SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6160175 | snp | G/T | 0.375 | 0.216506 | intron-variant | Hectd2 | Mm_Celera | 19:36604731 | TATAGGACATATTCG[G/T]ATTCACACAAACATT | 226098 |
rs6160835 | snp | C/T | 0.5 | 0 | intron-variant | Hectd2 | Mm_Celera | 19:36604873 | TGAAAGAGAAAGGGC[C/T]GTAAAAAGTTATTTT | 226098 |
rs6161400 | snp | C/T | 0.5 | 0 | intron-variant | Hectd2 | Mm_Celera | 19:36604946 | TCTTAGGGGCAATAC[C/T]CTTTGTCAAGGCATC | 226098 |
rs6251584 | snp | A/G | 0.5 | 0 | intron-variant | Hectd2 | Mm_Celera | 19:36583274 | ATAGCCAAGGACAGA[A/G]CTGTACTTGGTTCTG | 226098 |
rs6251644 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Hectd2 | Mm_Celera | 19:36583319 | ACATGTTCAAGTAAA[A/C]ATTAGCAGCANAAAG | 226098 |
rs6264283 | snp | A/C | 0.5 | 0 | intron-variant | Hectd2 | Mm_Celera | 19:36583330 | TAAANATTAGCAGCA[A/C]AAAGGNTCAATTACA | 226098 |
rs6264286 | snp | A/G | 0.5 | 0 | intron-variant | Hectd2 | Mm_Celera | 19:36583336 | TTAGCAGCANAAAGG[A/G]TCAATTACAAATTTT | 226098 |
rs6264830 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hectd2 | Mm_Celera | 19:36583478 | TGGGAGAATAAATGT[A/G]GGCCAGTACAAAACT | 226098 |
rs6265859 | snp | A/G | 0.5 | 0 | intron-variant | Hectd2 | Mm_Celera | 19:36583655 | AAGAGAAGGAGAGAA[A/G]GAACTATANATTTCA | 226098 |
rs6265873 | snp | C/G | 0.5 | 0 | intron-variant | Hectd2 | Mm_Celera | 19:36583664 | AGAGAANGAACTATA[C/G]ATTTCATCTATGAAG | 226098 |
rs6265917 | snp | C/G | 0.5 | 0 | intron-variant | Hectd2 | Mm_Celera | 19:36583692 | AAGGGCTTTGGGGAG[C/G]ANTGGAGATGAATGG | 226098 |
rs6265918 | snp | A/G | 0.5 | 0 | intron-variant | Hectd2 | Mm_Celera | 19:36583694 | GGGCTTTGGGGAGNA[A/G]TGGAGATGAATGGTG | 226098 |
rs6266384 | snp | G/T | 0.5 | 0 | intron-variant | Hectd2 | Mm_Celera | 19:36583727 | CAGCTCTAACTTTAT[G/T]CAAGGTATAGTCAAA | 226098 |
rs6266481 | snp | C/G | 0.5 | 0 | intron-variant | Hectd2 | Mm_Celera | 19:36583778 | TTTATGGAAAGCACC[C/G]TNTAAGAGCTGTTAG | 226098 |
rs6266488 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Hectd2 | Mm_Celera | 19:36583780 | TATGGAAAGCACCNT[C/G]TAAGAGCTGTTAGGA | 226098 |
rs13483609 | snp | C/T | 0.286243 | 0.247359 | intron-variant | Hectd2 | Mm_Celera | 19:36587224 | GTCTCAGGAGTGAAT[C/T]GGATACTGCTCTTAG | 226098 |
rs30306671 | snp | G/T | 0.375 | 0.216506 | intron-variant | Hectd2 | Mm_Celera | 19:36569726 | CTCTAGCCAAACAAC[G/T]TATGTGATGAATTAG | 226098 |
rs30317441 | snp | C/T | 0.444444 | 0.157135 | upstream-variant-2KB | Hectd2, LOC105246565 | GRCm38.p3 | 19:36553955 | AGAGGGAACGAAGGA[C/T]GGCGGGGGGCGGGGA | 226098 |
rs30318050 | snp | A/G | 0.46875 | 0.121031 | intron-variant | Hectd2 | GRCm38.p3 | 19:36584549 | TGAGAAAGGAAGGGC[A/G]CGTGTCAGGGTGAGG | 226098 |
rs30320425 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hectd2 | GRCm38.p3 | 19:36617244 | TCTTCCTCTGGTTTC[C/T]ATGTGTACACATAAG | 226098 |
rs30321076 | snp | A/G | 0.49827 | 0.0293608 | intron-variant | Hectd2 | GRCm38.p3 | 19:36607124 | AGAGTAAAAAGATGA[A/G]CAAGAACTGAAGCTG | 226098 |
rs30329627 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hectd2 | Mm_Celera | 19:36586134 | AATGTGATTAGTTAT[A/G]TTCATGTATTTCCAA | 226098 |
rs30348952 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hectd2 | Mm_Celera | 19:36615856 | TCAAACTCAGAGATC[C/T]GCCTCCCTCTCTATC | 226098 |
rs30349672 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hectd2 | GRCm38.p3 | 19:36566716 | ACTTAGCTAGACTGG[C/T]CAATTACCTGGGTGT | 226098 |
rs30352296 | snp | A/G | 0.415225 | 0.187619 | intron-variant | Hectd2 | Mm_Celera | 19:36583129 | CCTTCTTATCCCAGG[A/G]CACCCCATACTGAGT | 226098 |
rs30364005 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Hectd2 | Mm_Celera | 19:36593648 | ATAGGCATCTCATCC[G/T]TTAGGTTAGGAAATT | 226098 |
rs30365661 | snp | A/G | 0.387812 | 0.208586 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | Hectd2, 1500017E21Rik | Mm_Celera | 19:36619147 | TAGTTTGTCACAGGT[A/G]TCCACTGGGAAAGAC | 226098 |
rs30369314 | snp | G/T | 0.444444 | 0.157135 | upstream-variant-2KB | Hectd2 | GRCm38.p3 | 19:36552349 | CCCTTTAGGTCTTTT[G/T]CCTTCCTAAATCAGA | 226098 |
rs30370075 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hectd2 | Mm_Celera | 19:36593357 | CTCCATCTGTAGTGA[C/T]TGAGAGTCTTGCTGG | 226098 |
rs30374040 | snp | A/G | 0.484429 | 0.0868505 | intron-variant | Hectd2 | GRCm38.p3 | 19:36582954 | GAAGCTGTTTGGTGA[A/G]CCGTGGAATAAGAGA | 226098 |
rs30377274 | snp | G/T | 0.375 | 0.216506 | intron-variant | Hectd2 | GRCm38.p3 | 19:36590834 | ATATGCCCAAGAGTG[G/T]TAGAGCTGGATTGTA | 226098 |
rs30405308 | snp | A/G | 0.401235 | 0.199068 | intron-variant | Hectd2 | GRCm38.p3 | 19:36559550 | AGCACACCCACTGGA[A/G]TGTTGACCACAGGAT | 226098 |
rs30407513 | snp | C/T | 0.49827 | 0.0293608 | intron-variant | Hectd2 | Mm_Celera | 19:36617375 | TTTCTACATGAGTCA[C/T]AATTAAAAGAATGAG | 226098 |
rs30408432 | snp | C/T | 0.5 | 0 | intron-variant | Hectd2 | Mm_Celera | 19:36603736 | TTATTGATAATATTT[C/T]TATAAATATCTTGTG | 226098 |
rs30415801 | snp | A/G | 0.429688 | 0.173817 | intron-variant, upstream-variant-2KB | Hectd2, LOC105246565 | GRCm38.p3 | 19:36555888 | TGGAAATTGTTAAAG[A/G]CAACTCTTTTATCAT | 226098 |
rs30416578 | snp | C/G | 0.456747 | 0.140554 | intron-variant | Hectd2 | GRCm38.p3 | 19:36602830 | ATGATTGGTGACTCT[C/G]TGACACAGCTTATGC | 226098 |
rs30429814 | snp | C/T | 0.375 | 0.216506 | upstream-variant-2KB, nc-transcript-variant | Hectd2, LOC105246565 | GRCm38.p3 | 19:36553072 | AAAATGAAAGGTTGG[C/T]TTTACAATGTTTGTT | 226098 |
rs30441248 | snp | A/G | 0.415225 | 0.187619 | intron-variant | Hectd2 | Mm_Celera | 19:36601778 | TGAGGAGCTTGTTGG[A/G]ACTTCATTGTGTAAC | 226098 |
rs30499671 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hectd2 | Mm_Celera | 19:36592368 | GTTGTTTAGTTTTCA[A/G]TGATTTTGTAAGCTT | 226098 |
rs30510758 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hectd2 | GRCm38.p3 | 19:36617819 | TAGCAAATGCACCGG[C/T]TTTAGGGTCAGACCT | 226098 |
rs30554029 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hectd2 | GRCm38.p3 | 19:36617739 | ACTGTCATCCCCTCT[A/G]TAAGGCACACTGTTG | 226098 |
rs30606628 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Hectd2 | Mm_Celera | 19:36612744 | CCTTTCTACTATATA[G/T]AGAGAGAGAGAGAAA | 226098 |
rs30619016 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hectd2 | Mm_Celera | 19:36609193 | TTAGATCTAAAAGGA[A/G]ACTGGTGCATAATTC | 226098 |
rs30657771 | snp | C/T | 0.32 | 0.24 | intron-variant | Hectd2 | GRCm38.p3 | 19:36576911 | TGACCTCAAGCTGTA[C/T]TACAGAGCAATGGTG | 226098 |
rs30670562 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hectd2 | Mm_Celera | 19:36584747 | CCTACACATTTATAT[A/G]CTGTTTGTATCAACT | 226098 |
rs30696908 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Hectd2 | Mm_Celera | 19:36598521 | CTCCCTCATGCATGC[C/T]GAGGCCTCGGGGGTT | 226098 |
rs30710321 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hectd2 | Mm_Celera | 19:36557305 | CAGAAAATTAGTGTG[C/T]CATGGTTATGACGGT | 226098 |
rs30766662 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Hectd2 | Mm_Celera | 19:36595869 | ATAAATAAATCTTTT[A/T]AAAAAAAAAGAAAAG | 226098 |
rs30805300 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hectd2 | GRCm38.p3 | 19:36558415 | GTGAGTGTGCATGTA[C/T]GTGTGTGTACATGTG | 226098 |
rs30842320 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Hectd2 | GRCm38.p3 | 19:36592718 | GGGTAAGTAGTGTTT[A/C]TTTTACAAAGGTGGG | 226098 |
rs30850383 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Hectd2 | GRCm38.p3 | 19:36617730 | GAACTAAGAACTGTC[A/G]TCCCCTCTATAAGGC | 226098 |
rs30851162 | snp | A/C | 0.32 | 0.24 | intron-variant | Hectd2 | Mm_Celera | 19:36610667 | ACCACCCTGCCAGAT[A/C]TGAGGCTCTGGTCCC | 226098 |
rs30910268 | snp | A/G | 0.5 | 0 | intron-variant | Hectd2 | GRCm38.p3 | 19:36600751 | TTGTGATGGGAGTCT[A/G]ACCTCTCAGTGTTAC | 226098 |
rs30915485 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Hectd2 | Mm_Celera | 19:36606201 | ATCTTGTACATCCTT[A/G]TAAAAAGTCAGATAT | 226098 |
rs30917111 | snp | A/T | 0.415225 | 0.187619 | intron-variant | Hectd2 | GRCm38.p3 | 19:36616902 | CAGAGAGGGTAGGCC[A/T]TATGCATCTTATACT | 226098 |
rs30947361 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Hectd2 | GRCm38.p3 | 19:36597775 | TAATTCCTATTACTG[A/G]TAGTAGAATTCAAAT | 226098 |
rs30989214 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Hectd2 | Mm_Celera | 19:36612746 | TTTCTACTATATAGA[G/T]AGAGAGAGAGAAATG | 226098 |
rs30991176 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hectd2 | Mm_Celera | 19:36614633 | CCTGCTCTCCTACTC[A/G]CCCACTCCCACTTCT | 226098 |
rs30992107 | snp | C/T | 0.49827 | 0.0293608 | intron-variant | Hectd2 | GRCm38.p3 | 19:36600822 | GTAGTGTGTGGTTTT[C/T]ATACATAGTGTACGA | 226098 |
rs31008504 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hectd2 | Mm_Celera | 19:36562588 | GCTAGCATGCACAAA[A/G]TGATGTTCCATCCCC | 226098 |
rs31009339 | snp | A/T | 0.375 | 0.216506 | intron-variant | Hectd2 | Mm_Celera | 19:36593370 | GACTGAGAGTCTTGC[A/T]GGGTATAGTAGTGTG | 226098 |
rs31039933 | snp | A/G | 0.387812 | 0.208586 | intron-variant | Hectd2 | Mm_Celera | 19:36612018 | TGACACCTCTTCTTA[A/G]TATAATTGTCACTGG | 226098 |
rs31042743 | snp | A/G | 0.5 | 0 | upstream-variant-2KB, utr-variant-5-prime | Hectd2, LOC105246565 | GRCm38.p3 | 19:36554162 | GCCAGGAGAGGACAC[A/G]GGGAAAGAGTTAGTC | 226098 |
rs31044706 | snp | A/C | 0.359862 | 0.224567 | intron-variant | Hectd2 | GRCm38.p3 | 19:36595124 | TCTGGCTTCTCAGTT[A/C]TTACAAACACATAAT | 226098 |
rs31075415 | snp | C/G | 0.375 | 0.216506 | intron-variant | Hectd2 | GRCm38.p3 | 19:36586457 | CGAAGGAGTTGTGAC[C/G]CATTGGTTGAGAACT | 226098 |
rs31094642 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hectd2 | GRCm38.p3 | 19:36617735 | AAGAACTGTCATCCC[C/T]TCTATAAGGCACACT | 226098 |
rs31095513 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hectd2 | GRCm38.p3 | 19:36575603 | GCCTACACCTCTGTG[C/T]GCTCTTAACCATCTA | 226098 |
rs31137403 | snp | G/T | 0.375 | 0.216506 | intron-variant | Hectd2 | GRCm38.p3 | 19:36566109 | TAGGAACACAGACAG[G/T]AAGGAACCTGGAACA | 226098 |
rs31163762 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Hectd2 | Mm_Celera | 19:36604059 | GATTTTGGTACCTAC[G/T]GGCTACTAGGGTTCC | 226098 |
rs31184459 | snp | A/G | 0.375 | 0.216506 | upstream-variant-2KB, downstream-variant-500B | Hectd2, LOC105246565 | Mm_Celera | 19:36552730 | CTATATAGAGCTCCC[A/G]GCAGAATAAACCAAT | 226098 |
rs31196757 | snp | A/T | 0.493827 | 0.0552116 | utr-variant-3-prime, nc-transcript-variant | Hectd2, 1500017E21Rik | GRCm38.p3 | 19:36620175 | GCATTTAGTACCAGC[A/T]TATGGCCCATGTGCA | 226098 |
rs31205527 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hectd2 | GRCm38.p3 | 19:36617751 | TCTATAAGGCACACT[A/G]TTGAAGATTGATAGG | 226098 |
rs31227666 | snp | A/G | 0.401235 | 0.199068 | intron-variant | Hectd2 | GRCm38.p3 | 19:36584202 | ATATTAGACAAAAGT[A/G]AAGACACAAAAGACA | 226098 |
rs31240218 | snp | A/T | 0.46875 | 0.121031 | intron-variant | Hectd2 | GRCm38.p3 | 19:36601047 | TGATTAATAAATTGC[A/T]TATTCATTTGAACAT | 226098 |
rs31282759 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hectd2 | Mm_Celera | 19:36594001 | TTCCATTTTCAAGTA[C/T]TGAACAGTTTTATTC | 226098 |
rs31301780 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hectd2 | GRCm38.p3 | 19:36593080 | CAGTGCCCAATAAAT[A/G]TTGATTCCTGTTGTT | 226098 |
rs36240105 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Hectd2 | Mm_Celera | 19:36596465 | TGACTTTTATGGAAA[C/T]GTATGAAATGTATAC | 226098 |
rs36241859 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Hectd2 | Mm_Celera | 19:36588987 | GAACAAGTGAGAAAC[A/G]GTGGTCAGACTTGGG | 226098 |
rs36250511 | snp | C/G | 0.497041 | 0.0383476 | intron-variant | Hectd2 | GRCm38.p3 | 19:36607147 | TGAAGCTGTGTGGAA[C/G]AGAGGGAAGTTGCAG | 226098 |
rs36258980 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Hectd2 | Mm_Celera | 19:36595175 | GTGAAGTTAAACACT[C/T]ATCTGTAATCAATCA | 226098 |
rs36269472 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Hectd2 | Mm_Celera | 19:36598469 | AGGAGCACGGCATGA[A/G]CACTGAAACCAGGGT | 226098 |
rs36274882 | snp | A/G | 0.497041 | 0.0383476 | intron-variant | Hectd2 | Mm_Celera | 19:36582615 | AATTGCAAGTTCCCC[A/G]ATTATAAAAATACAA | 226098 |
rs36280695 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Hectd2 | Mm_Celera | 19:36578026 | CATCTTACTTCATTG[A/C]GCCTTCGTGTTTAGC | 226098 |
rs36281261 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Hectd2 | Mm_Celera | 19:36616592 | TACAGCTCCTTCTCC[A/G]TGTCGCTGACCTGGC | 226098 |
rs36294266 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Hectd2 | Mm_Celera | 19:36601627 | TAGTGTAATCAGGAA[A/G]TGTTAAAAATATCAT | 226098 |
rs36296687 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Hectd2 | Mm_Celera | 19:36580645 | CATGTTTTCACAAAT[A/G]TATTTTTGCTTTTTT | 226098 |
rs36309787 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hectd2 | Mm_Celera | 19:36587117 | AATTGTTGCTGGTCA[C/T]CAAAAGATCACCTTG | 226098 |
rs36316831 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Hectd2 | Mm_Celera | 19:36617634 | ATTGATTAAGTATAA[A/G]ATTAAATATAACTGT | 226098 |
rs36317045 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Hectd2 | Mm_Celera | 19:36599065 | TTCTCGCACTCTTCC[G/T]TTTCTCTTGAGAAGG | 226098 |
rs36325254 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Hectd2 | Mm_Celera | 19:36594843 | TCACTTCAGGAGTGG[A/G]CTATAAGCTGAAGTG | 226098 |
rs36336976 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Hectd2 | Mm_Celera | 19:36588479 | TTCACTATGCAGATA[G/T]AGGATGAGAACTGGT | 226098 |
rs36347243 | snp | A/C/G | 0.277778 | 0.248452 | intron-variant | Hectd2 | Mm_Celera | 19:36587252 | TAGTGTCGCTCTCTA[A/C/G]TCACTAAGTCTACTT | 226098 |
rs36350597 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Hectd2 | Mm_Celera | 19:36558595 | GAAAACACAAGGTGT[A/G]TGCAGAGGACAAGAG | 226098 |
rs36355545 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Hectd2 | Mm_Celera | 19:36578214 | TCTTCAAAAACGTCC[A/G]TTTGTTCTTTTGTTT | 226098 |
rs36356935 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hectd2 | Mm_Celera | 19:36568849 | GTTTTAGGAATTTTT[A/G]GAGTTGTTGAGATGG | 226098 |
rs36359206 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Hectd2 | Mm_Celera | 19:36579014 | TTCCAGAACTGTCCG[A/C]AGAGCATGTTGTAGA | 226098 |
rs36377686 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Hectd2 | Mm_Celera | 19:36612497 | TTAAGTATCATAGTA[C/G]ATAAGCTTTTAAAAG | 226098 |
rs36381255 | snp | A/T | 0.152778 | 0.230321 | intron-variant | Hectd2 | Mm_Celera | 19:36594815 | GCTTGTTGCCAGTTT[A/T]CAGATATTTCTGTCA | 226098 |
rs36383651 | snp | A/T | 0.5 | 0 | intron-variant | Hectd2 | Mm_Celera | 19:36567758 | TCAAGCCCTGTAATG[A/T]GTAAGGACTCTAGTG | 226098 |
rs36404468 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Hectd2 | Mm_Celera | 19:36611105 | TAACACCTGTTTGCT[A/T]AAGAGTGGGCTGTAG | 226098 |
rs36422582 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Hectd2 | Mm_Celera | 19:36587149 | GTATTTCTGCAAACT[A/G]TATACTGCACATTCC | 226098 |
rs36428729 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Hectd2 | Mm_Celera | 19:36608431 | TGTGGAGAATTATGA[A/G]TTATAACACTGTAAT | 226098 |
rs36432229 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Hectd2 | Mm_Celera | 19:36587203 | ACATCGCTGGTGCTC[C/T]CTGAGGTCTCAGGAG | 226098 |
rs36432948 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Hectd2 | Mm_Celera | 19:36603023 | ACGTCGCCATGTGAC[A/G]GCCACCTAGGGTCAA | 226098 |
rs36437090 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Hectd2 | Mm_Celera | 19:36588711 | TGCTTATGCCTAAAA[A/G]CTCATGTGAACATGA | 226098 |
rs36440346 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Hectd2 | Mm_Celera | 19:36585556 | TTGTTTATGGACATA[C/T]TTGAGTAGTATAATT | 226098 |
rs36447404 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Hectd2 | Mm_Celera | 19:36588465 | TGTGTATATTTGTAT[G/T]CACTATGCAGATATA | 226098 |
rs36448940 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Hectd2 | Mm_Celera | 19:36562742 | GTTATAAGAGGTACA[A/G]TAGTTAATTTGAAGT | 226098 |
rs36453027 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Hectd2 | Mm_Celera | 19:36611986 | AAGGATTAAAGACCT[C/G]CTATTTTACTTCAGA | 226098 |
rs36453051 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Hectd2 | Mm_Celera | 19:36618323 | CAACTTTCTGACAGT[C/T]GAGACTGAACTATAA | 226098 |
rs36456423 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hectd2 | Mm_Celera | 19:36573527 | AGTTTCCATTTAAGA[A/G]CACTGTGAACGGCAG | 226098 |
rs36457124 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Hectd2 | Mm_Celera | 19:36601807 | ACCATGATGAGAGCA[G/T]GAGTGTGTTAACACA | 226098 |
rs36466467 | snp | A/G | 0.132653 | 0.220748 | intron-variant, downstream-variant-500B | Hectd2 | Mm_Celera | 19:36611836 | CTAGCCTCGTACATT[A/G]CCCCAACACGGGAAG | 226098 |
rs36486051 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Hectd2 | Mm_Celera | 19:36584781 | ACTGATTTTTATTGT[C/T]TTCAGTATTAAAATT | 226098 |
rs36486368 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Hectd2 | Mm_Celera | 19:36582561 | GTTCTTAGTGTCTAC[A/G]TATGTTTCCGTGAAG | 226098 |
rs36487323 | snp | C/T | 0.142012 | 0.225474 | intron-variant, downstream-variant-500B | Hectd2 | Mm_Celera | 19:36611709 | TAATAGAGACGGTGC[C/T]GCAGACTCCTGCGGC | 226098 |
rs36507784 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Hectd2 | Mm_Celera | 19:36559249 | ACGAGCGAAAGGAAT[A/G]TGTAAACAGTGGGGA | 226098 |
rs36511440 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Hectd2 | Mm_Celera | 19:36602235 | TTCAAGAGTACAACA[A/C]AATATAAATGATGAT | 226098 |
rs36518893 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hectd2 | Mm_Celera | 19:36567350 | CTGCCGACTTTTATG[A/G]CTCTCAAGTGACTCC | 226098 |
rs36520874 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Hectd2 | Mm_Celera | 19:36584157 | ACATCTTTCCCTGAA[A/G]AATTAGCTGAACTTG | 226098 |
rs36524745 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Hectd2 | Mm_Celera | 19:36577704 | TGGAGATGAAAGTGG[C/T]CTCTTGATCATTTTT | 226098 |
rs36530291 | snp | A/G | 0.132653 | 0.220748 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | Hectd2, 1500017E21Rik | Mm_Celera | 19:36619093 | AACAGGTCTGAGTCC[A/G]GCAGTCTTTTTTATA | 226098 |
rs36532417 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Hectd2 | Mm_Celera | 19:36596568 | ATTTAAAAATTGTCA[A/G]AGTTCATGCTTGTTG | 226098 |
rs36533012 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Hectd2 | Mm_Celera | 19:36583651 | TTAAAAGAGAAGGAG[A/G]GAAGGAACTATACAT | 226098 |
rs36537395 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Hectd2 | Mm_Celera | 19:36564032 | CTAAAATTTTGTATA[A/C]AACAGAAATTGGCAC | 226098 |
rs36554759 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Hectd2 | Mm_Celera | 19:36559609 | AGTGTGGAACCTCGG[C/T]GACAGTAATGAAAGA | 226098 |
rs36557237 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hectd2 | Mm_Celera | 19:36599761 | TTACCTAACAGATGC[A/G]ATTAACGCAATAACT | 226098 |
rs36557691 | snp | G/T | 0.336735 | 0.234472 | intron-variant | Hectd2 | Mm_Celera | 19:36581774 | TAGTAAAACGTGAAA[G/T]CCATACTCTATGGCA | 226098 |
rs36570248 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Hectd2 | Mm_Celera | 19:36577222 | GTAATTTTTGTACCC[A/G]TGTCTTTAGTTATTA | 226098 |
rs36571246 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hectd2 | Mm_Celera | 19:36599771 | GATGCAATTAACGCA[A/G]TAACTGGATTTGAGG | 226098 |
rs36587416 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Hectd2 | Mm_Celera | 19:36586107 | TTAAGTAGAGATCAA[A/G]AATTCAGTTCTAATG | 226098 |
rs36591895 | snp | A/C | 0.132653 | 0.220748 | utr-variant-3-prime, nc-transcript-variant | Hectd2, 1500017E21Rik | Mm_Celera | 19:36619816 | ATTTTTGGAAAATGT[A/C]GGATATTTGACAAAA | 226098 |
rs36593926 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Hectd2 | Mm_Celera | 19:36559486 | AACTGGAGGAAGTAG[A/G]AGGAAGAAAGTGAAG | 226098 |
rs36595304 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Hectd2 | Mm_Celera | 19:36577893 | ACAAAGAGAGACCAA[C/G]TAGGGATCTAAGGTT | 226098 |
rs36597656 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Hectd2 | Mm_Celera | 19:36612089 | AGAACTGGTCTACAG[A/G]TGTAGCCACTGTGTA | 226098 |
rs36598186 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Hectd2 | Mm_Celera | 19:36588671 | TCAGCAACACTGAGA[C/T]GTCAAGCCCAAGCAC | 226098 |
rs36609964 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hectd2 | Mm_Celera | 19:36571890 | GTAAACTTATGGAGT[A/G]TGACAAAGTCAGAGT | 226098 |
rs36635913 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hectd2 | Mm_Celera | 19:36603489 | TCAGTGCTTATTTTT[A/G]GAGGAACATGAAAAC | 226098 |
rs36638198 | snp | G/T | 0.152778 | 0.230321 | intron-variant | Hectd2 | Mm_Celera | 19:36580987 | ACATGCATGTTAACA[G/T]TCTGTAGTTTTCATC | 226098 |
rs36643069 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Hectd2 | Mm_Celera | 19:36599343 | TACAAGAGATGACAC[C/G]AGTGGAGAAATGGCG | 226098 |
rs36667716 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Hectd2 | Mm_Celera | 19:36595381 | GGAACACAGAGACTA[A/G]CATTGTAACAAACAT | 226098 |
rs36670929 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Hectd2 | Mm_Celera | 19:36602740 | TTTCACAGACCGTGA[C/T]GGGAGCAGACTAAAG | 226098 |
rs36674604 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Hectd2 | Mm_Celera | 19:36580169 | TCTGCCAGGACTTCC[A/G]TGTCAGCAGCACAGA | 226098 |
rs36704469 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Hectd2 | Mm_Celera | 19:36581581 | TAATCTATAGTCTGC[A/G]TTTTCAGCATCACTA | 226098 |
rs36727257 | snp | C/T | 0.124444 | 0.216185 | intron-variant, downstream-variant-500B | Hectd2 | Mm_Celera | 19:36611801 | TTCCCATAACTGATT[C/T]GCCTTTTACCAAAAG | 226098 |
rs36727331 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Hectd2 | Mm_Celera | 19:36595303 | CTGCATGTGCAAATA[A/C]AATTATATCAGATAA | 226098 |
rs36738291 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Hectd2 | Mm_Celera | 19:36558737 | CACAGACAAGGCTTA[A/G]CCAGAATGTCGCACC | 226098 |
rs36742723 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Hectd2 | Mm_Celera | 19:36596541 | AGCTGAGCGTTCTTT[C/T]AGTTCTTTAACATTT | 226098 |
rs36746232 | snp | C/T | 0.497041 | 0.0383476 | intron-variant | Hectd2 | GRCm38.p3 | 19:36610146 | CTTCTTTTATTGTAC[C/T]AACAGAAAACACGCA | 226098 |
rs36759220 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hectd2 | Mm_Celera | 19:36572277 | ACTCTAAATGTGTTC[C/T]AACTAGCTAAATTTC | 226098 |
rs36764574 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Hectd2 | Mm_Celera | 19:36617671 | CACATGACATTCCAG[G/T]ACAGTGACAGTGTTC | 226098 |
rs36796432 | snp | C/T | 0.336735 | 0.234472 | synonymous-codon, nc-transcript-variant | Hectd2 | Mm_Celera | 19:36615552 | CTTCAGAAAAAGCTG[C/T]TACACTTTACTACAG | 226098 |
rs36817145 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Hectd2 | Mm_Celera | 19:36560426 | CCTCCACCTAAAGCA[A/G]TAATCCCAATTTGAA | 226098 |
rs36823235 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Hectd2 | Mm_Celera | 19:36579761 | ATTGTCTGATGTTCT[C/G]TATAGAGTTGCCTGT | 226098 |
rs36827151 | snp | A/G | 0.142012 | 0.225474 | synonymous-codon, nc-transcript-variant | Hectd2 | Mm_Celera | 19:36585455 | GCAGAAAGATGCCAC[A/G]GCCTCATTTAATACT | 226098 |
rs36831233 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Hectd2 | Mm_Celera | 19:36563974 | GAAATGTCTATCTTC[G/T]AAAGCAGTTTTGGAG | 226098 |
rs36831675 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Hectd2 | Mm_Celera | 19:36610460 | AAGAGATAGGCCCCT[G/T]CAGGAGAAGTAGCAA | 226098 |
rs36833916 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Hectd2 | Mm_Celera | 19:36600776 | TGTTACTGCTGCTGT[A/G]TTCATTCTTTCCATA | 226098 |
rs36850382 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Hectd2 | Mm_Celera | 19:36618642 | GTAGATCTCAATGTA[C/T]GCAGAGTTTTTTAAG | 226098 |
rs36871907 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Hectd2 | Mm_Celera | 19:36582928 | GGGCAGGAGGTATCA[A/G]GAGACTAAGTGAAGC | 226098 |
rs36884952 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Hectd2 | Mm_Celera | 19:36563520 | AGCTGTGGGAAAAGA[A/G]CATATTTTTGCCTGG | 226098 |
rs36890137 | snp | A/C | 0.277778 | 0.248452 | intron-variant | Hectd2 | Mm_Celera | 19:36597920 | TCTATGAGTGCTCAT[A/C]CTTGATGCCTTATTC | 226098 |
rs36894692 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Hectd2 | Mm_Celera | 19:36613287 | CCTGTCATATGTTCC[C/T]TCTGTTTTATCATGA | 226098 |
rs36900802 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Hectd2 | Mm_Celera | 19:36595057 | ATTTTCCAAGCACAC[C/T]GGAGACATGTTTATA | 226098 |
rs36917411 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Hectd2 | Mm_Celera | 19:36556792 | TGGAGGATAAAAACA[A/G]TTTGGAATAGAAAAC | 226098 |
rs36929188 | snp | A/T | 0.260355 | 0.249785 | intron-variant | Hectd2 | Mm_Celera | 19:36562472 | AGTTGTTTTAAGTTG[A/T]TATCCCAACATTAAG | 226098 |
rs36951469 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Hectd2 | Mm_Celera | 19:36579164 | TTCTAAGTCCTGTCT[A/G]CTTTGTTTTTGAATT | 226098 |
rs36968884 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Hectd2 | Mm_Celera | 19:36568043 | AACAGTCCAGAACCT[C/G]AGCTCTTAGCATCTG | 226098 |
rs36974553 | snp | A/C | 0.35503 | 0.226867 | intron-variant | Hectd2 | Mm_Celera | 19:36595013 | CCTCAGTAACTTACC[A/C]TTTAAGTGACACTCA | 226098 |
rs36991065 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Hectd2 | Mm_Celera | 19:36616357 | TACTCCTATTCCACT[A/G]TTCTGTGGCTTCAAA | 226098 |
rs36996511 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Hectd2 | Mm_Celera | 19:36575829 | CCTGTTTCTGATAGG[C/T]TTGCCTTCTGCTACT | 226098 |
rs37004993 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Hectd2 | Mm_Celera | 19:36579013 | CTTCCAGAACTGTCC[A/G]CAGAGCATGTTGTAG | 226098 |
rs37009045 | snp | C/G | 0.152778 | 0.230321 | intron-variant | Hectd2 | Mm_Celera | 19:36597306 | GGAATGATGTTTATA[C/G]TTTGAAATGCTTCAA | 226098 |
rs37017553 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Hectd2 | Mm_Celera | 19:36581304 | TATAGCCAGATTGGG[A/G]AAAGTGTGTGGGAAG | 226098 |
rs37040492 | snp | C/T | 0.152778 | 0.230321 | synonymous-codon, nc-transcript-variant | Hectd2 | Mm_Celera | 19:36605299 | TTTCCATCCAGATTA[C/T]GGTGAGTGTTTGTTT | 226098 |
rs37045069 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Hectd2 | Mm_Celera | 19:36610824 | TGAGCCAGTTCTACT[G/T]TTAAGTTTTGGTTCA | 226098 |
rs37054661 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Hectd2 | Mm_Celera | 19:36581813 | TTTGAAAATTCTACT[A/G]TCTTCTAACAGGAAA | 226098 |
rs37063673 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hectd2 | Mm_Celera | 19:36612804 | ATGCCTTTAGTTAGG[A/G]CATTAAAAGCTCTCT | 226098 |
rs37077684 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Hectd2 | Mm_Celera | 19:36600004 | GACCAAAAATGTATA[A/C]TGGCCCTCTGTTCAA | 226098 |
rs37083118 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Hectd2 | Mm_Celera | 19:36579828 | TTTCCCAGGTTCCCA[C/T]CACTAACTAGAGCAG | 226098 |
rs37085839 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Hectd2 | Mm_Celera | 19:36588511 | CATAATCTTGGGCTT[C/T]TTTGTAGCCAGTATA | 226098 |
rs37119885 | snp | A/C/T | 0.152778 | 0.230321 | intron-variant | Hectd2 | Mm_Celera | 19:36596598 | GTTCTCTGTGACAAA[A/C/T]GAAGCCAACTTATTT | 226098 |
rs37123801 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Hectd2 | Mm_Celera | 19:36600535 | ACTAGTACTGAGCAA[C/G]TTGTACTTATTACCA | 226098 |
rs37124004 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Hectd2 | Mm_Celera | 19:36582776 | CATTATGTAAAACAT[A/G]GGTTAACTATGTATC | 226098 |
rs37132291 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Hectd2 | Mm_Celera | 19:36600120 | TGTTTCTTTTACAGA[G/T]ATGCTCTCATTCCTG | 226098 |
rs37136202 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Hectd2 | Mm_Celera | 19:36584500 | ATAAAGTATAAAAGC[A/T]CCAGAAGGAGGACTG | 226098 |
rs37155780 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hectd2 | Mm_Celera | 19:36573671 | GTCTTCAGGTTTCCT[A/G]GACTAAATCTCTAAG | 226098 |
rs37162934 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hectd2 | Mm_Celera | 19:36570361 | TCTTAATAATATCAA[C/T]GCTATTCTTTCAAGG | 226098 |
rs37166243 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Hectd2 | Mm_Celera | 19:36599740 | ACCAATAGCTCATCT[A/G]ATTGTTTACCTAACA | 226098 |
rs37189148 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Hectd2 | Mm_Celera | 19:36560072 | AGACCAGACTCTTGA[A/G]CTGTAGGACAGTCAA | 226098 |
rs37196986 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Hectd2 | Mm_Celera | 19:36609555 | TTACTTTTTAAAAGT[C/T]CCTTCCTTGCAGAGA | 226098 |
rs37201775 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Hectd2 | Mm_Celera | 19:36581052 | ACTGTTGGCCTCTGG[C/T]GCTACCTCACTGGAC | 226098 |
rs37203720 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Hectd2 | Mm_Celera | 19:36601539 | CAAGGGTAAGCCAGC[C/T]ACGAAACATGTTTAT | 226098 |
rs37204054 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Hectd2 | Mm_Celera | 19:36560256 | CCACACAACAACCTC[A/G]TGGATAGAGTGTTAT | 226098 |
rs37207241 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Hectd2 | Mm_Celera | 19:36562416 | AGCCAACTCTCCAGC[A/C]CTGGATAAAATGTTT | 226098 |
rs37216572 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Hectd2 | Mm_Celera | 19:36588394 | GATCTGTAAATATTC[A/G]AAAGGAAATCAATCA | 226098 |
rs37227243 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Hectd2 | Mm_Celera | 19:36596548 | CGTTCTTTCAGTTCT[C/T]TAACATTTAAAAATT | 226098 |
rs37229332 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Hectd2 | Mm_Celera | 19:36588949 | AGAAAGTAACATCTG[C/T]GTATCTGTGTACTAT | 226098 |
rs37234097 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hectd2 | Mm_Celera | 19:36557638 | GGGAAGCACTATGAC[A/G]GCCTAAATGCAAGCT | 226098 |
rs37238154 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Hectd2 | Mm_Celera | 19:36599891 | CCTATCAAGAGGTTT[A/C]ACTTTTGCTACATTT | 226098 |
rs37263821 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Hectd2 | Mm_Celera | 19:36595086 | TATCTCAGTAAAAGT[A/G]ATGCATGTAGCCCCA | 226098 |
rs37282331 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Hectd2 | Mm_Celera | 19:36589092 | AATTAGCAGTTGGAT[A/G]TGAGTTGGCTTATAG | 226098 |
rs37293525 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Hectd2 | Mm_Celera | 19:36559021 | TTTATACATGGTTCA[A/G]AAAAGATGGTTGGTA | 226098 |
rs37295290 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Hectd2 | Mm_Celera | 19:36586116 | GATCAAGAATTCAGT[C/T]CTAATGTGATTAGTT | 226098 |
rs37296072 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Hectd2 | Mm_Celera | 19:36584197 | ATAACATATTAGACA[A/G]AAGTGAAGACACAAA | 226098 |
rs37305046 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Hectd2 | Mm_Celera | 19:36609186 | GCTGGTGTTAGATCT[A/G]AAAGGAGACTGGTGC | 226098 |
rs37320167 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Hectd2 | Mm_Celera | 19:36580362 | ATTTTCAACCAGAGT[A/C]AGCCCATAAATAGTG | 226098 |
rs37322619 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hectd2 | Mm_Celera | 19:36586864 | GGAATTAAATGCATC[C/T]CTAATGGCCAGATAC | 226098 |
rs37324915 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Hectd2 | Mm_Celera | 19:36611348 | TAAAAGACAGATCAC[A/G]GATTTATTTTTACAG | 226098 |
rs37325897 | snp | A/G | 0.336735 | 0.234472 | intron-variant, upstream-variant-2KB | Hectd2, LOC105246565 | Mm_Celera | 19:36555772 | CCTCCTAAATGACTA[A/G]GAACTTACTAAAATA | 226098 |
rs37326501 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Hectd2 | Mm_Celera | 19:36607826 | CTTCCTGGTATCACT[A/G]ATGAAGTTAGCTATT | 226098 |
rs37330395 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hectd2 | Mm_Celera | 19:36558394 | AAACTGTGTGTGTGT[A/G]CATGCGTGAGTGTGC | 226098 |
rs37336484 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Hectd2 | Mm_Celera | 19:36577470 | ATTTGCACTAGGGAA[A/C]AAAATAATTGAAATC | 226098 |
rs37339739 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Hectd2 | Mm_Celera | 19:36612432 | CCTAATGGTGAGTTT[A/G]AATTTTTAAGCTTTC | 226098 |
rs37370869 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Hectd2 | Mm_Celera | 19:36559211 | TTAAGCTGGCTGGCC[A/G]TTGAAGGAATGATAG | 226098 |
rs37376503 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hectd2 | Mm_Celera | 19:36577755 | TTCTTCCCGTATTTT[C/T]GATGCTCTTATCACT | 226098 |
rs37401405 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Hectd2 | Mm_Celera | 19:36579907 | CAAAGGAAGGTAAGT[A/G]CTTGTGGTCAAGCAG | 226098 |
rs37417857 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Hectd2 | Mm_Celera | 19:36613869 | CGCAGTGCACAGAGC[A/G]CAGCAGAGGTGGCAG | 226098 |
rs37425284 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Hectd2 | Mm_Celera | 19:36586018 | ACCTGCTTTACTTAG[G/T]TGACCTGAGTGATTC | 226098 |
rs37443069 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Hectd2 | Mm_Celera | 19:36577939 | TTTAGTTTCTATGGC[C/T]TCACTATTTAAATAG | 226098 |
rs37453305 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Hectd2 | Mm_Celera | 19:36608723 | GAAATTTGATCTGAA[C/T]GTCCTCTTTTGGCAA | 226098 |
rs37491165 | snp | C/T | 0.124444 | 0.216185 | intron-variant, nc-transcript-variant, downstream-variant-500B | Hectd2, 1500017E21Rik | Mm_Celera | 19:36621285 | TATATAGTCAGTTGC[C/T]TTAGCATATTCTTGG | 226098 |
rs37497348 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hectd2 | Mm_Celera | 19:36572415 | TCTACTTGAACAGTT[C/T]AGCAGACTTCTTTAC | 226098 |
rs37513896 | snp | A/G | 0.18 | 0.24 | intron-variant | Hectd2 | Mm_Celera | 19:36579120 | AGAGTAATTACTCTG[A/G]TGAGAGATTTTTTTT | 226098 |
rs37527250 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Hectd2 | Mm_Celera | 19:36575717 | ATAAGTAATAGCTAA[A/G]ATGGAATTTGTCAGT | 226098 |
rs37531769 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Hectd2 | GRCm38.p3 | 19:36610253 | TCAGTGGGTACCATC[G/T]ACCATCATAGGGCAA | 226098 |
rs37532327 | snp | C/T | 0.260355 | 0.249785 | synonymous-codon, nc-transcript-variant | Hectd2 | Mm_Celera | 19:36597142 | ACGACAGATAGCTAC[C/T]TTAGTGGAAGCTGAC | 226098 |
rs37535649 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hectd2 | Mm_Celera | 19:36571679 | AGAAGGCATGTTAAC[C/T]TTCTTGAGTTCTTGG | 226098 |
rs37560370 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Hectd2 | Mm_Celera | 19:36560334 | AAAGGGTAAAATGAT[A/C]CTGAGCTGCAAAGGT | 226098 |
rs37571849 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Hectd2 | Mm_Celera | 19:36559421 | GGGAAGCCTTTGGAA[C/T]TCCTCGAATAGAGGA | 226098 |
rs37601214 | snp | C/T | 0.375 | 0.216506 | utr-variant-3-prime, nc-transcript-variant | Hectd2, 1500017E21Rik | Mm_Celera | 19:36621049 | TTTCTGTATAAGTTT[C/T]TAGAAGTCCTTCTTT | 226098 |
rs37622264 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Hectd2 | Mm_Celera | 19:36589107 | GTGAGTTGGCTTATA[G/T]ACATTCTTCCCCTTT | 226098 |
rs37622899 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Hectd2 | Mm_Celera | 19:36616299 | AGACCATGATGTTAA[A/G]CAGTTTTCGAGTAGT | 226098 |
rs37643219 | snp | A/C | 0.32 | 0.24 | intron-variant | Hectd2 | Mm_Celera | 19:36616475 | CCTTTCATTTCCAAA[A/C]TTGAGTTGGTTCTGT | 226098 |
rs37651764 | snp | C/T | 0.336735 | 0.234472 | synonymous-codon, nc-transcript-variant | Hectd2 | Mm_Celera | 19:36614434 | GAGCACACAGTACGA[C/T]GGCTATGCGAAGACA | 226098 |
rs37657042 | snp | A/G | 0.132653 | 0.220748 | intron-variant, downstream-variant-500B | Hectd2 | GRCm38.p3 | 19:36611453 | GGTACTGATGAAAGC[A/G]TACCACTGTGAATGA | 226098 |
rs37675572 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Hectd2 | Mm_Celera | 19:36601028 | ACACATCAGAAATAG[C/T]CCTTGATTAATAAAT | 226098 |
rs37684009 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Hectd2 | Mm_Celera | 19:36575633 | AACCCTCATAGGGCT[C/T]TGTTTAATGGTCACA | 226098 |
rs37697859 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Hectd2 | Mm_Celera | 19:36613938 | GAAGAATGAGTTTGC[G/T]TCATGCTGAGTTGTT | 226098 |
rs37712263 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Hectd2 | Mm_Celera | 19:36556206 | TTGGTTGTCACCCCA[C/T]GCTTTGGCAGTTTTT | 226098 |
rs37722813 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hectd2 | Mm_Celera | 19:36565896 | GGTATAGACTTGATA[C/T]TCATTAGAGTGGAAT | 226098 |
rs37733974 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Hectd2 | Mm_Celera | 19:36585925 | TTTCAGAAAATTAGG[C/T]CATCCTTTTTCTAAT | 226098 |
rs37735105 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Hectd2 | GRCm38.p3 | 19:36602799 | CTGCTTCCCAGCTGC[C/T]GTGACACTTGAATTC | 226098 |
rs37739347 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Hectd2 | Mm_Celera | 19:36579973 | GCAGCCTTAGGAATG[A/G]CTGACCATTTCAATA | 226098 |
rs37749486 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hectd2 | Mm_Celera | 19:36572735 | GGTGTTAGAGAAGCT[A/G]TGGCAGCCTAGTGTG | 226098 |
rs37766061 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Hectd2 | Mm_Celera | 19:36583058 | AAGGGTAAACAAAGA[A/G]GTCCAGCAAAGGGAA | 226098 |
rs37825869 | snp | C/G | 0.260355 | 0.249785 | missense, nc-transcript-variant | Hectd2 | Mm_Celera | 19:36585486 | ATTGAGGACTCTGGG[C/G]TTAATGCCAATTTGG | 226098 |
rs37848194 | snp | A/C | 0.5 | 0 | intron-variant | Hectd2 | Mm_Celera | 19:36565219 | TTCTGGATTTTCCTA[A/C]TTTCATCACTTATTC | 226098 |
rs37873299 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Hectd2 | Mm_Celera | 19:36613684 | GTTGAGCTGTATCTA[A/C]GTTTTATGACTCTGG | 226098 |
rs37922002 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hectd2 | Mm_Celera | 19:36563943 | CTTTATCAGGTATTG[C/T]GTTAGAGTGTAAACA | 226098 |
rs37964729 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Hectd2 | Mm_Celera | 19:36618077 | AGTATAAACTCTGAT[C/T]GTACAGAATTCTTTT | 226098 |
rs37968905 | snp | C/T | 0.132653 | 0.220748 | intron-variant, downstream-variant-500B | Hectd2 | Mm_Celera | 19:36611454 | GTACTGATGAAAGCA[C/T]ACCACTGTGAATGAG | 226098 |
rs37983991 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Hectd2 | Mm_Celera | 19:36602535 | CTTGACATTTTGACT[A/T]AGTTGCATTTCTGTG | 226098 |
rs38041979 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Hectd2 | Mm_Celera | 19:36594960 | AGACTTTTAACCATT[C/T]CCATAGTCTGCCTGT | 226098 |
rs38064548 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Hectd2 | Mm_Celera | 19:36563407 | TTTTACTTTGTGCTG[A/G]TGCTATTTAGCTTAA | 226098 |
rs38092388 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Hectd2 | Mm_Celera | 19:36595544 | TCCTCACATAGTAGG[C/T]TTATGTTTTTACTAA | 226098 |
rs38096846 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Hectd2 | Mm_Celera | 19:36617787 | TTGAATGTGAGTGGC[A/G]ATGCTTTCTTACATC | 226098 |
rs38105215 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Hectd2 | Mm_Celera | 19:36582793 | GTTAACTATGTATCA[A/G]TGTTTAAAATCATGA | 226098 |
rs38121049 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Hectd2 | Mm_Celera | 19:36600315 | CTGGAACTCAGGGGA[A/C]GTCACCACTGACTGT | 226098 |
rs38181794 | snp | G/T | 0.21875 | 0.248039 | intron-variant | Hectd2 | Mm_Celera | 19:36598422 | TTAAAATAATGTGTT[G/T]ATTATTAGAATACAT | 226098 |
rs38201373 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Hectd2 | Mm_Celera | 19:36589041 | TGATAATGTTAAAAT[C/T]AAGATATTTCAGGAT | 226098 |
rs38206425 | snp | A/T | 0.260355 | 0.249785 | intron-variant | Hectd2 | Mm_Celera | 19:36583084 | GGGAAGCAATGAGAT[A/T]CCTGAGAATTCTCAG | 226098 |
rs38257619 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Hectd2 | Mm_Celera | 19:36563544 | TGCCTGGTTTCAAGA[C/T]CTGAAATAATTCTTC | 226098 |
rs38325246 | snp | C/G | 0.375 | 0.216506 | intron-variant | Hectd2 | Mm_Celera | 19:36570021 | CATTGCACCCTCACA[C/G]TAGTCAAAATCTCAT | 226098 |
rs38342361 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hectd2 | Mm_Celera | 19:36612952 | AACCTGGAGTCTAGA[A/G]TTCATCTCCAAAAGC | 226098 |
rs38348837 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Hectd2 | Mm_Celera | 19:36602199 | AAAAACAGAGTAGAC[A/G]GAAATTATTCCCATG | 226098 |
rs38359744 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Hectd2 | Mm_Celera | 19:36616438 | GCTCACACACTGAAC[A/G]TTTCTCACATCCTGT | 226098 |
rs38368496 | snp | A/G | 0.32 | 0.24 | intron-variant | Hectd2 | Mm_Celera | 19:36611188 | TTTTTCCAAGCCAAG[A/G]ATGGTAGAAATCATT | 226098 |
rs38372968 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Hectd2 | Mm_Celera | 19:36587162 | CTGTATACTGCACAT[C/T]CCAGAGAGCATCCTC | 226098 |
rs38380642 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Hectd2 | Mm_Celera | 19:36568890 | AGTGGATAGCTTCTT[A/T]AGCATGTTCTATGGT | 226098 |
rs38395153 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Hectd2 | Mm_Celera | 19:36563134 | TGAAGTGAATGAATA[C/T]ATCTCAGAGAGCCTT | 226098 |
rs38422094 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Hectd2 | Mm_Celera | 19:36585874 | TGTAATATAATTACA[C/T]GAAACAATCAGATAT | 226098 |
rs38432689 | snp | A/T | 0.497041 | 0.0383476 | intron-variant | Hectd2 | GRCm38.p3 | 19:36605077 | TTATGGAAGTAAAAA[A/T]AAAGTCTGTCTAATA | 226098 |
rs38464579 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Hectd2 | Mm_Celera | 19:36581335 | TGATAGAAAAGGGTA[A/G]TTCTAGTGAAGAACA | 226098 |
rs38476863 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hectd2 | Mm_Celera | 19:36612253 | TAGATGCCATTGTAA[A/G]CTGCAGTGAGTTAGT | 226098 |
rs38482227 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hectd2 | Mm_Celera | 19:36617711 | CAAGGACAGTATTCC[A/G]TCTGAACTAAGAACT | 226098 |
rs38528868 | snp | A/T | 0.132653 | 0.220748 | utr-variant-3-prime, nc-transcript-variant | Hectd2, 1500017E21Rik | Mm_Celera | 19:36620897 | TCAGCTAGAAAATTC[A/T]TGTAGCTTTTTAAAT | 226098 |
rs38540000 | snp | A/T | 0.408163 | 0.193609 | utr-variant-3-prime, nc-transcript-variant | Hectd2, 1500017E21Rik | Mm_Celera | 19:36620887 | TTTATTTTAATCAGC[A/T]AGAAAATTCATGTAG | 226098 |
rs38561743 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hectd2 | Mm_Celera | 19:36571747 | GTGTAAGATCCACTT[A/G]TAAGAGATTTGTGTA | 226098 |
rs38563984 | snp | A/G | 0.260355 | 0.249785 | synonymous-codon, nc-transcript-variant | Hectd2 | Mm_Celera | 19:36583997 | CATGTCTGTGGAAGC[A/G]TTACCATCTGAAGTG | 226098 |
rs38604273 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Hectd2 | Mm_Celera | 19:36616002 | GGTCAATGTGACCCT[A/G]TAACAGAGAAGGCTG | 226098 |
rs38688195 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Hectd2 | Mm_Celera | 19:36605344 | TCTAGACTTGTAGGC[C/G]CTCAGTAGTAGCCCT | 226098 |
rs38698595 | snp | G/T | 0.396694 | 0.202437 | intron-variant | Hectd2 | Mm_Celera | 19:36596954 | TTGCTTAAATAACAA[G/T]TTGTTTTTAAAGAAC | 226098 |
rs38790649 | snp | G/T | 0.260355 | 0.249785 | intron-variant | Hectd2 | Mm_Celera | 19:36598391 | AGAAGTTTAAGTTAA[G/T]GCTAGCCAGTAGATA | 226098 |
rs38829491 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Hectd2 | Mm_Celera | 19:36600188 | TGACCATTTCATTGT[C/T]AACTTTTAACGAGCT | 226098 |
rs39030169 | snp | C/G/T | 0.152778 | 0.230321 | intron-variant | Hectd2 | Mm_Celera | 19:36595447 | GTGAGTTCTTACCTC[C/G/T]CTTCCAGTGTTTGGA | 226098 |
rs39037859 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Hectd2 | Mm_Celera | 19:36599725 | ACTCTCACAGGTATG[A/G]CCAATAGCTCATCTA | 226098 |
rs39128660 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Hectd2 | Mm_Celera | 19:36575693 | AAACGTCTTCTGTAC[C/T]TAAGTTTTATAAGTA | 226098 |
rs39149070 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Hectd2 | Mm_Celera | 19:36577013 | TTGTTTTGTCTTTGG[A/G]GGAATATCCTTAAAT | 226098 |
rs39294001 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Hectd2 | Mm_Celera | 19:36599341 | CCTACAAGAGATGAC[A/G]CCAGTGGAGAAATGG | 226098 |
rs39330278 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Hectd2 | Mm_Celera | 19:36616400 | GAAGGCACAGCTTTC[A/T]TTATGATCACCCTTG | 226098 |
rs39404768 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Hectd2 | Mm_Celera | 19:36562533 | TTTAGGATGAGTAGA[G/T]TTGTGCTGGGGGGCA | 226098 |
rs39480435 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Hectd2 | Mm_Celera | 19:36595119 | TTCACTCTGGCTTCT[C/T]AGTTCTTACAAACAC | 226098 |
rs39616619 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Hectd2 | Mm_Celera | 19:36583431 | AGAATAAGAAAGTAA[G/T]ATCTTAAATACATGC | 226098 |
rs39631717 | snp | A/T | 0.132653 | 0.220748 | intron-variant, nc-transcript-variant, downstream-variant-500B | Hectd2, 1500017E21Rik | Mm_Celera | 19:36621347 | CATAGATAAGATGCC[A/T]CGCTGAATGCATACA | 226098 |
rs39693645 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Hectd2 | Mm_Celera | 19:36575050 | ATCTGTGTTTTATGT[A/T]GTCTGTAATTGTTAA | 226098 |
rs39988263 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Hectd2 | Mm_Celera | 19:36582656 | GGAAAGTTAGGTAAA[A/T]TTTGCTAATGGAGTT | 226098 |
rs45673289 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36577557 | CTTCTGTTTAGGGAC[A/G]TCTGATTAATTAACA | 226098 |
rs45773606 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36577833 | AAGAATGTAAATTTC[C/T]GGATTTCCACTGGAG | 226098 |
rs46057708 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36614236 | GACCAGGCTGGCCTC[A/G]AACTCAGAAATCCGC | 226098 |
rs46122785 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36577465 | CTATCATTTGCACTA[A/G]GGAACAAAATAATTG | 226098 |
rs46153536 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36577449 | ATATTTAGTTTTCTA[C/T]CTATCATTTGCACTA | 226098 |
rs46177781 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36614216 | GTCCTGGAACTCACT[C/T]TGTAGACCAGGCTGG | 226098 |
rs46271533 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36597268 | TAAACCTTTATAATA[C/T]TTAAATGTTTTTAAG | 226098 |
rs46519859 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36596989 | CATACTCAAATGTAG[C/T]TTCCTGAATTTGCCA | 226098 |
rs46617019 | snp | C/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36613585 | CAACATGAGAAACTG[C/T]ATTAAAGAGTCGTGG | 226098 |
rs46716888 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36582530 | TCTGAAGCTCATTTA[C/T]TACTCACTGAACATT | 226098 |
rs46890831 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36577810 | AAGTGCCAATTGTAT[C/T]CTCTCCAAAGAATGT | 226098 |
rs46980220 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36597249 | TTTTTATGATAAATT[A/G]TTGTAAACCTTTATA | 226098 |
rs47803367 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36577583 | TAACATCATTATTTC[C/T]TTTAATAATGATGCT | 226098 |
rs48202431 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36614249 | TCGAACTCAGAAATC[C/T]GCCTGCCTCTGCCTC | 226098 |
rs48245027 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36582855 | GTAGCCACTTAAACC[C/T]CTAAAAATAAACAGA | 226098 |
rs48594461 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36596971 | TGTTTTTAAAGAACT[A/G]CACATACTCAAATGT | 226098 |
rs49287899 | snp | C/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36590160 | AACTTATTGTCTAGG[C/T]AGCAGTTTGGGGTTT | 226098 |
rs49478539 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36614232 | TGTAGACCAGGCTGG[A/T]CTCGAACTCAGAAAT | 226098 |
rs49556648 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36577448 | TATATTTAGTTTTCT[A/G]TCTATCATTTGCACT | 226098 |
rs49723778 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36577654 | GGTGGGAGGCCTTAT[A/G]AAGTGAAGCTGAATT | 226098 |
rs49814951 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36614522 | GCTTGCTTGTTCATA[G/T]GACTTAGAATTCTTT | 226098 |
rs49887334 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36597004 | TTTCCTGAATTTGCC[A/G]CTTAGAATTCATGCT | 226098 |
rs49923615 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36597331 | CTTCAAAAGCCAGTT[A/T]TAAAATGCATACATT | 226098 |
rs50042160 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36596918 | CTGTCCTGACTCCAT[C/T]GCCTGTGACAGAAAC | 226098 |
rs50190475 | snp | C/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36597338 | AGCCAGTTATAAAAT[C/G]CATACATTAGTAATA | 226098 |
rs50252401 | snp | C/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36590510 | AGAGTGTATCTTGGT[C/T]ACCATTTACTCAGTG | 226098 |
rs50510827 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36577647 | GGTGTGGGGTGGGAG[A/G]CCTTATGAAGTGAAG | 226098 |
rs50547500 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36597247 | TATTTTTATGATAAA[C/T]TGTTGTAAACCTTTA | 226098 |
rs50778859 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36615131 | TAAATATACTGCAGC[C/T]CCACTCTGTCTTCAT | 226098 |
rs50884467 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36615025 | ATGGGATGGATCCCC[A/G]GGTGGGGCAGTCTCT | 226098 |
rs50892200 | snp | C/T | | | synonymous-codon, nc-transcript-variant | Hectd2 | Mm_Celera | 19:36614422 | TGCACTGCAGAGGAG[C/T]ACACAGTACGACGGC | 226098 |
rs50912446 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36615397 | TGTTATAAAATGTTA[C/T]TTTATTCTACTATCA | 226098 |
rs51260422 | snp | A/G | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36596314 | TGGACTACCCAGGAA[A/G]GTCAAAGTCAGACGC | 226098 |
rs51267627 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36596969 | GTTGTTTTTAAAGAA[C/T]TACACATACTCAAAT | 226098 |
rs51322156 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36582506 | TTAATCTGTTGATGG[C/T]GTGAGTACTCTGAAG | 226098 |
rs51874804 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36567234 | TCCACCTCCTCAATG[C/T]TAGGATTAAAAGCAT | 226098 |
rs52031662 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36594398 | GATATTCAAGATATC[A/T]GATATGTAACCCCTG | 226098 |
rs52163406 | snp | A/G | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36595900 | ATGTGTTAAAAAAAA[A/G]GAAAAAAAAGAAAAT | 226098 |
rs52219261 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36614210 | CTGGCTGTCCTGGGA[C/T]TCACTTTGTAGACCA | 226098 |
rs52297487 | snp | A/C/G | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36595901 | TGTGTTAAAAAAAAA[A/C/G]AAAAAAAAGAAAATA | 226098 |
rs52318451 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36582836 | ATAAAGTAAACTGAT[A/T]AAAGTAGCCACTTAA | 226098 |
rs52427227 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36572058 | GGGTTTCTCTGTGTA[A/G]CCCTGGCTGTCCTGG | 226098 |
rs211694788 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36599949 | GCTTTAATTAATAGC[A/G]TCTCTTCTACTTAAA | 226098 |
rs211696955 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36607792 | TACTATGTCACAGCT[C/T]AGCGTTGTGATATTT | 226098 |
rs211730851 | snp | C/T | | | upstream-variant-2KB, intron-variant | Hectd2, LOC105246565 | Mm_Celera | 19:36553783 | GGAAATTGTCTAAGT[C/T]GTCGTCGGGTGGTGG | 226098 |
rs211745123 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36562364 | AGGAATCGGACCTGG[A/G]TCTTCAACAAGAACA | 226098 |
rs211764618 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36561512 | ATATTAGCCCAAAAG[C/T]TCGGAGTACCCAAGA | 226098 |
rs211765473 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36569582 | TTATAAAAGAGCAAT[A/G]AACTATGTAAATATT | 226098 |
rs211820165 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36593310 | GATAGATCAATATTG[C/T]TTAAAATGTTTTTAA | 226098 |
rs211893314 | in-del | -/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36575506 | CTGAAGTAGTCAAAA[-/C]CAGCACAAGAGCTGC | 226098 |
rs211913669 | in-del | -/A | | | intron-variant | Hectd2 | Mm_Celera | 19:36576654 | TGAAGAAAGAAATTG[-/A]AAAAAAACTCTCAGA | 226098 |
rs211937901 | in-del | -/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36603850 | CTATAAACACATTAA[-/T]TTTTTTACTTTCTAT | 226098 |
rs211974622 | snp | C/T | | | synonymous-codon, nc-transcript-variant | Hectd2 | Mm_Celera | 19:36587414 | ATCATTAACAGCTTG[C/T]TACAAGAATGGAAAG | 226098 |
rs211984736 | snp | C/T | | | intron-variant, upstream-variant-2KB | Hectd2, LOC105246565 | GRCm38.p3 | 19:36554945 | GGCCGGGGGGCGCCC[C/T]GGGCGGTGGGTTGAA | 226098 |
rs212037783 | in-del | -/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36597520 | GTGTCTTTTTATTTA[-/T]TTTTTATGTCTCTCT | 226098 |
rs212046469 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36588016 | CCCATCCCTCAACGG[A/G]GGACCATGCCTCTGG | 226098 |
rs212088754 | in-del | -/GTC | | | upstream-variant-2KB, intron-variant | Hectd2, LOC105246565 | Mm_Celera | 19:36553781 | AAGGAAATTGTCTAA[-/GTC]GTCGTCGGGTGGTGG | 226098 |
rs212108186 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36617073 | AGCCAGGTATAGCTG[C/T]ATTAGCCTGTGACCC | 226098 |
rs212149009 | snp | C/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36570567 | TTGTTCCAGTCTAAA[C/G]ATTTATTTATTCTTA | 226098 |
rs212163118 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36563412 | CTTTGTGCTGATGCT[A/G]TTTAGCTTAAGAAGA | 226098 |
rs212183151 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36576554 | GGAAACCACATCCTT[C/T]ACAATAGTCACAAAT | 226098 |
rs212214468 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36570957 | TCAAGCATTAGCTGC[C/T]TTTTCCCTCATTGAG | 226098 |
rs212221645 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36609454 | CCACCTTGTGGTTGT[A/G]TTGTGCTAACTGCCA | 226098 |
rs212276106 | in-del | -/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36578357 | ACGAAGTTGTGATTG[-/C]CAGATGTGGTTGTTG | 226098 |
rs212383231 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36564177 | TATTCAAAGAAAATA[A/C]GCTTGAAAATATATG | 226098 |
rs212410106 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36602669 | TGTGCTGCCACTCAT[A/G]CGTAATGTGTCAGAT | 226098 |
rs212438748 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36595492 | CCCTTTCCACTCAGA[C/T]CCTTCCTTTGAGCTA | 226098 |
rs212447124 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36557983 | CTCATCCCAAATCTG[C/T]TTAGCAATAGCTGTC | 226098 |
rs212452846 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36609933 | TACACAGACACAAAT[A/G]AACATAACTTAAAAT | 226098 |
rs212530055 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36602303 | GCAGTTCAGTTCCTG[A/G]GTATATTTTTTTCCT | 226098 |
rs212549480 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36579479 | ACAGGCAGTCATGGC[A/T]CTAGAGAAGTAGCTA | 226098 |
rs212561061 | snp | C/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36573560 | AGAAATAGGTGCTCA[C/G]AGGAAACCTGGGGCA | 226098 |
rs212573774 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36557182 | TCAGGAACTTTGGGG[A/G]CCCTTTTAGTGATTC | 226098 |
rs212588202 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36578428 | CTTAACTGCTGAGCC[A/G]TCCCTTCAGCCCCTT | 226098 |
rs212589025 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36612796 | CTTCTGCTATGCCTT[A/T]AGTTAGGGCATTAAA | 226098 |
rs212621998 | in-del | -/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36617340 | AAACATAAATGAATA[-/T]TTTTTATGTAATTAA | 226098 |
rs212628111 | snp | C/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36573988 | CCCCCAGAGCAGGCA[C/G]TGTCTTACCAGAGCC | 226098 |
rs212641345 | in-del | -/A | | | intron-variant | Hectd2 | Mm_Celera | 19:36590289 | GACTTTGTTAGGATC[-/A]ACCTTCCTATCTTAC | 226098 |
rs212653375 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36605354 | TAGGCCCTCAGTAGT[A/C]GCCCTGACATTTTTA | 226098 |
rs212687887 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36560160 | TTTCAAAAAAGCATA[G/T]GTAAATAATATAACT | 226098 |
rs212728434 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36567567 | ACCAGAAGAGGGCAT[C/T]GGACCCCATTACAGA | 226098 |
rs212801427 | in-del | -/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36567785 | GTGCAGCATAATGGA[-/C]CAATATAAGGACAGT | 226098 |
rs212840516 | snp | C/G | | | synonymous-codon, nc-transcript-variant | Hectd2 | Mm_Celera | 19:36598947 | ATTTGTTTCTTTACG[C/G]CTGTTTCCAGCAAAA | 226098 |
rs212841613 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36591593 | CCATTCAAAGGAGTA[A/G]GATGGAATCTCAAAG | 226098 |
rs212884172 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36598347 | GAAGACTATAGAGAC[A/G]TTTCATTGGAACTGT | 226098 |
rs212888124 | snp | C/T | | | upstream-variant-2KB | Hectd2 | Mm_Celera | 19:36551979 | CACATCTGAGCTCCA[C/T]CCTCAGGGACTCAGA | 226098 |
rs212934986 | in-del | -/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36570435 | CTTTCTCTCTCTCTC[-/T]TTTTTTTAAGATTTA | 226098 |
rs212936787 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36566948 | AAGAAAATTGCATCA[A/G]TGTACTTGTGGAGGT | 226098 |
rs212950592 | snp | C/T | | | upstream-variant-2KB, downstream-variant-500B | Hectd2, LOC105246565 | Mm_Celera | 19:36552541 | ACACAAAAAGTTTTT[C/T]GTGACAGTTGCCTTA | 226098 |
rs212969451 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36580168 | GTCTGCCAGGACTTC[C/T]GTGTCAGCAGCACAG | 226098 |
rs213004417 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36592100 | TTTGCATTATTCTAC[A/G]TTCAACTTTTCAGTT | 226098 |
rs213009883 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36585948 | TTTCTAATTATCTGA[G/T]AATTAAACAGAAAAT | 226098 |
rs213014497 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36612442 | AGTTTGAATTTTTAA[G/T]CTTTCAATTAGGTTT | 226098 |
rs213101419 | in-del | -/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36596627 | TTCCCAGTGCAGGAG[-/T]TTTTACAATTTACAT | 226098 |
rs213157702 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36575115 | AATCTTCTGTGCTGG[C/T]TTGTTTGCCCTAGTA | 226098 |
rs213193109 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36574658 | ATATATATATTCTCA[A/T]ACATACATATCTTTC | 226098 |
rs213203033 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36607389 | GATTGGGTTCGAATG[A/G]AAGCTGAGCTGTTAC | 226098 |
rs213214084 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36568876 | ATGGAAAATATGTTA[A/G]TGGATAGCTTCTTAA | 226098 |
rs213247956 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36615893 | AGTGAGATTAAAGGC[A/G]TTGTACCACCACTGC | 226098 |
rs213259955 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36605996 | TAATAGTGTCAGGCC[A/T]TGGGACCTCCCCTGG | 226098 |
rs213285859 | snp | A/G | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36560847 | AGCAATTGGAGAAAA[A/G]CATGCTTATAAATTG | 226098 |
rs213343442 | snp | C/G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36557031 | GGCATCTGGGATGAC[C/G/T]GGATTCTCCAGTAGA | 226098 |
rs213387389 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36594823 | CCAGTTTACAGATAT[C/T]TCTGTCACTTCAGGA | 226098 |
rs213448325 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36589175 | GAATACAGTTTCCCC[A/T]CCCTCAGCTCCTCCC | 226098 |
rs213471984 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36591469 | AGGAACTGCAGTATT[G/T]GTTTCCATAGTCGCT | 226098 |
rs213506427 | in-del | -/GA | | | intron-variant | Hectd2 | Mm_Celera | 19:36587857 | GGCAGAGCCTCTCAG[-/GA]GACAGATGTCAGCTC | 226098 |
rs213531365 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36577611 | GCTAGATTCTCCAAG[A/C]AAGCTGTCATCTTCT | 226098 |
rs213555049 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36577015 | GTTTTGTCTTTGGGG[A/G]AATATCCTTAAATTC | 226098 |
rs213576043 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36571774 | TGTAATTGGGTTTTG[C/T]CTACCTGGATTGTCA | 226098 |
rs213622923 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36580570 | AAGGAAGGAAAATTA[C/T]TACTGCTTATCAATT | 226098 |
rs213681323 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36602856 | TATGCTATAGTCTGA[A/C]ATCGCAAAATTAAGT | 226098 |
rs213697197 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36558130 | ACTAAGGCTGGCAGA[C/T]TGAAATGGAGACAAA | 226098 |
rs213721119 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | Hectd2, 1500017E21Rik | Mm_Celera | 19:36619226 | GTGTGCTGGCAGCAC[A/G]CTGTAGCAAAGCAGA | 226098 |
rs213800014 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36596797 | AATGACCCCTGAGAT[C/T]GATATTATTTGTATG | 226098 |
rs213803295 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36611316 | TCCTTACAGTCTGAA[A/G]TAATGCTAGTTGATT | 226098 |
rs213832445 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36566180 | ATGTTCAGCTCTTTC[C/T]CTTGAACAGCTCACT | 226098 |
rs213835542 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36603702 | ACTAGATATACTTAG[A/G]ATAGTTTAAGCTTTG | 226098 |
rs213935393 | snp | C/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36588655 | GACAACAAACACCTC[C/G]TCAGCAACACTGAGA | 226098 |
rs213952163 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36597593 | AAAATACCAGAGTAT[G/T]AAAGCACATTACTTC | 226098 |
rs214043644 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36606619 | AATTCATATAGATGC[A/G]ATATCAAGCCTCCAT | 226098 |
rs214064350 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36561024 | CTGTAGTGAGAAATT[A/G]TAAGTCAGCCCTTGC | 226098 |
rs214074428 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36558506 | TTCCATCCCTAGTTT[A/G]GAATTCAAAGGGAAG | 226098 |
rs214165079 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36610795 | CATGAAGCTTGATTT[A/T]AAAAATGAAATATTG | 226098 |
rs214200398 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36607310 | CATAACATAAGTGTG[A/G]TGAGGTGGAGGAGAT | 226098 |
rs214220437 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36561404 | TTTTCACCTACTTAT[C/T]TCTAGCATTACAGTC | 226098 |
rs214222863 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36584516 | CCAGAAGGAGGACTG[G/T]GGAGGAAGAGGACAG | 226098 |
rs214245465 | snp | C/G/T | | | upstream-variant-2KB, intron-variant | Hectd2, LOC105246565 | GRCm38.p3 | 19:36554618 | GCGCACACGCGCGGG[C/G/T]GCGCGACGGGCCGCG | 226098 |
rs214281738 | snp | A/G | | | upstream-variant-2KB, nc-transcript-variant | Hectd2, LOC105246565 | Mm_Celera | 19:36553671 | TATTTTTAGTAAGTG[A/G]TACAGTGAATACTTC | 226098 |
rs214306669 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36565365 | GCCTTTGCTCCTTGT[C/T]TAGTTACTCACAAAC | 226098 |
rs214324296 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36600681 | ATACAGCTTAGATTG[A/G]TGGATTTGTTGCAAT | 226098 |
rs214370328 | in-del | -/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36590369 | TTCCCTTCCTCAGCC[-/T]CATCTCCCCTCCCAG | 226098 |
rs214403015 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36568331 | AAAAAGAACCTCTTC[A/G]TTTACTATGAAAGTA | 226098 |
rs214409120 | in-del | -/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36599726 | CTCTCACAGGTATGA[-/C]CAATAGCTCATCTAA | 226098 |
rs214410466 | in-del | -/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36581581 | AATCTATAGTCTGCA[-/T]TTTTCAGCATCACTA | 226098 |
rs214475851 | snp | C/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36581990 | GCTCACCTCAAGGCT[C/G]CTGGAAGGTGAGAGA | 226098 |
rs214476132 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36575563 | TCCATTATGCCTTGC[A/G]TGGTGCTCACGCTGT | 226098 |
rs214510852 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36581398 | TAAAAAATGTCCCTC[A/G]CTATTAATAAAAATG | 226098 |
rs214537102 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36576401 | GATGAAATGATTGTA[A/T]ACTTAAGTGACCCTA | 226098 |
rs214567974 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36589964 | CCGTTGCCCTAGCAT[A/G]TTTTTCAGGAAAGAC | 226098 |
rs214638882 | snp | C/T | | | missense, nc-transcript-variant | Hectd2 | Mm_Celera | 19:36584041 | TTCCAGAACCTTCTC[C/T]TCCTAGCCAGCCCAA | 226098 |
rs214707492 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36614292 | ATTAAAGGAGGGCAC[C/T]GCCACTGCCCGGCAA | 226098 |
rs214732292 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36568801 | TTTTTTATAATTCAT[A/G]TTTTATTTTTACAAA | 226098 |
rs214739076 | in-del | -/TT | | | intron-variant, upstream-variant-2KB | Hectd2, LOC105246565 | Mm_Celera | 19:36555334 | TGCCTCCCTGGATGC[-/TT]TTTTATTTTTTTCAT | 226098 |
rs214748904 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36586843 | AGTTACCAAGACTAA[C/T]TTATTGGAATTAAAT | 226098 |
rs214753257 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36602245 | CAACACAATATAAAT[G/T]ATGATATTTCAAACT | 226098 |
rs214775836 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36575101 | AAGAGTAGGAGATAA[A/T]TCTTCTGTGCTGGCT | 226098 |
rs214794251 | snp | C/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36601598 | AAATAAGTTAAATGT[C/G]TTGTGAATTGTTTTA | 226098 |
rs214875875 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36584411 | CATTCTCTAAAAGCT[A/G]TGTCACCATTCAGAA | 226098 |
rs214877512 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36578046 | TCGTGTTTAGCTGTC[A/C]TGAATCTAAGTCAGT | 226098 |
rs214914764 | snp | A/G | | | synonymous-codon, nc-transcript-variant | Hectd2 | Mm_Celera | 19:36584021 | TGAAGTGAAGGTCCC[A/G]CCCCTTCCAGAACCT | 226098 |
rs214937248 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36578279 | TGTAAATATTGTATA[C/T]ACATATAAACCTATC | 226098 |
rs214962883 | in-del | -/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36569509 | TCAGGAATGGTAATA[-/G]TCTGATTAAACTACT | 226098 |
rs214986773 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36616165 | TGTTGTCTAGCCCTC[A/T]GTAAATGATTTTTAT | 226098 |
rs215129054 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36593204 | GGATTTTGGTTGTTT[A/G]GATTGTTTATTTCCT | 226098 |
rs215147267 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36605343 | CTCTAGACTTGTAGG[A/C]CCTCAGTAGTAGCCC | 226098 |
rs215154174 | in-del | -/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36614534 | TAGGACTTAGAATTC[-/T]TTTTTTTTCCAATTT | 226098 |
rs215162931 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36594316 | ACAGTTCCTCATATT[G/T]TGGTGACCCCAACCA | 226098 |
rs215185013 | in-del | -/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36608996 | AAACCACCAACATAC[-/T]TGGTTAAACTTAGTA | 226098 |
rs215198328 | in-del | -/TA | | | intron-variant | Hectd2 | Mm_Celera | 19:36591619 | AAAGCCATTTTGATT[-/TA]TGTCTCCCTAATGGC | 226098 |
rs215208694 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36609877 | CTCCAGCTCCAGGGA[A/C]TCCAACACTTCTGGC | 226098 |
rs215229884 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36564021 | AGTAAATTGTACTAA[A/G]ATTTTGTATACAACA | 226098 |
rs215262223 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36560078 | GACTCTTGAGCTGTA[G/T]GACAGTCAAGACTAC | 226098 |
rs215356759 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36616967 | ATGACTATGTAAACT[A/G]ATGTCAAAATTATAC | 226098 |
rs215427159 | in-del | -/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36607712 | GTGTGTCCAACTTCT[-/G]GGTACCTTTTTACTA | 226098 |
rs215444339 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36580109 | CATTATTTATGACAC[A/G]TAGGGGATGATGTTT | 226098 |
rs215466970 | snp | C/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36563161 | CCTTACTTTCTGATG[C/G]TCAGTGAACACTGGA | 226098 |
rs215480076 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36585875 | GTAATATAATTACAT[A/G]AAACAATCAGATATA | 226098 |
rs215480135 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36579635 | TAGTGCCATTCCCTA[C/T]GAGGGCCATTTTCAT | 226098 |
rs215503123 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36566812 | GTCCAGATATGTTGA[A/C]CTTTTTATAAATAGT | 226098 |
rs215510011 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36570484 | TAATGTAAATGAGTA[C/T]ACTGTAGCTGTACTG | 226098 |
rs215569361 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36573537 | TAAGAGCACTGTGAA[C/T]GGCAGACAGAAATAG | 226098 |
rs215623029 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36563047 | ACCTAAAGCCTAAAA[A/G]AAGTATCTTGCTGAA | 226098 |
rs215662770 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36588092 | GCTAATGTCATCCCC[A/G]TGGGGTCCTGGGAGG | 226098 |
rs215704996 | in-del | -/ATGA | | | intron-variant | Hectd2 | Mm_Celera | 19:36556276 | TTTAGAAGCAATGTT[-/ATGA]ATGAGTTTAGTGTCT | 226098 |
rs215763929 | in-del | -/GAGCAAGTCATGGA | | | intron-variant | Hectd2 | Mm_Celera | 19:36607648 | CTCTCCAAGAAGGAT[-/GAGCAAGTCATGGA]GTCCTGTTTTCCTGT | 226098 |
rs215823833 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36582083 | TGAATGAGAATGGCC[C/T]TCCTAGGCTCATAGA | 226098 |
rs215823896 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36588519 | TGGGCTTCTTTGTAG[C/T]CAGTATATTTTATTT | 226098 |
rs215831220 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36572440 | CTTTACCTTAATAGA[A/G]CTCCAGTCTAGACGT | 226098 |
rs215855505 | in-del | -/GTCTGAGGCCT | | | intron-variant | Hectd2 | Mm_Celera | 19:36603990 | ACTTTGCTATTGAAG[-/GTCTGAGGCCT]GTGGAAATTGCAGTT | 226098 |
rs215879670 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36598297 | AGAATCATAAAAAAA[A/G]CATAAAATATTAAAA | 226098 |
rs215895334 | in-del | -/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36610773 | TATAAATTAAGAGTA[-/T]TTTTTTCATGAAGCT | 226098 |
rs215937023 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | Hectd2, 1500017E21Rik | Mm_Celera | 19:36619953 | GTAAATCCAAAAGTA[C/T]CCTTGTTTTCTATTT | 226098 |
rs215941579 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36610067 | TCACAGTATAAGTGA[A/C]AATGGTACTTTTTTA | 226098 |
rs215947328 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36591481 | ATTTGTTTCCATAGT[C/T]GCTGTACAAGTTTGC | 226098 |
rs215981703 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36564251 | GTATTTAACTTTTTA[A/G]GATTATTTAATACTA | 226098 |
rs216062605 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36602754 | ACGGGAGCAGACTAA[A/T]GACTGCAGCATAGTT | 226098 |
rs216096122 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36610674 | TGCCAGATATGAGGC[C/T]CTGGTCCCTGTGCTT | 226098 |
rs216116846 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36574578 | TGCCCTCTTCTGGTG[C/T]GTCTGAGGACAGCTT | 226098 |
rs216129644 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36597696 | TTCAAAATAAAAATT[A/T]AAAACTGTCAGTTCT | 226098 |
rs216130825 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36565281 | TACCCTTGTATTGTT[C/T]GTTGCTGTATACAAA | 226098 |
rs216142041 | snp | A/G | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36582069 | AGTAACTGGTGGTTT[A/G]AATGAGAATGGCCTT | 226098 |
rs216161587 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36613746 | ATACATGGCATAGTA[C/T]TGCCTATTTTTCAGA | 226098 |
rs216188711 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36558043 | GGGTTAGTGAAAGGG[A/G]TGGCTGTTTAAGTGT | 226098 |
rs216189862 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36567440 | ACTTAAATACTATGT[A/G]TATAGTATCTGGAAT | 226098 |
rs216236632 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36603446 | GTTACATATTTCTTA[C/T]AATTCTAATATGTTG | 226098 |
rs216300168 | in-del | -/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36576879 | AATAAAAGAACTTCT[-/G]GGGGAATCACCATCC | 226098 |
rs216330881 | in-del | -/TAA | | | intron-variant | Hectd2 | Mm_Celera | 19:36597016 | CCACTTAGAATTCAT[-/TAA]GCTTTGTGTTTTTCC | 226098 |
rs216348637 | snp | C/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36612870 | AGAGTTAATGCCTAG[C/G]TCCAGGGGTTGGGGG | 226098 |
rs216351024 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36592065 | ATTGGGTGTTGTGCA[G/T]GGTGTTAAGTCTGTA | 226098 |
rs216352898 | in-del | -/TA | | | intron-variant | Hectd2 | Mm_Celera | 19:36565645 | TTTAGCTTCCAACAC[-/TA]TGTTTCTCTCTTTAG | 226098 |
rs216361649 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36567613 | ATGTGGTTGCTGGGA[A/T]TTGAACTCAGGACCT | 226098 |
rs216379079 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36594775 | ATCTGAAAAAGCAGG[A/G]GTGAGGAGGGGCCGC | 226098 |
rs216411774 | in-del | -/CACTGAT | | | intron-variant | Hectd2 | Mm_Celera | 19:36589745 | GAGGGCTGAATAAGG[-/CACTGAT]CTATGAATATAGCAG | 226098 |
rs216424883 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36568140 | CCTTTCCAGAACTTA[G/T]AGATGTGATTTCTAC | 226098 |
rs216424916 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36560240 | TTAATACAATAGAAA[A/G]CCACACAACAACCTC | 226098 |
rs216494346 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36613634 | CCACTCTTTTAGAGT[A/G]CCCTTTGTAATATGT | 226098 |
rs216541539 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36561297 | TTTAAAATTAACTTG[C/T]TTATTTTTAGAGTTG | 226098 |
rs216575888 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36560976 | CACATAATAGATATG[A/G]AATCTAGAATAATGC | 226098 |
rs216598632 | in-del | -/CTCATTT | | | intron-variant | Hectd2 | Mm_Celera | 19:36610454 | TGGAGAAGAGATAGG[-/CTCATTT]CCCCTTCAGGAGAAG | 226098 |
rs216624839 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36592611 | GGTTTATAGCATCCA[C/T]TAGCTCTAGCACTTC | 226098 |
rs216660340 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36592124 | TTCAGTTTGGTCAGC[A/G]CCATTTGGTGGAGAT | 226098 |
rs216661456 | in-del | -/GG | | | intron-variant | Hectd2 | Mm_Celera | 19:36577850 | ATTTCCACTGGAGTA[-/GG]GGAATGGAGAGGCAT | 226098 |
rs216725128 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36618348 | CTATAACAATATTCT[A/C]TCTACTAGGTATTTT | 226098 |
rs216758758 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36556099 | ATGCCAATGTAGTTT[A/G]TTTGTTTCAAGTCTG | 226098 |
rs216767210 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36586587 | TATAGACATAATAAC[A/G]TTATACCGACTGTGT | 226098 |
rs216827266 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36614543 | AGAATTCTTTTTTTT[C/T]CAATTTTTTATTAGT | 226098 |
rs216834776 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36587101 | TTTTTTCAGTTACAA[A/G]AATTGTTGCTGGTCA | 226098 |
rs216839129 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36601331 | AGTAAAACACCATAC[A/G]AAAGTAATGTTTTAT | 226098 |
rs216868960 | in-del | -/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36560475 | AATATATTAATTCAA[-/T]TTTTTTCCAAATGTA | 226098 |
rs216885974 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36616011 | GACCCTGTAACAGAG[A/G]AGGCTGTGGCTGAGA | 226098 |
rs216911820 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36594249 | TGGAGTTGGGATGAT[C/T]GTAGGTCTAGTTTAG | 226098 |
rs216922798 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36569773 | TTTATAGAAATGCAT[A/G]CTAACATTAGACCTA | 226098 |
rs216944904 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36568921 | CTATACCTAAGGATC[C/T]CTATATGGTTAGAAA | 226098 |
rs216971253 | in-del | -/GCCACCATGCA | | | intron-variant | Hectd2 | Mm_Celera | 19:36574176 | GCCACATGGCTGCCT[-/GCCACCATGCA]GCCACCATGCAGCCA | 226098 |
rs216976979 | in-del | -/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36573757 | TGCATCTGAAAAAAA[-/T]ATTTTGCTGCATTAG | 226098 |
rs216996605 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36608965 | TGCTGTATTCTGCAC[C/T]CAAATACTTCTAACA | 226098 |
rs217020776 | in-del | -/CATGTATGTGTGTGTA | | | intron-variant | Hectd2 | Mm_Celera | 19:36558409 | ACATGCGTGAGTGTG[-/CATGTATGTGTGTGTA]CATGTGTATTTTGCT | 226098 |
rs217026421 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36616824 | TGTGACACCAAAAAG[C/T]CATCCTTTTTTTCAA | 226098 |
rs217027826 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36608061 | AGTGTTTTCAAGAAG[C/T]AGATCCATAAAACAA | 226098 |
rs217042682 | in-del | -/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36563982 | TATCTTCTAAAGCAG[-/T]TTTGGAGGATGGAGG | 226098 |
rs217086015 | snp | C/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36576934 | CAATGGTGATGAAAA[C/G]TGCATGGTACTGGTA | 226098 |
rs217133111 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36589210 | CCTTTCTACCGCCTC[A/T]TCTATCCAGATCCAT | 226098 |
rs217160273 | snp | A/C/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36614798 | GTTCATATTGTTGTT[A/C/T]CACCTATAAGGTTGC | 226098 |
rs217165950 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36618591 | GGCACTTGATCCTAA[A/G]TTCTCAATAAAGAAG | 226098 |
rs217171153 | in-del | -/GAG | | | intron-variant | Hectd2 | Mm_Celera | 19:36610420 | GACATCATACCAGAT[-/GAG]GAGGACCCAGGAGAC | 226098 |
rs217204980 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | Hectd2, 1500017E21Rik | Mm_Celera | 19:36619754 | TATATATTTTGATGT[A/T]CTGCTTATATCTACA | 226098 |
rs217209776 | in-del | -/A | | | intron-variant | Hectd2 | Mm_Celera | 19:36570403 | TTCTTTTCTTGATTT[-/A]TTTTTTCTTTTTGCT | 226098 |
rs217221710 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36589828 | GGTTTTACCCTAGGT[C/T]TCTGGACTATCTAGT | 226098 |
rs217274604 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36571007 | AGCTGTATATGTGTC[A/G]GGGGCCTGCCTGGTT | 226098 |
rs217291347 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36572315 | TGCCTGTTTTTTTTT[G/T]TTTTTTTTTCCTCAT | 226098 |
rs217309742 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36596691 | AAGAAAACCCACATT[A/G]TTGTCTTGCTATTTA | 226098 |
rs217317082 | snp | C/T | | | synonymous-codon, nc-transcript-variant | Hectd2 | Mm_Celera | 19:36611379 | GAATTGGCCCATGGA[C/T]TAAAGGAACTTTTAT | 226098 |
rs217325627 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36571909 | CAAAGTCAGAGTGTG[A/G]TGGATAGCAGTAACC | 226098 |
rs217349082 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36566355 | GTTGGCAACCAAGAG[A/T]AGCCACCACAAGTAC | 226098 |
rs217435550 | in-del | -/CA | | | intron-variant | Hectd2 | Mm_Celera | 19:36558704 | TTATGCTTAGCTTTG[-/CA]CTAACTGGGGTAGAA | 226098 |
rs217441902 | in-del | -/A | | | intron-variant | Hectd2 | Mm_Celera | 19:36568305 | ATCTGGCGACTAAAT[-/A]AAAGAAGTGAAAAAA | 226098 |
rs217506693 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36566728 | TGGTCAATTACCTGG[G/T]TGTCTGGATACAAAC | 226098 |
rs217540379 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36595634 | AATACTAGCTTTCTC[A/G]TGAGAGAGACATGGA | 226098 |
rs217566703 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36590564 | AACATAGCACACTTA[C/T]CTTTCAGGGGTCTGA | 226098 |
rs217584011 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36574049 | CTGCTTTTCTGAACT[A/T]CTTGGAAAACATAGT | 226098 |
rs217635929 | in-del | -/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36564687 | AACCCTGCAAGTCAG[-/T]TGTAGTCTTAAGTTT | 226098 |
rs217652287 | in-del | -/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36559087 | AAGCCCACTGGAACT[-/C]CCCCCCTCCCCAGAA | 226098 |
rs217704930 | snp | C/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36574485 | CAGCGGTTAAGAGCA[C/G]TGACTGCTCTTCCAG | 226098 |
rs217725320 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36591343 | AATATTTCCATGTTT[C/T]TAAAGAAACCAAAAT | 226098 |
rs217725376 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36584596 | GACGTGGTATTACTC[A/T]CCAGTGATTCTAGTG | 226098 |
rs217748933 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36579981 | AGGAATGACTGACCA[A/T]TTCAATAATTTTATA | 226098 |
rs217784158 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36585303 | TCTTATACATTAATT[C/T]TATTTTCAGTAATTG | 226098 |
rs217805356 | snp | A/G | | | upstream-variant-2KB, downstream-variant-500B | Hectd2, LOC105246565 | Mm_Celera | 19:36552624 | TCCCAGTCCTTACCC[A/G]GGGCTTGTATGAAAG | 226098 |
rs217825108 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36592365 | AGAGTTGTTTAGTTT[C/T]CAATGATTTTGTAAG | 226098 |
rs217832355 | in-del | -/TCTT | | | intron-variant, nc-transcript-variant, downstream-variant-500B | Hectd2, 1500017E21Rik | Mm_Celera | 19:36621198 | TTAAAATCACACTGC[-/TCTT]TCTTTATAAGATATC | 226098 |
rs217854880 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36605574 | GGAGATGGTTTAGTC[A/G]GTAAACAGCTGGCTG | 226098 |
rs217916349 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36569101 | TGATCATTAAAGCAG[C/T]ATTATTTAAATACTT | 226098 |
rs217943613 | in-del | -/AA | | | intron-variant | Hectd2 | Mm_Celera | 19:36591155 | AATATCCAATAAAAG[-/AA]AAAAAAAAAAGAGGT | 226098 |
rs217951598 | snp | A/G/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36575207 | TCATTAAAGATGAGC[A/G/T]TCTACAGAAATCACT | 226098 |
rs217966359 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36592811 | TGTCCTTCCCTGTCT[C/T]TTCTAATTAGTTTTG | 226098 |
rs218022099 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36607159 | GAAGAGAGGGAAGTT[G/T]CAGCGTTGACAAGTT | 226098 |
rs218055157 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36570101 | TTAAAAGAGCACTCA[A/G]GTATTAACTCACAGT | 226098 |
rs218099133 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36593642 | ACCTTTATAGGCATC[A/T]CATCCTTTAGGTTAG | 226098 |
rs218123357 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36580669 | CTTTTTTATACTGTA[C/T]TACAATATCCTCATA | 226098 |
rs218129403 | snp | G/T | | | upstream-variant-2KB, nc-transcript-variant | Hectd2, LOC105246565 | Mm_Celera | 19:36553429 | TACAAATTCTGGGCT[G/T]GAAAAACAACCTCAT | 226098 |
rs218160470 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36594418 | TGTAACCCCTGTGTG[A/G]GGGTCATGACCTGTC | 226098 |
rs218166933 | snp | A/C/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36615377 | TAGTTAAATAATGTT[A/C/T]AAAATGTTATAAAAT | 226098 |
rs218226196 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36575140 | CTAGTAAGATACCAA[A/C]TCCTTCTCTAGTCTT | 226098 |
rs218240923 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36587835 | CACATCTGTATTGGT[C/T]AGGATCTGGCAGAGC | 226098 |
rs218288630 | snp | C/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36581325 | GTGTGGGAAGTGATA[C/G]AAAAGGGTAATTCTA | 226098 |
rs218304141 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36588291 | CCACTCTCTGCTTCC[C/T]TTGATTATATTGTTC | 226098 |
rs218412372 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36572584 | CATATAATTCCTTGG[G/T]TTTTTTTGAGAAGCC | 226098 |
rs218444532 | in-del | -/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36567490 | TTAATACTAATAACC[-/T]TTTTTAAAAAAAAAG | 226098 |
rs218468453 | in-del | -/A | | | intron-variant | Hectd2 | Mm_Celera | 19:36561160 | ACACAGAATTAAGGG[-/A]TGCCTTGCACTCTGA | 226098 |
rs218470207 | in-del | -/A | | | intron-variant | Hectd2 | Mm_Celera | 19:36556760 | AGTTTAAGAATTTTT[-/A]AAAAAATCTTTGAAC | 226098 |
rs218485299 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36604035 | CTTCTCACTATAAAA[A/G]TTGAGCAAGATTTTG | 226098 |
rs218486193 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36575406 | TGCTAAATGTTCAGA[A/G]AAGTCCTCTTACAGG | 226098 |
rs218508645 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36597812 | TATCTGTGAAGTCAC[C/T]GTCAATGCTGAACTA | 226098 |
rs218553394 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36600789 | GTGTTCATTCTTTCC[A/G]TAGGCATTTATGTCT | 226098 |
rs218580348 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | Hectd2, 1500017E21Rik | Mm_Celera | 19:36620250 | TCGCTGTGCTTTCTG[C/T]ACCCAACCAGCAGAA | 226098 |
rs218618015 | in-del | -/A | | | intron-variant | Hectd2 | Mm_Celera | 19:36573731 | TTTCTTAACTATTCC[-/A]TAGAGAAAAGTGCAT | 226098 |
rs218653537 | snp | C/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36590916 | CCTTCCTACCCCCAG[C/G]CCCCAACACTAGGTA | 226098 |
rs218683486 | in-del | -/GTT | | | intron-variant | Hectd2 | Mm_Celera | 19:36604506 | CTAAGTTTATTAGTA[-/GTT]GTTGGTTAATTCCTC | 226098 |
rs218777903 | snp | C/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36577657 | GGGAGGCCTTATGAA[C/G]TGAAGCTGAATTGAG | 226098 |
rs218968424 | snp | C/T | | | upstream-variant-2KB | Hectd2 | Mm_Celera | 19:36552382 | AAAAACCTGATTGAT[C/T]AAGTCCAGTTGCATC | 226098 |
rs218970072 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36578925 | TATAAAAGAACTTAT[A/G]GGCATATTAAAAAAC | 226098 |
rs218997407 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36574154 | TCCTCTACTCCTTCG[A/C]CTCCCAGCCACATGG | 226098 |
rs219029250 | snp | A/G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36573733 | TTCTTAACTATTCCT[A/G/T]GAGAAAAGTGCATCT | 226098 |
rs219044975 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36578017 | GTTCCATTTCATCTT[A/C]CTTCATTGCGCCTTC | 226098 |
rs219045696 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36603822 | AGATCTGAACATTGA[C/T]AATGTCTTTGAACCT | 226098 |
rs219109029 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36568380 | AAGAGATGTTGGGCT[A/G]GAAAGATGCCTCACT | 226098 |
rs219138716 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36567803 | ATATAAGGACAGTTA[C/T]TTTCTCTGGAGTAGT | 226098 |
rs219188673 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36599194 | ATTTTACAAACTATA[A/C]ATTTTTATTTATAAA | 226098 |
rs219210771 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36558572 | GTAGGCAGTAGAAGC[A/G]TTTAAGAGAAAACAC | 226098 |
rs219222428 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36598499 | TTAAAGCACAGCCCT[A/G]CCGAATCTCCCTCAT | 226098 |
rs219228150 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36604525 | GGTTAATTCCTCAGA[A/G]GAGTTGATGTACAAT | 226098 |
rs219319767 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36581859 | AGACTGTGTTAGCTA[A/G]TTTTCTTATGACCGG | 226098 |
rs219327411 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36556761 | AGTTTAAGAATTTTT[A/T]AAAAATCTTTGAACA | 226098 |
rs219335153 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36576725 | ATATAGTGAAAATGG[A/C]CATCTTGCCGAAAGC | 226098 |
rs219370393 | in-del | -/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36611095 | AGTAGAGCTATAACA[-/C]CTGTTTGCTTAAGAG | 226098 |
rs219371374 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36576009 | CAATATACAGAAATC[C/T]ATCAATGTAATCCAC | 226098 |
rs219371437 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36582191 | ATGCAGGTGAGCTTT[G/T]AGGTTTTCAAAAGTT | 226098 |
rs219454568 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36557539 | CGAGACTGACTGTAG[A/T]GTTACTTTGGTAGGA | 226098 |
rs219489570 | in-del | -/TTAC | | | intron-variant | Hectd2 | Mm_Celera | 19:36564435 | AGGGAATGAATTCTA[-/TTAC]TTAGTGTGCTAGGTT | 226098 |
rs219494515 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36597663 | CAAGGTGGGAAAAAA[C/T]TAAAAGGGCAAAATA | 226098 |
rs219540114 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36602428 | GGCTCCAAAAAGAAT[G/T]CCAAAGCCATGCTGC | 226098 |
rs219569014 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36602010 | GAAAATGTAGCGCAA[G/T]GTGGAGTTTCTCCCT | 226098 |
rs219578135 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36578533 | ATTTGTATTATAACA[A/G]CCACCTCAAAATTTA | 226098 |
rs219589973 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36595100 | TGATGCATGTAGCCC[C/T]AAATTCACTCTGGCT | 226098 |
rs219626125 | in-del | -/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36566994 | TCATGTCTGATTTCA[-/T]TTTGGGCAAAGCCTG | 226098 |
rs219660870 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36578083 | ACATTCTTTTTAACT[C/T]TGAGGCTATATAGCC | 226098 |
rs219670047 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36572149 | AGTGCTGGGATTAAA[A/G]GCGTGCGCCACCACG | 226098 |
rs219697178 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36577777 | CTTATCACTTCAGAT[A/G]ACGTTTCTCCCAGGC | 226098 |
rs219711098 | snp | C/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36579550 | GAGACACTAGGTGTG[C/G]CTTGAGCATCTTGAG | 226098 |
rs219728015 | in-del | -/TT | | | intron-variant | Hectd2 | Mm_Celera | 19:36566152 | AACCGCCTTACTGGC[-/TT]GTTCCCAGGAGCATG | 226098 |
rs219734013 | snp | C/T | | | upstream-variant-2KB, nc-transcript-variant | Hectd2, LOC105246565 | Mm_Celera | 19:36552995 | AGAGATAACCCACCA[C/T]CATTTCAGAATTTAT | 226098 |
rs219761502 | snp | A/G | | | upstream-variant-2KB | Hectd2 | Mm_Celera | 19:36552322 | ATTTCATTGCCCCAT[A/G]CCACCCCGTTCCCCT | 226098 |
rs219787253 | in-del | -/TGTGTGTGTGTG | | | intron-variant | Hectd2 | Mm_Celera | 19:36586597 | TAACATTATACCGAC[-/TGTGTGTGTGTG]TGTGTGTGTGTGTGT | 226098 |
rs219796871 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36586863 | TGGAATTAAATGCAT[A/C]CCTAATGGCCAGATA | 226098 |
rs219896500 | in-del | -/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36613054 | TTGTATGATTCTTTC[-/T]TTTTTTTTAATCTAT | 226098 |
rs219901852 | snp | A/G | | | upstream-variant-2KB, downstream-variant-500B | Hectd2, LOC105246565 | Mm_Celera | 19:36552758 | AATGGGCTTGTTTCC[A/G]TTGCCTTATCTCGTC | 226098 |
rs219932330 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36598441 | ATTAGAATACATCAC[A/G]TACATGTTGGAAAGG | 226098 |
rs219994282 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36574780 | ATTAGACATACATGT[C/T]TATTCAGACCTCATT | 226098 |
rs219997509 | snp | C/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36580721 | AACGAAGATTTTCCT[C/G]TTTTATTTATGATAT | 226098 |
rs220002630 | snp | C/G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36580708 | TTGCATATGTCAGAA[C/G/T]GAAGATTTTCCTCTT | 226098 |
rs220004427 | in-del | -/ATGCTTATAAATT | | | intron-variant | Hectd2 | Mm_Celera | 19:36560848 | CAATTGGAGAAAAAC[-/ATGCTTATAAATT]ATGCTTATAAATTGT | 226098 |
rs220026753 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36580237 | CTTTTGATTATCTCT[A/G]AGCTACTGTTACTAT | 226098 |
rs220079445 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36580275 | AGCTATGCAGGAACA[A/G]CCTTTATATAACCAA | 226098 |
rs220082573 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36599114 | GGGTCGTGGAATACT[A/G]GAGAGATAGCTTTAA | 226098 |
rs220118462 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36575175 | TCTGTAAGACAATCT[A/G]GTATGAAACATCTAG | 226098 |
rs220119631 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36586285 | AGAGATACTGGTCTA[A/T]CCTAGTGGTTGTCAA | 226098 |
rs220154585 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36608187 | ATATAGTACAGTACA[A/G]GTTTTCAGACTGTCC | 226098 |
rs220181784 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36600244 | AACAGCTCACTTCAT[A/G]GGTCTTCCATTTGGT | 226098 |
rs220181882 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36608099 | AAGTTAAAATGTTAT[A/G]GAGTATTAATAACTG | 226098 |
rs220196058 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36562678 | TTTAAATATAAAATT[A/C]ATAGAAATTTTACTA | 226098 |
rs220212511 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36607632 | AGTGACTAATTCCAC[A/G]CTCTCCAAGAAGGAT | 226098 |
rs220234649 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36600825 | GTGTGTGGTTTTCAT[A/G]CATAGTGTACGACTT | 226098 |
rs220273375 | snp | A/G | | | intron-variant, upstream-variant-2KB | Hectd2, LOC105246565 | Mm_Celera | 19:36555373 | GACGTGTGATTTGAA[A/G]GAGCGAGGCTTTTTC | 226098 |
rs220345384 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36600908 | ATCTTTGTAAGTAAG[G/T]ATATTTCATATTTTA | 226098 |
rs220376145 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36607687 | CCTGTCATTTACAGG[C/T]CTCACTTGAGTGTGT | 226098 |
rs220430759 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36610205 | ACCAAGTAATACAAA[C/T]TTGCTTATCTCTTCA | 226098 |
rs220519013 | snp | A/T | | | intron-variant, upstream-variant-2KB | Hectd2, LOC105246565 | Mm_Celera | 19:36555319 | GGTAGTGGGAGGCAG[A/T]TGCCTCCCTGGATGC | 226098 |
rs220523826 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36582268 | ATATAGAACTCACAG[A/C]AGCTTGTCCAGCACC | 226098 |
rs220547943 | snp | C/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36562140 | GGGAAGGGGAGAGCA[C/G]ATAGGGGATAGGGGG | 226098 |
rs220548491 | snp | C/T | | | intron-variant, downstream-variant-500B | Hectd2 | Mm_Celera | 19:36611531 | TAGATGAGCAAGAAG[C/T]AATCAACATGTAAGG | 226098 |
rs220549646 | snp | C/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36603102 | CACACAAGACACTGT[C/G]CAGAAATACAGACGT | 226098 |
rs220557476 | snp | A/G | | | upstream-variant-2KB, intron-variant | Hectd2, LOC105246565 | Mm_Celera | 19:36554206 | GGTGAGCGGTCTCCC[A/G]GTCTCCCCGGCGCTG | 226098 |
rs220579248 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36611013 | TATATATGTGATTTG[A/G]AAATGAGAAGCACTA | 226098 |
rs220605142 | snp | C/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36603907 | TAAGTATCCACAATA[C/G]TTTAAGCCTGAGCTT | 226098 |
rs220628243 | in-del | -/AT | | | intron-variant | Hectd2 | Mm_Celera | 19:36574639 | TCTTTTAAAAAATTA[-/AT]ATATATATATATTCT | 226098 |
rs220630781 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36601767 | AAACCCAAATTTGAG[A/G]AGCTTGTTGGGACTT | 226098 |
rs220675470 | snp | C/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36611217 | TTAACGGGTATCATG[C/G]GTCTTAGAAAGTACA | 226098 |
rs220716091 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36565848 | TCTGTGAAGGCTACT[A/G]TAGCTAGAGAGTCTG | 226098 |
rs220771645 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36565628 | TCTTGGAATTGGATT[A/G]ATTTAGCTTCCAACA | 226098 |
rs220781949 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36604885 | GGCCGTAAAAAGTTA[C/T]TTTATATTATAGTCT | 226098 |
rs220813724 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36556485 | AAGCACATAGGTCTT[A/G]GTAATTTCAAGTTTT | 226098 |
rs220814884 | in-del | -/A | | | intron-variant | Hectd2 | Mm_Celera | 19:36591156 | AATATCCAATAAAAG[-/A]AAAAAAAAAGAGGTC | 226098 |
rs220857950 | in-del | -/CATCCATAA | | | intron-variant | Hectd2 | Mm_Celera | 19:36590429 | TGCCCCACTCCAGTC[-/CATCCATAA]CATCATCTGTTTCCC | 226098 |
rs220864957 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36590316 | TTACACCAGGTTTCC[A/T]TGGTGCCCCTCAAAT | 226098 |
rs220879523 | in-del | -/TAT | | | intron-variant | Hectd2 | Mm_Celera | 19:36573149 | CTCTTTCTCTTTTTG[-/TAT]TATTTTTCTTTCCCC | 226098 |
rs220892576 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36558782 | GCTAATGGATAACAA[A/G]CAAATCAGTATGTAA | 226098 |
rs220927269 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36558304 | GAGAGGTTCTCACTG[A/G]AATTGACTATACCAA | 226098 |
rs221007951 | snp | C/T | | | intron-variant, downstream-variant-500B | Hectd2 | Mm_Celera | 19:36611659 | TAAGACCCTTTCTCA[C/T]TTAACTAATGTTTAA | 226098 |
rs221049290 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36559794 | TATTAAAATAAAACA[A/G]TCCAGCCAGTAACAT | 226098 |
rs221055486 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36566537 | TATGATTCTGAGACT[G/T]CTGATTCCTTTCCCA | 226098 |
rs221138930 | in-del | -/TGTGTG | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36563074 | TGAAGCTTCAGTGCT[-/TGTGTG]TGTGTGTGTGTGTGT | 226098 |
rs221142613 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36578734 | GCTTCCTAACTGCTG[C/T]ACAGCATAATGACTG | 226098 |
rs221149251 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36558929 | AATTGGCAAATGTTC[A/G]GGGGGGTGTGTAGTA | 226098 |
rs221171502 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36578175 | TTTTGAGAGGAATTA[A/G]AAGTCTTCTCAACTG | 226098 |
rs221171736 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36584651 | CACCCCAAGTTTGAG[A/G]CCAACATGTGCTACA | 226098 |
rs221219863 | in-del | -/A | | | intron-variant | Hectd2 | Mm_Celera | 19:36615326 | CATTTTATAAAAAAC[-/A]AAAAAAAATGAGTTC | 226098 |
rs221229561 | in-del | -/GA | | | intron-variant | Hectd2 | Mm_Celera | 19:36590179 | AGTTTGGGGTTTGGG[-/GA]ATGTCTGTGGAACCC | 226098 |
rs221293328 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36579756 | GTATAATTGTCTGAT[A/G]TTCTCTATAGAGTTG | 226098 |
rs221368809 | snp | C/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36605603 | TGTGTAAACCTGAGT[C/G]TCAAGTTAGGTTCCA | 226098 |
rs221373166 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36613911 | ACACATCAGTGCTTC[C/T]TGCTGATTGGAGAAG | 226098 |
rs221387957 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36562763 | AATTTGAAGTTAATT[C/T]ATATGCTTTTATTAA | 226098 |
rs221415352 | snp | A/C | | | synonymous-codon, nc-transcript-variant | Hectd2 | Mm_Celera | 19:36605293 | CCAGATTTTCCATCC[A/C]GATTATGGTGAGTGT | 226098 |
rs221442617 | snp | A/T | | | missense, nc-transcript-variant | Hectd2 | Mm_Celera | 19:36584903 | TTTTTTAGGGAAGAT[A/T]TAGAAAAAGCTGAGG | 226098 |
rs221460824 | in-del | -/TTT | | | intron-variant | Hectd2 | Mm_Celera | 19:36590604 | GAGGATGAGGGTGTG[-/TTT]TTTTTTTTCTTTCTT | 226098 |
rs221471746 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36556604 | CTAAAACTGTAGCCA[A/G]TGTATTGTTTGTTCT | 226098 |
rs221498014 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36563622 | CTGGTAACTAGGAGA[G/T]TTTATTTTAGAAATT | 226098 |
rs221499297 | snp | C/G | | | intron-variant, upstream-variant-2KB | Hectd2, LOC105246565 | Mm_Celera | 19:36555442 | GTAATTTCCCAGCTG[C/G]ATTTTGCAAGGGTTA | 226098 |
rs221508156 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36561066 | TTTGGGCTTTTTTCT[C/T]ACCAGCCCTCTGTAT | 226098 |
rs221532005 | snp | C/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36586899 | GTACAATTTGTAATC[C/T]CAGCAATTAAGAAGC | 226098 |
rs221561261 | snp | C/T | | | upstream-variant-2KB, intron-variant | Hectd2, LOC105246565 | GRCm38.p3 | 19:36554354 | AGGTGAAGGGAAAGC[C/T]AGGGTTAGAATCCGT | 226098 |
rs221583238 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36557423 | ATTCTGAATGTTTAA[A/G]GAGGGGTGCCATGAT | 226098 |
rs221591087 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36587606 | CCCTATCCCATCCCC[A/C]CTTGCCTGATTCTAT | 226098 |
rs221592192 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36606695 | TATCTCAAAATGATT[A/G]TTTATATATCAGATT | 226098 |
rs221607162 | in-del | -/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36592150 | AGATGCTGTCTTTTT[-/G]ACAGTATATATTTCT | 226098 |
rs221649673 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36582498 | CCAGTCAATTAATCT[A/G]TTGATGGCGTGAGTA | 226098 |
rs221652342 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36588844 | TTTAGTGTCCTCAGG[A/G]GCTTCAGTGTCTGAG | 226098 |
rs221660291 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36616470 | CCAGGCCTTTCATTT[C/T]CAAAATTGAGTTGGT | 226098 |
rs221667299 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36583591 | TCTGAAAAGTTAAGT[A/G]TTAATAATGTTAAGT | 226098 |
rs221748954 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36559700 | GAAGAGGAAGAAGAG[A/G]AGGAAGAGGATGGAA | 226098 |
rs221771585 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36567084 | TGTACATGTGTGCAC[A/T]TGTATACACATGCAG | 226098 |
rs221805220 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36590979 | ATCAATATCATTATG[C/T]TACTTTCTGCTGACT | 226098 |
rs221811236 | in-del | -/TGAA | | | intron-variant | Hectd2 | Mm_Celera | 19:36584551 | GAAAGGAAGGGCACG[-/TGAA]TGTCAGGGTGAGGTG | 226098 |
rs221812775 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36609513 | TTTCTTTAAAATCAG[A/G]CTTTCCTTTTAGAAC | 226098 |
rs221866943 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36617108 | ACTGGAGTAAGGATG[C/T]GGAAACACATGAGGA | 226098 |
rs221869717 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36608429 | ATTGTGGAGAATTAT[A/G]AGTTATAACACTGTA | 226098 |
rs221900962 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36591719 | AATCTGTATCCCAAT[C/T]TTAATTGGGTTATTT | 226098 |
rs221901940 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36585046 | TCCCTTATTTTAAAT[A/T]TAAAAAAAGAGACTC | 226098 |
rs221912256 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36609548 | CTCTGTCTTACTTTT[A/T]AAAAGTCCCTTCCTT | 226098 |
rs221924482 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36605651 | CCAGGTACTGCCAGC[A/G]CTCCTTTAACAGTGC | 226098 |
rs221940304 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36585674 | ATATGTATAAGGGAG[C/T]CCACAGAGGCCAGCA | 226098 |
rs221958279 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36563802 | CCACCCTGATTCCTT[A/G]AGGCTGAAGGTTGGA | 226098 |
rs221962684 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36617202 | CAATGAAGTAAAGGC[A/G]GGGAGTGATAGGATA | 226098 |
rs221987040 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36613317 | AGAGTCTGGAGTAGC[C/T]TTTCTTTTGAATTGT | 226098 |
rs221988279 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36613027 | TTGAAGTTAGAATAC[A/C]ATTTTGTAAATATTG | 226098 |
rs222000644 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36570736 | TGAGCCATCTCTCCA[A/G]CCCTTTCTTTCTCTT | 226098 |
rs222022686 | in-del | -/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36608987 | CTTCTAACAAAACCA[-/C]CAACATACTTGGTTA | 226098 |
rs222093455 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36606961 | TTTAATTTCATAAAT[C/T]CAACTTCCTGTTTCT | 226098 |
rs222128763 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36613969 | TACTTGGTTTTCTAG[A/C]AAACTACTGATTACT | 226098 |
rs222151907 | snp | C/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36607435 | CAGTGATCACCCTGG[C/G]ACTGTGGGAAGTGCT | 226098 |
rs222202943 | snp | C/T | | | intron-variant, upstream-variant-2KB | Hectd2, LOC105246565 | GRCm38.p3 | 19:36554991 | GGACAACAGGGAAGT[C/T]GCGCCTCGAGGGCAA | 226098 |
rs222299767 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36583147 | CCCCATACTGAGTTT[A/T]CAGTCAAACTGAGCA | 226098 |
rs222352156 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36617252 | TGGTTTCCATGTGTA[C/T]ACATAAGTGTGTGTA | 226098 |
rs222410625 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36617795 | GAGTGGCAATGCTTT[C/T]TTACATCCTAGCAAA | 226098 |
rs222434673 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36571065 | GGGGGGTGGGGGGAT[C/T]CAGGTTAGATGAGAC | 226098 |
rs222505850 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36564507 | AAAGTTCAATTCCCT[A/G]CCCCCTCCAACCCCC | 226098 |
rs222515987 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36610932 | TAAAATGTATAAGCC[C/T]CTTAACATGTGAACT | 226098 |
rs222578409 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36610071 | AGTATAAGTGACAAT[A/G]GTACTTTTTTATCCC | 226098 |
rs222667150 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | Hectd2, 1500017E21Rik | Mm_Celera | 19:36619057 | ATATCAGAAATTTAT[C/T]GAATGAGAGCCTATG | 226098 |
rs222717724 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36589401 | AACTGAAAGCTGTAG[C/T]GTGTGTACGTGCATG | 226098 |
rs222742616 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36567952 | CTAAAAGGTTTTGCT[A/G]TTGTTAGTGTATATA | 226098 |
rs222807841 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36568453 | TCACTAGGATCTACA[C/T]GGTAGAAGGAGAGGG | 226098 |
rs222842417 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36592226 | GTCTGGATCTTACTT[C/T]AGTTGCCTCTCAGAA | 226098 |
rs222944717 | snp | C/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36561653 | AGTGTGGAGCAGAGA[C/G]TGAAGGATAGGCCAT | 226098 |
rs222972262 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36572761 | GTGTGGGTTACCCCA[A/G]TGTGGGTTACCCCAG | 226098 |
rs222978526 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36561100 | GCCTCAAGACCTGTA[C/T]CTGTCGCCTTTTCCG | 226098 |
rs223040946 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36566606 | TGCAGATTTTTGATG[A/T]CTGTGTTCTTGGGTG | 226098 |
rs223054051 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36586168 | TCAAATCTTCCTTGT[A/G]AAGTTGAACTAAATC | 226098 |
rs223103396 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36585757 | TGGTATACAGGTGAA[A/T]ACAGGGAGCTAAGAA | 226098 |
rs223140137 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36591746 | ATTTAGCTTTTTATA[G/T]CAACTTTTTTTAACT | 226098 |
rs223192221 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36614847 | GGGTGCTTTCTCTAG[C/T]TCCTACATTGGGGAC | 226098 |
rs223211097 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36568949 | AAATCCTGGTGTACC[A/T]ACAATTTAATTATAA | 226098 |
rs223235637 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36571194 | AATAAATATCTGCAT[A/C]TGGCTCTTTCAGCTG | 226098 |
rs223270975 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36570790 | CTTTTTTTTACAGTC[C/T]AGTCATTATCCCCTT | 226098 |
rs223275256 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36574467 | CAGGCTGCAGAGATG[A/G]CACAGCGGTTAAGAG | 226098 |
rs223293694 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36561823 | CAGAAGTGGATGCTT[A/G]GAGCCAAACATTGGA | 226098 |
rs223354374 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36565502 | TTCTCGCATAACTTA[C/T]TGGACAGTTTCTTCA | 226098 |
rs223387628 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36564686 | AAACCCTGCAAGTCA[G/T]TTGTAGTCTTAAGTT | 226098 |
rs223430179 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36596035 | GTGTATTAACTCATT[A/T]GAAGGTAAAAATATT | 226098 |
rs223432658 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36568105 | GGATTTTCCCCACCA[A/G]TCTTAAATGTGTCAT | 226098 |
rs223433006 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36574928 | TTCCATTTTGTTCAT[A/C]TGCAAAGTCTTTGTA | 226098 |
rs223484675 | snp | C/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36599444 | TATTTTTTTACCACA[C/G]AGTTTAAAATTGCCT | 226098 |
rs223493619 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36568698 | GGGATATATAGAGGC[C/T]TTGTCTCAAGATTTG | 226098 |
rs223511194 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36614118 | ATTTGATTCTGCAAT[A/G]AAAACACTTCAAATT | 226098 |
rs223534517 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36592593 | TATATATTAGGTCCA[C/T]TTGGTTTATAGCATC | 226098 |
rs223537833 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36568529 | CACACGTTTACATGG[A/G]CACACAGTGTGAGTT | 226098 |
rs223559911 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36589464 | CATGTAGGAGGCCCT[G/T]TGATTGCTGCTTCAG | 226098 |
rs223581672 | in-del | -/TT | | | intron-variant | Hectd2 | Mm_Celera | 19:36610887 | CCAGTACTCTCAGGC[-/TT]TTTTCTTGGAAGAGG | 226098 |
rs223584709 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36587670 | CCTCTCTGCCCTAGC[A/G]TTTCTCTACACTGGG | 226098 |
rs223595547 | in-del | -/TTTTGTTTTGTTTTG | | | utr-variant-3-prime, nc-transcript-variant | Hectd2, 1500017E21Rik | Mm_Celera | 19:36620013 | TTAAGCCCCAGGGAT[-/TTTTGTTTTGTTTTG]TTTTGTTTTGTTTTG | 226098 |
rs223628468 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36593567 | AATATTTTGATTATT[A/T]AGTGCTGAGGGGGCT | 226098 |
rs223630037 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36590034 | ACCATTCTCTTTTGG[C/T]AGCCTGCAGAGTACC | 226098 |
rs223630607 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36587068 | CTTACAATTTTGTCC[C/T]CTCAAGGAAAAAATG | 226098 |
rs223686829 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | Hectd2, 1500017E21Rik | Mm_Celera | 19:36620675 | GATGTGTGTGTATTG[A/G]TAGCTATGTCACTTT | 226098 |
rs223709647 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36592969 | GTTGAAGTATATTTC[C/T]TGGATGCAGCAAAAG | 226098 |
rs223770117 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36562548 | GTTGTGCTGGGGGGC[A/G]TGTAGCCCAATGGTA | 226098 |
rs223780907 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36617964 | TGCTTAAATGAAGCA[A/G]TGCATATCAGAGCAT | 226098 |
rs223812236 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36612464 | ATTAGGTTTTAAAAT[A/G]GTATAGAAGATAATT | 226098 |
rs223816048 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36571274 | TAGCGTTAGTAATAG[C/T]GTCAGGCCTTGGAGC | 226098 |
rs223872538 | snp | A/G | | | synonymous-codon, nc-transcript-variant | Hectd2 | Mm_Celera | 19:36618841 | AGGTTTTGGACTTGA[A/G]TAACCTAGAAGACTT | 226098 |
rs223890274 | snp | C/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36572078 | GGCTGTCCTGGAACT[C/G]ACTTTGGAGACGAGG | 226098 |
rs223905239 | in-del | -/GG | | | intron-variant | Hectd2 | Mm_Celera | 19:36572019 | TCTCTCTCTCTTTTT[-/GG]GGGGGGGTGGTTTTT | 226098 |
rs223921126 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36615894 | GTGAGATTAAAGGCG[G/T]TGTACCACCACTGCC | 226098 |
rs223931747 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36577695 | TTAGGAAGGTGGAGA[G/T]GAAAGTGGCCTCTTG | 226098 |
rs223943568 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36603148 | ACCCAAGGACCCAGA[A/G]AAGCAAAACTCTGCT | 226098 |
rs223944884 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36595413 | TAGAAGCTAAATTAT[C/T]TGAGGGATTAAATTT | 226098 |
rs223982849 | snp | C/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36602629 | ATAAAGTAGACAGCG[C/G]TATTTATCTAGATTT | 226098 |
rs223996728 | snp | C/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36596303 | AGCTACTTGTGTGGA[C/G]TACCCAGGAAAGTCA | 226098 |
rs224005404 | in-del | -/ACAGTTTATTGCCTCCT | | | intron-variant | Hectd2 | Mm_Celera | 19:36557085 | GGTGGAAAGAGAAAG[-/ACAGTTTATTGCCTCCT]AGTTTATTTCTGAAC | 226098 |
rs224066100 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36566482 | CAACAAGTAATTTGA[A/G]TAATTATTCTTTGTA | 226098 |
rs224087956 | snp | C/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36614193 | GGTTTCTCTGTGCAG[C/G]CCTGGCTGTCCTGGA | 226098 |
rs224159093 | in-del | -/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36587117 | AATTGTTGCTGGTCA[-/T]CAAAAGATCACCTTG | 226098 |
rs224173980 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36590076 | TAGACACTAGAACAT[A/G]GTGGTGAAGGTTCTT | 226098 |
rs224254857 | in-del | -/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36580965 | AAAGGATTCTGCGAC[-/T]TCATTAACATGCATG | 226098 |
rs224341303 | in-del | -/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36609612 | ACAGAACAGTACAGA[-/T]TTTTAGGTCTGATGG | 226098 |
rs224346432 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36590690 | ATTATGTAAACATAC[C/T]ATATTTTCTTTATCC | 226098 |
rs224412630 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | Hectd2, 1500017E21Rik | Mm_Celera | 19:36619410 | ACACTACACAGCAGC[C/T]GAAGAATCATGGGAT | 226098 |
rs224431346 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36612557 | ATGCCTTGTTTGTTT[A/C]TTTTGGTTGCTTATG | 226098 |
rs224449134 | in-del | -/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36606535 | TTTTTAAGTTTTTTT[-/C]CCCCCAATCTATAGT | 226098 |
rs224453660 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36567189 | AACTGATCTGGAGTT[C/T]GGCCAGCAAATTCCA | 226098 |
rs224484020 | snp | C/T | | | intron-variant, nc-transcript-variant, downstream-variant-500B | Hectd2, 1500017E21Rik | Mm_Celera | 19:36621243 | ACTAAATCATACACT[C/T]TCAAGAGCTATGTAG | 226098 |
rs224527195 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36574144 | TTGGCTTCACTCCTC[C/T]ACTCCTTCGCCTCCC | 226098 |
rs224543305 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36569690 | AAAACACAAATCTTT[G/T]AAGTTTGGAATGCCC | 226098 |
rs224576634 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36575340 | GCTAACGTTCTGTGA[A/G]TCACAGGGTTCCCTC | 226098 |
rs224613757 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36567686 | TTCAGCCTCCAATAC[G/T]AATAACCTTTTAAAA | 226098 |
rs224693984 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36612982 | CCTGGTAGACTTTTA[G/T]GGTGCTTTGACTTGT | 226098 |
rs224731248 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36575245 | GTCATGCTTAAGAGT[G/T]TTACGTACACTTCGC | 226098 |
rs224848922 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36576653 | TCTGAAGAAAGAAAT[C/T]GAAAAAAACTCTCAG | 226098 |
rs224908875 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36570693 | TGAACTTAGGACCTT[C/T]GGAAGAGCAGTCAGT | 226098 |
rs224934849 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36578209 | ATTTATCTTCAAAAA[C/T]GTCCGTTTGTTCTTT | 226098 |
rs224938370 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36572279 | TCTAAATGTGTTCCA[A/G]CTAGCTAAATTTCCA | 226098 |
rs224968481 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36577927 | TTCAGTTTTCACTTT[A/C]GTTTCTATGGCTTCA | 226098 |
rs225028803 | in-del | -/G | | | intron-variant, upstream-variant-2KB | Hectd2, LOC105246565 | GRCm38.p3 | 19:36555085 | TGTTTGCTTGTTTTC[-/G]GGGGGGTCTGGCTCC | 226098 |
rs225029364 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36570134 | TTTAGGTCAGAAGTC[A/G]GGGTGGATGTTGCTA | 226098 |
rs225090366 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36573278 | TTTGTTGGTAATTCA[A/G]GAAAGAGTGGATATG | 226098 |
rs225139563 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36597609 | AAAGCACATTACTTC[C/T]TCCCCTCAGGACTAT | 226098 |
rs225149129 | snp | C/T | | | intron-variant, upstream-variant-2KB | Hectd2, LOC105246565 | Mm_Celera | 19:36555599 | CTGGTTTTGACATTT[C/T]TATTTGACATAGTAT | 226098 |
rs225164534 | snp | C/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36602377 | AAATCATCTTGCATT[C/G]AATATGGGAATATTA | 226098 |
rs225190892 | snp | G/T | | | synonymous-codon, intron-variant, nc-transcript-variant, upstream-variant-2KB | Hectd2, LOC105246565 | GRCm38.p3 | 19:36554828 | CGGAGCGCCGCCGGC[G/T]GTAGCCGCGGCCGCC | 226098 |
rs225197235 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36598245 | GGATTACAGGTGGAC[A/C]CTGCCATGTGTGGCT | 226098 |
rs225325930 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36591837 | CCATTCTGTAGGCTG[A/C]CACTTTATCTGAATA | 226098 |
rs225354093 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36591273 | CTGCTGTTGTGGACA[A/G]TCGGAAGCAGTTCCA | 226098 |
rs225392117 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36605123 | TAAATAAATTCCCTT[C/T]TCATTGCTCTTCATT | 226098 |
rs225404911 | in-del | -/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36577636 | CTTCTCTCGTGGTGT[-/G]GGGGTGGGAGGCCTT | 226098 |
rs225434955 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36594643 | TGGTTTTAGAGGCTT[A/G]GATAATGGGTTGAGT | 226098 |
rs225464677 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36576856 | AGGGTAGTGAAGACT[A/C]TTCTCAACAATAAAA | 226098 |
rs225477177 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36575259 | TGTTACGTACACTTC[A/G]CTGTACTTGGTAAAA | 226098 |
rs225553109 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36598032 | ACTTTGTGAGTACAA[C/T]ACACCACGTCCTTCT | 226098 |
rs225599294 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36601085 | TTCTGACCTATTTCT[G/T]GGCCATCAACACTTG | 226098 |
rs225622614 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36577221 | TGTAATTTTTGTACC[C/T]GTGTCTTTAGTTATT | 226098 |
rs225640254 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36577414 | TCTTTTCCACATTGG[A/G]GACTTTCGATCAGAA | 226098 |
rs225640653 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36600714 | CTTCCATTGAGCTAT[A/G]TCCCACCTACACTGC | 226098 |
rs225646497 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36570941 | TGGGGCCTCAAGTCT[C/T]TCAAGCATTAGCTGC | 226098 |
rs225702850 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36579794 | ATGAAACTGTAGACC[C/T]CCTCATTTTAGGCCA | 226098 |
rs225712966 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36571534 | CTCTGGTACATTCTA[A/G]AGGGTCCCTCCACCT | 226098 |
rs225731930 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36594731 | CAGGTTTTCAGCTTC[C/T]AAGCTGGAGATAAGA | 226098 |
rs225758352 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36584440 | AAAATCAAAGTGCAT[A/C]ATTTGAAGCACTTAC | 226098 |
rs225768778 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36593874 | TCTGAGATTCTTTTT[C/T]CCATCTTTTATATTC | 226098 |
rs225801797 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36558995 | GTCTATGGACCAGAG[G/T]CCTTACAGAGTTTAT | 226098 |
rs225857623 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36574246 | CTCAAAGAGCTCAGC[C/T]GTTTTCCTTTTCCTC | 226098 |
rs225868883 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36579188 | TTGAATTGTTGTTGG[A/T]ACAGAAAATAAGACA | 226098 |
rs225891209 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36585088 | CAGTAGTGACTTAAA[A/C]AGTGTATATATTTTT | 226098 |
rs225893554 | in-del | -/AAA | | | intron-variant | Hectd2 | Mm_Celera | 19:36587305 | AAGTAAAATTAATGT[-/AAA]AAAAATCACAAAATA | 226098 |
rs225995490 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36579875 | TGTGAAAAATTCCAA[A/G]GGGCTGATAGTGTGA | 226098 |
rs226031573 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36599271 | CTTAAGTGCACATGA[C/T]TCACTACGTATTCAT | 226098 |
rs226069850 | snp | A/G | | | upstream-variant-2KB | Hectd2 | Mm_Celera | 19:36552066 | GCACATCAAGCGATA[A/G]ATTAATGTGATAGAA | 226098 |
rs226123648 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36607021 | TATTCCTACACTGGT[A/G]GAGCAAAGAGAGGTT | 226098 |
rs226123852 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36598730 | GAAATAGTATTGGTA[A/G]GATCTTACATCTTTT | 226098 |
rs226157491 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36605988 | AGCTTCAGTAATAGT[A/G]TCAGGCCATGGGACC | 226098 |
rs226215151 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36592423 | ATCCATCTTTAATCC[A/G]TGGTGGCCTGAGAGA | 226098 |
rs226264266 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36574672 | ATACATACATATCTT[C/T]CCTACATGTACATCA | 226098 |
rs226308252 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36580192 | AGCACAGAGACCCAG[A/G]TTGCTTCTCTTGAGC | 226098 |
rs226347293 | snp | C/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36582950 | AAGTGAAGCTGTTTG[C/G]TGAGCCGTGGAATAA | 226098 |
rs226431680 | in-del | -/TTAT | | | intron-variant | Hectd2 | Mm_Celera | 19:36569947 | ACTGGATAACGAAAC[-/TTAT]TTATATAGTTTAGAA | 226098 |
rs226433482 | in-del | -/TT | | | intron-variant | Hectd2 | Mm_Celera | 19:36580318 | TTTTCATTTTGATTA[-/TT]TTGCAGTTGTAGAAA | 226098 |
rs226446498 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36577166 | CCCCAAATTTATGAT[C/T]TTTCTCCTTCAACTT | 226098 |
rs226536526 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36609796 | AGTTAAGAGCTCTTA[C/T]TGCTTTGGTAGAACG | 226098 |
rs226625480 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36558281 | TATTTAATGGGCTGA[A/C]TGGGAAAGAGAGGTT | 226098 |
rs226627054 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36592917 | GAATATCTTTTTTTT[G/T]GTAACCCTTTACCCT | 226098 |
rs226630611 | snp | C/T | | | upstream-variant-2KB, downstream-variant-500B | Hectd2, LOC105246565 | Mm_Celera | 19:36552529 | TCCAGTAGGTACACA[C/T]AAAAAGTTTTTCGTG | 226098 |
rs226664245 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36560773 | CAGAATGCACATCTG[C/T]TTATTCTCCCATTCA | 226098 |
rs226682107 | snp | A/G | | | upstream-variant-2KB, nc-transcript-variant | Hectd2, LOC105246565 | Mm_Celera | 19:36553147 | ATGAGATAGTCCGGA[A/G]ATTTAAGAAGAGAGG | 226098 |
rs226822887 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36576763 | AGATTCAGTGCAATC[C/T]CCACCAACATTCCAA | 226098 |
rs226876710 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36610158 | TACCAACAGAAAACA[C/T]GCAGGCACAGCACCA | 226098 |
rs226925697 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36581131 | CTCTTAGGCTCTGCC[A/C]AAACCAAGTTCTCTT | 226098 |
rs226932736 | snp | C/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36575103 | GAGTAGGAGATAAAT[C/G]TTCTGTGCTGGCTTG | 226098 |
rs226948667 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36602500 | ACTGGCTTAAAAGTT[A/C]ATCTGTAATAGCCAG | 226098 |
rs226963291 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36580462 | ATATACTACCTACCA[A/G]CCCTCGTCATGCTTG | 226098 |
rs226990601 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36557659 | AATGCAAGCTTTTTT[G/T]TTTGTTTGGTTTTTG | 226098 |
rs227029414 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36556985 | AGCCTAAGGAAAAAA[A/T]ATGCTGACATCTGAA | 226098 |
rs227031410 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36564804 | TCTTGTCACTGCCTT[C/T]ATTCTCTAGCTTCCC | 226098 |
rs227068743 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36563991 | AAGCAGTTTTGGAGG[A/G]TGGAGGATAATCAAA | 226098 |
rs227073221 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36578133 | GTCATGAAAATAAGA[A/T]AACTTTTTGTTGTAG | 226098 |
rs227078191 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36559060 | TCTCTTTTTGTTAAT[C/T]GATCTCAATAAAAGC | 226098 |
rs227088255 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36557773 | CCACCTGCCTCTGCC[C/T]CCCAAGTGCTGGGAT | 226098 |
rs227110538 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36558430 | TGTGTGTGTACATGT[A/G]TATTTTGCTGAGGAT | 226098 |
rs227166681 | in-del | -/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36565452 | GTGAGGTGCCAAGAT[-/G]GTTTTTGAAATTTGA | 226098 |
rs227191196 | in-del | -/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36577293 | TTTCTTATGTCATGA[-/T]TTTTTTTAATCCATC | 226098 |
rs227219738 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36579546 | GGGTGAGACACTAGG[C/T]GTGGCTTGAGCATCT | 226098 |
rs227225571 | in-del | -/A | | | intron-variant | Hectd2 | Mm_Celera | 19:36556637 | CAGTGGAATAAGGTT[-/A]AAAAACTCTTACTTG | 226098 |
rs227260764 | in-del | -/T/TT/TTTT | | | intron-variant | Hectd2 | Mm_Celera | 19:36592908 | TTTGTTTAGAATATC[-/T/TT/TTTT]TTTTTTTTTGTAACC | 226098 |
rs227329021 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36568721 | AAGATTTGGGACAAC[A/G]GGTCAAAAGAATCCA | 226098 |
rs227339138 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36577827 | TCTCCAAAGAATGTA[A/C]ATTTCTGGATTTCCA | 226098 |
rs227342168 | in-del | -/A | | | intron-variant | Hectd2 | Mm_Celera | 19:36602573 | TCTTTTCTTTAAAGT[-/A]ATTTTTTTTCACTTT | 226098 |
rs227427601 | in-del | -/TGGGG | | | intron-variant | Hectd2 | Mm_Celera | 19:36597848 | ATCACTGAGCTTTGC[-/TGGGG]TGGGTTACTAGGAGC | 226098 |
rs227443453 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36562273 | TTTGTGTCTTTTATT[C/T]TATTATTTTATGTGT | 226098 |
rs227474430 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36561344 | CAGTGGATGAATGAG[A/G]AAGTGGGTGGAGCTG | 226098 |
rs227481588 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36606044 | GACCTGTCTCTGAAC[C/T]TTCTTTTCCTCAGGC | 226098 |
rs227492222 | in-del | -/A | | | intron-variant | Hectd2 | Mm_Celera | 19:36585279 | TTTTTAAAAATTACT[-/A]AAAATCATTCTTATA | 226098 |
rs227562719 | in-del | -/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36571057 | TGTGTGGTGGGGGGT[-/G]GGGGGATCCAGGTTA | 226098 |
rs227574528 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36611295 | GTAAGGGACCCACAG[C/T]CTGTATCCTTACAGT | 226098 |
rs227586020 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36573578 | GAAACCTGGGGCAGG[A/G]GTTGCTGTCTGGGGT | 226098 |
rs227605071 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36604383 | TTCCAAAATGGTTTA[A/G]CCTTATTTCTAACAT | 226098 |
rs227614111 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36560911 | GAGACCACTTTGCTA[A/T]TTTTAATTCTTTGTC | 226098 |
rs227617130 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36604128 | ATATGTAATTGATTT[A/G]TGAAATTATTTATGT | 226098 |
rs227648003 | snp | A/G | | | intron-variant, downstream-variant-500B | Hectd2 | Mm_Celera | 19:36611862 | GGAAGTTTAGGAGAA[A/G]GTGATGAGTCAGATT | 226098 |
rs227666105 | in-del | -/CCCAA | | | intron-variant | Hectd2 | Mm_Celera | 19:36594324 | TCATATTTTGGTGAC[-/CCCAA]CCATAAATTATTTTT | 226098 |
rs227675788 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36600370 | GCACATACTAATTTT[C/T]ATGTATTTTATTTTT | 226098 |
rs227684901 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36585803 | CTGGAAGATTAGCGG[A/G]TGTTCTTGACTTCAG | 226098 |
rs227722806 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36581974 | ACAGACAAGTAGGGT[A/T]GCTCACCTCAAGGCT | 226098 |
rs227727013 | snp | C/T | | | upstream-variant-2KB, intron-variant | Hectd2, LOC105246565 | Mm_Celera | 19:36554474 | TCTCCTCAGCGGTCC[C/T]CGCGCGTGACGCGGG | 226098 |
rs227753575 | snp | A/C/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36587917 | ATAGGGTTTGGTGTC[A/C/T]GCATGTGGGATGGAT | 226098 |
rs227755943 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36581326 | TGTGGGAAGTGATAG[A/G]AAAGGGTAATTCTAG | 226098 |
rs227883785 | snp | A/C/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36579929 | GTCAAGCAGCCCTTA[A/C/T]ACCCCCAGGTTGGCC | 226098 |
rs227910430 | snp | C/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36586513 | GACTTTGGGGCACTA[C/G]GATAAAACAGTTTTT | 226098 |
rs227932660 | in-del | -/CTA | | | intron-variant | Hectd2 | Mm_Celera | 19:36579162 | TTTTCTAAGTCCTGT[-/CTA]CTTTGTTTTTGAATT | 226098 |
rs227943121 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36614266 | CCTGCCTCTGCCTCC[C/T]GAGTGCTGGGATTAA | 226098 |
rs227943749 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36609113 | CAAAATATTTATAGT[A/G]TGTAAATAAAATGAA | 226098 |
rs227959756 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36589774 | AGAATATCATTAGGA[C/T]TCACTTTATTGTTAC | 226098 |
rs227970200 | in-del | -/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36592909 | TTGTTTAGAATATCT[-/G]TTTTTTTTGTAACCC | 226098 |
rs227972505 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36607731 | ACCTTTTTACTAACT[C/T]TGACCTATTTGAACT | 226098 |
rs228002428 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36607244 | TGACCAGGTAACATG[C/T]GTTAATAATCAGTAC | 226098 |
rs228005382 | snp | G/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36615730 | GTTGGTTGGTCGGTC[G/T]GTCAGTTGGTCAATC | 226098 |
rs228032091 | in-del | -/A | | | intron-variant | Hectd2 | Mm_Celera | 19:36576039 | TATATAAACAAACTC[-/A]AAAAAAAAAAAACCC | 226098 |
rs228082498 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36561209 | TTAGATGAATTTCTT[C/T]TTGAAGAAGAAAAAT | 226098 |
rs228086154 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36584397 | ATCTGCTATGTAACC[A/G]TTCTCTAAAAGCTGT | 226098 |
rs228102278 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36576228 | TGGAGAGAAACTTGA[A/G]TCAATCCCACTAAAA | 226098 |
rs228139436 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36590396 | CCAGTTCTCCCCTGA[C/T]CCTCCCATTCCTGTT | 226098 |
rs228142791 | snp | C/T | | | missense, nc-transcript-variant | Hectd2 | Mm_Celera | 19:36584001 | TCTGTGGAAGCGTTA[C/T]CATCTGAAGTGAAGG | 226098 |
rs228159909 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36581923 | AGGAAGATTCAATTT[A/G]AGTTACTGTCTTAGT | 226098 |
rs228192728 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36607143 | GAACTGAAGCTGTGT[A/G]GAAGAGAGGGAAGTT | 226098 |
rs228224447 | snp | C/G | | | intron-variant, downstream-variant-500B | Hectd2, 1500017E21Rik | Mm_Celera | 19:36621552 | CAAATAAATCTACTT[C/G]TAACATTAAGGGGTT | 226098 |
rs228233609 | in-del | -/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36577470 | ATTTGCACTAGGGAA[-/C]AAAATAATTGAAATC | 226098 |
rs228289341 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36563056 | CTAAAAAAAGTATCT[C/T]GCTGAAGCTTCAGTG | 226098 |
rs228344382 | snp | C/T | | | upstream-variant-2KB, nc-transcript-variant | Hectd2, LOC105246565 | Mm_Celera | 19:36553394 | ACAGTAGGCACTATC[C/T]GATTCACTTTATTGC | 226098 |
rs228353946 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36557799 | GGGATTAAAGGCGTG[A/C]GCCACCATGCCCGGC | 226098 |
rs228358550 | in-del | -/GAC | | | intron-variant, downstream-variant-500B | Hectd2 | Mm_Celera | 19:36611701 | AAGTGGTGTAATAGA[-/GAC]GGTGCCGCAGACTCC | 226098 |
rs228438271 | snp | C/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36589652 | GCTGTGTATTCTAAG[C/G]TCTCTCACTCTCTGC | 226098 |
rs228448332 | snp | C/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36612091 | AACTGGTCTACAGAT[C/G]TAGCCACTGTGTATG | 226098 |
rs228494327 | in-del | -/TTC | | | intron-variant | Hectd2 | Mm_Celera | 19:36560729 | GTCTCTCAACTCTTT[-/TTC]TCTTTTCTTTTTTTT | 226098 |
rs228513519 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36566743 | GTGTCTGGATACAAA[C/T]CCCAGTTCTCCTGCT | 226098 |
rs228534460 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36583894 | TTGCTAACTTGAAAA[A/G]GCGTTGATTCATTAC | 226098 |
rs228537866 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36612719 | AATAACAGTAGTGCT[C/T]TTCTTTCAGCCTTTC | 226098 |
rs228584049 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36560012 | TACATATGACCTGAT[C/T]TAGTGGTCCATGCTT | 226098 |
rs228615987 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36560649 | AAAGAGTTTTCAGTT[A/C]AGAAAAGAAGGCTGG | 226098 |
rs228659069 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36591367 | CCAAAATAACCACTA[C/T]ACTGGCTCTTGAGAT | 226098 |
rs228669058 | in-del | -/TT | | | intron-variant | Hectd2 | Mm_Celera | 19:36559653 | CAGGGGAAAAAAGAC[-/TT]AGTTCCAGAAAGAGT | 226098 |
rs228686393 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36605839 | ACATGTGAACATACA[A/G]ACATGTATACATGCA | 226098 |
rs228723495 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36592015 | ATCAGGTTCAGTTTA[C/T]CCTATTTTATGTTGA | 226098 |
rs228838831 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36586366 | CAACCGTAAAATTAT[C/T]TCCATCGCTACTTCA | 226098 |
rs228846511 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36558355 | AAGATAAATTTTATA[A/T]AACTAGGGAGGTGAA | 226098 |
rs228846959 | in-del | -/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36555921 | TCAGCACAGCAGATT[-/G]TGGACAGCAATGACA | 226098 |
rs228872743 | snp | C/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36585856 | TTTCAGATGCAGCCA[C/G]TTTGTAATATAATTA | 226098 |
rs228899817 | in-del | -/AGGAAGAAGAGA | | | intron-variant | Hectd2 | Mm_Celera | 19:36559689 | AGGAGGAAGAAGAAG[-/AGGAAGAAGAGA]AGGAAGAGGATGGAA | 226098 |
rs228901734 | in-del | -/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36587205 | TCGCTGGTGCTCCCT[-/G]GAGGTCTCAGGAGTG | 226098 |
rs228946193 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36616761 | GTTCATTTTTCATAT[A/T]TGTGCTTGCTAACTC | 226098 |
rs228971741 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36559240 | AGAATCTGAACGAGC[A/G]AAAGGAATATGTAAA | 226098 |
rs228975781 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36570326 | ATATACAGTTCCTTC[A/G]CACATGTCTTCTTAC | 226098 |
rs228998610 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36589201 | CTCCCAGATCCTTTC[C/T]ACCGCCTCTTCTATC | 226098 |
rs229020089 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36594006 | TTTTCAAGTATTGAA[C/T]AGTTTTATTCATTTC | 226098 |
rs229024372 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36566699 | AAAGGTCTCCCCTCA[C/T]CACTTAGCTAGACTG | 226098 |
rs229033418 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36562866 | AGATGGCTCAGTGGT[G/T]AAGAGCACTTATTGC | 226098 |
rs229057590 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36604410 | ACATTTTTAAACTAT[C/T]ATTTCTATGTGCAAA | 226098 |
rs229077999 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36594767 | GGTGTTGGATCTGAA[A/G]AAGCAGGAGTGAGGA | 226098 |
rs229186608 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36589083 | AATTCTTTTAATTAG[C/T]AGTTGGATGTGAGTT | 226098 |
rs229199111 | in-del | -/TGTG | | | intron-variant | Hectd2 | Mm_Celera | 19:36571031 | CTGGTTGAGAGATCT[-/TGTG]TGTGTGTGTGTGTGT | 226098 |
rs229222200 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36584253 | ATAAATAAATGTGTG[A/G]ATAATGAATAGTAGA | 226098 |
rs229273226 | in-del | -/A | | | intron-variant | Hectd2 | Mm_Celera | 19:36579198 | GTTGGAACAGAAAAT[-/A]AGACAAGAGTCTTGT | 226098 |
rs229290898 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36585201 | TTTAAATTATAAGTA[A/C]CAAAATACTAGATAT | 226098 |
rs229351665 | in-del | -/A | | | intron-variant, downstream-variant-500B | Hectd2 | Mm_Celera | 19:36611453 | GGTACTGATGAAAGC[-/A]TACCACTGTGAATGA | 226098 |
rs229358552 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36571601 | TGGCCCTCAGGGCTT[A/C]AGTCCCCCTCCCCCA | 226098 |
rs229415392 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36567256 | TAAAAGCATGTACTA[A/C]CATGAGAATCAAATT | 226098 |
rs229422968 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36618265 | GATGTTCAGTGTGCA[C/T]AGAGGACAACAGCTT | 226098 |
rs229447163 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36611288 | CTCATAGGTAAGGGA[C/T]CCACAGTCTGTATCC | 226098 |
rs229448339 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36605319 | AGTGTTTGTTTGTGA[C/T]CATTGACACTCTAGA | 226098 |
rs229468403 | in-del | -/AA | | | utr-variant-3-prime, nc-transcript-variant | Hectd2, 1500017E21Rik | Mm_Celera | 19:36621043 | TTATTTTTTCTGTAT[-/AA]GTTTTTAGAAGTCCT | 226098 |
rs229468759 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36565927 | TTTTAACTGATTCTC[A/G]TGGTCTGTGAACTTG | 226098 |
rs229478464 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36610619 | TTACAGATGGTGGTC[A/G]TGGGGAACCACAGTA | 226098 |
rs229494999 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36612633 | CAGACACGAGAGGAC[A/G]GGGAGATGAGTGGGA | 226098 |
rs229502278 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36572175 | CCACGCCCAGCTTGT[C/T]CCTTGCTTTCTTATC | 226098 |
rs229502566 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36565087 | GGGTTACATACAGAT[A/G]GTTGTAAGCTGCCAC | 226098 |
rs229545145 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36570232 | CACAAATATTCTTTT[C/T]CAACCTCCTTTTCCT | 226098 |
rs229610179 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36559942 | ATGTAGGGAGAGAAT[A/G]AAAAAATAATAGTGA | 226098 |
rs229651553 | in-del | -/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36593666 | AGGTTAGGAAATTTT[-/C]CTCCTATCATTATTT | 226098 |
rs229690886 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36573565 | TAGGTGCTCACAGGA[A/G]ACCTGGGGCAGGGGT | 226098 |
rs229726823 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36567570 | AGAAGAGGGCATTGG[A/G]CCCCATTACAGATGG | 226098 |
rs229744017 | in-del | -/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36606518 | CTACTAGACTAGGGA[-/T]TTTTTTTAAGTTTTT | 226098 |
rs229750440 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36567022 | CTGTGTGCATGTGTG[C/T]ACATTTTTTGTGTGT | 226098 |
rs229752411 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36608576 | TTTCTTATGTCTTCA[G/T]CCCTCATTTAGCCTT | 226098 |
rs229766810 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36574015 | AGCCACAGACATGCA[G/T]CTTCAGAGGTCTGTC | 226098 |
rs229820931 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36562835 | CTTATTCTAAAAGGA[A/G]TGTTTGGGTCTGGAG | 226098 |
rs229830756 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36598363 | TTTCATTGGAACTGT[A/G]GTTGTTTAAAACAGA | 226098 |
rs229857906 | in-del | -/A | | | intron-variant | Hectd2 | Mm_Celera | 19:36561506 | AGTGGATATTAGCCC[-/A]AAAAGCTCGGAGTAC | 226098 |
rs229907966 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36562326 | TGCTCTCCTAAGGAG[A/G]TGGTAAGCCTCAATG | 226098 |
rs229951635 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36569315 | GTCAGTTGCATGTAC[G/T]ACAGTTTCATCGTCT | 226098 |
rs229966861 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36592108 | ATTCTACGTTCAACT[C/T]TTCAGTTTGGTCAGC | 226098 |
rs229984576 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36607760 | CTTCTTCATGCATGT[A/G]TTATCTTGCTTTACA | 226098 |
rs229986097 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36588419 | CAATCAGTCTTTTAA[C/T]ATTATGTGTATTTTT | 226098 |
rs230000490 | snp | A/G | | | synonymous-codon, nc-transcript-variant | Hectd2 | Mm_Celera | 19:36598977 | ACCTGAAGAATTCCC[A/G]CCTCTAACGAAGTGT | 226098 |
rs230000567 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36591638 | CTCCCTAATGGCTAA[A/G]GATGTTGAAATTTCT | 226098 |
rs230019346 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36574659 | TATATATATTCTCAT[A/T]CATACATATCTTTCC | 226098 |
rs230163179 | in-del | -/GCTGCCGCT | | | utr-variant-5-prime, intron-variant, nc-transcript-variant, upstream-variant-2KB | Hectd2, LOC105246565 | GRCm38.p3 | 19:36554743 | CCGGCCGCCGCTGCC[-/GCTGCCGCT]GCCGCCGCCACCGCC | 226098 |
rs230167600 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36568384 | GATGTTGGGCTGGAA[A/T]GATGCCTCACTGGGT | 226098 |
rs230168005 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36575118 | CTTCTGTGCTGGCTT[A/G]TTTGCCCTAGTAAGA | 226098 |
rs230170449 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36587992 | AAATTTTGGAGATGG[A/G]TGGGTGGCCCCATCC | 226098 |
rs230230545 | snp | A/G | | | synonymous-codon, nc-transcript-variant | Hectd2 | Mm_Celera | 19:36614443 | GTACGACGGCTATGC[A/G]AAGACAGACCTGACC | 226098 |
rs230243150 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36582012 | GGTGAGAGAGACAAT[G/T]GTCTGGTGATAAGAT | 226098 |
rs230268767 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36613926 | CTGCTGATTGGAGAA[A/G]AATGAGTTTGCTTCA | 226098 |
rs230302962 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36618060 | TTTTTGTATGGTCTT[A/G]CAGTATAAACTCTGA | 226098 |
rs230354487 | snp | A/G | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36587795 | GGGGTCCCTGTGCTC[A/G]GTCAGATGGTTGGCT | 226098 |
rs230388428 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36577108 | GGGTTTTGAGTATAA[G/T]AGGCATGCACTGTAC | 226098 |
rs230442217 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36564941 | CTTGAATCTTTATAA[C/T]TTCCTCAGTTTTCTT | 226098 |
rs230445041 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36571111 | GGGGCCTGCCCCCTT[C/T]TTCAGCTTCTTCCAG | 226098 |
rs230509400 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36609884 | TCCAGGGAATCCAAC[A/C]CTTCTGGCCTCTACA | 226098 |
rs230546192 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36610318 | TGGACATATGGCCTC[A/C]TATGAGAGGCCTCAT | 226098 |
rs230586459 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36618457 | ATAGAAGTGAGGGAA[G/T]CAGTATTTAAATTCA | 226098 |
rs230587341 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36571803 | CATTTGTTTTAAGGT[C/T]ACATCTACAGGTTCC | 226098 |
rs230669965 | in-del | -/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36566239 | AGTAGGCTGAGCCCT[-/C]CTGCATTAATTAGCA | 226098 |
rs230678473 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36564051 | AGAAATTGGCACTTA[A/T]TGAAAACTGAATACC | 226098 |
rs230704042 | in-del | -/GGTTGGTTGGTTGGTTGGTTGGTC | | | intron-variant | Hectd2 | Mm_Celera | 19:36615702 | GTTGGTTGGTTGGTT[-/GGTTGGTTGGTTGGTTGGTTGGTC]GGTCGGTCAGTTGGT | 226098 |
rs230730196 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36591129 | GATAACATTTGAAAT[A/G]TAAATAAATAAAATA | 226098 |
rs230760571 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36612748 | TCTACTATATAGAGA[G/T]AGAGAGAGAAATGTG | 226098 |
rs230827547 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36573887 | TTATATGATTCAAAA[A/G]TGGGCTCACTTTAAG | 226098 |
rs230852026 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36589994 | CAGATTGTAGTTCAA[A/G]GGCTTTGTGATTGAG | 226098 |