429 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50859688 | GTTTTGCCTGCATGT[A/G]TGTCTGTGAACCACA | 21745 |
rs242445121 | snp | A/G | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | Tep1, Gm26782 | Mm_Celera | 14:50870137 | TCGTGGAGGCCTACC[A/G]CGTTGGCACCTTAGT | 21745 |
rs242477548 | in-del | -/TG | | | upstream-variant-2KB, intron-variant | Tep1, Gm26782 | Mm_Celera | 14:50872212 | ATTGTGAGAAATAAA[-/TG]TGTGTGTGGGGGGGA | 21745 |
rs242567081 | snp | A/C | | | intron-variant | Tep1 | Mm_Celera | 14:50836524 | GCCCCCGCCCCACCC[A/C]CACCCACCCCCGCCC | 21745 |
rs242570057 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50831176 | GAAGGTGCCCAAGGA[A/G]GGCAGAGGCTTCCTG | 21745 |
rs242570704 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50826122 | GGAGAGATGGCTCAG[C/T]AGGTAGGAGCAATTG | 21745 |
rs242575554 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50857374 | CGGAAGGGTTGGAGG[A/G]AAGAAAGGAAAAAGG | 21745 |
rs242601470 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50832159 | AGGCAGTACTGTATC[A/G]TGTTAGGAACACGGG | 21745 |
rs242657111 | snp | G/T | | | missense | Tep1 | Mm_Celera | 14:50855690 | GCCATGAAGGGCAGT[G/T]TCCCATTGTCTTCAG | 21745 |
rs242728972 | snp | A/C | | | intron-variant | Tep1 | Mm_Celera | 14:50853835 | CTCTCCTTACGCACT[A/C]TCCCATCCTCCCACA | 21745 |
rs242771950 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50825631 | TGTTGAATTTAGGCT[A/G]ACACAGACGTGTCTG | 21745 |
rs242811784 | snp | A/T | | | intron-variant | Tep1 | Mm_Celera | 14:50863446 | TCTAAAAATGTCCTC[A/T]ATGATCAAAAGGGGA | 21745 |
rs242951091 | snp | G/T | | | intron-variant | Tep1 | Mm_Celera | 14:50835014 | TGTAAGCATATAATA[G/T]GAAAATATAGTCTCT | 21745 |
rs243036717 | in-del | -/G | | | intron-variant | Tep1 | GRCm38.p3 | 14:50827880 | TGTCTCGAAGAAGAA[-/G]AAAAAAAAAAAAAAC | 21745 |
rs243162245 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50862654 | CTGTCAAACAGGAAG[C/T]GCGTTCACAGAGGTG | 21745 |
rs243165293 | snp | A/C | | | synonymous-codon | Tep1 | Mm_Celera | 14:50860612 | AGAAGCTTTGTTTCC[A/C]CGTAAACTCAGCTCC | 21745 |
rs243192177 | in-del | -/G | | | intron-variant | Tep1 | Mm_Celera | 14:50846309 | CCCTCTGAGAACGCA[-/G]GGAAGAAACCCCTCT | 21745 |
rs243310656 | snp | C/T | | | missense | Tep1 | Mm_Celera | 14:50862514 | TTAAGGGGCCAAAGG[C/T]TCTTTGGAAAACATT | 21745 |
rs243335035 | snp | C/G | | | intron-variant | Tep1 | Mm_Celera | 14:50846216 | ATGTCATTTAGTTGC[C/G]CAGGCTGGCCTGCAA | 21745 |
rs243383375 | in-del | -/TCT | | | intron-variant | Tep1 | Mm_Celera | 14:50848608 | CTCTCTCTCTCTCCC[-/TCT]TTCCCCCCCTCTCTC | 21745 |
rs243427291 | snp | C/G | | | intron-variant | Tep1 | Mm_Celera | 14:50865237 | ACTGGGCCTGAGGTA[C/G]CTTCTGTGAGAGACT | 21745 |
rs243475787 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50856075 | GCCACCTGCCACTGG[C/T]CTTTCCAAGACACTG | 21745 |
rs243528403 | snp | A/C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50825931 | TAATACTGACAGAAA[A/C/T]CAAAAAAAAAAAAAA | 21745 |
rs243594525 | in-del | -/GG | | | upstream-variant-2KB, intron-variant | Tep1, Gm26782 | Mm_Celera | 14:50872240 | GGAGAGAGAGAGAGA[-/GG]GTTCTAAAACCATCC | 21745 |
rs243691864 | snp | C/G | | | intron-variant | Tep1 | Mm_Celera | 14:50859366 | AAGGAGTTTCAAAGC[C/G]CATCCCCACAGTGAC | 21745 |
rs243736437 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50851075 | TTTTTGTTTGTTTTG[C/T]TTGTTTTTGAGGATC | 21745 |
rs243738998 | in-del | -/AA | | | intron-variant | Tep1 | Mm_Celera | 14:50837966 | GGTTTGAGTCAGAAG[-/AA]AAAGCTGTGGCTCTC | 21745 |
rs243753331 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50865770 | TCTAGTACACCTTCC[C/T]CCATCTCCCTTTTCT | 21745 |
rs243755394 | in-del | -/G | | | intron-variant | Tep1 | GRCm38.p3 | 14:50839473 | GAGAAACCCTGTCTC[-/G]AAAAAACAAACAAAC | 21745 |
rs243881870 | in-del | -/T | | | intron-variant | Tep1 | Mm_Celera | 14:50867027 | CTTTATCACACTACC[-/T]TTTCTCTACCCAGCC | 21745 |
rs243904804 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50867869 | TGATACCAAAAATGC[C/T]GAGAAAAGAAGGTCC | 21745 |
rs243966004 | snp | A/T | | | intron-variant | Tep1 | Mm_Celera | 14:50842749 | AATGAAACTAAGAAA[A/T]CATTATACCAGAAGT | 21745 |
rs243969398 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50828856 | TAACAAAATGCTAGG[C/T]GTGTGTGGCTTGCCA | 21745 |
rs244042735 | snp | G/T | | | intron-variant | Tep1 | Mm_Celera | 14:50825044 | CACTCTGGCCCTTCT[G/T]CTCCCACTAACCAGA | 21745 |
rs244120545 | snp | C/G | | | intron-variant | Tep1 | Mm_Celera | 14:50830480 | CCAAACAACCTGTCA[C/G]TAGCCCAAGTCTCCC | 21745 |
rs244132950 | in-del | -/A | | | intron-variant | Tep1 | Mm_Celera | 14:50857636 | AATAAATAAATCTTT[-/A]AAAAAAAAAAGAAAC | 21745 |
rs244249643 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50832533 | TCTTAACCACTCCAG[C/T]GCACAAATAATTCTT | 21745 |
rs244273143 | snp | C/T | | | intron-variant | Tep1 | GRCm38.p3 | 14:50838149 | CAACTGGATCCTGGC[C/T]CTCAGCCCTGTTCCT | 21745 |
rs244330833 | in-del | -/T/TA | | | intron-variant | Tep1 | Mm_Celera | 14:50826593 | CTAGGTGTCTGACTT[-/T/TA]AAAAAAAACTATACA | 21745 |
rs244369679 | snp | C/T | | | missense | Tep1 | Mm_Celera | 14:50838534 | CATACCTGCCAGGTT[C/T]TCAAGTTCAACAGGT | 21745 |
rs244408972 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50848195 | GCGATCAGCTCTGTA[C/T]AAACTACAATAGCTC | 21745 |
rs244438439 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50859125 | AAAATTGGAAGGTTT[C/T]CACTGTCTTATTTAG | 21745 |
rs244489089 | in-del | -/TCA | | | intron-variant, upstream-variant-2KB | Tep1, Gm26782 | Mm_Celera | 14:50869289 | TTAGGAGTTCAAAGG[-/TCA]TCATCCTTGGCTACA | 21745 |
rs244682558 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50828606 | TTGTTCTCTGACCTC[C/T]GAATACACAGGTGAG | 21745 |
rs244696422 | snp | C/T | | | missense | Tep1 | Mm_Celera | 14:50841630 | GACTGGCAGCCAGCA[C/T]TTCTTCCCAGCTCTT | 21745 |
rs244773156 | snp | A/G | | | missense | Tep1 | Mm_Celera | 14:50836773 | TGTGCAGGGAAGGCC[A/G]CCAGCCGGGCACCCT | 21745 |
rs244788206 | snp | A/G | | | intron-variant | Tep1 | GRCm38.p3 | 14:50839374 | ACCTTTAATTTCAGT[A/G]CTTGGGGGGCAGAGG | 21745 |
rs244828378 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50827278 | TCAAGGACTTCTCAT[A/G]AATGAAGTATAACGC | 21745 |
rs244860481 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50850498 | AGGCAAGATACAAAA[C/T]ATCAAACAAGTGAGA | 21745 |
rs244938207 | in-del | -/G | | | downstream-variant-500B | Tep1 | Mm_Celera | 14:50823670 | GTCCAAAGACTCATT[-/G]CTGCCTTTGGTGCCT | 21745 |
rs244951577 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50851735 | AAAGTTTGACAGATC[A/G]TTTAGAAAGGTCAAG | 21745 |
rs244981912 | snp | A/G | | | missense, downstream-variant-500B | Tep1 | Mm_Celera | 14:50841042 | GCATCAGGATCACAC[A/G]TCTTCCAGAGGTGAG | 21745 |
rs245110156 | snp | A/T | | | intron-variant | Tep1 | Mm_Celera | 14:50848029 | TAACCATAAGCCAGG[A/T]AAGTGTACTGGAAAA | 21745 |
rs245279011 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB | Tep1, Gm26782 | GRCm38.p3 | 14:50870456 | CAATGAGAGGCGCGT[C/T]GGTTCTCCGCAACGG | 21745 |
rs245309781 | snp | A/C | | | upstream-variant-2KB, intron-variant | Tep1, Gm26782 | Mm_Celera | 14:50871303 | GGCTGGCTTCTGACT[A/C]ACAGAGATCCGCCTG | 21745 |
rs245358656 | in-del | -/G | | | intron-variant | Tep1 | GRCm38.p3 | 14:50840135 | ATATACCAAGGGAGT[-/G]GGGGGTCAGAAAACA | 21745 |
rs245390379 | in-del | -/ATTAT | | | intron-variant | Tep1 | Mm_Celera | 14:50857401 | AGGGAAAATCATGTA[-/ATTAT]ATTTTGATTTCAAAA | 21745 |
rs245474076 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50857998 | ATAAAAGGGGGGAGG[A/G]GTAGAGAAATGTCTG | 21745 |
rs245505915 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50838187 | CTAAGTCACACGACT[C/T]AAAGGGAAGCCACAC | 21745 |
rs245665717 | snp | G/T | | | intron-variant | Tep1 | Mm_Celera | 14:50855179 | CAGATCCTCTGGAAA[G/T]TGAGTTATAGATGGT | 21745 |
rs245713954 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50833776 | AAGAAGAGAGAAAGT[A/G]TAAAGCATGCAGGTA | 21745 |
rs245738721 | snp | A/C | | | intron-variant | Tep1 | Mm_Celera | 14:50863832 | TCCTGGCCATCTTCT[A/C]CATCATCAACCAGGC | 21745 |
rs245794935 | snp | A/G | | | intron-variant, upstream-variant-2KB | Tep1, Gm26782 | Mm_Celera | 14:50869761 | TGGAACTACTATACA[A/G]ATTCCAACTCACAGA | 21745 |
rs245894186 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50860250 | ACAATATATTCTAGG[C/T]GTATTGCTACAAGTG | 21745 |
rs246104560 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50860854 | TGGGAGTGAGAACTA[C/T]CAGGCTTGGAGCCAT | 21745 |
rs246104590 | snp | A/G | | | synonymous-codon | Tep1 | Mm_Celera | 14:50853111 | CCATCATTCCGATCA[A/G]CAGCAGCACATAGTT | 21745 |
rs246172273 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50863355 | TTCCATTAGCCCACT[C/T]GGCTCTTAGAGAGAA | 21745 |
rs246182033 | snp | A/G | | | synonymous-codon | Tep1 | Mm_Celera | 14:50854241 | GTGCTTCCGACTGGC[A/G]GGCCTCCTATTTTTT | 21745 |
rs246256230 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50825175 | TCCTGTGAAGGGATA[A/G]GTAGAGAGGTAACTT | 21745 |
rs246288076 | in-del | -/GCACCAT | | | intron-variant | Tep1 | Mm_Celera | 14:50842602 | TAAGGAAGCTGAGCA[-/GCACCAT]GCATTCATCCTCTGA | 21745 |
rs246325248 | in-del | -/AAA | | | intron-variant | Tep1 | Mm_Celera | 14:50847202 | TGTGCCTCTTTCTTT[-/AAA]AAAAAAAATCATATT | 21745 |
rs246429238 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50864027 | AGAAAAAGATATTCA[A/G]TATCCAGATTATTGC | 21745 |
rs246440909 | snp | A/T | | | intron-variant, upstream-variant-2KB | Tep1, Gm26782 | Mm_Celera | 14:50869530 | GAGAAGCAATAGAAT[A/T]AGACACCTGGTGTGG | 21745 |
rs246455815 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50825734 | AGACAGACTTTGTAC[A/G]TAACTTTAGTAGGTA | 21745 |
rs246462428 | snp | A/C | | | intron-variant | Tep1 | Mm_Celera | 14:50856830 | AAAATTATCTTTATT[A/C]ATCTCTCTGTGTGTG | 21745 |
rs246462802 | snp | C/G/T | | | intron-variant | Tep1 | Mm_Celera | 14:50864983 | AGAACATCCCTCCAA[C/G/T]GGCTTCTGCATCAGC | 21745 |
rs246540738 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50857418 | TTTTGATTTCAAAAA[A/G]TAAAAAATATTTCTA | 21745 |
rs246557397 | snp | A/G | | | synonymous-codon | Tep1 | Mm_Celera | 14:50866821 | CATTGGGACTTCTGT[A/G]CTTTCTTCTTCTTGA | 21745 |
rs246576402 | snp | A/G | | | upstream-variant-2KB, intron-variant | Tep1, Gm26782 | Mm_Celera | 14:50871655 | CACAGACATACATAG[A/G]GGCAAAACTCATAAA | 21745 |
rs246577389 | snp | C/G | | | intron-variant | Tep1 | Mm_Celera | 14:50827594 | GACCTCAGCACCACT[C/G]CATAATGGCAGTGCC | 21745 |
rs246611354 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50828000 | ACAAAAACCACCAAA[C/T]CCACCACAGCTTTAG | 21745 |
rs246675739 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50861741 | AGAAGGAAAAAGAGG[C/T]AACTATTATCTAGAT | 21745 |
rs246728372 | snp | G/T | | | intron-variant | Tep1 | Mm_Celera | 14:50842371 | GCTCTTGCAGAGGAC[G/T]CGGGTTTAACTCCCA | 21745 |
rs246776475 | snp | C/G | | | intron-variant | Tep1 | Mm_Celera | 14:50829382 | CCTTTAATCCTAGCA[C/G]TAGGGACACAGTGGA | 21745 |
rs246778736 | snp | G/T | | | intron-variant | Tep1 | Mm_Celera | 14:50833712 | TGATTTTCTGAGTAC[G/T]GAGATTAAGGTAGGT | 21745 |
rs246789564 | snp | A/T | | | intron-variant | Tep1 | Mm_Celera | 14:50855584 | CTCCCCAGGGATCAC[A/T]CGTACCTCATGCTGG | 21745 |
rs246823673 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50855870 | GGCCTGAACTGGGGA[A/G]TAAAAACATATAACA | 21745 |
rs246903530 | snp | G/T | | | intron-variant | Tep1 | Mm_Celera | 14:50845215 | GGGGCCAGACTCAGG[G/T]GCAGGGCCAGACTCA | 21745 |
rs246942496 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50851438 | ATAATTCTCGAAATG[C/T]ATTACCTTCTAATTA | 21745 |
rs246958117 | snp | A/T | | | intron-variant | Tep1 | Mm_Celera | 14:50832042 | TACATACGGAAAATA[A/T]ACACCACAAACCCTG | 21745 |
rs247005371 | snp | C/T | | | synonymous-codon | Tep1 | Mm_Celera | 14:50824180 | TCTTCATTCCCAAGA[C/T]AGAAAATACAAGTTT | 21745 |
rs247158553 | snp | A/G | | | intron-variant | Tep1 | GRCm38.p3 | 14:50858314 | GGAAGTGTGTCCCTC[A/G]GGGTGGGCTTTAAGG | 21745 |
rs247190040 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50858847 | TCTCAAACTAGTCCT[C/T]CTCCTGCCTCAGTCC | 21745 |
rs247264726 | snp | G/T | | | intron-variant | Tep1 | Mm_Celera | 14:50850329 | GCAACCAATCTTGTC[G/T]TAATAGAATTATGTG | 21745 |
rs247280921 | snp | A/C | | | intron-variant | Tep1 | Mm_Celera | 14:50837495 | CTGCCCCAGGAAGAC[A/C]ATGTCAGGGTTCTGG | 21745 |
rs247452182 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50837328 | AGGCAGTCATGCCAC[A/G]TGGAACAACAAAATC | 21745 |
rs247452477 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50838891 | CTCTTCTGCCTCTTT[C/T]TCTGAAGGGCCGCTG | 21745 |
rs247460813 | in-del | -/CC | | | intron-variant | Tep1 | Mm_Celera | 14:50830990 | CAAATTCACAGAGCT[-/CC]ACCTGCCTCTGCTCC | 21745 |
rs247553074 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50827894 | AGAAAAAAAAAAAAA[A/G]CACTGAACTGATTCT | 21745 |
rs247554957 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50840561 | AAAAAAAAAAGGCTC[A/G]ACTCCAATGACTTAT | 21745 |
rs247619986 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50836996 | CCACTTTCACCACAG[C/T]CCTGCGTGTTCTCCT | 21745 |
rs247853760 | snp | A/C | | | intron-variant | Tep1 | Mm_Celera | 14:50838774 | CTGCCTCTTTCTCTG[A/C]ATCTCTGCCTGCACC | 21745 |
rs247932476 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50829152 | GGGTGGACAGAATTC[A/G]TATAGCCCAAGACAC | 21745 |
rs247968679 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50830102 | GGAAATAAAAGGGGA[A/G]GAAGGGGAAAGGCTG | 21745 |
rs248054080 | in-del | -/T | | | intron-variant | Tep1 | Mm_Celera | 14:50867475 | ACTTTTCCCCACGTA[-/T]TCCACAGAGGAAATG | 21745 |
rs248084733 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50829637 | TCTTCTTTTATGCTA[C/T]CTCCCCCTCCCTCCC | 21745 |
rs248180270 | snp | G/T | | | intron-variant | Tep1 | Mm_Celera | 14:50838098 | AGCCAAAGTTCTCTT[G/T]TATATACACAACTCT | 21745 |
rs248382296 | snp | A/G | | | missense | Tep1 | Mm_Celera | 14:50828920 | CTGGAACTGGTGGAC[A/G]TTGAACCTTTCCTCA | 21745 |
rs248440862 | in-del | -/ACACACACACACACACAT | | | intron-variant | Tep1 | Mm_Celera | 14:50826266 | CCCAAACACACACAC[-/ACACACACACACACACAT]ACACACACACACAAA | 21745 |
rs248461153 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50833886 | AGGCTGTGGGGCCAT[A/G]GGGTTGCATCTTCTG | 21745 |
rs248464466 | snp | C/G | | | intron-variant | Tep1 | Mm_Celera | 14:50825244 | AGACAGGATATATAT[C/G]ACACAAAATATTAGT | 21745 |
rs248471682 | in-del | -/CGTTC | | | intron-variant | Tep1 | Mm_Celera | 14:50857732 | ACCCAGCTCCATCCG[-/CGTTC]TGTTCTGGCCTTTCT | 21745 |
rs248528384 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50866600 | GGATCTTTTCCCTCT[A/G]CCATGTTCCACATGG | 21745 |
rs248552983 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50867290 | CAAACTGCAAATCAC[A/G]TAAGGGCAATAGCAG | 21745 |
rs248679042 | snp | A/G | | | synonymous-codon | Tep1 | Mm_Celera | 14:50841595 | GGCAAATGGACACAA[A/G]GGGAAAGGGTTTCCA | 21745 |
rs248684908 | snp | C/G | | | intron-variant | Tep1 | GRCm38.p3 | 14:50852757 | agaggcagaaagaga[C/G]agagagacagagaga | 21745 |
rs248782791 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50833131 | GACATCCATCTGCAC[A/G]CGTGCACTGATGCAC | 21745 |
rs248869688 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50855809 | GGAGAATGCAATCTG[C/T]TCTACTCAAAAGATT | 21745 |
rs248870987 | in-del | -/GG | | | intron-variant | Tep1 | Mm_Celera | 14:50846028 | TGTGTGTGTGTGTGT[-/GG]GGGGGGGTCCTCACT | 21745 |
rs248894161 | snp | A/G | | | upstream-variant-2KB, intron-variant | Tep1, Gm26782 | Mm_Celera | 14:50871415 | GATTTTGGGGATTTG[A/G]GCTTTTATTTTTAGA | 21745 |
rs248919587 | snp | A/C | | | intron-variant | Tep1 | Mm_Celera | 14:50850143 | ATCGATGCCTGGAGT[A/C]AGGGGTAGTGGCTTA | 21745 |
rs248928152 | snp | C/T | | | upstream-variant-2KB, intron-variant | Tep1, Gm26782 | Mm_Celera | 14:50872162 | AGCACTCTTAAGTCC[C/T]ACCTACTAAATATTA | 21745 |
rs249064343 | in-del | -/TCCTGGC | | | intron-variant | Tep1 | GRCm38.p3 | 14:50838142 | ATGTGAACAACTGGA[-/TCCTGGC]TCTCAGCCCTGTTCC | 21745 |
rs249077972 | snp | C/G | | | intron-variant | Tep1 | Mm_Celera | 14:50861122 | AAATAAAAACATAAG[C/G]CTACCTTACCCTATC | 21745 |
rs249111033 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50861965 | AAGGAATACATGTGA[C/T]ACACAGACACACAGA | 21745 |
rs249379261 | in-del | -/A | | | intron-variant | Tep1 | GRCm38.p3 | 14:50839346 | AGGTGGGAGCCGGGC[-/A]GTGGTGGCGCACACC | 21745 |
rs249485132 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50824310 | AACAGGAACAGAAAC[A/G]GGGGAAGTGAAACTA | 21745 |
rs249629812 | in-del | -/AA | | | intron-variant | Tep1 | Mm_Celera | 14:50863926 | TGCGTTGTAAATGAG[-/AA]AGAAATAACAGGCTG | 21745 |
rs249708244 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50855904 | TGTATCGGATAGCTG[C/T]TTATATAACAACTTA | 21745 |
rs249720895 | in-del | -/T | | | intron-variant | Tep1 | Mm_Celera | 14:50826591 | TCCTAGGTGTCTGAC[-/T]TTAAAAAAAACTATA | 21745 |
rs249733187 | snp | C/T | | | synonymous-codon | Tep1 | Mm_Celera | 14:50837661 | AGTGTCCGAAAGGAA[C/T]GCAAAAGAGGAAATC | 21745 |
rs249844892 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50833379 | AGATGCTAGAAAATG[C/T]TTGAGGCGGAGGTCA | 21745 |
rs249969263 | snp | C/G | | | intron-variant | Tep1 | Mm_Celera | 14:50846791 | TTCCACCACTCAATC[C/G]TCTCACCCCTGACCT | 21745 |
rs250019567 | snp | A/C/T | | | intron-variant | Tep1 | GRCm38.p3 | 14:50838148 | ACAACTGGATCCTGG[A/C/T]TCTCAGCCCTGTTCC | 21745 |
rs250121777 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50841410 | TCAGTGAACACATGT[A/G]CCAACGTTCCCATTG | 21745 |
rs250154869 | snp | A/C | | | synonymous-codon | Tep1 | Mm_Celera | 14:50846499 | GTGGGGATGATCAGG[A/C]AGATCATAGCTGGGG | 21745 |
rs250155922 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50843283 | ATCTGGTCAGATATG[A/G]AGGATTCAGCATTAT | 21745 |
rs250243261 | snp | A/C | | | intron-variant | Tep1 | Mm_Celera | 14:50844486 | TGCATAATCTCCCGG[A/C]TCTACCTCTTTAGCC | 21745 |
rs250250474 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50839748 | GACCAGGCTGGCCTC[A/G]AACTCAGAAATCCAC | 21745 |
rs250352504 | snp | A/T | | | intron-variant | Tep1 | Mm_Celera | 14:50826155 | AGCAAGCCTCACAAC[A/T]GAGTTTGATCTCTAG | 21745 |
rs250400541 | snp | A/T | | | intron-variant | Tep1 | Mm_Celera | 14:50832917 | TTGGGTTCAGTATCC[A/T]CCAGCAAAAGGGCAG | 21745 |
rs250497228 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50845647 | GTAATCTTGTGTCCT[C/T]CCCCGAAACACAGAC | 21745 |
rs250499432 | snp | C/G | | | intron-variant | Tep1 | Mm_Celera | 14:50856983 | CTAGAAGAGGATGCG[C/G]TATGCGCCCTGGAGC | 21745 |
rs250563579 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50859460 | CCCACTCCAACAAGG[C/T]CATACCTCCTAGTAG | 21745 |
rs250638772 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50864249 | GACTGGCCAGTGGGC[A/G]TGTCTGGGAGGAGAT | 21745 |
rs250684958 | in-del | -/GGACA | | | intron-variant | Tep1 | Mm_Celera | 14:50855713 | GTCTTCAGTCATGGG[-/GGACA]GGATAAAGCAAGTGA | 21745 |
rs250690693 | in-del | -/A | | | intron-variant | Tep1 | Mm_Celera | 14:50855074 | TTATTCATTTAATTG[-/A]AAAAATATTGTATGT | 21745 |
rs250692870 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50836495 | GTTTAAAGGTACTTC[C/T]CTGCCCCGTCCCTGC | 21745 |
rs250795408 | snp | C/T | | | synonymous-codon | Tep1 | Mm_Celera | 14:50844594 | CAGCCTCCCATGGGG[C/T]AGCAACAGCTGCTGC | 21745 |
rs250818550 | snp | A/T | | | intron-variant | Tep1 | GRCm38.p3 | 14:50839233 | GAGAGAGAGAGAGAG[A/T]GAGAATAGCTGAGGA | 21745 |
rs251010795 | snp | C/T | | | missense | Tep1 | Mm_Celera | 14:50868045 | TGGATTTCAGGGCCC[C/T]GGGTCCAGGTGGAAG | 21745 |
rs251044572 | snp | A/G | | | intron-variant, upstream-variant-2KB | Tep1, Gm26782 | Mm_Celera | 14:50869266 | GCACTTGAGGCCGAG[A/G]CAGAAGGGTTAGGAG | 21745 |
rs251090260 | snp | A/T | | | intron-variant | Tep1 | GRCm38.p3 | 14:50839592 | AGACAGGAGAACCAC[A/T]GGAGCTTGCTGGCCA | 21745 |
rs251113316 | snp | C/G | | | synonymous-codon | Tep1 | Mm_Celera | 14:50860935 | TCACCTGTAGCCCAG[C/G]AGGGCCTGGACGTGC | 21745 |
rs251171056 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50840321 | GAAGACCTAGGGAAG[C/T]GAAATCTTGTAATCT | 21745 |
rs251203857 | snp | C/G | | | intron-variant | Tep1 | Mm_Celera | 14:50853938 | AGCAAGGCAGAGTCC[C/G]TGGCAAAGCCGGTGC | 21745 |
rs251251630 | snp | C/T | | | intron-variant | Tep1 | Mm_Celera | 14:50858157 | AGCACAAATGTGATA[C/T]ACAGACATACATAAA | 21745 |
rs251447179 | snp | A/T | | | intron-variant | Tep1 | Mm_Celera | 14:50864192 | CTTGACAGCCTAGAG[A/T]CATCTGAGAGGGAAA | 21745 |
rs251584889 | snp | C/T | | | downstream-variant-500B | Tep1 | Mm_Celera | 14:50823692 | TTGGTGCCTGGGTTT[C/T]CCACTCTGGCCAGTT | 21745 |
rs251641729 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50830437 | TGACCTGTATGTATT[A/G]AGCATACTCCCCTCT | 21745 |
rs251681555 | in-del | -/GAACAAG | | | intron-variant | Tep1 | Mm_Celera | 14:50863103 | GTTACATAGGAACAA[-/GAACAAG]GAACAATTTCCTACT | 21745 |
rs251721550 | snp | G/T | | | intron-variant, upstream-variant-2KB | Tep1, Gm26782 | Mm_Celera | 14:50868908 | AACTCCAGTGGTCGG[G/T]ATTGCAGTGTTGTAC | 21745 |
rs251760050 | snp | C/T | | | downstream-variant-500B | Tep1 | Mm_Celera | 14:50823893 | CTTCCTTCCTTCTGA[C/T]AAGAGTGGACCTTAG | 21745 |
rs251880297 | snp | A/G | | | intron-variant | Tep1 | Mm_Celera | 14:50830900 | GCTTTTTGCTTGACT[A/G]TTGGTTTTTTGAGAC | 21745 |