SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3711677 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Ift122 | Mm_Celera | 6:115892764 | GGACGGGGCTACATG[G/T]CTACCAGTAGCCCAA | 81896 |
rs3712285 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ift122 | Mm_Celera | 6:115892833 | GCAGAGGGTTTAGGG[A/G]AAAGAACCTGCATTC | 81896 |
rs3721957 | snp | A/G | 0.5 | 0 | intron-variant | Ift122 | GRCm38.p3 | 6:115919848 | GGCTGTACTGCAGGC[A/G]GCCCCCGAGTACAGG | 81896 |
rs3722915 | snp | A/T | 0.5 | 0 | intron-variant | Ift122 | Mm_Celera | 6:115861698 | ACCACTACTACTACT[A/T]CTTCTTCTTCTCCTT | 81896 |
rs4137528 | snp | A/C | 0.5 | 0 | intron-variant | Ift122 | Mm_Celera | 6:115856084 | gcacctaattagaaa[A/C]aaaaaaaaaaaaaac | 81896 |
rs4138051 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Ift122 | Mm_Celera | 6:115901282 | TTGTGACTGACCACT[C/T]CGAATAGCACCCTGA | 81896 |
rs6204829 | snp | A/G | 0.433884 | 0.169371 | intron-variant | Ift122 | GRCm38.p3 | 6:115915535 | TTTTGTGAACCACCA[A/G]GCTCCATAGTGGGAC | 81896 |
rs6205405 | snp | A/C | 0.456747 | 0.140554 | intron-variant | Ift122 | Mm_Celera | 6:115915657 | GGTGCTTCAGGTTTT[A/C]TCTCTGCTGTGCCTT | 81896 |
rs6206408 | snp | C/T | 0.5 | 0 | intron-variant | Ift122 | Mm_Celera | 6:115915784 | GGCACATCTCGGCAG[C/T]GAGGCATCCCAGATG | 81896 |
rs6206441 | snp | A/G | 0.5 | 0 | intron-variant | Ift122 | Mm_Celera | 6:115915804 | CATCCCAGATGCTCC[A/G]ATGAGTGGCCTGCCT | 81896 |
rs6206524 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Ift122 | Mm_Celera | 6:115915849 | CTCGTGTAAGCCCTG[C/T]AGCCTCCCTGCTCCA | 81896 |
rs6274650 | snp | A/G | 0.5 | 0 | intron-variant | Ift122 | Mm_Celera | 6:115919211 | gggctacacagagaa[A/G]ccctgtctcagaaaa | 81896 |
rs6306141 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Ift122 | Mm_Celera | 6:115888355 | TCAGCACAGAGGCCT[C/G]CANGTGGCAGGTGCT | 81896 |
rs6306152 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ift122 | Mm_Celera | 6:115888358 | GCACAGAGGCCTNCA[C/T]GTGGCAGGTGCTCTG | 81896 |
rs6306784 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Ift122 | Mm_Celera | 6:115888524 | atggatactgggaat[C/G]aaacccaggtcttca | 81896 |
rs6307288 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Ift122 | Mm_Celera | 6:115888602 | TAAAGATTTTTGTAA[C/T]GAGAGTGTGTCACTT | 81896 |
rs6307844 | snp | C/T | 0.5 | 0 | intron-variant | Ift122 | Mm_Celera | 6:115888714 | GTCTCTTTTCCTCCG[C/T]TGACAGTTAGGATTA | 81896 |
rs6376941 | snp | C/T | 0.5 | 0 | intron-variant | Ift122 | Mm_Celera | 6:115863221 | TTCAAAGGCCACAGG[C/T]GCCCTCTGGATCTTG | 81896 |
rs6378569 | snp | A/G | 0.359862 | 0.224567 | intron-variant | Ift122 | GRCm38.p3 | 6:115863520 | TGTCCTCATTTCTCA[A/G]ATGCTGTGTTTTTTA | 81896 |
rs13478989 | snp | C/T | 0.4712 | 0.116493 | intron-variant | Ift122 | Mm_Celera | 6:115900841 | CCCTGCTATAGAGCA[C/T]GCGGCCAGATAAAGG | 81896 |
rs29825817 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ift122 | GRCm38.p3 | 6:115901164 | TGGAAGGAGGGGCCT[A/G]GCCTAGAAGGGTGCT | 81896 |
rs29829482 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Ift122 | GRCm38.p3 | 6:115917894 | CAACAAGCTGGGCCC[C/G]ACCAGGGTCCCCCGG | 81896 |
rs29832078 | snp | A/C | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Ift122, Mbd4 | Mm_Celera | 6:115855392 | AGCAGTTGAAGGAAT[A/C]TGCTGCCAAGGATAA | 81896 |
rs29870780 | snp | C/T | 0.484429 | 0.0868505 | intron-variant | Ift122 | GRCm38.p3 | 6:115907133 | CCCGTGGGCTGCTCC[C/T]GGTCCCTCCCCTTCA | 81896 |
rs29883157 | snp | A/C | 0.5 | 0 | intron-variant | Ift122 | GRCm38.p3 | 6:115905122 | AAGGAGTGCTACTCG[A/C]TGGCTTGCTCCTTAG | 81896 |
rs29919439 | snp | A/G | 0.432133 | 0.171253 | intron-variant | Ift122 | GRCm38.p3 | 6:115904641 | TGATGTACTTGATAG[A/G]AAACAAGCAAACGGC | 81896 |
rs29926803 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ift122 | GRCm38.p3 | 6:115895930 | TTTCAAGTTTAAAGG[C/T]AGCCTAGGATACATC | 81896 |
rs29964914 | snp | A/G | 0.5 | 0 | intron-variant | Ift122 | GRCm38.p3 | 6:115894646 | GCCATGACCAAAAAA[A/G]CAAGCTGGGGAGGAG | 81896 |
rs29967151 | snp | C/T | 0.5 | 0 | intron-variant | Ift122 | GRCm38.p3 | 6:115896482 | CCCACAGCAGTCTCC[C/T]CTGTCTTTGCCTCAG | 81896 |
rs30016529 | snp | C/T | 0.375 | 0.216506 | synonymous-codon | Ift122 | Mm_Celera | 6:115899529 | GTTCAAAGAAGCATA[C/T]CAGATCGCTTGCTTG | 81896 |
rs30021543 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ift122 | Mm_Celera | 6:115865793 | CTGGCCTCGAACTCA[A/G]AAATCCGCCTGCCTC | 81896 |
rs30021775 | snp | A/G | 0.5 | 0 | intron-variant | Ift122 | GRCm38.p3 | 6:115919010 | TGTGGCAGGCAGACT[A/G]TGGTCTGGCAAAGGC | 81896 |
rs30063276 | snp | C/T | 0.429688 | 0.173817 | intron-variant | Ift122 | GRCm38.p3 | 6:115901740 | CTTGCCTAATCCTGC[C/T]GTCTGCCACTGCTCA | 81896 |
rs30065415 | snp | C/G | 0.5 | 0 | intron-variant | Ift122 | Mm_Celera | 6:115861319 | AAAGATATTTTTGAT[C/G]AACAGTTATTTGAAT | 81896 |
rs30066043 | snp | A/G | 0.5 | 0 | intron-variant | Ift122 | GRCm38.p3 | 6:115903853 | GTCCAGTGGGGGAGA[A/G]AGGAGAGGCAGGAGA | 81896 |
rs30068652 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ift122 | Mm_Celera | 6:115885888 | ACCTACAACAGCCCA[C/T]CTCACCTACAACAGC | 81896 |
rs30069385 | snp | C/T | 0.5 | 0 | intron-variant | Ift122 | Mm_Celera | 6:115861258 | CCCACTCAGCCATCT[C/T]GCAAGCCCTAGTGCT | 81896 |
rs30113564 | snp | C/G | 0.432133 | 0.171253 | intron-variant | Ift122 | GRCm38.p3 | 6:115895127 | ACAGGAGAACAGGTA[C/G]AGTGGGCACTGACTG | 81896 |
rs30117352 | snp | A/T | 0.5 | 0 | intron-variant | Ift122 | GRCm38.p3 | 6:115910652 | TAGGTGCCCCTCAGG[A/T]GCTGTGTTGACCTTA | 81896 |
rs30127945 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Ift122 | GRCm38.p3 | 6:115879904 | CATTGTCTGTACCCG[C/T]TGTCACACCCTTTAT | 81896 |
rs30157042 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Ift122 | GRCm38.p3 | 6:115864673 | TGTCACTGAGTTACA[A/C]CTCTAGTCCTCAGGT | 81896 |
rs30164507 | snp | A/G | 0.486111 | 0.0821678 | intron-variant | Ift122 | GRCm38.p3 | 6:115916813 | CTGGCCAGGAGCTCT[A/G]CCCAGCTAAGGCCTA | 81896 |
rs30168576 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Ift122 | GRCm38.p3 | 6:115904217 | TGTGCTTAAGGAACT[A/G]TCTCTGAGGACAAGC | 81896 |
rs30214498 | snp | A/G | 0.5 | 0 | intron-variant | Ift122 | GRCm38.p3 | 6:115905223 | GACCTCCCCACATCA[A/G]TCAGAGAGCATGCCA | 81896 |
rs30215614 | snp | A/G | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Ift122, Rho | GRCm38.p3 | 6:115925592 | TGGCTTTCTCTAATG[A/G]CTGTGGTTCTGAGAG | 81896 |
rs30219690 | snp | A/G | 0.49827 | 0.0293608 | intron-variant | Ift122 | GRCm38.p3 | 6:115909755 | GTGGCAGCAAAGGAA[A/G]GCACAAGGGACCAAG | 81896 |
rs30228500 | snp | A/G | 0.401235 | 0.199068 | intron-variant | Ift122 | GRCm38.p3 | 6:115904809 | TGTTAGGAACTCTGC[A/G]TCACACGTTATGAAG | 81896 |
rs30265385 | snp | C/T | 0.5 | 0 | intron-variant | Ift122 | Mm_Celera | 6:115897816 | CCCGAGCAGCCAAGA[C/T]TCCAGGCTTTGCCAC | 81896 |
rs30270136 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Ift122 | Mm_Celera | 6:115877812 | AAGCAACCCCCCCCC[A/C]AAAAAAAGAAAGAAA | 81896 |
rs30313212 | snp | A/G | 0.46281 | 0.131194 | intron-variant | Ift122 | GRCm38.p3 | 6:115902571 | TCCCTTATGAGCAGT[A/G]TCTGGCAAGGGGTTC | 81896 |
rs30318130 | snp | A/G | 0.432133 | 0.171253 | intron-variant | Ift122 | GRCm38.p3 | 6:115875522 | AGCTTTCCTCTCCAG[A/G]ATGAGCTTGAATAGA | 81896 |
rs30348927 | snp | G/T | 0.375 | 0.216506 | intron-variant | Ift122 | GRCm38.p3 | 6:115917407 | CTGTTTTTTTTTTTT[G/T]TTTTGTTGTTGTTGT | 81896 |
rs30355523 | snp | A/G | 0.5 | 0 | intron-variant | Ift122 | GRCm38.p3 | 6:115862359 | GCCCACGCCCCTACC[A/G]TATCTGTTGGTGCCT | 81896 |
rs30361470 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ift122 | GRCm38.p3 | 6:115879891 | TTCCTACTAACTTCA[C/T]TGTCTGTACCCGTTG | 81896 |
rs30366882 | snp | A/G | 0.5 | 0 | intron-variant | Ift122 | Mm_Celera | 6:115874326 | GCATGACACACAGAC[A/G]TAGCTGACCCGCAGT | 81896 |
rs30414026 | snp | G/T | 0.415225 | 0.187619 | intron-variant | Ift122 | GRCm38.p3 | 6:115862238 | AGAGAGATTAAAAGG[G/T]GAAAAGGATATTCCT | 81896 |
rs30415304 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Ift122 | GRCm38.p3 | 6:115857278 | GACCTGCCTGTTTGC[A/C]CATCTTAGTCTCTGG | 81896 |
rs30418382 | snp | A/C | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Ift122, Rho | Mm_Celera | 6:115925961 | GTCGCCTCTTCTGCC[A/C]CTCCATTCTCCCTAT | 81896 |
rs30453788 | snp | C/T | 0.487535 | 0.077957 | intron-variant | Ift122 | GRCm38.p3 | 6:115903943 | CCCTAAGCTTTGGCA[C/T]GTTTGCCCTGTGAGC | 81896 |
rs30454830 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ift122 | GRCm38.p3 | 6:115901019 | GTGTGTATATTTCTT[A/G]TGGGTAGCATGATAT | 81896 |
rs30463269 | snp | A/G | 0.432133 | 0.171253 | intron-variant | Ift122 | GRCm38.p3 | 6:115898153 | TCCCTACAGTAAGAG[A/G]GGAAGTGTATGGTGT | 81896 |
rs30476098 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ift122 | GRCm38.p3 | 6:115875824 | TCTCTGCTGTAGCTG[C/T]CTTCGCTGCCAGCCC | 81896 |
rs30505859 | snp | C/G | 0.432133 | 0.171253 | intron-variant | Ift122 | GRCm38.p3 | 6:115892113 | CCTGTCTGGGAGGAA[C/G]AACAAGGGCCTGGGA | 81896 |
rs30508260 | snp | A/C/T | 0.444444 | 0.157135 | intron-variant | Ift122 | GRCm38.p3 | 6:115885660 | AGAAGAGAGAGAGAG[A/C/T]GAGGGCGAGAGGTCA | 81896 |
rs30509932 | snp | G/T | 0.5 | 0 | intron-variant | Ift122 | Mm_Celera | 6:115865681 | CTTTTTTTTTTTTGT[G/T]TTTTTTTTTTTGTTT | 81896 |
rs30514365 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ift122 | GRCm38.p3 | 6:115885869 | ACCTACAACAGCCCA[C/T]CTCACCTACAACAGC | 81896 |
rs30517068 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Ift122 | GRCm38.p3 | 6:115904085 | GGTCTTCATCCAGAT[C/T]TACAGAACATCACTT | 81896 |
rs30548411 | snp | C/T | 0.415225 | 0.187619 | intron-variant | Ift122 | GRCm38.p3 | 6:115888712 | GAGTCTCTTTTCCTC[C/T]GTTGACAGTTAGGAT | 81896 |
rs30569634 | snp | A/G | 0.432133 | 0.171253 | intron-variant | Ift122 | GRCm38.p3 | 6:115909075 | CAAGTGGGTTTCTGC[A/G]TGCATTGACTGCACT | 81896 |
rs30599733 | snp | A/G | 0.415225 | 0.187619 | intron-variant | Ift122 | GRCm38.p3 | 6:115862978 | GATAGGAACCCATGA[A/G]CAATGCCTCCTTTGG | 81896 |
rs30604446 | snp | A/G | 0.42 | 0.183303 | intron-variant | Ift122 | GRCm38.p3 | 6:115912938 | TGGCATTAAAAACCT[A/G]TGTGGCATTTTGGCA | 81896 |
rs30606358 | snp | A/C/T | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Ift122, Rho | GRCm38.p3 | 6:115924820 | TCAAGCTGAGAGAAT[A/C/T]GAGTGTGAGGCTCCC | 81896 |
rs30611519 | snp | A/G | 0.456747 | 0.140554 | intron-variant | Ift122 | GRCm38.p3 | 6:115904798 | CACCAGGTGTGTGTT[A/G]GGAACTCTGCGTCAC | 81896 |
rs30656657 | snp | A/G | 0.5 | 0 | intron-variant | Ift122 | GRCm38.p3 | 6:115863222 | TCAAAGGCCACAGGC[A/G]CCCTCTGGATCTTGT | 81896 |
rs30657994 | snp | A/G | 0.48 | 0.0979796 | upstream-variant-2KB, intron-variant | Ift122, Mbd4 | Mm_Celera | 6:115852262 | TCCACCAACACCTAC[A/G]TATATAGACAAACAC | 81896 |
rs30664360 | snp | G/T | 0.432133 | 0.171253 | intron-variant | Ift122 | GRCm38.p3 | 6:115893476 | CCCTTCACATGGGAA[G/T]TACCAATATTCCTCA | 81896 |
rs30666878 | snp | A/G | 0.455 | 0.143091 | intron-variant | Ift122 | GRCm38.p3 | 6:115907895 | GCACTTCCTGAACCC[A/G]TGGCCTTCTACCCAG | 81896 |
rs30668809 | snp | C/T | 0.5 | 0 | intron-variant | Ift122 | GRCm38.p3 | 6:115864810 | TAGGTAAGATGAAGA[C/T]AGTCACTCAGATAAC | 81896 |
rs30712079 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ift122 | GRCm38.p3 | 6:115908728 | TGCTTTTATCATGCC[C/T]GTCTCTGTTGCTAAC | 81896 |
rs30715565 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ift122 | Mm_Celera | 6:115885881 | CCATCTCACCTACAA[C/T]AGCCCACCTCACCTA | 81896 |
rs30715644 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ift122 | GRCm38.p3 | 6:115876269 | TGGGATCATAATAGT[A/G]TTTGGCATTTTGTGA | 81896 |
rs30719341 | snp | A/G | 0.492188 | 0.0620098 | intron-variant | Ift122 | Mm_Celera | 6:115874316 | CCTTAAAAGAGCATG[A/G]CACACAGACATAGCT | 81896 |
rs30759472 | snp | A/G | 0.49827 | 0.0293608 | intron-variant | Ift122 | GRCm38.p3 | 6:115899347 | CCAGGTGGCCAGGGC[A/G]AGGCTGCAAAGATGC | 81896 |
rs30759684 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Ift122 | GRCm38.p3 | 6:115911795 | GGTAGATTCCTCACC[C/T]TGCGAGGGCTGCTTT | 81896 |
rs30800627 | snp | A/G | 0.415225 | 0.187619 | intron-variant | Ift122 | GRCm38.p3 | 6:115898278 | GGGGGCAAAAGAACC[A/G]GAAATGTCAAAGATA | 81896 |
rs30805199 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Ift122 | GRCm38.p3 | 6:115915048 | CCTATCCATCTGTCT[G/T]TGTCGCCCTTCCAAG | 81896 |
rs30807037 | snp | A/G | 0.387812 | 0.208586 | utr-variant-5-prime, upstream-variant-2KB, intron-variant | Ift122, Mbd4 | GRCm38.p3 | 6:115853611 | GAAGTGGTTTGTGGA[A/G]AGAAGCCTGTTGCTG | 81896 |
rs30808639 | snp | C/T | 0.5 | 0 | intron-variant | Ift122 | GRCm38.p3 | 6:115865894 | AGTGTAATGAGAAGC[C/T]GCCGGCACTGAGAGT | 81896 |
rs30852515 | snp | A/G | 0.415225 | 0.187619 | intron-variant | Ift122 | GRCm38.p3 | 6:115890625 | TCCTGCACTACCATC[A/G]AGCTTGCTGTCCGGG | 81896 |
rs30857334 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ift122 | GRCm38.p3 | 6:115884536 | TAGTGAGCTTGACTT[C/T]AGGTCCTGGGCCCAG | 81896 |
rs30900638 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ift122 | GRCm38.p3 | 6:115857165 | TACCCTCTACGAGAG[C/T]AAAGAGTACTCTTAA | 81896 |
rs30906811 | snp | A/C/G | 0.493827 | 0.0552116 | intron-variant | Ift122 | GRCm38.p3 | 6:115898051 | TCCAGGAAGATGGGT[A/C/G]CTTTGCCCTTTTCAG | 81896 |
rs30943580 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ift122 | GRCm38.p3 | 6:115924591 | AGACTGGGGAGGTCC[C/T]CACATAGTGAGGACC | 81896 |
rs30945767 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Ift122 | GRCm38.p3 | 6:115881961 | TTCTTGCTTCATCGG[C/T]CCTTCCCTCATGTCC | 81896 |
rs31503030 | snp | A/T | 0.391111 | 0.206368 | upstream-variant-2KB, intron-variant | Ift122, Mbd4 | Mm_Celera | 6:115851758 | ATTTTACTCTTATTG[A/T]CAAATTGTGTGATAA | 81896 |
rs31503032 | snp | C/T | 0.124444 | 0.216185 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | Ift122, Mbd4 | Mm_Celera | 6:115852872 | TGCAAATACGTGCAT[C/T]ATTTTAGCCCGGACA | 81896 |
rs31503764 | snp | A/G | 0.444444 | 0.157135 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | Ift122, Mbd4 | Mm_Celera | 6:115852942 | CTGAGGGTCCCTTCC[A/G]GCCCAGGCTAACCTG | 81896 |
rs31503766 | snp | A/C | 0.336735 | 0.234472 | upstream-variant-2KB, utr-variant-5-prime | Ift122, Mbd4 | Mm_Celera | 6:115853306 | CGAATCCAAACACCG[A/C]CGTGAAAGTCAATCA | 81896 |
rs31503768 | snp | A/G | 0.444444 | 0.157135 | upstream-variant-2KB, utr-variant-5-prime | Ift122, Mbd4 | Mm_Celera | 6:115853360 | ACCGCTTCAGCTACA[A/G]ATGCCACAGCCAGGG | 81896 |
rs31503770 | snp | C/T | 0.32 | 0.24 | upstream-variant-2KB, utr-variant-5-prime | Ift122, Mbd4 | Mm_Celera | 6:115853377 | TGCCACAGCCAGGGT[C/T]CCGCCAATCAAACCC | 81896 |