SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs230874298 | in-del | -/A | | | intron-variant | Hectd2 | Mm_Celera | 19:36568315 | CTAAATAAAGAAGTG[-/A]AAAAAGAACCTCTTC | 226098 |
rs230885018 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36567496 | CTAATAACCTTTTTT[A/T]AAAAAAAAGATTTAT | 226098 |
rs230905757 | snp | C/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36596853 | ACTTTAAAGCCATGC[C/G]TAATGGTGCACAGCT | 226098 |
rs230940962 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36590529 | ATTTACTCAGTGGTT[A/C]ATATCCAGATATAAG | 226098 |
rs230957148 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36561184 | ACTCTGAACTCCTCA[A/G]TGTAAGAATTTAGAT | 226098 |
rs231072156 | in-del | -/CCATTCCATTCCATTCCATT | | | intron-variant | Hectd2 | Mm_Celera | 19:36564851 | TTCACATGATTTCTG[-/CCATTCCATTCCATTCCATT]CCATTCCATTCCATT | 226098 |
rs231102807 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36592078 | CAGGGTGTTAAGTCT[A/G]TATCAATTTGCATTA | 226098 |
rs231108164 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36568032 | CCAAGCTCATGAACA[A/G]TCCAGAACCTGAGCT | 226098 |
rs231156042 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36574301 | GCTGAGGTTTACAGT[G/T]TGTCTGTCTGGGGCT | 226098 |
rs231190786 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36613470 | CAACCCTTTCACAGG[A/G]ATAACATATCAGATG | 226098 |
rs231195966 | snp | C/G | | | upstream-variant-2KB, nc-transcript-variant | Hectd2, LOC105246565 | Mm_Celera | 19:36553683 | GTGGTACAGTGAATA[C/G]TTCCTCTCTCCCTTC | 226098 |
rs231229614 | snp | C/T | | | upstream-variant-2KB, downstream-variant-500B | Hectd2, LOC105246565 | Mm_Celera | 19:36552788 | CTGGAGCAGTAGAAA[C/T]GAACACTTCTGACTT | 226098 |
rs231240105 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36607321 | TGTGGTGAGGTGGAG[A/G]AGATGGGATATGTGT | 226098 |
rs231242221 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36599123 | AATACTGGAGAGATA[A/G]CTTTAACTTTTAAAC | 226098 |
rs231275000 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36587010 | TGTACATATCTAAAA[A/T]ATATGCCAAACATTT | 226098 |
rs231290330 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36606621 | TTCATATAGATGCAA[G/T]ATCAAGCCTCCATAG | 226098 |
rs231320100 | in-del | -/GGTCAAAGGCCACCAGCTG | | | upstream-variant-2KB, intron-variant | Hectd2, LOC105246565 | Mm_Celera | 19:36554289 | GAGCGCGAGTTTAAA[-/GGTCAAAGGCCACCAGCTG]GGTCAAAGGTCCCCG | 226098 |
rs231367900 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36592516 | CAATTTTAGAGAAAG[C/T]CTCATAAGGTATAGA | 226098 |
rs231389956 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36581409 | CCTCGCTATTAATAA[A/G]AATGTTTAAACATAA | 226098 |
rs231422733 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36580712 | ATATGTCAGAACGAA[G/T]ATTTTCCTCTTTTAT | 226098 |
rs231442162 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36595322 | TATATCAGATAACTA[C/T]TACATGGCAATAGTA | 226098 |
rs231442693 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36586436 | CTTTTGCAGATAGAG[A/G]TTTGCCGAAGGAGTT | 226098 |
rs231472814 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36599785 | AATAACTGGATTTGA[A/G]GTTTATATAAATAAA | 226098 |
rs231478566 | in-del | -/A | | | intron-variant | Hectd2 | Mm_Celera | 19:36602448 | AGCCATGCTGCCCTT[-/A]AAGAATGACATTAAA | 226098 |
rs231494381 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36589123 | ACATTCTTCCCCTTT[C/T]ATTAAACATAGATTC | 226098 |
rs231552125 | in-del | -/GGGGGG | | | upstream-variant-2KB, intron-variant | Hectd2, LOC105246565 | Mm_Celera | 19:36554568 | GCGCACGCAGGGGGT[-/GGGGGG]GGGCGGCGGAGCCTG | 226098 |
rs231586706 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36576424 | TGACCCTAAAAATTC[C/T]ACCAGAGAACTCCTA | 226098 |
rs231648500 | in-del | -/A | | | intron-variant | Hectd2 | Mm_Celera | 19:36561856 | AAGCACGGGGTCCCC[-/A]ATGGAGAAGCTAGAG | 226098 |
rs231702511 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | Hectd2, 1500017E21Rik | Mm_Celera | 19:36619167 | CTGGGAAAGACAAGT[A/G]CAGTAAGAATGCATC | 226098 |
rs231780491 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36566141 | AAACTATGGAGGAAC[C/T]GCCTTACTGGCGTTC | 226098 |
rs231783110 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36594372 | TGTTATGAATCACAA[C/T]GTAAATATCTGATAT | 226098 |
rs231787856 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36602259 | TGATGATATTTCAAA[A/C]TATAAAAATAAGAAT | 226098 |
rs231798118 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36578050 | GTTTAGCTGTCATGA[A/G]TCTAAGTCAGTGTTT | 226098 |
rs231812131 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36572201 | TTATCGGTACAGATA[A/C]TTTGATTTGTGAACT | 226098 |
rs231845471 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36588548 | TTCAAAAAATAAGTT[A/G]CTGGCTTTAAAGAAA | 226098 |
rs231892509 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36594786 | CAGGAGTGAGGAGGG[A/G]CCGCTGTCAACCTGC | 226098 |
rs231945089 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36578285 | TATTGTATATACATA[C/T]AAACCTATCACATAC | 226098 |
rs231983143 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36590457 | CCCTTCCCAGGGAGA[A/G]CATGCACCTCCTCCT | 226098 |
rs231999207 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36604788 | TCTTGCATGTACACT[A/G]CTGCAGTCAGACCAT | 226098 |
rs232018304 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36597425 | ATTATTGAAAATATC[A/G]ACCACTTGCAGTTTT | 226098 |
rs232033821 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36603910 | GTATCCACAATAGTT[C/T]AAGCCTGAGCTTAGC | 226098 |
rs232061994 | in-del | -/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36577321 | ATCAGAAGAAAAACC[-/G]ATAGCTTTCTAAGAT | 226098 |
rs232120455 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36574560 | ATCTGTAATGGGATC[C/T]GATGCCCTCTTCTGG | 226098 |
rs232126838 | snp | A/C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36589604 | GTTCCCTGAGCTCTG[A/C/T]GGGAGGGATTTGATG | 226098 |
rs232147630 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36597772 | TAATAATTCCTATTA[C/T]TGATAGTAGAATTCA | 226098 |
rs232190854 | in-del | -/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36585327 | TAATTGCCTTAATTC[-/T]TTTTTTGGTCATCAG | 226098 |
rs232204734 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36598305 | AAAAAAAGCATAAAA[G/T]ATTAAAAATATGATA | 226098 |
rs232245595 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36618364 | TCTACTAGGTATTTT[A/G]CATAGATCACAGTCT | 226098 |
rs232248754 | snp | A/G | | | upstream-variant-2KB, nc-transcript-variant | Hectd2, LOC105246565 | Mm_Celera | 19:36553461 | CCAGGAAGAACTGTA[A/G]CTATTTATTTAGTTC | 226098 |
rs232269509 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36556284 | GCAATGTTATGAGTT[C/T]AGTGTCTAACAGCAA | 226098 |
rs232276466 | in-del | -/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36582700 | CCTATTTTTCTAAGA[-/T]TAAAAAAGGGCAAGT | 226098 |
rs232283973 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36569188 | TATTTTATGAGTAGA[C/T]CTTGTTAAACTCATA | 226098 |
rs232305435 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36572859 | TAGGTAAGCCTGTCA[A/C]GTTGGCTGTCTTTTG | 226098 |
rs232410055 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36596719 | TTAATTGGATAATAA[C/T]GATTGCCAGCATTTA | 226098 |
rs232413498 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36593666 | AGGTTAGGAAATTTT[C/T]CTCCTATCATTATTT | 226098 |
rs232481796 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36566651 | CCATTCCTGCTACAC[G/T]TCCTCATTTGTTCTC | 226098 |
rs232567913 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36598188 | ATGTATCCCAGGGGA[C/T]TTCTAACTCACAATC | 226098 |
rs232603030 | in-del | -/GCTCGTTCCAG | | | intron-variant | Hectd2 | Mm_Celera | 19:36561121 | GCCTTTTCCGATCGA[-/GCTCGTTCCAG]TCTCGTTCCAGTCCA | 226098 |
rs232613654 | in-del | -/A | | | intron-variant | Hectd2 | Mm_Celera | 19:36568362 | AACTATCATTAGATT[-/A]AAAAGAGATGTTGGG | 226098 |
rs232679126 | in-del | -/TA | | | intron-variant | Hectd2 | Mm_Celera | 19:36592174 | TATTTCTGGCCTCTT[-/TA]TCAAATATCAGGTGT | 226098 |
rs232693993 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36570825 | GTCTGCCCTCCGACA[G/T]TTTCTCATCCCATTT | 226098 |
rs232709322 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36558834 | TCCTAGTTATACAGG[A/G]CCAGTTAGTTCTACT | 226098 |
rs232733053 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36576795 | TCAGTTCTTCACCGA[G/T]GTAGAAAGAGCAATT | 226098 |
rs232740931 | in-del | -/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36556934 | TATTTTTCAAGAGGA[-/T]TTTCAGAGCTGAAAT | 226098 |
rs232749087 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36560124 | GTCAGTCAATCAGTC[A/G]GTCTGTCTGTCTCTC | 226098 |
rs232754456 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36580408 | GCTAATAATCTCACT[C/T]CTTTATACATAACTA | 226098 |
rs232768774 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36617432 | GCAGGGTTATTTGCT[C/T]AACAGAATTTTTTGG | 226098 |
rs232810039 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36559426 | GCCTTTGGAATTCCT[C/T]GAATAGAGGAACAAC | 226098 |
rs232872607 | in-del | -/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36600967 | TAAATTTATGACTGC[-/T]TTTTTATGCTATAAT | 226098 |
rs232898756 | snp | C/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36582205 | TGAGGTTTTCAAAAG[C/T]TCAAGCCAGGGCCAG | 226098 |
rs232927851 | in-del | -/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36590603 | TGAGGATGAGGGTGT[-/G]GTTTTTTTTCTTTCT | 226098 |
rs232965839 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36564264 | TAAGATTATTTAATA[C/T]TATAATCTTACATAT | 226098 |
rs232987118 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36558086 | TGCTCAAGAGGCCCC[A/G]GGTGATGGAAATTAG | 226098 |
rs233005713 | snp | C/G | | | upstream-variant-2KB, intron-variant | Hectd2, LOC105246565 | Mm_Celera | 19:36554572 | CACGCAGGGGGTGGG[C/G]GGCGGAGCCTGGCGG | 226098 |
rs233022808 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36557441 | GGGGTGCCATGATGG[A/G]AGAGAGAATGGTAGA | 226098 |
rs233046128 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36578236 | CTTTTGTTTTGTTTT[A/T]AATTTATTGTGTATA | 226098 |
rs233053634 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36579647 | CTATGAGGGCCATTT[A/T]CATTTGAACCACCAG | 226098 |
rs233065028 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36593181 | TCATGCTTGTGTTTC[A/G]CTTCCTTGGATTTTG | 226098 |
rs233080597 | in-del | -/A | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36556978 | ATAAAAAGCCTAAGG[-/A]AAAAAAAATGCTGAC | 226098 |
rs233095515 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36573433 | CACTCTGAAATAGCC[A/G]AAGGGAAGAAAGGTT | 226098 |
rs233137820 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36580147 | GTGCATTAAAGCAAC[C/T]ACTCTGTCTGCCAGG | 226098 |
rs233145062 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36574147 | GCTTCACTCCTCTAC[A/T]CCTTCGCCTCCCAGC | 226098 |
rs233158591 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36605330 | GTGATCATTGACACT[C/T]TAGACTTGTAGGCCC | 226098 |
rs233181544 | snp | A/G | | | synonymous-codon, nc-transcript-variant | Hectd2 | Mm_Celera | 19:36584033 | CCCGCCCCTTCCAGA[A/G]CCTTCTCTTCCTAGC | 226098 |
rs233215296 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36583594 | GAAAAGTTAAGTGTT[A/G]ATAATGTTAAGTTTC | 226098 |
rs233290334 | in-del | -/TA | | | intron-variant | Hectd2 | Mm_Celera | 19:36593233 | CTATGTTTTTGTGGT[-/TA]TAGTTTTCCTCCTTA | 226098 |
rs233311038 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36598282 | CCATTTTAAAATAAC[A/T]GAATCATAAAAAAAG | 226098 |
rs233318885 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36567638 | GGACCTCTGGAAGAG[C/T]AGTCAGTGCTCTTTA | 226098 |
rs233341329 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36560991 | GAATCTAGAATAATG[A/C]ACATGAAAAAGCTAC | 226098 |
rs233354828 | in-del | -/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36609824 | CGCTCGAGTTCAGTT[-/C]ATGGTGCCCATGTTA | 226098 |
rs233361934 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36574579 | GCCCTCTTCTGGTGT[A/G]TCTGAGGACAGCTTT | 226098 |
rs233376925 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36568161 | TGATTTCTACTTCTA[A/G]CCTATCAGAGTTAAT | 226098 |
rs233376949 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36560246 | CAATAGAAAACCACA[C/T]AACAACCTCGTGGAT | 226098 |
rs233415184 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36587622 | CTTGCCTGATTCTAT[A/G]AGGGTGCTCCCCCAC | 226098 |
rs233453142 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36580028 | AGGAGCCTCAGTGAC[C/T]AAGGTTAACAGAGTA | 226098 |
rs233484412 | in-del | -/TAT | | | intron-variant | Hectd2 | Mm_Celera | 19:36597226 | TCATTTTAACTGTGA[-/TAT]TATTATTTTTATGAT | 226098 |
rs233499882 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36576359 | ATGCAAACTGGAAAG[A/G]AAGAAGTCAAAATAT | 226098 |
rs233503836 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36556171 | TGTGTATGGAGGTCA[C/T]ATATACATGTGACCT | 226098 |
rs233540077 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36580206 | GGTTGCTTCTCTTGA[A/G]CAATCTACATAGATA | 226098 |
rs233541955 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36586702 | GAATTTGAAAGAGAG[A/G]AAACAGGGCTATTTG | 226098 |
rs233562683 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36570381 | TTCTTTCAAGGCCAG[C/T]AGCAGGGTTCTTTTC | 226098 |
rs233568148 | snp | A/G | | | upstream-variant-2KB, intron-variant | Hectd2, LOC105246565 | Mm_Celera | 19:36554427 | GCGACCAACATGGCG[A/G]CCAGGCGCCCCCCAG | 226098 |
rs233591572 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36582130 | CCAGGGAGTAGCACT[A/G]TTGGAAAGGATTAGG | 226098 |
rs233596818 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36580680 | TGTATTACAATATCC[A/T]CATATATTGCAGTTG | 226098 |
rs233645381 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36588118 | GGAGGCTCTTGCTTT[C/T]CTGACAGCCTGGTCT | 226098 |
rs233653870 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36602086 | AGTGAGCGCTCACAC[A/G]GTTCCTCTACACGCT | 226098 |
rs233674838 | in-del | -/ATT | | | intron-variant | Hectd2 | Mm_Celera | 19:36590973 | GGGAGCATCAATATC[-/ATT]ATGCTACTTTCTGCT | 226098 |
rs233685734 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36609676 | GGCTTTGTAAACTTG[A/G]GTGAGTTATTTAACC | 226098 |
rs233686707 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36582792 | GGTTAACTATGTATC[A/G]ATGTTTAAAATCATG | 226098 |
rs233773746 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36556856 | AAAATTTCTTTTGAC[A/C]TTGATACTGCTGTTG | 226098 |
rs233796475 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36608085 | AAAACAAAATAATAA[A/T]GTTAAAATGTTATGG | 226098 |
rs233800260 | in-del | -/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36592206 | CCATGGGTGTGCGGG[-/T]TTATGTCTGGATCTT | 226098 |
rs233804472 | in-del | -/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36590941 | TAGGTAGGAGAGAAA[-/G]AAGGTTAGGAGAGGA | 226098 |
rs233830577 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36616033 | TGGCTGAGAGTTCCC[A/G]GAGTGTTGACACATC | 226098 |
rs233831962 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36607481 | TAAGGCCATGTCACA[G/T]TTACTATGGTTAAAT | 226098 |
rs233958822 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36583512 | AAATAAGAGGACAAA[A/G]GCAAATAAAGTCTTA | 226098 |
rs233978822 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36602403 | TATTAGAAGAAATTT[C/T]ATTGCCTATGGCTCC | 226098 |
rs233979027 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36610678 | AGATATGAGGCTCTG[G/T]TCCCTGTGCTTTTAA | 226098 |
rs234005848 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36573869 | ACTTTCTGAATAGCA[A/C]ATTTATATGATTCAA | 226098 |
rs234030453 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36610068 | CACAGTATAAGTGAC[A/G]ATGGTACTTTTTTAT | 226098 |
rs234044778 | in-del | -/CATGTGTACATGCACGTGCA | | | intron-variant | Hectd2 | Mm_Celera | 19:36568529 | ACACGTTTACATGGG[-/CATGTGTACATGCACGTGCA]CACACAGTGTGAGTT | 226098 |
rs234056801 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36579033 | GCATGTTGTAGAGCA[A/G]GACCCCAGACCTGAA | 226098 |
rs234184841 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36558393 | TAAACTGTGTGTGTG[C/T]ACATGCGTGAGTGTG | 226098 |
rs234192513 | snp | C/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36610946 | CTCTTAACATGTGAA[C/G]TGTATGTCTGATGTT | 226098 |
rs234259336 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36603285 | TATTATGTCATAGCA[C/T]ATTAGTGTACTTCAG | 226098 |
rs234309509 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36612446 | TGAATTTTTAAGCTT[C/T]CAATTAGGTTTTAAA | 226098 |
rs234369817 | in-del | -/ACTAAT | | | intron-variant | Hectd2 | Mm_Celera | 19:36595616 | TTTGTTACAAAGCAA[-/ACTAAT]ACTAGCTTTCTCGTG | 226098 |
rs234415593 | snp | C/T | | | upstream-variant-2KB, downstream-variant-500B | Hectd2, LOC105246565 | Mm_Celera | 19:36552468 | TCTTCAGCACATCTT[C/T]ATGCATAGCAGCCAG | 226098 |
rs234428782 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36605581 | GTTTAGTCAGTAAAC[A/G]GCTGGCTGTGTAAAC | 226098 |
rs234433288 | in-del | -/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36617824 | AATGCACCGGCTTTA[-/G]GGTCAGACCTGACTG | 226098 |
rs234470724 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36612918 | GTAATTGCCCCTGCC[C/T]ACTCAAGGGTCTACC | 226098 |
rs234549068 | in-del | -/TTT | | | intron-variant | Hectd2 | Mm_Celera | 19:36587517 | CTCTTAGGAAATATC[-/TTT]TTTTTTTAATTGGAT | 226098 |
rs234563527 | snp | C/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36608914 | CACAGTCTTACTTAA[C/G]CTTTAAATAACTAAA | 226098 |
rs234595689 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36606216 | ATAAAAAGTCAGATA[A/T]AAATATGCCTTCTAT | 226098 |
rs234622994 | snp | C/T | | | upstream-variant-2KB, downstream-variant-500B | Hectd2, LOC105246565 | Mm_Celera | 19:36552567 | CCTTACAAGTTCTGC[C/T]AGAGTTATCATTCTA | 226098 |
rs234646153 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36585617 | TTTTTTAAAAAGATT[A/C]ATTTTTTTAATTTAT | 226098 |
rs234705977 | in-del | -/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36589789 | TTCACTTTATTGTTA[-/C]TTTTTTAAAGACAAA | 226098 |
rs234706219 | in-del | -/TTCAAG | | | intron-variant | Hectd2 | Mm_Celera | 19:36616243 | CTACTGTATTAATAC[-/TTCAAG]TTCAAGTCTCGTGCT | 226098 |
rs234767399 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36601283 | TCATAGGTTTGTAGA[A/G]ATGAACTTATGCACA | 226098 |
rs234835316 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36580626 | CTGAATGAAACCTAA[A/G]TGGCATGTTTTCACA | 226098 |
rs234939272 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36582618 | TGCAAGTTCCCCGAT[A/T]ATAAAAATACAAAGT | 226098 |
rs235019902 | in-del | -/AGGATAGGATA | | | intron-variant | Hectd2 | Mm_Celera | 19:36590793 | TGAGTAAGTGTTCCT[-/AGGATAGGATA]AAGTGTCCTTTGTGT | 226098 |
rs235044471 | in-del | -/AA | | | intron-variant, downstream-variant-500B | Hectd2 | Mm_Celera | 19:36611884 | AGTCAGATTAAAAAC[-/AA]AAAAAAAGAAACACT | 226098 |
rs235096615 | snp | A/G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36576923 | GTATTACAGAGCAAT[A/G/T]GTGATGAAAAGTGCA | 226098 |
rs235111216 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36561801 | CTCTGCCAGAGCCTG[A/T]CATATACAGAAGTGG | 226098 |
rs235138715 | snp | G/T | | | intron-variant, upstream-variant-2KB | Hectd2, LOC105246565 | Mm_Celera | 19:36555179 | GAGGTTTTCCCTGAG[G/T]GGGAGAACCTGCCTG | 226098 |
rs235174624 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36562531 | TGTTTAGGATGAGTA[G/T]AGTTGTGCTGGGGGG | 226098 |
rs235208715 | in-del | -/A | | | intron-variant | Hectd2 | Mm_Celera | 19:36599562 | TCACGTGCATGGTGG[-/A]AAAAGAGCACTATAT | 226098 |
rs235238737 | in-del | -/ATC | | | intron-variant | Hectd2 | Mm_Celera | 19:36616406 | ACAGCTTTCATTATG[-/ATC]ACCCTTGCCCTACGG | 226098 |
rs235260308 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36602735 | TGTCCTTTCACAGAC[C/T]GTGACGGGAGCAGAC | 226098 |
rs235299139 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36570646 | ATATCTCATTACAGA[A/T]GGTTGTAAGTCACCA | 226098 |
rs235303616 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36557990 | CAAATCTGCTTAGCA[A/G]TAGCTGTCAAAGTGG | 226098 |
rs235322542 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36564193 | GCTTGAAAATATATG[A/T]TTACATGTTATTACA | 226098 |
rs235328270 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36571918 | AGTGTGGTGGATAGC[A/G]GTAACCTTTGTTTCA | 226098 |
rs235352738 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36570972 | CTTTTCCCTCATTGA[A/G]GCCATACCAGGCAGT | 226098 |
rs235409019 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36594987 | CTGTTACCTTAAAAT[A/G]CTACAGCTTTCCTCA | 226098 |
rs235418195 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36565452 | GTGAGGTGCCAAGAT[G/T]GTTTTTGAAATTTGA | 226098 |
rs235462591 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36565520 | GACAGTTTCTTCATC[C/T]TCACTGTGCATCAGA | 226098 |
rs235510333 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36589245 | TTTCTATCTCTCATT[A/G]GCAAAGAATAGACTT | 226098 |
rs235514904 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36566367 | GAGAAGCCACCACAA[A/G]TACCTATATCATAAG | 226098 |
rs235519076 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36602956 | CAAACACATTTCCAG[A/T]GAAAAGGACCTCAGA | 226098 |
rs235536127 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36588734 | GAACATGAATGGCAC[A/G]GCCAGTGTGGTGACG | 226098 |
rs235547293 | snp | C/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36558187 | TATTAGAAAAACATG[C/G]TAAATAAAGGAGAAA | 226098 |
rs235567483 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36590035 | CCATTCTCTTTTGGT[A/T]GCCTGCAGAGTACCT | 226098 |
rs235623967 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36559275 | GGGGAAAATAACTTG[A/C]GAGGCCTTAAAGAGA | 226098 |
rs235632075 | snp | C/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36584125 | GTCATCTGCATGTCA[C/G]GGCTATGCATCCGTT | 226098 |
rs235664691 | snp | C/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36618423 | TGGAGATTGGAAACA[C/T]TGAGCAATTCGAAAT | 226098 |
rs235689391 | snp | C/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36584632 | GAGTCTGAGGCAGGA[C/G]AAACACCCCAAGTTT | 226098 |
rs235732036 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36590620 | TTTTTTTTCTTTCTT[C/T]CTAGTTCCATTTATT | 226098 |
rs235741584 | in-del | -/GGC | | | intron-variant | Hectd2 | Mm_Celera | 19:36572892 | AAGCTGAAAAGTGTA[-/GGC]GGCGTTTTACCTACT | 226098 |
rs235744440 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36590950 | GAGAAAGAAGGTTAG[A/G]AGAGGAAGGGAGCAT | 226098 |
rs235766625 | snp | C/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36590340 | CTCAAATGCCCTTCA[C/G]TTCCAGCTGTCTATT | 226098 |
rs235768234 | in-del | -/TGGA | | | intron-variant | Hectd2 | Mm_Celera | 19:36605030 | TATTGTCTGGCAAAT[-/TGGA]TAGATGGATAGATGT | 226098 |
rs235773446 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36585312 | TTAATTTTATTTTCA[A/G]TAATTGCCTTAATTC | 226098 |
rs235814523 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36578091 | TTTAACTTTGAGGCT[A/C]TATAGCCTTTTGAAT | 226098 |
rs235897244 | in-del | -/TCATATCAGCTGGTGTATAA | | | intron-variant | Hectd2 | Mm_Celera | 19:36571013 | TATGTGTCAGGGGCC[-/TCATATCAGCTGGTGTATAA]TGCCTGGTTGAGAGA | 226098 |
rs235912022 | in-del | -/TGATT | | | intron-variant | Hectd2 | Mm_Celera | 19:36587612 | CCATCCCCCCTTGCC[-/TGATT]TGATTCTATGAGGGT | 226098 |
rs235974505 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36561468 | TTTTCTGTCAAAAAT[A/G]CACATGGTATGCACT | 226098 |
rs236007840 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36613149 | CAGATGTTTGTGAGC[C/T]ACCATGTGGTTGCTG | 226098 |
rs236043446 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36593245 | GGTTATAGTTTTCCT[C/T]CTTAGGTTGGAGTTT | 226098 |
rs236047293 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36592814 | CCTTCCCTGTCTCTT[C/T]TAATTAGTTTTGGTC | 226098 |
rs236080672 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36605471 | GACACTGAGAATTTG[A/G]AAGCAAGCCTGTAGG | 226098 |
rs236101862 | in-del | -/AT | | | intron-variant | Hectd2 | Mm_Celera | 19:36579446 | ATTTTCATTATGGCA[-/AT]GAAAGTGTGGTGGCC | 226098 |
rs236118331 | in-del | -/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36557275 | GCCCTGTAATCATGT[-/G]GGGGTTTTTTCCCTC | 226098 |
rs236127455 | snp | C/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36560190 | TGTTGAGTGCATATT[C/G]TGTACTATACATTTT | 226098 |
rs236142758 | in-del | -/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36590724 | TTCTGTTGAGGGACA[-/T]CTAGGCTGTTTCCAA | 226098 |
rs236153134 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36587572 | GTGATCCCCTTTCCC[A/G]GTTTCCCCTCTGCAA | 226098 |
rs236185101 | in-del | -/TTTTT | | | intron-variant | Hectd2 | Mm_Celera | 19:36614149 | CATTTAAGACTATCA[-/TTTTT]TTTTTTTAAATTTGG | 226098 |
rs236193999 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36593334 | TTTTTAATGGAATAT[C/T]TTATTTCCTCCATCT | 226098 |
rs236206306 | snp | A/G | | | upstream-variant-2KB | Hectd2 | Mm_Celera | 19:36552048 | CTCCACATGTGCAAC[A/G]TGGCACATCAAGCGA | 226098 |
rs236217443 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36588033 | GACCATGCCTCTGGA[C/T]ATGGTCTCTGAAAGG | 226098 |
rs236226990 | in-del | -/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36572027 | CTTTTTGGGGGGGGG[-/T]TGGTTTTTTGAGACA | 226098 |
rs236356240 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36570539 | GCTGGAAATTTGAAT[G/T]CAGGTCCTCTGCTTG | 226098 |
rs236404246 | in-del | -/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36592337 | TTCTGTTTTGACACA[-/T]TTTTTTCAGTAGAGA | 226098 |
rs236417798 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36616970 | ACTATGTAAACTGAT[A/G]TCAAAATTATACTTT | 226098 |
rs236475013 | snp | A/G | | | missense, nc-transcript-variant | Hectd2 | Mm_Celera | 19:36609415 | GACGACTTGTGCCAG[A/G]TTATGCCTGTAAGTA | 226098 |
rs236480281 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36617080 | TATAGCTGTATTAGC[C/T]TGTGACCCCTGAACT | 226098 |
rs236507837 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36563238 | TAATTGCATTAATTG[A/G]CCTTTATAGTGGAAA | 226098 |
rs236586576 | in-del | -/AT | | | intron-variant | Hectd2 | Mm_Celera | 19:36613277 | GCCATCATGCCTGTC[-/AT]ATATGTTCCTTCTGT | 226098 |
rs236599108 | in-del | -/A | | | intron-variant | Hectd2 | Mm_Celera | 19:36571062 | GTGGGGGGTGGGGGG[-/A]ATCCAGGTTAGATGA | 226098 |
rs236615617 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36609953 | TAACTTAAAATAAAT[G/T]TTTATGGTAATAGCC | 226098 |
rs236651356 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | Hectd2, 1500017E21Rik | Mm_Celera | 19:36620096 | ATTTTCATCTCAAGA[A/C]TTATTCTTTGATAGT | 226098 |
rs236670374 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36561516 | TAGCCCAAAAGCTCG[A/G]AGTACCCAAGATACA | 226098 |
rs236696633 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36576607 | CTCGAACCAAGCAAG[A/T]GAAAGATCTGTACGA | 226098 |
rs236718693 | snp | C/G | | | intron-variant, downstream-variant-500B | Hectd2 | Mm_Celera | 19:36611603 | AGGGGTCCTGGCACT[C/G]GGGAGTCTCAGACAC | 226098 |
rs236751940 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36566513 | GTTCTAACCTTTAAT[A/G]TGTATGCCTATGATT | 226098 |
rs236773260 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36607407 | GCTGAGCTGTTACTG[A/G]CTTGCTACAAAGCAG | 226098 |
rs236791916 | snp | C/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36572462 | TCTAGACGTCTGGCT[C/G]TTCTGTCTGGATACC | 226098 |
rs236809999 | in-del | -/TT | | | intron-variant | Hectd2 | Mm_Celera | 19:36567489 | TTAATACTAATAACC[-/TT]TTTTTTAAAAAAAAA | 226098 |
rs236932206 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36577780 | ATCACTTCAGATAAC[A/G]TTTCTCCCAGGCCAA | 226098 |
rs236968630 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36583443 | TAAGATCTTAAATAC[A/G]TGCAACTACTTCAAG | 226098 |
rs237056325 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36572720 | ATCTGATCTCCAAGT[A/G]GTGTTAGAGAAGCTA | 226098 |
rs237093628 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36572163 | AGGCGTGCGCCACCA[C/T]GCCCAGCTTGTCCCT | 226098 |
rs237125302 | in-del | -/CATCCATAAGCA | | | intron-variant | Hectd2 | Mm_Celera | 19:36571253 | AGGTGGGGTGGTAGG[-/CATCCATAAGCA]CATTATAGCGTTAGT | 226098 |
rs237143910 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36617796 | AGTGGCAATGCTTTC[G/T]TACATCCTAGCAAAT | 226098 |
rs237195652 | in-del | -/GTGTCT | | | intron-variant | Hectd2 | Mm_Celera | 19:36587904 | TTGGCATCCACAATA[-/GTGTCT]GGGTTTGGTGTCCGC | 226098 |
rs237223708 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36573736 | TTAACTATTCCTAGA[A/G]AAAAGTGCATCTGAA | 226098 |
rs237228367 | snp | G/T | | | upstream-variant-2KB | Hectd2 | Mm_Celera | 19:36552330 | GCCCCATGCCACCCC[G/T]TTCCCCTTTAGGTCT | 226098 |
rs237262274 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36613015 | TGGCCATATAACTTG[A/G]AGTTAGAATACCATT | 226098 |
rs237277363 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36579910 | AGGAAGGTAAGTACT[C/T]GTGGTCAAGCAGCCC | 226098 |
rs237345851 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36611332 | TAATGCTAGTTGATT[A/G]TAAAAGACAGATCAC | 226098 |
rs237354676 | snp | C/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36574364 | GTTTAGAAAACACAG[C/G]TAAGAATTAGTAGCT | 226098 |
rs237363501 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36567883 | AAAACATGGAACAGA[A/G]TTGTTATGAGTTGTT | 226098 |
rs237371956 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36566215 | CCTGCCTAGGGATAG[C/T]ACTCCTCACAGTAGG | 226098 |
rs237372301 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36580255 | CTACTGTTACTATAT[C/T]CAATAGCTATGCAGG | 226098 |
rs237412210 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36558553 | AGATGAGGAACTGTG[C/T]CAAGTAGGCAGTAGA | 226098 |
rs237413642 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36574182 | TGGCTGCCTGCCACC[A/T]TGCAGCCACCATGCA | 226098 |
rs237413739 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36567265 | GTACTAACATGAGAA[C/T]CAAATTTAAGTCTAC | 226098 |
rs237499852 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36594260 | TGATTGTAGGTCTAG[C/T]TTAGTGATTCTTGGC | 226098 |
rs237526986 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36578469 | AGAGATGAGGCATGA[A/G]ATTCTGAGAGATGAC | 226098 |
rs237549707 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36575189 | TAGTATGAAACATCT[A/C]GTTCATTAAAGATGA | 226098 |
rs237558970 | snp | C/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36601367 | AAGGAGGGTACCTTA[C/G]AATCCCTTAGTGTAC | 226098 |
rs237588157 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36574819 | TGAGTTGTGTCCATC[A/C]TTTTTTAAAGAGCAG | 226098 |
rs237660760 | in-del | -/TGCCTC | | | intron-variant | Hectd2 | Mm_Celera | 19:36590461 | CCCAGGGAGAACATG[-/TGCCTC]CACCTCCTCCTCCTC | 226098 |
rs237684677 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36591878 | TTGCCTTGCAGAAAC[G/T]TTTGAGTTTCATGAG | 226098 |
rs237695628 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36576051 | ACTCAAAAAAAAAAA[A/C]CCCAAAACCCCACAT | 226098 |
rs237715556 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36561046 | AGCCCTTGCTATTCC[C/T]ATTATTTGGGCTTTT | 226098 |
rs237805581 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36617786 | GTTGAATGTGAGTGG[C/T]AATGCTTTCTTACAT | 226098 |
rs237807271 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36600293 | TCAGCTGGAATCGGA[A/G]TGGCATCTGGAACTC | 226098 |
rs237819927 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36570754 | CTTTCTTTCTCTTTT[G/T]TAAAATTATTATTCT | 226098 |
rs237827958 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36593614 | TCTACTTAGTGTTCT[A/G]TATGCTTCTTGTACC | 226098 |
rs237840111 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36571054 | GTGTGTGTGGTGGGG[G/T]GTGGGGGGATCCAGG | 226098 |
rs237858730 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36570235 | AAATATTCTTTTCCA[A/G]CCTCCTTTTCCTCCT | 226098 |
rs237858814 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36576726 | TATAGTGAAAATGGA[C/T]ATCTTGCCGAAAGCA | 226098 |
rs237861211 | snp | C/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36586850 | AAGACTAACTTATTG[C/G]AATTAAATGCATCCC | 226098 |
rs237864151 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36593038 | TCTTTTTATTGGGGA[A/T]TTATGACCATTGACA | 226098 |
rs237868042 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36600835 | TTCATACATAGTGTA[C/T]GACTTAGCTCTGATC | 226098 |
rs237869892 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36577007 | TTTACATTGTTTTGT[A/C]TTTGGGGGAATATCC | 226098 |
rs237908266 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36592733 | ATTTTACAAAGGTGG[A/G]TGGCATAGATGTTAA | 226098 |
rs237921286 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36602024 | AGGTGGAGTTTCTCC[C/T]TGGGCCTCTGCTCTG | 226098 |
rs238042577 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36602551 | AGTTGCATTTCTGTG[C/T]CATGTGTCTTTTCTT | 226098 |
rs238048395 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36611127 | GGGCTGTAGAGTTAA[A/G]TCTCTGTAGAATAAA | 226098 |
rs238082520 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36594732 | AGGTTTTCAGCTTCC[A/G]AGCTGGAGATAAGAC | 226098 |
rs238086873 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36602472 | CATTAAACTGGCATA[C/T]TTGACACCAGATACT | 226098 |
rs238100033 | in-del | -/ACTT | | | intron-variant | Hectd2 | Mm_Celera | 19:36565182 | GTCTCTAGCCCACCC[-/ACTT]AGTTTTTAATACACT | 226098 |
rs238110907 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36603112 | ACTGTCCAGAAATAC[A/C]GACGTCCTTGGGAAG | 226098 |
rs238119599 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36589349 | AGAAAGCACAAGAAT[C/T]GGAGACCCACAGGTT | 226098 |
rs238147786 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36616212 | AGCTTGGGGCTTTTG[A/C]AAGGAGCAGAGGTAA | 226098 |
rs238155831 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36595640 | AGCTTTCTCGTGAGA[A/G]AGACATGGATTCAAA | 226098 |
rs238212476 | in-del | -/GAGGAAGAGGAGGAAGAA | | | intron-variant | Hectd2 | Mm_Celera | 19:36559746 | AAAAAGGAGGAAGAG[-/GAGGAAGAGGAGGAAGAA]GAGGAAGAGGAAGCA | 226098 |
rs238328221 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36570050 | ATCGTATTTATCTTC[C/T]GTTGCTGCACAATGA | 226098 |
rs238340144 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | Hectd2, 1500017E21Rik | Mm_Celera | 19:36619060 | TCAGAAATTTATTGA[A/G]TGAGAGCCTATGGCA | 226098 |
rs238362392 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36608128 | TGATATTTTAAAAGT[A/C]GAAATACCTATACCA | 226098 |
rs238384492 | in-del | -/TTTTTTTTTT | | | intron-variant | Hectd2 | Mm_Celera | 19:36570775 | TATTATTCTTTAATC[-/TTTTTTTTTT]TTTTTTTTACAGTCC | 226098 |
rs238405594 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | Hectd2, 1500017E21Rik | Mm_Celera | 19:36620295 | AACTCATCAGCGTCC[C/T]ATAGTTCCGAAGCCC | 226098 |
rs238418565 | snp | C/G | | | upstream-variant-2KB | Hectd2 | Mm_Celera | 19:36552294 | CTCTTTGGATATAAT[C/G]TCTCTAAATCCCATT | 226098 |
rs238419792 | in-del | -/ATAGCAGCAAA | | | intron-variant | Hectd2 | Mm_Celera | 19:36582731 | CTAGATTCTGTGAAT[-/ATAGCAGCAAA]CAAACAAAAGTTTTT | 226098 |
rs238447120 | in-del | -/TACTAGATATT | | | intron-variant | Hectd2 | Mm_Celera | 19:36585207 | TTATAAGTACCAAAA[-/TACTAGATATT]TACTAGATATTTTAT | 226098 |
rs238493491 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36598426 | AATAATGTGTTTATT[A/T]TTAGAATACATCACA | 226098 |
rs238539837 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36557060 | GAGTGGGGAAGACTT[A/G]ATGGAATGTGGTGGA | 226098 |
rs238566074 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36588225 | TCCTCCATCTCCTCC[C/T]ATACTTGATTCTTCC | 226098 |
rs238666369 | in-del | -/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36612549 | AAAATAAATGCCTTG[-/T]TTTGTTTATTTTGGT | 226098 |
rs238684263 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36592664 | GACTTGTCTATTGGT[A/G]ATAGTGGTGAATTGA | 226098 |
rs238781611 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36559796 | TTAAAATAAAACAAT[C/T]CAGCCAGTAACATTT | 226098 |
rs238801669 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36573544 | ACTGTGAACGGCAGA[C/T]AGAAATAGGTGCTCA | 226098 |
rs238830337 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36575507 | CTGAAGTAGTCAAAA[A/C]AGCACAAGAGCTGCA | 226098 |
rs238923452 | snp | A/G | | | synonymous-codon, nc-transcript-variant | Hectd2 | Mm_Celera | 19:36612402 | TGGATTTCATAGTGT[A/G]TGTGCTTCAAATGCC | 226098 |
rs238947245 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36566844 | TTCTCTTCACTAAAT[C/T]TAACACAGAAATATT | 226098 |
rs239003560 | snp | G/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36569850 | TCTATCTTCAATAAC[G/T]TCTTTCTTCCTTTGA | 226098 |
rs239037173 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36591487 | TTCCATAGTCGCTGT[A/T]CAAGTTTGCGCTCCT | 226098 |
rs239097214 | snp | C/T | | | upstream-variant-2KB, nc-transcript-variant | Hectd2, LOC105246565 | Mm_Celera | 19:36553269 | GGCTACTTTATTCTA[C/T]TTATTGTACACCTTT | 226098 |
rs239161601 | in-del | -/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36592471 | AATGTTCTTGATCTG[-/T]TGAGACTTGCTTTGT | 226098 |
rs239189218 | snp | C/T | | | intron-variant, upstream-variant-2KB | Hectd2, LOC105246565 | Mm_Celera | 19:36555447 | TTCCCAGCTGGATTT[C/T]GCAAGGGTTAATTTG | 226098 |
rs239189259 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36563748 | ATCATTTATTCTTTT[A/G]TAAAAGTAGTTTTTA | 226098 |
rs239223436 | snp | A/C | | | intron-variant, upstream-variant-2KB | Hectd2, LOC105246565 | Mm_Celera | 19:36555323 | GTGGGAGGCAGTTGC[A/C]TCCCTGGATGCTTTT | 226098 |
rs239225809 | snp | G/T | | | synonymous-codon, nc-transcript-variant | Hectd2 | Mm_Celera | 19:36585485 | TATTGAGGACTCTGG[G/T]CTTAATGCCAATTTG | 226098 |
rs239226773 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36562810 | TAATAATTAGATGTA[A/G]AATTATGACCTTATT | 226098 |
rs239231993 | in-del | -/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36590434 | CACTCCAGTCCATCA[-/T]TCTGTTTCCCTTCCC | 226098 |
rs239288491 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36577666 | TATGAAGTGAAGCTG[A/C]ATTGAGTGATTTATT | 226098 |
rs239354109 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36556613 | TAGCCAATGTATTGT[C/T]TGTTCTGTTCAGTGG | 226098 |
rs239373659 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36613855 | CAGACTACCCAGGCC[A/G]CAGTGCACAGAGCAC | 226098 |
rs239418147 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36568352 | TATGAAAGTAAACTA[C/T]CATTAGATTAAAAAG | 226098 |
rs239443653 | in-del | -/A | | | intron-variant | Hectd2 | Mm_Celera | 19:36557711 | TGTATAGCCCTGGCT[-/A]TCCTGGAACTCACTC | 226098 |
rs239469911 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36558311 | TCTCACTGGAATTGA[A/C]TATACCAAGGAATTA | 226098 |
rs239471031 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36576834 | CATTTGGAATAACAA[A/C]AAAGCCAGGGTAGTG | 226098 |
rs239502876 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36557777 | CTGCCTCTGCCTCCC[A/G]AGTGCTGGGATTAAA | 226098 |
rs239506439 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36603868 | TTTTACTTTCTATAA[A/G]TAGACTATTCTTTTA | 226098 |
rs239571606 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36593414 | GGTTTCTTATAGTCT[G/T]CAGCACATCTGTCCA | 226098 |
rs239728674 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36583842 | TGAATGCATTATAAA[A/G]TGCTTATTTTCTGTT | 226098 |
rs239735627 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36578627 | GACCTAGAGTGACCT[C/T]TGAGGGCTTGCTGAA | 226098 |
rs239737775 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36559718 | GAAGAGGATGGAAGG[A/G]AAAAGAAGGCAGAAA | 226098 |
rs239756411 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36578184 | GAATTAGAAGTCTTC[A/T]CAACTGGCCATTTAT | 226098 |
rs239757185 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36576690 | GAAAGATCTCCCATG[C/T]TCATGGATTGGAAAG | 226098 |
rs239795273 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36584243 | AGTTGAAGGTATAAA[C/T]AAATGTGTGAATAAT | 226098 |
rs239807429 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36617143 | TGCTTGCCAGCCAAG[C/T]TCAAAGAAAAGGCAA | 226098 |
rs239835186 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36591013 | GGCATTGAATTCCTT[A/G]GAGCAAGTTTGATCT | 226098 |
rs239861307 | snp | C/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36585703 | CAGAGGGCACCTGAT[C/G]CCCTGGGGCTGGAAT | 226098 |
rs239889570 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36573616 | GGACTTGCCACTTGA[A/G]GATTTTTACTTTGGA | 226098 |
rs239900516 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36585047 | CCCTTATTTTAAATT[A/T]AAAAAAAGAGACTCC | 226098 |
rs239919971 | in-del | -/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36615290 | TTTACTGGCACTGTG[-/T]TTTAAAAAAAAAGAC | 226098 |
rs239922642 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36578771 | AAACTGAATATCCCC[A/G]AGGAGGAAGCCAAAC | 226098 |
rs239966013 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36570731 | ACCACTGAGCCATCT[C/T]TCCAGCCCTTTCTTT | 226098 |
rs239988955 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36607804 | GCTTAGCGTTGTGAT[A/C]TTTTGACTTCCTGGT | 226098 |
rs240011043 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36562396 | CAAGTGCCCTTTGAC[C/T]ATTGAGCCAACTCTC | 226098 |
rs240027450 | snp | C/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36579795 | TGAAACTGTAGACCC[C/G]CTCATTTTAGGCCAC | 226098 |
rs240092788 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36605947 | TTTTGGAGGGCAGTC[A/G]TGATAGATCACTGTG | 226098 |
rs240093041 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36614080 | GTAATTTTATTTACT[G/T]AGACAGTGTCATAAT | 226098 |
rs240132733 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36613353 | AAGAAGAAAGAAATG[A/G]ACTATCAAAGTTCCA | 226098 |
rs240145043 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36598223 | TCTCTCAGTCTCCCA[G/T]TTATAGGGATTACAG | 226098 |
rs240146897 | snp | C/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36605612 | CTGAGTGTCAAGTTA[C/G]GTTCCAAGTATCCAT | 226098 |
rs240158303 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36606982 | TCCTGTTTCTCATCC[C/T]TATCTCAGGTATGTT | 226098 |
rs240199852 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36565299 | TGCTGTATACAAAGC[C/T]CCATTAGAAAACACC | 226098 |
rs240200124 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36586939 | TCAAAAGATCTTGGC[C/T]AGCCTGGTTTACATA | 226098 |
rs240252293 | in-del | -/ATAT | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | Hectd2, 1500017E21Rik | Mm_Celera | 19:36619031 | TTTAAAAATATATAA[-/ATAT]ATATATATATATATC | 226098 |
rs240308283 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36582072 | AACTGGTGGTTTGAA[A/T]GAGAATGGCCTTCCT | 226098 |
rs240453260 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36609519 | TAAAATCAGGCTTTC[C/T]TTTTAGAACTCTTCT | 226098 |
rs240473724 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36589855 | TAGTCTCTGGTTCTT[A/G]GCCACCCAAGCAGTG | 226098 |
rs240506149 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36617917 | TCCTCATCCATACAG[C/T]GGAAATAATAACCAC | 226098 |
rs240506184 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36609729 | TGGCAATACTAGGTT[A/G]TTTTAAAAATAATAA | 226098 |
rs240519495 | in-del | -/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36563841 | ACACTAGAAATTCAA[-/T]TTAAAATATTTTATT | 226098 |
rs240542183 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36617371 | GAAATTTCTACATGA[A/G]TCACAATTAAAAGAA | 226098 |
rs240561851 | in-del | -/A | | | intron-variant | Hectd2 | Mm_Celera | 19:36572955 | AAAAGAAAAGAAAAG[-/A]AAAGAAAAAGGCCTA | 226098 |
rs240566118 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36610161 | CAACAGAAAACACGC[A/G]GGCACAGCACCATGA | 226098 |
rs240607777 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36602332 | CTGTTAAAGAAAAAG[A/G]CAAAGGTTTGGGTGC | 226098 |
rs240608310 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36601813 | ATGAGAGCAGGAGTG[C/T]GTTAACACAGATCAT | 226098 |
rs240633662 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36557289 | GTGGGGTTTTTTCCC[C/T]CAGAAAATTAGTGTG | 226098 |
rs240659373 | in-del | -/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36612690 | AGAATCAATACAAAG[-/T]TTTCAAAAATATAAA | 226098 |
rs240818059 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36592181 | GGCCTCTTTATCAAA[C/T]ATCAGGTGTCCATGG | 226098 |
rs240828066 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36603255 | TAAGTCTCAAACTCA[A/G]TTTGGGGCATGAGAT | 226098 |
rs240849745 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36558356 | AGATAAATTTTATAT[A/T]ACTAGGGAGGTGAAA | 226098 |
rs240863193 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36599080 | GTTTCTCTTGAGAAG[G/T]AGTAGGGACATATTT | 226098 |
rs240892938 | in-del | -/A | | | intron-variant | Hectd2 | Mm_Celera | 19:36597689 | AAATATTTTCAAAAT[-/A]AAAATTTAAAACTGT | 226098 |
rs240899032 | snp | A/G | | | upstream-variant-2KB, downstream-variant-500B | Hectd2, LOC105246565 | Mm_Celera | 19:36552663 | AGTGGTACATTATGA[A/G]TCATGTATTTAGTAG | 226098 |
rs240977619 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36584266 | TGAATAATGAATAGT[A/G]GATATGTTATAGCAA | 226098 |
rs241003227 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36605144 | GCTCTTCATTCTGTC[A/T]TACTACATAACTTCT | 226098 |
rs241054420 | in-del | -/CAAA | | | intron-variant | Hectd2 | Mm_Celera | 19:36582732 | CTAGATTCTGTGAAT[-/CAAA]CAAAAGTTTTTCAGT | 226098 |
rs241137738 | in-del | -/TGGGAATTACCTT | | | intron-variant | Hectd2 | Mm_Celera | 19:36613653 | TTGTAATATGTTTAC[-/TGGGAATTACCTT]TGAAAAAGATGTACT | 226098 |
rs241145616 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36567153 | TTCCCACCTTTGTGT[C/T]TTCAAGGCAGGGTCT | 226098 |
rs241181669 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36566623 | TGTGTTCTTGGGTGT[A/T]GAAGCAGCCCTGCCA | 226098 |
rs241183301 | in-del | -/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36591749 | AGCTTTTTATATCAA[-/G]CTTTTTTTAACTCTT | 226098 |
rs241278659 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36612640 | GAGAGGACGGGGAGA[G/T]GAGTGGGACTGGGGT | 226098 |
rs241288373 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36568944 | GTTAGAAATCCTGGT[A/G]TACCTACAATTTAAT | 226098 |
rs241295991 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36567984 | CCTGTGGGTCAGGAG[A/T]GGGTCTGCTTTATAT | 226098 |
rs241341317 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36575150 | ACCAACTCCTTCTCT[A/G]GTCTTTAATTCTGTA | 226098 |
rs241410092 | snp | C/G/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36561119 | TCGCCTTTTCCGATC[C/G/T]AGCTCGTTCCAGTCT | 226098 |
rs241434343 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36560689 | AAATACATATTCTGG[A/G]TGTCTAATTTTGAGT | 226098 |
rs241514856 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36562153 | CACATAGGGGATAGG[A/G]GGTTTTCAGAGGGGA | 226098 |
rs241515235 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36570103 | AAAAGAGCACTCAGG[C/T]ATTAACTCACAGTTC | 226098 |
rs241522316 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36606709 | TGTTTATATATCAGA[A/T]TTATCAAAAATTTAA | 226098 |
rs241531648 | in-del | -/AT | | | intron-variant | Hectd2 | Mm_Celera | 19:36590552 | GATATAAGGGAAAAC[-/AT]AGCACACTTATCTTT | 226098 |
rs241541806 | in-del | -/TTTTG | | | utr-variant-3-prime, nc-transcript-variant | Hectd2, 1500017E21Rik | Mm_Celera | 19:36620014 | TTAAGCCCCAGGGAT[-/TTTTG]TTTTGTTTTGTTTTG | 226098 |
rs241551671 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36569114 | AGTATTATTTAAATA[C/T]TTAATTAAAGTGGTT | 226098 |
rs241558548 | snp | A/G | | | upstream-variant-2KB, nc-transcript-variant | Hectd2, LOC105246565 | Mm_Celera | 19:36553106 | AGTTTTCAGCATGCT[A/G]GCCTGCTAAAAGAAA | 226098 |
rs241607972 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | Hectd2, LOC105246565 | Mm_Celera | 19:36554170 | AGGACACGGGGAAAG[A/G]GTTAGTCATAAGGAT | 226098 |
rs241619203 | in-del | -/AAGT | | | intron-variant | Hectd2 | Mm_Celera | 19:36557329 | TGACGGTGTAGAAAC[-/AAGT]AAGAGTGACAGCTCA | 226098 |
rs241623743 | snp | C/T | | | upstream-variant-2KB, nc-transcript-variant | Hectd2, LOC105246565 | Mm_Celera | 19:36553035 | CTAGACACAGTAGCA[C/T]GGTACATCTTGAATC | 226098 |
rs241626395 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36600795 | ATTCTTTCCATAGGC[A/G]TTTATGTCTGAGTAG | 226098 |
rs241649289 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36586374 | AAATTATTTCCATCG[C/T]TACTTCATAACTAAT | 226098 |
rs241658453 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36570809 | CATTATCCCCTTCTT[G/T]GTCTGCCCTCCGACA | 226098 |
rs241666687 | snp | A/C/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36561086 | GCCCTCTGTATCAAG[A/C/T]CTCAAGACCTGTACC | 226098 |
rs241712184 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36599209 | AATTTTTATTTATAA[A/G]TGTTTTACAAAGCTG | 226098 |
rs241775790 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36564731 | ATTCTTTAACTTTTC[C/T]GTCTCCATCCCCCCA | 226098 |
rs241793962 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36588309 | GATTATATTGTTCCC[C/T]CTTCTAAGGGATTAA | 226098 |
rs241803569 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36563947 | ATCAGGTATTGCGTT[A/C]GAGTGTAAACAGAAA | 226098 |
rs241803998 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36571198 | AATATCTGCATATGG[C/T]TCTTTCAGCTGCTTA | 226098 |
rs241826887 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36594496 | TCTTTGTTGAATGGG[A/G]GTTTTGTTTCTTGGT | 226098 |
rs241828689 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36587862 | GAGCCTCTCAGGACA[A/G]ATGTCAGCTCCTGTC | 226098 |
rs241877983 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36617220 | GAGTGATAGGATAGA[C/T]ACCCAGTATCTTCCT | 226098 |
rs241947675 | in-del | -/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36590176 | AGCAGTTTGGGGTTT[-/G]GGGAATGTCTGTGGA | 226098 |
rs241979849 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36572320 | GTTTTTTTTTTTTTT[G/T]TTTTCCTCATAAGAG | 226098 |
rs241993761 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36589205 | CAGATCCTTTCTACC[A/G]CCTCTTCTATCCAGA | 226098 |
rs241995743 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36596535 | TTGCTTAGCTGAGCG[C/T]TCTTTCAGTTCTTTA | 226098 |
rs242071180 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36589505 | TTCATATGAGCTTTG[C/T]TCAGTTGCTTTAGAG | 226098 |
rs242093463 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36563891 | GGGAGATGTTACCAT[A/C]TTATAGCATTGTGTG | 226098 |
rs242133085 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | Hectd2, 1500017E21Rik | Mm_Celera | 19:36619110 | CAGTCTTTTTTATAG[C/T]GTTTTGTTGTTTTTC | 226098 |
rs242140260 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36597682 | AAGGGCAAAATATTT[C/T]CAAAATAAAAATTTA | 226098 |
rs242148143 | snp | C/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36589678 | TCTGCATAATGTCTG[C/G]CTGTGAGTCTCTGTA | 226098 |
rs242163861 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36556762 | GTTTAAGAATTTTTA[A/T]AAAATCTTTGAACAT | 226098 |
rs242189825 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36604582 | AGTGTGCTACCTGGA[C/T]TCTAGACCTGCCATC | 226098 |
rs242204805 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36584186 | TGTAGATTTTTATAA[A/C]ATATTAGACAAAAGT | 226098 |
rs242292435 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | Hectd2, 1500017E21Rik | Mm_Celera | 19:36619622 | GTTACTTGAGTATTC[G/T]GTAATGTTTGTATAA | 226098 |
rs242417397 | in-del | -/TATA | | | intron-variant | Hectd2 | Mm_Celera | 19:36612737 | TTTCAGCCTTTCTAC[-/TATA]TATATAGAGAGAGAG | 226098 |
rs242427453 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36583148 | CCCATACTGAGTTTA[C/T]AGTCAAACTGAGCAG | 226098 |
rs242434282 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36586353 | TTGTGGTGACCCCCA[A/G]CCGTAAAATTATTTC | 226098 |
rs242509255 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36574128 | GGGCTTCCCCAGCAC[G/T]TTGGCTTCACTCCTC | 226098 |
rs242563767 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36611273 | AGTTTACTTTTTATT[C/T]TCATAGGTAAGGGAC | 226098 |
rs242576691 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36579580 | GCCTCATTGCCTACT[C/T]CCAGTGATACACTTC | 226098 |
rs242578844 | in-del | -/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36602574 | TTTTCTTTAAAGTAA[-/T]TTTTTTTTCACTTTG | 226098 |
rs242634392 | in-del | -/GCCTTT | | | intron-variant | Hectd2 | Mm_Celera | 19:36565350 | CATGTTTGTTAGTGA[-/GCCTTT]GCTCCTTGTCTAGTT | 226098 |
rs242675503 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36600057 | TCAAAACTGAAAAAC[A/G]GTTTCCTCTAAGGAC | 226098 |
rs242687436 | in-del | -/AT | | | intron-variant | Hectd2 | Mm_Celera | 19:36562741 | GTTATAAGAGGTACA[-/AT]GTAGTTAATTTGAAG | 226098 |
rs242700668 | snp | A/T | | | upstream-variant-2KB, intron-variant | Hectd2, LOC105246565 | Mm_Celera | 19:36553834 | GACGATTTAAAGTAA[A/T]TTTTTAAACGTTCTT | 226098 |
rs242756974 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36591236 | AATCACACCCTTGCC[A/C]GGGCATAAGGTAAAT | 226098 |
rs242768743 | in-del | -/TTTT | | | intron-variant | Hectd2 | Mm_Celera | 19:36572305 | TCCACCTCTTGCCTG[-/TTTT]TTTTTTTTTTTTTTT | 226098 |
rs242839108 | snp | C/T | | | missense, intron-variant, nc-transcript-variant, upstream-variant-2KB | Hectd2, LOC105246565 | GRCm38.p3 | 19:36554844 | GTAGCCGCGGCCGCC[C/T]CGGAGGAGAGGAAGG | 226098 |
rs242856068 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36581707 | TGTCCTGCCCCCACC[A/G]GCTTCACCCAGACCC | 226098 |
rs242908395 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36592296 | TTCATTACCATTCAG[A/T]TTTAGAAAGTCTTTA | 226098 |
rs242985193 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36586204 | TGGCCATAGTGCATA[A/T]TTTTTAAAAATATTT | 226098 |
rs243050439 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36575681 | CTAATGAACTATAAA[C/T]GTCTTCTGTACCTAA | 226098 |
rs243119939 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36576543 | AAAGAAATTAGGGAA[A/G]CCACATCCTTTACAA | 226098 |
rs243123696 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36609495 | AGTCTTCTAATGCTA[G/T]TCTTTCTTTAAAATC | 226098 |
rs243185515 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36569069 | AACTCATAAATTATT[A/T]AAATTTATAGTTTTA | 226098 |
rs243221765 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36607640 | ATTCCACACTCTCCA[A/G]GAAGGATGAGCAAGT | 226098 |
rs243224268 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36556532 | TAATCCTTTTAAGTA[G/T]TACCACATGTAATAA | 226098 |
rs243227586 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36570956 | CTCAAGCATTAGCTG[C/T]CTTTTCCCTCATTGA | 226098 |
rs243262476 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36570555 | CAGGTCCTCTGCTTG[C/T]TCCAGTCTAAAGATT | 226098 |
rs243268334 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36576884 | AAAGAACTTCTGGGG[A/G]ATCACCATCCCTGAC | 226098 |
rs243288082 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36571540 | TACATTCTAAAGGGT[C/T]CCTCCACCTCCTGCC | 226098 |
rs243372136 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36561832 | ATGCTTGGAGCCAAA[C/T]ATTGGACTAAGCACG | 226098 |
rs243386462 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36594932 | AATGTTTTTAAATTA[C/T]TGATGATTTATTAGA | 226098 |
rs243403176 | in-del | -/TTCTTC | | | intron-variant | Hectd2 | Mm_Celera | 19:36572313 | TTGCCTGTTTTTTTT[-/TTCTTC]TTTTTTTTTTTCCTC | 226098 |
rs243488858 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36578293 | ATACATATAAACCTA[C/T]CACATACATGCAAGC | 226098 |
rs243492654 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36566263 | ATTAGCAATCAAGGA[A/C]ATGCATCATAGATGT | 226098 |
rs243492668 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36573365 | GTTTATTCTTAGCAG[A/G]GCCTTGGTGTGGCAT | 226098 |
rs243526012 | snp | C/G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36572310 | CCTCTTGCCTGTTTT[C/G/T]TTTTTTTTTTTTTTC | 226098 |
rs243542211 | snp | C/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36595539 | GAATTTCCTCACATA[C/G]TAGGCTTATGTTTTT | 226098 |
rs243602126 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36581873 | AGTTTTCTTATGACC[A/G]GAACAAAATACCTGA | 226098 |
rs243607505 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36573889 | ATATGATTCAAAAGT[A/G]GGCTCACTTTAAGCC | 226098 |
rs243637681 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36573558 | ACAGAAATAGGTGCT[C/T]ACAGGAAACCTGGGG | 226098 |
rs243638624 | snp | C/T | | | intron-variant, downstream-variant-500B | Hectd2 | Mm_Celera | 19:36611770 | AAGGGCACGGTACTC[C/T]CCAGGTAGTTGCATC | 226098 |
rs243639148 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36579330 | CATATGCCTGTCTTG[A/G]TTAGGGTTTCTATTG | 226098 |
rs243644798 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36597618 | TACTTCCTCCCCTCA[A/G]GACTATATTTCCATT | 226098 |
rs243664464 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36566592 | GTTACATAATGAAGT[A/G]CAGATTTTTGATGTC | 226098 |
rs243688829 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36564892 | GAAGATTTTGTAATC[A/G]TTGAGATAGACACAC | 226098 |
rs243699849 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36605353 | GTAGGCCCTCAGTAG[A/T]AGCCCTGACATTTTT | 226098 |
rs243738415 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36558936 | AAATGTTCAGGGGGG[G/T]GTGTAGTATGTTTTT | 226098 |
rs243769535 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36605993 | CAGTAATAGTGTCAG[A/G]CCATGGGACCTCCCC | 226098 |
rs243769561 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36598346 | AGAAGACTATAGAGA[C/T]ATTTCATTGGAACTG | 226098 |
rs243773226 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36591277 | TGTTGTGGACAGTCG[A/G]AAGCAGTTCCATATC | 226098 |
rs243800968 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36590537 | AGTGGTTAATATCCA[A/G]ATATAAGGGAAAACA | 226098 |
rs243806971 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36598247 | ATTACAGGTGGACAC[A/T]GCCATGTGTGGCTGG | 226098 |
rs243831290 | in-del | -/GAA | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36590344 | ATGCCCTTCAGTTCC[-/GAA]AGCTGTCTATTCCCT | 226098 |
rs243919027 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36598860 | AAATGAAAGTTTTGA[C/T]TGGAATTCTTTCAAA | 226098 |
rs243926532 | in-del | -/TT | | | intron-variant | Hectd2 | Mm_Celera | 19:36591763 | AACTTTTTTTAACTC[-/TT]TATATATTTTATAAA | 226098 |
rs243944525 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36589610 | TGAGCTCTGTGGGAG[A/G]GATTTGATGGAGATA | 226098 |
rs243981472 | in-del | -/AATA | | | intron-variant | Hectd2 | Mm_Celera | 19:36574638 | TTCTTTTAAAAAATT[-/AATA]TATATATATATTCTC | 226098 |
rs244025571 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36600742 | TGCAGCTACTTGTGA[C/T]GGGAGTCTGACCTCT | 226098 |
rs244028156 | snp | A/G | | | synonymous-codon, nc-transcript-variant | Hectd2 | Mm_Celera | 19:36584926 | AGCTGAGGCCACAGG[A/G]AATTGGAAGACAGTA | 226098 |
rs244037691 | in-del | -/GAGGAAGAGGAAGAGGAGGAAGAA | | | intron-variant | Hectd2 | Mm_Celera | 19:36559745 | AAAAAGGAGGAAGAG[-/GAGGAAGAGGAAGAGGAGGAAGAA]GAGGAAGAGGAGGAA | 226098 |
rs244144703 | in-del | -/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36590352 | CAGTTCCAGCTGTCT[-/C]ATTCCCTTCCTCAGC | 226098 |
rs244145802 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36593960 | TTCAGAATTCCCTCA[G/T]TTTGGGTTTTCTTTA | 226098 |
rs244177867 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36601175 | TGGAAATGACTTGTG[G/T]GAACAATGTAAGTGA | 226098 |
rs244181008 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36593278 | CTTCCAGCACCCTCT[A/G]CAGGACTGGATTTGT | 226098 |
rs244212108 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | Hectd2, 1500017E21Rik | Mm_Celera | 19:36621014 | GTCTTGTCCTTTTTT[A/T]AAAAACCTATTATTT | 226098 |
rs244286384 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36611939 | ATACAAGTTTTGTGG[A/G]CTTTATTAAAGTATT | 226098 |
rs244324130 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36566689 | GTTTGTAAGAAAAGG[A/T]CTCCCCTCACCACTT | 226098 |
rs244345808 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36598501 | AAAGCACAGCCCTAC[C/T]GAATCTCCCTCATGC | 226098 |
rs244369189 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36572927 | CAGCTGCTAGGGATG[A/G]TGCAGCATCTTCAAA | 226098 |
rs244388476 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36605765 | ACTCTTTCAAAAATA[C/T]AATGGACCATGACTG | 226098 |
rs244424702 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36560439 | CAATAATCCCAATTT[A/G]AAAAAGAGGATGTGG | 226098 |
rs244452407 | in-del | -/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36575307 | CAGGGAATGTGTTAC[-/T]TTTTTTTGGCTCTGA | 226098 |
rs244462996 | in-del | -/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36583180 | TAGCACTAAAGAAAA[-/C]TAACACCTGAGTGCA | 226098 |
rs244496908 | snp | A/G | | | upstream-variant-2KB, downstream-variant-500B | Hectd2, LOC105246565 | Mm_Celera | 19:36552442 | ATTACATTTGGTGTC[A/G]CTGAAAAGCGTCTTC | 226098 |
rs244516615 | in-del | -/TAAG | | | intron-variant | Hectd2 | Mm_Celera | 19:36559300 | AAGAGAAAAATAAAT[-/TAAG]TAACAATAAAACAAG | 226098 |
rs244585074 | snp | C/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36560340 | TAAAATGATACTGAG[C/G]TGCAAAGGTTGTTTC | 226098 |
rs244625183 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36616616 | ACCTGGCCCTGACGC[A/G]TTGGGCATTAGTAGC | 226098 |
rs244690256 | in-del | -/A | | | intron-variant | Hectd2 | Mm_Celera | 19:36585975 | AATACCTCTGTATCT[-/A]AATATGTATTTAGAA | 226098 |
rs244706676 | in-del | -/GAAAA | | | intron-variant | Hectd2 | Mm_Celera | 19:36572944 | GCAGCATCTTCAAAA[-/GAAAA]GAAAAGAAAAGAAAA | 226098 |
rs244709737 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36608644 | TATATGTTTAGGTTT[C/T]CTTTTGGATCTATAA | 226098 |
rs244710480 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36558464 | ACTCAGGGCTTTGTG[C/T]ACATGCATTCTATCA | 226098 |
rs244766660 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36559087 | AAGCCCACTGGAACT[C/T]CCCCCCTCCCCAGAA | 226098 |
rs244859955 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36610095 | TTATCCCACTTCTCC[C/T]ATCCGAGACTATTCT | 226098 |
rs244879920 | in-del | -/A | | | intron-variant | Hectd2 | Mm_Celera | 19:36582880 | ACAGAATAAATAACC[-/A]AAAAATGTAAGTTCT | 226098 |
rs244894322 | in-del | -/AAT | | | intron-variant | Hectd2 | Mm_Celera | 19:36599426 | TTTTGTAAAGCAAGA[-/AAT]AATATTTTTTTACCA | 226098 |
rs244900349 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36575728 | CTAAGATGGAATTTG[C/T]CAGTATAATGATTTT | 226098 |
rs244978188 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36557586 | CATCCCACCCTAAGA[C/T]ACCAGTTTTCAATCT | 226098 |
rs245001094 | snp | A/G | | | intron-variant, upstream-variant-2KB | Hectd2, LOC105246565 | GRCm38.p3 | 19:36555050 | ACGCTCGGGGAGTGG[A/G]GTCCGCTGCCTGATG | 226098 |
rs245002533 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36570212 | GGGCTGGACTCTGCA[A/C]AAATCACAAATATTC | 226098 |
rs245020381 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36564614 | GTTTGCAGGCTGGCC[A/G]TATTCCAAGACTTCA | 226098 |
rs245028756 | snp | A/G | | | upstream-variant-2KB, downstream-variant-500B | Hectd2, LOC105246565 | Mm_Celera | 19:36552531 | CAGTAGGTACACACA[A/G]AAAGTTTTTCGTGAC | 226098 |
rs245064006 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36561402 | GTTTTTCACCTACTT[A/T]TCTCTAGCATTACAG | 226098 |
rs245123200 | snp | C/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36562291 | TTATTTTATGTGTCT[C/G]CATTTGTACACCATT | 226098 |
rs245123289 | snp | A/C | | | upstream-variant-2KB, nc-transcript-variant | Hectd2, LOC105246565 | Mm_Celera | 19:36553503 | AATTATATAAAATGA[A/C]AGTCACCAAATCCCC | 226098 |
rs245227428 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36583658 | AGAAGGAGAGAAGGA[A/G]CTATACATTTCATCT | 226098 |
rs245232697 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36580517 | TGTTTTACTTAATGT[C/T]TCTAAGCAACAAGCT | 226098 |
rs245264834 | snp | A/G | | | upstream-variant-2KB, intron-variant | Hectd2, LOC105246565 | Mm_Celera | 19:36554590 | CGGAGCCTGGCGGCC[A/G]GCCCGGGGGCGCGCG | 226098 |
rs245267018 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36580163 | ACTCTGTCTGCCAGG[A/G]CTTCCGTGTCAGCAG | 226098 |
rs245270175 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36589410 | CTGTAGTGTGTGTAC[A/G]TGCATGCGTGTATGC | 226098 |
rs245314466 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36594644 | GGTTTTAGAGGCTTA[A/G]ATAATGGGTTGAGTT | 226098 |
rs245345406 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36575275 | CTGTACTTGGTAAAA[A/C]GTCCATCTCCCCAAC | 226098 |
rs245371224 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36575108 | GGAGATAAATCTTCT[G/T]TGCTGGCTTGTTTGC | 226098 |
rs245398702 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36557005 | TGACATCTGAAGATG[A/T]GGAAAGCCAGGGCAT | 226098 |
rs245426826 | in-del | -/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36602136 | TGCTTAGGAGAGTAT[-/G]TCCGGTGTTAAAGAT | 226098 |
rs245464347 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36581987 | GTTGCTCACCTCAAG[A/G]CTGCTGGAAGGTGAG | 226098 |
rs245522476 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36576377 | GAAGTCAAAATATCA[A/C]TATTTGCAGATGAAA | 226098 |
rs245554053 | snp | C/G | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36591750 | AGCTTTTTATATCAA[C/G]TTTTTTTAACTCTTT | 226098 |
rs245557130 | snp | C/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36588408 | CGAAAGGAAATCAAT[C/G]AGTCTTTTAACATTA | 226098 |
rs245571731 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36609815 | TTTGGTAGAACGCTC[A/G]AGTTCAGTTATGGTG | 226098 |
rs245572080 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36601541 | AGGGTAAGCCAGCTA[C/T]GAAACATGTTTATGC | 226098 |
rs245597129 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36583417 | AGAAATGCATGGCCA[A/G]AATAAGAAAGTAAGA | 226098 |
rs245666863 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36590407 | CTGACCCTCCCATTC[C/T]TGTTCCCTGCCCCAC | 226098 |
rs245669177 | snp | A/T | | | missense, nc-transcript-variant | Hectd2 | Mm_Celera | 19:36584004 | GTGGAAGCGTTACCA[A/T]CTGAAGTGAAGGTCC | 226098 |
rs245679619 | in-del | -/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36572582 | TGCATATAATTCCTT[-/G]GGTTTTTTTGAGAAG | 226098 |
rs245702337 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36589820 | TAGCATTTGGTTTTA[C/T]CCTAGGTCTCTGGAC | 226098 |
rs245739285 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36585801 | TTCTGGAAGATTAGC[A/G]GATGTTCTTGACTTC | 226098 |
rs245743586 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36618008 | TATCATAATCCAGAG[A/T]CTCCATAAGTGGTAA | 226098 |
rs245746897 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36577591 | TTATTTCTTTTAATA[A/C]TGATGCTAGATTCTC | 226098 |
rs245794260 | in-del | -/A | | | intron-variant | Hectd2 | Mm_Celera | 19:36585365 | ATTAGTTGAGATTAT[-/A]AAAAAAGTATAATTC | 226098 |
rs245796434 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36571291 | TCAGGCCTTGGAGCC[A/T]CCCCTTGAGCTGGAC | 226098 |
rs245802003 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36577895 | AAAGAGAGACCAACT[A/G]GGGATCTAAGGTTGT | 226098 |
rs245814629 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36584409 | ACCATTCTCTAAAAG[A/C]TGTGTCACCATTCAG | 226098 |
rs245850686 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36603656 | GCATAGTTTTCCTAC[C/T]CATTTTTAGTAGCTG | 226098 |
rs245887482 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36614165 | TTTTTTTAAATTTGG[A/T]TTTTCAAGACAGGGT | 226098 |
rs245926358 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36604729 | TATATAGGACATATT[A/C]GTATTCACACAAACA | 226098 |
rs245927946 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36568611 | CATGTGGTATAGATC[A/G]GTGATCTTAGCATTG | 226098 |
rs245958386 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36597554 | AACATATCTTACTGC[A/G]TATGTGATACTTTCT | 226098 |
rs245960975 | snp | C/G | | | synonymous-codon, nc-transcript-variant | Hectd2 | Mm_Celera | 19:36612176 | TGGAGTAATTAAATC[C/G]TATAACTTAAAACCA | 226098 |
rs245995728 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36596793 | TCAAAATGACCCCTG[A/G]GATTGATATTATTTG | 226098 |
rs246000525 | snp | C/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36561197 | CAGTGTAAGAATTTA[C/G]ATGAATTTCTTCTTG | 226098 |
rs246001003 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36604384 | TCCAAAATGGTTTAG[C/T]CTTATTTCTAACATT | 226098 |
rs246069569 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36607027 | TACACTGGTGGAGCA[A/G]AGAGAGGTTAGATTT | 226098 |
rs246078106 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36605339 | GACACTCTAGACTTG[C/T]AGGCCCTCAGTAGTA | 226098 |
rs246159792 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36614289 | GGGATTAAAGGAGGG[C/T]ACCGCCACTGCCCGG | 226098 |
rs246164746 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36580423 | CCTTTATACATAACT[A/G]TATTACAGTCTACAC | 226098 |
rs246182030 | in-del | -/TATT | | | intron-variant | Hectd2 | Mm_Celera | 19:36613066 | TTCTTTTTTTTAATC[-/TATT]TATTTTATGTATTGA | 226098 |
rs246190559 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36613720 | GGAGGATGGAGAAAG[A/G]GAAAATAAAAATACA | 226098 |
rs246198033 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36579056 | GACCTGAAGGGAGCC[A/T]TTTAGATAACATGCA | 226098 |
rs246215220 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36607301 | CAAGATTAGCATAAC[A/G]TAAGTGTGGTGAGGT | 226098 |
rs246245376 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36587040 | TTAAATTAATAAATA[C/T]AATACTGTTAGACTT | 226098 |
rs246255353 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36591720 | ATCTGTATCCCAATT[C/T]TAATTGGGTTATTTA | 226098 |
rs246295600 | in-del | -/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36612575 | TTGGTTGCTTATGTG[-/T]TTTTTTATTTTCTTT | 226098 |
rs246336565 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36600583 | AGGCTGTCTAATGTT[C/T]GGTATATAGGGCTAC | 226098 |
rs246373441 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36607741 | TAACTTTGACCTATT[C/T]GAACTTCTTCATGCA | 226098 |
rs246431499 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36581209 | TGAGTGGGTATAAAA[A/C]TGTGCATGCATATAG | 226098 |
rs246435662 | snp | C/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36608964 | GTGCTGTATTCTGCA[C/G]CCAAATACTTCTAAC | 226098 |
rs246463573 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36574725 | TTCAGCTGTCTTATT[G/T]GAGGTATCTTTCTTG | 226098 |
rs246465070 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36572085 | CTGGAACTCACTTTG[G/T]AGACGAGGCTGGCCC | 226098 |
rs246523173 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | Hectd2 | Mm_Celera | 19:36618908 | TTACTGTGCCTTTAA[C/T]ACTTTCATGCTTCTG | 226098 |
rs246573498 | in-del | -/A | | | intron-variant | Hectd2 | Mm_Celera | 19:36587076 | TTTGTCCCCTCAAGG[-/A]AAAAATGAATTTTTT | 226098 |
rs246634571 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36565757 | AGGCTTTGTTTTTAT[G/T]AAGACAGGGTAAAGG | 226098 |
rs246650919 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36568467 | ATGGTAGAAGGAGAG[G/T]GCAGCTTCTCTGAGG | 226098 |
rs246798142 | in-del | -/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36594549 | AGAGTGTGATTGCTG[-/T]TATGCTGCCTGATAG | 226098 |
rs246854150 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36556196 | TGACCTGGTGTTGGT[C/T]GTCACCCCATGCTTT | 226098 |
rs246890243 | in-del | -/TTTC | | | intron-variant | Hectd2 | Mm_Celera | 19:36594862 | TAAGCTGAAGTGTAG[-/TTTC]TTTCTTTAATGTATA | 226098 |
rs246910346 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36557993 | ATCTGCTTAGCAATA[G/T]CTGTCAAAGTGGTTC | 226098 |
rs246922068 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36592957 | TCTATCTTTGATGTT[A/G]AAGTATATTTCTTGG | 226098 |
rs246971152 | in-del | -/AGAG | | | intron-variant | Hectd2 | Mm_Celera | 19:36612743 | GCCTTTCTACTATAT[-/AGAG]AGAGAGAGAGAAATG | 226098 |
rs247067303 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36558406 | TGTACATGCGTGAGT[A/G]TGCATGTATGTGTGT | 226098 |
rs247072303 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36573672 | TCTTCAGGTTTCCTG[A/G]ACTAAATCTCTAAGA | 226098 |
rs247099229 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36574023 | ACATGCATCTTCAGA[A/G]GTCTGTCTGTCTGCT | 226098 |
rs247213408 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36568107 | ATTTTCCCCACCAGT[A/C]TTAAATGTGTCATCA | 226098 |
rs247216109 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36612609 | GAGGAGGTTTCAAGG[A/G]GCATTGGGCAGACAC | 226098 |
rs247220780 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36567418 | CAAAAGTCACTTAAA[C/T]CCAGACACTTAAATA | 226098 |
rs247222399 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36559341 | GAAACTTGCCGAGGA[C/T]TTGTGGGAGTTATGT | 226098 |
rs247247170 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36574469 | GGCTGCAGAGATGGC[A/T]CAGCGGTTAAGAGCA | 226098 |
rs247254573 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36566756 | AACCCCAGTTCTCCT[A/G]CTTATGCATCAAACA | 226098 |
rs247272605 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36568711 | GCCTTGTCTCAAGAT[C/T]TGGGACAACGGGTCA | 226098 |
rs247312850 | in-del | -/A | | | intron-variant | Hectd2 | Mm_Celera | 19:36596369 | CTCAGTGCTAGAACC[-/A]AACTTACGAACTCTG | 226098 |
rs247322282 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36602507 | TAAAAGTTAATCTGT[A/G]ATAGCCAGTCATCTT | 226098 |
rs247352928 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36557664 | AAGCTTTTTTGTTTG[G/T]TTGGTTTTTGGTTTT | 226098 |
rs247354353 | in-del | -/A | | | intron-variant | Hectd2 | Mm_Celera | 19:36568972 | ATTATAATGCTTTGG[-/A]AAAAATCAACACTCA | 226098 |
rs247486534 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36615737 | GGTCGGTCGGTCAGT[C/T]GGTCAATCAGTCTGA | 226098 |
rs247490811 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36586572 | TTCCCTGAGAACATG[C/T]ATAGACATAATAACA | 226098 |
rs247492916 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36593120 | TTATTGGTGGTGGTG[A/G]TGATTGTGTGTACAC | 226098 |
rs247527944 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36569285 | GCTGCGGCTCTCTAT[A/G]CTTATGCTGATTTGG | 226098 |
rs247529490 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36585400 | ATTATTAAGAATAAT[A/C]CATGAAATGTTAAAC | 226098 |
rs247532092 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36592609 | TTGGTTTATAGCATC[C/T]ATTAGCTCTAGCACT | 226098 |
rs247563753 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36575249 | TGCTTAAGAGTGTTA[C/T]GTACACTTCGCTGTA | 226098 |
rs247601827 | in-del | -/TAGGGA | | | intron-variant | Hectd2 | Mm_Celera | 19:36569215 | ATAATAACTGTGAAG[-/TAGGGA]TATTGTTGCCATCAC | 226098 |
rs247629992 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36572191 | CCTTGCTTTCTTATC[A/G]GTACAGATACTTTGA | 226098 |
rs247650295 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36580088 | TTTTTCAAGCTGGGG[C/T]TTTCCCATTATTTAT | 226098 |
rs247653806 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36587083 | CCTCAAGGAAAAAAT[G/T]AATTTTTTCAGTTAC | 226098 |
rs247657784 | snp | C/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36563014 | TGTGTACACACCTAT[C/G]CACAGAGGTACACAC | 226098 |
rs247763501 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36616787 | AACTCTCATGAAGAT[A/C]TTTTTTAATGTTGAC | 226098 |
rs247883600 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36604198 | TTAAGTGTTTTAAGT[A/G]TAATTATACTTTAAA | 226098 |
rs247890014 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36588043 | CTGGATATGGTCTCT[A/G]AAAGGTTCTCCTTCT | 226098 |
rs247893586 | in-del | -/ATTA | | | intron-variant | Hectd2 | Mm_Celera | 19:36566243 | GGCTGAGCCCTCTGC[-/ATTA]ATTAATTAGCAATCA | 226098 |
rs247918003 | snp | C/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36593715 | TTTTGAGCTGGAATT[C/G]TCCTTCCTCTCCTTC | 226098 |
rs247944371 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36617801 | CAATGCTTTCTTACA[G/T]CCTAGCAAATGCACC | 226098 |
rs248090393 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36583278 | CCAAGGACAGAGCTG[A/T]ACTTGGTTCTGAGAG | 226098 |
rs248100632 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36618476 | TATTTAAATTCAGAT[C/T]TGTCTGACTCCAAAC | 226098 |
rs248127398 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36580722 | ACGAAGATTTTCCTC[C/T]TTTATTTATGATATT | 226098 |
rs248170559 | snp | C/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36575212 | AAAGATGAGCGTCTA[C/T]AGAAATCACTTGTAT | 226098 |
rs248203890 | in-del | -/TATACCACC | | | intron-variant | Hectd2 | Mm_Celera | 19:36600640 | ACTAGTGGCCACAAA[-/TATACCACC]TACTAGGTTCAGGTG | 226098 |
rs248271605 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36588913 | CTTCATGATTTCATG[C/T]TCATGAATCGTTTTT | 226098 |
rs248300130 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36611292 | TAGGTAAGGGACCCA[C/T]AGTCTGTATCCTTAC | 226098 |
rs248332646 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36589323 | ACAATTGAAAATGAA[A/G]GATCCCTAAGAGAAA | 226098 |
rs248396481 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36600924 | ATATTTCATATTTTA[A/C]AGTTTCTCATTTTTA | 226098 |
rs248408573 | in-del | -/ACTA | | | intron-variant | Hectd2 | Mm_Celera | 19:36597791 | TAGTAGAATTCAAAT[-/ACTA]ACTATCTGTGAAGTC | 226098 |
rs248409831 | in-del | -/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36580073 | AGATTAAGTTCCTGA[-/T]TTTTCAAGCTGGGGC | 226098 |
rs248423372 | in-del | -/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36588052 | GTCTCTGAAAGGTTC[-/T]CCTTCTCCTTTGTGG | 226098 |
rs248429669 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36608356 | TTACTATAGGCATCC[A/T]GCTTTTAGGTTTTAG | 226098 |
rs248494069 | snp | C/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36598074 | TAACATCACAACTTT[C/G]TTCTTCATTGGAACT | 226098 |
rs248526208 | snp | C/T | | | intron-variant, upstream-variant-2KB | Hectd2, LOC105246565 | Mm_Celera | 19:36555416 | TCGGCTATCCAAGCT[C/T]AATAAGCGTGGTAAT | 226098 |
rs248543139 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36613620 | AGAAAGGTTGATAAC[C/T]ACTCTTTTAGAGTGC | 226098 |
rs248585630 | snp | A/G | | | upstream-variant-2KB, nc-transcript-variant | Hectd2, LOC105246565 | Mm_Celera | 19:36552983 | GTAGACAATAGGAGA[A/G]ATAACCCACCATCAT | 226098 |
rs248637377 | in-del | -/TCT | | | intron-variant | Hectd2 | Mm_Celera | 19:36591025 | TTAGAGCAAGTTTGA[-/TCT]TCTTCAGCAGCAGCA | 226098 |
rs248710357 | snp | C/T | | | upstream-variant-2KB, nc-transcript-variant | Hectd2, LOC105246565 | Mm_Celera | 19:36553690 | AGTGAATACTTCCTC[C/T]CTCCCTTCTCCTCCA | 226098 |
rs248750357 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36576783 | CAACATTCCAACTCA[A/G]TTCTTCACCGAGGTA | 226098 |
rs248776018 | in-del | -/CACG | | | intron-variant | Hectd2 | Mm_Celera | 19:36579104 | TACTCTACAGCAGGT[-/CACG]AGAGTAATTACTCTG | 226098 |
rs248792338 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36582309 | GCATGTAGCCATGCT[A/T]CCCACCATGAAAATG | 226098 |
rs248879668 | in-del | -/CCGCCA | | | cds-indel, intron-variant, upstream-variant-2KB | Hectd2, LOC105246565 | GRCm38.p3 | 19:36554748 | CCGCCGCTGCCGCCG[-/CCGCCA]CCGCCTCGCGCCTCA | 226098 |
rs248926623 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36574269 | TTTTCCTCTCCATTC[A/T]CTGCCTCTGGGCAGC | 226098 |
rs248931422 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36575190 | AGTATGAAACATCTA[A/G]TTCATTAAAGATGAG | 226098 |
rs248956539 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36570060 | TCTTCCGTTGCTGCA[C/T]AATGAATTGTCACAA | 226098 |
rs248987654 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36569093 | AGTTTTAGTGATCAT[A/T]AAAGCAGTATTATTT | 226098 |
rs248992765 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36575604 | CCTACACCTCTGTGT[A/G]CTCTTAACCATCTAA | 226098 |
rs249001406 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36583445 | AGATCTTAAATACAT[A/G]CAACTACTTCAAGAA | 226098 |
rs249036715 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36600872 | ACAAGTTATTTCCAT[G/T]CCCTTTGATAATACT | 226098 |
rs249101810 | in-del | -/CATTTTGTCTAT | | | intron-variant | Hectd2 | Mm_Celera | 19:36559897 | ATGTAACCTTTTGTG[-/CATTTTGTCTAT]CATATTCTAAATGAG | 226098 |
rs249142876 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36578210 | TTTATCTTCAAAAAC[A/G]TCCGTTTGTTCTTTT | 226098 |
rs249159520 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36570342 | CACATGTCTTCTTAC[A/T]GGTTCTTAATAATAT | 226098 |
rs249202207 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36593638 | TTGTACCTTTATAGG[A/C]ATCTCATCCTTTAGG | 226098 |
rs249202306 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36601681 | AACCCTGTTCACAGT[A/G]TGGAAGATAGAACAC | 226098 |
rs249213436 | in-del | -/GCGCTTCCATA | | | intron-variant | Hectd2 | Mm_Celera | 19:36610543 | TGAGGCTCAGAGCCT[-/GCGCTTCCATA]CAGTTCGGATGACAG | 226098 |
rs249221255 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36605323 | TTTGTTTGTGATCAT[C/T]GACACTCTAGACTTG | 226098 |
rs249244729 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36559993 | TAAACTAAGATTTTT[A/T]AAATACATATGACCT | 226098 |
rs249272151 | snp | A/G/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36576735 | AATGGACATCTTGCC[A/G/T]AAAGCAATCTACAGA | 226098 |
rs249347031 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36572508 | TGCTCACATGTCACG[G/T]GTGCTACAGAAAGAA | 226098 |
rs249382144 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36578071 | GTCAGTGTTTACACA[C/T]TCTTTTTAACTTTGA | 226098 |
rs249382338 | in-del | -/AA | | | intron-variant | Hectd2 | Mm_Celera | 19:36603075 | AAGAAAGGATAAGAC[-/AA]AAAGATCTGTCACAC | 226098 |
rs249431356 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36577120 | TAATAGGCATGCACT[A/G]TACAGAATCTAGCAA | 226098 |
rs249443608 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36604026 | CAGTTCAGCCTTCTC[A/G]CTATAAAAATTGAGC | 226098 |
rs249453746 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36592450 | GAGAATAAAGTGAGT[G/T]AGTTCAATGTTCTTG | 226098 |
rs249485491 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36571122 | CCTTCTTCAGCTTCT[C/T]CCAGCCTTTCCCTAA | 226098 |
rs249501864 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36599313 | CATGAGTCCCCACTA[A/G]TTACTGGGCACTCCT | 226098 |
rs249524369 | snp | C/T | | | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | Hectd2 | Mm_Celera | 19:36569450 | CCAGAAGAAGGAAGC[C/T]GCTGAGAACAGAAGC | 226098 |
rs249561345 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36607773 | GTATTATCTTGCTTT[A/G]CAATACTATGTCACA | 226098 |
rs249600641 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36604794 | ATGTACACTGCTGCA[A/G]TCAGACCATCATGTA | 226098 |
rs249601670 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36615857 | CAAACTCAGAGATCT[A/G]CCTCCCTCTCTATCC | 226098 |
rs249635233 | in-del | -/A | | | intron-variant | Hectd2 | Mm_Celera | 19:36595892 | AAGAAAAGATGTGTT[-/A]AAAAAAAAGAAAAAA | 226098 |
rs249675757 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36596872 | TGGTGCACAGCTAAT[A/G]TAGGTGGTAGGATCA | 226098 |
rs249675950 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36589428 | CATGCGTGTATGCAG[A/G]GGACTGGTGTCCAGA | 226098 |
rs249682781 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36562357 | TGGTGGTAGGAATCG[A/G]ACCTGGGTCTTCAAC | 226098 |
rs249699994 | snp | C/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36577172 | ATTTATGATTTTTCT[C/G]CTTCAACTTCCTGAC | 226098 |
rs249707725 | in-del | -/AGTT | | | intron-variant | Hectd2 | Mm_Celera | 19:36558837 | TAGTTATACAGGACC[-/AGTT]AGTTCTACTTTAAAC | 226098 |
rs249713440 | snp | C/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36596019 | TACCAAAGTTGTTCA[C/G]GTGTATTAACTCATT | 226098 |
rs249739696 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36590022 | GAGTTGGTGTTTACC[A/G]TTCTCTTTTGGTAGC | 226098 |
rs249827740 | in-del | -/A | | | intron-variant | Hectd2 | Mm_Celera | 19:36565546 | TCAGACTTAGGCTGG[-/A]AGTACTGCTTTCCAT | 226098 |
rs249926943 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36588013 | GGCCCCATCCCTCAA[C/T]GGGGGACCATGCCTC | 226098 |
rs249943614 | snp | C/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36587812 | TCAGATGGTTGGCTG[C/T]GAGCATCCACATCTG | 226098 |
rs249957030 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36603053 | AGAACAGGGTCAGAA[A/G]ATGAGAAAGAAAGGA | 226098 |
rs249978090 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36582013 | GTGAGAGAGACAATG[A/G]TCTGGTGATAAGATA | 226098 |
rs249978986 | in-del | -/A | | | intron-variant | Hectd2 | Mm_Celera | 19:36594702 | GTTGGACCAGAAAAG[-/A]AAAGAGACCAGAGCA | 226098 |
rs249999735 | in-del | -/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36586346 | CTCATGTTGTGGTGA[-/C]CCCCCAACCGTAAAA | 226098 |
rs249999758 | in-del | -/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36583210 | AAGTAGAAGGGGGGT[-/G]GGGGGCACATGGGTC | 226098 |
rs250015207 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | Hectd2, 1500017E21Rik | Mm_Celera | 19:36620559 | ACAAAGAATTATGTA[C/T]AGGAAACCAGATTTA | 226098 |
rs250039686 | in-del | -/AATC | | | intron-variant | Hectd2 | Mm_Celera | 19:36565162 | TGCTCTTAACTACTG[-/AATC]ATGTCTCTAGCCCAC | 226098 |
rs250101694 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36558289 | GGGCTGAATGGGAAA[G/T]AGAGGTTCTCACTGG | 226098 |
rs250106945 | in-del | -/G | | | upstream-variant-2KB | Hectd2, LOC105246565 | Mm_Celera | 19:36553958 | GGAACGAAGGACGGC[-/G]GGGGGGCGGGGAGAG | 226098 |
rs250107215 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36592313 | TTAGAAAGTCTTTAA[C/T]TTCTTTATTTCTGTT | 226098 |
rs250124916 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36564126 | AATTTGACTCAGATA[A/C]TGTTCCTCAGTAAAT | 226098 |
rs250143579 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36599152 | ACCATTATTTTGAAG[A/G]AAACAAAGTAACTTA | 226098 |
rs250159450 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36602276 | ATAAAAATAAGAATA[C/T]TTTATTTCTCAGCAG | 226098 |
rs250161583 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36592794 | CTTTGATGAGTATGT[C/T]GTGTCCTTCCCTGTC | 226098 |
rs250185597 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36596042 | AACTCATTTGAAGGT[A/G]AAAATATTAAGCTAT | 226098 |
rs250199862 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36609916 | TCTTATATACATACT[A/T]ATACACAGACACAAA | 226098 |
rs250284888 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36557071 | ACTTGATGGAATGTG[A/G]TGGAAAGAGAAAGAC | 226098 |
rs250344555 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36585178 | TTGACTTAAAAAGTG[C/T]ATATATTTTTAAATT | 226098 |
rs250376319 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36578149 | AACTTTTTGTTGTAG[C/T]TTTAATGGAATTTTG | 226098 |
rs250436313 | snp | C/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36572796 | GGTTACCCCAGTGTG[C/G]GTTCCCTAACAGCTG | 226098 |
rs250508963 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36557447 | CCATGATGGGAGAGA[A/G]AATGGTAGAAACTGT | 226098 |
rs250584332 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36613546 | AAGTAGTAACAAATA[C/T]AATTTTGTGTTTGAG | 226098 |
rs250679659 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36560775 | GAATGCACATCTGTT[C/T]ATTCTCCCATTCATG | 226098 |
rs250680201 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36558123 | TGAATTCACTAAGGC[A/T]GGCAGATTGAAATGG | 226098 |
rs250726035 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36583601 | TAAGTGTTAATAATG[C/T]TAAGTTTCACTGAAC | 226098 |
rs250913672 | snp | C/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36574937 | GTTCATCTGCAAAGT[C/G]TTTGTAAGATATTCC | 226098 |
rs250922564 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36592532 | CTCATAAGGTATAGA[A/G]AAGAATGTGTATATT | 226098 |
rs250940175 | in-del | -/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36592486 | TGAGACTTGCTTTGT[-/G]TCTGAGTGTATGATC | 226098 |
rs250989454 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36586442 | CAGATAGAGGTTTGC[C/T]GAAGGAGTTGTGACC | 226098 |
rs250990577 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36580276 | GCTATGCAGGAACAG[C/T]CTTTATATAACCAAC | 226098 |
rs251005376 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36558903 | GGAAAGGGAAAATTG[A/G]CTTTCTGTTTAATTG | 226098 |
rs251053900 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36561006 | CACATGAAAAAGCTA[C/T]ATCTGTAGTGAGAAA | 226098 |
rs251053967 | snp | C/T | | | upstream-variant-2KB | Hectd2 | Mm_Celera | 19:36552306 | AATCTCTCTAAATCC[C/T]ATTTCATTGCCCCAT | 226098 |
rs251084939 | in-del | -/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36571788 | CCTACCTGGATTGTC[-/T]ATTTGTTTTAAGGTT | 226098 |
rs251099919 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36586146 | TATATTCATGTATTT[C/T]CAAAGGTCAAATCTT | 226098 |
rs251129017 | in-del | -/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36595947 | AAAAGCAAATTTTTA[-/T]TTTAAAAAAATTATA | 226098 |
rs251166926 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36586717 | AAAACAGGGCTATTT[A/G]GGAGGTTTTGGAGGA | 226098 |
rs251192008 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36607691 | TCATTTACAGGTCTC[A/G]CTTGAGTGTGTCCAA | 226098 |
rs251243486 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36580221 | GCAATCTACATAGAT[A/G]CTTTTGATTATCTCT | 226098 |
rs251271297 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36578913 | TGATTGAAGAAATAT[A/C]AAAGAACTTATGGGC | 226098 |
rs251319043 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36580695 | TCATATATTGCAGTT[A/G]CATATGTCAGAACGA | 226098 |
rs251336454 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36588551 | AAAAAATAAGTTGCT[A/G]GCTTTAAAGAAAACT | 226098 |
rs251371125 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36607626 | GGCCAGAGTGACTAA[G/T]TCCACACTCTCCAAG | 226098 |
rs251418299 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36579708 | TCTTTGTGGTTGTGT[A/G]CTTTACTTGGGTGAC | 226098 |
rs251437099 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36574583 | TCTTCTGGTGTGTCT[G/T]AGGACAGCTTTAGTG | 226098 |
rs251456661 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36600406 | AACCAAAATGGCAAA[A/G]ATTGAGAAGCACTGT | 226098 |
rs251463026 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36618408 | ATACCAGTGAGGAAA[C/T]GGAGATTGGAAACAT | 226098 |
rs251471877 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36574152 | ACTCCTCTACTCCTT[C/T]GCCTCCCAGCCACAT | 226098 |
rs251486440 | in-del | -/A | | | intron-variant | Hectd2 | Mm_Celera | 19:36557881 | TTTTAACTTCTTGGT[-/A]AAAACTAAGAGTGAA | 226098 |
rs251509862 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36600243 | CAACAGCTCACTTCA[C/T]GGGTCTTCCATTTGG | 226098 |
rs251509951 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36608087 | AACAAAATAATAAAG[G/T]TAAAATGTTATGGAG | 226098 |
rs251510456 | snp | C/T | | | upstream-variant-2KB, intron-variant | Hectd2, LOC105246565 | Mm_Celera | 19:36554503 | GGGCCGCGGTCTGAG[C/T]CCCGGCCGGCGGACC | 226098 |
rs251559861 | snp | G/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36565355 | TTGTTAGTGAGCCTT[G/T]GCTCCTTGTCTAGTT | 226098 |
rs251594635 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36571769 | ATTTGTGTAATTGGG[A/T]TTTGCCTACCTGGAT | 226098 |
rs251623267 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36610748 | CCCATGACATTACTT[A/T]TACAATTTAATATAA | 226098 |
rs251644296 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36581818 | AAATTCTACTGTCTT[C/T]TAACAGGAAAAGTTT | 226098 |
rs251671585 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36583568 | CATATATAAGGGATT[C/T]GCATATTTCTGAAAA | 226098 |
rs251711447 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36581945 | TGTCTTAGTCCATTA[C/T]ACACGGGACAAATAC | 226098 |
rs251727334 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36610989 | CATAAAATAGTAGCA[C/T]ATTTAAAATATATAT | 226098 |
rs251754839 | snp | A/G | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36598134 | TCTTTGGATTTTGAG[A/G]CAGGTGAGTCTGTAC | 226098 |
rs251755106 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36589950 | CAAGCTTTATGCCAC[C/T]GTTGCCCTAGCATAT | 226098 |
rs251779134 | in-del | -/TT | | | intron-variant | Hectd2 | Mm_Celera | 19:36585598 | TTTATTGTACAACTC[-/TT]TTGTTTTTTAAAAAG | 226098 |
rs251829193 | in-del | -/A | | | intron-variant | Hectd2 | Mm_Celera | 19:36573972 | TATCCTAGAATTCCT[-/A]CCCCCAGAGCAGGCA | 226098 |
rs251839803 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36582156 | TTAGGAGGAGTGGCA[C/T]TGTTGGATGAAGTAT | 226098 |
rs251879523 | snp | G/T | | | intron-variant, downstream-variant-500B | Hectd2 | Mm_Celera | 19:36611530 | TTAGATGAGCAAGAA[G/T]TAATCAACATGTAAG | 226098 |
rs251923533 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36603903 | AAATTAAGTATCCAC[A/G]ATAGTTTAAGCCTGA | 226098 |
rs251932757 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36575063 | GTAGTCTGTAATTGT[C/T]AAGTGATTTACTGAG | 226098 |
rs251933929 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36576717 | AAAGGTTAATATAGT[A/G]AAAATGGACATCTTG | 226098 |
rs251996929 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36610070 | CAGTATAAGTGACAA[C/T]GGTACTTTTTTATCC | 226098 |
rs252036898 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36609520 | AAAATCAGGCTTTCC[G/T]TTTAGAACTCTTCTC | 226098 |
rs252084572 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36568798 | TTGTTTTTTATAATT[C/T]ATGTTTTATTTTTAC | 226098 |
rs252143870 | in-del | -/GCCATCTTGTGATTAG | | | intron-variant | Hectd2 | Mm_Celera | 19:36604592 | CTGGACTCTAGACCT[-/GCCATCTTGTGATTAG]GTGTAGAACAAGTCA | 226098 |
rs252150281 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36602407 | AGAAGAAATTTTATT[G/T]CCTATGGCTCCAAAA | 226098 |
rs252181274 | in-del | -/A | | | intron-variant | Hectd2 | Mm_Celera | 19:36585428 | ACATCGTTAATTCCT[-/A]TAATTGAATTTGCAG | 226098 |
rs252198117 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36593189 | GTGTTTCGCTTCCTT[A/G]GATTTTGGTTGTTTA | 226098 |
rs252324205 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36567157 | CACCTTTGTGTTTTC[A/C]AGGCAGGGTCTCTCT | 226098 |
rs252385583 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36583897 | CTAACTTGAAAAGGC[G/T]TTGATTCATTACATG | 226098 |
rs252504227 | snp | C/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36606585 | GAAAATTAAACATCA[C/G]ATTTATTAGATTTTC | 226098 |
rs252527219 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36570436 | TTTCTCTCTCTCTCT[C/T]TTTTTTAAGATTTAT | 226098 |
rs252539967 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36605602 | CTGTGTAAACCTGAG[G/T]GTCAAGTTAGGTTCC | 226098 |
rs252616700 | in-del | -/TATT | | | intron-variant | Hectd2 | Mm_Celera | 19:36617450 | CAGAATTTTTTGGAA[-/TATT]TATAGCAATAAAAAT | 226098 |
rs252623194 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36616931 | CTCCATGTAGGCACA[C/T]ATGGAGTAACTGTTT | 226098 |
rs252644199 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36570118 | TATTAACTCACAGTT[C/T]TTTAGGTCAGAAGTC | 226098 |
rs252687236 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36570684 | GCTGGGATTTGAACT[C/T]AGGACCTTCGGAAGA | 226098 |
rs252716734 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36604439 | AATATGTATACTTGC[A/G]TAAATTCTGATATAG | 226098 |
rs252766812 | in-del | -/A | | | intron-variant | Hectd2 | Mm_Celera | 19:36567236 | CACCTCCTCAATGCT[-/A]GGATTAAAAGCATGT | 226098 |
rs252776254 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36564224 | AGTGGAACAGGTATT[C/T]TAAATATTTTTGTAT | 226098 |
rs252793802 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36612072 | TGTGTTAAGGGAGAG[A/G]CAGAACTGGTCTACA | 226098 |
rs252814334 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36588739 | TGAATGGCACAGCCA[G/T]TGTGGTGACGTCTCA | 226098 |
rs252852793 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36582994 | TAAGTAATAGATATT[C/T]ATTGTTAAGCTCAGA | 226098 |
rs252853694 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36589257 | ATTAGCAAAGAATAG[A/G]CTTCTAGGAGATAAT | 226098 |
rs252923991 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36567041 | TTTTTTGTGTGTTTG[A/G]GTACACATGTGTGTG | 226098 |
rs252956201 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36573577 | GGAAACCTGGGGCAG[A/G]GGTTGCTGTCTGGGG | 226098 |
rs252974040 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36578042 | GCCTTCGTGTTTAGC[C/T]GTCATGAATCTAAGT | 226098 |
rs252986456 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36559247 | GAACGAGCGAAAGGA[A/G]TATGTAAACAGTGGG | 226098 |
rs253014296 | in-del | -/A | | | intron-variant | Hectd2 | Mm_Celera | 19:36565784 | AGGAAGGGAGAAGAG[-/A]AAACACCCGGAAGTC | 226098 |
rs253030613 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36567571 | GAAGAGGGCATTGGA[C/T]CCCATTACAGATGGT | 226098 |
rs253071915 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36591701 | GTTTGAAAAGTCTGT[G/T]TAAATCTGTATCCCA | 226098 |
rs253097631 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36562543 | GTAGAGTTGTGCTGG[A/G]GGGCATGTAGCCCAA | 226098 |
rs253102378 | snp | A/G | | | upstream-variant-2KB, intron-variant | Hectd2, LOC105246565 | Mm_Celera | 19:36554198 | GATGCTCAGGTGAGC[A/G]GTCTCCCAGTCTCCC | 226098 |
rs253115329 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36592123 | TTTCAGTTTGGTCAG[C/T]ACCATTTGGTGGAGA | 226098 |
rs253116748 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36585657 | TGTGAATGAATGTGT[A/G]CATATGTATAAGGGA | 226098 |
rs253139857 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36561814 | TGACATATACAGAAG[C/T]GGATGCTTGGAGCCA | 226098 |
rs253180739 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36573875 | TGAATAGCACATTTA[G/T]ATGATTCAAAAGTGG | 226098 |
rs253254187 | snp | C/T | | | intron-variant, upstream-variant-2KB | Hectd2, LOC105246565 | Mm_Celera | 19:36555242 | GCGGTCCTTTCTCCC[C/T]TCGGGTTGAACAGTC | 226098 |
rs253267925 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36586068 | CAGTCACAGGAAGTG[A/G]CACAGGCTCAGAGAC | 226098 |
rs253290959 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36598615 | AGAAATCTTAGTCTT[C/T]AAGACAGAATCTGTA | 226098 |
rs253306711 | in-del | -/TGTT | | | intron-variant | Hectd2 | Mm_Celera | 19:36564872 | CCATTCCATTGAATC[-/TGTT]TGAAGATTTTGTAAT | 226098 |
rs253316503 | snp | G/T | | | upstream-variant-2KB, downstream-variant-500B | Hectd2, LOC105246565 | Mm_Celera | 19:36552479 | TCTTTATGCATAGCA[G/T]CCAGAGCTCTGTCTG | 226098 |
rs253444300 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36592060 | TTGGAATTGGGTGTT[A/G]TGCAGGGTGTTAAGT | 226098 |
rs253466775 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36558301 | AAAGAGAGGTTCTCA[A/C]TGGAATTGACTATAC | 226098 |
rs253469787 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36566431 | AGAAGAGGGTATACA[A/G]CCACTCAACAAATGA | 226098 |
rs253474906 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36585296 | AAATCATTCTTATAC[A/G]TTAATTTTATTTTCA | 226098 |
rs253492012 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36561507 | AGTGGATATTAGCCC[A/C]AAAGCTCGGAGTACC | 226098 |
rs253501607 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36565568 | GCTTTCCATTTTGTC[C/T]TTGGCTAGCCAGGCT | 226098 |
rs253562698 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36616691 | TTTTACAGCCACATA[A/T]GATTTTGGTTCATCC | 226098 |
rs253619229 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36601313 | ATAAAATCTTTTGTG[A/G]ATAGTAAAACACCAT | 226098 |
rs253629656 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36607366 | GTAGGAATTTAAACT[A/G]AGAGGATGATTGGGT | 226098 |
rs253676801 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36594171 | GGTAGGATAGCAGGC[C/T]TCCAATGGAGACAAA | 226098 |
rs253705670 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36590039 | TCTCTTTTGGTAGCC[A/T]GCAGAGTACCTTTCT | 226098 |
rs253719686 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36562852 | GTTTGGGTCTGGAGA[A/G]ATGGCTCAGTGGTTA | 226098 |
rs253729657 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36556060 | TGCACAGGGTTTTCA[C/T]AGCTTTTTATGTAGG | 226098 |
rs253731132 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36584633 | AGTCTGAGGCAGGAC[A/G]AACACCCCAAGTTTG | 226098 |
rs253841624 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36579589 | CCTACTCCCAGTGAT[A/G]CACTTCCTCCATCAA | 226098 |
rs253876147 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36578719 | TGGCCTTTTTATGTG[A/G]CTTCCTAACTGCTGC | 226098 |
rs253962033 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36570977 | CCCTCATTGAGGCCA[G/T]ACCAGGCAGTCCTCA | 226098 |
rs253962644 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36612528 | TAGAAAATGTTTTCT[A/T]CTTTTAAAAATAAAT | 226098 |
rs253989735 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36576929 | CAGAGCAATGGTGAT[A/G]AAAAGTGCATGGTAC | 226098 |
rs253995218 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36587340 | CTAATAATTATTTTA[C/T]CTTAATTATTTTCTT | 226098 |
rs254036606 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36586886 | GCCAGATACAATTGT[A/G]CAATTTGTAATCCCA | 226098 |
rs254069820 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36592834 | TAGTTTTGGTCTGAA[A/G]TCTGTTTTATTTGAT | 226098 |
rs254085086 | snp | A/T | | | intron-variant, upstream-variant-2KB | Hectd2, LOC105246565 | Mm_Celera | 19:36555725 | TATACATTTAAAAAA[A/T]TTTCTACTTGCAATT | 226098 |
rs254095181 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36587580 | CTTTCCCGGTTTCCC[C/T]TCTGCAAACTCCCTA | 226098 |
rs254136065 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36565076 | CCTTGGAACTGGGGT[A/T]ACATACAGATGGTTG | 226098 |
rs254138123 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36572168 | TGCGCCACCACGCCC[A/G]GCTTGTCCCTTGCTT | 226098 |
rs254168361 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36571567 | TGCCTCCCATGGTTG[C/T]CTGTTTCCATTTTTC | 226098 |
rs254261608 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36582569 | TGTCTACGTATGTTT[C/T]CGTGAAGAAAAACAC | 226098 |
rs254279510 | snp | A/C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36565921 | TGGAATTTTTAACTG[A/C/T]TTCTCATGGTCTGTG | 226098 |
rs254310142 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36588453 | TGCTTAAAATTATGT[A/G]TATATTTGTATTCAC | 226098 |
rs254348859 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36617107 | AACTGGAGTAAGGAT[A/G]CGGAAACACATGAGG | 226098 |
rs254396916 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36616426 | CCTTGCCCTACGGCT[C/T]ACACACTGAACGTTT | 226098 |
rs254397825 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36617066 | TATAAGAAGCCAGGT[A/G]TAGCTGTATTAGCCT | 226098 |
rs254401436 | snp | C/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36579911 | GGAAGGTAAGTACTT[C/G]TGGTCAAGCAGCCCT | 226098 |
rs254402512 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36585817 | GATGTTCTTGACTTC[A/G]GATCCATCTCTACAG | 226098 |
rs254494282 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36574849 | GAAACAGTACCACAA[C/T]AAGTGACTTTATATA | 226098 |
rs254524020 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36574438 | CTGTGTAAATAGGAA[A/C]ATAGGTATTTTCTCA | 226098 |
rs254539146 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36609509 | ATTCTTTCTTTAAAA[C/T]CAGGCTTTCCTTTTA | 226098 |
rs254556185 | in-del | -/A | | | intron-variant | Hectd2 | Mm_Celera | 19:36600050 | GAACAGTCAAAACTG[-/A]AAAAACGGTTTCCTC | 226098 |
rs254587147 | in-del | -/A | | | intron-variant | Hectd2 | Mm_Celera | 19:36605872 | AACCACAGACAAAGG[-/A]AAATAGAAATTCATA | 226098 |
rs254602648 | snp | C/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36609960 | AAATAAATGTTTATG[C/G]TAATAGCCATATCAA | 226098 |
rs254617670 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36602631 | AAAGTAGACAGCGCT[A/G]TTTATCTAGATTTCC | 226098 |
rs254639577 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36568688 | TAGGCCACCAGGGAT[A/T]TATAGAGGCCTTGTC | 226098 |
rs254646700 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36557851 | CAGAATTTCTGAGAC[C/T]GGAGACATATTTTTC | 226098 |
rs254647057 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36599551 | TATTAGAATAAATCA[C/T]GTGCATGGTGGAAAA | 226098 |
rs254667157 | snp | C/T | | | upstream-variant-2KB, nc-transcript-variant | Hectd2, LOC105246565 | Mm_Celera | 19:36553401 | GCACTATCCGATTCA[C/T]TTTATTGCTTGCTAC | 226098 |
rs254697363 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36565068 | GTCAGATCCCTTGGA[A/T]CTGGGGTTACATACA | 226098 |
rs254702346 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36561273 | AAATTAGCAACTTCT[C/T]TGTTGCATTTTAAAA | 226098 |
rs254723805 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36599393 | CTTTCTCTAAATATT[G/T]TTATGATCCTCATCA | 226098 |
rs254744909 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36593040 | TTTTTATTGGGGATT[C/T]ATGACCATTGACATT | 226098 |
rs254776997 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36592544 | AGAGAAGAATGTGTA[C/T]ATTCTTTTGTGTTTG | 226098 |
rs254846860 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36584461 | AAGCACTTACATGGG[A/G]ATGGGAAAGGAGAGA | 226098 |
rs254915106 | in-del | -/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36586745 | GGAAAGAAAGGGAAA[-/G]GGGGGGTGACATAAT | 226098 |
rs254935451 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36575389 | TCCTTCAGCTTTCTT[C/T]TTGCTAAATGTTCAG | 226098 |
rs254974621 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36612460 | TTCAATTAGGTTTTA[A/T]AATGGTATAGAAGAT | 226098 |
rs254975190 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36581314 | TTGGGGAAAGTGTGT[A/G]GGAAGTGATAGAAAA | 226098 |
rs254995675 | in-del | -/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36573188 | GACTTGCCTAAAACA[-/T]TTTTTTAAAAACTTC | 226098 |
rs255026971 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36567514 | AAAAAAGATTTATTT[A/G]TTTTATACTTATGAG | 226098 |
rs255041101 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36612843 | TGCGACTTAGGAGCA[A/C]AGCATAGCAGGAGAG | 226098 |
rs255107319 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36602628 | AATAAAGTAGACAGC[A/G]CTATTTATCTAGATT | 226098 |
rs255122451 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36596397 | CTGGAAGGGCAGCAG[G/T]CGCTCTGAACCACTG | 226098 |
rs255136621 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36612772 | AAATGTGACTTTAGC[G/T]CTTTCTCTCTTCTGC | 226098 |
rs255152765 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36603124 | TACAGACGTCCTTGG[G/T]AAGATAGGACCCAAG | 226098 |
rs255154844 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36595394 | TAGCATTGTAACAAA[C/T]ATTTAGAAGCTAAAT | 226098 |
rs255200348 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36582246 | TTCCTGCTGCCTGCA[A/G]ACCTGAATATAGAAC | 226098 |
rs255251535 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36560146 | CTGTCTCTCCTCTTT[C/T]TCAAAAAAGCATAGG | 226098 |
rs255314685 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36592095 | ATCAATTTGCATTAT[C/T]CTACGTTCAACTTTT | 226098 |
rs255347162 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36564629 | GTATTCCAAGACTTC[A/G]TCTCTAGTATTCAAC | 226098 |
rs255397633 | in-del | -/TGTTGAAATG | | | intron-variant | Hectd2 | Mm_Celera | 19:36579244 | AAAACACAGACCTGT[-/TGTTGAAATG]TGTTTTCATGCTCCT | 226098 |
rs255471983 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36602484 | ATATTTGACACCAGA[C/T]ACTGGCTTAAAAGTT | 226098 |
rs255497322 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36561094 | TATCAAGCCTCAAGA[C/T]CTGTACCTGTCGCCT | 226098 |
rs255497658 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36568911 | GTTCTATGGTCTATA[C/T]CTAAGGATCTCTATA | 226098 |
rs255516242 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36558561 | AACTGTGCCAAGTAG[G/T]CAGTAGAAGCGTTTA | 226098 |
rs255534939 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36568406 | TCACTGGGTAAAGGT[A/G]CTTGCCACTGAGATT | 226098 |
rs255543117 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36585929 | AGAAAATTAGGTCAT[C/T]CTTTTTCTAATTATC | 226098 |
rs255594068 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36603758 | TATCTTGTGGAATAA[A/C]TTTATTTCTAATCTT | 226098 |
rs255660073 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36561518 | GCCCAAAAGCTCGGA[A/G]TACCCAAGATACAAT | 226098 |
rs255694784 | snp | C/T | | | synonymous-codon, nc-transcript-variant | Hectd2 | Mm_Celera | 19:36614431 | GAGGAGCACACAGTA[C/T]GACGGCTATGCGAAG | 226098 |
rs255714308 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36570249 | AACCTCCTTTTCCTC[C/T]TCCTCCTGGCAAAAT | 226098 |
rs255722642 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36568850 | TTTTAGGAATTTTTA[A/G]AGTTGTTGAGATGGA | 226098 |
rs255735579 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36584551 | AGAAAGGAAGGGCAC[A/G]TGTCAGGGTGAGGTG | 226098 |
rs255736961 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36576052 | CTCAAAAAAAAAAAA[A/C]CCAAAACCCCACATG | 226098 |
rs255831992 | snp | C/T | | | intron-variant, downstream-variant-500B | Hectd2 | Mm_Celera | 19:36611776 | ACGGTACTCTCCAGG[C/T]AGTTGCATCTTCCCA | 226098 |
rs255854563 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36570755 | TTTCTTTCTCTTTTG[A/T]AAAATTATTATTCTT | 226098 |
rs255891371 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36578499 | CTTGATTTTCCCAAT[A/G]TTACATTTTCCATTA | 226098 |
rs256002773 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36594742 | CTTCCAAGCTGGAGA[G/T]AAGACTGGAGGTGTT | 226098 |
rs256074689 | snp | A/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36588200 | TCAATTTCCTGCCCC[A/T]CTGTGCATCTCCTCC | 226098 |
rs256132487 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36580716 | GTCAGAACGAAGATT[A/T]TCCTCTTTTATTTAT | 226098 |
rs256135129 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36589143 | AACATAGATTCCTTT[C/T]TCATACAATATACTC | 226098 |
rs256170684 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36586860 | TATTGGAATTAAATG[C/T]ATCCCTAATGGCCAG | 226098 |
rs256175487 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36562316 | ACCATTTATGTGCTC[G/T]CCTAAGGAGGTGGTA | 226098 |
rs256179508 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36618249 | AAGGATTCAAGGACT[A/G]GATGTTCAGTGTGCA | 226098 |
rs256180677 | in-del | -/A | | | intron-variant | Hectd2 | Mm_Celera | 19:36582426 | AATAGAATGCTGACT[-/A]AAACAGTAACCTTGA | 226098 |
rs256237618 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | Hectd2, 1500017E21Rik | Mm_Celera | 19:36619076 | TGAGAGCCTATGGCA[A/G]AAACAGGTCTGAGTC | 226098 |
rs256265408 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36556653 | AAAAACTCTTACTTG[C/T]CTTATGGCATTTCAA | 226098 |
rs256307102 | in-del | -/AGA | | | intron-variant | Hectd2 | Mm_Celera | 19:36583643 | AGGCACCTTTAAAAG[-/AGA]AGGAGAGAAGGAACT | 226098 |
rs256316322 | snp | C/T | | | intron-variant, upstream-variant-2KB | Hectd2, LOC105246565 | Mm_Celera | 19:36555544 | CCTTCCCCCTGTTTG[C/T]ACTTAGTGGTTGGGA | 226098 |
rs256329717 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36572271 | TTTTTTACTCTAAAT[A/G]TGTTCCAACTAGCTA | 226098 |
rs256368204 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36611301 | GACCCACAGTCTGTA[A/T]CCTTACAGTCTGAAG | 226098 |
rs256398966 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36616340 | TTAATTCTTGTCTTC[A/G]TTACTCCTATTCCAC | 226098 |
rs256413149 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | Hectd2, 1500017E21Rik | Mm_Celera | 19:36619212 | GCCCAGTGGCAGATG[C/T]GTGCTGGCAGCACAC | 226098 |
rs256443126 | snp | A/T | | | intron-variant, upstream-variant-2KB | Hectd2, LOC105246565 | Mm_Celera | 19:36555350 | TTTTATTTTTTTCAT[A/T]CGGTACTGACGTGTG | 226098 |
rs256460342 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36608170 | GAAACTGTATAGAGA[C/T]AATATAGTACAGTAC | 226098 |
rs256484297 | snp | C/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36562590 | TAGCATGCACAAAAT[C/G]ATGTTCCATCCCCAG | 226098 |
rs256500633 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36591802 | TCTGTCAGATGTAGA[A/G]TTGGTAAAAGCCTTT | 226098 |
rs256530644 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36566153 | AACCGCCTTACTGGC[A/G]TTCCCAGGAGCATGT | 226098 |
rs256610671 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36577273 | GCATATTTCTTTTAC[A/G]GAACTTTCTTATGTC | 226098 |
rs256624725 | in-del | -/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36557279 | TGTAATCATGTGGGG[-/T]TTTTTTCCCTCAGAA | 226098 |
rs256626497 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36588283 | ATTCCCTCCCACTCT[A/C]TGCTTCCTTTGATTA | 226098 |
rs256650859 | snp | C/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36576847 | AACAAAGCCAGGGTA[C/G]TGAAGACTCTTCTCA | 226098 |
rs256771846 | snp | C/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36572090 | ACTCACTTTGGAGAC[C/G]AGGCTGGCCCCGAAC | 226098 |
rs256772441 | snp | A/G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36590463 | CCAGGGAGAACATGC[A/G/T]CCTCCTCCTCCTCCC | 226098 |
rs256800757 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36568283 | TTCTAAAAGAGTAAA[A/T]GGAATCAATCTGGCG | 226098 |
rs256816705 | snp | A/G | | | upstream-variant-2KB, nc-transcript-variant | Hectd2, LOC105246565 | Mm_Celera | 19:36553296 | CTTTTGTTATTAATA[A/G]AGAAACGATGGTGAC | 226098 |
rs256851805 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36574561 | TCTGTAATGGGATCT[A/G]ATGCCCTCTTCTGGT | 226098 |
rs256858752 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36566919 | GTCAATGAGCAGCCA[A/G]AGATATTGCATATAA | 226098 |
rs256870360 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36559792 | CATATTAAAATAAAA[C/T]AATCCAGCCAGTAAC | 226098 |
rs256915221 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36559454 | AACATAATGAAGTTG[C/T]TGGTAGTGTGTAGTT | 226098 |
rs256926449 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36585078 | ATTTTATAGTCAGTA[G/T]TGACTTAAACAGTGT | 226098 |
rs257017362 | in-del | -/AC | | | intron-variant | Hectd2 | Mm_Celera | 19:36598003 | GCCAATATAACCATA[-/AC]ACACACACACACACT | 226098 |
rs257086409 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36575328 | TTGGCTCTGATGGCT[A/G]ACGTTCTGTGAGTCA | 226098 |
rs257087493 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36592674 | TTGGTAATAGTGGTG[A/T]ATTGAAGTCTCCCAC | 226098 |
rs257106982 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36585732 | ATTACAGGTGGTGAT[A/G]GGCAGTGTGTGGTAT | 226098 |
rs257175245 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36613442 | CTGTAGGTCATGACC[C/T]TATTGGGTCTAACAA | 226098 |
rs257177045 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36591503 | CAAGTTTGCGCTCCT[A/G]CTAGCAATGGAGGAG | 226098 |
rs257199161 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36557796 | GCTGGGATTAAAGGC[A/G]TGCGCCACCATGCCC | 226098 |
rs257201713 | in-del | -/GGTC | | | intron-variant | Hectd2 | Mm_Celera | 19:36574023 | ACATGCATCTTCAGA[-/GGTC]TGTCTGTCTGCTTTT | 226098 |
rs257284517 | in-del | -/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36596661 | CTGGTTTTCCTTTTG[-/T]TTTTTTTTAAAATCA | 226098 |
rs257315176 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36587964 | TTCCTTTAGACAGGA[A/G]TAATCCTGGGTTAAA | 226098 |
rs257357535 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36558331 | CCAAGGAATTAAATA[G/T]ATTCAAAAAAGATAA | 226098 |
rs257363526 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36605976 | TGAGCGCTCCATAGC[C/T]TCAGTAATAGTGTCA | 226098 |
rs257396420 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36599329 | TTACTGGGCACTCCT[A/G]CAAGAGATGACACCA | 226098 |
rs257419477 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36606651 | GTCTCAATACATTTA[A/G]AGAAAATGTCTGACT | 226098 |
rs257431117 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36606998 | TATCTCAGGTATGTT[A/T]TGTAATTTATTCCTA | 226098 |
rs257438948 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36561058 | TCCTATTATTTGGGC[A/T]TTTTTCTCACCAGCC | 226098 |
rs257473595 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36568372 | AGATTAAAAAGAGAT[A/G]TTGGGCTGGAAAGAT | 226098 |
rs257480320 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36577906 | AACTAGGGATCTAAG[A/G]TTGTCTTCAGTTTTC | 226098 |
rs257531977 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36575519 | AAACAGCACAAGAGC[C/T]GCACTGAGAGAGGGA | 226098 |
rs257561158 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36587635 | ATGAGGGTGCTCCCC[C/T]ACCCACCTACCCACT | 226098 |
rs257591730 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36573178 | CCCCCTTTTAGACTT[A/G]CCTAAAACATTTTTT | 226098 |
rs257638960 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36578185 | AATTAGAAGTCTTCT[A/C]AACTGGCCATTTATC | 226098 |
rs257693843 | in-del | -/TGTT | | | intron-variant | Hectd2 | Mm_Celera | 19:36605306 | CCAGATTATGGTGAG[-/TGTT]TGTTTGTGATCATTG | 226098 |
rs257694899 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36604396 | TAGCCTTATTTCTAA[A/C]ATTTTTAAACTATTA | 226098 |
rs257709862 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36570732 | CCACTGAGCCATCTC[G/T]CCAGCCCTTTCTTTC | 226098 |
rs257725785 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36564017 | TCAAAGTAAATTGTA[C/T]TAAAATTTTGTATAC | 226098 |
rs257751929 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36573732 | TTTCTTAACTATTCC[A/T]AGAGAAAAGTGCATC | 226098 |
rs257778669 | snp | C/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36570844 | CTCATCCCATTTTTC[C/G]TCCCTCCTCCCCACT | 226098 |
rs257785549 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36617165 | AAAAGGCAAGTTTTC[A/G]GTTCAGTCAGAGACC | 226098 |
rs257802117 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36617920 | TCATCCATACAGTGG[A/G]AATAATAACCACTTT | 226098 |
rs257802160 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36609773 | ATGGGCTGGAAAGAT[A/G]GCTCAGCAGTTAAGA | 226098 |
rs257835180 | in-del | -/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36616829 | ACCAAAAAGCCATCC[-/T]TTTTTTTCAATAAAT | 226098 |
rs257858842 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36605310 | ATTATGGTGAGTGTT[A/T]GTTTGTGATCATTGA | 226098 |
rs257866105 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36610166 | GAAAACACGCAGGCA[C/T]AGCACCATGATCTGA | 226098 |
rs257868449 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36563799 | AGTCCACCCTGATTC[C/T]TTGAGGCTGAAGGTT | 226098 |
rs257888179 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36598494 | CAGGGTTAAAGCACA[A/G]CCCTACCGAATCTCC | 226098 |
rs257891854 | in-del | -/A | | | intron-variant | Hectd2 | Mm_Celera | 19:36602992 | TCTCCATTAGCATCC[-/A]GGGGTAAATAAATAT | 226098 |
rs257922520 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36598244 | GGGATTACAGGTGGA[C/T]ACTGCCATGTGTGGC | 226098 |
rs257940545 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36595096 | AAAGTGATGCATGTA[A/G]CCCCAAATTCACTCT | 226098 |
rs258000010 | in-del | -/GGG | | | upstream-variant-2KB, intron-variant | Hectd2, LOC105246565 | Mm_Celera | 19:36554562 | AGCCGGGCGCACGCA[-/GGG]GGGGGTGGGCGGCGG | 226098 |
rs258000125 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36588923 | TCATGTTCATGAATC[A/G]TTTTTAAATTAGAAA | 226098 |
rs258009026 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36575256 | GAGTGTTACGTACAC[G/T]TCGCTGTACTTGGTA | 226098 |
rs258046368 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36581091 | AGCCTCAGCGTTACT[A/G]TCTCTCTTATATAAG | 226098 |
rs258095481 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36578265 | TATATCTAAATGCAT[A/G]TAAATATTGTATATA | 226098 |
rs258106800 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36607747 | TGACCTATTTGAACT[C/T]CTTCATGCATGTATT | 226098 |
rs258109592 | in-del | -/A | | | intron-variant | Hectd2 | Mm_Celera | 19:36573241 | AAGCAGTTCTTCCGT[-/A]AGCCTTTTGAAATGT | 226098 |
rs258123145 | in-del | -/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36602935 | TCATTTGAAGCATTC[-/T]TGTAGCAAACACATT | 226098 |
rs258143417 | snp | A/G | | | intron-variant, downstream-variant-500B | Hectd2, 1500017E21Rik | Mm_Celera | 19:36621617 | TTATGGGTGAGGGAA[A/G]AGTGAGGCACAGAGA | 226098 |
rs258165046 | in-del | -/A | | | intron-variant | Hectd2 | Mm_Celera | 19:36580110 | TTATTTATGACACGT[-/A]AGGGGATGATGTTTT | 226098 |
rs258207914 | snp | A/T | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | Hectd2, 1500017E21Rik | Mm_Celera | 19:36619031 | ATTTAAAAATATATA[A/T]ATATATATATATATC | 226098 |
rs258257207 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36608571 | AGCTCTTTCTTATGT[C/T]TTCAGCCCTCATTTA | 226098 |
rs258267307 | in-del | -/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36590605 | GAGGATGAGGGTGTG[-/T]TTTTTTTCTTTCTTT | 226098 |
rs258268739 | snp | A/T | | | missense, nc-transcript-variant | Hectd2 | Mm_Celera | 19:36584037 | CCCCTTCCAGAACCT[A/T]CTCTTCCTAGCCAGC | 226098 |
rs258283345 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36601832 | AACACAGATCATTCA[C/T]ACTAGAGCACTTTCT | 226098 |
rs258316945 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36601057 | ATTGCATATTCATTT[G/T]AACATGTAAATATTC | 226098 |
rs258336031 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36598290 | AAATAACAGAATCAT[A/C]AAAAAAGCATAAAAT | 226098 |
rs258336549 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36567678 | GCCATCTCTTCAGCC[C/T]CCAATACGAATAACC | 226098 |
rs258376099 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36566634 | GTGTTGAAGCAGCCC[C/T]GCCATTCCTGCTACA | 226098 |
rs258384656 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36599097 | GTAGGGACATATTTT[A/C]AGGGTCGTGGAATAC | 226098 |
rs258416729 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36566122 | AGGAAGGAACCTGGA[A/G]CAGAAACTATGGAGG | 226098 |
rs258472597 | in-del | -/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36561157 | TCCACACAGAATTAA[-/G]GGGTGCCTTGCACTC | 226098 |
rs258511933 | in-del | -/A | | | intron-variant | Hectd2 | Mm_Celera | 19:36583565 | AAGCATATATAAGGG[-/A]TTTGCATATTTCTGA | 226098 |
rs258544324 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36592208 | ATGGGTGTGCGGGTT[A/T]ATGTCTGGATCTTAC | 226098 |
rs258552613 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36559046 | TTGGTAAAATCTTAT[C/T]TCTTTTTGTTAATTG | 226098 |
rs258605409 | in-del | -/A | | | intron-variant | Hectd2 | Mm_Celera | 19:36610013 | TAAAATAGGTGCTTT[-/A]AAAAAAGAAAACCCA | 226098 |
rs258701487 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36575171 | TAATTCTGTAAGACA[A/G]TCTAGTATGAAACAT | 226098 |
rs258824855 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36569151 | GGTGGACTATATACT[A/T]TGTACAAGAAATGGT | 226098 |
rs258859806 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36568948 | GAAATCCTGGTGTAC[C/T]TACAATTTAATTATA | 226098 |
rs258873483 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36568714 | TTGTCTCAAGATTTG[A/G]GACAACGGGTCAAAA | 226098 |
rs258905227 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36602117 | TGCGCATATCCGGTG[C/T]CTACTGCTTAGGAGA | 226098 |
rs258930113 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36556897 | TGGAAATTTTAAGAG[A/G]AAAATGCAAGTATGT | 226098 |
rs258968759 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36593519 | TCTTTTCCCCTTGTA[A/G]CTTTTAATATTCTCC | 226098 |
rs258971290 | in-del | -/GT | | | intron-variant | Hectd2 | Mm_Celera | 19:36616092 | TCCTTTTAAATGCCC[-/GT]GTGTCAAGTATTTGA | 226098 |
rs259030132 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36562242 | TTAATTAAAGAATAA[C/T]TGAATTAAAAATATT | 226098 |
rs259096711 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36562756 | AGTAGTTAATTTGAA[A/G]TTAATTCATATGCTT | 226098 |
rs259111014 | snp | C/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36577219 | CATGTAATTTTTGTA[C/G]CCGTGTCTTTAGTTA | 226098 |
rs259123663 | snp | A/C/G | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36594768 | GTGTTGGATCTGAAA[A/C/G]AGCAGGAGTGAGGAG | 226098 |
rs259130372 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36560746 | CTTTTCTTTTTTTTT[C/T]GGCTGCAAGGCCAGA | 226098 |
rs259160877 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36587892 | CAGCAAGCACTTCTT[A/G]GCATCCACAATAGGG | 226098 |
rs259167967 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | Hectd2, 1500017E21Rik | Mm_Celera | 19:36619884 | TAGCTTGATATAAAA[A/G]AGAAGTTTGACATTT | 226098 |
rs259226605 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36577508 | TGGGTAAGGTTATTA[A/G]CCTTAAGCTTTATCA | 226098 |
rs259269850 | in-del | -/TCAATAACG | | | intron-variant | Hectd2 | Mm_Celera | 19:36569842 | TCTGAACCTCTATCT[-/TCAATAACG]TCTTTCTTCCTTTGA | 226098 |
rs259287288 | in-del | -/AAAA | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | Hectd2, 1500017E21Rik | Mm_Celera | 19:36619019 | GTGAAGGCATGATTT[-/AAAA]AAAAATATATAAATA | 226098 |
rs259287359 | snp | A/G | | | upstream-variant-2KB, nc-transcript-variant | Hectd2, LOC105246565 | Mm_Celera | 19:36553144 | TCTATGAGATAGTCC[A/G]GAGATTTAAGAAGAG | 226098 |
rs259323513 | snp | A/G | | | upstream-variant-2KB, downstream-variant-500B | Hectd2, LOC105246565 | Mm_Celera | 19:36552520 | ACCCCCAGATCCAGT[A/G]GGTACACACAAAAAG | 226098 |
rs259324820 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36561121 | GCCTTTTCCGATCGA[G/T]CTCGTTCCAGTCTCG | 226098 |
rs259326286 | snp | A/C/G | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36582410 | TGGTGTTTCATAACA[A/C/G]CAATAGAATGCTGAC | 226098 |
rs259355647 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36588358 | AAAGCTATTTAGTGT[A/T]CTGAGATTTGGATTT | 226098 |
rs259357621 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36581950 | TAGTCCATTATACAC[A/G]GGACAAATACAGACA | 226098 |
rs259363428 | in-del | -/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36614165 | TTTTTTAAATTTGGA[-/T]TTTTCAAGACAGGGT | 226098 |
rs259375881 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36603089 | CAAAAAGATCTGTCA[C/T]ACAAGACACTGTCCA | 226098 |
rs259387024 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36586384 | CATCGCTACTTCATA[A/G]CTAATTTTGCTACTG | 226098 |
rs259410864 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36571660 | CCTGTCTTCTCTCCC[A/T]CCCAGAAGGCATGTT | 226098 |
rs259439657 | in-del | -/TGTGTGTG | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36586598 | TAACATTATACCGAC[-/TGTGTGTG]TGTGTGTGTGTGTGT | 226098 |
rs259452847 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36580440 | ATTACAGTCTACACA[A/C]ATTTTAATATACTAC | 226098 |
rs259474404 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36603327 | ACTGATCCTTAATTG[A/C]ACAGAATTCATTTTC | 226098 |
rs259492564 | in-del | -/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36558023 | CTATGAAAGATGGGG[-/T]GCAGGGGTTAGTGAA | 226098 |
rs259530102 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36590664 | CATGATGTCATTTTT[A/T]AAAATACCTGATTAT | 226098 |
rs259531536 | in-del | -/A | | | intron-variant | Hectd2 | Mm_Celera | 19:36589796 | TATTGTTACTTTTTT[-/A]AAGACAAATAGCATT | 226098 |
rs259547863 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36566593 | TTACATAATGAAGTG[C/T]AGATTTTTGATGTCT | 226098 |
rs259569160 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36597693 | ATTTTCAAAATAAAA[A/T]TTTAAAACTGTCAGT | 226098 |
rs259605432 | snp | C/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36590344 | AATGCCCTTCAGTTC[C/T]AGCTGTCTATTCCCT | 226098 |
rs259641619 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36589705 | TGTATTTGCTCCCAT[A/C]TTCTGCAGGAGGAAG | 226098 |
rs259734271 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36556978 | GATAAAAAGCCTAAG[A/G]AAAAAAAATGCTGAC | 226098 |
rs259736277 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36564744 | TCTGTCTCCATCCCC[C/T]CACGCCCACCCTAGC | 226098 |
rs259763560 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36590970 | GAAGGGAGCATCAAT[A/G]TCATTATGCTACTTT | 226098 |
rs259793728 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36579547 | GGTGAGACACTAGGT[A/G]TGGCTTGAGCATCTT | 226098 |
rs259798303 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36557726 | TTCCTGGAACTCACT[C/T]TGTAGACCAGGCTGG | 226098 |
rs259853898 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36589519 | GCTCAGTTGCTTTAG[A/G]GGGCTTTGTTCTCCT | 226098 |
rs259867506 | snp | A/G | | | intron-variant, downstream-variant-500B | Hectd2, 1500017E21Rik | Mm_Celera | 19:36621532 | AGAATGTTATGATCA[A/G]TATGCAAATAAATCT | 226098 |
rs259885271 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36574138 | AGCACTTTGGCTTCA[C/T]TCCTCTACTCCTTCG | 226098 |
rs259894954 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36612672 | CATGATGGGAACCTC[A/T]CAAAGAATCAATACA | 226098 |
rs259966077 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36560970 | CTACCTCACATAATA[G/T]ATATGGAATCTAGAA | 226098 |
rs260011101 | snp | A/G | | | synonymous-codon, nc-transcript-variant | Hectd2 | Mm_Celera | 19:36599031 | TAAAGTTCTGGCTTT[A/G]CTTAGTAGGTTTTGA | 226098 |
rs260062542 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36606154 | ATTATATGTATCATA[C/T]ATATTATGGATAAAA | 226098 |
rs260083540 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36611293 | AGGTAAGGGACCCAC[A/G]GTCTGTATCCTTACA | 226098 |
rs260155308 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36581765 | AAGCTTGCTTAGTAA[A/G]ACGTGAAATCCATAC | 226098 |
rs260177668 | snp | C/T | | | upstream-variant-2KB, downstream-variant-500B | Hectd2, LOC105246565 | Mm_Celera | 19:36552619 | CTACCTCCCAGTCCT[C/T]ACCCGGGGCTTGTAT | 226098 |
rs260237825 | snp | A/G | | | intron-variant, downstream-variant-500B | Hectd2 | Mm_Celera | 19:36611846 | ACATTACCCCAACAC[A/G]GGAAGTTTAGGAGAA | 226098 |
rs260264822 | snp | A/C | | | synonymous-codon, nc-transcript-variant | Hectd2 | Mm_Celera | 19:36605278 | CCTTCTTCTAATTCG[A/C]CAGATTTTCCATCCA | 226098 |
rs260300995 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36604221 | ACTTTAAATAAAAAT[A/G]AAAAATATCTGCTTT | 226098 |
rs260383476 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36594608 | CCTGTTCAGCTGATG[C/T]TTGCCCAGGGTGTGC | 226098 |
rs260393371 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36586362 | CCCCCAACCGTAAAA[C/T]TATTTCCATCGCTAC | 226098 |
rs260411204 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36601793 | GACTTCATTGTGTAA[A/C]CATGATGAGAGCAGG | 226098 |
rs260436926 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36556601 | TATCTAAAACTGTAG[A/C]CAATGTATTGTTTGT | 226098 |
rs260572836 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36576295 | CTATTCATTATAGTA[C/T]TCAAAGTTCTAGCTA | 226098 |
rs260588067 | in-del | -/AT | | | intron-variant | Hectd2 | Mm_Celera | 19:36613064 | CTTTCTTTTTTTTAA[-/AT]TCTATTTTATGTATT | 226098 |
rs260597510 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36608357 | TACTATAGGCATCCT[G/T]CTTTTAGGTTTTAGC | 226098 |
rs260623798 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36607730 | TACCTTTTTACTAAC[C/T]TTGACCTATTTGAAC | 226098 |
rs260641587 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36588678 | CACTGAGACGTCAAG[A/C]CCAAGCACACTCTCT | 226098 |
rs260687193 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36605534 | ATTAAATAGTCATTT[C/T]ACAAAATAGAAGTCT | 226098 |
rs260703925 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36560226 | TGTCATTTAGTCAGT[A/T]AATACAATAGAAAAC | 226098 |
rs260752482 | snp | A/G | | | upstream-variant-2KB | Hectd2 | Mm_Celera | 19:36552050 | CCACATGTGCAACAT[A/G]GCACATCAAGCGATA | 226098 |
rs260842653 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36602968 | CAGAGAAAAGGACCT[C/T]AGAGCTTGTCTCCAT | 226098 |
rs260859931 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36558275 | CTTCAGTATTTAATG[A/G]GCTGAATGGGAAAGA | 226098 |
rs260877063 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36610872 | AAGAAAATATTTCTC[C/T]CAGTACTCTCAGGCT | 226098 |
rs260893458 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36565453 | TGAGGTGCCAAGATG[G/T]TTTTTGAAATTTGAA | 226098 |
rs260924501 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36580189 | AGCAGCACAGAGACC[C/T]AGGTTGCTTCTCTTG | 226098 |
rs261059466 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36574669 | CTCATACATACATAT[C/T]TTTCCTACATGTACA | 226098 |
rs261094104 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36578115 | TTTGAATCTGCAGGT[C/T]ATGTCATGAAAATAA | 226098 |
rs261124543 | snp | C/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36584137 | TCAGGGCTATGCATC[C/G]GTTAACATCTTTCCC | 226098 |
rs261149195 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36600105 | ATATTTTCTTGGTAG[C/T]GTTTCTTTTACAGAT | 226098 |
rs261178014 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36607414 | TGTTACTGACTTGCT[A/G]CAAAGCAGTGATCAC | 226098 |
rs261183660 | in-del | -/C | | | upstream-variant-2KB, nc-transcript-variant | Hectd2, LOC105246565 | Mm_Celera | 19:36553179 | CTAAAAACAAAAATT[-/C]AAGAAAAAGGAGACA | 226098 |
rs261187853 | in-del | -/TTT | | | intron-variant | Hectd2 | Mm_Celera | 19:36572306 | TCCACCTCTTGCCTG[-/TTT]TTTTTTTTTTTTTTT | 226098 |
rs261220241 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36573366 | TTTATTCTTAGCAGA[A/G]CCTTGGTGTGGCATG | 226098 |
rs261308752 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36601240 | TATAGAAAATTAAAA[G/T]ACTGTACTTAAAGGG | 226098 |
rs261317245 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36567339 | TTACTTGTCAGCTGC[C/T]GACTTTTATGACTCT | 226098 |
rs261336039 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36586224 | TAAAAATATTTTTGG[C/T]TCAATTTGCTAGTAT | 226098 |
rs261344731 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36573757 | TGCATCTGAAAAAAA[A/T]ATTTTGCTGCATTAG | 226098 |
rs261365229 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36562865 | GAGATGGCTCAGTGG[C/T]TAAGAGCACTTATTG | 226098 |
rs261436047 | in-del | -/GAT | | | intron-variant | Hectd2 | Mm_Celera | 19:36597360 | TAGTAATACATAAAA[-/GAT]AAATAAACATCTATT | 226098 |
rs261442653 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36567949 | GATCTAAAAGGTTTT[A/G]CTGTTGTTAGTGTAT | 226098 |
rs261523640 | in-del | -/TGTT | | | intron-variant | Hectd2 | Mm_Celera | 19:36584749 | TACACATTTATATAC[-/TGTT]TGTATCAACTATAAC | 226098 |
rs261525189 | in-del | -/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36586541 | TTCTTTATTTGGTTA[-/T]TCAATACCAAAGGTC | 226098 |
rs261537973 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36592403 | TTATTTCTTTTGTTG[A/T]TGATATCCATCTTTA | 226098 |
rs261539081 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36585826 | GACTTCAGATCCATC[G/T]CTACAGCTCCTCTTT | 226098 |
rs261564674 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36591996 | ATCCTCCACTTTCTC[A/T]TTTATCAGGTTCAGT | 226098 |
rs261571263 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36581478 | AAATTAAGTCTTAAT[C/T]AAATCTTTGTTTATA | 226098 |
rs261642791 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36609438 | TGTAAGTATGTTATT[A/G]CCACCTTGTGGTTGT | 226098 |
rs261653785 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36610487 | GCAAAGAATGGAGCT[A/G]GAGGTATCATCCCAT | 226098 |
rs261687892 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36556407 | TCAGTGGAACTGAAA[A/G]AAAGGTTTGGAACTT | 226098 |
rs261779619 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36585802 | TCTGGAAGATTAGCG[A/G]ATGTTCTTGACTTCA | 226098 |
rs261891063 | snp | C/T | | | intron-variant, downstream-variant-500B | Hectd2 | Mm_Celera | 19:36611644 | ATTTGAGCTGCGCAG[C/T]AAGACCCTTTCTCAC | 226098 |
rs261902895 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36566528 | GTGTATGCCTATGAT[C/T]CTGAGACTGCTGATT | 226098 |
rs261938739 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36614190 | CAGGGTTTCTCTGTG[C/T]AGCCCTGGCTGTCCT | 226098 |
rs261980973 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36590855 | CTGGATTGTAACCAG[A/T]CCTTTGGCTACTTCT | 226098 |
rs261982687 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36561202 | TAAGAATTTAGATGA[A/C]TTTCTTCTTGAAGAA | 226098 |
rs262079191 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36581213 | TGGGTATAAAAATGT[A/G]CATGCATATAGGCTT | 226098 |
rs262099912 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36587051 | AATACAATACTGTTA[A/G]ACTTACAATTTTGTC | 226098 |
rs262136997 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36567765 | CTGTAATGTGTAAGG[A/T]CTCTAGTGCAGCATA | 226098 |
rs262178600 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36613018 | CCATATAACTTGAAG[C/T]TAGAATACCATTTTG | 226098 |
rs262187341 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36565836 | TGGAAGTCTCCCTCT[A/G]TGAAGGCTACTGTAG | 226098 |
rs262217253 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36605631 | CCAAGTATCCATGTG[A/T]AAAGCCAGGTACTGC | 226098 |
rs262228991 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36560410 | GATGTGGCACAAAGA[A/G]CCTCCACCTAAAGCA | 226098 |
rs262258344 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36588186 | CTACATACCTCTGTT[A/C]AATTTCCTGCCCCTC | 226098 |
rs262259646 | in-del | -/CAGC | | | intron-variant | Hectd2 | Mm_Celera | 19:36613886 | GCAGAGGTGGCAGGA[-/CAGC]CAGCTCAGGACACAT | 226098 |
rs262275906 | snp | A/T | | | utr-variant-5-prime, intron-variant, nc-transcript-variant, upstream-variant-2KB | Hectd2, LOC105246565 | GRCm38.p3 | 19:36554753 | gctgccgccgccgcc[A/T]ccgccTCGCGCCTCA | 226098 |
rs262280072 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36594313 | AATACAGTTCCTCAT[A/G]TTTTGGTGACCCCAA | 226098 |
rs262285467 | in-del | -/TC | | | intron-variant | Hectd2 | Mm_Celera | 19:36566320 | TACTTCAGCTGAAGT[-/TC]TCTTTTCTACATGTG | 226098 |
rs262306494 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36590260 | GTGGGGGTTTCGGCT[C/T]CTTCATTATTTGGAG | 226098 |
rs262335076 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36584248 | AAGGTATAAATAAAT[G/T]TGTGAATAATGAATA | 226098 |
rs262433779 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36564283 | AATCTTACATATTAC[A/C]TACATATTTATATGA | 226098 |
rs262451194 | snp | C/G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36612632 | GCAGACACGAGAGGA[C/G/T]GGGGAGATGAGTGGG | 226098 |
rs262452885 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36571063 | GTGGGGGGTGGGGGG[A/G]TCCAGGTTAGATGAG | 226098 |
rs262494926 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36559813 | AGCCAGTAACATTTT[A/T]AAAAAATGTTGTGTG | 226098 |
rs262515201 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36567250 | TAGGATTAAAAGCAT[A/G]TACTAACATGAGAAT | 226098 |
rs262599163 | in-del | -/TAAAC | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36605076 | TTATGGAAGTAAAAA[-/TAAAC]TAAAGTCTGTCTAAT | 226098 |
rs262615685 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36589350 | GAAAGCACAAGAATT[A/G]GAGACCCACAGGTTT | 226098 |
rs262676065 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36615746 | GTCAGTTGGTCAATC[A/G]GTCTGATGGTTGGTT | 226098 |
rs262687309 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36569292 | CTCTCTATGCTTATG[A/C]TGATTTGGTCAGTTG | 226098 |
rs262715442 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36598438 | ATTATTAGAATACAT[C/T]ACATACATGTTGGAA | 226098 |
rs262750796 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36591727 | TCCCAATTTTAATTG[A/G]GTTATTTAGCTTTTT | 226098 |
rs262752421 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36593769 | TTGGTCTTTTCATGG[A/G]GCTTCAAATTTCCTG | 226098 |
rs262823930 | in-del | -/TT | | | intron-variant | Hectd2 | Mm_Celera | 19:36573123 | TCCTTCCTTCCTTCC[-/TT]TTCTTTCTTTCTCTT | 226098 |
rs262831151 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36587965 | TCCTTTAGACAGGAA[C/T]AATCCTGGGTTAAAT | 226098 |
rs262889512 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36617661 | CTGTCAAAGGCACAT[A/G]ACATTCCAGTACAGT | 226098 |
rs262902513 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36570891 | GTGTCCCCACCCCCA[A/T]CCTCTACCCTGCCCC | 226098 |
rs262922245 | in-del | -/A | | | intron-variant | Hectd2 | Mm_Celera | 19:36559987 | ATTTAATAAACTAAG[-/A]TTTTTTAAATACATA | 226098 |
rs262944881 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36574769 | TATTCCATTATATTA[A/G]ACATACATGTCTATT | 226098 |
rs262983002 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36616061 | ATCTCAGTACTAAAG[G/T]TGACACCCTTCTGTC | 226098 |
rs262986832 | in-del | -/TCT | | | intron-variant | Hectd2 | Mm_Celera | 19:36575453 | ACCTGTCACAACTAA[-/TCT]TCTCTGGTCTTTCCC | 226098 |
rs263010726 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36591087 | AATGCCCTTTCAAGG[A/G]TTTCTGGAGGGGAAA | 226098 |
rs263055990 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36569880 | ATTTATTTATACCTA[C/T]ACCCACACATATTTG | 226098 |
rs263127950 | in-del | -/A | | | intron-variant | Hectd2 | Mm_Celera | 19:36575639 | CATAGGGCTCTGTTT[-/A]ATGGTCACAAAATGG | 226098 |
rs263130199 | in-del | -/TA | | | intron-variant | Hectd2 | Mm_Celera | 19:36569075 | TAAATTATTAAAATT[-/TA]TAGTTTTAGTGATCA | 226098 |
rs263153979 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36577688 | TGATTTATTAGGAAG[A/G]TGGAGATGAAAGTGG | 226098 |
rs263187624 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36574297 | AGCTGCTGAGGTTTA[C/T]AGTGTGTCTGTCTGG | 226098 |
rs263219562 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36568029 | GACCCAAGCTCATGA[A/G]CAGTCCAGAACCTGA | 226098 |
rs263225988 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36618684 | TTTCATGTCTGTTTT[A/T]AAGACCTAGTAACCC | 226098 |
rs263328143 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36592465 | TAGTTCAATGTTCTT[A/G]ATCTGTTGAGACTTG | 226098 |
rs263398501 | snp | C/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36571224 | GCTTATTGGAGCTCT[C/G]GAACAGGGGGTGGCA | 226098 |
rs263459922 | snp | C/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36602177 | CTTAGCTTCTTAAAA[C/G]AGAAAGAAAAACAGA | 226098 |
rs263503241 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36596149 | TCAGCTGTAAGTCCT[A/G]CTCACGCATCACCCT | 226098 |
rs263505776 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36573633 | ATTTTTACTTTGGAA[A/G]TATCTCTAAGGCCTC | 226098 |
rs263602206 | snp | A/G | | | intron-variant, upstream-variant-2KB | Hectd2, LOC105246565 | GRCm38.p3 | 19:36555002 | AAGTTGCGCCTCGAG[A/G]GCAACGGCCATCACT | 226098 |
rs263636450 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36600781 | CTGCTGCTGTGTTCA[G/T]TCTTTCCATAGGCAT | 226098 |
rs263672655 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36578161 | TAGCTTTAATGGAAT[C/T]TTGAGAGGAATTAGA | 226098 |
rs263682423 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36582082 | TTGAATGAGAATGGC[C/T]TTCCTAGGCTCATAG | 226098 |
rs263686339 | in-del | -/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36583647 | ACCTTTAAAAGAGAA[-/G]GAGAGAAGGAACTAT | 226098 |
rs263707867 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | Hectd2, 1500017E21Rik | Mm_Celera | 19:36620896 | ATCAGCTAGAAAATT[C/T]ATGTAGCTTTTTAAA | 226098 |
rs263755210 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36576620 | AGAGAAAGATCTGTA[C/T]GACAAGAACTTCAAG | 226098 |
rs263779658 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36572810 | GGGTTCCCTAACAGC[C/T]GAGGGATCCATTCCT | 226098 |
rs263830223 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36602354 | TTTGGGTGCCTGAAA[A/T]GTTCCCCAAATCATC | 226098 |
rs263874104 | in-del | -/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36576051 | CTCAAAAAAAAAAAA[-/C]CCCAAAACCCCACAT | 226098 |
rs263888251 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36574945 | GCAAAGTCTTTGTAA[A/G]ATATTCCTGGAAGTG | 226098 |
rs263993651 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36600519 | TAACTCAGTATTTGT[G/T]ACTAGTACTGAGCAA | 226098 |
rs264024536 | in-del | -/GGT | | | intron-variant | Hectd2 | Mm_Celera | 19:36608639 | AGGCCTATATGTTTA[-/GGT]TTCCTTTTGGATCTA | 226098 |
rs264062622 | snp | C/T | | | upstream-variant-2KB, intron-variant | Hectd2, LOC105246565 | GRCm38.p3 | 19:36554568 | GGCGCACGCAGGGGG[C/T]GGGCGGCGGAGCCTG | 226098 |
rs264068580 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36597958 | ATTGATTAGTTAAAT[C/T]GAAATCATAATGGTT | 226098 |
rs264076730 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36593142 | TGTGTACACACATGT[G/T]CATTCATGTGTGCAT | 226098 |
rs264094108 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36605100 | GTCTAATATTGTTCC[C/T]TAAAAAATAAATAAA | 226098 |
rs264157192 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36576346 | GGAGGTCAAAGGGAT[A/G]CAAACTGGAAAGAAA | 226098 |
rs264248646 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36558962 | TTTTTGTTGGGATGT[A/G]TTACGTTGTATGTAC | 226098 |
rs264269288 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36579790 | GTTCATGAAACTGTA[A/G]ACCCCCTCATTTTAG | 226098 |
rs264279293 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36604118 | AGGTTAAAATATATG[C/T]AATTGATTTATGAAA | 226098 |
rs264359088 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36585027 | TACAAAAGATACTTT[C/T]CCTTCCCTTATTTTA | 226098 |
rs264378188 | snp | C/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36575136 | TGCCCTAGTAAGATA[C/G]CAACTCCTTCTCTAG | 226098 |
rs264388729 | in-del | -/A | | | intron-variant | Hectd2 | Mm_Celera | 19:36572939 | TGATGCAGCATCTTC[-/A]AAAAGAAAAGAAAAG | 226098 |
rs264394712 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36606735 | TTTAATAAAAGTTTT[A/T]AAAATCTAGAGTATT | 226098 |
rs264499851 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36605766 | CTCTTTCAAAAATAC[A/G]ATGGACCATGACTGA | 226098 |
rs264535710 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36609645 | ATTGATTTGAATGCC[A/G]ACCATGCCATTTATG | 226098 |
rs264546017 | snp | C/T | | | upstream-variant-2KB, downstream-variant-500B | Hectd2, LOC105246565 | Mm_Celera | 19:36552451 | GGTGTCACTGAAAAG[C/T]GTCTTCAGCACATCT | 226098 |
rs264565688 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36560520 | AATAAATATATTCTA[A/G]ATATATGATCATTTG | 226098 |
rs264579002 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36598509 | GCCCTACCGAATCTC[A/C]CTCATGCATGCTGAG | 226098 |
rs264606588 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36563894 | AGATGTTACCATCTT[A/C]TAGCATTGTGTGATG | 226098 |
rs264630151 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36602036 | TCCCTGGGCCTCTGC[A/T]CTGCCTACCAGTGTT | 226098 |
rs264668820 | snp | C/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36583156 | GAGTTTACAGTCAAA[C/G]TGAGCAGCATAGCAC | 226098 |
rs264744560 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36603278 | CATGAGATATTATGT[C/T]ATAGCATATTAGTGT | 226098 |
rs264754221 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36611277 | TACTTTTTATTCTCA[C/T]AGGTAAGGGACCCAC | 226098 |
rs264783671 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36585181 | ACTTAAAAAGTGCAT[A/G]TATTTTTAAATTATA | 226098 |
rs264817295 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36613554 | ACAAATATAATTTTG[A/T]GTTTGAGGGTCACCA | 226098 |
rs264822838 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36568044 | ACAGTCCAGAACCTG[A/G]GCTCTTAGCATCTGT | 226098 |
rs264835224 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36580258 | CTGTTACTATATCCA[A/G]TAGCTATGCAGGAAC | 226098 |
rs264871368 | snp | C/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36561948 | CCAGTACCCCCAGAG[C/G]TCCCAGGAACTAAAC | 226098 |
rs264891862 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36607679 | CCTGTTTTCCTGTCA[C/T]TTACAGGTCTCACTT | 226098 |
rs264946255 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36581908 | ATCAACTTAAAGGAA[A/C]GGAAGATTCAATTTG | 226098 |
rs264986554 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36564912 | GATAGACACACTCTC[A/G]ATTGTTTCATATTCT | 226098 |
rs265038594 | snp | G/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36583881 | ATTATTCTGTTATTT[G/T]CTAACTTGAAAAGGC | 226098 |
rs265047842 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36589633 | TGGAGATATCTCATT[C/T]AGAGCTGTGTATTCT | 226098 |
rs265083724 | in-del | -/CGT | | | intron-variant | Hectd2 | Mm_Celera | 19:36610130 | CTAGAAACAGGGAGA[-/CGT]CTTCTTTTATTGTAC | 226098 |
rs265126880 | in-del | -/TGACTC | | | intron-variant | Hectd2 | Mm_Celera | 19:36613691 | TGTATCTACGTTTTA[-/TGACTC]TGGTAGTGGGAGGAT | 226098 |
rs265128832 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36566695 | AAGAAAAGGTCTCCC[A/C]TCACCACTTAGCTAG | 226098 |
rs265161621 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36591271 | GTCTGCTGTTGTGGA[C/T]AGTCGGAAGCAGTTC | 226098 |
rs265219900 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36616504 | GTGCTTTCCCAGTTG[C/T]TCCCACCCTGGTGCT | 226098 |
rs265243651 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36562815 | ATTAGATGTAGAATT[A/G]TGACCTTATTCTAAA | 226098 |
rs265253214 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36570222 | CTGCACAAATCACAA[A/G]TATTCTTTTCCAACC | 226098 |
rs265306475 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36588410 | AAAGGAAATCAATCA[A/G]TCTTTTAACATTATG | 226098 |
rs265317076 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36594713 | AAAGAAAAGAGACCA[A/G]AGCAGGTTTTCAGCT | 226098 |
rs265385437 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36610310 | AGGCATCTTGGACAT[A/G]TGGCCTCATATGAGA | 226098 |
rs265395533 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36618017 | CCAGAGACTCCATAA[A/G]TGGTAACTGACCTAG | 226098 |
rs265401416 | snp | C/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36571513 | AGCGTCTCTCACCTC[C/G]CAGGTCTCTGGTACA | 226098 |
rs265425655 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36590439 | CCAGTCCATCATCTG[C/T]TTCCCTTCCCAGGGA | 226098 |
rs265465046 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36573886 | TTTATATGATTCAAA[A/T]GTGGGCTCACTTTAA | 226098 |
rs265515212 | snp | C/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36568528 | GCACACGTTTACATG[C/G]GCACACAGTGTGAGT | 226098 |
rs265531222 | in-del | -/GGG | | | intron-variant | Hectd2 | Mm_Celera | 19:36617128 | CACATGAGGATCACT[-/GGG]GCTTGCCAGCCAAGT | 226098 |
rs265535741 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36614085 | TTTATTTACTGAGAC[A/G]GTGTCATAATTTCTA | 226098 |
rs265553264 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36598676 | TTATCAACTATATTA[A/G]TGACACTGCAGTAAT | 226098 |
rs265575012 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36592964 | TTGATGTTGAAGTAT[A/G]TTTCTTGGATGCAGC | 226098 |
rs265591735 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36586994 | ATAACTTGAATCAGT[A/G]TGTACATATCTAAAA | 226098 |
rs265618091 | in-del | -/A | | | intron-variant | Hectd2 | Mm_Celera | 19:36560148 | TCTCTCCTCTTTTTC[-/A]AAAAAAGCATAGGTA | 226098 |
rs265634520 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36570820 | TCTTTGTCTGCCCTC[C/T]GACATTTTCTCATCC | 226098 |
rs265648369 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36602522 | AATAGCCAGTCATCT[C/T]GACATTTTGACTAAG | 226098 |
rs265690265 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36595319 | AATTATATCAGATAA[A/C]TACTACATGGCAATA | 226098 |
rs265728880 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36577865 | AGGAATGGAGAGGCA[C/T]TGTGACCCTGTGACA | 226098 |
rs265748426 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36572200 | CTTATCGGTACAGAT[A/G]CTTTGATTTGTGAAC | 226098 |
rs265852545 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36580764 | TAATTAATCACTATA[A/C]TTATTGGTTCTCTCA | 226098 |
rs265875446 | in-del | -/TGTAG | | | intron-variant | Hectd2 | Mm_Celera | 19:36584171 | AGAATTAGCTGAACT[-/TGTAG]ATTTTTATAACATAT | 226098 |
rs265897024 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36575219 | AGCGTCTACAGAAAT[A/C]ACTTGTATCAGTCAT | 226098 |
rs265916229 | in-del | -/TTCT | | | intron-variant | Hectd2 | Mm_Celera | 19:36603740 | GATAATATTTCTATA[-/TTCT]AATATCTTGTGGAAT | 226098 |
rs265937648 | snp | A/G | | | intron-variant, upstream-variant-2KB | Hectd2, LOC105246565 | Mm_Celera | 19:36555418 | GGCTATCCAAGCTTA[A/G]TAAGCGTGGTAATTT | 226098 |
rs265955117 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36601009 | TTATTCATTTCTGAA[A/G]CTCACACATCAGAAA | 226098 |
rs265964546 | in-del | -/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36606528 | AGGGATTTTTTTAAG[-/T]TTTTTTTCCCCCAAT | 226098 |
rs265971892 | snp | A/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36593662 | CTTTAGGTTAGGAAA[A/T]TTTCCTCCTATCATT | 226098 |
rs266012018 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36576793 | ACTCAGTTCTTCACC[A/G]AGGTAGAAAGAGCAA | 226098 |
rs266053177 | snp | C/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36558384 | AAATCAGTTTAAACT[C/G]TGTGTGTGTACATGC | 226098 |
rs266108590 | in-del | -/A | | | intron-variant | Hectd2 | Mm_Celera | 19:36585953 | AATTATCTGAGAATT[-/A]AACAGAAAATACCTC | 226098 |
rs266109507 | in-del | -/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36591673 | CTATTTCTTAGCCAC[-/T]CGAGTTTCCCCTGTT | 226098 |
rs266113030 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36584293 | GCAAAAGACAGCAAA[C/T]ACCAAGAGAATGAGT | 226098 |
rs266147218 | in-del | -/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36590224 | CTCAGTTAGAGGAAA[-/C]CCATCCCCAGCACTG | 226098 |
rs266155725 | snp | A/C | | | intron-variant | Hectd2 | Mm_Celera | 19:36574227 | GACCTTCCTGCCACC[A/C]GAACTCAAAGAGCTC | 226098 |
rs266181559 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36598258 | ACACTGCCATGTGTG[A/G]CTGGAGGGCCATTTT | 226098 |
rs266191793 | snp | A/C/G | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36605324 | TTGTTTGTGATCATT[A/C/G]ACACTCTAGACTTGT | 226098 |
rs266201084 | snp | A/G | | | intron-variant | Hectd2 | Mm_Celera | 19:36560010 | AATACATATGACCTG[A/G]TCTAGTGGTCCATGC | 226098 |
rs266244747 | snp | C/T | | | intron-variant | Hectd2 | Mm_Celera | 19:36599266 | GTAGTCTTAAGTGCA[C/T]ATGACTCACTACGTA | 226098 |
rs266253207 | snp | A/T | | | upstream-variant-2KB, nc-transcript-variant | Hectd2, LOC105246565 | Mm_Celera | 19:36553039 | ACACAGTAGCATGGT[A/T]CATCTTGAATCGTAT | 226098 |
rs386966077 | in-del | -/GT | | | intron-variant | Hectd2 | Mm_Celera | 19:36563115 | TGTGTGTGTGTGTGT[-/GT]TCTGAAGTGAATGAA | 226098 |
rs387029831 | in-del | -/TGGT | | | intron-variant | Hectd2 | Mm_Celera | 19:36615721 | GGTTGGTTGGTTGGT[-/TGGT]CGGTCGGTCAGTTGG | 226098 |
rs387403810 | in-del | -/AT | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | Hectd2, 1500017E21Rik | Mm_Celera | 19:36619045 | AATATATATATATAT[-/AT]CAGAAATTTATTGAA | 226098 |
rs387468199 | in-del | -/ATT | | | intron-variant | Hectd2 | Mm_Celera | 19:36573153 | TTCTCTTTTTGTATT[-/ATT]TTTCTTTCCCCCTTT | 226098 |
rs387506312 | in-del | -/C | | | upstream-variant-2KB, downstream-variant-500B | Hectd2, LOC105246565 | Mm_Celera | 19:36552457 | ACTGAAAAGCGTCTT[-/C]AGCACATCTTTATGC | 226098 |
rs387618637 | in-del | -/GT | | | intron-variant | Hectd2 | Mm_Celera | 19:36586640 | TGTGTGTGTGTGTGT[-/GT]ACCATATTACCTATA | 226098 |
rs578287645 | snp | C/G | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36557690 | GTTTTTCGGGACAGG[C/G]TTTCTCTGTATAGCC | 226098 |
rs578373310 | snp | A/G | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36614807 | GTTGTTACACCTATA[A/G]GGTTGCAGACTCCTT | 226098 |
rs578400591 | snp | C/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36590731 | TGAGGGACACTAGGC[C/T]GTTTCCAATTTCTGG | 226098 |
rs578404164 | snp | C/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36602440 | AATTCCAAAGCCATG[C/T]TGCCCTTAAAGAATG | 226098 |
rs578408231 | snp | C/G | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36566156 | CGCCTTACTGGCGTT[C/G]CCAGGAGCATGTTCA | 226098 |
rs578488679 | snp | A/G | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36561099 | AGCCTCAAGACCTGT[A/G]CCTGTCGCCTTTTCC | 226098 |
rs578494001 | snp | G/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36572019 | TCTCTCTCTCTTTTT[G/T]GGGGGGGGTGGTTTT | 226098 |
rs578501061 | snp | A/C | | | intron-variant, downstream-variant-500B | Hectd2 | GRCm38.p3 | 19:36611717 | ACGGTGCCGCAGACT[A/C]CTGCGGCACTGAAAA | 226098 |
rs578537256 | snp | A/G | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36594469 | ACTGGTCTAGGTGCT[A/G]TACTGGGTTTTTCTT | 226098 |
rs578589731 | snp | C/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36566064 | AAAAGGTTTGTTATG[C/T]CTTATAGCCCATCAT | 226098 |
rs578705227 | snp | A/G | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36571263 | GGTAGGCATTATAGC[A/G]TTAGTAATAGCGTCA | 226098 |
rs578727846 | snp | A/C | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36560137 | TCAGTCTGTCTGTCT[A/C]TCCTCTTTTTCAAAA | 226098 |
rs578951817 | snp | C/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36583184 | CACTAAAGAAAATAA[C/T]ACCTGAGTGCAAGTA | 226098 |
rs579048329 | snp | G/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36602701 | CAGCAATTTTCCTAT[G/T]GGAAAGGAGAGCCCC | 226098 |
rs579071918 | snp | A/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36614732 | ATGGCCGACTAGGCC[A/T]TCTTCTGCTACATAT | 226098 |
rs579094893 | snp | A/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36565179 | TCATGTCTCTAGCCC[A/T]CCCAGTTTTTAATAC | 226098 |
rs579157208 | snp | C/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36602700 | GCAGCAATTTTCCTA[C/T]GGGAAAGGAGAGCCC | 226098 |
rs579160560 | snp | A/G | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36582420 | TAACACCAATAGAAT[A/G]CTGACTAAACAGTAA | 226098 |
rs579166632 | snp | A/G | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36610537 | TTATCAGTGAGGCTC[A/G]GAGCCTCAGTTCGGA | 226098 |
rs579166855 | snp | A/C | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36594712 | AAAAGAAAAGAGACC[A/C]GAGCAGGTTTTCAGC | 226098 |
rs579194114 | snp | A/G | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36585594 | TCTTCTTTATTGTAC[A/G]ACTCTTGTTTTTTAA | 226098 |
rs579195058 | snp | A/G | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36559687 | TCAGGAGGAAGAAGA[A/G]GAGGAAGAAGAGAAG | 226098 |
rs579202154 | snp | A/G | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36572152 | GCTGGGATTAAAGGC[A/G]TGCGCCACCACGCCC | 226098 |
rs579261718 | snp | G/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36574530 | TTCCCAGCAACCACA[G/T]GGGGGCTCACAACCA | 226098 |
rs579561852 | snp | A/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36576287 | CTCCCTATCTATTCA[A/T]TATAGTATTCAAAGT | 226098 |
rs579565441 | snp | A/C | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36606296 | AAAGGTGATTTGTAA[A/C]AGAATTGTTGTTAGT | 226098 |
rs579582268 | snp | C/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36573097 | CCTTCCTTCCTTCCT[C/T]CCTCCCTCCCTTCCT | 226098 |
rs579624662 | snp | C/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36596376 | GCTAGAACCAACTTA[C/T]GAACTCTGGAAGGGC | 226098 |
rs579684375 | snp | A/G | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36603397 | TCTAGATAAGGAAAT[A/G]CATAAGCATATTGGT | 226098 |
rs579726182 | snp | A/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36575318 | TTACTTTTTTTTGGC[A/T]CTGATGGCTAACGTT | 226098 |
rs579799162 | snp | C/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36591747 | TTTAGCTTTTTATAT[C/T]AACTTTTTTTAACTC | 226098 |
rs579821971 | snp | A/G | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36568519 | TGCAGCACGGCACAC[A/G]TTTACATGGGCACAC | 226098 |
rs580074760 | snp | A/G | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36586595 | TAATAACATTATACC[A/G]ACTGTGTGTGTGTGT | 226098 |
rs580081178 | snp | A/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36613062 | ATTCTTTCTTTTTTT[A/T]AATCTATTTTATGTA | 226098 |
rs580099802 | snp | A/G | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36561167 | AATTAAGGGTGCCTT[A/G]CACTCTGAACTCCTC | 226098 |
rs580147707 | snp | A/G | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36614966 | GGTCCCTTCAGCAAA[A/G]TCTTTCTGGCATATG | 226098 |
rs580176453 | snp | C/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36566328 | GCTGAAGTTCTTTTC[C/T]ACATGTGTCAAGTTG | 226098 |
rs580219740 | snp | A/C | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36572961 | AAAGAAAAGAAAAGA[A/C]AAAGGCCTAGAAGGT | 226098 |
rs580223041 | snp | C/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36591143 | TGTAAATAAATAAAA[C/T]ATCCAATAAAAGAAA | 226098 |
rs580246316 | snp | C/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36577631 | TGTCATCTTCTCTCG[C/T]GGTGTGGGGTGGGAG | 226098 |
rs580249106 | snp | A/G | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36596720 | TAATTGGATAATAAT[A/G]ATTGCCAGCATTTAT | 226098 |
rs580252306 | snp | C/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36608519 | CTATCTTCTTACACA[C/T]ACTGGTCAGCCTGTG | 226098 |
rs580327506 | snp | C/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36573109 | CCTCCCTCCCTCCCT[C/T]CCTTCCTTCCTTCCT | 226098 |
rs580357623 | snp | C/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36585176 | TATTGACTTAAAAAG[C/T]GCATATATTTTTAAA | 226098 |
rs580361563 | snp | A/C | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36612686 | CACAAAGAATCAATA[A/C]AAAGTTTCAAAAATA | 226098 |
rs580611652 | snp | G/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36592155 | GCTGTCTTTTTACAG[G/T]ATATATTTCTGGCCT | 226098 |
rs580703878 | snp | A/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36574204 | CACCATGCAGCCACC[A/T]TGCAGCCGACCTTCC | 226098 |
rs580749382 | snp | C/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36610534 | TGTTTATCAGTGAGG[C/T]TCAGAGCCTCAGTTC | 226098 |
rs580777402 | snp | C/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36558828 | TAATGTTCCTAGTTA[C/T]ACAGGACCAGTTAGT | 226098 |
rs580864375 | snp | G/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36613881 | AGCACAGCAGAGGTG[G/T]CAGGACAGCTCAGGA | 226098 |
rs580885687 | snp | A/G | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36562155 | CATAGGGGATAGGGG[A/G]TTTTCAGAGGGGAAA | 226098 |
rs580890778 | snp | A/C | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36587688 | TCTCTACACTGGGGC[A/C]TCAAACCTTCACAGG | 226098 |
rs581074897 | snp | A/G | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36610063 | CATTTCACAGTATAA[A/G]TGACAATGGTACTTT | 226098 |
rs581162095 | snp | A/G | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36589738 | TCTGTGGTGAGGGCT[A/G]AATAAGGCTATGAAT | 226098 |
rs581201498 | snp | A/C | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36571607 | TCAGGGCTTCAGTCC[A/C]CCTCCCCCAATAGCT | 226098 |
rs581263618 | snp | A/C | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36570720 | CAGTGCTCTTAACCA[A/C]TGAGCCATCTCTCCA | 226098 |
rs581310847 | snp | C/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36574134 | CCCCAGCACTTTGGC[C/T]TCACTCCTCTACTCC | 226098 |
rs581320975 | snp | A/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36597782 | TATTACTGATAGTAG[A/T]ATTCAAATACTAACT | 226098 |
rs581349338 | snp | A/G | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36592217 | CGGGTTTATGTCTGG[A/G]TCTTACTTCAGTTGC | 226098 |
rs581382293 | snp | C/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36564838 | CATTTGTCAGTTCAT[C/T]CACATGATTTCTGCC | 226098 |
rs581442624 | snp | C/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36582687 | GTGAGAGAATTTTCC[C/T]ATTTTTCTAAGATTA | 226098 |
rs581446616 | snp | G/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36610550 | TCAGAGCCTCAGTTC[G/T]GATGACAGACTTTCA | 226098 |
rs581729534 | snp | A/G | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36587789 | TCCATTGGGGTCCCT[A/G]TGCTCAGTCAGATGG | 226098 |
rs581730119 | snp | C/G | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36594472 | GGTCTAGGTGCTGTA[C/G]TGGGTTTTTCTTTGT | 226098 |
rs581781750 | snp | C/G | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36576149 | GAAAGATCAGGAATT[C/G]AAGGCCCATACTAAA | 226098 |
rs581833056 | snp | A/G | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36572067 | TGTGTAGCCCTGGCT[A/G]TCCTGGAACTCACTT | 226098 |
rs581848261 | snp | A/G | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36614659 | CTTCTTGGCCCTGGT[A/G]TTCCCCTGTACTGAG | 226098 |
rs581867388 | snp | C/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36561105 | AAGACCTGTACCTGT[C/T]GCCTTTTCCGATCGA | 226098 |
rs581873093 | snp | A/G | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36584543 | ACAGCCTGAGAAAGG[A/G]AGGGCACGTGTCAGG | 226098 |
rs581881290 | snp | A/G | | | intron-variant, downstream-variant-500B | Hectd2 | GRCm38.p3 | 19:36611868 | TTAGGAGAAGGTGAT[A/G]AGTCAGATTAAAAAC | 226098 |
rs581930388 | snp | A/T | | | upstream-variant-2KB, intron-variant | Hectd2, LOC105246565 | GRCm38.p3 | 19:36553774 | GAGGAGAAAGGAAAT[A/T]GTCTAAGTCGTCGTC | 226098 |
rs581975781 | snp | C/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36566069 | GTTTGTTATGTCTTA[C/T]AGCCCATCATCAGTG | 226098 |
rs581989753 | snp | C/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36590399 | GTTCTCCCCTGACCC[C/T]CCCATTCCTGTTCCC | 226098 |
rs581994886 | snp | C/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36614799 | TTCATATTGTTGTTA[C/T]ACCTATAAGGTTGCA | 226098 |
rs582123055 | snp | A/G | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36614755 | CTACATATGCAGCTA[A/G]AGACACGAGCTCCAG | 226098 |
rs582182908 | snp | A/G | | | intron-variant, downstream-variant-500B | Hectd2 | GRCm38.p3 | 19:36611686 | TTAAAGTATCAAAGC[A/G]AGTGGTGTAATAGAG | 226098 |
rs582313467 | snp | C/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36583559 | ATAAGAAAGCATATA[C/T]AAGGGATTTGCATAT | 226098 |
rs582386718 | snp | C/G | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36615021 | GATTATGGGATGGAT[C/G]CCCAGGTGGGGCAGT | 226098 |
rs582406048 | snp | C/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36573049 | CCTTCCTTCCTTCCT[C/T]CCTCCCTCCCTCCCT | 226098 |
rs582486446 | snp | A/G | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36602939 | TTGAAGCATTCTTGT[A/G]GCAAACACATTTCCA | 226098 |
rs582509258 | snp | G/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36575295 | ATCTCCCCAACCCAG[G/T]GAATGTGTTACTTTT | 226098 |
rs582538964 | snp | A/G | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36559763 | GGAAGAGGAGGAAGA[A/G]GAGGAAGAGGAAGCA | 226098 |
rs582593605 | snp | A/G | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36572885 | TTTTGAAAAAGCTGA[A/G]AAGTGTAGGCGTTTT | 226098 |
rs582718466 | snp | A/G | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36614891 | TTATAGATAACTATG[A/G]GCATCCACTTCTGTA | 226098 |
rs582743978 | snp | A/G | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36566230 | CACTCCTCACAGTAG[A/G]CTGAGCCCTCTGCAT | 226098 |
rs582815172 | snp | G/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36596390 | ACGAACTCTGGAAGG[G/T]CAGCAGGCGCTCTGA | 226098 |
rs582880140 | snp | A/G | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36592494 | TGCTTTGTTCTGAGT[A/G]TATGATCAATTTTAG | 226098 |
rs582909018 | snp | A/G | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36590732 | GAGGGACACTAGGCT[A/G]TTTCCAATTTCTGGC | 226098 |
rs582966560 | snp | C/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36573101 | CCTTCCTTCCTCCCT[C/T]CCTCCCTTCCTTCCT | 226098 |
rs582977283 | snp | C/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36602694 | TCAGATGCAGCAATT[C/T]TCCTATGGGAAAGGA | 226098 |
rs583010298 | snp | C/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36574566 | AATGGGATCTGATGC[C/T]CTCTTCTGGTGTGTC | 226098 |
rs583029445 | snp | A/G | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36587693 | ACACTGGGGCATCAA[A/G]CCTTCACAGGACCAA | 226098 |
rs583034358 | snp | G/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36614145 | AATTTCATTTAAGAC[G/T]ATCATTTTTTTAAAT | 226098 |
rs583054143 | snp | A/G | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36563968 | TAAACAGAAATGTCT[A/G]TCTTCTAAAGCAGTT | 226098 |
rs583166692 | snp | A/G | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36569204 | CTTGTTAAACTCATA[A/G]TAACTGTGAAGTATT | 226098 |
rs583271816 | snp | C/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36613072 | TTTTTTAATCTATTT[C/T]ATGTATTGAGTACAC | 226098 |
rs583299377 | snp | C/G | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36561170 | TAAGGGTGCCTTGCA[C/G]TCTGAACTCCTCAGT | 226098 |
rs583340858 | snp | A/C | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36610121 | ATTCTCTTTGCTAGA[A/C]ACAGGGAGACTTCTT | 226098 |
rs583372053 | snp | A/G | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36555918 | TAAGTCAGCACAGCA[A/G]ATTTGGACAGCAATG | 226098 |
rs583403948 | snp | C/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36591417 | TGAGGAACTGCACTA[C/T]ACTGGCTCTTGAGAT | 226098 |
rs583431741 | snp | C/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36617329 | AATTATATTTTAAAA[C/T]ATAAATGAATATTTT | 226098 |
rs583572065 | snp | C/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36578342 | TCCCTTGAACCATCC[C/T]ACGAAGTTGTGATTG | 226098 |
rs583654809 | snp | C/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36567597 | ATGGTTGTGAGCCAC[C/T]ATGTGGTTGCTGGGA | 226098 |
rs583660274 | snp | C/G | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36609820 | TAGAACGCTCGAGTT[C/G]AGTTATGGTGCCCAT | 226098 |
rs583675538 | snp | A/C | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36561141 | TTCCAGTCTCGTTCC[A/C]GTCCACACAGAATTA | 226098 |
rs583857721 | snp | A/G | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36569943 | TGTCAACTGGATAAC[A/G]AAACTTATATAGTTT | 226098 |
rs583902799 | snp | C/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36602139 | CTTAGGAGAGTATTC[C/T]GGTGTTAAAGATGAG | 226098 |
rs584037300 | snp | G/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36592161 | TTTTTACAGTATATA[G/T]TTCTGGCCTCTTTAT | 226098 |
rs584040380 | snp | G/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36613051 | AATATTGTATGATTC[G/T]TTCTTTTTTTTAATC | 226098 |
rs584045737 | snp | C/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36573114 | CTCCCTCCCTTCCTT[C/T]CTTCCTTCCTTCTTT | 226098 |
rs584046956 | snp | C/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36597003 | GTTTCCTGAATTTGC[C/T]ACTTAGAATTCATGC | 226098 |
rs584129075 | snp | A/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36574490 | GTTAAGAGCACTGAC[A/T]GCTCTTCCAGAGGTC | 226098 |
rs584157310 | snp | C/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36606302 | GATTTGTAACAGAAT[C/T]GTTGTTAGTAATTTG | 226098 |
rs584323160 | snp | A/G | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36580084 | CTGATTTTTCAAGCT[A/G]GGGCTTTCCCATTAT | 226098 |
rs584391511 | snp | A/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36614788 | GTACTGGTTAGTTCA[A/T]ATTGTTGTTACACCT | 226098 |
rs584477359 | snp | C/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36610876 | AAATATTTCTCCCAG[C/T]ACTCTCAGGCTTTTT | 226098 |
rs584501179 | snp | A/C | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36559888 | GTCTTATATATGTAA[A/C]CTTTTGTGCATTTTG | 226098 |
rs584582374 | snp | A/G | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36602123 | TATCCGGTGCCTACT[A/G]CTTAGGAGAGTATTC | 226098 |
rs584602810 | snp | G/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36590213 | TCAGCCAGCAGCTCA[G/T]TTAGAGGAAACCCAT | 226098 |
rs584617899 | snp | C/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36571785 | TTTGCCTACCTGGAT[C/T]GTCATTTGTTTTAAG | 226098 |
rs584622189 | snp | C/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36594339 | CCCAACCATAAATTA[C/T]TTTTATGATTTGGCT | 226098 |
rs584633307 | snp | C/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36557681 | TGGTTTTTGGTTTTT[C/T]GGGACAGGGTTTCTC | 226098 |
rs584687014 | snp | A/G | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36582696 | TTTTCCTATTTTTCT[A/G]AGATTAAAAAAGGGC | 226098 |
rs584701448 | snp | A/G | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36566063 | GAAAAGGTTTGTTAT[A/G]TCTTATAGCCCATCA | 226098 |
rs584725620 | snp | C/G | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36574199 | GCAGCCACCATGCAG[C/G]CACCATGCAGCCGAC | 226098 |
rs584740028 | snp | G/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36600655 | TATACCACCTACTAG[G/T]TTCAGGTGGAATACA | 226098 |
rs584815415 | snp | C/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36571006 | CAGCTGTATATGTGT[C/T]AGGGGCCTGCCTGGT | 226098 |
rs584827134 | snp | A/C | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36592476 | TCTTGATCTGTTGAG[A/C]CTTGCTTTGTTCTGA | 226098 |
rs584848952 | snp | C/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36587841 | TGTATTGGTCAGGAT[C/T]TGGCAGAGCCTCTCA | 226098 |
rs584938709 | snp | C/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36572144 | TCCCGAGTGCTGGGA[C/T]TAAAGGCGTGCGCCA | 226098 |
rs585027807 | snp | A/G | | | upstream-variant-2KB, intron-variant | Hectd2, LOC105246565 | GRCm38.p3 | 19:36554540 | AGCGGAGCGCGGCCG[A/G]GGGCGCGAGCCGGGC | 226098 |
rs585059114 | snp | A/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36583641 | AAAGGCACCTTTAAA[A/T]GAGAAGGAGAGAAGG | 226098 |
rs585113050 | snp | C/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36614710 | CAAGGGGCCTCTCTT[C/T]CCAATGATGGCCGAC | 226098 |
rs585138621 | snp | A/G | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36564842 | TGTCAGTTCATTCAC[A/G]TGATTTCTGCCATTC | 226098 |
rs585210736 | snp | A/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36594473 | GTCTAGGTGCTGTAC[A/T]GGGTTTTTCTTTGTT | 226098 |
rs585281528 | snp | C/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36610536 | TTTATCAGTGAGGCT[C/T]AGAGCCTCAGTTCGG | 226098 |
rs585283051 | snp | A/G | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36606285 | TTTTTAACATGAAAG[A/G]TGATTTGTAACAGAA | 226098 |
rs585304881 | snp | A/G | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36559666 | GACAGTTCCAGAAAG[A/G]GTTTCTCAGGAGGAA | 226098 |
rs585308951 | snp | C/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36582419 | ATAACACCAATAGAA[C/T]GCTGACTAAACAGTA | 226098 |
rs585379107 | snp | A/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36583626 | CTGAACTATTCCTTG[A/T]AAGGCACCTTTAAAA | 226098 |
rs585421537 | snp | A/C | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36566147 | TGGAGGAACCGCCTT[A/C]CTGGCGTTCCCAGGA | 226098 |
rs585423519 | snp | A/G | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36590722 | TTCTTCTGTTGAGGG[A/G]CACTAGGCTGTTTCC | 226098 |
rs585429769 | snp | A/G | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36614804 | ATTGTTGTTACACCT[A/G]TAAGGTTGCAGACTC | 226098 |
rs585457178 | snp | A/G | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36575296 | TCTCCCCAACCCAGG[A/G]AATGTGTTACTTTTT | 226098 |
rs585578662 | snp | C/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36576265 | ACTAGACAAGGCTGC[C/T]CACTCTCTCCCTATC | 226098 |
rs585696975 | snp | A/C | | | intron-variant, downstream-variant-500B | Hectd2 | GRCm38.p3 | 19:36611696 | AAAGCAAGTGGTGTA[A/C]TAGAGACGGTGCCGC | 226098 |
rs585698968 | snp | C/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36573070 | CTCCCTCCCTCCCTT[C/T]CTTCCTTCCTTCCTT | 226098 |
rs585725932 | snp | A/G | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36595960 | TTATTTAAAAAAATT[A/G]TATTATCTTAGCTAA | 226098 |
rs585780478 | snp | A/G | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36602988 | CTTGTCTCCATTAGC[A/G]TCCAGGGGTAAATAA | 226098 |
rs585803999 | snp | A/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36613061 | GATTCTTTCTTTTTT[A/T]TAATCTATTTTATGT | 226098 |
rs585811686 | snp | A/G | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36591617 | CTCAAAGCCATTTTG[A/G]TTTGTCTCCCTAATG | 226098 |
rs585826282 | snp | A/G | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36561151 | GTTCCAGTCCACACA[A/G]AATTAAGGGTGCCTT | 226098 |
rs585837179 | snp | A/G | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36567609 | CACTATGTGGTTGCT[A/G]GGAATTGAACTCAGG | 226098 |
rs585893818 | snp | C/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36614916 | TCTGTATTTGCCAGG[C/T]ACTGGCATAGCTTCA | 226098 |
rs585945581 | snp | A/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36591134 | CATTTGAAATGTAAA[A/T]AAATAAAATATCCAA | 226098 |
rs585952973 | snp | C/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36572937 | GGATGATGCAGCATC[C/T]TCAAAAGAAAAGAAA | 226098 |
rs586173925 | snp | C/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36585816 | GGATGTTCTTGACTT[C/T]AGATCCATCTCTACA | 226098 |
rs586220823 | snp | C/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36595633 | TAATACTAGCTTTCT[C/T]GTGAGAGAGACATGG | 226098 |
rs586281309 | snp | C/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36566232 | CTCCTCACAGTAGGC[C/T]GAGCCCTCTGCATTA | 226098 |
rs586347642 | snp | A/G | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36610126 | CTTTGCTAGAAACAG[A/G]GAGACTTCTTTTATT | 226098 |
rs586395613 | snp | A/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36606525 | GACTAGGGATTTTTT[A/T]AAGTTTTTTTCCCCC | 226098 |
rs586402982 | snp | C/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36569225 | GTGAAGTATTGTTGC[C/T]ATCACCTTTGCAAAC | 226098 |
rs586477400 | snp | A/G | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36600661 | ACCTACTAGGTTCAG[A/G]TGGAATACAGCTTAG | 226098 |
rs586492529 | snp | C/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36561114 | ACCTGTCGCCTTTTC[C/T]GATCGAGCTCGTTCC | 226098 |
rs586503954 | snp | A/C | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36584548 | CTGAGAAAGGAAGGG[A/C]ACGTGTCAGGGTGAG | 226098 |
rs586510091 | snp | C/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36612556 | AATGCCTTGTTTGTT[C/T]ATTTTGGTTGCTTAT | 226098 |
rs586576247 | snp | C/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36579113 | AGCAGGTAGAGTAAT[C/T]ACTCTGATGAGAGAT | 226098 |
rs586753429 | snp | A/G | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36592143 | TTTGGTGGAGATGCT[A/G]TCTTTTTACAGTATA | 226098 |
rs586755142 | snp | A/G | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36558042 | GGGGTTAGTGAAAGG[A/G]ATGGCTGTTTAAGTG | 226098 |
rs586768615 | snp | G/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36581320 | AAAGTGTGTGGGAAG[G/T]GATAGAAAAGGGTAA | 226098 |
rs586850872 | snp | A/G | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36613708 | ACTCTGGTAGTGGGA[A/G]GATGGAGAAAGGGAA | 226098 |
rs586857137 | snp | A/C | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36574203 | CCACCATGCAGCCAC[A/C]ATGCAGCCGACCTTC | 226098 |
rs586881203 | snp | C/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36561171 | AAGGGTGCCTTGCAC[C/T]CTGAACTCCTCAGTG | 226098 |
rs586882648 | snp | A/G | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36587686 | TTTCTCTACACTGGG[A/G]CATCAAACCTTCACA | 226098 |
rs586969200 | snp | A/G | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36557318 | TGTCATGGTTATGAC[A/G]GTGTAGAAACAAGTA | 226098 |
rs586977165 | snp | C/G | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36610025 | CTTTAAAAAAGAAAA[C/G]CCAGCTGCCAATTTT | 226098 |
rs587021606 | snp | A/C | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36592202 | GTGTCCATGGGTGTG[A/C]GGGTTTATGTCTGGA | 226098 |
rs587075160 | snp | C/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36592481 | ATCTGTTGAGACTTG[C/T]TTTGTTCTGAGTGTA | 226098 |
rs587131359 | snp | C/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36573105 | CCTTCCTCCCTCCCT[C/T]CCTTCCTTCCTTCCT | 226098 |
rs587397602 | snp | A/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36570470 | TTTATTTATTTATTT[A/T]ATGTAAATGAGTACA | 226098 |
rs587427841 | snp | C/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36574127 | TGGGCTTCCCCAGCA[C/T]TTTGGCTTCACTCCT | 226098 |
rs587430165 | snp | A/G | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36597778 | TTCCTATTACTGATA[A/G]TAGAATTCAAATACT | 226098 |
rs587431880 | snp | C/G | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36587766 | CCTTCAGTCCTTCCC[C/G]TAACTCCTCCATTGG | 226098 |
rs587434287 | snp | C/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36614252 | AACTCAGAAATCCGC[C/T]TGCCTCTGCCTCCCG | 226098 |
rs587454819 | snp | A/G | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36564699 | CAGTTGTAGTCTTAA[A/G]TTTAAGAAGGTGTAA | 226098 |
rs587488244 | snp | A/C | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36596718 | TTTAATTGGATAATA[A/C]TGATTGCCAGCATTT | 226098 |
rs587506013 | snp | C/T | | | utr-variant-5-prime, intron-variant, nc-transcript-variant, upstream-variant-2KB | Hectd2, LOC105246565 | GRCm38.p3 | 19:36554743 | TCCGGCCGCCGCTGC[C/T]GCCGCCGCCACCGCC | 226098 |
rs587509066 | snp | A/T | | | intron-variant | Hectd2 | GRCm38.p3 | 19:36576898 | GAATCACCATCCCTG[A/T]CCTCAAGCTGTATTA | 226098 |