SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3675549 | snp | A/C | 0.5 | 0 | intron-variant | E4f1 | Mm_Celera | 17:24449375 | ACCCCGAGATTCCCA[A/C]TGCCCACAAGTACTC | 13560 |
rs3675553 | snp | C/T | 0.5 | 0 | intron-variant | E4f1 | Mm_Celera | 17:24449380 | GAGATTCCCAATGCC[C/T]ACAAGTACTCTGGGC | 13560 |
rs3676180 | snp | C/T | 0.5 | 0 | intron-variant | E4f1 | Mm_Celera | 17:24449500 | GAGGCTGGGGCCCCT[C/T]GGTGGACAGGACACT | 13560 |
rs3676747 | snp | A/C | 0.5 | 0 | intron-variant | E4f1 | Mm_Celera | 17:24449583 | CAGCCATCAAGCAAT[A/C]CCTCGGAATTGAGGG | 13560 |
rs13460332 | snp | C/T | | | synonymous-codon, upstream-variant-2KB, nc-transcript-variant, utr-variant-3-prime | E4f1, Dnase1l2 | GRCm38.p3 | 17:24444945 | ACACTTCCGGACACA[C/T]CTGGAAGAAAAGCCC | 13560 |
rs29497273 | snp | A/T | 0.444444 | 0.157135 | intron-variant | E4f1 | Mm_Celera | 17:24453413 | TCACTGAGCTGAGTC[A/T]GCCAGACTCAAGCTT | 13560 |
rs29500354 | snp | C/T | 0.375 | 0.216506 | intron-variant | E4f1 | Mm_Celera | 17:24453937 | ATGTCATAAGTAGAC[C/T]CAAGAACCTACAAGC | 13560 |
rs29502458 | snp | A/G | 0.375 | 0.216506 | intron-variant | E4f1 | Mm_Celera | 17:24452017 | GTATAAGACCTCTGA[A/G]TTTGGATCCCCAGAA | 13560 |
rs29505717 | snp | A/G | 0.375 | 0.216506 | downstream-variant-500B, upstream-variant-2KB, utr-variant-5-prime | E4f1, Dnase1l2 | Mm_Celera | 17:24443696 | GCTAGAGGGTGGCCT[A/G]AGCAGGCAAGTGTGT | 13560 |
rs29520691 | snp | C/T | 0.444444 | 0.157135 | intron-variant | E4f1 | Mm_Celera | 17:24452236 | AGCAGGAGCCCTCAC[C/T]TATGACCAAACAATC | 13560 |
rs33104243 | snp | A/G | 0.375 | 0.216506 | intron-variant | E4f1 | Mm_Celera | 17:24450994 | ATAGGGAGCTGTCTA[A/G]TTTAGTAAGACAGTG | 13560 |
rs33112831 | snp | C/G | 0.444444 | 0.157135 | missense, upstream-variant-2KB, nc-transcript-variant, downstream-variant-500B | E4f1, Dnase1l2 | Mm_Celera | 17:24444591 | CCACAGACGAGAACT[C/G]CACCAGCACGGTGTG | 13560 |
rs33244151 | snp | C/T | 0.375 | 0.216506 | intron-variant | E4f1 | Mm_Celera | 17:24450194 | ATTTTCTAGCAAAGC[C/T]CCTCCACCTTCCTAA | 13560 |
rs33245804 | snp | C/T | 0.375 | 0.216506 | intron-variant | E4f1 | Mm_Celera | 17:24452068 | GCTGGTGATTGAATG[C/T]ATAAGCATCTCACTT | 13560 |
rs33269047 | snp | C/T | 0.444444 | 0.157135 | intron-variant | E4f1 | Mm_Celera | 17:24453445 | CAAAACAGTCTGTCT[C/T]GTTTCCACTGTCTTA | 13560 |
rs33297238 | snp | A/G | 0.375 | 0.216506 | intron-variant | E4f1 | Mm_Celera | 17:24446713 | ATGAGTCCTTAAAGA[A/G]CCTGGCAGCCAATTT | 13560 |
rs33301251 | snp | C/T | 0.375 | 0.216506 | intron-variant | E4f1 | Mm_Celera | 17:24453850 | GTAGCAACAAAACAA[C/T]TTTCCGGTTGGGAGT | 13560 |
rs33343747 | snp | C/T | 0.375 | 0.216506 | intron-variant | E4f1 | Mm_Celera | 17:24446719 | CCTTAAAGAACCTGG[C/T]AGCCAATTTGGGAAA | 13560 |
rs33396019 | snp | A/G | 0.375 | 0.216506 | intron-variant | E4f1 | Mm_Celera | 17:24452069 | CTGGTGATTGAATGC[A/G]TAAGCATCTCACTTG | 13560 |
rs33406933 | snp | C/T | 0.375 | 0.216506 | intron-variant | E4f1 | Mm_Celera | 17:24453868 | TCCGGTTGGGAGTTC[C/T]AGAATATAAGGAACT | 13560 |
rs33412635 | snp | A/G | 0.375 | 0.216506 | intron-variant | E4f1 | Mm_Celera | 17:24447223 | GCCCTGTGGGGAGGG[A/G]CAGTAAGGCTCAAGG | 13560 |
rs33416733 | snp | A/C | 0.375 | 0.216506 | intron-variant | E4f1 | Mm_Celera | 17:24453804 | ATATCTACATTACAA[A/C]TCAGCACAGTAGCAA | 13560 |
rs33462229 | snp | C/G | 0.32 | 0.24 | intron-variant, upstream-variant-2KB, downstream-variant-500B | E4f1, Dnase1l2 | Mm_Celera | 17:24444751 | CCTCACGCCCTCACC[C/G]TCTCCTGCCACGTGT | 13560 |
rs33498884 | snp | C/G | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | E4f1, Dnase1l2 | Mm_Celera | 17:24445403 | CAGCTGCCAGCCCAC[C/G]GGACCACCCTACCCA | 13560 |
rs33512516 | snp | C/T | 0.375 | 0.216506 | intron-variant | E4f1 | Mm_Celera | 17:24450465 | CTTGGAGCAAGGGTA[C/T]GAAAGACTGAACCTG | 13560 |
rs33531001 | snp | C/T | 0.444444 | 0.157135 | intron-variant | E4f1 | Mm_Celera | 17:24453411 | GGTCACTGAGCTGAG[C/T]CTGCCAGACTCAAGC | 13560 |
rs33531682 | snp | A/G | 0.375 | 0.216506 | intron-variant | E4f1 | Mm_Celera | 17:24446708 | GTTCAATGAGTCCTT[A/G]AAGAACCTGGCAGCC | 13560 |
rs33562976 | snp | C/T | 0.375 | 0.216506 | intron-variant | E4f1 | Mm_Celera | 17:24446391 | AGGCCATCTACTAAG[C/T]TCTCCCCACAGCCTG | 13560 |
rs33573727 | snp | A/T | 0.375 | 0.216506 | intron-variant | E4f1 | Mm_Celera | 17:24450595 | TGTATATGAGTGTTC[A/T]GCTTGTATGTATGTA | 13560 |
rs33589631 | snp | C/G | 0.375 | 0.216506 | intron-variant | E4f1 | Mm_Celera | 17:24446283 | CTGGAGCCCCATGCT[C/G]CACAGCCAGCTAGCT | 13560 |
rs33592591 | snp | C/T | 0.444444 | 0.157135 | downstream-variant-500B, upstream-variant-2KB, utr-variant-5-prime | E4f1, Dnase1l2 | Mm_Celera | 17:24443385 | AAGCAGGCTGAGAAA[C/T]TAAGAAAGCCCAGCC | 13560 |
rs33639637 | snp | A/G | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | E4f1, Dnase1l2 | Mm_Celera | 17:24445420 | GACCACCCTACCCAC[A/G]GACCCCTCACCTCCC | 13560 |
rs45678397 | snp | A/C | | | missense, nc-transcript-variant | E4f1 | Mm_Celera | 17:24447437 | GCCTCTGCCATCTCG[A/C]CATCCCCTGGCTCTG | 13560 |
rs45750760 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime | E4f1 | Mm_Celera | 17:24455497 | CGCCAGACATCAGGG[C/T]GGAAGTGGGCGTGGC | 13560 |
rs45810982 | snp | A/G | | | upstream-variant-2KB | E4f1 | Mm_Celera | 17:24457509 | GCACTTAATGCTCTT[A/G]CAAAAGACCAGAGTT | 13560 |
rs45812213 | snp | A/G | | | intron-variant, upstream-variant-2KB | E4f1, Dnase1l2 | Mm_Celera | 17:24445619 | ATGGTACCAAAAGCA[A/G]CAGTCAGCCCTCTTC | 13560 |
rs45863415 | snp | G/T | | | upstream-variant-2KB | E4f1 | Mm_Celera | 17:24456014 | TGCCTAGCGCCCGTG[G/T]GGCCCAGAAGAGGGT | 13560 |
rs46013014 | snp | C/T | | | synonymous-codon, nc-transcript-variant | E4f1 | Mm_Celera | 17:24445988 | AGGCAGTTCAGGGGA[C/T]CCATCTCCCAGGCAC | 13560 |
rs46119864 | snp | C/T | | | upstream-variant-2KB | E4f1 | Mm_Celera | 17:24456563 | GAGCCAGCGAGCCAG[C/T]CCCAAGACTTTTATT | 13560 |
rs46127613 | snp | A/G | | | intron-variant | E4f1 | GRCm38.p3 | 17:24448426 | CTGTTCTTTACCCAG[A/G]CCATTAGAAATGCTG | 13560 |
rs46221870 | snp | C/T | | | upstream-variant-2KB | E4f1 | Mm_Celera | 17:24457022 | AATAATATTGAAATG[C/T]ATCGTATAAACAATG | 13560 |
rs46264934 | snp | C/T | | | intron-variant | E4f1 | Mm_Celera | 17:24448716 | GAGGAATGAGTGTCC[C/T]TGTTGCAGGAACATT | 13560 |
rs46304395 | snp | A/C | | | intron-variant | E4f1 | Mm_Celera | 17:24448121 | GGAACCAGCCACACA[A/C]CAGTCTTAGAAGCCA | 13560 |
rs46376412 | snp | G/T | | | upstream-variant-2KB | E4f1 | Mm_Celera | 17:24456726 | GGCTTTGTAGCTCCC[G/T]GTGGCCAGTAACTCG | 13560 |
rs46480873 | snp | A/T | | | intron-variant | E4f1 | Mm_Celera | 17:24449187 | GAGGCTCGGCGTTAT[A/T]TGCTCATAAAAGCCC | 13560 |
rs46522663 | snp | A/C | | | intron-variant | E4f1 | Mm_Celera | 17:24453205 | GACTGGCCACAAACT[A/C]AGAAATCCACCTGCC | 13560 |
rs46684574 | snp | A/T | | | upstream-variant-2KB, utr-variant-5-prime | E4f1 | Mm_Celera | 17:24455491 | CATCAGCGCCAGACA[A/T]CAGGGCGGAAGTGGG | 13560 |
rs46843180 | snp | A/G | | | intron-variant | E4f1 | Mm_Celera | 17:24454079 | CAGGAACTCAGCTGG[A/G]TAGTGGTGGCTCATG | 13560 |
rs46870872 | snp | C/G | | | intron-variant | E4f1 | Mm_Celera | 17:24449470 | TGAAGGGACTGCCTA[C/G]GGGAAGGCTCACATG | 13560 |
rs46883664 | snp | A/G | | | upstream-variant-2KB | E4f1 | Mm_Celera | 17:24455683 | ATTTTTAGGACCTCT[A/G]CTTGCTCCGGTTGCT | 13560 |
rs46895499 | snp | A/C/T | | | intron-variant | E4f1 | GRCm38.p3 | 17:24445787 | TAACACTGGCTACAC[A/C/T]GTAAATTTGAGGCTA | 13560 |
rs46926214 | snp | C/T | | | intron-variant | E4f1 | Mm_Celera | 17:24454395 | GTCTGATCAAATCTA[C/T]AGCTCCGTGGAACTA | 13560 |
rs46935862 | snp | C/T | | | upstream-variant-2KB | E4f1 | GRCm38.p3 | 17:24455606 | AAAAAGATTTATTTA[C/T]TTTATGTATATGAGT | 13560 |
rs47077755 | snp | A/G | | | intron-variant | E4f1 | Mm_Celera | 17:24454301 | AGCTGAAATAAGGGA[A/G]AAAAAAATTACAGTG | 13560 |
rs47134808 | snp | A/G | | | upstream-variant-2KB | E4f1 | Mm_Celera | 17:24455962 | TTTTTTTAATGTAGT[A/G]TGGTTTGTCTGCATA | 13560 |
rs47173406 | snp | A/C | | | intron-variant | E4f1 | Mm_Celera | 17:24451745 | GTCTAGGGTCTAACC[A/C]CATCCTTTAGAGGTC | 13560 |
rs47293197 | snp | A/C/T | | | intron-variant | E4f1 | GRCm38.p3 | 17:24451023 | TGAGTACATCCACCA[A/C/T]TGGGATCCAATCAAG | 13560 |
rs47406354 | snp | C/T | | | upstream-variant-2KB | E4f1 | Mm_Celera | 17:24456849 | TAGCCAGCTCACCTA[C/T]CAAGCACAAAATGAA | 13560 |
rs47464200 | snp | C/T | | | intron-variant | E4f1 | Mm_Celera | 17:24454992 | TCTGGCCCAACGGGT[C/T]AGAGGCAGTCCGAAG | 13560 |
rs47561774 | snp | C/G | | | intron-variant | E4f1 | Mm_Celera | 17:24451601 | GTGGGCAATCAGGTC[C/G]TTATCCAGCTTCCCT | 13560 |
rs47584968 | snp | C/T | | | intron-variant | E4f1 | Mm_Celera | 17:24448045 | GGATTCTGCCCTTCC[C/T]AGAGGATGCTGAGTA | 13560 |
rs47641346 | snp | A/G | | | intron-variant | E4f1 | Mm_Celera | 17:24454290 | GACTCTCTCCAAGCT[A/G]AAATAAGGGAAAAAA | 13560 |
rs47678431 | snp | A/G | | | intron-variant | E4f1 | Mm_Celera | 17:24448955 | AGCATCATCTTCCCA[A/G]CATCCATTATCCTTC | 13560 |
rs47690895 | snp | A/G | | | utr-variant-5-prime, nc-transcript-variant | E4f1 | Mm_Celera | 17:24455299 | TCCATGTCGCAACGC[A/G]CCACAGGAAGATGGC | 13560 |
rs47758026 | snp | G/T | | | intron-variant | E4f1 | Mm_Celera | 17:24455048 | TTACAGACACTCGAG[G/T]AGCCAGGATCCGGGC | 13560 |
rs47776590 | snp | C/T | | | intron-variant | E4f1 | Mm_Celera | 17:24448498 | TATAGAAGCAGAGGG[C/T]CCCTGAAAGGGGAAT | 13560 |
rs47908015 | snp | C/T | | | synonymous-codon, upstream-variant-2KB, nc-transcript-variant, downstream-variant-500B | E4f1, Dnase1l2 | Mm_Celera | 17:24444655 | AGGGCTCTCCTCAGA[C/T]ACCAGCAACTCCTCC | 13560 |
rs48077882 | snp | A/T | | | intron-variant | E4f1 | Mm_Celera | 17:24448123 | AACCAGCCACACAAC[A/T]GTCTTAGAAGCCATT | 13560 |
rs48132400 | snp | A/T | | | upstream-variant-2KB | E4f1 | Mm_Celera | 17:24456081 | TGTAGGTGTTGGGAA[A/T]TGAACCTAGATACAC | 13560 |
rs48145740 | snp | C/G | | | upstream-variant-2KB | E4f1 | Mm_Celera | 17:24457334 | CATCAGATCTCATTA[C/G]AGGTGGTTGTGAGTC | 13560 |
rs48227967 | snp | A/G | | | intron-variant | E4f1 | Mm_Celera | 17:24454884 | GAGAAGCAGAAGCTA[A/G]GGCTGATGGGCGCTG | 13560 |
rs48323365 | snp | A/G | | | intron-variant | E4f1 | Mm_Celera | 17:24450098 | CTCAGTGAGGGGCAC[A/G]TACTAAGGGCAGGAC | 13560 |
rs48342652 | snp | A/C | | | intron-variant | E4f1 | GRCm38.p3 | 17:24452724 | CTTAGTGGTTAAGAG[A/C]ACTGGCTGCGCTTCC | 13560 |
rs48381940 | snp | A/T | | | upstream-variant-2KB | E4f1 | Mm_Celera | 17:24457581 | CTTCAATTTCAGGGT[A/T]TCTGATGCTCTCTTC | 13560 |
rs48393522 | snp | C/T | | | intron-variant | E4f1 | Mm_Celera | 17:24449224 | AACCAGGGCACCAAT[C/T]CTCATGTCAGTGTAA | 13560 |
rs48449293 | snp | A/G | | | intron-variant | E4f1 | Mm_Celera | 17:24454268 | AGAGTTCCCTGAGAC[A/G]GTAACTGACTCTCTC | 13560 |
rs48449623 | snp | A/G | | | intron-variant | E4f1 | Mm_Celera | 17:24448216 | GTCAGAAACAATTAA[A/G]GGCATCCATCTCTCA | 13560 |
rs48542366 | snp | A/G | | | upstream-variant-2KB | E4f1 | Mm_Celera | 17:24457366 | CCATGTGGTTGCTAG[A/G]ATTTGAACTCAGGAC | 13560 |
rs48611264 | snp | A/G | | | utr-variant-5-prime, nc-transcript-variant | E4f1 | Mm_Celera | 17:24455382 | CGACAGGCAGGGGGC[A/G]GGACAAAAACGAATT | 13560 |
rs48839408 | snp | A/G | | | upstream-variant-2KB | E4f1 | Mm_Celera | 17:24456004 | ACCACGTGCATGCCT[A/G]GCGCCCGTGGGGCCC | 13560 |
rs48853361 | snp | A/C | | | intron-variant | E4f1 | Mm_Celera | 17:24449776 | ATGCACCTGTGGGTT[A/C]CAGAATTGAGAGAAG | 13560 |
rs48944043 | snp | A/G | | | intron-variant | E4f1 | Mm_Celera | 17:24448231 | GGGCATCCATCTCTC[A/G]CCCATGCTCCAGCCC | 13560 |
rs49067803 | snp | A/C | | | upstream-variant-2KB | E4f1 | Mm_Celera | 17:24456740 | CTGTGGCCAGTAACT[A/C]GGTGGCCCCGGTAAC | 13560 |
rs49113961 | snp | C/T | | | upstream-variant-2KB | E4f1 | Mm_Celera | 17:24457569 | AATTGCCTGTAACTT[C/T]AATTTCAGGGTATCT | 13560 |
rs49177633 | snp | C/T | | | intron-variant | E4f1 | Mm_Celera | 17:24448593 | TAGAGCCTGATTATA[C/T]ATCAAAACCCAGTGA | 13560 |
rs49233988 | snp | A/G | | | intron-variant | E4f1 | Mm_Celera | 17:24453012 | TGCCCACAAAGAACA[A/G]AAGAAGGTATCAGAT | 13560 |
rs49321939 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | E4f1 | Mm_Celera | 17:24455457 | CGTCAGTAGAGGTGG[A/G]GCTTGGCTCTTTGAG | 13560 |
rs49379323 | snp | C/T | | | intron-variant, upstream-variant-2KB, downstream-variant-500B | E4f1, Dnase1l2 | Mm_Celera | 17:24444509 | GGTCATCATGGGCTG[C/T]CCCGAGTCCAAACCT | 13560 |
rs49393235 | snp | C/T | | | intron-variant | E4f1 | Mm_Celera | 17:24446994 | GTGTTGAGGGGACAC[C/T]GGGTCTTTTCATCTA | 13560 |
rs49399986 | snp | C/G | | | intron-variant | E4f1 | Mm_Celera | 17:24455002 | CGGGTTAGAGGCAGT[C/G]CGAAGGGAAACCTGT | 13560 |
rs49428423 | snp | C/T | | | upstream-variant-2KB | E4f1 | Mm_Celera | 17:24457469 | AACTCAGTCATGGGC[C/T]GAAAGGGTGGCTCAT | 13560 |
rs49535514 | snp | A/G | | | upstream-variant-2KB | E4f1 | Mm_Celera | 17:24456333 | TCATGTGGTTGTTGG[A/G]TATTGAATTTAGGAC | 13560 |
rs49609620 | snp | A/G | | | intron-variant | E4f1 | Mm_Celera | 17:24449182 | TCAAAGAGGCTCGGC[A/G]TTATATGCTCATAAA | 13560 |
rs49676439 | snp | C/T | | | intron-variant | E4f1 | Mm_Celera | 17:24452911 | ACTCCTGCCCTCTCC[C/T]CCTTTTGCTTTAAGA | 13560 |
rs49750988 | snp | A/G | | | intron-variant | E4f1 | Mm_Celera | 17:24448490 | GCAAAGAATATAGAA[A/G]CAGAGGGCCCCTGAA | 13560 |
rs50045407 | snp | A/G/T | | | upstream-variant-2KB | E4f1 | GRCm38.p3 | 17:24455775 | AGATTTATTCATTAA[A/G/T]TACACTGTAGCTATC | 13560 |
rs50099085 | snp | C/T | | | downstream-variant-500B, upstream-variant-2KB, utr-variant-5-prime | E4f1, Dnase1l2 | Mm_Celera | 17:24443605 | TCCAGCTAGGTAGGG[C/T]AGGAGGCTGTCTGTC | 13560 |
rs50120254 | snp | A/G | | | intron-variant | E4f1 | GRCm38.p3 | 17:24449817 | CCCTCTGTGGAAGAA[A/G]GGAGCTTCCTTCTAG | 13560 |
rs50147764 | snp | C/G | | | intron-variant | E4f1 | Mm_Celera | 17:24445880 | GCTAGCAGCTCCCAC[C/G]CCCACATGAGAAGCA | 13560 |
rs50148577 | snp | C/G | | | upstream-variant-2KB | E4f1 | Mm_Celera | 17:24457432 | CCATCTTTCCAGCAG[C/G]CCCTGGAAGGGATTT | 13560 |