SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs31049135 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Fbxl19 | Mm_Celera | 7:127753680 | GAATTATACCATAAG[A/C]CATCTTTTCTTTTTT | 233902 |
rs31096011 | snp | A/G | 0.32 | 0.24 | intron-variant | Fbxl19 | Mm_Celera | 7:127764243 | GGTCGACTGAGCTGC[A/G]GCCAGTCTGTAAATG | 233902 |
rs31205356 | snp | A/G | 0.387812 | 0.208586 | intron-variant | Fbxl19 | Mm_Celera | 7:127760248 | TCCTTATGCAGAAAA[A/G]TAGATAGGGAGTAGA | 233902 |
rs31230513 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Fbxl19 | Mm_Celera | 7:127760468 | CGGTGTGGGCCTTAT[C/T]TGATAAAATATTTGG | 233902 |
rs31235888 | snp | G/T | 0.375 | 0.216506 | intron-variant | Fbxl19 | Mm_Celera | 7:127762784 | TGAACTAAGTCTTTT[G/T]TTGTTGTTGTTTTTT | 233902 |
rs31246903 | snp | A/G | 0.387812 | 0.208586 | intron-variant | Fbxl19 | Mm_Celera | 7:127763801 | GCCAAATTCTCTCCA[A/G]GTCTGGGGCCATTTT | 233902 |
rs31323160 | snp | C/T | 0.387812 | 0.208586 | intron-variant | Fbxl19 | Mm_Celera | 7:127762346 | ATGAGTCAGGACAGA[C/T]GGACATAGAGGTAGG | 233902 |
rs31341961 | snp | A/G | 0.375 | 0.216506 | intron-variant | Fbxl19 | Mm_Celera | 7:127754797 | CTCCAGACCTTAAGG[A/G]AAAGAGAGATGGTAC | 233902 |
rs31418024 | snp | C/T | 0.32 | 0.24 | intron-variant | Fbxl19 | Mm_Celera | 7:127753038 | CCCCACAGCATGCTG[C/T]TCCCCTAATGGAGCA | 233902 |
rs31428211 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Fbxl19 | Mm_Celera | 7:127763687 | GATGCTCTGCATCCC[A/G]AGTATTGAGCTTAGG | 233902 |
rs31429796 | snp | C/G | 0.304688 | 0.243945 | intron-variant | Fbxl19 | Mm_Celera | 7:127759243 | AAAGTCTATTGGGAG[C/G]TATTGTATCATTAGT | 233902 |
rs31431379 | snp | C/T | 0.387812 | 0.208586 | intron-variant | Fbxl19 | Mm_Celera | 7:127756142 | AGAGAGAGAGGGTGA[C/T]AAAGGCATCAGCAGC | 233902 |
rs31512421 | snp | C/G/T | 0.625 | 0.0931695 | utr-variant-3-prime, upstream-variant-2KB | Fbxl19, Orai3 | Mm_Celera | 7:127768778 | GGGGGACTTGGGGGA[C/G/T]TTGAGGGGACCAGCT | 233902 |
rs31514302 | snp | A/G | 0.375 | 0.216506 | intron-variant | Fbxl19 | Mm_Celera | 7:127763900 | AGAAGTATTTCTTTG[A/G]AGGGGAAGACACCAC | 233902 |
rs31543493 | snp | A/G | 0.304688 | 0.243945 | intron-variant | Fbxl19 | Mm_Celera | 7:127755228 | CCCAGACGGGAATTT[A/G]GAGATGGGACTTAGC | 233902 |
rs31557944 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Fbxl19 | Mm_Celera | 7:127753276 | TGGAGACCAGTCTAC[A/C]TAGGAGACGTTCTTC | 233902 |
rs31557951 | snp | A/C | 0.375 | 0.216506 | intron-variant | Fbxl19 | Mm_Celera | 7:127763529 | GACCAGGCTGGCTTC[A/C]AACTCAAGAGAGATG | 233902 |
rs31590816 | snp | C/T | 0.375 | 0.216506 | intron-variant | Fbxl19 | Mm_Celera | 7:127754467 | TTGTTTTGAATTCAT[C/T]CTTGGGCGGTTGATC | 233902 |
rs31610653 | snp | C/T | 0.375 | 0.216506 | intron-variant | Fbxl19 | Mm_Celera | 7:127767270 | AGCTCTCCCGGAAGG[C/T]TTCCCTGAGGGGATA | 233902 |
rs31646636 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Fbxl19 | Mm_Celera | 7:127748147 | TCTCTGAGGGTAGAA[A/G]CAGAAGCTCTGCCCC | 233902 |
rs31833740 | snp | C/T | 0.387812 | 0.208586 | intron-variant | Fbxl19 | Mm_Celera | 7:127762401 | GGGGCACAGAGGCGG[C/T]TGTTGGTGAAGGTCT | 233902 |
rs31885436 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Fbxl19 | Mm_Celera | 7:127764490 | GGGCGTGGTGATGCA[C/T]GCCTTTAATTCCAGC | 233902 |
rs31887994 | snp | A/G | 0.32 | 0.24 | intron-variant | Fbxl19 | Mm_Celera | 7:127752919 | TACCCCTTCCCTCCT[A/G]ACCCTCAGCCCCCAA | 233902 |
rs31976186 | snp | A/C | 0.401235 | 0.199068 | intron-variant | Fbxl19 | Mm_Celera | 7:127760666 | ACACTGGCTTGATTC[A/C]TTCAGTCAGTGTGTG | 233902 |
rs31980860 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Fbxl19 | Mm_Celera | 7:127763686 | TGATGCTCTGCATCC[C/T]AAGTATTGAGCTTAG | 233902 |
rs32002385 | snp | A/C | 0.375 | 0.216506 | intron-variant | Fbxl19 | Mm_Celera | 7:127757917 | CAGCCAAGAAACAAT[A/C]GGAGCGACTTCCCAA | 233902 |
rs32005424 | snp | C/T | 0.375 | 0.216506 | intron-variant | Fbxl19 | Mm_Celera | 7:127750598 | AATCTTTGAGAGACC[C/T]GGAGGATTAGGGAGG | 233902 |
rs32097872 | snp | G/T | 0.387812 | 0.208586 | intron-variant | Fbxl19 | Mm_Celera | 7:127764435 | GTTTTCAAGAAAACC[G/T]CTGTATCCAAATTTC | 233902 |
rs32114958 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Fbxl19 | Mm_Celera | 7:127748996 | CTCTTCTGCCTCCCT[C/T]ATCCTTTCAGCAGCC | 233902 |
rs32130434 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Fbxl19 | GRCm38.p3 | 7:127764478 | TACTTTTAGCTGGGC[A/G]TGGTGATGCATGCCT | 233902 |
rs32142945 | snp | A/G | 0.375 | 0.216506 | intron-variant | Fbxl19 | Mm_Celera | 7:127762682 | TCTGAGGGGCCAGGG[A/G]GTCAGAGTAGTTAAT | 233902 |
rs32159292 | snp | C/T | 0.375 | 0.216506 | intron-variant | Fbxl19 | Mm_Celera | 7:127764303 | AACCTGGGCTTGCCA[C/T]GTTGAATGCGCACAG | 233902 |
rs32163699 | snp | A/G | 0.375 | 0.216506 | intron-variant | Fbxl19 | Mm_Celera | 7:127750549 | CTCACTATGAGGAAG[A/G]AACACAAGCGAAGGG | 233902 |
rs32252595 | snp | C/T | 0.375 | 0.216506 | intron-variant | Fbxl19 | Mm_Celera | 7:127748472 | CTTGAGCCCCATGCC[C/T]GGGGTATGTGGAACC | 233902 |
rs32263715 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Fbxl19 | Mm_Celera | 7:127754167 | CAGCTTGGGCCCTGC[G/T]CCTGGCCTGTGGTTT | 233902 |
rs32270893 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Fbxl19 | Mm_Celera | 7:127754228 | CTCTATTCTCACTTA[A/T]AAGTCTGGGATATAT | 233902 |
rs32293306 | snp | C/T | 0.375 | 0.216506 | intron-variant | Fbxl19 | Mm_Celera | 7:127766775 | AAAGCCTAACCTGCA[C/T]ACACCACCAGAAAAG | 233902 |
rs32308910 | snp | C/T | 0.265928 | 0.249492 | intron-variant | Fbxl19 | Mm_Celera | 7:127763924 | ACACCACACTTGGTA[C/T]TTTTTAGTCTTACTT | 233902 |
rs32354515 | snp | C/T | 0.32 | 0.24 | intron-variant | Fbxl19 | Mm_Celera | 7:127754828 | CTGGACTTGGGGTGC[C/T]GGTCTGGAATTCTAC | 233902 |
rs32371226 | snp | A/C | 0.5 | 0 | intron-variant | Fbxl19 | Mm_Celera | 7:127765616 | GTGGCTTCCTTCTTA[A/C]ATTTTTTTTTAAATT | 233902 |
rs32396790 | snp | A/G | 0.32 | 0.24 | intron-variant | Fbxl19 | Mm_Celera | 7:127750797 | AAGAAGACGACGAGG[A/G]ACCCTAGTTTGGTTG | 233902 |
rs32527991 | snp | A/G | 0.32 | 0.24 | intron-variant | Fbxl19 | Mm_Celera | 7:127752863 | AAAACCTTTACAGGT[A/G]GCCTCTGGCCTCTAA | 233902 |
rs33163786 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl19 | Mm_Celera | 7:127756226 | GGTATTCATTGGCCA[C/T]GGAGACAGTATTGAG | 233902 |
rs33163789 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxl19 | Mm_Celera | 7:127756446 | CGTTTTCAAGGACGT[A/G]GGCAGAGAAGGAAGT | 233902 |
rs33163792 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fbxl19 | Mm_Celera | 7:127756666 | GGGTTTGAAACTGCA[A/G]TGGAGGTTTTACAGG | 233902 |
rs33163805 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxl19 | Mm_Celera | 7:127764068 | GAGTCTTCCATCTTT[A/G]CTGTCCTCTTCTTCT | 233902 |
rs33163808 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxl19 | Mm_Celera | 7:127764264 | TCTGTAAATGTGCTC[A/G]TCAGAGTCATGTGGA | 233902 |
rs33163813 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxl19 | Mm_Celera | 7:127764323 | AATGCGCACAGAGGT[A/G]GAGCTAACAGAAGCT | 233902 |
rs33164585 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Fbxl19 | Mm_Celera | 7:127757398 | TCTCTCTGGCCCTTG[A/G]ATACTTGTTTTTTAA | 233902 |
rs33164588 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxl19 | Mm_Celera | 7:127757435 | TGGGCCTTAAGTTGT[A/G]CAAAGGCCGTGATTA | 233902 |
rs33164591 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Fbxl19 | Mm_Celera | 7:127757639 | TGGGCAAACCCCTGC[C/T]TTTGTCCACCTTCCC | 233902 |
rs33164688 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Fbxl19 | Mm_Celera | 7:127765369 | AGTTTTGGCAACTTA[C/T]CTTGGACTGTGATGT | 233902 |
rs33165404 | snp | G/T | 0.297521 | 0.245442 | intron-variant | Fbxl19 | Mm_Celera | 7:127757664 | CTTCCCCTCCTGGAG[G/T]AAGGCTGCTTTCTTC | 233902 |
rs33165409 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fbxl19 | Mm_Celera | 7:127757931 | TAGGAGCGACTTCCC[A/G]AACATGAAGGTCTAG | 233902 |
rs33165412 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Fbxl19 | Mm_Celera | 7:127757996 | CCCAGGGACACAGAA[C/T]GTATCAGAGTGTATT | 233902 |
rs33165857 | snp | A/G | 0.231111 | 0.249285 | upstream-variant-2KB | Fbxl19 | GRCm38.p3 | 7:127742114 | AGAGAGAGAGAGAGA[A/G]AATGGCCCTTAGTTC | 233902 |
rs33165860 | snp | A/C | 0.231111 | 0.249285 | upstream-variant-2KB | Fbxl19 | GRCm38.p3 | 7:127742168 | ACAGATAGGATAGGG[A/C]CTACAGACTGTGGGA | 233902 |
rs33165863 | snp | A/G | 0.231111 | 0.249285 | upstream-variant-2KB | Fbxl19 | GRCm38.p3 | 7:127742325 | AGCCCTGGCAGCCTG[A/G]AGTACTGAGATTAAA | 233902 |
rs33166295 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Fbxl19 | Mm_Celera | 7:127758007 | AGAACGTATCAGAGT[G/T]TATTGGTACTAGATG | 233902 |
rs33166298 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fbxl19 | Mm_Celera | 7:127758417 | CTTCAGATTGGAGCC[C/T]GATTTGTAGCCTTCG | 233902 |
rs33166301 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Fbxl19 | Mm_Celera | 7:127759009 | AAAGTAAATCTGTTG[G/T]TTTTGAAAAGGAAGT | 233902 |
rs33166646 | snp | C/G | 0.124444 | 0.216185 | upstream-variant-2KB | Fbxl19 | GRCm38.p3 | 7:127742733 | AACAACAAACAACAA[C/G]AAAAGGGAAGCAGGT | 233902 |
rs33166649 | snp | C/T | 0.231111 | 0.249285 | upstream-variant-2KB | Fbxl19 | GRCm38.p3 | 7:127742748 | CAAAAGGGAAGCAGG[C/T]ACTTGGCTCCAGCTG | 233902 |
rs33166652 | snp | C/T | 0.124444 | 0.216185 | upstream-variant-2KB | Fbxl19 | GRCm38.p3 | 7:127743009 | GAATTTTTGAAGATA[C/T]ATTAGAAGTCTAACT | 233902 |
rs33167206 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Fbxl19 | Mm_Celera | 7:127759663 | GCTTGCACAGCGAGC[C/G]TTTACTGCCCAGGCA | 233902 |
rs33167209 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fbxl19 | Mm_Celera | 7:127759689 | AGGCATCCCTGGCCT[C/T]ACGGTTAGTTTAAGC | 233902 |
rs33167212 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fbxl19 | Mm_Celera | 7:127759918 | CAGCACAGGCTCACA[A/G]TCCTGGTTGAAGTAG | 233902 |
rs33167475 | snp | A/G | 0.231111 | 0.249285 | upstream-variant-2KB | Fbxl19 | GRCm38.p3 | 7:127743163 | TATCTGTTGTGTATA[A/G]CTGAGTGTAAAAAAA | 233902 |
rs33167478 | snp | A/C | 0.231111 | 0.249285 | upstream-variant-2KB | Fbxl19 | GRCm38.p3 | 7:127743209 | TTCCTTTCTGTATCA[A/C]ACACGATAAAAATGT | 233902 |
rs33167481 | snp | C/T | 0.277778 | 0.248452 | upstream-variant-2KB | Fbxl19 | GRCm38.p3 | 7:127743229 | GATAAAAATGTGTGT[C/T]CTGGAGAAGGACTTA | 233902 |
rs33167997 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxl19 | Mm_Celera | 7:127760505 | TTCTAGTAACTGCTA[A/G]TTGAATCTTTTGGTG | 233902 |
rs33168000 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fbxl19 | Mm_Celera | 7:127760528 | TTTTGGTGTGCTGGA[C/T]TCAGGCCTGTTTACC | 233902 |
rs33168003 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxl19 | Mm_Celera | 7:127760638 | AAGTGGGAAGGAGTC[A/G]TTGAAGTAGTTCACA | 233902 |
rs33168084 | snp | A/G | 0.231111 | 0.249285 | upstream-variant-2KB | Fbxl19 | GRCm38.p3 | 7:127743324 | GTCAAACCTTTGTCT[A/G]CACAGAGGCCCACTA | 233902 |
rs33168087 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fbxl19 | Mm_Celera | 7:127754777 | TGCCTCAGTATTGCT[C/T]CTGGCTCCAGACCTT | 233902 |
rs33168092 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fbxl19 | Mm_Celera | 7:127754916 | AAAGGACTAGGAGCT[A/G]AGCAGTGGTGGGCAC | 233902 |
rs33168777 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Fbxl19 | Mm_Celera | 7:127755320 | CTTGCTGATTGGTTG[C/G]CTGTGAAGGCTGATT | 233902 |
rs33168780 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fbxl19 | Mm_Celera | 7:127755382 | CTGGGTGGGAGAGAG[C/T]CATAGTCTTGAAGCC | 233902 |
rs33168783 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Fbxl19 | Mm_Celera | 7:127755470 | GTCTGAGAAAAGCTT[G/T]CGAGCCAGTCAGAGT | 233902 |
rs33169098 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl19 | Mm_Celera | 7:127761193 | GAGAACTGGGTTTTC[C/T]TGACTGGGTTCCTAG | 233902 |
rs33169101 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Fbxl19 | Mm_Celera | 7:127761761 | GATGGTGATGAGTTG[A/G]GACAGATGGACACAG | 233902 |
rs33169616 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Fbxl19 | Mm_Celera | 7:127755471 | TCTGAGAAAAGCTTG[C/T]GAGCCAGTCAGAGTC | 233902 |
rs33169618 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Fbxl19 | Mm_Celera | 7:127755485 | GCGAGCCAGTCAGAG[G/T]CCACTGCTGAGAACA | 233902 |
rs33169620 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Fbxl19 | Mm_Celera | 7:127755885 | GTGGTAGAGCAGAGA[A/C]CACGAGTGTGAGCTA | 233902 |
rs33169623 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Fbxl19 | Mm_Celera | 7:127756054 | ACTGTCAAGGCCTGG[A/G]AGGAGTGTTTGCCTA | 233902 |
rs33169844 | snp | G/T | 0.277778 | 0.248452 | intron-variant | Fbxl19 | Mm_Celera | 7:127762144 | ACAGACAGACACAGA[G/T]GTAGGATGATGAGTT | 233902 |
rs33169847 | snp | G/T | 0.260355 | 0.249785 | intron-variant | Fbxl19 | GRCm38.p3 | 7:127762214 | ACAGACAGACACAGA[G/T]GTAGGATGATGAGTT | 233902 |
rs33169850 | snp | A/G | 0.375 | 0.216506 | intron-variant | Fbxl19 | GRCm38.p3 | 7:127762267 | GATGGTGATGAGTTG[A/G]GACAGATGGACACAG | 233902 |
rs33169853 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Fbxl19 | Mm_Celera | 7:127762306 | GGTGATGAGTTGGGA[C/T]GGATGGACACAGAGA | 233902 |
rs33170186 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Fbxl19 | Mm_Celera | 7:127756059 | CAAGGCCTGGGAGGA[C/G]TGTTTGCCTAATATC | 233902 |
rs33170480 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Fbxl19 | Mm_Celera | 7:127763735 | GGATAAACCAGCATT[A/G]CCTCCTCCTGCCTTA | 233902 |
rs45669899 | snp | C/T | | | upstream-variant-2KB | Fbxl19 | GRCm38.p3 | 7:127743866 | TATCTGGTTTGATTC[C/T]CAGCAGGGCAAAACC | 233902 |
rs46250087 | snp | C/T | | | intron-variant | Fbxl19 | Mm_Celera | 7:127766299 | AGAGGCCATGGAGGT[C/T]CACATCTTACTGGCT | 233902 |
rs46922967 | snp | A/G/T | | | intron-variant | Fbxl19 | GRCm38.p3 | 7:127748678 | CTACACAGAAGAGTC[A/G/T]GCCTCAGGTCTGTAG | 233902 |
rs47001497 | snp | C/T | | | intron-variant | Fbxl19 | Mm_Celera | 7:127766656 | TGCTGGGATTAAAGG[C/T]GTGAGTCACCACTGC | 233902 |
rs47082371 | snp | A/G | | | intron-variant | Fbxl19 | Mm_Celera | 7:127757259 | TTATGTGCACCACAG[A/G]CATGCATGAGCGTGT | 233902 |
rs47765493 | snp | A/T | | | utr-variant-5-prime | Fbxl19 | GRCm38.p3 | 7:127744486 | AATTCAGGTTGAGAA[A/T]ATTTGGTCAGTGTGT | 233902 |
rs47972978 | snp | A/G | | | intron-variant | Fbxl19 | Mm_Celera | 7:127761139 | AATCCAGTCCTTTGG[A/G]CTGAAGGCCAGAAGA | 233902 |
rs48138335 | snp | G/T | | | intron-variant | Fbxl19 | Mm_Celera | 7:127760936 | GCCCAGAGATAGATT[G/T]TGGGGGCTGCTTTTA | 233902 |
rs48508068 | snp | C/T | | | intron-variant | Fbxl19 | Mm_Celera | 7:127747619 | GGGAAGACCTAAAGC[C/T]GAGCCCACCTTGAAT | 233902 |