SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs30129626 | snp | C/T | 0.5 | 0 | intron-variant | Trim52 | Mm_Celera | 14:106121060 | TTCTCCTGCCTCTAT[C/T]TAAGGATTGCTGGAA | 212085 |
rs30158467 | snp | A/C | 0.375 | 0.216506 | intron-variant | Trim52 | Mm_Celera | 14:106133731 | AGGGAGGAAAGCAGG[A/C]ATAATAGTGAAATAC | 212085 |
rs30158743 | snp | A/C | 0.33241 | 0.236027 | utr-variant-3-prime, intron-variant | Trim52 | Mm_Celera | 14:106108926 | GCTATTTCAAGGAAA[A/C]AAAAATAATATTCAG | 212085 |
rs30201722 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Trim52 | Mm_Celera | 14:106122501 | TCTGGGCTCTTTCCA[G/T]CTTCTGGCTATTATA | 212085 |
rs30207203 | snp | A/C | 0.375 | 0.216506 | intron-variant | Trim52 | Mm_Celera | 14:106130127 | TTCCAGATTTCTTTT[A/C]TAGGGTTTTTTTCTC | 212085 |
rs30211682 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Trim52 | Mm_Celera | 14:106134914 | AGGGTACATGGCACT[A/C]ATTAGGCATGTATGC | 212085 |
rs30216432 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Trim52 | Mm_Celera | 14:106125423 | GGCATTAAAGGCATG[C/T]GCCACCATGCCCAAC | 212085 |
rs30262295 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Trim52 | Mm_Celera | 14:106134842 | GCTATAAAGAGCTAC[C/T]ATGATAAAGATAACA | 212085 |
rs30305997 | snp | A/C | 0.375 | 0.216506 | intron-variant | Trim52 | Mm_Celera | 14:106124549 | GCCACAGCCACATGA[A/C]TGAAGCTGCTGAATT | 212085 |
rs30308367 | snp | C/T | 0.197531 | 0.244432 | downstream-variant-500B, intron-variant | Trim52 | Mm_Celera | 14:106109412 | AGAGCCTGCAAGTAG[C/T]ATGCCTATAGAACAG | 212085 |
rs30340501 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Trim52 | Mm_Celera | 14:106126350 | ACAAGCCATTGCTGT[C/T]CTATTCAGAAAGTTT | 212085 |
rs30387836 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Trim52 | Mm_Celera | 14:106124700 | CACAACTGGAGTTAT[C/G]ACAGAGAAAGGAGCT | 212085 |
rs30490436 | snp | A/G | 0.5 | 0 | intron-variant | Trim52 | Mm_Celera | 14:106124971 | CAGCAGCATGAAAGT[A/G]TAAGCCAAATAAACC | 212085 |
rs30509114 | snp | C/T | 0.5 | 0 | intron-variant | Trim52 | Mm_Celera | 14:106135355 | TTTTGTTCCATTGAG[C/T]TATGTTTGTACTAGT | 212085 |
rs30524595 | snp | A/C | 0.5 | 0 | intron-variant | Trim52 | Mm_Celera | 14:106121120 | TTATATATACTCTTA[A/C]AATGTTACAATTATT | 212085 |
rs30556122 | snp | C/T | 0.375 | 0.216506 | intron-variant | Trim52 | Mm_Celera | 14:106134010 | CTTGGCCTCCACAGA[C/T]ACATATCTGGTCTCA | 212085 |
rs30567613 | snp | A/G/T | 0.5 | 0 | intron-variant | Trim52 | GRCm38.p3 | 14:106118528 | AACAGTTTATTCAGC[A/G/T]TACACTTTCACATTG | 212085 |
rs30586644 | snp | C/T | 0.375 | 0.216506 | intron-variant | Trim52 | Mm_Celera | 14:106133391 | GCTGAGCTCAAAGCT[C/T]ACCCAAGTGAAACAA | 212085 |
rs30648277 | snp | A/C | 0.290657 | 0.246672 | utr-variant-3-prime, intron-variant, downstream-variant-500B | Trim52 | Mm_Celera | 14:106107996 | GTTCAGTTTTAGGAA[A/C]TATTACTCCTTTGTT | 212085 |
rs30652185 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Trim52 | Mm_Celera | 14:106110046 | CAGAGAATGGGAAAG[C/T]TGGTAAGATGTTCTA | 212085 |
rs30654033 | snp | G/T | 0.375 | 0.216506 | intron-variant | Trim52 | Mm_Celera | 14:106130236 | CATCTGTTTTGTTGT[G/T]TTTTCCTATTTTCCT | 212085 |
rs30703430 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Trim52 | Mm_Celera | 14:106120704 | AAGTGCTACTGTTTT[C/T]TTCTGTACTTCCCTG | 212085 |
rs30734640 | snp | A/C | 0.375 | 0.216506 | intron-variant | Trim52 | Mm_Celera | 14:106134260 | TTAGATGGGTGGAAT[A/C]TCACCCAAGGGCACC | 212085 |
rs30753787 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Trim52 | GRCm38.p3 | 14:106111723 | TTGATTTTGCTTTGT[A/G]ACTGTGCCCTAGTTT | 212085 |
rs30779425 | snp | A/G | 0.375 | 0.216506 | nc-transcript-variant | Trim52 | Mm_Celera | 14:106135672 | CTGTTACCTCGATCT[A/G]CACGTACAGTTTGCT | 212085 |
rs30798669 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Trim52 | Mm_Celera | 14:106122561 | TGTGTCCTTCATACC[A/G]GTTGGGGCATCTACT | 212085 |
rs30874377 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Trim52 | GRCm38.p3 | 14:106111995 | TTTCAGGAAGTGTTT[A/C]ATCAAAGTCAACAGG | 212085 |
rs30924685 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Trim52 | Mm_Celera | 14:106135154 | CAAATATATGAACTT[A/G]CAGGAATCATTCTTA | 212085 |
rs30946235 | snp | G/T | 0.375 | 0.216506 | upstream-variant-2KB | Trim52 | Mm_Celera | 14:106106148 | AATGGGGGCGGGGTG[G/T]CAGGAAGAACCTATG | 212085 |
rs30960763 | snp | A/T | 0.5 | 0 | intron-variant | Trim52 | GRCm38.p3 | 14:106111653 | GGGGTTTTTGTTTGT[A/T]TGTTTGTTTGTTTTT | 212085 |
rs31025566 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Trim52 | Mm_Celera | 14:106124814 | GGTGCCATCTCTGGG[C/T]TGGTAGTCTTGGGTT | 212085 |
rs31044684 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Trim52 | Mm_Celera | 14:106125958 | AACATTTAATTGGGG[A/C]TGGTTTACAGGTTCA | 212085 |
rs31073687 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Trim52 | Mm_Celera | 14:106131929 | GTACATGATCTAGGT[A/G]GAATGCAGACATACT | 212085 |
rs31082868 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Trim52 | GRCm38.p3 | 14:106128079 | ATCCAGGTATTCCAG[A/T]ATGTTGAGTATAGCC | 212085 |
rs31141045 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Trim52 | Mm_Celera | 14:106122568 | TTCATACCAGTTGGG[A/G]CATCTACTGGATATA | 212085 |
rs31164956 | snp | A/C/T | 0.375 | 0.216506 | utr-variant-3-prime, intron-variant, downstream-variant-500B | Trim52 | GRCm38.p3 | 14:106107947 | CCTAGCATGCCCCCA[A/C/T]TTTCCAATTTATTTT | 212085 |
rs31206654 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Trim52 | Mm_Celera | 14:106125438 | CGCCACCATGCCCAA[C/G]TTGAACCATACATTT | 212085 |
rs31222256 | snp | G/T | 0.375 | 0.216506 | intron-variant | Trim52 | Mm_Celera | 14:106130092 | CTCTTGTATTCTGTT[G/T]CTGATGCTTGCATCT | 212085 |
rs31237379 | snp | C/T | 0.375 | 0.216506 | intron-variant | Trim52 | Mm_Celera | 14:106130142 | ATAGGGTTTTTTTCT[C/T]CAGTGTTGCCTCCCT | 212085 |
rs31255605 | snp | A/G | 0.5 | 0 | intron-variant | Trim52 | Mm_Celera | 14:106124966 | ATGAACAGCAGCATG[A/G]AAGTGTAAGCCAAAT | 212085 |
rs31321495 | snp | A/T | 0.32 | 0.24 | intron-variant | Trim52 | Mm_Celera | 14:106132065 | TCTCCAAGATCCATG[A/T]CTTCACTAGCCTTGG | 212085 |
rs31330360 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Trim52 | Mm_Celera | 14:106124785 | TGATCAAGGGGGAAA[G/T]TCCTCTTGTGGGTGG | 212085 |
rs31335456 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Trim52 | Mm_Celera | 14:106131890 | CTACTCTGGTAAGGG[A/T]TAATATCCAAAGGCC | 212085 |
rs31349488 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Trim52 | Mm_Celera | 14:106125105 | AATGCTGAGATCAGC[A/G]TGCCTGTCTATGAGA | 212085 |
rs31418406 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Trim52 | Mm_Celera | 14:106122574 | CCAGTTGGGGCATCT[A/T]CTGGATATATGCCCA | 212085 |
rs31436571 | snp | A/C | 0.375 | 0.216506 | intron-variant | Trim52 | Mm_Celera | 14:106134211 | TGCTCTTTAGGAACA[A/C]ATAATTCCTTAGGGC | 212085 |
rs31469013 | snp | C/T | 0.32 | 0.24 | intron-variant | Trim52 | Mm_Celera | 14:106132550 | ATATATATATATATA[C/T]ATATATATATATACA | 212085 |
rs31469796 | snp | A/T | 0.375 | 0.216506 | intron-variant | Trim52 | Mm_Celera | 14:106124617 | CTATTACATTATCAC[A/T]GGCTTTATGTTTTCT | 212085 |
rs31473257 | snp | C/T | 0.375 | 0.216506 | intron-variant | Trim52 | Mm_Celera | 14:106134149 | TGATCAGGATAGAAA[C/T]TGGCTCCCTTCTTGA | 212085 |
rs31503688 | snp | C/T | 0.32 | 0.24 | intron-variant | Trim52 | Mm_Celera | 14:106132530 | ATATATATATATATA[C/T]ATATATATATATATA | 212085 |
rs31528402 | snp | A/G | 0.375 | 0.216506 | upstream-variant-2KB | Trim52 | GRCm38.p3 | 14:106106129 | TTCGCCCCCGCCCCC[A/G]GGCAATGGGGGCGGG | 212085 |
rs45632442 | snp | G/T | | | intron-variant | Trim52 | Mm_Celera | 14:106121594 | CACTTCTGTGTTTGT[G/T]AGGCCCCGGCATAGT | 212085 |
rs45675456 | snp | A/T | 0.32 | 0.24 | intron-variant | Trim52 | Mm_Celera | 14:106120166 | GTTTCCTGAATAGGA[A/T]CTGATTAAAATATGA | 212085 |
rs45722468 | snp | A/T | 0.231111 | 0.249285 | upstream-variant-2KB | Trim52 | Mm_Celera | 14:106105767 | TATTTAGCTGTGAGG[A/T]GAAGCAGTTGACGAT | 212085 |
rs45893569 | snp | C/G/T | | | intron-variant | Trim52 | GRCm38.p3 | 14:106130971 | AGAAGCTGTGTTGCT[C/G/T]CTGCCTGTCCCAGAA | 212085 |
rs45930658 | snp | G/T | | | intron-variant | Trim52 | Mm_Celera | 14:106123297 | TGAACTCATAAGTCC[G/T]CCTGTCTCTGCCTCC | 212085 |
rs45970011 | snp | A/T | 0.32 | 0.24 | intron-variant | Trim52 | Mm_Celera | 14:106120256 | TATTGACATTTCTGA[A/T]AGGTAGAAACATTGA | 212085 |
rs45970210 | snp | G/T | | | upstream-variant-2KB | Trim52 | Mm_Celera | 14:106105230 | GGAAGAAACAAGAGT[G/T]TACTTCATTTGTAAA | 212085 |
rs45971629 | snp | C/T | 0.132653 | 0.220748 | utr-variant-5-prime, nc-transcript-variant | Trim52 | Mm_Celera | 14:106106316 | GCCAGCGCCTTCTGG[C/T]TTCGGAGCGACGGCT | 212085 |
rs46126203 | snp | G/T | 0.152778 | 0.230321 | upstream-variant-2KB | Trim52 | Mm_Celera | 14:106105303 | TTAATAAAATGTGAT[G/T]ATTTGAAAATGTTGA | 212085 |
rs46152408 | snp | C/T | | | intron-variant | Trim52 | Mm_Celera | 14:106122666 | TGATTTCCAGAGTGG[C/T]TCTACAAGCTTGCAA | 212085 |
rs46245898 | snp | A/G | | | intron-variant | Trim52 | Mm_Celera | 14:106130404 | GTGCTTTTAAACTCG[A/G]GTATATTTTAGGGTG | 212085 |
rs46454178 | snp | C/G | | | intron-variant | Trim52 | Mm_Celera | 14:106110924 | TTGCCCTGTGTCATG[C/G]ACATCCTTCAGCTTG | 212085 |
rs46460357 | snp | C/T | | | intron-variant | Trim52 | Mm_Celera | 14:106122073 | CTTTACTGGCTTGCT[C/T]ACCCTGGCTTGCTCA | 212085 |
rs46540553 | snp | A/G | | | intron-variant | Trim52 | Mm_Celera | 14:106110759 | TGTGGAAGTTGTAGT[A/G]TGTGACAGTGTGTCC | 212085 |
rs46572165 | snp | A/T | | | intron-variant | Trim52 | Mm_Celera | 14:106135405 | TTACTATTGCTCTGT[A/T]ATGTATTTTAGGATC | 212085 |
rs46640169 | snp | C/T | 0.244898 | 0.249948 | upstream-variant-2KB | Trim52 | Mm_Celera | 14:106104665 | GAAGCTGCTTCCTAC[C/T]TAGTTCCTCCACTGT | 212085 |
rs46735472 | snp | C/G | | | nc-transcript-variant | Trim52 | Mm_Celera | 14:106135568 | CTAGCCATAAAGATA[C/G]GGAAGGCATACAAGA | 212085 |
rs46854758 | snp | A/C | 0.244898 | 0.249948 | upstream-variant-2KB | Trim52 | Mm_Celera | 14:106104937 | GTAAACCTCAGTTTT[A/C]TACTCAGGAAGGGCC | 212085 |
rs46986545 | snp | C/G | | | intron-variant | Trim52 | Mm_Celera | 14:106128878 | AGTTTCTGTTTCCAT[C/G]ATCTGTCCATTTATG | 212085 |
rs46990071 | snp | A/C | 0.124444 | 0.216185 | upstream-variant-2KB | Trim52 | Mm_Celera | 14:106105779 | AGGAGAAGCAGTTGA[A/C]GATGACGATGACTGC | 212085 |
rs47037338 | snp | A/G | | | intron-variant | Trim52 | Mm_Celera | 14:106131085 | AAAGCCCTCCCGGGC[A/G]GAGCAGACACCTCTT | 212085 |
rs47086678 | snp | A/T | 0.336735 | 0.234472 | intron-variant | Trim52 | Mm_Celera | 14:106119109 | TAGTGAGACTCTTTT[A/T]AAAATGGCTTATTAC | 212085 |
rs47098065 | snp | A/G | 0.244898 | 0.249948 | upstream-variant-2KB | Trim52 | Mm_Celera | 14:106105526 | ATGTAGGAATTTGCA[A/G]TTTTCTCGGCAGACC | 212085 |
rs47101598 | snp | A/T | | | nc-transcript-variant | Trim52 | Mm_Celera | 14:106135418 | GTTATGTATTTTAGG[A/T]TCTACTGCAACAAGG | 212085 |
rs47166985 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Trim52 | Mm_Celera | 14:106118839 | ATTGTCCAAAGCTGG[G/T]CTGCTTAACGTAGCT | 212085 |
rs47360384 | snp | A/G | | | intron-variant | Trim52 | Mm_Celera | 14:106129215 | TTTTCCCTGAGTTGC[A/G]TTTCCTGTGAGCAGC | 212085 |
rs47368151 | snp | G/T | | | upstream-variant-2KB | Trim52 | Mm_Celera | 14:106104909 | CTTTTCTCAGATTCA[G/T]CCTCTATAGTAGGTA | 212085 |
rs47400482 | snp | A/G | | | intron-variant | Trim52 | Mm_Celera | 14:106130427 | TTAGGGTGTGTTGGG[A/G]TGCTCAGGACTGGCT | 212085 |
rs47582352 | snp | A/G | | | intron-variant | Trim52 | Mm_Celera | 14:106124548 | AGCCACAGCCACATG[A/G]ATGAAGCTGCTGAAT | 212085 |
rs47601653 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Trim52 | Mm_Celera | 14:106118887 | GTAGGAACTGGATTA[A/G]CTTTAAGAAATAATA | 212085 |
rs47707459 | snp | C/T | | | upstream-variant-2KB | Trim52 | Mm_Celera | 14:106105180 | CTTGCTGTGATTTAA[C/T]TAAAAACCTGGATAG | 212085 |
rs47747203 | snp | A/G | | | intron-variant | Trim52 | Mm_Celera | 14:106128789 | ATCCTTTTGTTTTAG[A/G]ATAAAATGTTCTCTA | 212085 |
rs47841224 | snp | C/T | | | intron-variant | Trim52 | Mm_Celera | 14:106123108 | CAGGTTCAGAGGTTC[C/T]GTCCATTATCATCAA | 212085 |
rs47841298 | snp | A/G | | | intron-variant | Trim52 | Mm_Celera | 14:106121536 | TTCTCTAGCTCCTCC[A/G]TTGGGGGCCCTGTGA | 212085 |
rs47863050 | snp | A/G | | | intron-variant | Trim52 | Mm_Celera | 14:106118381 | AAGCCAAAGTTCGAA[A/G]GCCCCTCCACAATCC | 212085 |
rs47884686 | snp | A/T | | | upstream-variant-2KB | Trim52 | Mm_Celera | 14:106105250 | TCATTTGTAAACTAT[A/T]AACAATTTACATCCT | 212085 |
rs47891172 | snp | A/C | | | intron-variant | Trim52 | Mm_Celera | 14:106131243 | TGTTGTTTTTTACTT[A/C]CTTGGTGATATTGAG | 212085 |
rs47934315 | snp | A/C | 0.231111 | 0.249285 | upstream-variant-2KB | Trim52 | Mm_Celera | 14:106105336 | TCAGTATGGAAATAA[A/C]AATGCTGAGTGTTTT | 212085 |
rs48080223 | snp | C/G | | | intron-variant | Trim52 | Mm_Celera | 14:106121032 | TGGCTAGAGGGTGAT[C/G]TTGAACTCAGTATTC | 212085 |
rs48212669 | snp | C/T | 0.124444 | 0.216185 | missense, intron-variant | Trim52 | Mm_Celera | 14:106107481 | CCCAGGTTCCTTCTC[C/T]ACCTCGGCCCACACC | 212085 |
rs48246329 | snp | A/C | 0.244898 | 0.249948 | upstream-variant-2KB | Trim52 | Mm_Celera | 14:106106170 | GAACCTATGTTAGAG[A/C]GCCTTGACGTCACTT | 212085 |
rs48260347 | snp | C/T | | | intron-variant | Trim52 | Mm_Celera | 14:106129142 | TCCAGCTTGTTTCTT[C/T]AGACCATTTGCTTGA | 212085 |
rs48297547 | snp | C/T | | | intron-variant | Trim52 | Mm_Celera | 14:106123342 | ACAGGCATGTGCCAC[C/T]GAGCTGAGAGTTCTA | 212085 |
rs48341770 | snp | C/T | 0.244898 | 0.249948 | utr-variant-5-prime, intron-variant | Trim52 | Mm_Celera | 14:106106558 | GTCCTTAGCGCCCAT[C/T]GGCTTGGCAGCAAGG | 212085 |
rs48365020 | snp | A/C | | | upstream-variant-2KB | Trim52 | Mm_Celera | 14:106105392 | GTGTCCGTCCCCCCC[A/C]CCCCCCCAAGAAACC | 212085 |
rs48393875 | snp | C/T | | | intron-variant | Trim52 | Mm_Celera | 14:106130973 | AAGCTGTGTTGCTTC[C/T]GCCTGTCCCAGAAGC | 212085 |
rs48455396 | snp | C/T | 0.244898 | 0.249948 | utr-variant-5-prime, intron-variant | Trim52 | Mm_Celera | 14:106106626 | GTCCTCAGCGCCCGT[C/T]GGCTAGGCAGTGAGG | 212085 |
rs48546671 | snp | C/T | | | intron-variant | Trim52 | Mm_Celera | 14:106133468 | ATGAGCCTATGGGGG[C/T]CATTCTTATTGAAAC | 212085 |
rs48553249 | snp | C/T | | | intron-variant | Trim52 | Mm_Celera | 14:106131185 | TGCCTGTCCAAGAAG[C/T]TGTTGGCTACTGTAG | 212085 |