SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3697467 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Hectd1 | Mm_Celera | 12:51774432 | TTTAATCCCAGCACT[C/T]GGGAGGCAGAGGCAG | 207304 |
rs3697471 | snp | C/T | 0.5 | 0 | intron-variant | Hectd1 | Mm_Celera | 12:51774439 | CCAGCACTCGGGAGG[C/T]AGAGGCAGGCGGATT | 207304 |
rs3699306 | snp | G/T | 0.410864 | 0.191371 | synonymous-codon | Hectd1 | GRCm38.p3 | 12:51774763 | AAACAAATGAGGATC[G/T]GTCAAAGTCGTACCA | 207304 |
rs3707792 | snp | C/T | 0.32 | 0.24 | intron-variant | Hectd1 | Mm_Celera | 12:51771085 | ATAAACAGGTAGTTC[C/T]ACCAACACAGAGACT | 207304 |
rs3708328 | snp | A/C | 0.362812 | 0.2231 | intron-variant | Hectd1 | Mm_Celera | 12:51771131 | GGGTATACCTGATGC[A/C]ATGTGGGAATATACT | 207304 |
rs4138206 | snp | C/T | 0.5 | 0 | intron-variant | Hectd1 | Mm_Celera | 12:51774468 | TTTCTGAGTTCGAGG[C/T]CTGGTCTACAAAGTG | 207304 |
rs6217162 | snp | A/G | 0.5 | 0 | intron-variant | Hectd1 | Mm_Celera | 12:51821203 | taatctcattactca[A/G]gaggcagagcagaca | 207304 |
rs6218676 | snp | A/G | 0.5 | 0 | intron-variant | Hectd1 | Mm_Celera | 12:51821426 | AAATTTAGCCTGTCT[A/G]CAAGAAATGCAGGAA | 207304 |
rs6218734 | snp | A/G | 0.5 | 0 | intron-variant | Hectd1 | Mm_Celera | 12:51821463 | aagagcagccgacca[A/G]taacaggccaaatca | 207304 |
rs6226854 | snp | C/T | 0.30839 | 0.243086 | intron-variant | Hectd1 | Mm_Celera | 12:51809769 | ATGTCTCTATAGGCC[C/T]AAATTTTCCTCACAG | 207304 |
rs6226928 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Hectd1 | Mm_Celera | 12:51809812 | AATCAGAAAACCTAA[A/C]CCAGAGAATCATCCT | 207304 |
rs6226931 | snp | A/C/T | 0.5 | 0 | intron-variant | Hectd1 | Mm_Celera | 12:51809815 | CAGAAAACCTAANCC[A/C/T]GAGAATCATCCTCNT | 207304 |
rs6257400 | snp | C/T | 0.255 | 0.24995 | intron-variant | Hectd1 | Mm_Celera | 12:51751848 | CTGCTTTATAGGCGG[C/T]TCCTCACCTCGAGAA | 207304 |
rs6270102 | snp | C/G | 0.255 | 0.24995 | synonymous-codon | Hectd1 | Mm_Celera | 12:51751937 | TCCACGGGGAACTTT[C/G]ACTCTTTCGTGCTTG | 207304 |
rs6270608 | snp | A/C/T | 0.345679 | 0.230967 | synonymous-codon | Hectd1 | GRCm38.p3 | 12:51752009 | ACTGCTCGTGGTCCG[A/C/T]GTTCGCTCCACAGTG | 207304 |
rs6271725 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Hectd1 | Mm_Celera | 12:51824323 | CCAGACTGGATTATA[A/G]AGTGATACCCCCTCT | 207304 |
rs6271774 | snp | C/G | 0.489796 | 0.070696 | intron-variant | Hectd1 | Mm_Celera | 12:51824350 | CTCTCTAAAAACAAA[C/G]AAAAGACAGCGGCGC | 207304 |
rs6272333 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Hectd1 | Mm_Celera | 12:51824445 | CAAATTTCAGGCCAG[C/G]CCAGGTTACATGAGA | 207304 |
rs6358084 | snp | G/T | 0.5 | 0 | intron-variant | Hectd1 | GRCm38.p3 | 12:51801985 | TTGGGTGTTTTGGGG[G/T]TTTTTTTGCTtttgc | 207304 |
rs6358591 | snp | C/T | 0.5 | 0 | intron-variant | Hectd1 | Mm_Celera | 12:51802073 | ctgtagagcagactg[C/T]ccttgaactcacaga | 207304 |
rs6382273 | snp | C/G/T | 0.226562 | 0.268709 | intron-variant | Hectd1 | Mm_Celera | 12:51764202 | AATACAATTAGCAAA[C/G/T]GGCACAGCAAGGTCA | 207304 |
rs6382881 | snp | A/G | 0.456747 | 0.140554 | intron-variant | Hectd1 | Mm_Celera | 12:51764361 | ATGATCTCAAAGTAT[A/G]TTTCAGTCAANAAAA | 207304 |
rs6382896 | snp | C/T | 0.5 | 0 | intron-variant | Hectd1 | Mm_Celera | 12:51764372 | GTATNTTTCAGTCAA[C/T]AAAATCTATGAAAGG | 207304 |
rs6383952 | snp | C/T | 0.456747 | 0.140554 | intron-variant | Hectd1 | Mm_Celera | 12:51764507 | CCTGCTGAGCATATA[C/T]TGTGTGCCCAGAACT | 207304 |
rs6384627 | snp | A/T | 0.415225 | 0.187619 | intron-variant | Hectd1 | Mm_Celera | 12:51764640 | GCGAGACAAGACCTT[A/T]TGGAGACATACAAAA | 207304 |
rs6385781 | snp | A/T | 0.5 | 0 | intron-variant | Hectd1 | GRCm38.p3 | 12:51764857 | CCTAGTGATGATGCA[A/T]ACCTGTGACACAAGC | 207304 |
rs6390007 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Hectd1 | Mm_Celera | 12:51809829 | CAGAGAATCATCCTC[A/G]TTTCCTCCCATTCCC | 207304 |
rs6390072 | snp | A/C | 0.304688 | 0.243945 | intron-variant | Hectd1 | Mm_Celera | 12:51809874 | CAAGGAATCCGTTGA[A/C]CCCTATCAGTCTTTT | 207304 |
rs6391661 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Hectd1 | Mm_Celera | 12:51810135 | acctaaaatgcagca[C/T]tcgaatggctagaac | 207304 |
rs6391738 | snp | A/G | 0.5 | 0 | intron-variant | Hectd1 | Mm_Celera | 12:51810172 | gtttcatgtgaggtt[A/G]tggctagtaagagac | 207304 |
rs6399920 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Hectd1 | Mm_Celera | 12:51771706 | TGCCTACTAAGCGAT[C/T]GGGAAACTATTCCTT | 207304 |
rs6399921 | snp | A/G | 0.46281 | 0.131194 | intron-variant | Hectd1 | Mm_Celera | 12:51771708 | CCTACTAAGCGATTG[A/G]GAAACTATTCCTTAT | 207304 |
rs13481451 | snp | A/G | 0.440089 | 0.162377 | intron-variant | Hectd1 | Mm_Celera | 12:51810798 | CCACAAGATCATGAG[A/G]GTAAACAACCCACAC | 207304 |
rs29124021 | snp | C/T | 0.5 | 0 | downstream-variant-500B | Hectd1 | Mm_Celera | 12:51743621 | ATTTTATTTTGTTTT[C/T]AAAAAAGAGAATTTG | 207304 |
rs29124495 | snp | A/C | 0.375 | 0.216506 | intron-variant | Hectd1 | Mm_Celera | 12:51779809 | ACTATCCTTCAATTT[A/C]CTCAGCAAGGATAAA | 207304 |
rs29125668 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Hectd1 | Mm_Celera | 12:51813871 | TTCCAGGCTACCCAG[C/T]GGTACATAAACACTC | 207304 |
rs29125698 | snp | C/T | 0.5 | 0 | intron-variant | Hectd1 | Mm_Celera | 12:51763825 | CTGGGATTACAGGTG[C/T]GCGCCACCACGCCTG | 207304 |
rs29126138 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Hectd1 | Mm_Celera | 12:51807624 | AACAAACCAACCAAC[C/T]TAGGATACTCTATAT | 207304 |
rs29126305 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Hectd1 | Mm_Celera | 12:51746047 | AGCAGTGTTGATTGT[A/T]GATGTTAATGTCAAA | 207304 |
rs29126405 | snp | A/T | 0.345679 | 0.230967 | intron-variant | Hectd1 | Mm_Celera | 12:51763646 | CTACAAAGCGTTTTT[A/T]AAAGCTCTTCATTTC | 207304 |
rs29126411 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hectd1 | Mm_Celera | 12:51788758 | ACATCACAGGATAAC[C/T]CAGAATATTTACAAC | 207304 |
rs29126589 | snp | A/G | 0.432133 | 0.171253 | intron-variant | Hectd1 | Mm_Celera | 12:51765780 | AGCAAATCCCAGCAT[A/G]CCTGGCAACAATGTG | 207304 |
rs29127248 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hectd1 | Mm_Celera | 12:51783004 | GTCCTCTTCTGGCCT[C/T]TGAGGGTAGTAGTAC | 207304 |
rs29127369 | snp | C/T | 0.444444 | 0.157135 | upstream-variant-2KB, synonymous-codon | Hectd1, Gm5785 | GRCm38.p3 | 12:51829691 | GGGGCGCCGGGCTCC[C/T]TCGGCGGTCGGCTAC | 207304 |
rs29127649 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hectd1 | Mm_Celera | 12:51779759 | AGACATTAGCAATCC[C/T]ACATAGATTCGAGGA | 207304 |
rs29128245 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Hectd1 | Mm_Celera | 12:51761277 | AAGTAATTCTTTAAC[G/T]GTTAAATTACATTTA | 207304 |
rs29128408 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Hectd1 | Mm_Celera | 12:51761688 | TTGTAGTACTTTGAG[A/C]CTATTATTTTAAAAT | 207304 |
rs29129711 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Hectd1 | Mm_Celera | 12:51815400 | CTGCCAGACTTTCAG[A/G]CCAGACTGAGACATC | 207304 |
rs29130781 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hectd1 | Mm_Celera | 12:51787729 | AGGGCTTCTGAGTGA[C/T]GATGCCTTCTGACCG | 207304 |
rs29131339 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Hectd1 | Mm_Celera | 12:51805444 | CCTTGTCTCAAAAAC[G/T]TCAACTAGGGAACTG | 207304 |
rs29131344 | snp | A/T | 0.345679 | 0.230967 | intron-variant | Hectd1 | Mm_Celera | 12:51772217 | ATACAATTTACACAG[A/T]ATCCGAAGACAGAAG | 207304 |
rs29132323 | snp | A/G | 0.5 | 0 | intron-variant | Hectd1 | Mm_Celera | 12:51752691 | TGTGTGTGTGTGTGA[A/G]TATGCATGTGGAGAT | 207304 |
rs29132392 | snp | A/T | 0.48 | 0.0979796 | upstream-variant-2KB, downstream-variant-500B | Hectd1, Gm5785 | Mm_Celera | 12:51831313 | AAAAACCTTAATTAG[A/T]AATTGTAAAAGACTG | 207304 |
rs29133002 | snp | C/T | 0.265928 | 0.249492 | intron-variant | Hectd1 | Mm_Celera | 12:51777479 | GAATCTATTTACTTA[C/T]TGATGTGCGTGTGCG | 207304 |
rs29133560 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hectd1 | Mm_Celera | 12:51802920 | AGCAAAGTGATAAAG[A/G]ACGTGCCCCATGGGG | 207304 |
rs29133958 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hectd1 | Mm_Celera | 12:51818533 | CAGTTAACGCTAGTA[A/G]CAGTATCCTTCACTG | 207304 |
rs29135134 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hectd1 | Mm_Celera | 12:51777050 | CTCCTTTAATCCTAG[C/T]GGTTGGGAGGCATAA | 207304 |
rs29135197 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hectd1 | Mm_Celera | 12:51816943 | CAGAAGGGACCAGAG[A/G]GACTTCACTCCCTGT | 207304 |
rs29135737 | snp | C/T | 0.401235 | 0.199068 | synonymous-codon | Hectd1 | GRCm38.p3 | 12:51759293 | CAGTTGAAGCAGTTT[C/T]TGTACATAGTAAAAG | 207304 |
rs29136454 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Hectd1 | Mm_Celera | 12:51820832 | TCATTTGGTAAAGGT[A/G]CTCGTCTCACACCTG | 207304 |
rs29136676 | snp | C/G | 0.444444 | 0.157135 | downstream-variant-500B | Hectd1 | Mm_Celera | 12:51743664 | GAGTTTAAAAAGCAC[C/G]TGGTTAAGCTCGTAG | 207304 |
rs29136719 | snp | A/G | 0.188366 | 0.242283 | intron-variant | Hectd1 | Mm_Celera | 12:51799260 | CTCTGTCACTTCTTC[A/G]AACTCCTCCCGGTTT | 207304 |
rs29137113 | snp | C/T | 0.5 | 0 | intron-variant | Hectd1 | Mm_Celera | 12:51766710 | TTCAAGGACAGAGGG[C/T]TCTCCTAACCTGTGA | 207304 |
rs29138269 | snp | C/G | 0.387812 | 0.208586 | intron-variant | Hectd1 | Mm_Celera | 12:51777501 | GCGTGTGCGTGTGTG[C/G]GTGTTTAAGTGCACA | 207304 |
rs29138322 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hectd1 | Mm_Celera | 12:51798863 | TGGAGAGATGGCTGC[A/G]CAGTCAGGAGCACTT | 207304 |
rs29138783 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hectd1 | Mm_Celera | 12:51816794 | TTTGAGACAAAGTCC[A/G]CAGTGTGTATCTAGG | 207304 |
rs29139428 | snp | A/C | 0.5 | 0 | intron-variant | Hectd1 | Mm_Celera | 12:51822972 | CCCAGAAGCACAGAA[A/C]GAAATACTATAAAAG | 207304 |
rs29139483 | snp | G/T | 0.375 | 0.216506 | intron-variant | Hectd1 | Mm_Celera | 12:51783700 | TCTTTTTTAAAGAGA[G/T]TAAGCCAGGAATTCT | 207304 |
rs29139958 | snp | A/T | 0.42 | 0.183303 | intron-variant | Hectd1 | Mm_Celera | 12:51765733 | GGTAAGCATTTTAAC[A/T]CTGTGAAGTCAGTGT | 207304 |
rs29140469 | snp | A/C | 0.375 | 0.216506 | intron-variant | Hectd1 | Mm_Celera | 12:51803125 | GCAACTTGCCAATAT[A/C]ATCTATGAATGTGAG | 207304 |
rs29140981 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hectd1 | Mm_Celera | 12:51777943 | GATGTGGGCAGCCCC[A/G]TTTTGAAAGTAAAGA | 207304 |
rs29141111 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Hectd1 | Mm_Celera | 12:51780013 | TTGTTTTTTGGTTGG[C/T]TGGGTTTGGTTTCCT | 207304 |
rs29141962 | snp | G/T | 0.265928 | 0.249492 | intron-variant | Hectd1 | Mm_Celera | 12:51759019 | CTGAGCCCAGATTAG[G/T]ATGGACTATTTCTAA | 207304 |
rs29142012 | snp | C/G | 0.455 | 0.143091 | intron-variant | Hectd1 | Mm_Celera | 12:51746514 | ATGCTGGAGCTCAAA[C/G]GCAGGGCTTGGAGAA | 207304 |
rs29142249 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hectd1 | Mm_Celera | 12:51803089 | TGAGCAGTAGAAACG[C/T]GGAAAGAGTAACTAT | 207304 |
rs29142791 | snp | A/G | 0.5 | 0 | intron-variant | Hectd1 | Mm_Celera | 12:51801328 | GACACTGTTGAGATT[A/G]GAGGGAAGATGAGGG | 207304 |
rs29142809 | snp | A/T | 0.489796 | 0.070696 | intron-variant | Hectd1 | Mm_Celera | 12:51823038 | CTACTGATACTCTTG[A/T]AGGATAGGATCCAAA | 207304 |
rs29143142 | snp | G/T | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Hectd1, Gm5785 | Mm_Celera | 12:51827208 | TTACTAGGGTTCCAT[G/T]AACCACAGACAACTG | 207304 |
rs29143518 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Hectd1 | GRCm38.p3 | 12:51798484 | AGTGCGCTCGCGCTC[G/T]CTCTCTCTCTCTCTC | 207304 |
rs29143664 | snp | A/G | 0.5 | 0 | intron-variant | Hectd1 | Mm_Celera | 12:51820942 | TTCACGCCATGGCAA[A/G]TGCAGGCACCGCCCC | 207304 |
rs29143920 | snp | C/G | 0.498615 | 0.0262793 | intron-variant | Hectd1 | Mm_Celera | 12:51792577 | GTACCTCAAAGGGTA[C/G]GGATCCAATGAATCT | 207304 |
rs29143957 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Hectd1 | Mm_Celera | 12:51783958 | ATAATTCCGTGTGTA[C/T]ATAAACACAGACTTA | 207304 |
rs29144433 | snp | C/G | 0.375 | 0.216506 | intron-variant | Hectd1 | Mm_Celera | 12:51782766 | CTCCTTTCACCATGT[C/G]AATTTCTGGGATTGA | 207304 |
rs29144513 | snp | A/G | 0.5 | 0 | intron-variant | Hectd1 | Mm_Celera | 12:51763864 | TATTTTATTTAAGAC[A/G]CCGTTTTATGCAGCC | 207304 |
rs29145987 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Hectd1 | GRCm38.p3 | 12:51791623 | TTTAAATAATATCTT[A/T]AATTATATCATATCC | 207304 |
rs29146803 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Hectd1 | Mm_Celera | 12:51751625 | AGGCTAGAATTTAGC[C/T]GGACAGAAAGAATTC | 207304 |
rs29147698 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hectd1 | Mm_Celera | 12:51789075 | GCAGAGGCAGGAAGA[C/T]CTCGGAGAGTTGAGT | 207304 |
rs29147724 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Hectd1 | Mm_Celera | 12:51785656 | AGGTTCAATTATCTC[A/G]TTCCATTGATTTAAT | 207304 |
rs29147845 | snp | C/T | 0.32 | 0.24 | intron-variant | Hectd1 | Mm_Celera | 12:51769684 | CCCAAGACTGGTAAA[C/T]TTTTTTCTTTTATTC | 207304 |
rs29148401 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Hectd1 | Mm_Celera | 12:51797641 | GTGAATTGCTAGTCT[G/T]GTCTACACAGTGAGT | 207304 |
rs29148752 | snp | G/T | 0.456747 | 0.140554 | intron-variant | Hectd1 | Mm_Celera | 12:51789007 | GCCACATACACTGTA[G/T]TTTTTAAAGTATTTC | 207304 |
rs29148863 | snp | A/C | 0.5 | 0 | intron-variant | Hectd1 | Mm_Celera | 12:51811141 | GTGTTAAATGTATTT[A/C]TATCTGATGTTATTT | 207304 |
rs29148974 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hectd1 | Mm_Celera | 12:51777977 | CTACCTGATGAACAA[A/G]CAATCAGGCAGCACG | 207304 |
rs29149211 | snp | A/T | 0.375 | 0.216506 | intron-variant | Hectd1 | Mm_Celera | 12:51822783 | AAAAGGTAATGTAAT[A/T]AAAAAAAAAAAAACT | 207304 |
rs29150114 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hectd1 | Mm_Celera | 12:51787282 | GTAATGGGGATCCAA[C/T]GCACTCTTCTGGTGT | 207304 |
rs29150571 | snp | A/T | 0.5 | 0 | intron-variant | Hectd1 | Mm_Celera | 12:51768128 | AAAAAAAAAAAAAAA[A/T]TAAAAAAAGAAAAAA | 207304 |
rs29150626 | snp | A/C | 0.265928 | 0.249492 | intron-variant | Hectd1 | Mm_Celera | 12:51799721 | CCCAAGGAACATTAT[A/C]AGAATCTCTATCATG | 207304 |
rs29150683 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hectd1 | Mm_Celera | 12:51785038 | TCCAGGGGCTCCAAT[A/G]CCCTCTTGTGGCCTG | 207304 |
rs29150793 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Hectd1 | Mm_Celera | 12:51817040 | CAAGCAGTGGCCACT[C/G]AGGAAACAGTCTGCA | 207304 |
rs29151536 | snp | C/T | 0.32 | 0.24 | intron-variant | Hectd1 | Mm_Celera | 12:51800398 | TTACCAGAACAAAAT[C/T]TTTTACCATTCTAAT | 207304 |
rs29151806 | snp | C/T | 0.465374 | 0.126941 | intron-variant | Hectd1 | Mm_Celera | 12:51792607 | TGTAAGGACATTTTA[C/T]TGTAGCCTAGAAGCT | 207304 |
rs29152066 | snp | C/T | 0.5 | 0 | intron-variant | Hectd1 | Mm_Celera | 12:51788948 | GGGTTTTTTTTTTGC[C/T]CCAACTAAAACTCAC | 207304 |
rs29153683 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Hectd1 | Mm_Celera | 12:51803519 | AGTCCTGCACCACCA[C/T]GCCTGCCTTATAACA | 207304 |
rs29153684 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hectd1 | Mm_Celera | 12:51774834 | CTCTTAAGAACTCCA[C/T]TTTAAACAACATTGA | 207304 |
rs29154099 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hectd1 | Mm_Celera | 12:51790294 | AAAGCACTTCACAGA[A/G]TACACATTCTTATGC | 207304 |
rs29155322 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hectd1 | Mm_Celera | 12:51822824 | TGGGTCTGGAAAGAT[A/G]GCTTATTGGTTAAGA | 207304 |
rs29155474 | snp | A/C/T | 0.5 | 0 | intron-variant | Hectd1 | GRCm38.p3 | 12:51798138 | AAAGCCCTACCTACA[A/C/T]TGAAAACTTAAAAAA | 207304 |
rs29156636 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hectd1 | Mm_Celera | 12:51748028 | ATGATTAATGTTTTC[A/G]TCTTGTTTTTTTGTT | 207304 |
rs29156743 | snp | A/G | 0.5 | 0 | intron-variant | Hectd1 | Mm_Celera | 12:51814077 | GTTTTTTGGAGACAA[A/G]GTCTAACAAGCTGGC | 207304 |
rs29157106 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Hectd1 | Mm_Celera | 12:51801734 | GACAGACAGACTGAC[A/T]GACAGACAGACAGAC | 207304 |
rs29157769 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hectd1 | Mm_Celera | 12:51785515 | TAGGATTTCAGAACT[A/G]AGGTGCTTTATTTCA | 207304 |
rs29157882 | snp | A/G | 0.188366 | 0.242283 | synonymous-codon | Hectd1 | GRCm38.p3 | 12:51803828 | GTCACGAATGAAGGT[A/G]AGAACACAATTCAAA | 207304 |
rs29158161 | snp | A/G | 0.5 | 0 | intron-variant | Hectd1 | Mm_Celera | 12:51811470 | AGTCACCCAGTGTGG[A/G]AACTGGGAACTGAGT | 207304 |
rs29158855 | snp | A/G | 0.33241 | 0.236027 | intron-variant | Hectd1 | Mm_Celera | 12:51761625 | TTTGTAGTATATTAC[A/G]AACCACTGGGGCAAA | 207304 |
rs29159809 | snp | A/C | 0.375 | 0.216506 | intron-variant | Hectd1 | Mm_Celera | 12:51745183 | AGCCACTTAAGAGAC[A/C]GTGATTAATCTCAGT | 207304 |
rs29159855 | snp | A/G | 0.42 | 0.183303 | intron-variant | Hectd1 | Mm_Celera | 12:51799573 | AGAATTCTCTCTAAA[A/G]TAAAGACCTGCTTTG | 207304 |
rs29160713 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Hectd1 | Mm_Celera | 12:51823479 | AAAGCATCTCCCTCT[C/G]TCCCTCCAAAAGGAC | 207304 |
rs29160886 | snp | C/G | 0.375 | 0.216506 | intron-variant | Hectd1 | Mm_Celera | 12:51761880 | ACTTGACTGCTAGAA[C/G]TTTTTCTTTTTTTCT | 207304 |
rs29160934 | snp | A/T | 0.444444 | 0.157135 | synonymous-codon | Hectd1 | Mm_Celera | 12:51754082 | GGTGATTTTTTTACT[A/T]GTAAATTCATCAGGT | 207304 |
rs29161092 | snp | A/G | 0.48 | 0.0979796 | downstream-variant-500B | Hectd1 | Mm_Celera | 12:51743313 | GGAGAAATGAGGCAT[A/G]AATGAAGAGACTAGG | 207304 |
rs29161493 | snp | A/G | 0.5 | 0 | intron-variant | Hectd1 | Mm_Celera | 12:51792705 | TAAGTCTGACAACCG[A/G]AGAACCTCGGGAACC | 207304 |
rs29161739 | snp | A/C | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Hectd1, Gm5785 | GRCm38.p3 | 12:51827945 | ACAAAAACAAAACAA[A/C]AAAAAAAAACTTTCC | 207304 |
rs29161964 | snp | G/T | 0.33241 | 0.236027 | intron-variant | Hectd1 | Mm_Celera | 12:51746622 | ATAAAAACACAGTTT[G/T]CCATGAATCACTTTT | 207304 |
rs29162193 | snp | C/T | 0.265928 | 0.249492 | intron-variant | Hectd1 | Mm_Celera | 12:51803927 | AAGGTTAGTAGAGGA[C/T]AGCAACACTAAACTG | 207304 |
rs29162513 | snp | A/T | 0.444444 | 0.157135 | upstream-variant-2KB, utr-variant-3-prime | Hectd1, Gm5785 | Mm_Celera | 12:51830145 | CATGGGCGTTGAAAA[A/T]TCAAATACTAGCCGC | 207304 |
rs29163208 | snp | C/T | 0.32 | 0.24 | upstream-variant-2KB, downstream-variant-500B | Hectd1, Gm5785 | Mm_Celera | 12:51831364 | CATCCCAGTGGCTGG[C/T]GAGAAAGCATATGAA | 207304 |
rs29165046 | snp | C/T | 0.5 | 0 | intron-variant | Hectd1 | GRCm38.p3 | 12:51788417 | GTCCTGGAACTCTTA[C/T]GTCGAGGAGGCTGGC | 207304 |
rs29165453 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Hectd1 | Mm_Celera | 12:51796909 | AATTGGAGCATGGCC[G/T]GGCGTGGTGGCTCAC | 207304 |
rs29165970 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Hectd1 | GRCm38.p3 | 12:51773048 | AAATTAAATATCAAA[A/T]TTTAAAGATAATTAG | 207304 |
rs29166758 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Hectd1 | Mm_Celera | 12:51817072 | AGGAATTTCAAGATT[A/C]AGTGGAAAATATAGT | 207304 |
rs29166964 | snp | A/G | 0.290657 | 0.246672 | intron-variant | Hectd1 | Mm_Celera | 12:51812203 | ATAATGGAATAGAGT[A/G]GGGCAAAACATGGCA | 207304 |
rs29167809 | snp | A/G | 0.265928 | 0.249492 | intron-variant | Hectd1 | Mm_Celera | 12:51774264 | AAATTATAAACTGAG[A/G]ACGGTCGTCCACTTC | 207304 |
rs29168495 | snp | C/T | 0.32 | 0.24 | intron-variant | Hectd1 | Mm_Celera | 12:51805590 | CTTACTTGGTGCTGA[C/T]ACTTTAAAAGATGCA | 207304 |
rs29168953 | snp | A/G | 0.32 | 0.24 | intron-variant | Hectd1 | Mm_Celera | 12:51763980 | CCATGCCTGGCTTTT[A/G]CTACCCTACATTAGT | 207304 |
rs29168990 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hectd1 | Mm_Celera | 12:51787052 | TGCAGGTCAGTCAGA[C/T]ACAGTGGTGACTGCC | 207304 |
rs29169008 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hectd1 | Mm_Celera | 12:51788386 | AAATGAACACCAACT[C/T]TCCCCTAAAAAGGCT | 207304 |
rs29169553 | snp | C/T | 0.5 | 0 | intron-variant | Hectd1 | Mm_Celera | 12:51812448 | AAAAACCAAAAGAGC[C/T]CCTGGGAGCTGAAGA | 207304 |
rs29169723 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Hectd1 | Mm_Celera | 12:51769659 | TTTTATTAGATTTAT[C/T]TCTGGACAGCCCAAG | 207304 |
rs29169767 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Hectd1 | Mm_Celera | 12:51815392 | ACAGGAGTCTGCCAG[A/G]CTTTCAGGCCAGACT | 207304 |
rs29169969 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Hectd1 | Mm_Celera | 12:51799883 | GCTTTTTTGAACATG[A/G]GCTGAAACTTGAAGC | 207304 |
rs29170981 | snp | A/G | 0.444444 | 0.157135 | upstream-variant-2KB, utr-variant-3-prime | Hectd1, Gm5785 | Mm_Celera | 12:51830152 | GTTGAAAAATCAAAT[A/G]CTAGCCGCTGCTAGT | 207304 |
rs29171218 | snp | C/G | 0.444444 | 0.157135 | upstream-variant-2KB, missense | Hectd1, Gm5785 | GRCm38.p3 | 12:51829714 | TCGGCTACGGCTCTC[C/G]TCAGCCCGGCCTCCC | 207304 |
rs29171748 | snp | C/T | 0.32 | 0.24 | synonymous-codon | Hectd1 | GRCm38.p3 | 12:51769214 | CAAGCTGCTCCATGA[C/T]TGCGTTGTGCCTGAA | 207304 |
rs29172220 | snp | A/G | 0.375 | 0.216506 | upstream-variant-2KB, intron-variant | Hectd1, Gm5785 | Mm_Celera | 12:51830939 | AATTCTTACTGCTAA[A/G]TAATAGTAAGTTGTT | 207304 |
rs29172425 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Hectd1 | Mm_Celera | 12:51810620 | GACAATCTTGGCCCA[C/T]ACTGTACTGTCTCAA | 207304 |
rs29172747 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Hectd1 | Mm_Celera | 12:51812071 | AAGGCTCCTGTGATC[A/C]AGAGCCTGAGAAAAA | 207304 |
rs29173504 | snp | C/T | 0.265928 | 0.249492 | intron-variant | Hectd1 | Mm_Celera | 12:51803405 | TTTTATTTTGTGCCT[C/T]ATCCTGTAACCCTGT | 207304 |
rs29173719 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hectd1 | Mm_Celera | 12:51789745 | TCAAGAACCAAGCAG[C/T]TAAGCTGCACCACTT | 207304 |
rs29174638 | snp | A/G | 0.444444 | 0.157135 | upstream-variant-2KB, utr-variant-3-prime | Hectd1, Gm5785 | Mm_Celera | 12:51830540 | ACCCTGTTCTGTATC[A/G]TGTGTTCCTGGCCAG | 207304 |
rs29174973 | snp | A/C | 0.5 | 0 | intron-variant | Hectd1 | Mm_Celera | 12:51763580 | TGGCAATTGTTTTTA[A/C]CCACCCATCACTCTT | 207304 |
rs29175071 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Hectd1 | Mm_Celera | 12:51815662 | GAATACTCTAGTTTT[A/T]AAGAATCTTTTTCCT | 207304 |
rs29175077 | snp | A/G | 0.290657 | 0.246672 | intron-variant | Hectd1 | GRCm38.p3 | 12:51752996 | CATTTATCACAACAG[A/G]CCCAGAGACTAATAT | 207304 |
rs29175607 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | Hectd1, Gm5785 | Mm_Celera | 12:51827803 | AGCCGGGCATGGTGG[C/T]ACACTCCTTTAATCC | 207304 |
rs29176148 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hectd1 | Mm_Celera | 12:51798430 | ACACACACACACACA[C/T]TCTAAGGATATAAAT | 207304 |
rs29176341 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Hectd1 | Mm_Celera | 12:51823682 | AGCTCTAGACCATTT[C/T]AAAGGCACATGGGCC | 207304 |
rs29176897 | snp | A/C | 0.277778 | 0.248452 | synonymous-codon | Hectd1 | GRCm38.p3 | 12:51802802 | TGCAAAACACCGCAG[A/C]GCTCCATCGGAAACC | 207304 |
rs29176991 | snp | C/T | 0.401235 | 0.199068 | synonymous-codon | Hectd1 | GRCm38.p3 | 12:51754306 | TCCACAGGGGCTCTG[C/T]CCGTTGCCTGCTTTA | 207304 |
rs29177142 | snp | A/G | 0.265928 | 0.249492 | intron-variant | Hectd1 | Mm_Celera | 12:51775975 | GCATCCTTAGCAAGT[A/G]CAGGACACCCTGGCT | 207304 |
rs29177654 | snp | G/T | 0.375 | 0.216506 | upstream-variant-2KB, missense | Hectd1, Gm5785 | Mm_Celera | 12:51829893 | CCCTCCTCCGGACTT[G/T]TAAAGCCAGCGGTTT | 207304 |
rs29177695 | snp | A/C | 0.359862 | 0.224567 | intron-variant | Hectd1 | Mm_Celera | 12:51772163 | TTCATTTTAATGTGC[A/C]GTCATTATCAGTTCT | 207304 |
rs29177707 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Hectd1 | Mm_Celera | 12:51823150 | CACGGCTTCTTCCCA[A/C]AAGTCCTGGCCTCCT | 207304 |
rs29178695 | snp | A/G | 0.32 | 0.24 | intron-variant | Hectd1 | Mm_Celera | 12:51813845 | TCAAAGTTATCCTTA[A/G]CTATAGCAAATTCCA | 207304 |
rs29179038 | snp | A/T | 0.375 | 0.216506 | intron-variant | Hectd1 | Mm_Celera | 12:51802944 | CATGGGGCTTGAATG[A/T]CAGCACCATACACTG | 207304 |
rs29179994 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hectd1 | Mm_Celera | 12:51755570 | TCACTAAGAATGTGG[C/T]TGCCTTTTGCTCTTC | 207304 |
rs29180744 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hectd1 | Mm_Celera | 12:51798407 | GCACAGGTACTGCAT[C/T]CATATGTACACACAC | 207304 |
rs29181751 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hectd1 | Mm_Celera | 12:51824788 | CCACATTGTCCCTCA[C/T]ACCCATATACAGCTC | 207304 |
rs29181997 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hectd1 | Mm_Celera | 12:51755251 | TCAACTGTTTCTCTC[C/T]GTGTTGGTTGGAGTA | 207304 |
rs29182157 | snp | C/T | 0.401235 | 0.199068 | synonymous-codon | Hectd1 | GRCm38.p3 | 12:51797881 | TGTCTGTGCAAACAC[C/T]GGCAGCAACCTCTTC | 207304 |
rs29182350 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hectd1 | GRCm38.p3 | 12:51791694 | ACAGAATGAAATCCC[A/G]TTACTGCAACACCAT | 207304 |
rs29185236 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Hectd1 | Mm_Celera | 12:51823425 | TCTTCTCCTGCCTCA[C/G]TAACTCAGGCAGTGT | 207304 |
rs29185885 | snp | A/C | 0.375 | 0.216506 | intron-variant | Hectd1 | Mm_Celera | 12:51769781 | TCAGAAATCTGCCTG[A/C]CACTGCCTCTCAAGT | 207304 |
rs29185961 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Hectd1 | Mm_Celera | 12:51789798 | GAAGCAACATGATCA[C/T]CTTTAGTTTATTATT | 207304 |
rs29186027 | snp | C/T | 0.455 | 0.143091 | intron-variant | Hectd1 | Mm_Celera | 12:51800082 | TGTATCTGTGCACCA[C/T]GCCTGTATATGATGC | 207304 |
rs29186704 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Hectd1 | Mm_Celera | 12:51752394 | TTATAGCTGTAAGCC[A/T]ATAGGTCTAAGTAGT | 207304 |
rs29187464 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hectd1 | Mm_Celera | 12:51797311 | TGCTCAACTGCTGTT[C/T]TATTTATAGTAACCA | 207304 |
rs29187543 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Hectd1 | Mm_Celera | 12:51806208 | GGAAGCATATCTCTA[C/T]CTTTAGCCGTCATCA | 207304 |
rs29188169 | snp | C/G | 0.375 | 0.216506 | intron-variant | Hectd1 | Mm_Celera | 12:51775407 | GATGCCCTCACCCCC[C/G]ATTCCCCAGCCCACC | 207304 |
rs29188339 | snp | C/G | 0.375 | 0.216506 | upstream-variant-2KB, missense | Hectd1, Gm5785 | Mm_Celera | 12:51829866 | GCAGGCGCTCGGCGT[C/G]CCCGGGTCACCCCCT | 207304 |
rs29188476 | snp | A/G | 0.5 | 0 | intron-variant | Hectd1 | Mm_Celera | 12:51778138 | GCCTTGTTGGAGGAA[A/G]TGTATGACAGTGGGG | 207304 |
rs29188576 | snp | C/T | 0.387812 | 0.208586 | intron-variant | Hectd1 | Mm_Celera | 12:51765767 | TCCTATAGTTACCAG[C/T]AAATCCCAGCATACC | 207304 |
rs29189331 | snp | A/G | 0.46875 | 0.121031 | intron-variant | Hectd1 | Mm_Celera | 12:51790300 | CTTCACAGAGTACAC[A/G]TTCTTATGCTACAGT | 207304 |
rs29189826 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hectd1 | Mm_Celera | 12:51805635 | ATTCTTACAAGGAGC[A/G]TGTGTGTGTGTGTGT | 207304 |
rs29189996 | snp | A/G | 0.455 | 0.143091 | intron-variant | Hectd1 | Mm_Celera | 12:51771578 | TATTATTTGGATAAG[A/G]ACTTTTGCTAAAATC | 207304 |
rs29190351 | snp | C/T | 0.375 | 0.216506 | synonymous-codon | Hectd1 | GRCm38.p3 | 12:51768800 | TTCCTTATTGGTTAA[C/T]TCAGATACCGAACTA | 207304 |
rs29191056 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hectd1 | Mm_Celera | 12:51801672 | ACATACATACATCAG[A/G]CAAACACCCACACAC | 207304 |
rs29192307 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Hectd1 | Mm_Celera | 12:51772266 | ACCAGGTTCTAACCA[C/T]GACTCACCATTGTGG | 207304 |
rs29192629 | snp | C/T | 0.455 | 0.143091 | intron-variant | Hectd1 | Mm_Celera | 12:51771809 | AGGCATTGCCTAAAT[C/T]CTAAAACTACCAAGA | 207304 |
rs29192943 | snp | A/T | 0.375 | 0.216506 | intron-variant | Hectd1 | Mm_Celera | 12:51793845 | TCAGGTTCACCCTCC[A/T]AAGAGAATTAGAGGC | 207304 |
rs29193328 | snp | C/G | 0.5 | 0 | intron-variant | Hectd1 | Mm_Celera | 12:51812234 | AAAAACCCCCTCAGA[C/G]TTAGCTTTCTAAGAC | 207304 |
rs29193522 | snp | G/T | 0.375 | 0.216506 | intron-variant | Hectd1 | Mm_Celera | 12:51803097 | AGAAACGCGGAAAGA[G/T]TAACTATTATGTGCA | 207304 |
rs29194504 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Hectd1 | Mm_Celera | 12:51823104 | ACTACTCCACAAGGC[C/T]AAGTGCTCCTGCACC | 207304 |
rs29194796 | snp | A/T | 0.46875 | 0.121031 | intron-variant | Hectd1 | Mm_Celera | 12:51814163 | GCTTATCATGCCTAA[A/T]TCTTCTGTCCATTTA | 207304 |
rs29195465 | snp | C/T | 0.265928 | 0.249492 | intron-variant | Hectd1 | Mm_Celera | 12:51758986 | ATTATAAAAATCCAA[C/T]TGACATTCTTTTCAA | 207304 |
rs29195814 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Hectd1 | Mm_Celera | 12:51806172 | TAAACCCCCCTCCCC[C/G]CCCCCGCCCCAAGCA | 207304 |
rs29195826 | snp | C/T | 0.32 | 0.24 | intron-variant | Hectd1 | Mm_Celera | 12:51824248 | GCACAACTTGAATAG[C/T]AGCGCTCAGAAGTTC | 207304 |
rs29196826 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Hectd1 | Mm_Celera | 12:51771447 | TACATTTTTAATGCT[C/T]AGTATAATTGGTAAG | 207304 |
rs29197040 | snp | A/C | 0.33241 | 0.236027 | intron-variant | Hectd1 | Mm_Celera | 12:51775958 | TCAAAGACAACTCAG[A/C]TGCATCCTTAGCAAG | 207304 |
rs29198020 | snp | A/T | 0.5 | 0 | upstream-variant-2KB, missense | Hectd1, Gm5785 | Mm_Celera | 12:51829945 | CCTGGGAACTCGGCG[A/T]GCGCTGCGCAGCCGG | 207304 |
rs29198446 | snp | C/T | 0.265928 | 0.249492 | intron-variant | Hectd1 | Mm_Celera | 12:51802955 | AATGTCAGCACCATA[C/T]ACTGCTAACTCCATA | 207304 |
rs29198963 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Hectd1 | Mm_Celera | 12:51820919 | AAACCTGTCCTCTGA[A/C]TGGTAAGTTCACGCC | 207304 |
rs29199519 | snp | A/G | 0.415225 | 0.187619 | downstream-variant-500B | Hectd1 | Mm_Celera | 12:51743636 | CAAAAAAGAGAATTT[A/G]TGTTACCGTGAAGAG | 207304 |
rs29199651 | snp | C/T | 0.401235 | 0.199068 | intron-variant | Hectd1 | Mm_Celera | 12:51797705 | CAAAATAAAATAAAC[C/T]GGAAGAGATGATGTT | 207304 |
rs29200061 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hectd1 | Mm_Celera | 12:51779550 | ATTTGGTGGCTATTA[C/T]ACATAAGAATTTTTC | 207304 |
rs29200074 | snp | A/G | 0.188366 | 0.242283 | intron-variant | Hectd1 | Mm_Celera | 12:51767823 | ATACGCAGTATTGAA[A/G]GAACCTTTAAAAAAA | 207304 |
rs29202011 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Hectd1 | Mm_Celera | 12:51761401 | TTTGGGTTTGTCAGG[C/G]TTGGTGGCAAAAGCT | 207304 |
rs29203786 | snp | C/T | 0.265928 | 0.249492 | intron-variant | Hectd1 | Mm_Celera | 12:51803543 | TATAACACATTCCAC[C/T]GCCCTCCCAAAGGCT | 207304 |
rs29204400 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hectd1 | Mm_Celera | 12:51815044 | TTGACAACTGGATCA[C/T]AAACTAGTTGGCTGT | 207304 |
rs29204614 | snp | C/T | 0.265928 | 0.249492 | missense | Hectd1 | GRCm38.p3 | 12:51768910 | CTAACTTCCTTTCCG[C/T]ATTTTCACTTCCCGT | 207304 |
rs29205099 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hectd1 | Mm_Celera | 12:51797581 | GTGTGGTGGTGCACA[A/G]CTTTTAAGGCCAGTT | 207304 |
rs29205664 | snp | A/T | 0.375 | 0.216506 | intron-variant | Hectd1 | Mm_Celera | 12:51759674 | TCTCAAGTACTGGAA[A/T]AACATGATCACTGAC | 207304 |
rs29206735 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hectd1 | Mm_Celera | 12:51778496 | GCCAGGCATGGTAGC[A/G]CACACCTTTAATCCC | 207304 |
rs29206767 | snp | C/G | 0.5 | 0 | intron-variant | Hectd1 | Mm_Celera | 12:51778303 | TGAACCTCTGAACCT[C/G]TTAAGCAGCCTTAAT | 207304 |
rs29206834 | snp | A/G | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Hectd1, Gm5785 | Mm_Celera | 12:51827860 | GATTTCTGAGTTCAA[A/G]GCCAGCCTGGTCTAC | 207304 |
rs29207317 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hectd1 | Mm_Celera | 12:51761443 | AGCCAAGTTACTGTC[C/T]TTTAGTTCTTTATAG | 207304 |
rs29207616 | snp | A/G | 0.5 | 0 | intron-variant | Hectd1 | Mm_Celera | 12:51814134 | GCCTCCCAAATGTTG[A/G]CATTACAGGAACAGC | 207304 |
rs29207736 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Hectd1 | Mm_Celera | 12:51785523 | CAGAACTGAGGTGCT[C/T]TATTTCATGTAACCT | 207304 |
rs29208131 | snp | A/T | 0.375 | 0.216506 | intron-variant | Hectd1 | Mm_Celera | 12:51759988 | AACAGAACAGGTATA[A/T]GTATATGAAATATAT | 207304 |
rs29208181 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Hectd1 | Mm_Celera | 12:51820896 | AGCCAGGAGGAAACC[A/C]CCTCCACAAACCTGT | 207304 |
rs29208345 | snp | C/T | 0.32 | 0.24 | intron-variant | Hectd1 | Mm_Celera | 12:51823562 | CTATTGTGCAAGATG[C/T]ACTGAGAGGAATAAA | 207304 |
rs29210901 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hectd1 | Mm_Celera | 12:51815884 | TCTTTTGAAACTATT[A/G]TTAATTAAACTTCTT | 207304 |
rs29210919 | snp | G/T | 0.265928 | 0.249492 | intron-variant | Hectd1 | Mm_Celera | 12:51803434 | GTCCGGCCTGAGAGC[G/T]TAGTACGTAGACTAG | 207304 |
rs29211943 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Hectd1 | Mm_Celera | 12:51801730 | TATAGACAGACAGAC[A/T]GACTGACAGACAGAC | 207304 |
rs29212455 | snp | A/C | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Hectd1, Gm5785 | Mm_Celera | 12:51828033 | GCTTAATGCAAAAAC[A/C]CTCAAGGCAAAACAG | 207304 |
rs29213003 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Hectd1 | Mm_Celera | 12:51799959 | ATTATCTCAAATAAA[C/T]AGACTCAAGTCCCAT | 207304 |
rs29213039 | snp | C/T | 0.265928 | 0.249492 | intron-variant | Hectd1 | Mm_Celera | 12:51799279 | TCCTCCCGGTTTTCA[C/T]GTAACAGGAGTATGG | 207304 |
rs29213098 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hectd1 | Mm_Celera | 12:51803974 | AGAAAACATAACAAA[C/T]GCTCCAAATTCAGTG | 207304 |
rs29214457 | snp | A/G | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Hectd1, Gm5785 | Mm_Celera | 12:51827993 | TTCAAAAAGTATGCT[A/G]CATATGCAGCAGTCT | 207304 |
rs29215912 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Hectd1 | Mm_Celera | 12:51800106 | ATGATGCCCTGAGAG[A/T]CCGTCAGATCCCCTG | 207304 |
rs29216887 | snp | C/T | 0.5 | 0 | intron-variant | Hectd1 | Mm_Celera | 12:51792324 | CAGGGTGGGAGAATA[C/T]CCAGGGCTTCCACCC | 207304 |
rs29217198 | snp | C/T | 0.42 | 0.183303 | intron-variant | Hectd1 | Mm_Celera | 12:51766128 | GGCAGGAAGATCAAA[C/T]ATGCAAGGCTAGGGT | 207304 |
rs29217781 | snp | C/T | 0.32 | 0.24 | intron-variant | Hectd1 | Mm_Celera | 12:51799747 | TCATGGTCAACATGG[C/T]GGCCATCGCTCCAAC | 207304 |
rs29217885 | snp | C/T | 0.432133 | 0.171253 | synonymous-codon | Hectd1 | GRCm38.p3 | 12:51772350 | CTTCCAATCAAGGCC[C/T]CTGATAACACGTGCT | 207304 |
rs29218123 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Hectd1 | Mm_Celera | 12:51787792 | ATATACATGTAGGCA[A/C]AACACACAAACACAG | 207304 |
rs29218547 | snp | A/C/T | 0.444444 | 0.157135 | intron-variant | Hectd1 | GRCm38.p3 | 12:51791526 | AAAACATGAACCAGG[A/C/T]TTATAATTAAGACAT | 207304 |
rs29218551 | snp | C/T | 0.387812 | 0.208586 | intron-variant | Hectd1 | Mm_Celera | 12:51751484 | CTTCATGTGGCCTTC[C/T]TCTTTAGAACTCCTT | 207304 |
rs29218585 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hectd1 | Mm_Celera | 12:51805446 | TTGTCTCAAAAACTT[C/T]AACTAGGGAACTGAG | 207304 |
rs29220056 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hectd1 | Mm_Celera | 12:51779722 | ACTGCTGAGACATCC[C/T]TCCAGCCCAAGAATT | 207304 |
rs29220669 | snp | A/T | 0.48 | 0.0979796 | downstream-variant-500B | Hectd1 | Mm_Celera | 12:51743227 | CCAGAGAGAGAAATA[A/T]GGGATATATTTGCTT | 207304 |
rs29221020 | snp | A/G | 0.32 | 0.24 | intron-variant | Hectd1 | Mm_Celera | 12:51824316 | CTCTAGGCCAGACTG[A/G]ATTATAGAGTGATAC | 207304 |
rs29221261 | snp | C/G | 0.42 | 0.183303 | intron-variant | Hectd1 | Mm_Celera | 12:51775926 | CAGGAGGGAATGAAG[C/G]AGGAGGACCGGGGAG | 207304 |
rs29222071 | snp | A/T | 0.33241 | 0.236027 | intron-variant | Hectd1 | Mm_Celera | 12:51751387 | TGTAGCATGTTATGC[A/T]GACATCCAAAGATTG | 207304 |
rs29222476 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hectd1 | Mm_Celera | 12:51797670 | GTTTCAGGTCAGTCA[A/G]GGCTACATAGTACAA | 207304 |
rs29223403 | snp | A/C | 0.5 | 0 | intron-variant | Hectd1 | Mm_Celera | 12:51792076 | GTATGCTGTATCCAA[A/C]AATGTAATTATGTGC | 207304 |
rs29223577 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hectd1 | Mm_Celera | 12:51797220 | TCAAAAGGCTAGAAA[C/T]GAATCTATCTATGAT | 207304 |
rs29223836 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hectd1 | Mm_Celera | 12:51802822 | CATCGGAAACCTAAC[A/G]GTGTACAACAATGTA | 207304 |
rs29483805 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Hectd1 | Mm_Celera | 12:51800108 | GATGCCCTGAGAGTC[C/T]GTCAGATCCCCTGTA | 207304 |
rs29484469 | snp | A/C | 0.345679 | 0.230967 | intron-variant | Hectd1 | Mm_Celera | 12:51748004 | ATCAGATAATCCTTC[A/C]AAAATAAAATGATTA | 207304 |
rs29486511 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Hectd1 | Mm_Celera | 12:51810437 | TGGGGGAGAAGAGCC[A/G]CTGAGGAAGATTGGC | 207304 |
rs29487073 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Hectd1 | Mm_Celera | 12:51761475 | GACTGTACTTCCTTT[A/G]TATGAACTGATTGCG | 207304 |
rs29487427 | snp | A/G | 0.188366 | 0.242283 | intron-variant | Hectd1 | Mm_Celera | 12:51783550 | GCAGAAAATGATAGT[A/G]TGCCATTCCTTCCAA | 207304 |
rs29487545 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hectd1 | Mm_Celera | 12:51759716 | AAAATAAAAATAAAC[A/G]ATTAAAAATTTTTTC | 207304 |
rs29487804 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Hectd1 | Mm_Celera | 12:51790023 | ATTTTAATGTTGGTA[C/T]AGATATACAAGCTAA | 207304 |
rs29489348 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hectd1 | Mm_Celera | 12:51751754 | GTCACAGAAACCCTC[C/T]CCTTGTTTTCCTGCC | 207304 |
rs29489493 | snp | G/T | 0.197531 | 0.244432 | intron-variant | Hectd1 | Mm_Celera | 12:51796835 | GTATACGTCTGACAG[G/T]GCTGGTACCTAGAAT | 207304 |
rs29489723 | snp | C/T | 0.5 | 0 | intron-variant | Hectd1 | Mm_Celera | 12:51752897 | GCAGGAGAGAACACA[C/T]GCACACACATGCAGT | 207304 |
rs29490141 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Hectd1 | Mm_Celera | 12:51769613 | GTATGCATTATATAC[A/G]ATGTTTCTGGGATAT | 207304 |
rs29490668 | snp | A/G | 0.32 | 0.24 | intron-variant | Hectd1 | Mm_Celera | 12:51799644 | TCTAAAAACCAGCCA[A/G]TTCAAATTACTAGCC | 207304 |
rs29490703 | snp | A/T | 0.345679 | 0.230967 | intron-variant | Hectd1 | Mm_Celera | 12:51775255 | GATTCGGATGTGTAA[A/T]TTATTGCTCTTTCTT | 207304 |
rs29490800 | snp | A/C | 0.277778 | 0.248452 | intron-variant | Hectd1 | Mm_Celera | 12:51761489 | TATATGAACTGATTG[A/C]GAAAGAATAAAACAA | 207304 |
rs29490897 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hectd1 | Mm_Celera | 12:51803122 | TGTGCAACTTGCCAA[C/T]ATCATCTATGAATGT | 207304 |
rs29491507 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hectd1 | Mm_Celera | 12:51823974 | AAAAAAATAAAATAA[A/G]ATAAAATAAAATTTT | 207304 |
rs33843462 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Hectd1 | Mm_Celera | 12:51775604 | AGGTTAATTGAGACT[G/T]CTGGTCCTCCCACAT | 207304 |
rs33843792 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Hectd1 | Mm_Celera | 12:51823132 | ACCTCCCCTGCCGGG[A/T]ACCACGGCTTCTTCC | 207304 |
rs33844013 | snp | C/G | 0.33241 | 0.236027 | intron-variant | Hectd1 | Mm_Celera | 12:51782690 | AGGGTGCATTAGACA[C/G]CTCCCTTCCTTACAT | 207304 |
rs33844689 | snp | A/T | 0.32 | 0.24 | intron-variant | Hectd1 | Mm_Celera | 12:51769447 | CAAACGGGATCAGCG[A/T]TTCATGGCGCTGTAC | 207304 |
rs33845254 | snp | A/G | 0.465374 | 0.126941 | intron-variant | Hectd1 | Mm_Celera | 12:51803419 | TCATCCTGTAACCCT[A/G]TCCGGCCTGAGAGCT | 207304 |
rs33845307 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hectd1 | Mm_Celera | 12:51777488 | TACTTACTGATGTGC[A/G]TGTGCGTGTGTGGGT | 207304 |
rs33845768 | snp | A/T | 0.265928 | 0.249492 | intron-variant | Hectd1 | Mm_Celera | 12:51790085 | AAGGCATAACTAAAA[A/T]TTGTGTCGAGCCTTT | 207304 |
rs33857908 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Hectd1 | Mm_Celera | 12:51797625 | GCAGGCAGACAGACT[A/T]GTGAATTGCTAGTCT | 207304 |
rs33858172 | snp | C/G | 0.5 | 0 | intron-variant | Hectd1 | Mm_Celera | 12:51815714 | TTGGGAATACTGACT[C/G]TATCTGCAGATTATC | 207304 |
rs33881976 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hectd1 | Mm_Celera | 12:51783772 | TCATCTCCTCAGGCA[C/T]AGGACTACAGGTGTG | 207304 |
rs45650783 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Hectd1 | Mm_Celera | 12:51776914 | GCTTGTAAAAAAGTT[C/G]AATGACAGACATCAA | 207304 |
rs45669185 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hectd1 | Mm_Celera | 12:51794166 | GGGGCCAACTGCAGC[A/G]AGCAGAGGTTCTAAA | 207304 |
rs45670767 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Hectd1 | Mm_Celera | 12:51781971 | ACAGTGCAACTGAAC[G/T]AAGACCAAACCAAAC | 207304 |
rs45676270 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Hectd1 | Mm_Celera | 12:51765453 | TTATATTGTCCAAAA[C/T]AAAGACATTAATAAC | 207304 |
rs45676608 | snp | C/T | | | intron-variant, missense | Hectd1, Gm5785 | Mm_Celera | 12:51828251 | AAACTCCACCAAAAA[C/T]CGGAGCTTCAGATAC | 207304 |
rs45680870 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hectd1 | Mm_Celera | 12:51781618 | GAGTGTAAATGTGTT[A/G]GGCAGAACTCTGGCA | 207304 |
rs45702383 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Hectd1 | Mm_Celera | 12:51752195 | TATATCTGTCACCTA[C/G]TTCCCAGGATCATGG | 207304 |
rs45717390 | snp | G/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51817622 | ACAGGGATGTGGAAT[G/T]TTCTGGTGAATTGTC | 207304 |
rs45771075 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hectd1 | Mm_Celera | 12:51758174 | CAACATCCCTAAATC[C/T]AGAGGGCTAAAGGTA | 207304 |
rs45800474 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon | Hectd1 | Mm_Celera | 12:51746330 | ATATATTCTTGAAGA[C/T]GGGCAAAACTGGAAA | 207304 |
rs45825151 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Hectd1 | Mm_Celera | 12:51763140 | TTTAATTTGTCATGT[A/G]TTAAATATTAACCTT | 207304 |
rs45841310 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hectd1 | Mm_Celera | 12:51757709 | CAGCAAGTAGGCTTC[A/G]GGAGCCGGCCTGTTG | 207304 |
rs45852064 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51772899 | CCAGCACCCAGGAAA[C/T]AGAGGCAGATAGAGA | 207304 |
rs45865665 | snp | A/G | | | intron-variant | Hectd1, Gm5785 | Mm_Celera | 12:51828536 | ACCACCCCCCCCCAG[A/G]CAGACGGACAGACAG | 207304 |
rs45879065 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51758030 | CTCTCTCTCTCTTTT[C/T]TTTTTTTGATTAAAT | 207304 |
rs45901583 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hectd1 | Mm_Celera | 12:51774964 | ATAACCAAAGAGCCT[C/T]GCTATCAGAAACAGT | 207304 |
rs45917774 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hectd1 | Mm_Celera | 12:51781072 | CGTTATAGTGGACAG[C/T]TCTATAGCACATGCA | 207304 |
rs45929255 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hectd1 | Mm_Celera | 12:51753307 | ACGCAGGGAGAAAGC[A/G]GTCATCAGACCCAGA | 207304 |
rs45930621 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51809176 | TAAAATTCCCCTACT[A/G]TCTGCAATAAATATT | 207304 |
rs45956271 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51756279 | GAAAGGAGTTAGAGA[C/T]CTGAAGCCCATTTTG | 207304 |
rs46005095 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Hectd1 | Mm_Celera | 12:51758569 | TCATTGCATTTCTAT[A/C]TCAAAAAACTACTAT | 207304 |
rs46054603 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hectd1 | Mm_Celera | 12:51752259 | AAGAATGTGTTCAGT[C/T]GGTAATTTTCTGTTT | 207304 |
rs46056590 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hectd1 | Mm_Celera | 12:51797779 | CAAATCCCAGATCCT[C/T]CTGAAAAGCGGGTGT | 207304 |
rs46071627 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hectd1 | Mm_Celera | 12:51764203 | ATACAATTAGCAAAC[A/G]GCACAGCAAGGTCAT | 207304 |
rs46083368 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51819719 | GGGGCTGAAAAGTTG[A/G]AGCCATAGCTCACTT | 207304 |
rs46155909 | snp | A/G | 0.32 | 0.24 | intron-variant | Hectd1 | Mm_Celera | 12:51806821 | TAGTTAAGTATTCCT[A/G]TTCCTTAAACCTAAT | 207304 |
rs46176181 | snp | A/C | | | intron-variant | Hectd1 | Mm_Celera | 12:51809178 | AAATTCCCCTACTGT[A/C]TGCAATAAATATTTA | 207304 |
rs46215275 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51758084 | TAAAGAAGGCCCCCA[A/G]CTGTGTGTGCATATG | 207304 |
rs46251137 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Hectd1 | Mm_Celera | 12:51776883 | AAGGAATTAAAACAA[C/T]ACATGTTTCTACGTG | 207304 |
rs46300601 | snp | A/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51809272 | TCCTATTATTTTTTT[A/T]AAGGTTTATTTATTC | 207304 |
rs46350803 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hectd1 | Mm_Celera | 12:51782422 | GCCTTGTTCCATAAA[A/G]GTAAAGCCTATCGCT | 207304 |
rs46391901 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51819767 | GAAGGAACAAAGTCC[C/T]GAGTCCAATCTTCAG | 207304 |
rs46432898 | snp | A/G | | | synonymous-codon | Hectd1 | GRCm38.p3 | 12:51757056 | ACTTACCATTTTCCC[A/G]TTTTCCTTTTCTTTA | 207304 |
rs46444128 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hectd1 | Mm_Celera | 12:51753974 | AATGAAAGAAGAGCT[A/G]ATCAGAGGCACAAGG | 207304 |
rs46458342 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Hectd1 | Mm_Celera | 12:51795402 | TTCATTACTGTCACT[A/G]GGAACACAATAGGAA | 207304 |
rs46460171 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Hectd1 | Mm_Celera | 12:51784051 | TCATTTTTGTTTTGG[A/G]CGCTAGGTATTAAAT | 207304 |
rs46484170 | snp | A/G | 0.132653 | 0.220748 | synonymous-codon | Hectd1 | Mm_Celera | 12:51750390 | AGTCCTCTGAAACTC[A/G]GCCGCCACAAGAGCA | 207304 |
rs46510171 | snp | G/T | 0.489796 | 0.070696 | intron-variant | Hectd1 | Mm_Celera | 12:51782036 | TTAAAAAATAGTCTA[G/T]AAAATATATCTTACT | 207304 |
rs46531424 | snp | A/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51798976 | CTGCAGGAAATCCTA[A/T]CCCCTCTGACCTACA | 207304 |
rs46535549 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hectd1 | Mm_Celera | 12:51754608 | GACAAGCTTTGGTTT[A/G]CTCAGATCCAAGGCC | 207304 |
rs46549340 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hectd1 | Mm_Celera | 12:51783388 | TACACTCAGTAAAAG[C/T]CACTCATTGTAGAAG | 207304 |
rs46552642 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Hectd1 | Mm_Celera | 12:51748322 | AGACTTCACTGACAG[C/T]CTACAGATTCATAGG | 207304 |
rs46563172 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hectd1 | Mm_Celera | 12:51782101 | CATAATACCATACAA[A/G]ACAGATTTGAAATAA | 207304 |
rs46579089 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51811193 | GAGCTACAACCCCAT[C/T]TTAAGTCAAAGAGTA | 207304 |
rs46588844 | snp | C/T | 0.142012 | 0.225474 | synonymous-codon | Hectd1 | Mm_Celera | 12:51748772 | GCGGGACTCATAGAT[C/T]AGTTTGCTCATATTG | 207304 |
rs46599145 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hectd1 | Mm_Celera | 12:51762180 | CTTCTATGAGAAACA[A/G]CAGAATTACTACGAC | 207304 |
rs46600474 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Hectd1 | Mm_Celera | 12:51747387 | TGTTACTTTGCTGAA[A/T]ACTGTAGACAAGTGT | 207304 |
rs46616787 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51815586 | GTGTTTGTCATTATG[A/G]CTCTGGAGTATAATT | 207304 |
rs46644121 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hectd1 | Mm_Celera | 12:51814695 | ACAGCTGAACACCAT[C/T]GTTATTAGCCTCGGA | 207304 |
rs46683793 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hectd1 | Mm_Celera | 12:51751642 | GACAGAAAGAATTCA[A/G]CCCAACTTAGGTAAG | 207304 |
rs46707467 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Hectd1 | Mm_Celera | 12:51801248 | GCAGAGGCAAGAGAG[G/T]TACTACAAGTTTATG | 207304 |
rs46708625 | snp | A/C | | | intron-variant | Hectd1, Gm5785 | Mm_Celera | 12:51828527 | TAACAGGTTACCACC[A/C]CCCCCCAGGCAGACG | 207304 |
rs46710648 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hectd1 | Mm_Celera | 12:51748267 | AAGCCATACATATTC[A/G]AACAGACAATCAGCA | 207304 |
rs46717869 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hectd1 | Mm_Celera | 12:51793626 | GGGGCTCAACCTCCA[C/T]ATATCGTTCATATTT | 207304 |
rs46724725 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Hectd1 | Mm_Celera | 12:51760438 | GTACTCCTTAAGTAA[C/T]TGTTCTTGTGTCAAG | 207304 |
rs46754038 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Hectd1 | Mm_Celera | 12:51801092 | GATAGATTGATATGA[A/C]TATTTCATTAACTAC | 207304 |
rs46770920 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Hectd1 | Mm_Celera | 12:51805112 | GATGAACATAACTAA[A/T]TTTCAAGGGATCAGA | 207304 |
rs46800176 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Hectd1 | Mm_Celera | 12:51782448 | TCGCTGCTCTTACAC[A/T]CTTGGCTGTGACAGC | 207304 |
rs46808571 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Hectd1 | Mm_Celera | 12:51794128 | GCAGGGACTGAGTGA[C/G]TGGAGTTGAGACCAG | 207304 |
rs46814076 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hectd1 | Mm_Celera | 12:51786926 | AATGCAAACTGAAAG[C/T]CATTATTCACCTTAA | 207304 |
rs46902522 | snp | C/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51748305 | TAGTCTATCGCTGCC[C/G]TAGACTTCACTGACA | 207304 |
rs46916172 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hectd1 | Mm_Celera | 12:51800835 | GATGATAAAGAGTCA[C/T]AAAGTTGCTCTATTA | 207304 |
rs46921547 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hectd1 | Mm_Celera | 12:51770629 | ACTTATCTATTCATG[A/G]GTTATTTGAAAGGAA | 207304 |
rs46930339 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51787663 | GGTGCAGCTCCCAGT[A/G]CCCACATGGTGGTTC | 207304 |
rs46931285 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Hectd1 | Mm_Celera | 12:51790072 | TTAACAAAGAGAAAA[A/G]GCATAACTAAAAATT | 207304 |
rs46936421 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hectd1 | Mm_Celera | 12:51816962 | TTCACTCCCTGTTGG[A/G]TAAGTGAGGAAACAA | 207304 |
rs46945908 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Hectd1 | Mm_Celera | 12:51790926 | CAAGGAATTTGTGAA[G/T]TATTTTCTTAATACA | 207304 |
rs46984255 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Hectd1 | GRCm38.p3 | 12:51749420 | ACTAAGGTTATTTAG[G/T]TATAAAAGTAGAGGC | 207304 |
rs47012554 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon | Hectd1 | Mm_Celera | 12:51802535 | AAGAAGCATCCTTAC[A/G]TGTGTTACTAGTGGA | 207304 |
rs47026187 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Hectd1 | Mm_Celera | 12:51745744 | TCACTATAGTCAACT[C/G]ACAAACTCTCATTTA | 207304 |
rs47037290 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Hectd1 | Mm_Celera | 12:51747745 | GAGTGCAGAACCAAA[C/T]ACTGTTTCTTACAAT | 207304 |
rs47040196 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hectd1 | Mm_Celera | 12:51793804 | TGGTGGCTGTGCCTG[C/T]AATTTCAGTACTTAG | 207304 |
rs47046562 | snp | C/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51817758 | CTAACACCCATGTGG[C/G]GACTCATAAGTGTCT | 207304 |
rs47110884 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hectd1 | Mm_Celera | 12:51795337 | TCTCAAATAAACAAA[A/G]ACACAAGATACTAAT | 207304 |
rs47151253 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51819410 | AAGTAACAAATGTAA[A/G]CTTTTTATACTGTTA | 207304 |
rs47159582 | snp | G/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51820155 | TGACTCAATGGTCAA[G/T]GACATTTCCTTCTCT | 207304 |
rs47165716 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51813554 | GCCTCTTGAGTGCTG[A/G]GATTAAACACATACC | 207304 |
rs47169831 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51808766 | CGACCGCTCCGCTTG[A/G]CGTCCCGAGCTCATA | 207304 |
rs47259318 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Hectd1 | Mm_Celera | 12:51789704 | AGCTAAGTCAGCCAT[C/G]AAAACAAGCATTAAA | 207304 |
rs47266002 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hectd1 | Mm_Celera | 12:51800096 | ACGCCTGTATATGAT[A/G]CCCTGAGAGTCCGTC | 207304 |
rs47318274 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Hectd1 | Mm_Celera | 12:51746014 | CAGAACTTAGGGGCA[A/C]ATTTGACGACAATAC | 207304 |
rs47322378 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hectd1 | Mm_Celera | 12:51795662 | TCCCTGCACCAGGAC[C/T]GCCACCACCCATCGT | 207304 |
rs47349403 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hectd1 | Mm_Celera | 12:51766346 | CCATGGTCCGTCAGT[A/G]TCAGGCACAGAGAAG | 207304 |
rs47368053 | snp | G/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51801095 | AGATTGATATGAATA[G/T]TTCATTAACTACAGA | 207304 |
rs47402206 | snp | C/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51822414 | CTGTCACCATCAGTT[C/G]TTTGTCACCAGAAGA | 207304 |
rs47430339 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Hectd1 | Mm_Celera | 12:51752165 | TTTTAAATGTTGTTT[G/T]GAGACAGGCTTTTCT | 207304 |
rs47455196 | snp | A/G | 0.32 | 0.24 | intron-variant | Hectd1 | Mm_Celera | 12:51768299 | TATAGTGAATACAGG[A/G]GCTGAGTGAGAGGCG | 207304 |
rs47491420 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Hectd1 | Mm_Celera | 12:51785477 | ATACTTTCTAACACT[A/G]TCTTACAGAGTAGCT | 207304 |
rs47501008 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51794165 | TGGGGCCAACTGCAG[C/T]GAGCAGAGGTTCTAA | 207304 |
rs47504072 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hectd1 | Mm_Celera | 12:51768368 | TGTGTAGCCGTCTCT[C/T]ATAAAATGCAAGCTA | 207304 |
rs47505696 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hectd1 | GRCm38.p3 | 12:51794668 | CACCTGGGCCAGGGA[A/G]AGCTGCATCTGAATG | 207304 |
rs47545398 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Hectd1 | Mm_Celera | 12:51788597 | GAAGCACACAGAGGC[A/T]AAATAATAATAATAA | 207304 |
rs47554735 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51790766 | CCTAAAGCAACTCTC[C/T]AGACATTTTTTTTCT | 207304 |
rs47575258 | snp | A/C/G/T | | | intron-variant, upstream-variant-2KB | Hectd1, Gm5785 | Mm_Celera | 12:51826883 | AGCATACACGAAAGT[A/C/G/T]CACACACACACACAC | 207304 |
rs47609652 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Hectd1 | Mm_Celera | 12:51781019 | CCTAGCTGGGAAACT[C/G]CAGACTCTCAAGGGC | 207304 |
rs47610901 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Hectd1 | Mm_Celera | 12:51780580 | CTGAAAGCTCTAACT[A/T]ACGATACAGAAAGCT | 207304 |
rs47615628 | snp | G/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51756234 | TGGAACCAGCCCAAC[G/T]AAAAGAAGTATGTTG | 207304 |
rs47616680 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Hectd1 | GRCm38.p3 | 12:51749666 | AAAGTTTAAAAGTGA[A/G]TAAAAAAATGTTTAA | 207304 |
rs47622041 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Hectd1 | Mm_Celera | 12:51781651 | TGATTAATGCAGCGG[C/T]ACAGCCCTCAGGAAC | 207304 |
rs47668199 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hectd1 | Mm_Celera | 12:51777842 | CTTACATTACATAGA[C/T]TCACATGAGAGGAGA | 207304 |
rs47672852 | snp | A/G | | | intron-variant | Hectd1, Gm5785 | Mm_Celera | 12:51828387 | GCCCAAATACAAACA[A/G]TAATTAGATATGAAA | 207304 |
rs47681782 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51819849 | ACATGAGTCTGGGGG[A/G]CTGAGAAATGTACTC | 207304 |
rs47726217 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Hectd1 | Mm_Celera | 12:51768204 | AAAAATAAGCAACAG[A/G]ATTAATTTTATTGTA | 207304 |
rs47789229 | snp | G/T | | | intron-variant, upstream-variant-2KB | Hectd1, Gm5785 | Mm_Celera | 12:51827344 | AGGTGATGCAGGAAT[G/T]CACTTACGTTTCAAA | 207304 |
rs47801443 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hectd1 | Mm_Celera | 12:51774895 | TGTGTTATGACATAA[C/T]CATCTAGCCAGGAGT | 207304 |
rs47829446 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hectd1 | Mm_Celera | 12:51799495 | AATTTAAAAATAGCT[A/G]AAACAGAGTAGACCC | 207304 |
rs47850648 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51792042 | ATCTGATCATCACAC[A/G]TTGAATATACTAATC | 207304 |
rs47856811 | snp | C/G | 0.391111 | 0.206368 | intron-variant | Hectd1 | Mm_Celera | 12:51758728 | CGAGAAAAAGCAGCT[C/G]AAAAGACTACATGTG | 207304 |
rs47859902 | snp | A/C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51749120 | AAACATCTTTTCAAA[A/C/T]TTTGTCATCTGAAGA | 207304 |
rs47862187 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hectd1 | Mm_Celera | 12:51811293 | TATCCACAAAAATTA[C/T]CTACTCAAAGACTCT | 207304 |
rs47891739 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Hectd1 | Mm_Celera | 12:51784038 | AGAAATTTGGGGTTC[A/G]TTTTTGTTTTGGACG | 207304 |
rs47928176 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hectd1 | Mm_Celera | 12:51746215 | GTTTGCCAGTATTAG[C/T]GTTTTGCTGAGAGGA | 207304 |
rs47933739 | snp | A/C | | | intron-variant | Hectd1 | Mm_Celera | 12:51805489 | TGGTGAATTCAAGGC[A/C]AGTCTGAGCTACATA | 207304 |
rs47971354 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51823919 | TTAAAAGATTTTAAG[C/T]CGGGGGCTAAACAGA | 207304 |
rs47975073 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hectd1 | Mm_Celera | 12:51788713 | TTTAAAAACTGAGAT[A/G]AATTCTTAGAAGAAC | 207304 |
rs47981248 | snp | A/G | 0.396694 | 0.202437 | intron-variant | Hectd1 | Mm_Celera | 12:51811421 | TAATTTAGTGTGTAT[A/G]TATGCCATCGGGCTA | 207304 |
rs48025893 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon | Hectd1 | Mm_Celera | 12:51767641 | AGTATTACTTAATGA[C/T]TGACCCACTGATAAA | 207304 |
rs48049568 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Hectd1 | Mm_Celera | 12:51765518 | ACCCAACAGAATAAT[C/G]AGATTAAATAAGAGA | 207304 |
rs48059399 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hectd1 | Mm_Celera | 12:51792830 | TTAAAAAGCAGAGTT[A/G]ATATTATGTCAGATA | 207304 |
rs48079736 | snp | A/C | | | intron-variant | Hectd1 | Mm_Celera | 12:51787640 | CCACTGCTCTTGCCG[A/C]AGCTCCAGGTGCAGC | 207304 |
rs48138514 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hectd1 | Mm_Celera | 12:51781945 | GTATCTGGTGTCTGT[C/T]TTTTCTTATGACAGT | 207304 |
rs48157175 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51756175 | CCTCAAGATCTTGGA[A/G]ATGCCAGAGTTGTGG | 207304 |
rs48164884 | snp | G/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51782181 | AGATGGTTCAATAGC[G/T]AAGAGCATTTGTTCC | 207304 |
rs48184403 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hectd1 | Mm_Celera | 12:51793381 | GCCTAATACATCCTA[C/T]GCCTGAGTTCTGCAC | 207304 |
rs48217042 | snp | C/T | | | intron-variant, upstream-variant-2KB | Hectd1, Gm5785 | Mm_Celera | 12:51826876 | ACACCATAGCATACA[C/T]GAAAGTACACACACA | 207304 |
rs48225507 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hectd1 | Mm_Celera | 12:51795149 | TTAACCAGCCTGGCT[A/G]CTGAAACAGCATGTT | 207304 |
rs48232062 | snp | A/G | 0.32 | 0.24 | intron-variant | Hectd1 | Mm_Celera | 12:51804230 | CTCAACCCTGACCTC[A/G]GTGGCCTTGAGGAGT | 207304 |
rs48291990 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Hectd1 | Mm_Celera | 12:51773804 | ACTGATTTTCCCCAA[A/T]TTTCAAAGACTCCTC | 207304 |
rs48307701 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Hectd1 | Mm_Celera | 12:51767158 | TCTACTTGTTTTATT[A/C]ATTTTTTTTCTAAAA | 207304 |
rs48323306 | snp | A/G | 0.231111 | 0.249285 | synonymous-codon | Hectd1 | Mm_Celera | 12:51798711 | CTCGAGCTTTATCCA[A/G]TGGTGTTTTCCCATC | 207304 |
rs48330617 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51757500 | TCAAGAGTAGGAGAG[C/T]CGGGCAAAAGGACTG | 207304 |
rs48365879 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hectd1 | GRCm38.p3 | 12:51794638 | GTCATGGGAAAGAGC[A/G]CACAACACATCGGCC | 207304 |
rs48435494 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51801573 | AATTCCCAGCACCTA[C/T]CTACACAGTGGCTCA | 207304 |
rs48462565 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hectd1 | Mm_Celera | 12:51761244 | TTAGCCATCTACCAA[A/G]TAAGTTACCTATATG | 207304 |
rs48480507 | snp | A/G | 0.132653 | 0.220748 | synonymous-codon | Hectd1 | Mm_Celera | 12:51748736 | CGACTGACTTTCAGT[A/G]CAGTGCAAGTCTCTG | 207304 |
rs48487700 | snp | A/G | 0.391111 | 0.206368 | synonymous-codon | Hectd1 | GRCm38.p3 | 12:51797898 | GCAGCAACCTCTTCA[A/G]GTAGAGCGGTGCCAT | 207304 |
rs48563720 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51781955 | TCTGTCTTTTCTTAT[A/G]ACAGTGCAACTGAAC | 207304 |
rs48578911 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51794223 | AGCTCACCACCATCT[A/G]TACAGCTACAGTATA | 207304 |
rs48631859 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Hectd1 | Mm_Celera | 12:51783671 | GACAATGCTCAAATT[A/T]TCTTCCTTTGTCTTC | 207304 |
rs48643196 | snp | C/T | 0.5 | 0 | intron-variant | Hectd1 | Mm_Celera | 12:51823676 | GAACTCAGCTCTAGA[C/T]CATTTCAAAGGCACA | 207304 |
rs48660001 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Hectd1 | Mm_Celera | 12:51784137 | GTAACAAGCACGTGA[A/C]AAGGTGACAGCATGC | 207304 |
rs48691635 | snp | C/T | | | intron-variant | Hectd1, Gm5785 | GRCm38.p3 | 12:51828672 | GACCAAAGGACAGCG[C/T]TGCGTCCCACGCAAT | 207304 |
rs48712235 | snp | C/T | | | missense | Hectd1 | GRCm38.p3 | 12:51748497 | TCATCTTCAGAAAGA[C/T]TTTTATTGCCTAGAA | 207304 |
rs48712332 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hectd1 | Mm_Celera | 12:51770450 | GAAAGTTCAGTGTTA[C/T]GTTAGTTAGAGGCTG | 207304 |
rs48750281 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Hectd1 | Mm_Celera | 12:51765411 | ATAAAGAAAGACAAT[A/G]TAGAATAATTTTAAA | 207304 |
rs48792044 | snp | C/G/T | | | intron-variant | Hectd1 | GRCm38.p3 | 12:51817987 | GGCTGGCACTGGAGC[C/G/T]GCTCAGTGTGCAGCC | 207304 |
rs48815212 | snp | G/T | | | intron-variant, upstream-variant-2KB | Hectd1, Gm5785 | Mm_Celera | 12:51826564 | AGTGACTTATTGGAA[G/T]TCACAACTCAGATGA | 207304 |
rs48823674 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hectd1 | Mm_Celera | 12:51777439 | TGAAGCCACAACATA[C/T]ATAATGAACCTTTCA | 207304 |
rs48839519 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Hectd1 | Mm_Celera | 12:51803513 | GATTAAAGTCCTGCA[C/T]CACCACGCCTGCCTT | 207304 |
rs48863954 | snp | A/G | 0.32 | 0.24 | intron-variant | Hectd1 | Mm_Celera | 12:51745305 | AAATGTGGTTACTAC[A/G]TCACAGTTCTTTAGA | 207304 |
rs48887525 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51819478 | CCAGTAGAAAGTATT[C/T]TCCACGTGACCAATG | 207304 |
rs48891753 | snp | G/T | 0.260355 | 0.249785 | intron-variant | Hectd1 | Mm_Celera | 12:51760540 | CACAGTATCTTTATA[G/T]CAATAAAACATGTTA | 207304 |
rs49012426 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hectd1 | Mm_Celera | 12:51783449 | GGTGCAGCGAAGGGT[C/T]GTCAATCAGAACCAC | 207304 |
rs49039715 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hectd1 | Mm_Celera | 12:51747392 | CTTTGCTGAATACTG[C/T]AGACAAGTGTATTAC | 207304 |
rs49055696 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Hectd1 | Mm_Celera | 12:51795061 | TTTTTAGTTGGCTTA[C/T]TTCATATTAATACGT | 207304 |
rs49070146 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51787639 | CCCACTGCTCTTGCC[A/G]CAGCTCCAGGTGCAG | 207304 |
rs49078713 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Hectd1 | Mm_Celera | 12:51804562 | AGCGGGAGCTAACAT[A/T]GTGAGACCCTGTTTC | 207304 |
rs49089407 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hectd1 | Mm_Celera | 12:51769627 | CGATGTTTCTGGGAT[A/G]TCTCTAAAATTCTTC | 207304 |
rs49129597 | snp | A/C | 0.165289 | 0.235211 | intron-variant | Hectd1 | Mm_Celera | 12:51752614 | CTGAACAACCAACCA[A/C]CATTAAGGTAGTTAT | 207304 |
rs49145087 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hectd1 | Mm_Celera | 12:51823055 | GGATAGGATCCAAAG[C/T]CTGTGCATCATCACA | 207304 |
rs49146157 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Hectd1 | Mm_Celera | 12:51786477 | GCATGGTATGTACAA[A/T]AAAACAAATCCAACA | 207304 |
rs49155813 | snp | A/G | 0.375 | 0.216506 | intron-variant | Hectd1 | Mm_Celera | 12:51780338 | AGAGTATGGGGTATA[A/G]ATCCACAGAGTATGT | 207304 |
rs49173094 | snp | A/C | | | intron-variant | Hectd1 | Mm_Celera | 12:51784557 | GAACGAGAGTCAATT[A/C]ATTTCCATTTTTATT | 207304 |
rs49180645 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hectd1 | Mm_Celera | 12:51788162 | GCCAAGGCGAAACCT[C/T]TCCTCCACACGACAT | 207304 |
rs49205485 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Hectd1 | Mm_Celera | 12:51746846 | TTTAACATGTGTTTA[C/T]CTAATACTTTTTTGT | 207304 |
rs49260953 | snp | A/G | | | intron-variant | Hectd1 | GRCm38.p3 | 12:51806927 | TGTGTGTGTGTGTGT[A/G]TGTGTGTGCATATGT | 207304 |
rs49327190 | snp | G/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51756329 | AGAACCTGAAGCCTG[G/T]CCGCGGGCTTTCAGC | 207304 |
rs49369166 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hectd1 | Mm_Celera | 12:51782007 | ATTTTCAATCTTTTA[A/G]CTTGATTTTCAACTT | 207304 |
rs49405923 | snp | A/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51809489 | TCACTCTCTTTATTT[A/T]ACTGTGGGTTTGTAT | 207304 |
rs49420126 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon | Hectd1 | GRCm38.p3 | 12:51768587 | GTCACTGCTGCTTCG[A/G]CTTAGGTTCATGTTG | 207304 |
rs49421183 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Hectd1 | Mm_Celera | 12:51808697 | GTTAGAAGGACTACA[A/G]TCATGTTAGATGAAA | 207304 |
rs49435960 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hectd1 | Mm_Celera | 12:51809221 | TGCCTCTAGGTTATG[C/T]ATTCTAATCTCTTCC | 207304 |
rs49443384 | snp | A/G | | | intron-variant, missense | Hectd1, Gm5785 | Mm_Celera | 12:51828255 | TCCACCAAAAATCGG[A/G]GCTTCAGATACGGGT | 207304 |
rs49451844 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Hectd1 | Mm_Celera | 12:51805228 | CACCCTTTCCACTGC[A/G]GGTCTCAACTTTATA | 207304 |
rs49497839 | snp | C/G/T | 0.244898 | 0.249948 | intron-variant | Hectd1 | GRCm38.p3 | 12:51785150 | AAAAAGAAATTAAAA[C/G/T]GGCAAGTAGAACTGA | 207304 |
rs49507768 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hectd1 | Mm_Celera | 12:51810910 | TGCAAAGTAAGCTGC[C/T]ACCAATAGAATGAGA | 207304 |
rs49520745 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hectd1 | Mm_Celera | 12:51753050 | TTAAACGGCAGAAAA[C/T]TGTAACTCAGTAAGA | 207304 |
rs49524825 | snp | C/T | 0.32 | 0.24 | intron-variant | Hectd1 | GRCm38.p3 | 12:51749123 | CATCTTTTCAAATTT[C/T]GTCATCTGAAGATGC | 207304 |
rs49532099 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hectd1 | Mm_Celera | 12:51785802 | TTGTAGCCCTAAATA[C/T]ACTTACATTGTTTAG | 207304 |
rs49534545 | snp | A/C | | | intron-variant, upstream-variant-2KB | Hectd1, Gm5785 | Mm_Celera | 12:51826477 | GGCATTAATTATACC[A/C]AGCTTTAAGCCAATA | 207304 |
rs49545022 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Hectd1 | Mm_Celera | 12:51777052 | CCTTTAATCCTAGCG[C/G]TTGGGAGGCATAAGC | 207304 |
rs49545262 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon | Hectd1 | Mm_Celera | 12:51762445 | CCCAACAGGCCGGCT[C/T]CCTGCTCCAGAAGGG | 207304 |
rs49558416 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Hectd1 | Mm_Celera | 12:51781939 | AAAACTGTATCTGGT[A/G]TCTGTCTTTTCTTAT | 207304 |
rs49562972 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51756446 | GCAGCTTGGCTTTAC[A/G]AAGGGTTACAGTTAA | 207304 |
rs49636127 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51808426 | CTGCGGTTTCCACAT[A/G]TGTGTGCCCCCCCCC | 207304 |
rs49638168 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51756376 | CTAACTCTGCTCCCT[C/T]CCTCCTTCTGAAATG | 207304 |
rs49673233 | snp | A/T | | | downstream-variant-500B | Hectd1 | Mm_Celera | 12:51743404 | AACTCTTGTGAACTC[A/T]TGGGGACTGAAGCAG | 207304 |
rs49700969 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Hectd1 | Mm_Celera | 12:51809209 | ACATATCATTTTTGC[C/T]TCTAGGTTATGCATT | 207304 |
rs49712144 | snp | A/G | 0.132653 | 0.220748 | synonymous-codon | Hectd1 | Mm_Celera | 12:51748757 | CAAGTCTCTGTCGCC[A/G]CGGGACTCATAGATT | 207304 |
rs49731060 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Hectd1 | Mm_Celera | 12:51775001 | GTGTCTGTTTGGTTT[G/T]GTTGCAGTGCTGGAG | 207304 |
rs49770471 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon | Hectd1 | Mm_Celera | 12:51764123 | ATCTAGTTCAGCTAA[A/G]AGAGTACTGGCACGG | 207304 |
rs49792671 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Hectd1 | Mm_Celera | 12:51747314 | CAGATGATACATTTT[A/T]CTGCACATACAGACT | 207304 |
rs49845433 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hectd1 | Mm_Celera | 12:51777521 | TTAAGTGCACATCTA[C/T]ACAAGCAGTAATCAA | 207304 |
rs49882636 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hectd1 | Mm_Celera | 12:51745118 | CTGGTGCGTCTCACT[C/T]ACACTTCAGTAAAAA | 207304 |
rs49884880 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Hectd1 | Mm_Celera | 12:51809127 | CTGACCTCACTATAA[C/G]TTTATGACATCAATG | 207304 |
rs49923015 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51757804 | GGGTGGGGCTGTCAG[C/T]TACAGAAAACAACTT | 207304 |
rs49946339 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51819864 | ACTGAGAAATGTACT[C/T]ACAGTGTATTTTACA | 207304 |
rs49949953 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51812653 | CAGGCCTCCCTGGGT[A/G]CCAGGAACACACATG | 207304 |
rs49963996 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51756399 | CTGAAATGGTAATAC[A/G]TATCCTGTTCCATAT | 207304 |
rs49973916 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hectd1 | Mm_Celera | 12:51803649 | TGAAAACTAAATGTA[C/T]ACAACAGCACTTTAC | 207304 |
rs50045874 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51757609 | ACACAAATCGCCACT[A/G]TCTGTGTGTGCATGT | 207304 |
rs50074700 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Hectd1 | Mm_Celera | 12:51808152 | GGAGTATATTCACAT[A/G]TGCATTTAAAATTAC | 207304 |
rs50075652 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Hectd1 | GRCm38.p3 | 12:51750476 | AAAACGACAAAAGAA[C/T]GATAAAGACAGGGTC | 207304 |
rs50091074 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Hectd1 | Mm_Celera | 12:51746030 | ATTTGACGACAATAC[A/T]TAGCAGTGTTGATTG | 207304 |
rs50114049 | snp | G/T | | | upstream-variant-2KB, downstream-variant-500B | Hectd1, Gm5785 | GRCm38.p3 | 12:51831219 | TCTGAGTTGAGGCCA[G/T]CCTGGACTACAGAGT | 207304 |
rs50187762 | snp | A/G | 0.32 | 0.24 | intron-variant | Hectd1 | Mm_Celera | 12:51790296 | AGCACTTCACAGAGT[A/G]CACGTTCTTATGCTA | 207304 |
rs50194916 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Hectd1 | Mm_Celera | 12:51795045 | AACAGTTTATACTTA[C/T]TTTTTAGTTGGCTTA | 207304 |
rs50205562 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hectd1 | Mm_Celera | 12:51823560 | AACTATTGTGCAAGA[C/T]GCACTGAGAGGAATA | 207304 |
rs50214007 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hectd1 | Mm_Celera | 12:51765960 | AGGTTTTAAGGTATA[C/T]TCTTAGCTTCCTATA | 207304 |
rs50224277 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Hectd1 | Mm_Celera | 12:51771669 | CAGTTTAAATTCCCT[C/G]CAGAGGCTGGTAGAC | 207304 |
rs50261437 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hectd1 | Mm_Celera | 12:51769612 | AGTATGCATTATATA[C/T]GATGTTTCTGGGATA | 207304 |
rs50262563 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hectd1 | Mm_Celera | 12:51768432 | ACCCTGACTTCATAG[C/T]TCCCAAGTGCTGCAT | 207304 |
rs50353917 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51756516 | TTTAAACAGTGTGGA[A/G]ACTTTTAATAGACCA | 207304 |
rs50386977 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Hectd1 | Mm_Celera | 12:51753479 | TGACAATAATCTAGG[A/T]AAGTTACAAAGAAAC | 207304 |
rs50391478 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51822501 | AACTCAGGACCTCTG[C/T]AAGAGCAGTCAGTGC | 207304 |
rs50404137 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Hectd1 | Mm_Celera | 12:51818030 | AAGGCCCGAGGTCTT[A/C]CCCTAGAACTGAAAG | 207304 |
rs50422460 | snp | C/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51808653 | ATAGATCTAGTGCTC[C/G]TAACCATGGAGCCAT | 207304 |
rs50450068 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Hectd1 | Mm_Celera | 12:51749027 | CTTCACAAAGGAAAA[C/T]GACACATTAATACAT | 207304 |
rs50498486 | snp | A/G | 0.32 | 0.24 | intron-variant | Hectd1 | Mm_Celera | 12:51768390 | TGCAAGCTAGTCTCA[A/G]GTCCTGAACTACTGT | 207304 |
rs50516376 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51787666 | GCAGCTCCCAGTGCC[C/T]ACATGGTGGTTCACA | 207304 |
rs50550812 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51756785 | AGGCCCAGTCTCTCC[C/T]CTCTCCCTGTTGCCT | 207304 |
rs50581996 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Hectd1 | Mm_Celera | 12:51803450 | TAGTACGTAGACTAG[C/G]CCAGCCTGGAATTCA | 207304 |
rs50714968 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hectd1 | Mm_Celera | 12:51776062 | GCCTACACCTGTAAG[C/T]AGCGATACCTTTATT | 207304 |
rs50725578 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hectd1 | Mm_Celera | 12:51795313 | AACTCCACACTCAAT[A/G]TAGCTATTTCTCAAA | 207304 |
rs50729288 | snp | C/T | 0.32 | 0.24 | intron-variant | Hectd1 | Mm_Celera | 12:51755144 | GCCTTCCCAGTGATA[C/T]GGTCTATGACGCTTC | 207304 |
rs50767247 | snp | A/G | 0.495868 | 0.0452663 | intron-variant | Hectd1 | Mm_Celera | 12:51808802 | TCATGCTGCCTCTGC[A/G]GAAGACTTACTGGCT | 207304 |
rs50773572 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Hectd1 | Mm_Celera | 12:51796697 | CCTAGTGTGGTGGCT[C/T]AGACCTATAGTTCTA | 207304 |
rs50821228 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hectd1 | Mm_Celera | 12:51783790 | GACTACAGGTGTGTG[C/T]TACACCCAGCGTTAT | 207304 |
rs50836228 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hectd1 | Mm_Celera | 12:51777876 | TCCACTAAGAGGTCT[A/G]GATCAGTGTGTCCTG | 207304 |
rs50849673 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Hectd1 | Mm_Celera | 12:51775020 | GCAGTGCTGGAGAAG[C/G]ACCCCCAGGATTTTA | 207304 |
rs50868072 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hectd1 | Mm_Celera | 12:51757976 | GTCGTAGTAATTCTG[C/T]TGTTTCTCATAGAAG | 207304 |
rs50868580 | snp | A/G | 0.132653 | 0.220748 | synonymous-codon | Hectd1 | Mm_Celera | 12:51759380 | CGTCACTTTCAGTGT[A/G]AGAGCCAAGCGAGGT | 207304 |
rs50878951 | snp | C/G | 0.32 | 0.24 | synonymous-codon | Hectd1 | Mm_Celera | 12:51768908 | GCCTAACTTCCTTTC[C/G]GCATTTTCACTTCCC | 207304 |
rs50879920 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hectd1 | GRCm38.p3 | 12:51749492 | AACTAGGGCTGCCAA[C/T]TGTCTAGCTGGGTAA | 207304 |
rs50881291 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Hectd1 | Mm_Celera | 12:51754627 | AGATCCAAGGCCACA[C/G]GCAGCATTTGTAATT | 207304 |
rs50952517 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hectd1 | Mm_Celera | 12:51805268 | GGAAATATAACTCAA[C/T]GGGTAAAGCACTCGC | 207304 |
rs51010742 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hectd1 | GRCm38.p3 | 12:51749436 | TATAAAAGTAGAGGC[C/T]AACCTGGGCAAATAT | 207304 |
rs51011111 | snp | A/C | | | intron-variant | Hectd1 | Mm_Celera | 12:51820360 | TCCCATGTGGTAGAT[A/C]AGAAACAACTCCAGA | 207304 |
rs51019557 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Hectd1 | Mm_Celera | 12:51801532 | TGGAAGTTAAGAGAA[A/C]TTGCTATGCTTGCCA | 207304 |
rs51030995 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51795396 | CTGTCCTTCATTACT[A/G]TCACTAGGAACACAA | 207304 |
rs51050928 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hectd1 | Mm_Celera | 12:51786386 | TGTAGTCCTGTGGTA[C/T]TATATATAGCACTTC | 207304 |
rs51066118 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Hectd1 | Mm_Celera | 12:51751770 | CCTTGTTTTCCTGCC[A/G]TGGCTTTACACAGAT | 207304 |
rs51095754 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Hectd1 | Mm_Celera | 12:51748355 | CAGAGAAACAGAAAC[C/T]TTTAGCTTTCCTCAT | 207304 |
rs51123349 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Hectd1 | Mm_Celera | 12:51818248 | ACAAAGAACACCTTA[C/T]GTCTTCCCTCTACTT | 207304 |
rs51161124 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Hectd1 | Mm_Celera | 12:51774266 | ATTATAAACTGAGAA[C/T]GGTCGTCCACTTCTT | 207304 |
rs51162769 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hectd1 | Mm_Celera | 12:51811667 | TGGGAAGTAAGGCTT[A/G]GTAGAGAAAGCTAGG | 207304 |
rs51177762 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51773493 | CCAAGGACACATACC[C/T]GTTAAAGAACAACTT | 207304 |
rs51187710 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Hectd1 | Mm_Celera | 12:51802161 | AACAGAAAAAGTTCT[C/G]ACCTCCTGTGTCAAT | 207304 |
rs51269878 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Hectd1 | Mm_Celera | 12:51758577 | TTTCTATCTCAAAAA[A/G]CTACTATTATCAGAT | 207304 |
rs51277280 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51758392 | ACCCATAATGAGATC[C/T]GAGGCCCTCTTCTGG | 207304 |
rs51289936 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Hectd1 | Mm_Celera | 12:51772498 | AGTCACTTTACTAAA[A/C]AGTTGTAGAAAGCTG | 207304 |
rs51318452 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Hectd1 | Mm_Celera | 12:51812005 | TTCCCTCCTAAACTG[A/G]CCCCAGAGCTGGCTC | 207304 |
rs51365214 | snp | C/G | 0.497778 | 0.0332592 | intron-variant | Hectd1 | Mm_Celera | 12:51808879 | GTTAAATTTTACTGG[C/G]TTGCATAAAACGGTG | 207304 |
rs51414099 | snp | A/C | | | intron-variant | Hectd1 | Mm_Celera | 12:51819580 | GTTCAAGCCTGTAAT[A/C]CCTGCTCTGGGAGGC | 207304 |
rs51420165 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hectd1 | Mm_Celera | 12:51796872 | AGGGAAAAACACCTA[A/G]CCATGGAAAAAAGAA | 207304 |
rs51428025 | snp | G/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51782307 | TGTGATGTGTTTAAA[G/T]GAAGCCAGAACATTC | 207304 |
rs51443048 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51812483 | AAAGATGGGGGAAGA[A/G]AGAAAAGAACAACAA | 207304 |
rs51499424 | snp | C/T | 0.132653 | 0.220748 | synonymous-codon | Hectd1 | Mm_Celera | 12:51750387 | GTCAGTCCTCTGAAA[C/T]TCAGCCGCCACAAGA | 207304 |
rs51576941 | snp | C/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51796166 | AAAAATTACTGAGTA[C/G]AGTAGTTTTTGATAA | 207304 |
rs51588521 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hectd1 | Mm_Celera | 12:51772164 | TCATTTTAATGTGCC[A/G]TCATTATCAGTTCTT | 207304 |
rs51591834 | snp | A/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51797588 | GGTGCACAACTTTTA[A/T]GGCCAGTTCGTGGAG | 207304 |
rs51602403 | snp | C/T | | | intron-variant, upstream-variant-2KB | Hectd1, Gm5785 | Mm_Celera | 12:51827964 | AAAAAACTTTCCAAA[C/T]TGCAAAGTATTACTT | 207304 |
rs51636995 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hectd1 | Mm_Celera | 12:51761580 | TCCATACTATATGCA[A/G]CCTGTATTTCCTAGT | 207304 |
rs51673795 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hectd1 | Mm_Celera | 12:51768420 | TAGGTTCTTCAGACC[C/T]TGACTTCATAGTTCC | 207304 |
rs51675463 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hectd1 | Mm_Celera | 12:51777089 | GCACACTAGGTTCCA[C/T]GACAGCCATACTGAG | 207304 |
rs51679290 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon | Hectd1 | Mm_Celera | 12:51806421 | GTTCAACTACCACCA[A/G]GCGATTACAAAGTGC | 207304 |
rs51687777 | snp | A/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51784558 | AACGAGAGTCAATTC[A/T]TTTCCATTTTTATTG | 207304 |
rs51716516 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hectd1 | Mm_Celera | 12:51817997 | GGAGCGGCTCAGTGT[A/G]CAGCCCTTATCTAAA | 207304 |
rs51732086 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hectd1 | Mm_Celera | 12:51808891 | TGGCTTGCATAAAAC[A/G]GTGAGGAAATTTCTT | 207304 |
rs51769306 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51819742 | GCTCACTTGGTAGGG[C/T]GCCTGCCTGGAAGGA | 207304 |
rs51779643 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hectd1 | Mm_Celera | 12:51774906 | ATAATCATCTAGCCA[A/G]GAGTTATTCACTTGA | 207304 |
rs51817063 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51819764 | CTGGAAGGAACAAAG[C/T]CCTGAGTCCAATCTT | 207304 |
rs51828269 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Hectd1 | Mm_Celera | 12:51804492 | GAATAGCACCTTATA[A/G]ATAAAGTTTTCAGAA | 207304 |
rs51831199 | snp | C/T | | | intron-variant, upstream-variant-2KB | Hectd1, Gm5785 | Mm_Celera | 12:51826640 | AGGAAAATCATGGCC[C/T]AAGTGCCGAGCTAGT | 207304 |
rs51849593 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Hectd1 | Mm_Celera | 12:51745351 | TTTTGGACATGAAAA[A/C]GTCTGTACCTTAGAA | 207304 |
rs51850673 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51815771 | AGAGCTCTGGCAGTG[C/T]CCCCCACTTCCTAGC | 207304 |
rs51852631 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Hectd1 | Mm_Celera | 12:51805287 | TAAAGCACTCGCCTA[C/G]AACACTCATTATAAA | 207304 |
rs51865498 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Hectd1 | GRCm38.p3 | 12:51794627 | AGAGCGAGAAAGTCA[C/T]GGGAAAGAGCGCACA | 207304 |
rs51866592 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Hectd1 | Mm_Celera | 12:51795127 | TAAATGCTATTTTAT[G/T]TATCATTTAACCAGC | 207304 |
rs51872156 | snp | A/G | | | intron-variant | Hectd1 | GRCm38.p3 | 12:51794597 | ATCCTGGGGAGGAAA[A/G]AGGGGGAGCAGATGA | 207304 |
rs51918332 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hectd1 | Mm_Celera | 12:51777021 | TTCTCAGATGAGCCA[A/G]GAGTGGTGGGACACT | 207304 |
rs51919945 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hectd1 | Mm_Celera | 12:51795300 | TCGGCAATTTGAAAA[C/T]TCCACACTCAATGTA | 207304 |
rs51937675 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hectd1 | Mm_Celera | 12:51762317 | ATTTTCTGTAAAGTG[C/T]AGGACCTAAGCATCA | 207304 |
rs51999180 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Hectd1 | Mm_Celera | 12:51756988 | ACAGAGGCTAAGATA[C/T]CCTTTTACTTTTTTC | 207304 |
rs52025490 | snp | A/C | 0.277778 | 0.248452 | intron-variant | Hectd1 | Mm_Celera | 12:51801064 | TTCTAAAGTTTAAAC[A/C]ATTTTAAAGATCGAT | 207304 |
rs52027115 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51824845 | CAAGCCACATGTCCA[C/T]ACATACAAGCAAAAC | 207304 |
rs52039288 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hectd1 | Mm_Celera | 12:51788202 | AGGACCATTTTGTCC[C/T]ATATCAGCTTCCACA | 207304 |
rs52043018 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Hectd1 | Mm_Celera | 12:51777420 | TCTAATCGACTTATT[A/C]CTTTGAAGCCACAAC | 207304 |
rs52045860 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51758196 | CTAAAGGTATGAATG[C/T]TTTCTATAATAAGTG | 207304 |
rs52065421 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hectd1 | Mm_Celera | 12:51757839 | TGATGCTTAGGTCCT[A/G]CACTTTACAGAAAAT | 207304 |
rs52101685 | snp | A/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51822355 | AATAAATGAATAAAA[A/T]TTTTTTTTCTTTTTT | 207304 |
rs52122794 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51775357 | GGGGAGGAGGTATGG[A/G]ATGTGGAACAGTCTG | 207304 |
rs52179218 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51813092 | CCAGGCAGTGGCGCA[C/T]GCCTTTGATCCCACA | 207304 |
rs52183574 | snp | A/T | 0.391111 | 0.206368 | intron-variant | Hectd1 | Mm_Celera | 12:51768156 | AAAGGAAAAAAAAAG[A/T]CCATAATTACCTTTT | 207304 |
rs52202434 | snp | A/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51770718 | AAGCATATTATATAT[A/T]TTTTGTATTCGTATT | 207304 |
rs52219446 | snp | A/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51817867 | ATGCAGGCAAAACAC[A/T]CACACACACACACAC | 207304 |
rs52241627 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51820642 | AAAAAAAAAAAAAAA[A/G]AAAAAAAAGAAAAGA | 207304 |
rs52246103 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51795838 | ggattaaagtcatAT[A/G]tgtgtgtgtgtgtgt | 207304 |
rs52259699 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51820640 | AAAAAAAAAAAAAAA[A/G]AAAAAAAAAAGAAAA | 207304 |
rs52261983 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51776169 | TAAGGCAAGTTCTCT[C/T]TTTTTTTTTTTTTCT | 207304 |
rs52277507 | snp | A/T | | | intron-variant | Hectd1 | GRCm38.p3 | 12:51749266 | ACAGGGTTTCTCTGT[A/T]TAGCCCTGGCTGCCA | 207304 |
rs52282156 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51825653 | GAACTCTCAGATAAA[C/T]AAAAATAAACACATC | 207304 |
rs52309377 | snp | A/T | | | intron-variant | Hectd1 | GRCm38.p3 | 12:51749193 | AGAAATATATATATA[A/T]ATATATATATATATA | 207304 |
rs52311953 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Hectd1 | Mm_Celera | 12:51787543 | AGAAAGCCAGTAAAA[G/T]AAGAGAAATTCAGCA | 207304 |
rs52333403 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51820634 | AAAAAAAAAAAAAAA[A/G]AAAAAAAAAAAAAAA | 207304 |
rs52339375 | snp | A/C | | | intron-variant | Hectd1 | Mm_Celera | 12:51799059 | ATAAAAAATAAAAGC[A/C]AAAAAAAAAAAAAAA | 207304 |
rs52353895 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Hectd1 | Mm_Celera | 12:51746837 | ACAAAGTCCTTTAAC[A/G]TGTGTTTATCTAATA | 207304 |
rs52355512 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51820629 | AAAAAAAAAAAAAAA[A/G]AAAAAAAAAAAAAAA | 207304 |
rs52359734 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51773435 | TTTGGTGTGTGTGGT[A/G]TGTGTGTGTGGTGTG | 207304 |
rs52386962 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51807845 | AAACACAAAACACCT[A/G]ATGTATAGTTGATTT | 207304 |
rs52455626 | snp | C/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51754713 | CCATTCCTTTATGct[C/G]tctctctctctctct | 207304 |
rs52475618 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Hectd1 | Mm_Celera | 12:51804392 | TTGGATTATTCGTTG[C/T]TTCTGAAGTAGCAAA | 207304 |
rs52511778 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51799102 | AAATCATTAAAAAGA[C/T]TTCCCAGAATCAAAA | 207304 |
rs52519205 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51813194 | AGACAGCCAGGGCTA[C/T]ACAGAGAAACCTTGT | 207304 |
rs52520968 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51820623 | CCTAAAAAAAAAAAA[A/G]AAAAAAAAAAAAAAA | 207304 |
rs52529595 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51813088 | TAAGCCAGGCAGTGG[C/T]GCACGCCTTTGATCC | 207304 |
rs52559859 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Hectd1 | Mm_Celera | 12:51775245 | TGGGTGCAGTGATTC[A/G]GATGTGTAAATTATT | 207304 |
rs52597152 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Hectd1 | Mm_Celera | 12:51776147 | ATCTTTATGTTGAGG[G/T]TGCTGTTAAGGCAAG | 207304 |
rs52611749 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Hectd1 | Mm_Celera | 12:51786809 | CAACGACACTAAACT[C/T]AGGTGTGAGAAAGAC | 207304 |
rs52618227 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Hectd1 | Mm_Celera | 12:51751001 | ATCACCTTGAAGGTT[G/T]CTGAAAACACTGATA | 207304 |
rs52618909 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Hectd1 | Mm_Celera | 12:51779949 | TGGATAAGCTCTGTA[C/G]TCTAAGCTGGAGTCT | 207304 |
rs52625212 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Hectd1 | Mm_Celera | 12:51770764 | TTTTGAAGAACCAAC[A/G]TTTAACTTTCTCATT | 207304 |
rs52630481 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Hectd1 | Mm_Celera | 12:51784600 | TGAATTTAAGTGAAA[A/G]AAATAAAAACCATGG | 207304 |
rs52648740 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Hectd1 | Mm_Celera | 12:51800558 | CTGATCCTGCAAGTT[A/G]TCATCTGACCATGCA | 207304 |
rs108164619 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51812866 | GGGGAGCTGGAGAGA[C/T]GGCTCAGCAGTTAAG | 207304 |
rs108166400 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51812898 | GCACTGACTGCTCTT[C/T]CAGAGGTCCTGAGTT | 207304 |
rs108168932 | snp | C/T | | | intron-variant, upstream-variant-2KB | Hectd1, Gm5785 | Mm_Celera | 12:51826890 | ACGAAAGTACACACA[C/T]ACACACACACACACA | 207304 |
rs108267575 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51812875 | GAGAGACGGCTCAGC[A/G]GTTAAGAGCACTGAC | 207304 |
rs108295581 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51812874 | GGAGAGACGGCTCAG[C/T]AGTTAAGAGCACTGA | 207304 |
rs108497927 | snp | C/T | | | intron-variant, upstream-variant-2KB | Hectd1, Gm5785 | Mm_Celera | 12:51826884 | GCATACACGAAAGTA[C/T]ACACACACACACACA | 207304 |
rs108852506 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51814809 | GCACACCTTTAATCC[C/T]AGCACTCGAGAGCAG | 207304 |
rs211718134 | snp | A/T | | | intron-variant | Hectd1 | GRCm38.p3 | 12:51750547 | TTTCAAGACAGAGTT[A/T]CTCTCTGTAGTCCTG | 207304 |
rs211752651 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51812075 | CTCCTGTGATCAAGA[A/G]CCTGAGAAAAATCCT | 207304 |
rs211783711 | snp | A/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51820292 | ACATTCAGACAGACA[A/T]ATCTATAAAGACACA | 207304 |
rs211785966 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51759042 | ATTTCTAAAGGTTCT[C/T]CAGTTCTAAAGTTCA | 207304 |
rs211845912 | snp | G/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51769697 | AATTTTTTTCTTTTA[G/T]TCAAGACAGGGTTTC | 207304 |
rs211868951 | snp | C/T | | | intron-variant, upstream-variant-2KB | Hectd1, Gm5785 | Mm_Celera | 12:51828000 | AGTATGCTACATATG[C/T]AGCAGTCTACTTCCT | 207304 |
rs211970792 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51779318 | ACTTAGATGCAGACA[C/T]AATACTTATACACAG | 207304 |
rs211974552 | snp | C/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51816759 | AATTTGGTTTCTTAA[C/G]TATCCTTTAGTGCAG | 207304 |
rs212033707 | snp | A/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51786730 | CACACATGAAGGTAC[A/T]CATACACATAAAACA | 207304 |
rs212051611 | snp | C/T | | | intron-variant, upstream-variant-2KB | Hectd1, Gm5785 | Mm_Celera | 12:51827657 | ACACACACACACACA[C/T]GCATGTGTATATGTA | 207304 |
rs212097803 | snp | G/T | | | upstream-variant-2KB, utr-variant-3-prime | Hectd1, Gm5785 | Mm_Celera | 12:51830520 | ACAGAGAATAAGTTA[G/T]GGCTACCCTGTTCTG | 207304 |
rs212124800 | in-del | -/TCTCTCTCTCTCTCTCTCTC | | | intron-variant | Hectd1 | Mm_Celera | 12:51807879 | TTTACACAGAAACGT[-/TCTCTCTCTCTCTCTCTCTC]TCTCTCTCTCTCTCT | 207304 |
rs212243827 | snp | A/G/T | | | intron-variant | Hectd1 | GRCm38.p3 | 12:51788611 | CTAAATAATAATAAT[A/G/T]ATGATGATAATCACA | 207304 |
rs212355726 | in-del | -/CA | | | intron-variant | Hectd1 | GRCm38.p3 | 12:51750095 | ACACACCACCACCAC[-/CA]CACACACACACACAC | 207304 |
rs212444768 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51805155 | GAAGAGAAGGAAGTG[A/G]AGGAAAAGAAAAACT | 207304 |
rs212452904 | snp | C/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51789195 | GATACACCTATTTGT[C/G]ACTAAAAAATGTTCA | 207304 |
rs212458320 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51750759 | CCATCAGACACCACA[C/T]TGAGTACTGTGCAAA | 207304 |
rs212509519 | snp | G/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51804331 | CTTTTTCTGGTTGTT[G/T]TTTTTTGTTGTTGTT | 207304 |
rs212509651 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51812746 | ACCAGGTAAACGCCA[A/G]CAAGCCTGATGATCT | 207304 |
rs212511323 | in-del | -/A | | | intron-variant | Hectd1 | GRCm38.p3 | 12:51779432 | CCCCCCCCACCCCCC[-/A]CCCCCGCCCCAGTGT | 207304 |
rs212523077 | in-del | -/A | | | intron-variant | Hectd1 | Mm_Celera | 12:51823066 | AAGCCTGTGCATCAT[-/A]CACAAGACTCAGCAA | 207304 |
rs212614702 | snp | C/T | | | synonymous-codon | Hectd1 | Mm_Celera | 12:51746279 | AATCTTTACCTCATC[C/T]TCCCCACTTGGCTTG | 207304 |
rs212634157 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51808395 | GAGAATGACTGGGAA[A/G]ACTCCCTGTGTCAAC | 207304 |
rs212677433 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51745607 | AAAGAGCAAAGCACA[A/G]ACTCAGTTCCTAAGT | 207304 |
rs212694056 | snp | C/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51807235 | TTTTATATAAGCAGG[C/G]ACCTCTTTGAAACCT | 207304 |
rs212780581 | in-del | -/A | | | intron-variant | Hectd1 | Mm_Celera | 12:51800315 | ACTGAATCTATTTTT[-/A]AAAAAATGAATTAAA | 207304 |
rs212790440 | snp | A/G | | | synonymous-codon | Hectd1 | Mm_Celera | 12:51791347 | AGCATCACTCCAAAT[A/G]TATAAGCAGTCCCTT | 207304 |
rs212802738 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51761793 | CTTAAATTTCTATAT[A/G]ACAAACAGATGAAGC | 207304 |
rs212809705 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51813800 | CCTTTAGTCCCAGCG[A/G]TCAGAGGTAGAGAGA | 207304 |
rs212822818 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51774409 | gccagacagtggtgg[C/T]gcacgcctttaatcc | 207304 |
rs212832613 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51821722 | GGGGCTCTCAGAGAC[C/T]GAACAACCAACCAAA | 207304 |
rs212852341 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51773020 | AAACAAATTGTTTAC[A/G]AACCTGAATAAAAAA | 207304 |
rs212885869 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51756043 | TAGAATCAAGGATAC[A/G]AGAAAGGGGTTGCGG | 207304 |
rs212906483 | snp | C/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51817227 | ACCTACTAACTTAAA[C/G]AAAGAAAGAAAGAAA | 207304 |
rs212959225 | in-del | -/ATAA | | | intron-variant | Hectd1 | Mm_Celera | 12:51747591 | ACTCATATACATGAG[-/ATAA]ATAAATCCTTCAACA | 207304 |
rs212966050 | snp | C/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51809121 | ACAAAACTGACCTCA[C/G]TATAACTTTATGACA | 207304 |
rs213065889 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51752843 | TCCTTTTATTAACTG[C/T]GTGTGTGACAGTCAG | 207304 |
rs213066904 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51746021 | TAGGGGCAAATTTGA[C/T]GACAATACTTAGCAG | 207304 |
rs213071807 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51765077 | GCTCCCTACCATCTG[C/T]AATGGGATTCAACAC | 207304 |
rs213098436 | in-del | -/GATG | | | intron-variant | Hectd1 | Mm_Celera | 12:51787726 | CTAGGGCTTCTGAGT[-/GATG]GACGATGCCTTCTGA | 207304 |
rs213117631 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51814595 | TTACAAGTACCTCCA[C/T]CCTGTGGCCTGATGC | 207304 |
rs213153793 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51763029 | GAGTGTCCAAAGACA[A/G]CTATAGTGTACTTAC | 207304 |
rs213160142 | in-del | -/TTTTTTTTTTTTT | | | intron-variant | Hectd1 | GRCm38.p3 | 12:51826168 | GACTTTTTCTTTTTC[-/TTTTTTTTTTTTT]TTTTTTCTTTTTTTG | 207304 |
rs213197087 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51774879 | CCTTTTCCAAGTCAA[C/T]TGTGTTATGACATAA | 207304 |
rs213269941 | in-del | -/ACACACACACACACAC | | | intron-variant | Hectd1 | Mm_Celera | 12:51800594 | GGCATACACATGCAA[-/ACACACACACACACAC]ACACACACACACACA | 207304 |
rs213290076 | in-del | -/TGTGTGTG | | | intron-variant | Hectd1 | Mm_Celera | 12:51805635 | TTCTTACAAGGAGCA[-/TGTGTGTG]TGTGTGTGTGTGTGT | 207304 |
rs213338009 | snp | C/T | | | intron-variant | Hectd1 | GRCm38.p3 | 12:51745546 | TCTACATTACATATA[C/T]AGAAAGAAAAAAAAA | 207304 |
rs213387949 | in-del | -/A | | | intron-variant | Hectd1 | Mm_Celera | 12:51773719 | TCTTATCTTAATATT[-/A]AAAAAAAAAACAACA | 207304 |
rs213394848 | snp | A/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51752494 | TGGTGATATAGTTCC[A/T]TTCATATCAATTAAA | 207304 |
rs213399477 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51755271 | TGGTTGGAGTAAGAT[A/G]GCCCCCAAAGGTTCA | 207304 |
rs213406789 | in-del | -/A | | | intron-variant | Hectd1 | GRCm38.p3 | 12:51749668 | AGTTTAAAAGTGAGT[-/A]AAAAAATGTTTAAAG | 207304 |
rs213410975 | snp | A/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51823628 | AGGAGTCAGGCTTAA[A/T]GCATGACTACTCAAC | 207304 |
rs213412056 | snp | C/T | | | synonymous-codon | Hectd1 | Mm_Celera | 12:51744898 | AACCCTCACAAACCG[C/T]AGGAAGCCAGGACTG | 207304 |
rs213424821 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51814471 | TCCTTTGCTGTACAG[C/T]GGTTTACTTTTATAC | 207304 |
rs213425401 | snp | A/G | | | intron-variant | Hectd1 | GRCm38.p3 | 12:51816319 | GAGGAAGAAGAACAG[A/G]AGGAGGAAAAGAAAG | 207304 |
rs213468168 | snp | A/C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51806156 | TAGTGACGACCAGAA[A/C/T]TAAACCCCCCTCCCC | 207304 |
rs213483074 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51813624 | TTAGGCTGGTGGTGC[A/G]CCTCAGTGATGGAGT | 207304 |
rs213539362 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51821514 | CCATGACACTATTAA[C/T]GACATTCTGTTTTGC | 207304 |
rs213594199 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51820483 | GCCAGGCGTGGTGGC[A/G]CACGCCTTAAATCCC | 207304 |
rs213620440 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51781619 | AGTGTAAATGTGTTA[A/G]GCAGAACTCTGGCAG | 207304 |
rs213675882 | in-del | -/A | | | intron-variant, upstream-variant-2KB | Hectd1, Gm5785 | Mm_Celera | 12:51827937 | TGAAAAAACAAAAAC[-/A]AAAACAACAAAAAAA | 207304 |
rs213692554 | snp | C/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51783475 | ACCACAGCTTACCCA[C/G]CCTGCTACTAATGGC | 207304 |
rs213696458 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51753989 | AATCAGAGGCACAAG[A/G]GGACAAGGCACACCA | 207304 |
rs213770375 | snp | C/T | | | intron-variant, synonymous-codon | Hectd1, Gm5785 | Mm_Celera | 12:51828899 | AAGCCGCCGAGCGGC[C/T]GGGGTGCGGGTCTCC | 207304 |
rs213770645 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51798577 | TTCTAAGAACAATGC[A/G]TTCATATAATGTTAG | 207304 |
rs213805837 | in-del | -/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51799795 | TCCACATGCACTATA[-/T]TTTTTTCTAGTTCTC | 207304 |
rs213824586 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51765027 | TAATGACTGCTCTTC[C/T]AGAGACCCTGAATTC | 207304 |
rs213860436 | in-del | -/T | | | intron-variant | Hectd1 | GRCm38.p3 | 12:51812493 | AAGAGAGAAAAGAAC[-/T]AACAAAGGAATCCCT | 207304 |
rs213869339 | snp | C/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51783445 | AAATGGTGCAGCGAA[C/G]GGTCGTCAATCAGAA | 207304 |
rs213875728 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51824111 | AGCCAGGGCTATACA[A/G]AGAAACCCTGCCTCG | 207304 |
rs213938656 | snp | C/T | | | synonymous-codon | Hectd1 | Mm_Celera | 12:51791317 | ATTACTGCCATTAGA[C/T]AATTCCAAAGCTGCA | 207304 |
rs213963285 | in-del | -/AAC | | | intron-variant | Hectd1 | Mm_Celera | 12:51750792 | TTAATTACTTCTCAT[-/AAC]AACTGTGGAGATTTT | 207304 |
rs214046701 | in-del | -/GCGT | | | intron-variant | Hectd1 | Mm_Celera | 12:51798487 | AGTGCGCTCGCGCTC[-/GCGT]TCTCTCTCTCTCTCT | 207304 |
rs214088557 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51771583 | TTTGGATAAGGACTT[C/T]TGCTAAAATCTATAG | 207304 |
rs214103594 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51773522 | TTGTAGGAGTTGGCT[C/T]TCTGTCCACCATATA | 207304 |
rs214118790 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51784899 | CAATACACTGAGAAA[C/T]TCTGTCTTAGAAAAA | 207304 |
rs214121815 | in-del | -/AAC | | | intron-variant | Hectd1 | Mm_Celera | 12:51777705 | ATGTGGCAGTCAGAA[-/AAC]AACTGTGGAAATCAG | 207304 |
rs214199680 | in-del | -/GACAAAA | | | intron-variant | Hectd1 | Mm_Celera | 12:51764581 | AATCTCTAAGAAACT[-/GACAAAA]GACAAAGGATTCAAT | 207304 |
rs214243100 | in-del | -/A | | | intron-variant | Hectd1 | GRCm38.p3 | 12:51749445 | GAGGCCAACCTGGGC[-/A]AAATATTAATACCCT | 207304 |
rs214279520 | in-del | -/A | | | intron-variant | Hectd1 | Mm_Celera | 12:51796878 | AACACCTAACCATGG[-/A]AAAAAAGAACTCAAA | 207304 |
rs214299842 | in-del | -/ACAGAGG | | | intron-variant | Hectd1 | Mm_Celera | 12:51821441 | ACAAGAAATGCAGGA[-/ACAGAGG]AAGAGCAGCCGACCA | 207304 |
rs214325459 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51764179 | ACAAAGCCAACAACC[A/G]CATTGTGAATACAAT | 207304 |
rs214325637 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51747230 | GACTGCGCTCTTAAC[C/T]GCTGAGCCATCTCTC | 207304 |
rs214361823 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51809025 | TCAAATATCGTCTAT[C/T]GCTTCCTGACTACAA | 207304 |
rs214370526 | snp | A/C | | | intron-variant | Hectd1 | Mm_Celera | 12:51823348 | TTCTCAAAAGCCACC[A/C]TTATCTAATGACTAC | 207304 |
rs214384671 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51746532 | AGGGCTTGGAGAAGC[A/G]TTAAGGGCGAAAACC | 207304 |
rs214399702 | snp | A/G | | | synonymous-codon | Hectd1 | Mm_Celera | 12:51774656 | TTTAGCTTACTTTGC[A/G]TTTGTTCCAATCCAG | 207304 |
rs214420214 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51816010 | TAGACCAGGCTGGCC[C/T]TGAACTCAGAAATCC | 207304 |
rs214420557 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51808536 | CACATGGGTATCTGA[C/T]GCCCACGGAGGCCAG | 207304 |
rs214494914 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51792581 | CTCAAAGGGTAGGGA[C/T]CCAATGAATCTGTAA | 207304 |
rs214497498 | in-del | -/AA | | | intron-variant | Hectd1 | Mm_Celera | 12:51762691 | CAGGGCCCCCAATTG[-/AA]AAAAAAAAAAAAAAA | 207304 |
rs214503511 | in-del | -/TTTA | | | intron-variant | Hectd1 | Mm_Celera | 12:51753104 | GTATAAAATTATGAT[-/TTTA]TACCTACTTTGCCAG | 207304 |
rs214516439 | in-del | -/A | | | intron-variant | Hectd1 | Mm_Celera | 12:51745801 | GATACGCTCTATCAT[-/A]AAAGCAGCCAAGGTT | 207304 |
rs214522480 | snp | A/C | | | intron-variant | Hectd1 | GRCm38.p3 | 12:51749390 | GTCAAGCTCCTTTAG[A/C]AATATTTTAATGGCA | 207304 |
rs214549187 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51811081 | CAAAAAATTCACATT[C/T]CCAACAATCTCTTTG | 207304 |
rs214571116 | snp | G/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51801500 | AAAATTCCATAATAG[G/T]TGCTGGAGAGAGAGC | 207304 |
rs214612156 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51810383 | GACTAGCCTAATAGG[C/T]GGACTTTGGTTTTGA | 207304 |
rs214617307 | in-del | -/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51807858 | CTAATGTATAGTTGA[-/T]TTTTTTTTACACAGA | 207304 |
rs214735052 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51817648 | TTGTCTTTGCATTAC[C/T]TAGACGTGTATTAGG | 207304 |
rs214761468 | snp | A/C | | | intron-variant | Hectd1 | Mm_Celera | 12:51823983 | aaataaaataaaata[A/C]aatTTTAagccgggc | 207304 |
rs214765981 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51777924 | ATATAGAAGATCCAG[C/T]CAAGATGTGGGCAGC | 207304 |
rs214774324 | in-del | -/A | | | intron-variant, upstream-variant-2KB | Hectd1, Gm5785 | Mm_Celera | 12:51826757 | GATGGCTCAGCTGGT[-/A]AAAGTACTTACCACG | 207304 |
rs214831375 | in-del | -/A | | | intron-variant | Hectd1 | Mm_Celera | 12:51823956 | CTGTCTCGAAAAACC[-/A]AAAAAAAAATAAAAT | 207304 |
rs214862716 | in-del | -/GTGTGTGTGTGTGTAGTGTGTGTT | | | intron-variant | Hectd1 | Mm_Celera | 12:51773286 | CTGCTAGTGTGTGTG[-/GTGTGTGTGTGTGTAGTGTGTGTT]GTGTGTGTGGTATGT | 207304 |
rs214882802 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51792012 | GCGTTTGAAGTAAAA[A/G]TGTGAATCACCCTGA | 207304 |
rs214944686 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51800693 | AAGTGACTAAAGGTA[C/T]TTTTTTTAATCCAAA | 207304 |
rs214950665 | snp | A/C | | | intron-variant | Hectd1 | Mm_Celera | 12:51791468 | AGAATGATTCCATGA[A/C]ATATTTGTAATAATT | 207304 |
rs215005442 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51800153 | GGCTGTGAGCAGTAC[C/T]GGTGTTAGGAATTGA | 207304 |
rs215014712 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51801076 | AACAATTTTAAAGAT[C/T]GATAGATTGATATGA | 207304 |
rs215026457 | in-del | -/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51745579 | AAAGAAAGAAAGAAA[-/G]GAAAAGAAAAGAAAA | 207304 |
rs215047724 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51756665 | ATACTTAGTCACCCA[A/G]CAGGGAATGAAATCC | 207304 |
rs215104495 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51753570 | CATGCTGTACCAACA[A/G]AGCATATATATGTAT | 207304 |
rs215124424 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51767474 | CATTCCTCATCAAGA[A/G]TTCCAGGAAAAATGC | 207304 |
rs215160228 | snp | A/C | | | intron-variant | Hectd1 | Mm_Celera | 12:51826026 | ACTCGAAGATGCTAG[A/C]GATGTTAGAGAGGTT | 207304 |
rs215284713 | in-del | -/AAAAAT | | | intron-variant | Hectd1 | Mm_Celera | 12:51762703 | TTGAAAAAAAAAAAA[-/AAAAAT]AACTCTTTTAGTTAG | 207304 |
rs215318382 | snp | A/C | | | intron-variant | Hectd1 | Mm_Celera | 12:51817890 | ACACACACACACACA[A/C]TATCAACAACTCAAT | 207304 |
rs215366040 | snp | G/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51756089 | AGGTGTGTGTCGTAA[G/T]CATGCCTCATGGAGG | 207304 |
rs215380836 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51817604 | CTCTCAAATGCTGGG[A/G]TTACAGGGATGTGGA | 207304 |
rs215428583 | snp | G/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51765832 | CAATTAATGGTCTCT[G/T]AATTTAATAAAATAC | 207304 |
rs215435819 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51764932 | TGAACTATACAGTAA[A/G]ATTCTCTTTTAAAAT | 207304 |
rs215435915 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51747074 | CTCTTTTTTTTAATA[C/T]TTATTTATTTATTTA | 207304 |
rs215438219 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51825200 | GGTAAAGTCTAATTC[C/T]CTAGGAGCAATCCCC | 207304 |
rs215460436 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51808986 | ATCTAGTACTTGAAT[A/G]CTATCCACAAACAAA | 207304 |
rs215490078 | snp | A/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51765188 | AAAAAAAACAACGCA[A/T]GGACAATCAAGAAGG | 207304 |
rs215588043 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51757880 | TCTGCTACAATGCAA[A/G]CAGGAGTTTCTTACT | 207304 |
rs215631907 | in-del | -/GAGA | | | intron-variant | Hectd1 | Mm_Celera | 12:51753130 | TTTGCCAGAATAGGT[-/GAGA]TATAAAATCATTCCA | 207304 |
rs215633435 | snp | A/C | | | intron-variant | Hectd1 | Mm_Celera | 12:51818469 | AGCACCTGCCTCTAA[A/C]ACAAACACCTGCCAG | 207304 |
rs215633473 | snp | A/G | | | intron-variant, upstream-variant-2KB | Hectd1, Gm5785 | Mm_Celera | 12:51827966 | AAAACTTTCCAAACT[A/G]CAAAGTATTACTTCA | 207304 |
rs215648604 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51765991 | ATAAAAATTTCTGAT[A/G]TGTTACAATTCACTT | 207304 |
rs215659647 | in-del | -/TTG | | | intron-variant | Hectd1 | Mm_Celera | 12:51748039 | TTTCATCTTGTTTTT[-/TTG]TTGTTGTTTTTTGTT | 207304 |
rs215691486 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51825274 | CTTTGACCTCCACCC[A/G]CACCACTACATAAAG | 207304 |
rs215703711 | in-del | -/A | | | intron-variant | Hectd1 | Mm_Celera | 12:51814125 | CTGTCTTAGCCTCCC[-/A]AAATGTTGACATTAC | 207304 |
rs215716887 | snp | A/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51783913 | AGACTGAAAATTTTT[A/T]AATTTTATATTTATC | 207304 |
rs215724907 | in-del | -/A | | | intron-variant, upstream-variant-2KB | Hectd1, Gm5785 | Mm_Celera | 12:51826645 | ATCATGGCCTAAGTG[-/A]CCGAGCTAGTAGAGT | 207304 |
rs215739347 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51814667 | AGATCACAAAGTCAC[A/G]TTACAATGCCAAACA | 207304 |
rs215766801 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51786684 | AATTCCAGGAAACCC[C/T]ATGGCCACTTCTGAC | 207304 |
rs215799557 | snp | C/T | | | synonymous-codon | Hectd1 | Mm_Celera | 12:51748604 | TTCCCAAGTTAAAAT[C/T]CCATTAAACCAGGCT | 207304 |
rs215804817 | in-del | -/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51762150 | GAGAGAGAAATAAAA[-/G]AAAGACTACTACTTC | 207304 |
rs215828336 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51786092 | ATTTTGAATAGGTCA[A/G]CAATATTTGTTTGTA | 207304 |
rs215828869 | snp | A/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51810255 | CGGCAGTTAAGCTTG[A/T]CATGTTGGAGTTTGG | 207304 |
rs215886591 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51793460 | CTGAATCAAGGCCCT[A/G]ACATCTTTTTGTAAT | 207304 |
rs215892486 | in-del | -/TCT | | | intron-variant | Hectd1 | GRCm38.p3 | 12:51758024 | TTATTTCTCTCTCTC[-/TCT]TTTTTTTTTTTGATT | 207304 |
rs215930924 | in-del | -/TTT | | | intron-variant | Hectd1 | GRCm38.p3 | 12:51798220 | CCCCTTAAATTTAGA[-/TTT]TTTTTTTTTTCATTC | 207304 |
rs215997814 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51746388 | ATTACTATTCAGCAG[C/T]CGTCAGTGTTTATAA | 207304 |
rs216007147 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51788483 | AGTACTGGGATTAAA[A/G]GTGTATGACAGAACT | 207304 |
rs216021941 | snp | C/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51808457 | AAACACACACACACA[C/G]AAATCACTAACATTT | 207304 |
rs216049571 | in-del | -/TTTTGTG | | | intron-variant | Hectd1 | Mm_Celera | 12:51817511 | TTGCCACCCAATAGC[-/TTTTGTG]TTTTGTGTTTTTTGT | 207304 |
rs216061252 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51796684 | AAAGGCCAGAAACCC[C/T]AGTGTGGTGGCTTAG | 207304 |
rs216095636 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51777268 | CTGATGCCCTCTTCC[A/G]GTGTGTCTGAAGACA | 207304 |
rs216107632 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51815320 | TGTTTCTATTACTGC[C/T]ATCTTTTGCTAACAT | 207304 |
rs216108517 | in-del | -/C | | | intron-variant | Hectd1 | Mm_Celera | 12:51758006 | GAAGTAGTAGTCTTT[-/C]TTTTATTTCTCTCTC | 207304 |
rs216131649 | in-del | -/TT | | | intron-variant | Hectd1 | Mm_Celera | 12:51790771 | GCAACTCTCCAGACA[-/TT]TTTTTTTTCTTGGTA | 207304 |
rs216164068 | in-del | -/TGTGTG | | | intron-variant | Hectd1 | Mm_Celera | 12:51805636 | TTCTTACAAGGAGCA[-/TGTGTG]TGTGTGTGTGTGTGT | 207304 |
rs216167367 | snp | C/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51784843 | TAGATCTCTCAGGTC[C/G]AGGCCAGCCTGGCTT | 207304 |
rs216174743 | in-del | -/TA | | | intron-variant | Hectd1 | GRCm38.p3 | 12:51749421 | CTAAGGTTATTTAGT[-/TA]TAAAAGTAGAGGCCA | 207304 |
rs216236566 | snp | A/G | | | synonymous-codon | Hectd1 | Mm_Celera | 12:51750384 | CAAGTCAGTCCTCTG[A/G]AACTCAGCCGCCACA | 207304 |
rs216294183 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51758834 | TGGGGGTATAGCTTG[A/G]GTAGAGATTTAACTG | 207304 |
rs216313016 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51748161 | CCTTCCCAGCGCTGG[A/G]ATTTTGTCATATGTC | 207304 |
rs216316242 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51819397 | ATGTTTTTGATATAA[A/G]TAACAAATGTAAACT | 207304 |
rs216332196 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51768470 | GGCAGTCTGTCTGAC[A/G]TGGCTAGCCTCAGCT | 207304 |
rs216351491 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51778968 | TTGGCTCACAATTTT[C/T]ATCCCAATACTTGGG | 207304 |
rs216351517 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51767530 | GGATGGATTGTATAG[C/T]TAATAAACTTTGATC | 207304 |
rs216355503 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51826142 | AGCCCCCTCCATAGA[C/T]ACCCTTACTTTGACT | 207304 |
rs216373400 | snp | A/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51754507 | AATATGACTGTTGAA[A/T]TTTTTTCTTTGTTTG | 207304 |
rs216405942 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51779114 | ATCACTGAATAAGAA[C/T]AAAATAAAAGACACT | 207304 |
rs216408761 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51777991 | AGCAATCAGGCAGCA[C/T]GAGCACATTCGCTCT | 207304 |
rs216591536 | snp | A/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51763415 | TGTCATCAACATTTT[A/T]AAAAATATATACTAT | 207304 |
rs216614205 | snp | A/G | | | upstream-variant-2KB, utr-variant-3-prime | Hectd1, Gm5785 | Mm_Celera | 12:51831159 | ccaggcagtggtggc[A/G]cacacctttaatccc | 207304 |
rs216628965 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51801520 | GGAGAGAGAGCATGG[A/G]AGTTAAGAGAACTTG | 207304 |
rs216673555 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51754763 | tctctctctctctct[C/T]tctttctttctttct | 207304 |
rs216685688 | snp | C/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51809522 | AATCCTAATCCTAAC[C/G]CTAACCCACATACCA | 207304 |
rs216685762 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51801098 | TTGATATGAATATTT[C/T]ATTAACTACAGAAAT | 207304 |
rs216724798 | snp | C/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51780932 | CAACAACTGTGGTTG[C/G]CTCCATAACGTCTGC | 207304 |
rs216803796 | snp | A/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51809598 | GCTTGTTCAGTAACC[A/T]TAAAGCTCAGGCTGA | 207304 |
rs216816654 | snp | A/C | | | intron-variant | Hectd1 | Mm_Celera | 12:51804021 | AAAACATGTGAAATT[A/C]AATTTCATATCAAGC | 207304 |
rs216817550 | snp | C/T | | | intron-variant | Hectd1 | GRCm38.p3 | 12:51794714 | TACTTATGGATGGCG[C/T]GCCAAAGGAAGATGA | 207304 |
rs216871059 | in-del | -/CT | | | intron-variant | Hectd1 | Mm_Celera | 12:51809477 | GACTGATTTTGTTCA[-/CT]CTCTTTATTTTACTG | 207304 |
rs216873050 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51803440 | CCTGAGAGCTTAGTA[C/T]GTAGACTAGCCCAGC | 207304 |
rs216963804 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51778014 | TTCGCTCTGCTCCTG[A/G]CTATGATGTGACTTG | 207304 |
rs217012709 | snp | C/T | | | downstream-variant-500B | Hectd1 | Mm_Celera | 12:51743500 | gattttcgggtgtgt[C/T]gaggagtgggtctct | 207304 |
rs217032005 | snp | C/T | | | intron-variant, upstream-variant-2KB | Hectd1, Gm5785 | Mm_Celera | 12:51827184 | GTATTTACATAATCA[C/T]GATTATCATTACTAG | 207304 |
rs217042704 | in-del | -/GAAGAG | | | intron-variant | Hectd1 | GRCm38.p3 | 12:51816381 | AAGGAGGAGAAGGAA[-/GAAGAG]GAAGAGGAAGAGGAG | 207304 |
rs217101613 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51804126 | ACCAGGTAGGGTGAT[A/G]CAAGTCTGCCATGCC | 207304 |
rs217155571 | snp | G/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51775460 | ctccagtctcttgag[G/T]gttaggtgtgttttc | 207304 |
rs217171234 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51760227 | TCTTCTTTATATCAT[A/G]CAACTCTTAAAATAG | 207304 |
rs217208330 | in-del | -/AAAAAAAAAAAT | | | intron-variant | Hectd1 | Mm_Celera | 12:51762697 | CCCCAATTGAAAAAA[-/AAAAAAAAAAAT]AACTCTTTTAGTTAG | 207304 |
rs217213711 | snp | A/C | | | intron-variant | Hectd1 | Mm_Celera | 12:51770600 | GGGGCTCCGAGGAGC[A/C]CTGAGCCGCCTGCAC | 207304 |
rs217256425 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51812027 | AGCTGGCTCCAGCAT[A/G]TGTTTCAAAACCCCT | 207304 |
rs217258665 | snp | A/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51769783 | AGAAATCTGCCTGAC[A/T]CTGCCTCTCAAGTGT | 207304 |
rs217283772 | snp | A/C | | | intron-variant | Hectd1, Gm5785 | Mm_Celera | 12:51828763 | GCGGGGCTGCCCCAT[A/C]GTCCTCGGCCTGATC | 207304 |
rs217341962 | snp | A/G | | | intron-variant, upstream-variant-2KB | Hectd1, Gm5785 | Mm_Celera | 12:51828028 | CCTGGGCTTAATGCA[A/G]AAACCCTCAAGGCAA | 207304 |
rs217366605 | snp | A/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51822898 | TCCACATGACAGCTC[A/T]TAACTGTCTGTAACT | 207304 |
rs217422001 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51805088 | TTAAAATATTTATAT[A/G]TGAGTTGTGATGAAC | 207304 |
rs217463501 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51763090 | TAAAAGTTCCTTCAT[C/T]GGTCATCTTCAGCAA | 207304 |
rs217480236 | snp | C/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51789985 | AGTTTCACTATTTTT[C/G]TCACTAATTCCAATT | 207304 |
rs217493754 | in-del | -/ATC | | | intron-variant | Hectd1 | GRCm38.p3 | 12:51774560 | AAAGTTCCTTAAGTA[-/ATC]GAAGGATGTTCAGTG | 207304 |
rs217520630 | snp | A/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51798480 | ATTTCTGTAGTGCGC[A/T]CGCGCTCTCTCTCTC | 207304 |
rs217520811 | in-del | -/TTTG | | | intron-variant | Hectd1 | Mm_Celera | 12:51813454 | TGAATTTTATTTACT[-/TTTG]TTTGTTTGTTTGTTG | 207304 |
rs217521744 | snp | A/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51773059 | CAAATTTTAAAGATA[A/T]TTAGTTTATTTACAG | 207304 |
rs217613606 | in-del | -/CTTTTAAC | | | intron-variant | Hectd1 | GRCm38.p3 | 12:51817382 | TAGATATAAACAATT[-/CTTTTAAC]CTCCTACCTCAAAGA | 207304 |
rs217628236 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51805907 | GTCCTAAAACCAGAC[C/T]TCCTAATCTTCAAAT | 207304 |
rs217654958 | in-del | -/GTTTTTTTTTAAACAT | | | intron-variant | Hectd1 | Mm_Celera | 12:51781846 | TACTAGAGCTTGTTC[-/GTTTTTTTTTAAACAT]GTGAACACATGGTGT | 207304 |
rs217674687 | snp | A/C | | | synonymous-codon | Hectd1 | Mm_Celera | 12:51785890 | GTTCTCATCCTTCAG[A/C]AGTACAATTAGGTTT | 207304 |
rs217678558 | in-del | -/AAAG | | | intron-variant | Hectd1 | Mm_Celera | 12:51745560 | ACAGAAAGAAAAAAA[-/AAAG]AAAGAAAGAAAGAAA | 207304 |
rs217726713 | in-del | -/AGTC | | | intron-variant, upstream-variant-2KB | Hectd1, Gm5785 | Mm_Celera | 12:51826442 | TTTAGCAAGTAATAT[-/AGTC]AGTCTATTTCCACCT | 207304 |
rs217730358 | in-del | -/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51767245 | CCTATAATCAGATAA[-/T]TTTTTTAATCTTCTC | 207304 |
rs217745217 | snp | A/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51811446 | GGGCTAGATTTACAC[A/T]TAGTATTGAGTCACC | 207304 |
rs217755928 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51793158 | ATAAATCTTTGGGCC[A/G]GAGCAAGCAGGGACT | 207304 |
rs217809737 | in-del | -/AC | | | intron-variant, upstream-variant-2KB | Hectd1, Gm5785 | Mm_Celera | 12:51826883 | AGCATACACGAAAGT[-/AC]ACACACACACACACA | 207304 |
rs217893662 | in-del | -/AG | | | intron-variant | Hectd1 | Mm_Celera | 12:51753541 | AACCCCACGCTGTAT[-/AG]ACTGATGCAATCCAT | 207304 |
rs217895862 | snp | C/G | | | intron-variant | Hectd1 | GRCm38.p3 | 12:51749840 | ATTTAACTTAAAAAG[C/G]GATCTCCGAGGTTCA | 207304 |
rs217913043 | snp | A/C | | | intron-variant | Hectd1 | Mm_Celera | 12:51785097 | CACATGCAGGCAAAA[A/C]CCCATACACATAAAA | 207304 |
rs217932152 | snp | A/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51778227 | TGGATCAGGATATAG[A/T]AAACTCAGGTCCTTT | 207304 |
rs217954707 | snp | G/T | | | intron-variant | Hectd1 | GRCm38.p3 | 12:51749231 | TTTTTTTGTTTGTTT[G/T]TTTTTTTTTGTTTTT | 207304 |
rs217995251 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51792659 | AGAATGAGAATGGTG[A/G]AACCGTCCATCACTT | 207304 |
rs218058974 | snp | C/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51791898 | taggtacaacatata[C/G]aaagttctaattttc | 207304 |
rs218068539 | snp | A/G/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51787708 | CTGTATCGGCTATCT[A/G/T]TATCTAGGGCTTCTG | 207304 |
rs218213762 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51812421 | AGAGAAACCCAGTCT[C/T]GAAAAAAACCAAAAA | 207304 |
rs218221826 | snp | A/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51786911 | GCAAGAAGAGGATAC[A/T]ATGCAAACTGAAAGT | 207304 |
rs218224614 | in-del | -/C | | | intron-variant | Hectd1 | GRCm38.p3 | 12:51749819 | TCCTCTGGCCTCCCT[-/C]CCCCCATTTAACTTA | 207304 |
rs218233770 | in-del | -/C | | | intron-variant | Hectd1 | Mm_Celera | 12:51799058 | CATAAAAAATAAAAG[-/C]CAAAAAAAAAAAAAA | 207304 |
rs218243870 | snp | C/T | | | intron-variant | Hectd1 | GRCm38.p3 | 12:51770894 | CAATCTCTCTCTCTC[C/T]ACACACACACACACA | 207304 |
rs218304427 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51770031 | TTTGACCTGTTAAAT[A/G]TGACTATATGATTAT | 207304 |
rs218335077 | snp | A/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51782692 | GGTGCATTAGACACC[A/T]CCCTTCCTTACATTT | 207304 |
rs218335347 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51772222 | ATTTACACAGAATCC[A/G]AAGACAGAAGGAAGA | 207304 |
rs218346680 | snp | A/G | | | intron-variant | Hectd1 | GRCm38.p3 | 12:51750032 | GCATTAGGCATGCAT[A/G]TAGTACATACACACA | 207304 |
rs218362925 | snp | G/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51750935 | TCTTTTTTCTACCTG[G/T]GTTTTTGTGACCCAA | 207304 |
rs218371985 | snp | A/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51812001 | GGCTTTCCCTCCTAA[A/T]CTGGCCCCAGAGCTG | 207304 |
rs218391943 | snp | A/G | | | intron-variant | Hectd1 | GRCm38.p3 | 12:51749585 | ACACTCTTCCCACAC[A/G]TTGCTTTTCACATGC | 207304 |
rs218392091 | snp | A/C/T | | | intron-variant | Hectd1 | GRCm38.p3 | 12:51781920 | ATACAAATGCTCAGG[A/C/T]TCCAAAACTGTATCT | 207304 |
rs218410630 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51779609 | CACTGTTACTCTCTT[C/T]AGACACACCAGAAGA | 207304 |
rs218477425 | in-del | -/C | | | intron-variant | Hectd1 | Mm_Celera | 12:51811787 | AATCCCGACCACACA[-/C]CCCAAAGCCAAATGA | 207304 |
rs218501883 | snp | A/G | | | synonymous-codon | Hectd1 | Mm_Celera | 12:51748937 | ATCACTGTCCTGTGG[A/G]AATGGCGCTGTGAAC | 207304 |
rs218523079 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51818442 | TTCCAGGCTAGCCAC[A/G]GCTACACGGTGAGCA | 207304 |
rs218529456 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51810448 | AGCCACTGAGGAAGA[C/T]TGGCAACATCAACAT | 207304 |
rs218532358 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51745048 | TTGTGCCTTACTCTG[A/G]CATCTGTTGCCCAGG | 207304 |
rs218533431 | in-del | -/CTGGAC | | | intron-variant | Hectd1 | Mm_Celera | 12:51815090 | TGGTTATCAACTTAA[-/CTGGAC]CTAGAACCAACTAAG | 207304 |
rs218538336 | in-del | -/GA | | | intron-variant, upstream-variant-2KB | Hectd1, Gm5785 | Mm_Celera | 12:51826818 | CCCACATGCTAAAAT[-/GA]GAGATCAACTCCCAA | 207304 |
rs218587118 | snp | G/T | | | downstream-variant-500B | Hectd1 | Mm_Celera | 12:51743490 | ATTTTTGTAGGATTT[G/T]CGGGTGTGTTGAGGA | 207304 |
rs218588237 | in-del | -/AAAAAAAAAAAA | | | intron-variant | Hectd1 | Mm_Celera | 12:51758457 | ATAATAAATAAATCT[-/AAAAAAAAAAAA]AAAAAAAAAAAAAAG | 207304 |
rs218663803 | snp | A/C | | | intron-variant | Hectd1 | Mm_Celera | 12:51751677 | AACCCAGGCTCTGCT[A/C]TCAAGAGAAGAGGAG | 207304 |
rs218815360 | snp | A/C | | | intron-variant | Hectd1 | Mm_Celera | 12:51805380 | ATACCTAGAAACAAC[A/C]GGCAAAAGAATCTTT | 207304 |
rs218824251 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51812867 | GGGAGCTGGAGAGAC[A/G]GCTCAGCAGTTAAGA | 207304 |
rs218889382 | in-del | -/TTT | | | intron-variant | Hectd1 | GRCm38.p3 | 12:51794359 | AAACACACACACACA[-/TTT]CCTTTAAAACAAAAC | 207304 |
rs218903818 | in-del | -/C | | | intron-variant | Hectd1 | Mm_Celera | 12:51760061 | TAAAATTATCACTGA[-/C]CCTACACTCAAGGAA | 207304 |
rs218910428 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51820418 | TGCAGACACATGCAC[A/G]CATGAGCACACAAAT | 207304 |
rs218968964 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51746749 | GCTTCATTATTCACA[A/G]TTATACAAAGTGTAT | 207304 |
rs218986155 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51780867 | CAGCGGTCAGGAAGA[A/G]CTAGTAAAAGATGTG | 207304 |
rs218996684 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51773617 | CTGGCCTCCAATCTG[A/G]TTTTTTTTCATACTT | 207304 |
rs219019590 | in-del | -/A | | | intron-variant | Hectd1 | Mm_Celera | 12:51757762 | TCCAGCCTGTCATAC[-/A]CGGTTTACATTCTGC | 207304 |
rs219024677 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51746005 | CTGCTGGACCAGAAC[C/T]TAGGGGCAAATTTGA | 207304 |
rs219055452 | snp | C/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51788421 | TGGAACTCTTACGTC[C/G]AGGAGGCTGGCTTTA | 207304 |
rs219057664 | snp | A/C | | | intron-variant | Hectd1 | Mm_Celera | 12:51781423 | CCAATGAAAACATGT[A/C]ATTTGCACCCACTGG | 207304 |
rs219059755 | snp | A/C | | | intron-variant | Hectd1 | Mm_Celera | 12:51789484 | GCCTCCTGAGTGGCT[A/C]GGTTATAAGCCCATG | 207304 |
rs219110167 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51788794 | TACAATGAGTATCTT[A/G]TGATACAGATGGCCT | 207304 |
rs219113033 | in-del | -/AATAATAATTA | | | intron-variant | Hectd1 | GRCm38.p3 | 12:51788601 | ACACAGAGGCTAAAT[-/AATAATAATTA]AATAATAATAATGAT | 207304 |
rs219250981 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51751212 | AGAAGCTCCACTTTA[C/T]CCTAGGCATCCATCT | 207304 |
rs219276660 | in-del | -/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51788747 | CAATCAGGACACATC[-/T]ACAGGATAACTCAGA | 207304 |
rs219300968 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51782230 | GACAGCCCACAACCA[C/T]CTATGATCCTGGTTC | 207304 |
rs219306249 | snp | A/G | | | intron-variant | Hectd1 | GRCm38.p3 | 12:51750623 | GGTCTGCCTGCCTCT[A/G]TCTCTAAGGTCTGTG | 207304 |
rs219351202 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51759486 | AGAGCACAAAGAGCA[C/T]AGACAAGGCCATACA | 207304 |
rs219380838 | in-del | -/GCTGGCCTCAAACTTTCGCTATA | | | intron-variant | Hectd1 | Mm_Celera | 12:51788812 | ATACAGATGGCCTAG[-/GCTGGCCTCAAACTTTCGCTATA]GCTGGCCTAGAACTC | 207304 |
rs219496822 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51814798 | GCAGTGGTGGCGCAC[A/G]CCTTTAATCCCAGCA | 207304 |
rs219516962 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51812272 | AAGAGCTCCTGGGGT[A/G]CCAAGTGGTGGTAGT | 207304 |
rs219531518 | in-del | -/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51787612 | GCTGGAGCGACTCAG[-/T]CGGTCATAGCACCCA | 207304 |
rs219535083 | in-del | -/AT | | | intron-variant | Hectd1 | Mm_Celera | 12:51822195 | GATGTGCCCAGCCTC[-/AT]AGAGACTTCACATGA | 207304 |
rs219547566 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51822977 | AAGCACAGAAAGAAA[C/T]ACTATAAAAGACTGT | 207304 |
rs219547630 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51813881 | CCCAGCGGTACATAA[A/G]CACTCTGTTCCAGGA | 207304 |
rs219555550 | snp | C/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51781710 | TGGTGGCTCACGGCT[C/G]TATTCCCAGTATTAG | 207304 |
rs219595527 | snp | A/G | | | utr-variant-3-prime | Hectd1 | Mm_Celera | 12:51744518 | TCTTCTGCATTTCAA[A/G]ACTCAATTGAGATGA | 207304 |
rs219603401 | snp | A/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51822225 | AGAGGGTGAGAAGAT[A/T]CCCAAGGGGGCCCCC | 207304 |
rs219612181 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51745682 | GGGCCAGGGATCAGT[C/T]CTCAGCACCCTAACC | 207304 |
rs219644310 | in-del | -/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51748277 | TATTCAAACAGACAA[-/T]CAGCATTTGCTATAG | 207304 |
rs219645655 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51789388 | CTTCTTGAGATAGGA[C/T]CTCACTAAGTTACAC | 207304 |
rs219688091 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51781783 | AAGACCATAGAGTGA[A/G]AAACCTTGTCTCAAC | 207304 |
rs219688364 | in-del | -/GCTCA | | | intron-variant | Hectd1 | Mm_Celera | 12:51781913 | CTGCTATATACAAAT[-/GCTCA]GGTTCCAAAACTGTA | 207304 |
rs219750528 | snp | C/T | | | missense | Hectd1 | Mm_Celera | 12:51754407 | ATCCAGACTTTGTTC[C/T]ATGCTCACAAAAATC | 207304 |
rs219861276 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51818526 | TAAACTACAGTTAAC[A/G]CTAGTAGCAGTATCC | 207304 |
rs219972604 | snp | A/C | | | intron-variant | Hectd1 | Mm_Celera | 12:51815758 | CCATTTTCCCAACAG[A/C]GCTCTGGCAGTGCCC | 207304 |
rs220047973 | in-del | -/AA | | | intron-variant | Hectd1 | Mm_Celera | 12:51768146 | AAAAAAGAAAAAAGG[-/AA]AAAAAAAGTCCATAA | 207304 |
rs220049273 | snp | G/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51777583 | TCACCACCTTGGTTC[G/T]AAGAATCAGGCTTGG | 207304 |
rs220049663 | snp | A/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51786148 | GGGTTTTTTAAAAAA[A/T]ATTTTAATTATGTGG | 207304 |
rs220102018 | snp | A/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51825605 | CTCTTCTGGCCTCCG[A/T]GGGCACCTGCACACA | 207304 |
rs220108066 | snp | A/C | | | intron-variant | Hectd1 | Mm_Celera | 12:51785495 | TTACAGAGTAGCTTC[A/C]TGAGTAGGATTTCAG | 207304 |
rs220112791 | in-del | -/TT | | | intron-variant | Hectd1 | Mm_Celera | 12:51791203 | AAGCTAAGAAAATAC[-/TT]TTAATTAGAGTTTTA | 207304 |
rs220118963 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51783561 | TAGTGTGCCATTCCT[C/T]CCAAAGGTATTCTAA | 207304 |
rs220156746 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51760622 | AAGCACAATCAGGTA[C/T]GAGAAGTAAAGATTC | 207304 |
rs220179339 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51782990 | GCAGTGGATCTGATG[C/T]CCTCTTCTGGCCTCT | 207304 |
rs220190311 | snp | C/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51820810 | ATGGGTGGGACTGGT[C/G]AGAGGCTCATTTGGT | 207304 |
rs220210642 | snp | C/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51818187 | GACTCCTGAGCTCAT[C/G]CAAATCTGCCCTCAT | 207304 |
rs220237645 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51790670 | TTTCAAATCTACCAC[C/T]TTAATGAAATGTAAC | 207304 |
rs220255671 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51748195 | AGGCTAGGTTCTAGG[C/T]GGTGTTGGAGACCCA | 207304 |
rs220269938 | snp | G/T | | | intron-variant, missense | Hectd1, Gm5785 | Mm_Celera | 12:51829055 | GAACAAAGGGCCCGA[G/T]ACGCAGAGGCGACGG | 207304 |
rs220310213 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51747449 | AGGTAAACAGAGGCT[C/T]GAGAGAGCACTGTCC | 207304 |
rs220368163 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51755686 | CCTATAAATATTAGT[A/G]ATCACTCTTATGCAT | 207304 |
rs220400396 | in-del | -/A | | | intron-variant | Hectd1 | Mm_Celera | 12:51753412 | GACTCTGCGCTAAAT[-/A]AAAAAAAAAAAGGCT | 207304 |
rs220439372 | snp | A/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51788163 | CCAAGGCGAAACCTC[A/T]CCTCCACACGACATA | 207304 |
rs220534189 | snp | A/G | | | intron-variant | Hectd1 | GRCm38.p3 | 12:51795582 | TGTTACCCTTGAGGT[A/G]ACCAGACAGAAGGAT | 207304 |
rs220543483 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51759660 | TTTTTCCCTGAGCCT[C/T]TCAAGTACTGGAAAA | 207304 |
rs220550497 | in-del | -/CACACACACA | | | intron-variant | Hectd1 | Mm_Celera | 12:51818958 | CAAGATTCATTGTGG[-/CACACACACA]CACACACACACACAC | 207304 |
rs220569779 | snp | A/C | | | intron-variant | Hectd1 | Mm_Celera | 12:51819993 | GCTGTCTTGGACCTC[A/C]CTCTATAGACCAGGC | 207304 |
rs220577570 | in-del | -/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51762393 | GCAGAATGTAAACCG[-/T]GTATGACAGGCTGGA | 207304 |
rs220612580 | snp | C/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51809215 | CATTTTTGCCTCTAG[C/G]TTATGCATTCTAATC | 207304 |
rs220619434 | in-del | -/TGTGTGTGTGTGTGTGTGTGTGTGTG | | | intron-variant | Hectd1 | Mm_Celera | 12:51807007 | CACAGTGTGTGTTTC[-/TGTGTGTGTGTGTGTGTGTGTGTGTG]TGTGTGTGTGTGTGT | 207304 |
rs220627467 | in-del | -/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51821768 | GGACCTGGGGGAGGA[-/G]GGGCTATCCCAAAAG | 207304 |
rs220663971 | snp | A/C | | | intron-variant | Hectd1 | Mm_Celera | 12:51816696 | AAAACACTAAAAATA[A/C]AATTATATAAATGCA | 207304 |
rs220781734 | snp | A/C | | | intron-variant | Hectd1 | Mm_Celera | 12:51789563 | GATAAATAAAACTTT[A/C]AAGTTAATACTCTGG | 207304 |
rs220815173 | in-del | -/AAA | | | intron-variant | Hectd1 | Mm_Celera | 12:51768145 | AAAAAAGAAAAAAGG[-/AAA]AAAAAAAAAGTCCAT | 207304 |
rs220843625 | in-del | -/AAA | | | intron-variant | Hectd1 | Mm_Celera | 12:51765170 | TCTCTAAATATAATT[-/AAA]AAAAAAAAAACAACG | 207304 |
rs220844788 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51798098 | TAAATTACCTAGAAC[A/G]AGGTCCAATTTTGAA | 207304 |
rs220885613 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51801203 | ACTTTAGGCGTGGTG[A/G]CACACGCCTGTAACC | 207304 |
rs220914545 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51798952 | GCTCACAACCACCTG[C/T]CATTCTCACTGCAGG | 207304 |
rs220916330 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51789680 | CTTGGTCTCTAGCAT[C/T]CTAAGTTCAGCTAAG | 207304 |
rs220955883 | snp | G/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51800486 | CTAAAGGGGTGAAGG[G/T]GCTTGCCATCAAACC | 207304 |
rs220968283 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51798274 | GAAACAGAAAAGGGG[C/T]CAGTGTTTACAAGCA | 207304 |
rs220989047 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51795066 | AGTTGGCTTACTTCA[C/T]ATTAATACGTTGTTA | 207304 |
rs220999655 | in-del | -/A | | | intron-variant | Hectd1 | Mm_Celera | 12:51766790 | TCAAGGCTATGTGGT[-/A]AAAAAATAAAAAATA | 207304 |
rs221038197 | snp | C/T | | | synonymous-codon | Hectd1 | Mm_Celera | 12:51754273 | CAGAATCCGCAGAAG[C/T]TGAAGGACGTCCTCT | 207304 |
rs221048223 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51751266 | TGACTCCGGTCCCTG[A/G]AAGGTAAGGAAGTTC | 207304 |
rs221073452 | in-del | -/AAA | | | intron-variant | Hectd1 | Mm_Celera | 12:51767832 | ATTGAAGGAACCTTT[-/AAA]AAAAAAAAAATCAAG | 207304 |
rs221085184 | snp | A/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51764291 | ACAGTTAATAATGCC[A/T]CCTCTTTACCCTAAC | 207304 |
rs221130217 | in-del | -/A | | | intron-variant | Hectd1 | Mm_Celera | 12:51784037 | AGAAATTTGGGGTTC[-/A]ATTTTTGTTTTGGAC | 207304 |
rs221241557 | snp | A/C | | | intron-variant | Hectd1 | Mm_Celera | 12:51818131 | CTTAAAACTCAAAGA[A/C]GCTTTCCATAAGTTT | 207304 |
rs221247108 | snp | C/G | | | intron-variant, upstream-variant-2KB | Hectd1, Gm5785 | Mm_Celera | 12:51828129 | TCAAACACTATGAAA[C/G]AAGTTTTGGATCCCA | 207304 |
rs221251438 | snp | A/G | | | intron-variant | Hectd1 | GRCm38.p3 | 12:51816369 | GGAAGAAGAGGGAAA[A/G]GAGGAGAAGGAAGAA | 207304 |
rs221261601 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51788882 | ACTCAAAGGTACAGT[C/T]ATCATGCCTTACCAC | 207304 |
rs221299592 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51817815 | GTTCTCTCTGGCCAC[C/T]AAGAACACCAGACAC | 207304 |
rs221301480 | snp | A/G | | | intron-variant, upstream-variant-2KB | Hectd1, Gm5785 | Mm_Celera | 12:51826339 | GAGATTAAAAGCATG[A/G]GCCATATCCAGCTAA | 207304 |
rs221353960 | in-del | -/AAAAATAAATAAAAG | | | intron-variant | Hectd1 | GRCm38.p3 | 12:51820671 | AAAAGAAAAAGAGAA[-/AAAAATAAATAAAAG]AAAAATAAACAAAAG | 207304 |
rs221374146 | snp | G/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51753104 | GTATAAAATTATGAT[G/T]TTATACCTACTTTGC | 207304 |
rs221405218 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51814863 | AGGCCAGCCTGGTCT[A/G]CAGAGTGAGTTCCAG | 207304 |
rs221406531 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51785195 | TCTAGCCAGGCGTGG[C/T]GGCGCATGCCTTTAG | 207304 |
rs221447220 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51792703 | GCTAAGTCTGACAAC[C/T]GAAGAACCTCGGGAA | 207304 |
rs221454575 | snp | C/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51763376 | TTCCTGCTTCAGGCA[C/G]AAAGTGCTGGGACTA | 207304 |
rs221485381 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51823013 | CCCTCACTGGCAGTA[C/T]TCCAATGCCCTACTG | 207304 |
rs221519596 | snp | C/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51756900 | ACTAAATGTCTGAAA[C/G]TGTAAGTGAGCCCCC | 207304 |
rs221581577 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51756302 | CCATTTTGACATCAG[A/G]CACAGGAATACAGAA | 207304 |
rs221646068 | snp | A/C | | | intron-variant | Hectd1 | Mm_Celera | 12:51766277 | CGTTAGGTTTATGCT[A/C]ATGAAAGCTTTAGAG | 207304 |
rs221738545 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51818935 | tccaaagttgtactg[C/T]aacctctgcaAGATT | 207304 |
rs221775907 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51824361 | caaaGAAAAGACAGC[A/G]GCGCCAgcatggtgg | 207304 |
rs221786949 | snp | A/C | | | intron-variant | Hectd1 | Mm_Celera | 12:51825350 | GAAAAATTATTAACA[A/C]AGGTTAATAAGAGGG | 207304 |
rs221805849 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51796986 | GTTCGAGGCCAGTCC[A/G]GTGTATAGAGTGAGT | 207304 |
rs221862900 | snp | G/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51815511 | GGAGCTGTGTAGCTT[G/T]ACTTCTGGGTCCTCT | 207304 |
rs221896984 | in-del | -/TTTTTCT | | | intron-variant | Hectd1 | Mm_Celera | 12:51826162 | TACTTTGACTTTTTC[-/TTTTTCT]TTTTTCTTTTTTCTT | 207304 |
rs221951032 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51818844 | TGGTAAGATGGTTCA[A/G]CAAGCAAAGAAACTT | 207304 |
rs222008021 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51787650 | tgccgcagctccagg[C/T]gcagctcccagtgcc | 207304 |
rs222097744 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51787097 | GTGGGAGCCCTGGGT[C/T]AGAGGACTTCCTAAA | 207304 |
rs222103209 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51762340 | AAGCATCAGGGGAAA[C/T]TGTTTTCTGTAACTG | 207304 |
rs222132687 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51822385 | TAAAAGACTTATTTA[C/T]TTATATGAATAGACT | 207304 |
rs222153915 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51786319 | ACATGTAACCACTGA[A/G]CTATCTCTCCAGCCC | 207304 |
rs222191769 | in-del | -/AAA | | | intron-variant | Hectd1 | Mm_Celera | 12:51761637 | ACGAACCACTGGGGC[-/AAA]AAAAAAAAAACTCGT | 207304 |
rs222330757 | snp | A/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51809304 | TTTATGTTAGTAAGT[A/T]AACTGTTGCTCTCCT | 207304 |
rs222347237 | in-del | -/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51756381 | CTGCTCCCTCCCTCC[-/T]TTCTGAAATGGTAAT | 207304 |
rs222377583 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51766130 | CAGGAAGATCAAATA[C/T]GCAAGGCTAGGGTGA | 207304 |
rs222381317 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51795765 | CTGAAACTCAATCTA[C/T]AGAAAATATGCTGGT | 207304 |
rs222389417 | in-del | -/A | | | intron-variant | Hectd1 | Mm_Celera | 12:51811300 | AAAAATTACCTACTC[-/A]AAGACTCTGAAACAG | 207304 |
rs222420041 | in-del | -/AC | | | intron-variant | Hectd1 | Mm_Celera | 12:51800627 | CACACACCATGGCAT[-/AC]ACACACACACACACA | 207304 |
rs222425799 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51762198 | GAATTACTACGACTA[C/T]TATAAACCTCAGCTG | 207304 |
rs222432830 | snp | G/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51795146 | CATTTAACCAGCCTG[G/T]CTGCTGAAACAGCAT | 207304 |
rs222432918 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51804388 | TCCTTTGGATTATTC[A/G]TTGTTTCTGAAGTAG | 207304 |
rs222444724 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51765522 | AACAGAATAATGAGA[C/T]TAAATAAGAGAAGTT | 207304 |
rs222454886 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51804451 | TTCCAATGCTATAAA[A/G]TATGAATTATGTAAC | 207304 |
rs222486706 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51803630 | ATGTATTTAAAGCCC[C/T]TTTTGAAAACTAAAT | 207304 |
rs222502823 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51776354 | GCTGGGATTAAAGGC[A/G]TGTGCCACCACATGT | 207304 |
rs222514766 | in-del | -/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51787613 | CTGGAGCGACTCAGC[-/G]GGTCATAGCACCCAC | 207304 |
rs222561208 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51775470 | TTGAGGGTTAGGTGT[A/G]TTTTCTCTGTCTAAA | 207304 |
rs222589107 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51758262 | GGTAAAACATTTTTC[C/T]TATGACTAGAAAGGC | 207304 |
rs222653325 | in-del | -/GTGTGTGT | | | intron-variant | Hectd1 | Mm_Celera | 12:51746773 | GTGTATGTATGTGTG[-/GTGTGTGT]GTGTGTGTGTGTGTG | 207304 |
rs222658450 | in-del | -/A | | | intron-variant | Hectd1 | Mm_Celera | 12:51758458 | ATAATAAATAAATCT[-/A]AAAAAAAAAAAAAGA | 207304 |
rs222691573 | in-del | -/CGGAGCACGGCAGGATAAAA | | | intron-variant | Hectd1 | Mm_Celera | 12:51818338 | ACGCACTAATAACCT[-/CGGAGCACGGCAGGATAAAA]CTGCTGAAACTGCTG | 207304 |
rs222714280 | snp | A/G | | | synonymous-codon | Hectd1 | Mm_Celera | 12:51806530 | TGTCACCTCTAAGAC[A/G]TTGTCTGGAGCACTT | 207304 |
rs222745725 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51763176 | TAAGAATATACCTAG[A/G]TTTTTTTTCTTTCTT | 207304 |
rs222818027 | snp | A/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51776775 | ccaatgtggtggcat[A/T]tctgcaatatcaaca | 207304 |
rs222827072 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51821772 | CTGGGGGAGGAGGGG[C/T]TATCCCAAAAGCTGT | 207304 |
rs222866025 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51775399 | ACCACGAGGATGCCC[C/T]CACCCCCCATTCCCC | 207304 |
rs222889182 | snp | A/G | | | upstream-variant-2KB, intron-variant | Hectd1, Gm5785 | Mm_Celera | 12:51830593 | CCCACTGATCTCTTT[A/G]TTTATGGTTTTGCCC | 207304 |
rs222908267 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51793856 | CTCCTAAGAGAATTA[A/G]AGGCTAGATGGGATC | 207304 |
rs222921696 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51771418 | CCAGTCCCGTAATTT[C/T]TATTATAGCATTTTA | 207304 |
rs222956331 | snp | G/T | | | utr-variant-5-prime, synonymous-codon | Hectd1, Gm5785 | Mm_Celera | 12:51829481 | CCAGGTCCGCGCGGG[G/T]CCGTCGGCGGCAGCG | 207304 |
rs222965239 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51802919 | GAGCAAAGTGATAAA[A/G]AACGTGCCCCATGGG | 207304 |
rs222993371 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51765310 | AGCCTGACAACATGA[A/G]TTCCATTCCCAGAGC | 207304 |
rs223005812 | in-del | -/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51761820 | AGCGTTGGTTGTTAA[-/G]AAATCAAATGACATA | 207304 |
rs223021920 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51824384 | CATGGTGGCACATGC[C/T]TGAGAGGTGGAGGCA | 207304 |
rs223032094 | snp | C/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51801671 | CACATACATACATCA[C/G]GCAAACACCCACACA | 207304 |
rs223045700 | snp | A/G | | | intron-variant | Hectd1, Gm5785 | Mm_Celera | 12:51828412 | ATGAAATCTACCTAT[A/G]CGGAAGTAAATACTG | 207304 |
rs223057709 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51776318 | CGAACTCAGAAATCT[A/G]CCTGCCTCTGCCTCC | 207304 |
rs223061232 | snp | C/T | | | intron-variant | Hectd1 | GRCm38.p3 | 12:51817389 | AAACAATTCTTTTAA[C/T]CTCCTACCTCAAAGA | 207304 |
rs223115637 | in-del | -/AA | | | intron-variant | Hectd1 | Mm_Celera | 12:51765171 | TCTCTAAATATAATT[-/AA]AAAAAAAACAACGCA | 207304 |
rs223168949 | in-del | -/AAGCCTA | | | intron-variant | Hectd1 | Mm_Celera | 12:51808719 | AGATGAAAGTCATAC[-/AAGCCTA]AAGCCTAAAGTAAGG | 207304 |
rs223198818 | in-del | -/A | | | intron-variant | Hectd1 | Mm_Celera | 12:51809568 | GAAGAGCTTGCTCAC[-/A]AAAAATATTTAAGAG | 207304 |
rs223299179 | in-del | -/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51812850 | TGAAAAAGTGAGCCA[-/G]GGGGAGCTGGAGAGA | 207304 |
rs223345772 | snp | G/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51800246 | TTTCAATTTCTCAAA[G/T]TATAGAGAGGAATCT | 207304 |
rs223359290 | in-del | -/T | | | intron-variant | Hectd1 | GRCm38.p3 | 12:51824938 | AATAACAAGATAACC[-/T]TGTGTGTGTGGAGGT | 207304 |
rs223372513 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51810028 | ACAGGGTACCTGAGG[A/G]ACACAAGAGGAAGAG | 207304 |
rs223382478 | snp | A/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51792398 | TGGGATAAGAAGGGG[A/G]AAGTGACTAGGATGC | 207304 |
rs223439446 | snp | C/G | | | intron-variant | Hectd1 | Mm_Celera | 12:51809432 | GAACTGCTGAATCAT[C/G]TCTCCAGCCCTTCTC | 207304 |
rs223439477 | in-del | -/GTGGA | | | intron-variant | Hectd1 | Mm_Celera | 12:51756510 | GGACTTTTAAACAGT[-/GTGGA]GTGGAAACTTTTAAT | 207304 |
rs223468028 | snp | C/T | | | intron-variant | Hectd1 | Mm_Celera | 12:51801295 | TCTCAAGCTCTAGGC[C/T]AGCCAGAGTTACGAA | 207304 |