SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6356655 | snp | C/T | 0.5 | 0 | upstream-variant-2KB, utr-variant-5-prime | Tle6 | Mm_Celera | 10:81601110 | AGAATGCTCATTGCT[C/T]AGTTTGTGGCCGTGC | 114606 |
rs6358176 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | Tle6 | Mm_Celera | 10:81601428 | TCCTGGCTGGCCCGC[A/G]TGTgccctgggccct | 114606 |
rs6358228 | snp | A/T | 0.5 | 0 | upstream-variant-2KB | Tle6 | Mm_Celera | 10:81601462 | cccagcaccacttga[A/T]gacaccttcattatc | 114606 |
rs13473087 | snp | A/G | | | missense, upstream-variant-2KB | Tle6, Gm32024 | Mm_Celera | 10:81594348 | CAGAGACCCAGAAAG[A/G]CACTTGAAATGCAGC | 114606 |
rs46419870 | snp | A/C | | | intron-variant | Tle6, Gm32024 | Mm_Celera | 10:81597216 | TCACCAAAGGTGATG[A/C]TGCACTTGAGACCTG | 114606 |
rs46519550 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Tle6, Tle2 | Mm_Celera | 10:81592612 | CTGTGACTTCTCAAA[A/C]ATTCCTTGAGCTGAC | 114606 |
rs46695054 | snp | C/T | 0.231111 | 0.249285 | synonymous-codon, intron-variant | Tle6, Tle2 | Mm_Celera | 10:81592016 | CAGCCAGTCTTCGGT[C/T]GGACTGTGAGCCAGG | 114606 |
rs47379030 | snp | A/G | 0.32 | 0.24 | intron-variant | Tle6, Tle2 | Mm_Celera | 10:81591646 | GTTGGAGTGTGGACA[A/G]TACCCAAGCCCTGAC | 114606 |
rs49447054 | snp | A/C | | | intron-variant | Tle6, Gm32024 | Mm_Celera | 10:81597234 | CACTTGAGACCTGAT[A/C]ATCCCCACCCCCCTC | 114606 |
rs49528472 | snp | A/G | 0.231111 | 0.249285 | intron-variant, downstream-variant-500B | Tle6, Tle2 | Mm_Celera | 10:81592915 | GATTCCCTCAAAGCC[A/G]TGGGACTAACCCAAC | 114606 |
rs50096865 | snp | C/T | 0.124444 | 0.216185 | downstream-variant-500B, missense, intron-variant | Tle2, Tle6 | Mm_Celera | 10:81591094 | TGATGATGAGCCTGC[C/T]GTTCTCAGTCATGTC | 114606 |
rs50110733 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Tle6, Tle2 | Mm_Celera | 10:81592641 | ACCTGGGCTGTTCCC[G/T]CTCCTGACACTGAGT | 114606 |
rs50131868 | snp | C/T | 0.124444 | 0.216185 | downstream-variant-500B, missense, intron-variant | Tle2, Tle6 | Mm_Celera | 10:81591310 | CCGTGATGAAGTTGC[C/T]CATACCGACGCTCGC | 114606 |
rs50135314 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tle6, Tle2 | Mm_Celera | 10:81592635 | GAGCTGACCTGGGCT[A/G]TTCCCTCTCCTGACA | 114606 |
rs50433282 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Tle6, Tle2 | Mm_Celera | 10:81592633 | TTGAGCTGACCTGGG[C/T]TGTTCCCTCTCCTGA | 114606 |
rs50489750 | snp | A/C | | | intron-variant | Tle6 | Mm_Celera | 10:81600302 | GACACACACCCCCAG[A/C]TAAGGGCCTCATTAG | 114606 |
rs50762235 | snp | C/T | | | upstream-variant-2KB | Tle6 | Mm_Celera | 10:81602767 | TAGTGCTGGTAACTG[C/T]TGAGCCGCCTCTCCA | 114606 |
rs51115039 | snp | C/G | | | intron-variant | Tle6 | Mm_Celera | 10:81599964 | GGGCAGAGAGAACTA[C/G]TCTCCAAAACCCCAA | 114606 |
rs51416360 | snp | C/G | 0.32 | 0.24 | downstream-variant-500B, intron-variant, synonymous-codon | Tle2, Tle6 | Mm_Celera | 10:81590493 | TTTCTGTGTGTGTGT[C/G]AAGCGTACAGGTGAG | 114606 |
rs51458785 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Tle6, Tle2 | Mm_Celera | 10:81591877 | GCCCAGGCTCAGTGG[A/G]CTCCTTACCATTTGG | 114606 |
rs51867465 | snp | C/T | 0.142012 | 0.225474 | downstream-variant-500B, utr-variant-3-prime, intron-variant, synonymous-codon | Tle2, Tle6 | Mm_Celera | 10:81590670 | CCTTATCCTGCCTGG[C/T]GTGGGCTTTACCAAC | 114606 |
rs52049036 | snp | A/T | | | intron-variant, upstream-variant-2KB, downstream-variant-500B | Tle6, Gm32024 | Mm_Celera | 10:81598963 | CGGGCTTAAAAACAA[A/T]CCCAAACAACATTTC | 114606 |
rs211867574 | snp | A/G | | | missense, upstream-variant-2KB | Tle6, Gm32024 | Mm_Celera | 10:81595238 | TTATCAGCTCTTCCA[A/G]AAGATTCCTGTGGTA | 114606 |
rs211914147 | snp | C/T | | | synonymous-codon, upstream-variant-2KB | Tle6, Gm32024 | Mm_Celera | 10:81594432 | GGTGAAGACGTGCCG[C/T]GTGAAGGAGCTCACA | 114606 |
rs212018247 | in-del | -/G | | | upstream-variant-2KB, utr-variant-5-prime | Tle6 | Mm_Celera | 10:81601009 | CAGGGCCCAGGCCAC[-/G]GGTGCACGTGGGCCC | 114606 |
rs212248150 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | Tle6 | Mm_Celera | 10:81601046 | CAGCGAACCGCCCCT[A/G]CAGGCCCTGACCAAT | 114606 |
rs212397023 | snp | A/G | | | downstream-variant-500B, utr-variant-3-prime, intron-variant | Tle2, Tle6 | GRCm38.p3 | 10:81591017 | CACTGTGCAGTTAGG[A/G]GAGGGGAGTTGAAGT | 114606 |
rs212720845 | snp | A/G | | | upstream-variant-2KB | Tle6 | Mm_Celera | 10:81601748 | CCTGGGTTAGAGTGG[A/G]CTCTCTGGACCTCCC | 114606 |
rs212747146 | in-del | -/CGCCCGAA | | | intron-variant | Tle6, Tle2 | Mm_Celera | 10:81592102 | AGGCTGCAAGGTCCC[-/CGCCCGAA]CGCCCGCCCACCCAA | 114606 |
rs212768799 | snp | C/G | | | missense, intron-variant | Tle6, Tle2 | Mm_Celera | 10:81591956 | CACCTGGTCCCTCTT[C/G]CTGCTGTTGAACAGG | 114606 |
rs212798925 | snp | A/C | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | Tle6, Gm32024 | Mm_Celera | 10:81597675 | GACACCCCCACCCCC[A/C]CCCCCCCCACCCCCC | 114606 |
rs213043614 | snp | G/T | | | intron-variant, downstream-variant-500B | Tle6, Gm32024 | Mm_Celera | 10:81596766 | CCTCCCCTGGGAGCT[G/T]TTGGAGAGCACCCAG | 114606 |
rs213279336 | in-del | -/C | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | Tle6, Gm32024 | Mm_Celera | 10:81597509 | TAGTTCACACTCCAG[-/C]CCCTGCCTGGAGCTC | 114606 |
rs213464829 | snp | A/G | | | upstream-variant-2KB | Tle6 | Mm_Celera | 10:81601987 | ACCCACACAGTAGAA[A/G]GTGAGAATGTGTTCT | 114606 |
rs213686184 | snp | C/T | | | intron-variant | Tle6 | Mm_Celera | 10:81600159 | GGCAGAAAAGCCGAC[C/T]CCCACCCCCATCCCC | 114606 |
rs213811626 | snp | A/G | | | intron-variant | Tle6 | Mm_Celera | 10:81600695 | CAAATCACTCAACCT[A/G]GGTAAACTCCCCGCT | 114606 |
rs214056530 | snp | C/G/T | | | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | Tle6, Gm32024 | Mm_Celera | 10:81595326 | TCTCCCACTCACCTG[C/G/T]GTCTCAGGTTGGGGC | 114606 |
rs214091806 | snp | A/G | | | intron-variant, downstream-variant-500B | Tle6, Gm32024 | Mm_Celera | 10:81596462 | CTTTGGCTATAGACC[A/G]ACTTTGAGATCCTAT | 114606 |
rs214449371 | snp | A/T | | | downstream-variant-500B, utr-variant-3-prime, intron-variant | Tle2, Tle6 | Mm_Celera | 10:81590721 | CTTTAAAACAAAAAC[A/T]GGGTGGGGCTAGTTT | 114606 |
rs214629795 | snp | A/G | | | upstream-variant-2KB | Tle6 | Mm_Celera | 10:81602965 | TGGCAGGAAGCTGAA[A/G]GGGGAGGGGTAGTCT | 114606 |
rs215026810 | snp | C/G | | | intron-variant, upstream-variant-2KB, downstream-variant-500B | Tle6, Gm32024 | Mm_Celera | 10:81598736 | CCAAGAGGATGAGCC[C/G]CCTAATCTATAAATG | 114606 |
rs215033474 | snp | A/G | | | intron-variant | Tle6, Tle2 | Mm_Celera | 10:81592046 | GCTCATGATCTGGGT[A/G]AGCCAGGCAGAGGTA | 114606 |
rs215377693 | snp | A/C | | | intron-variant, upstream-variant-2KB | Tle6, Gm32024 | Mm_Celera | 10:81597929 | CAGGGCACCTGGAAG[A/C]CAGGCAGGAAGGATG | 114606 |
rs215499646 | snp | C/T | | | synonymous-codon, downstream-variant-500B | Tle6, Tle2 | Mm_Celera | 10:81592770 | CAGGTCCCAGCATCG[C/T]AGGCAGGCGTCCAGA | 114606 |
rs215714969 | in-del | -/A | | | downstream-variant-500B, intron-variant, frameshift-variant | Tle2, Tle6 | Mm_Celera | 10:81590524 | GACCCGACTGGGTAT[-/A]CAGCCTTCATTTCTC | 114606 |
rs215721904 | snp | A/T | | | intron-variant, downstream-variant-500B | Tle6, Tle2 | Mm_Celera | 10:81593209 | GAGCCATCCTAGGCT[A/T]CAGAGCAAGTTCAGC | 114606 |
rs215967893 | snp | A/T | | | downstream-variant-500B, intron-variant | Tle2, Tle6 | Mm_Celera | 10:81590898 | CCTGGGTAAAGGACA[A/T]ATCTCTGCCATTTCA | 114606 |
rs216005177 | snp | C/T | | | intron-variant | Tle6, Tle2 | Mm_Celera | 10:81591815 | CTGAACTCAGATCCA[C/T]CTGCCTCTGCCTCCC | 114606 |
rs216263523 | snp | A/T | | | intron-variant | Tle6 | Mm_Celera | 10:81600230 | CCTTCCCCATCCCCA[A/T]GTCTTCTGCGCTCCC | 114606 |
rs216297811 | snp | C/T | | | upstream-variant-2KB, intron-variant | Tle6 | Mm_Celera | 10:81600947 | CCACGCCCTACTAGG[C/T]CACACCCACACACCA | 114606 |
rs216373131 | in-del | -/CAG | | | intron-variant, upstream-variant-2KB | Tle6, Gm32024 | Mm_Celera | 10:81595596 | GGGGACACGTCACCC[-/CAG]GGGGGGACACCCAGC | 114606 |
rs216649816 | snp | A/G | | | intron-variant, upstream-variant-2KB | Tle6, Gm32024 | Mm_Celera | 10:81595623 | CCCAGCAGATGCCTG[A/G]GGGTTCCTGGCTGCA | 114606 |
rs216683168 | snp | C/T | | | intron-variant, downstream-variant-500B | Tle6, Gm32024 | Mm_Celera | 10:81596548 | CACCATCATCAAGGG[C/T]TTAGATGCAGCCCTT | 114606 |
rs216890312 | snp | A/G | | | upstream-variant-2KB | Tle6 | Mm_Celera | 10:81603044 | CTAAGACACGTTAAC[A/G]ACAAATTTACATCAG | 114606 |
rs218139503 | in-del | -/GGGGGT | | | intron-variant, upstream-variant-2KB | Tle6, Gm32024 | Mm_Celera | 10:81597839 | GTCTTGGCTTGGGCA[-/GGGGGT]GGGGGTGGGGGTGCG | 114606 |
rs219248715 | snp | C/T | | | intron-variant | Tle6 | Mm_Celera | 10:81600504 | TCTACAAAGTGAGTT[C/T]CAGGACAGCCAGGAA | 114606 |
rs219296383 | in-del | -/AAAGAAAAG | | | intron-variant, downstream-variant-500B | Tle6, Gm32024 | Mm_Celera | 10:81596502 | CTTCAAAAAAAAAAA[-/AAAGAAAAG]AAAAGAAAAGAAAAC | 114606 |
rs219361794 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime | Tle6 | Mm_Celera | 10:81601093 | CACGTGGGCTGCGAG[C/T]CAGAATGCTCATTGC | 114606 |
rs219364929 | snp | C/T | | | missense | Tle6 | Mm_Celera | 10:81600054 | ATTCCACCAAAGGTG[C/T]CACTGCTCTGTCTGT | 114606 |
rs219461841 | snp | A/G | | | intron-variant, upstream-variant-2KB, downstream-variant-500B | Tle6, Gm32024 | Mm_Celera | 10:81599015 | CCACTGTCCAGGCAC[A/G]GCTGGTTCTTTGGGG | 114606 |
rs219847488 | snp | C/T | | | intron-variant, upstream-variant-2KB | Tle6, Gm32024 | Mm_Celera | 10:81593519 | CTGTTCTCCCTTGTC[C/T]TACAAGAATTACAAT | 114606 |
rs220012236 | snp | A/G | | | intron-variant, upstream-variant-2KB | Tle6, Gm32024 | Mm_Celera | 10:81593707 | AAAAACAAGATTTAC[A/G]AATAAGCCAGGCACA | 114606 |
rs220038484 | snp | C/T | | | intron-variant, upstream-variant-2KB | Tle6, Gm32024 | Mm_Celera | 10:81594704 | CCTGCCTCTACCTCA[C/T]GAGCGCTAGGAGCCA | 114606 |
rs220059214 | snp | A/G | | | upstream-variant-2KB | Tle6 | Mm_Celera | 10:81602244 | CTTCTGACTTATAGA[A/G]CACTCACATATATTA | 114606 |
rs220062971 | in-del | -/TACCTAGC | | | intron-variant, upstream-variant-2KB, nc-transcript-variant | Tle6, Gm32024 | Mm_Celera | 10:81598098 | CTACCAGGGGACGTG[-/TACCTAGC]TCCAGTCCCCAGTTC | 114606 |
rs220110326 | snp | C/T | | | intron-variant | Tle6, Tle2 | Mm_Celera | 10:81592240 | CCCTGGTTGGTTTTA[C/T]TGGGACATGGTCTTG | 114606 |
rs220188042 | in-del | -/GA | | | intron-variant, upstream-variant-2KB | Tle6, Gm32024 | Mm_Celera | 10:81595791 | GCAAGGTGGGGGGAG[-/GA]GAGAGAGGGAAGAAG | 114606 |
rs220198494 | snp | A/G | | | upstream-variant-2KB | Tle6 | Mm_Celera | 10:81602474 | ATATTTTAAGGCCAG[A/G]CAGTGGTGGTGCATG | 114606 |
rs220297652 | snp | C/T | | | upstream-variant-2KB | Tle6 | Mm_Celera | 10:81601550 | ATAGCAAATTCCAGG[C/T]TAGCTTGGAGTACAG | 114606 |
rs220366661 | in-del | -/GTGT | | | intron-variant, downstream-variant-500B | Tle6, Tle2 | Mm_Celera | 10:81592895 | TAGGCTCGACAGTCC[-/GTGT]CTAAGATTCCCTCAA | 114606 |
rs220504976 | in-del | -/GT | | | upstream-variant-2KB | Tle6 | Mm_Celera | 10:81602976 | GAAAGGGGAGGGGTA[-/GT]GTCTCTCTCTCTCTC | 114606 |
rs220572915 | snp | G/T | | | intron-variant, upstream-variant-2KB, nc-transcript-variant | Tle6, Gm32024 | Mm_Celera | 10:81598507 | CCCAACCAGCCAGGC[G/T]CCCTCCTGCCCCAGG | 114606 |
rs221043952 | snp | A/G | | | missense, intron-variant | Tle6, Gm32024 | Mm_Celera | 10:81596125 | GTCTGGGCAGAGCCC[A/G]TTGGGGCCTCATGAG | 114606 |
rs221154742 | snp | A/G | | | intron-variant | Tle6, Gm32024 | Mm_Celera | 10:81597021 | AATGGGGGGGGGGGG[A/G]AGGACACTGGCACAG | 114606 |
rs221282718 | snp | C/T | | | intron-variant, upstream-variant-2KB | Tle6, Gm32024 | Mm_Celera | 10:81594836 | CTAATTATTACAGCC[C/T]CTTCTCCAAGACATC | 114606 |
rs221438034 | in-del | -/ACC | | | intron-variant, upstream-variant-2KB, downstream-variant-500B | Tle6, Gm32024 | Mm_Celera | 10:81598707 | AAAGCCCCTGCATTT[-/ACC]CTAGGGTGGAACCCC | 114606 |
rs221445205 | snp | A/G | | | intron-variant | Tle6, Tle2 | Mm_Celera | 10:81591459 | TGAGAATGAGTCTAG[A/G]CTACATGAGACCTTG | 114606 |
rs221579539 | snp | A/G | | | intron-variant | Tle6, Tle2 | Mm_Celera | 10:81592230 | AAGTCTGTCTCCCTG[A/G]TTGGTTTTATTGGGA | 114606 |
rs221590440 | snp | C/T | | | intron-variant, upstream-variant-2KB | Tle6 | Mm_Celera | 10:81599366 | TTTTGTTCCTATAAC[C/T]GTAACATTACTAGCG | 114606 |
rs221852345 | snp | G/T | | | intron-variant, upstream-variant-2KB | Tle6, Gm32024 | Mm_Celera | 10:81594763 | CACAGCCACACATGC[G/T]TCCCTACTCTAAAAC | 114606 |
rs221859166 | snp | C/T | | | downstream-variant-500B, missense, intron-variant | Tle2, Tle6 | Mm_Celera | 10:81591309 | ACCGTGATGAAGTTG[C/T]CCATACCGACGCTCG | 114606 |
rs221865789 | snp | A/C | | | missense, nc-transcript-variant | Tle6, Gm32024 | Mm_Celera | 10:81595999 | TCACTCTCTGAGAGG[A/C]ACCGACGTCTGGTGG | 114606 |
rs222120082 | snp | A/C | | | intron-variant, upstream-variant-2KB | Tle6, Gm32024 | Mm_Celera | 10:81593925 | GCTCCACTCTGGGGG[A/C]GTGGGGTTTGGGTAA | 114606 |
rs222656214 | snp | C/T | | | intron-variant, upstream-variant-2KB | Tle6 | Mm_Celera | 10:81599169 | GTCAAAACTATAAAG[C/T]CTGCATCTCCCTGAA | 114606 |
rs222812445 | in-del | -/A | | | upstream-variant-2KB | Tle6 | Mm_Celera | 10:81601360 | CACACACACACACAC[-/A]CCCACACACACTTTT | 114606 |
rs222919317 | snp | C/T | | | intron-variant, upstream-variant-2KB, nc-transcript-variant | Tle6, Gm32024 | Mm_Celera | 10:81598388 | CTTACTATATTGTTC[C/T]TAATGAAAAGCCAAG | 114606 |
rs224253993 | in-del | -/T | | | intron-variant | Tle6 | Mm_Celera | 10:81599943 | GGTGCGGGGTGGGGG[-/T]GGGGGGGGCAGAGAG | 114606 |
rs224622249 | snp | C/T | | | upstream-variant-2KB | Tle6 | Mm_Celera | 10:81602164 | TGATCTTCTAGAGGA[C/T]CCAGGCTCAATTCCC | 114606 |
rs225715754 | snp | C/T | | | intron-variant, upstream-variant-2KB, downstream-variant-500B | Tle6, Gm32024 | Mm_Celera | 10:81598587 | CCCCCACCCCCACCT[C/T]GGCTGCCACCAGGGT | 114606 |
rs225753092 | snp | A/G | | | intron-variant | Tle6 | Mm_Celera | 10:81599872 | GGCACTGAGGGGCTC[A/G]GGCTGGGGTGCAGGC | 114606 |
rs226195616 | snp | A/C | | | upstream-variant-2KB, intron-variant | Tle6 | Mm_Celera | 10:81600927 | CCCCGCCCCTCCAGC[A/C]TAGGCCACGCCCTAC | 114606 |
rs226233908 | snp | A/G | | | upstream-variant-2KB | Tle6 | Mm_Celera | 10:81601642 | CCCCCATATTCAAGG[A/G]CAGGAAGTGAAGCAG | 114606 |
rs226412575 | snp | C/G | | | intron-variant, upstream-variant-2KB | Tle6 | Mm_Celera | 10:81599421 | CAGGGTATGGAACCA[C/G]CAAAGGGTCACGACC | 114606 |
rs226578992 | snp | C/T | | | intron-variant, downstream-variant-500B | Tle6, Gm32024 | Mm_Celera | 10:81596464 | TTGGCTATAGACCGA[C/T]TTTGAGATCCTATCT | 114606 |
rs226615563 | snp | C/T | | | intron-variant, utr-variant-5-prime | Tle6, Gm32024 | Mm_Celera | 10:81597316 | CAACACTTAGAACTC[C/T]GCAGCCTCCAAGTCC | 114606 |
rs226899996 | snp | C/T | | | intron-variant | Tle6 | Mm_Celera | 10:81600368 | CCTCCAACTCCCTAG[C/T]GGGATCAGCCAGAAA | 114606 |
rs227181394 | snp | C/T | | | intron-variant | Tle6, Gm32024 | Mm_Celera | 10:81597068 | AGGCTCAGGGGCAGT[C/T]AAAAGCCTGGGAGCT | 114606 |
rs227203110 | snp | A/C | | | intron-variant, upstream-variant-2KB, nc-transcript-variant | Tle6, Gm32024 | Mm_Celera | 10:81598172 | CACCTGAAATCACAC[A/C]GCAGGTGAGAGGTAG | 114606 |
rs227720265 | snp | A/G | | | intron-variant, missense, upstream-variant-2KB | Tle6, Gm32024 | Mm_Celera | 10:81594322 | CCCCGTCCCTGCCCC[A/G]TCACCTGGACGCTGC | 114606 |
rs227746737 | snp | C/T | | | intron-variant, upstream-variant-2KB | Tle6, Gm32024 | Mm_Celera | 10:81594933 | TACAAGTTGTTCTTA[C/T]ATTTACTCATTAATG | 114606 |