SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3671191 | snp | A/G | 0.489796 | 0.070696 | downstream-variant-500B | Ints12 | Mm_Celera | 3:133111466 | TATTATAAATTAACT[A/G]GCTCATAGGCCTTTA | 71793 |
rs30005815 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Gstcd, Ints12 | Mm_Celera | 3:133090568 | CCCTTACTAGTTTAA[A/T]GGTGTTTTTCATTAG | 71793 |
rs30012842 | snp | A/T | 0.473373 | 0.11227 | intron-variant | Ints12 | Mm_Celera | 3:133107616 | AGATGTTTTTCCTAA[A/T]CAGGATATCATGAGA | 71793 |
rs30076360 | snp | A/C | 0.5 | 0 | intron-variant | Gstcd, Ints12 | Mm_Celera | 3:133090494 | TTCTTTCCACTCCCC[A/C]GGCCCCGGACCTCAC | 71793 |
rs30161359 | snp | A/G | 0.5 | 0 | intron-variant | Ints12 | Mm_Celera | 3:133099247 | CAAGGTGAAGGAGTC[A/G]GCTCTCCCATTCTAA | 71793 |
rs30303763 | snp | C/T | 0.487535 | 0.077957 | utr-variant-3-prime | Ints12 | Mm_Celera | 3:133110163 | CCAGCTTCTTCCTCA[C/T]GGTGAAAGGACAAGC | 71793 |
rs30308760 | snp | C/G | 0.5 | 0 | intron-variant | Ints12 | Mm_Celera | 3:133104837 | ACACACACACACACA[C/G]ACAGACACACACACA | 71793 |
rs30314777 | snp | A/C | 0.5 | 0 | intron-variant | Ints12 | Mm_Celera | 3:133105925 | TATTATTTCAATATT[A/C]AATATTTCAATGCAT | 71793 |
rs30363460 | snp | A/G | 0.475309 | 0.108333 | intron-variant | Ints12 | Mm_Celera | 3:133108317 | CAACTTGATTATTTT[A/G]AGTGAGTGTAGAACT | 71793 |
rs30411931 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ints12 | Mm_Celera | 3:133101329 | AGATCCTTTGGTTGG[A/G]GGTTTTGGCTTCGTT | 71793 |
rs30454671 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ints12 | Mm_Celera | 3:133107769 | AGTAGTCATATACAG[A/G]CTATGTTGAAGGCAA | 71793 |
rs30495153 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ints12 | Mm_Celera | 3:133094347 | GGCCTGGCCCTAATA[C/T]TATGTAAATAAACCC | 71793 |
rs30506904 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Gstcd, Ints12 | Mm_Celera | 3:133091013 | GTTAGAGAGGTATGT[A/G]TTAGGGTATTCTTTT | 71793 |
rs30524401 | snp | C/T | 0.46875 | 0.121031 | intron-variant | Ints12 | Mm_Celera | 3:133107407 | ACCTTGCTTTCCTGT[C/T]CATCCTTCATTGACC | 71793 |
rs30555722 | snp | A/G | 0.46875 | 0.121031 | intron-variant | Ints12 | Mm_Celera | 3:133095566 | TCTGTCTGTCTGCGC[A/G]GGGTATGAGGAGGAA | 71793 |
rs30596901 | snp | A/T | 0.5 | 0 | intron-variant | Ints12 | Mm_Celera | 3:133108447 | TGGTTGTTTTTTTTT[A/T]AATTAAAGTAGATTG | 71793 |
rs30599592 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Gstcd, Ints12 | Mm_Celera | 3:133090578 | TTTAAAGGTGTTTTT[C/T]ATTAGTACTATAGAA | 71793 |
rs30736639 | snp | C/T | 0.231111 | 0.249285 | upstream-variant-2KB, intron-variant | Gstcd, Ints12 | Mm_Celera | 3:133093427 | CTGCAAGAGGTCCTG[C/T]TCAGTAGGAAAATGT | 71793 |
rs30736641 | snp | C/T | 0.231111 | 0.249285 | upstream-variant-2KB, intron-variant | Gstcd, Ints12 | Mm_Celera | 3:133093475 | AGATGGGAAGTGAGT[C/T]GACCAAACAAGCATG | 71793 |
rs30736643 | snp | A/G | 0.487535 | 0.077957 | intron-variant, upstream-variant-2KB | Ints12, Gstcd | Mm_Celera | 3:133093746 | AGAGGTAAGCGATGC[A/G]GGGAGATTATTGTGT | 71793 |
rs30737345 | snp | A/G | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Ints12, Gstcd | Mm_Celera | 3:133093854 | AGCTATCACTGCCAC[A/G]TCCTAGGTTATTGAT | 71793 |
rs30737347 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Ints12 | Mm_Celera | 3:133094208 | AATGGTGTAGCAGAC[G/T]TCACATTTCACTAGC | 71793 |
rs30737349 | snp | A/G/T | 0.231111 | 0.249285 | intron-variant | Ints12 | GRCm38.p3 | 3:133094707 | GGAGAAAAGGGAAAT[A/G/T]GGAAGTTGCTGGATA | 71793 |
rs30737351 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ints12 | Mm_Celera | 3:133094839 | ATTTATGGCAGGGGT[A/G]CACAGCATGTTAAGT | 71793 |
rs30737353 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ints12 | Mm_Celera | 3:133095291 | ATTTAAAGCAGCAGT[A/G]GAGCCGATTTCATTT | 71793 |
rs30737784 | snp | A/G | 0.244898 | 0.249948 | missense | Ints12 | Mm_Celera | 3:133109250 | GTGGGAATGGAAATA[A/G]TGCTACAACGGGGCC | 71793 |
rs30737786 | snp | A/T | 0.132653 | 0.220748 | synonymous-codon | Ints12 | Mm_Celera | 3:133109341 | TAAAGGTCCAACTTC[A/T]CAAGAATCACAGCTC | 71793 |
rs30737788 | snp | A/G | 0.152778 | 0.230321 | utr-variant-3-prime | Ints12 | Mm_Celera | 3:133109433 | AATATGGCCAGATAG[A/G]TTTTTATATCATATT | 71793 |
rs30737790 | snp | A/G | 0.132653 | 0.220748 | utr-variant-3-prime | Ints12 | Mm_Celera | 3:133109679 | CTGATGCATGACAAG[A/G]GCTTCAAGAAATTGA | 71793 |
rs30737792 | snp | A/T | 0.124444 | 0.216185 | utr-variant-3-prime | Ints12 | Mm_Celera | 3:133109701 | AGAAATTGATGGCGC[A/T]TACAGATGAAAAGAA | 71793 |
rs30737804 | snp | C/T | 0.336735 | 0.234472 | synonymous-codon | Ints12 | Mm_Celera | 3:133098559 | GAAGAGACCTGCTGA[C/T]AAGGTAAGCTTTGCT | 71793 |
rs30737806 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ints12 | Mm_Celera | 3:133098643 | TTATGTAGCAGTGGG[C/T]GGAGTTACATCACGA | 71793 |
rs30737808 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Ints12 | Mm_Celera | 3:133098743 | ATATGTAACCATGGT[G/T]TGAGATAGTTGTTGT | 71793 |
rs30737810 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Ints12 | Mm_Celera | 3:133098790 | AAGGGAAAGTAATGA[C/T]GACTCTAATCCCTAA | 71793 |
rs30737812 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Ints12 | Mm_Celera | 3:133098838 | TTTGAGAAGTAAAAC[A/G]AAGAAACCACAGTGA | 71793 |
rs30738135 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Ints12 | Mm_Celera | 3:133095364 | CTTTCTAGAACTCTA[G/T]CCTTCAAACTCACTA | 71793 |
rs30738137 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Ints12 | Mm_Celera | 3:133095382 | TTCAAACTCACTATC[C/T]AGGCAATCCAGACAG | 71793 |
rs30738140 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ints12 | Mm_Celera | 3:133095803 | TCGATCAAAGAATTG[A/G]ACACCAAGGGTATGT | 71793 |
rs30738141 | snp | A/G | 0.495868 | 0.0452663 | intron-variant | Ints12 | Mm_Celera | 3:133096138 | GGGATATTAAAAATA[A/G]CAGAGGACTGGGGAG | 71793 |
rs30738142 | snp | A/C/G | 0.35503 | 0.226867 | intron-variant | Ints12 | GRCm38.p3 | 3:133096167 | AGGAAGGAAAATACA[A/C/G]AGAAGCAAAACAAGA | 71793 |
rs30738704 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Ints12 | Mm_Celera | 3:133099336 | CAAGGAGTCTCTGTG[A/G]CCAAACTGTGTCTTT | 71793 |
rs30738706 | snp | A/G | 0.297521 | 0.245442 | intron-variant | Ints12 | Mm_Celera | 3:133099895 | TAAAGTGTTTTTTAC[A/G]TATAGTCTTTTACAT | 71793 |
rs30738708 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Ints12 | Mm_Celera | 3:133100305 | ATAATACAAAGCGGA[A/G]TACAGATATTATACT | 71793 |
rs30738710 | snp | A/G | 0.18 | 0.24 | intron-variant | Ints12 | Mm_Celera | 3:133100346 | ATTTATATCTTGCTA[A/G]TTTAGCATACTAATT | 71793 |
rs30738712 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Ints12 | Mm_Celera | 3:133100580 | ATTTAGAGTTTATGT[C/T]ATGTTACTTTCACAA | 71793 |
rs30738774 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime | Ints12 | Mm_Celera | 3:133109773 | TAGAAAGTGTTCCAG[C/T]GTTTTATAAAATCTG | 71793 |
rs30738776 | snp | C/T | 0.277778 | 0.248452 | utr-variant-3-prime | Ints12 | Mm_Celera | 3:133109786 | AGCGTTTTATAAAAT[C/T]TGAAATGTTCAGTGT | 71793 |
rs30738778 | snp | A/G | 0.231111 | 0.249285 | utr-variant-3-prime | Ints12 | Mm_Celera | 3:133109973 | ATGAATGCTCATACA[A/G]TATACTTTCTCACGT | 71793 |
rs30738781 | snp | C/T | 0.244898 | 0.249948 | utr-variant-3-prime | Ints12 | Mm_Celera | 3:133110212 | AACGTTTGGTGTGGT[C/T]TATCTTTGTATGAAA | 71793 |
rs30738783 | snp | C/T | 0.231111 | 0.249285 | utr-variant-3-prime | Ints12 | Mm_Celera | 3:133110251 | TACCTAATGATTAGT[C/T]CTTGAGGTTTCTGTC | 71793 |
rs30739284 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Ints12 | Mm_Celera | 3:133096206 | TAAAAGCTACACAGC[A/G]ACTGCGACATGAACC | 71793 |
rs30739286 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ints12 | Mm_Celera | 3:133096341 | GTAAACTTGACTTAA[A/G]AGCAGGCAAGTTACG | 71793 |
rs30739287 | snp | C/T | 0.429688 | 0.173817 | intron-variant | Ints12 | Mm_Celera | 3:133096920 | CTCAAAAGGTATCGA[C/T]CTGAATACAAAGTTT | 71793 |
rs30739289 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Ints12 | Mm_Celera | 3:133096943 | CAAAGTTTGGAAAGT[C/G]TTGGAAGTGTTCAGT | 71793 |
rs30739291 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Ints12 | Mm_Celera | 3:133096983 | TAGATTGTCTCCAAA[C/T]ACTCTATGTAATCAT | 71793 |
rs30739293 | snp | G/T | 0.46875 | 0.121031 | intron-variant | Ints12 | Mm_Celera | 3:133097333 | CTGGTGTGCAAAAAT[G/T]CCTTCTTTGCAATTT | 71793 |
rs30739554 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Ints12 | Mm_Celera | 3:133100603 | TTTCACAATCGTTCA[A/G]CATCTCGTTCTTTTC | 71793 |
rs30739556 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Ints12 | Mm_Celera | 3:133100610 | ATCGTTCAACATCTC[A/G]TTCTTTTCATAGATG | 71793 |
rs30739558 | snp | A/C | 0.132653 | 0.220748 | missense | Ints12 | Mm_Celera | 3:133100644 | GATGTCACTGAAGGA[A/C]TTGATGTTCCAAAGA | 71793 |
rs30739560 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Ints12 | Mm_Celera | 3:133101028 | GCTAGTTTATCTTCC[A/G]GACCACAGCTTCTTT | 71793 |
rs30739562 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ints12 | Mm_Celera | 3:133101267 | CCTGAGTGACACTTT[C/T]ACGCTGGAATGCATA | 71793 |
rs30739785 | snp | A/G | 0.231111 | 0.249285 | utr-variant-3-prime | Ints12 | Mm_Celera | 3:133110520 | CTGAACTCTTGCCGT[A/G]ATGTGATCCTATATA | 71793 |
rs30739787 | snp | C/T | 0.429688 | 0.173817 | utr-variant-3-prime | Ints12 | Mm_Celera | 3:133110554 | GGTCCAAGCCATTGT[C/T]TTGTAAGCTAATGAA | 71793 |
rs30740215 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Ints12 | Mm_Celera | 3:133097893 | ACCTAGTACAGGCAG[A/G]CTTTCAGCTAGAAGT | 71793 |
rs30740217 | snp | A/C | 0.260355 | 0.249785 | intron-variant | Ints12 | Mm_Celera | 3:133097940 | TCTGAAACTCCAGGT[A/C]ACCCAGGTGTGGAGA | 71793 |
rs30740219 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ints12 | Mm_Celera | 3:133097976 | CTGCCCAACTAAGAC[A/G]GAAGACAACTATGGC | 71793 |
rs30740221 | snp | A/G | 0.32 | 0.24 | intron-variant | Ints12 | Mm_Celera | 3:133098141 | GGTGGCTGTCTCATC[A/G]ACATGCACACCATGA | 71793 |
rs30740223 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Ints12 | Mm_Celera | 3:133098379 | TTTGAGTAAAATGAA[G/T]GCCTCTTACCTTTTT | 71793 |
rs30740564 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ints12 | Mm_Celera | 3:133101300 | TAGAGAAGCATGTAA[C/T]TCTGCCTGGTGGGAG | 71793 |
rs30740566 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Ints12 | Mm_Celera | 3:133102169 | TTGTAATTATTGACT[A/G]AGTATTACCTATCAG | 71793 |
rs30740568 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ints12 | Mm_Celera | 3:133102296 | TTACCAGAAGAATGT[A/G]GAAACAGCTTTAAAT | 71793 |
rs30740570 | snp | C/T | 0.46875 | 0.121031 | intron-variant | Ints12 | Mm_Celera | 3:133102624 | AATAATGCTGAAAAA[C/T]AAGCTAACATTTAAG | 71793 |
rs30740572 | snp | C/T | 0.32 | 0.24 | intron-variant | Ints12 | Mm_Celera | 3:133102741 | AAACAGGGTTGAAGA[C/T]ACATAGGACACTATG | 71793 |
rs30741444 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ints12 | Mm_Celera | 3:133102773 | TTTTCAATCATGAAG[C/T]TTTAATCACAAACAT | 71793 |
rs30741446 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ints12 | Mm_Celera | 3:133102960 | GCCCAGATTCACCAG[C/T]CTTCCTCCTCATTGG | 71793 |
rs30741448 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ints12 | Mm_Celera | 3:133103025 | CCCAGTGTGCTCACA[C/T]TAACTACTAATACTG | 71793 |
rs30741450 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Ints12 | Mm_Celera | 3:133103750 | ACACATACATGCACA[C/T]AACCAGCACACACAT | 71793 |
rs30741452 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Ints12 | Mm_Celera | 3:133103941 | ATCCCCAGAAATAGC[A/G]CAGCAACACGGTGAT | 71793 |
rs30742274 | snp | A/C | 0.5 | 0 | intron-variant | Ints12 | Mm_Celera | 3:133104053 | TCCCTAGCAACTGTT[A/C]ACTTGTTTTCATACT | 71793 |
rs30742276 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Ints12 | Mm_Celera | 3:133104355 | CTAAATTTCCTCAAG[A/G]TTTTCTTCTCTTATT | 71793 |
rs30742278 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ints12 | Mm_Celera | 3:133105231 | TTACATAACTACAAT[C/T]CGTCCTCATAAACAC | 71793 |
rs30742280 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Ints12 | Mm_Celera | 3:133105327 | GTCAGCCCTGGGTCT[C/G]TTTGATACTAAACAC | 71793 |
rs30742281 | snp | A/C | 0.486111 | 0.0821678 | intron-variant | Ints12 | Mm_Celera | 3:133105405 | GTAAACACTCAGAAT[A/C]TGAAAGAGGATCCAC | 71793 |
rs30742283 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Ints12 | Mm_Celera | 3:133105411 | ACTCAGAATCTGAAA[A/G]AGGATCCACGTTTAT | 71793 |
rs30742995 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Ints12 | Mm_Celera | 3:133105553 | ATTTATAAACTTTTC[A/T]AAGGATTTGATTCAC | 71793 |
rs30742997 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Ints12 | Mm_Celera | 3:133105662 | AATTACCAGAGTTGT[C/T]TTTAACTCATCTTCA | 71793 |
rs30742998 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ints12 | Mm_Celera | 3:133105793 | TTCCATGATTGTCTC[C/T]CACTTTCTGTGAACT | 71793 |
rs30743000 | snp | C/G | 0.244898 | 0.249948 | synonymous-codon | Ints12 | Mm_Celera | 3:133107076 | AGCATTCAAGAGAAC[C/G]GAAGTTAAGGTAAAG | 71793 |
rs30743002 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Ints12 | Mm_Celera | 3:133107286 | TGCTAGGTTCCCAAG[G/T]TTGTAGTGCTTCATG | 71793 |
rs30743844 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Ints12 | Mm_Celera | 3:133107321 | TGCATCCTGGTTGTG[C/T]TCTACACCATCTGTC | 71793 |
rs30743846 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Ints12 | Mm_Celera | 3:133107376 | CGGTCATTAGAGTCA[A/G]GTGCTCAGCACAGCC | 71793 |
rs30743849 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Ints12 | Mm_Celera | 3:133107467 | CTCTTTGGTGGAGCA[C/G]ATAGTTTCATGTCTT | 71793 |
rs30743851 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Ints12 | Mm_Celera | 3:133107572 | TTTCTGTCACCAGCA[A/G]TGTGTGTCCCAGGAA | 71793 |
rs30744855 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Ints12 | Mm_Celera | 3:133108119 | GAGTGTGTCAAACCT[C/T]CCCAAAATGCCTGTG | 71793 |
rs30744857 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Ints12 | Mm_Celera | 3:133108131 | CCTCCCCAAAATGCC[A/T]GTGCCACCCAAGAGG | 71793 |
rs30744860 | snp | G/T | 0.277778 | 0.248452 | intron-variant | Ints12 | Mm_Celera | 3:133108325 | TTATTTTAAGTGAGT[G/T]TAGAACTTCTATATA | 71793 |
rs30744862 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Ints12 | Mm_Celera | 3:133108361 | TTCCTTTAACACATC[C/T]ATCAATGATTGAATC | 71793 |
rs30745814 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Ints12 | Mm_Celera | 3:133108712 | GAACCTAATTTTGTT[G/T]TGTTGTCCATATTGT | 71793 |
rs30745816 | snp | A/G | 0.244898 | 0.249948 | synonymous-codon | Ints12 | Mm_Celera | 3:133108885 | CAACGTGTCCTCTTC[A/G]GTAACTAGTGGCCTA | 71793 |
rs30745818 | snp | G/T | 0.132653 | 0.220748 | synonymous-codon | Ints12 | Mm_Celera | 3:133109239 | CAGCCAATTGAGTGG[G/T]AATGGAAATAGTGCT | 71793 |