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 |