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 |