SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs11105 | snp | A/G | 0.418491 | 0.184691 | utr-variant-3-prime | RAB40B | GRCh38.p7 | 17:82657414 | TTTCAATGTCAAAGC[A/G]CCAATTTATAAAACG | 10966 |
rs744991 | snp | C/G | 0.426201 | 0.177351 | | | GRCh38.p7 | 17:82655541 | TCCGTTCCCAGCTCG[C/G]TGATGGTGAAGGGTA | 10966 |
rs756072 | snp | A/G | 0.315758 | 0.241197 | intron-variant | RAB40B | GRCh38.p7 | 17:82664225 | GGTGCTGGGCAGATG[A/G]TGGTGGGGGGAGCTT | 10966 |
rs878878 | snp | C/T | 0.39214 | 0.205661 | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82666173 | GGTCAACCTCCTGGA[C/T]TCAAGTGATCCTCCC | 10966 |
rs1057423 | snp | A/T | 0 | 0 | | | GRCh38.p7 | 17:82655675 | CCCTTCTCTCTGCTG[A/T]GCCTCAGGTGGGGTG | 10966 |
rs1057424 | snp | A/T | 0 | 0 | | | GRCh38.p7 | 17:82655671 | TCTCTCTGCTGAGCC[A/T]CAGGTGGGGTGAGAA | 10966 |
rs1210094 | snp | C/T | 0 | 0 | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82666264 | agagcgaaattccat[C/T]tcaaaaaaaaaaaaT | 10966 |
rs1985249 | snp | C/T | 0.302435 | 0.244439 | | | GRCh38.p7 | 17:82655335 | GAATGCACGGGCCGC[C/T]CGGAGGCCTTGGCCC | 10966 |
rs2004642 | snp | A/C | 0.0733688 | 0.176922 | | | GRCh38.p7 | 17:82654702 | ctatagacgtgcacc[A/C]ccatgcccggctagt | 10966 |
rs2011631 | snp | A/C | 0.305186 | 0.243833 | | | GRCh38.p7 | 17:82655185 | AGCTACGAGAAAATA[A/C]ATATTTGTTATTTAA | 10966 |
rs2015031 | snp | A/G | 0.40595 | 0.195396 | intron-variant | RAB40B | GRCh38.p7 | 17:82664288 | GGGAGGGTGCTCCCC[A/G]GGGTGCTGTGCTGAT | 10966 |
rs2087049 | snp | A/C | 0.000714909 | 0.0188929 | intron-variant | RAB40B | GRCh38.p7 | 17:82664598 | TTCCAGCGTCCTGTT[A/C]GCTGCAGCCTCAGGC | 10966 |
rs2087050 | snp | A/C | | | intron-variant | RAB40B | GRCh38.p7 | 17:82664582 | GCTGCAGCCTCAGGC[A/C]TAAGCCGTCTCTAAC | 10966 |
rs2243606 | snp | G/T | 0.444444 | 0.157135 | upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82698740 | CGCTGACAGCGCGCA[G/T]CCCCGCCCGGCCCCG | 10966 |
rs2244094 | snp | A/G | 0.457853 | 0.138915 | intron-variant | RAB40B | GRCh38.p7 | 17:82689618 | TTTCAAATGCATAGA[A/G]ACATTTAATGTATTT | 10966 |
rs2244208 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | RAB40B | GRCh38.p7 | 17:82687988 | GAGGTGAGAGGACTG[C/T]TTGAGCCCAGGAGGT | 10966 |
rs2244304 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | RAB40B | GRCh38.p7 | 17:82687722 | CAAGCACAGGGTTCC[C/T]GGAAAACCAGCCCTC | 10966 |
rs2244312 | snp | C/G | 0.463343 | 0.130326 | intron-variant | RAB40B | GRCh38.p7 | 17:82687410 | AGTCAAACAAAATGC[C/G]AGTCCTATCACGAGT | 10966 |
rs2244323 | snp | A/G | 0.331642 | 0.236293 | intron-variant | RAB40B | GRCh38.p7 | 17:82687122 | ATGACGCTGGCCTCT[A/G]TGTCTCTCCAAAGTC | 10966 |
rs2244551 | snp | A/G | 0.497881 | 0.0324789 | intron-variant | RAB40B | GRCh38.p7 | 17:82685867 | GGAGTGCGATGGTGC[A/G]ATCTCAGCTCACTGC | 10966 |
rs2244565 | snp | G/T | 0.495174 | 0.0488838 | intron-variant | RAB40B | GRCh38.p7 | 17:82685518 | GCAGTGAAACGCTCA[G/T]ATGGGGCGGGCCCCA | 10966 |
rs2244566 | snp | A/C | 0.288646 | 0.246995 | intron-variant | RAB40B | GRCh38.p7 | 17:82685490 | GCCCGTAGGGTCCCA[A/C]GGAGACAGCCCAGCA | 10966 |
rs2245043 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | RAB40B | GRCh38.p7 | 17:82681832 | GCTGAGAGCTTTTGT[C/T]GTGAAAAGGTATTGG | 10966 |
rs2247740 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40B | GRCh38.p7 | 17:82680797 | TGATGCAACTGCCTC[A/G]GCCTTCCAAAGTGCT | 10966 |
rs2247767 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | RAB40B | GRCh38.p7 | 17:82680334 | CCCTCTTTGGCAGGT[C/G]GTGGCCAAGGTGGGT | 10966 |
rs2247910 | snp | C/T | 0.47726 | 0.104176 | intron-variant | RAB40B | GRCh38.p7 | 17:82679008 | gtagtcccagctacc[C/T]gggaggctgaggcag | 10966 |
rs2247989 | snp | C/T | 0.47726 | 0.104176 | intron-variant | RAB40B | GRCh38.p7 | 17:82678506 | AATATTTTAGGAATC[C/T]GTTTTAAGTCATCTA | 10966 |
rs2247996 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | RAB40B | GRCh38.p7 | 17:82678304 | CTGATTAACTTACCA[C/T]GTACTCTGTCCATCA | 10966 |
rs2248124 | snp | C/T | 0.47885 | 0.100637 | intron-variant | RAB40B | GRCh38.p7 | 17:82677678 | GGGCCAGCACCCAAG[C/T]GTTTGGGGTTTCCAG | 10966 |
rs2248257 | snp | C/T | 0.489837 | 0.0705577 | intron-variant | RAB40B | GRCh38.p7 | 17:82676115 | GTCCCACGAGGCGGT[C/T]GGTTCCCCATTCATA | 10966 |
rs2248357 | snp | A/G | 0.499958 | 0.00459246 | intron-variant | RAB40B | GRCh38.p7 | 17:82675718 | TGGGATGAGTGAAGC[A/G]TCCAAGAGCTCCCTC | 10966 |
rs2248358 | snp | C/T | 0.499831 | 0.00918375 | intron-variant | RAB40B | GRCh38.p7 | 17:82675712 | AGGGGCGAGGGAGCT[C/T]TTGGATGCTTCACTC | 10966 |
rs2248361 | snp | A/G | 0.247905 | 0.249991 | intron-variant | RAB40B | GRCh38.p7 | 17:82675650 | TCTGACGAGGGCTGC[A/G]TCCTGGTTCATGGAG | 10966 |
rs2248369 | snp | C/T | 0.487305 | 0.0786545 | intron-variant | RAB40B | GRCh38.p7 | 17:82675401 | CTGCTGTGAAGGAAG[C/T]CAGCGCTTGGTGGAG | 10966 |
rs2248370 | snp | C/T | 0.48679 | 0.0801892 | intron-variant | RAB40B | GRCh38.p7 | 17:82675395 | TGAAGGAAGCCAGCG[C/T]TTGGTGGAGACCACG | 10966 |
rs2248371 | snp | A/C | 0.48679 | 0.0801892 | intron-variant | RAB40B | GRCh38.p7 | 17:82675394 | ACGTGGTCTCCACCA[A/C]GCGCTGGCTTCCTTC | 10966 |
rs2248467 | snp | G/T | 0.389715 | 0.207315 | intron-variant | RAB40B | GRCh38.p7 | 17:82674897 | CGATGCCGTCAGGAT[G/T]ATCTCGTGTTGTTCT | 10966 |
rs2254045 | snp | A/T | 0.0391387 | 0.134304 | upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82698983 | GCGGGGTGGGGGCGA[A/T]CAGGGGGTGGGGCCG | 10966 |
rs2254271 | snp | A/G | 0.0387552 | 0.1337 | intron-variant | RAB40B | GRCh38.p7 | 17:82697068 | CACTCTGCACCCACC[A/G]GCTGCCAGAGACTCC | 10966 |
rs2254862 | snp | C/G | 0.390651 | 0.206682 | intron-variant | RAB40B | GRCh38.p7 | 17:82692389 | TGTTCCCTTTGCTCC[C/G]ATACGGTCAGCGAGG | 10966 |
rs2264373 | snp | C/T | 0.365646 | 0.221644 | upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82699547 | gcacacgcagacaca[C/T]agatgtgcagacatc | 10966 |
rs2264374 | snp | C/T | 0.486464 | 0.0811471 | intron-variant | RAB40B | GRCh38.p7 | 17:82682866 | aaaaacgaacccggc[C/T]gggcacggtgactca | 10966 |
rs2264576 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | RAB40B | GRCh38.p7 | 17:82682097 | gtgtgtgtATAGTAa[C/T]gtcatctggtaatcg | 10966 |
rs2279392 | snp | C/T | 0.409319 | 0.192659 | intron-variant | RAB40B | GRCh38.p7 | 17:82664468 | GAGGTGCGAGCGTCC[C/T]GCACCCCCAGGGAGT | 10966 |
rs2279393 | snp | C/T | 0.331179 | 0.236453 | intron-variant | RAB40B | GRCh38.p7 | 17:82664414 | CCCCTGTCAGCACAG[C/T]GCCCCGGGGAGCACC | 10966 |
rs2279394 | snp | C/T | 0.392696 | 0.205275 | intron-variant | RAB40B | GRCh38.p7 | 17:82660153 | GGTATGCACTGTGTG[C/T]GTCTGTGCATGAGTA | 10966 |
rs2279395 | snp | C/T | 0.279411 | 0.248264 | intron-variant | RAB40B | GRCh38.p7 | 17:82659676 | GTTCTGCGTGCTGAG[C/T]CTGTGACCTCTCCCC | 10966 |
rs2306756 | snp | A/G | 0.119281 | 0.213102 | intron-variant | RAB40B | GRCh38.p7 | 17:82658430 | CCGAGGTGGGTCAGC[A/G]GCCCCCTGGATAAGT | 10966 |
rs2306911 | snp | C/T | 0.497855 | 0.0326773 | | | GRCh38.p7 | 17:82655712 | GGTCTTTGCAGCGTG[C/T]CTGCACGAGGCTGGC | 10966 |
rs2306912 | snp | C/T | 0.286825 | 0.247273 | | | GRCh38.p7 | 17:82655768 | AGGGTTCACCTTCTG[C/T]CCACAGACCACACCC | 10966 |
rs2379119 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82666589 | CTGGTGTCTGGGGGG[G/T]GATGGGGGCGGGGAA | 10966 |
rs2451197 | snp | C/G | | | intron-variant | RAB40B | GRCh38.p7 | 17:82694019 | ctcagctcactgcaa[C/G]ctctgcctcccaggt | 10966 |
rs2451198 | snp | C/T | 0.449853 | 0.150196 | intron-variant | RAB40B | GRCh38.p7 | 17:82693066 | gcagtgagctgagat[C/T]gcaccactgcacacc | 10966 |
rs2451199 | snp | A/C | 0.437965 | 0.164831 | intron-variant | RAB40B | GRCh38.p7 | 17:82690881 | TGCTCCCCCGGGGCA[A/C]ACGTGCACACTCCGT | 10966 |
rs2451200 | snp | A/C | 0.0119091 | 0.0762411 | intron-variant | RAB40B | GRCh38.p7 | 17:82690143 | GAGGTGGATTTGCTG[A/C]TTAATACAGCTACTC | 10966 |
rs2451201 | snp | A/G | 0.479177 | 0.0998894 | intron-variant | RAB40B | GRCh38.p7 | 17:82678906 | TTTTTTTTTTGAGAC[A/G]GAGTCTCGCTCTGTC | 10966 |
rs2451202 | snp | A/C | 0.284733 | 0.247575 | intron-variant | RAB40B | GRCh38.p7 | 17:82685307 | AGGAGGAGGAGAAAC[A/C]CCACAGAAAGAGACA | 10966 |
rs2451203 | snp | C/T | 0.45946 | 0.136478 | intron-variant | RAB40B | GRCh38.p7 | 17:82688050 | GCACTCCAGCCTGGG[C/T]AATAAGCCAGACCCG | 10966 |
rs2459708 | snp | C/G | 0.330249 | 0.23677 | intron-variant | RAB40B | GRCh38.p7 | 17:82685235 | GAGGGGGAGGGAGGA[C/G]GGAGGAGGGAGGGGG | 10966 |
rs2459709 | snp | C/T | 0.495891 | 0.0451408 | intron-variant | RAB40B | GRCh38.p7 | 17:82686387 | aaagtgatgggatta[C/T]aggcatgagccaccg | 10966 |
rs2459718 | snp | A/G | 0.430136 | 0.173352 | intron-variant | RAB40B | GRCh38.p7 | 17:82690790 | AATTGGAGGGAGATG[A/G]AGTGTGCATGTGTGT | 10966 |
rs2459719 | snp | A/T | 0.448963 | 0.151372 | intron-variant | RAB40B | GRCh38.p7 | 17:82694091 | CCATCTCAAAAAAAA[A/T]AAAAAAAAAAAGGAA | 10966 |
rs2677921 | snp | A/G | 0.389527 | 0.207442 | intron-variant | RAB40B | GRCh38.p7 | 17:82685948 | ggtgtggtggcgggc[A/G]cctgtaatcccagct | 10966 |
rs2677924 | snp | A/G | 0.273587 | 0.248885 | intron-variant | RAB40B | GRCh38.p7 | 17:82683432 | aaagacttacatcca[A/G]aacgtatttaaacat | 10966 |
rs2677928 | snp | A/T | 0.476833 | 0.105105 | intron-variant | RAB40B | GRCh38.p7 | 17:82677239 | GGCGTGAGCCACCGC[A/T]CCCGGCCAGCCTACT | 10966 |
rs3078848 | in-del | -/GT | | | intron-variant | RAB40B | GRCh38.p7 | 17:82682133 | tgtgtgtgtgtgtgt[-/GT]gcatgcgtgtgtgtg | 10966 |
rs3751910 | snp | A/G | 9.0203e-05 | 0.00671516 | utr-variant-3-prime | RAB40B | GRCh38.p7 | 17:82657741 | CACACGGAAGGCGTC[A/G]CACACATTCGCAAGC | 10966 |
rs3751911 | snp | A/G | 0.271847 | 0.249044 | utr-variant-3-prime | RAB40B | GRCh38.p7 | 17:82657767 | CAAGCAGCATTCGCC[A/G]AGAGGAACCGGGATC | 10966 |
rs3751912 | snp | A/G | 0.00874735 | 0.0655527 | utr-variant-3-prime | RAB40B | GRCh38.p7 | 17:82657842 | TGGAGAGATTCCGCC[A/G]TGTTTCTTTCAGTGC | 10966 |
rs3794725 | snp | C/T | 0.422787 | 0.180679 | downstream-variant-500B | RAB40B | GRCh38.p7 | 17:82657057 | ATTCGAAAGAACCGG[C/T]CGCCAACTCTACCAA | 10966 |
rs3794726 | snp | A/C | 0.216349 | 0.247725 | intron-variant, utr-variant-3-prime | RAB40B | GRCh38.p7 | 17:82661712 | GCCAACATAGTGAAA[A/C]CCCGTCTCTACTAAA | 10966 |
rs3794727 | snp | C/T | 0.388021 | 0.208447 | intron-variant | RAB40B | GRCh38.p7 | 17:82663551 | GAGGGAGAGGTGCCC[C/T]GGGCTTGCCCCAAGG | 10966 |
rs3794728 | snp | C/T | 0.3744 | 0.216852 | intron-variant | RAB40B | GRCh38.p7 | 17:82663740 | CATCACTGAGCCAGG[C/T]GTGGGGGACCCAGGA | 10966 |
rs3848402 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | RAB40B | GRCh38.p7 | 17:82681685 | aaTAGATTGCCGAAT[C/T]TGGTATATTTTTTAT | 10966 |
rs3859203 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | RAB40B | GRCh38.p7 | 17:82679568 | aggtgggagccactg[C/T]gcccggccGCCACAA | 10966 |
rs3898431 | snp | C/T | 0.128976 | 0.218754 | upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82700463 | AGGATGGAAGGTGGA[C/T]GCTAGAAAACTATGA | 10966 |
rs3933871 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | RAB40B | GRCh38.p7 | 17:82679503 | G[A/G] | 10966 |
rs4258659 | snp | A/G | 0.106987 | 0.205054 | intron-variant | RAB40B | GRCh38.p7 | 17:82682869 | aacgaacccggccgg[A/G]cacggtgactcatgc | 10966 |
rs4789706 | snp | C/T | 0.0584853 | 0.160693 | intron-variant, utr-variant-5-prime, utr-variant-3-prime | RAB40B | GRCh38.p7 | 17:82661204 | ACTTTCCAATGTCCC[C/T]GAAGGGATCCGGGTG | 10966 |
rs4789708 | snp | A/T | 0.202651 | 0.245475 | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82670961 | CCCTGGCCCACCCGA[A/T]CCCCTGTCTCCCTTC | 10966 |
rs4789709 | snp | C/T | 0.375 | 0.216506 | intron-variant | RAB40B | GRCh38.p7 | 17:82672363 | ACACGCTCCCTGTAC[C/T]CACTGACACACCTCA | 10966 |
rs4789818 | snp | A/C | 0.204803 | 0.245881 | intron-variant, utr-variant-3-prime | RAB40B | GRCh38.p7 | 17:82661366 | TCTGAAGATAAATCT[A/C]TGCAGTAAGGAGTGT | 10966 |
rs4789819 | snp | A/C | 0.244898 | 0.249948 | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82665893 | CAAGAACAACAACAA[A/C]AAAAAAAAAAAAAAA | 10966 |
rs4789820 | snp | A/C | 0.361894 | 0.223562 | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82665896 | GAACAACAACAAAAA[A/C]AAAAAAAAAAAAAAA | 10966 |
rs4789821 | snp | A/C | 0.197531 | 0.244432 | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82665905 | CAAAAAAAAAAAAAA[A/C]AAAAAAAAACTACAC | 10966 |
rs4789822 | snp | C/T | 0.5 | 0 | intron-variant | RAB40B | GRCh38.p7 | 17:82672247 | CACACTCACACGCTC[C/T]CTGTACTCACTGACA | 10966 |
rs4789823 | snp | A/C | 0.5 | 0 | intron-variant | RAB40B | GRCh38.p7 | 17:82672290 | TAACTCTAACACACA[A/C]ACTCACACGCTCCCT | 10966 |
rs4789824 | snp | C/T | 0 | 0 | intron-variant | RAB40B | GRCh38.p7 | 17:82672298 | ACACACAAACTCACA[C/T]GCTCCCTGTACTGAC | 10966 |
rs5822541 | in-del | -/G | 0.429837 | 0.173662 | | | GRCh38.p7 | 17:82654899 | TCTTAAGAGAAGAAA[-/G]GTGTGTAAGAATCTG | 10966 |
rs5822542 | in-del | -/TT | | | upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82700169 | CATTTTTTTTTTTTT[-/TT]GAGACAGAGTCTTGC | 10966 |
rs7208066 | snp | C/T | 0.277067 | 0.24853 | intron-variant, upstream-variant-2KB | RAB40B, MIR4525 | GRCh38.p7 | 17:82669470 | acaagagcgaaactc[C/T]gtctcaaaaaaataa | 10966 |
rs7209718 | snp | A/G | 0.428333 | 0.175206 | intron-variant, utr-variant-3-prime | RAB40B | GRCh38.p7 | 17:82662391 | CCGAAGGGCCAGCAC[A/G]TGCTGTCAGAGTGCC | 10966 |
rs7210081 | snp | A/G | 0.271162 | 0.249103 | intron-variant, synonymous-codon | RAB40B | GRCh38.p7 | 17:82662641 | CTTGCTCAGACGACA[A/G]TGTGGACAGAGCTGG | 10966 |
rs7210502 | snp | C/T | 0.0744748 | 0.178019 | intron-variant | RAB40B | GRCh38.p7 | 17:82693127 | cctgcctcagtctcc[C/T]gagtagctgggaata | 10966 |
rs7211237 | snp | G/T | 0.0235055 | 0.105844 | intron-variant | RAB40B | GRCh38.p7 | 17:82664566 | CGATGCCTGCGGAAG[G/T]GTTAGAGACGGCTTA | 10966 |
rs7211499 | snp | A/G | 0.419776 | 0.18351 | intron-variant | RAB40B | GRCh38.p7 | 17:82667303 | CACCGGTGGCCTCCC[A/G]CTTGGCTTGGACAGC | 10966 |
rs7214687 | snp | C/G | 0.0744748 | 0.178019 | intron-variant | RAB40B | GRCh38.p7 | 17:82693191 | tttgtatttttagta[C/G]agatggggtttcacc | 10966 |
rs7215144 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant, upstream-variant-2KB | RAB40B, MIR4525 | GRCh38.p7 | 17:82669532 | gtggtgcacacctgt[C/T]gtcccagcttctcag | 10966 |
rs7218760 | snp | A/T | 0.390464 | 0.206809 | intron-variant | RAB40B | GRCh38.p7 | 17:82693519 | cagggaaacctgtgc[A/T]gacatttgcgtgcct | 10966 |
rs7219091 | snp | A/G | 0.274393 | 0.248807 | intron-variant, upstream-variant-2KB | RAB40B, MIR4525 | GRCh38.p7 | 17:82669471 | caagagcgaaactct[A/G]tctcaaaaaaataaa | 10966 |
rs7219561 | snp | C/T | | | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82671761 | TAACACACACTCACA[C/T]GCTCCCTGTACCCAC | 10966 |
rs7221877 | snp | C/T | 0 | 0 | intron-variant, upstream-variant-2KB | RAB40B, MIR4525 | GRCh38.p7 | 17:82668334 | gtcctccttccagtc[C/T]gcaggactggcagcc | 10966 |
rs7222888 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant, upstream-variant-2KB | RAB40B, MIR4525 | GRCh38.p7 | 17:82669511 | taaaaaaattggcca[A/G]tcatggtggtgcaca | 10966 |
rs7224226 | snp | A/C | 0.00358779 | 0.0422022 | utr-variant-3-prime | RAB40B | GRCh38.p7 | 17:82657164 | CAGCTCTTCCTTGAC[A/C]TGTCGAAACTGTGCT | 10966 |
rs7224369 | snp | G/T | 0.0150606 | 0.0854603 | intron-variant | RAB40B | GRCh38.p7 | 17:82684685 | ggttcaaaggCCTCC[G/T]GGATGCAGGCACGTT | 10966 |
rs7225035 | snp | A/C | 0.454182 | 0.144256 | intron-variant, utr-variant-3-prime | RAB40B | GRCh38.p7 | 17:82662394 | AAGGGCCAGCACGTG[A/C]TGTCAGAGTGCCCCA | 10966 |
rs7225599 | snp | A/C | 0 | 0 | intron-variant | RAB40B | GRCh38.p7 | 17:82685672 | GGTGCCCAGCTCTTC[A/C]TTCATGAGAACGAAA | 10966 |
rs7225680 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | RAB40B | GRCh38.p7 | 17:82662862 | CTGGGAGAGGGCACG[C/T]GCCAGCCCTGATGCA | 10966 |
rs7226102 | snp | C/G | | | intron-variant | RAB40B | GRCh38.p7 | 17:82679776 | TCCACCAAGCACAGG[C/G]CAGGGGCCAGCTTCC | 10966 |
rs8064270 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | RAB40B | GRCh38.p7 | 17:82679982 | GGGAGGGACAGAGGG[A/G]CCAGATCCCAGAGCT | 10966 |
rs8064541 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | RAB40B | GRCh38.p7 | 17:82680364 | GGTGTGGGCTCTGGG[C/T]GGGGCCGCTCGGGGG | 10966 |
rs8068138 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | RAB40B | GRCh38.p7 | 17:82680143 | GGCCTGGCAGGGTTC[A/G]AGGGCTCAACTCAGG | 10966 |
rs8071828 | snp | C/T | 0.0543475 | 0.155628 | intron-variant | RAB40B | GRCh38.p7 | 17:82690977 | CAACTGTGTCACTTT[C/T]CATAACGGAGGCTCT | 10966 |
rs8079119 | snp | A/C/T | 0.000854285 | 0.02065 | synonymous-codon, missense | RAB40B | GRCh38.p7 | 17:82658492 | GCCCCTGGGCCTACC[A/C/T]TTGCTCGGCCGCCAG | 10966 |
rs8080937 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | RAB40B | GRCh38.p7 | 17:82684852 | ggcacggtggcccac[A/G]cctgtaatcctagaa | 10966 |
rs8081139 | snp | C/T | 0.444666 | 0.15686 | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82665315 | tggagtgcagtggcg[C/T]gatcacagctcactg | 10966 |
rs9303032 | snp | A/G | 0.494651 | 0.0514399 | intron-variant | RAB40B | GRCh38.p7 | 17:82691414 | CAAAAGGCCGGGCGC[A/G]GTGGCTCACGCCTGT | 10966 |
rs9890381 | snp | G/T | 0 | 0 | intron-variant | RAB40B | GRCh38.p7 | 17:82691221 | GCTCTTAGCAAAAAT[G/T]AAACAAAGAAAGAAC | 10966 |
rs9890713 | snp | C/T | 0.39121 | 0.2063 | intron-variant | RAB40B | GRCh38.p7 | 17:82674679 | AAAAGAAAAAGCAAC[C/T]TAAAACACCTGGGGA | 10966 |
rs9891087 | snp | A/G | 0.256061 | 0.249927 | intron-variant | RAB40B | GRCh38.p7 | 17:82691544 | ATACAAAAATTAGCC[A/G]GGCATGGTACACCTG | 10966 |
rs9893830 | snp | A/T | 0.262435 | 0.249691 | intron-variant | RAB40B | GRCh38.p7 | 17:82673645 | AGAGTTCCTTTTGAG[A/T]TCGGCCGTAAACTCA | 10966 |
rs9895695 | snp | A/G | 0.466721 | 0.124627 | intron-variant | RAB40B | GRCh38.p7 | 17:82674271 | ctgaggctgggaggc[A/G]gaggttgcagtgagc | 10966 |
rs9896156 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RAB40B | GRCh38.p7 | 17:82674466 | gaaaccccgtctcta[C/G]taaaaatacaaaaaa | 10966 |
rs9896615 | snp | C/G | 0.405082 | 0.196086 | intron-variant | RAB40B | GRCh38.p7 | 17:82674633 | gacagagcaagactc[C/G]tcttaaaaaaaaaaa | 10966 |
rs9898182 | snp | C/T | | | intron-variant | RAB40B | GRCh38.p7 | 17:82685809 | Cttcttcttcttctt[C/T]ttttttttttttgag | 10966 |
rs9900923 | snp | A/G | 0.337841 | 0.23406 | intron-variant | RAB40B | GRCh38.p7 | 17:82674354 | tcaaaagaaaagacc[A/G]ggcgtggtggttcac | 10966 |
rs9905734 | snp | C/T | 0.288646 | 0.246995 | intron-variant, upstream-variant-2KB | RAB40B, MIR4525 | GRCh38.p7 | 17:82669203 | attagggcctgggcg[C/T]ggtggctcacgcctg | 10966 |
rs9912679 | snp | C/T | 0.0429648 | 0.14013 | intron-variant | RAB40B | GRCh38.p7 | 17:82691423 | gggcgcggtggctca[C/T]gcctgtaatcccagc | 10966 |
rs9912932 | snp | A/G | 0.382279 | 0.212137 | intron-variant, upstream-variant-2KB | RAB40B, MIR4525 | GRCh38.p7 | 17:82669763 | AATTACGCTTTGAGC[A/G]ACGACCAAAAATCTC | 10966 |
rs9914549 | snp | A/G | 0.31721 | 0.240796 | intron-variant | RAB40B | GRCh38.p7 | 17:82667081 | CAGCTCTCCTTCCAG[A/G]GAAGCCCACGATGTA | 10966 |
rs9914583 | snp | C/T | 0.0349115 | 0.127424 | intron-variant, utr-variant-5-prime | RAB40B | GRCh38.p7 | 17:82696606 | CCTCCAGGCGCTCAA[C/T]CTCCAGCCCTGTCCT | 10966 |
rs10438709 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RAB40B | GRCh38.p7 | 17:82679676 | GACAAGTGCTGCAGA[A/G]GCCACGCCAACCCTG | 10966 |
rs10685757 | in-del | -/CACT | | | intron-variant | RAB40B | GRCh38.p7 | 17:82672310 | CACGCTCCCTGTACT[-/CACT]GACACACCCCACCCC | 10966 |
rs10710873 | in-del | -/G | 0.361474 | 0.223771 | intron-variant, upstream-variant-2KB | RAB40B, MIR4525 | GRCh38.p7 | 17:82669136 | TGAGCCCAGGAATTC[-/G]AAACCAGCCTGGGCA | 10966 |
rs10852798 | snp | G/T | 0.321292 | 0.23962 | intron-variant | RAB40B | GRCh38.p7 | 17:82694981 | caatgaacagagaca[G/T]aaatggtaaaaggac | 10966 |
rs11323271 | in-del | -/T | | | intron-variant | RAB40B | GRCh38.p7 | 17:82672105 | GACACACCCCACCCC[-/T]TGTAACTCTAACACA | 10966 |
rs11326382 | in-del | -/T | 0.423726 | 0.179776 | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82665259 | ATGCCTTTCTTCTTC[-/T]TTTTTTTTTTTGAGA | 10966 |
rs11357202 | in-del | -/A | 0.0535932 | 0.154675 | intron-variant | RAB40B | GRCh38.p7 | 17:82673462 | ATCCTTCCCTCTCTT[-/A]AGCTGACTCCTCTTT | 10966 |
rs11449157 | in-del | -/T | | | intron-variant | RAB40B | GRCh38.p7 | 17:82672273 | GACACACCCCACCCC[-/T]CGTAACTCTAACACA | 10966 |
rs11449158 | in-del | -/ACTC | 0.498481 | 0.027514 | intron-variant | RAB40B | GRCh38.p7 | 17:82672307 | TCACACGCTCCCTGT[-/ACTC]ACTGACACACCCCAC | 10966 |
rs11548172 | snp | A/C | | | missense, utr-variant-5-prime | RAB40B | GRCh38.p7 | 17:82698506 | GGCAAGGGCGAGATC[A/C]TGGCGAGCCTGCAGG | 10966 |
rs11650031 | snp | C/T | 0.100231 | 0.200173 | intron-variant | RAB40B | GRCh38.p7 | 17:82674891 | GGAGAAAGAACAACA[C/T]GAGATAATCCTGACG | 10966 |
rs11653433 | snp | A/C | 0.266819 | 0.249434 | intron-variant | RAB40B | GRCh38.p7 | 17:82693132 | ctcagtctcccgagt[A/C]gctgggaatacaggt | 10966 |
rs11653879 | snp | C/T | 0.16911 | 0.236552 | intron-variant | RAB40B | GRCh38.p7 | 17:82677469 | TGGCCCATCCTGCAG[C/T]GGCCAGCTCAACACA | 10966 |
rs11654159 | snp | C/T | 0.125182 | 0.216612 | intron-variant | RAB40B | GRCh38.p7 | 17:82695073 | gccacaatacagaag[C/T]aagggctataaacct | 10966 |
rs11655071 | snp | A/G | 0.110872 | 0.20771 | intron-variant | RAB40B | GRCh38.p7 | 17:82694989 | agagacataaatggt[A/G]aaaggactttggtga | 10966 |
rs11656597 | snp | A/G | 0.225005 | 0.248747 | intron-variant | RAB40B | GRCh38.p7 | 17:82687798 | CGCCCCCagccaggc[A/G]cggtggctcatgtct | 10966 |
rs11656603 | snp | C/T | 0.5 | 0 | intron-variant | RAB40B | GRCh38.p7 | 17:82672242 | ACACACACACTCACA[C/T]GCTCCCTGTACTCAC | 10966 |
rs11656644 | snp | A/G | 0.234109 | 0.249494 | intron-variant | RAB40B | GRCh38.p7 | 17:82687885 | aagacaagcctgggc[A/G]gcatagcaagaccct | 10966 |
rs11658763 | snp | C/T | 0.389715 | 0.207315 | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82666554 | CCGGCCAATAAATAT[C/T]TTTAAAGGGAAAAAT | 10966 |
rs11867441 | snp | A/G | 0.483995 | 0.0880135 | intron-variant | RAB40B | GRCh38.p7 | 17:82673039 | tgaaacctcatctct[A/G]ctaaaaatacaaaaa | 10966 |
rs11868984 | snp | A/C | 0.147321 | 0.227941 | intron-variant, utr-variant-5-prime | RAB40B | GRCh38.p7 | 17:82664867 | CCGGTGGGTTTGCCG[A/C]GGGGCTGTGGCCGCT | 10966 |
rs11870880 | snp | C/T | 0.0744748 | 0.178019 | intron-variant | RAB40B | GRCh38.p7 | 17:82697086 | TGCCAGAGACTCCCC[C/T]GCATGCTGCAGTTTC | 10966 |
rs11870950 | snp | A/C/G/T | 0.0726307 | 0.176182 | intron-variant | RAB40B | GRCh38.p7 | 17:82660047 | gcaggtacgtgcact[A/C/G/T]tgtgtgcgtgcatct | 10966 |
rs11871968 | snp | C/T | 0.0955749 | 0.196603 | intron-variant | RAB40B | GRCh38.p7 | 17:82696961 | ACGGTCCTAGAGACC[C/T]GCCACCGAGCGGGGA | 10966 |
rs12451351 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82670360 | AAGCTAATTTGTGTA[C/T]TTTTAGTAGACACGG | 10966 |
rs12600399 | snp | A/G | | | intron-variant | RAB40B | GRCh38.p7 | 17:82682799 | ctgctggaacaatta[A/G]acatccctgtgcaaa | 10966 |
rs12936937 | snp | A/G | | | intron-variant | RAB40B | GRCh38.p7 | 17:82698338 | ccccggcctcttccc[A/G]acccctgcccggtct | 10966 |
rs12937622 | snp | A/C | 0.167158 | 0.235875 | intron-variant | RAB40B | GRCh38.p7 | 17:82681872 | atacaattcccttaa[A/C]ctgataaagtgcatc | 10966 |
rs12938630 | snp | A/G | 0.286825 | 0.247273 | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82671426 | CTGTAACTCTAACAC[A/G]CACACGCTCCCTGTA | 10966 |
rs12938650 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82671444 | CACGCTCCCTGTACT[A/C]ACTGACACACCCCAC | 10966 |
rs12938705 | snp | A/T | | | intron-variant | RAB40B | GRCh38.p7 | 17:82686541 | caggagagaaggctg[A/T]gtgacgacagacagc | 10966 |
rs12940682 | snp | A/T | 0.353371 | 0.227628 | intron-variant | RAB40B | GRCh38.p7 | 17:82672746 | CAGCCTCCAGAACTG[A/T]AAGAAATGCATTTAT | 10966 |
rs12942304 | snp | A/C | 0 | 0 | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82671459 | AACTGACACACCCCA[A/C]CCCTGTAACTCTAAC | 10966 |
rs12942653 | snp | C/T | 0 | 0 | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82671610 | ACATGCTCCCTGTAC[C/T]CACTGACACAGCTCA | 10966 |
rs12943213 | snp | C/G | | | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82671729 | GTACCCACTGACACA[C/G]CCCACCCCTGTAACT | 10966 |
rs12943214 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82671731 | ACCCACTGACACACC[C/T]CACCCCTGTAACTCT | 10966 |
rs12943248 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | RAB40B | GRCh38.p7 | 17:82678990 | caggttcacaccatt[C/T]tcctgcctcagcctc | 10966 |
rs12944925 | snp | C/T | 0.170084 | 0.236883 | intron-variant | RAB40B | GRCh38.p7 | 17:82680786 | cctttaatcccagca[C/T]tttggaaggctgagg | 10966 |
rs12947411 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82671469 | CCCCACCCCTGTAAC[C/T]CTAACACACACTCAC | 10966 |
rs12947930 | snp | C/T | | | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82671623 | ACCCACTGACACAGC[C/T]CACCCCGTAACTCTA | 10966 |
rs12948616 | snp | C/T | | | upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82698835 | TTACTCTCGTCACCG[C/T]CTCCGGGCTGTCGCC | 10966 |
rs12948621 | snp | A/C | 0.392325 | 0.205532 | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82665230 | AAACAAACAAACAAA[A/C]AAAAAACCCGAGAAT | 10966 |
rs12949107 | snp | A/G | 0.368733 | 0.220005 | intron-variant | RAB40B | GRCh38.p7 | 17:82681047 | AAAAAAAAAAAAAAA[A/G]AAAGAAAGAGAAAAG | 10966 |
rs12949425 | snp | C/G | 0.294064 | 0.246086 | intron-variant, upstream-variant-2KB | RAB40B, MIR4525 | GRCh38.p7 | 17:82670252 | GTGCAGTGACGTGAT[C/G]TCGCTCACTGCAACC | 10966 |
rs12950387 | snp | C/G | | | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82671621 | GTACCCACTGACACA[C/G]CTCACCCCGTAACTC | 10966 |
rs12951296 | snp | C/G | | | intron-variant | RAB40B | GRCh38.p7 | 17:82686538 | acccaggagagaagg[C/G]tgtgtgacgacagac | 10966 |
rs12952159 | snp | C/T | 0.375 | 0.216506 | intron-variant, downstream-variant-500B, utr-variant-5-prime | RAB40B, MIR4525 | GRCh38.p7 | 17:82668228 | AGTCTGGGGTTTTTG[C/T]GGTCTTCAGGGTGGG | 10966 |
rs12952494 | snp | A/G | 0.388775 | 0.207946 | intron-variant | RAB40B | GRCh38.p7 | 17:82659140 | TCTGTTGTTCAGGAC[A/G]CCCAGGTTGTGGTCG | 10966 |
rs17855477 | snp | A/G/T | 0.000153988 | 0.00877327 | missense, utr-variant-5-prime | RAB40B | GRCh38.p7 | 17:82698473 | CCGGGTGGCCGTACG[A/G/T]GGACTCGGCCGCGCC | 10966 |
rs28879120 | snp | A/G | | | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82666056 | ACCACACCTGCCACC[A/G]CACCTGCCACCGCAC | 10966 |
rs28970460 | snp | C/T | | | intron-variant | RAB40B | GRCh38.p7 | 17:82672155 | ACCCACTGACACAGC[C/T]CACCCCTGTAACTCT | 10966 |
rs28970534 | snp | C/G | | | intron-variant | RAB40B | GRCh38.p7 | 17:82672153 | GTACCCACTGACACA[C/G]CTCACCCCTGTAACT | 10966 |
rs34004249 | snp | A/G | 0.151334 | 0.229706 | intron-variant | RAB40B | GRCh38.p7 | 17:82691758 | AATCTGGTGTTGGAA[A/G]CACCAGCTGGGGTGG | 10966 |
rs34066713 | in-del | -/A | 0 | 0 | intron-variant | RAB40B | GRCh38.p7 | 17:82694102 | AAAAAAAAAAAAAAA[-/A]GGAAAACTCCAAAAC | 10966 |
rs34107393 | in-del | -/G | | | intron-variant | RAB40B | GRCh38.p7 | 17:82682244 | ACAAGGCCAACATGG[-/G]AAAAAAACAGTTGTA | 10966 |
rs34107818 | in-del | -/A | 0.391769 | 0.205917 | intron-variant | RAB40B | GRCh38.p7 | 17:82674638 | AGCAAGACTCGTCTT[-/A]AAAAAAAAAAAAAAG | 10966 |
rs34189304 | snp | A/C/G/T | 0.0306411 | 0.119928 | missense | RAB40B | GRCh38.p7 | 17:82657912 | AGCTCGTCCGCCCCC[A/C/G/T]CCAGAGCCCCCCCAA | 10966 |
rs34212418 | in-del | -/TTTT | 0.389903 | 0.207189 | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82666250 | CCTGGCCACAATACA[-/TTTT]TTTTTTTTGAGATGG | 10966 |
rs34309377 | snp | A/G | 0.20511 | 0.245937 | intron-variant | RAB40B | GRCh38.p7 | 17:82677018 | CAGTGGCACGATCTC[A/G]GCTCACCGCAAGCTC | 10966 |
rs34411310 | in-del | -/C | | | intron-variant | RAB40B | GRCh38.p7 | 17:82673372 | GGGGCATCTTTCCAG[-/C]ACCTTCTGTCCTGCT | 10966 |
rs34618580 | snp | C/G | | | intron-variant | RAB40B | GRCh38.p7 | 17:82663945 | AGAAGCCCTGGTGCA[C/G]CTGGGGCTGGGGGTG | 10966 |
rs34648826 | snp | G/T | 0.165853 | 0.235413 | intron-variant | RAB40B | GRCh38.p7 | 17:82676196 | GTCAGCTCAGCAAAG[G/T]CTCCAACTCCTCCCC | 10966 |
rs34711227 | in-del | -/C | | | intron-variant, nc-transcript-variant, upstream-variant-2KB | RAB40B, MIR4525 | GRCh38.p7 | 17:82668295 | AACCAGCATGCACAT[-/C]CCCCCCTCTGACAAA | 10966 |
rs34764023 | in-del | -/G | | | intron-variant | RAB40B | GRCh38.p7 | 17:82686091 | CAGGCGTGAGCCACC[-/G]GCACCCAGCCTTCTT | 10966 |
rs34778953 | in-del | -/A/AA/AAA | | | intron-variant | RAB40B | GRCh38.p7 | 17:82684220 | GTGAGACTCTGTCTC[-/A/AA/AAA]AAAAAAAAAAAAAAA | 10966 |
rs34923378 | in-del | -/A/AA/AAA | 0.361474 | 0.223771 | intron-variant | RAB40B | GRCh38.p7 | 17:82689966 | AAAAAAAAAAAAAAA[-/A/AA/AAA]GAAGTAGAAAACCAT | 10966 |
rs35145848 | in-del | -/A | 0.492823 | 0.0594727 | intron-variant | RAB40B | GRCh38.p7 | 17:82683823 | AAAAAAAAAAAAAAA[-/A]GAAAAGAAAAGAAAA | 10966 |
rs35151088 | in-del | -/G | | | intron-variant, utr-variant-5-prime, utr-variant-3-prime | RAB40B | GRCh38.p7 | 17:82661221 | AGGGATCCGGGTGTT[-/G]GGGATGTCCTCCCAG | 10966 |
rs35199691 | in-del | -/T/TT | 0.383632 | 0.211288 | upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82700156 | CATTTTTTTTTTTTT[-/T/TT]GAGACAGAGTCTTGC | 10966 |
rs35212440 | in-del | -/T | | | upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82699641 | TTGCATGTGTGTGTC[-/T]TGCGTGTGCTGCTTC | 10966 |
rs35231107 | snp | A/C | | | intron-variant | RAB40B | GRCh38.p7 | 17:82663944 | GAGAAGCCCTGGTGC[A/C]GCTGGGGCTGGGGGT | 10966 |
rs35236038 | in-del | -/CA | 0.5 | 0 | intron-variant | RAB40B | GRCh38.p7 | 17:82682122 | ACACACACACGCATG[-/CA]CACACACACACACAC | 10966 |
rs35256137 | in-del | -/T/TT | 0 | 0 | intron-variant | RAB40B | GRCh38.p7 | 17:82686105 | CGCACCCAGCCTTCT[-/T/TT]TTTTTTTTTTTTTTT | 10966 |
rs35309316 | in-del | -/T | | | intron-variant | RAB40B | GRCh38.p7 | 17:82693122 | TTCTCCTGCCTCAGT[-/T]CTCCCGAGTCGCTGG | 10966 |
rs35332089 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | RAB40B | GRCh38.p7 | 17:82694560 | ACATACACACACACA[C/T]ACACACACACACCTG | 10966 |
rs35406298 | in-del | -/C | | | intron-variant | RAB40B | GRCh38.p7 | 17:82685085 | ACCATTGCACTCCAG[-/C]CTGGGTGACAAGAGT | 10966 |
rs35495504 | in-del | -/C | | | intron-variant, frameshift-variant | RAB40B | GRCh38.p7 | 17:82662743 | CCCTGGGATCTCACT[-/C]CTGAGGTGAGAGGGA | 10966 |
rs35569013 | in-del | -/G | | | intron-variant | RAB40B | GRCh38.p7 | 17:82660519 | AGGCACTCATGCACA[-/G]GATGCATACACAGTG | 10966 |
rs35597028 | in-del | -/G | | | intron-variant | RAB40B | GRCh38.p7 | 17:82692427 | CAGCTGCCTGAGCAA[-/G]GGACAAGATGCATCT | 10966 |
rs35622820 | in-del | -/G | | | frameshift-variant | RAB40B | GRCh38.p7 | 17:82658049 | GAGGTGGCTTCTTAA[-/G]GCAATGGGGAGCGGG | 10966 |
rs35636736 | in-del | -/G | | | intron-variant | RAB40B | GRCh38.p7 | 17:82696992 | GGGGGTAGGACATGC[-/G]GGGGGCAGCGGCGCC | 10966 |
rs35692329 | in-del | -/G | | | intron-variant | RAB40B | GRCh38.p7 | 17:82683383 | AGAAAAGGCACAGAT[-/G]GGGGTGAAAATACTT | 10966 |
rs35702047 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | RAB40B | GRCh38.p7 | 17:82693418 | GACAGAGACAGCCCC[A/G]TGCTGAGAGGGAAGA | 10966 |
rs35765887 | in-del | -/A | | | intron-variant | RAB40B | GRCh38.p7 | 17:82682353 | CTTGAGTATAAATCT[-/A]AAAAAAAGTGCAAGA | 10966 |
rs35826981 | in-del | -/C | | | intron-variant | RAB40B | GRCh38.p7 | 17:82663422 | GAGGCACCGCAGGAG[-/C]CCCCCCATCCCCACC | 10966 |
rs35834449 | in-del | -/T | | | | | GRCh38.p7 | 17:82656549 | TGCCTGGGTGCCAGC[-/T]TTTAACTCTCCGCTC | 10966 |
rs35842117 | in-del | -/C | | | intron-variant | RAB40B | GRCh38.p7 | 17:82675742 | ATCCCATCCACAAAG[-/C]CCCCACGTGACCTAA | 10966 |
rs35848277 | in-del | -/T | 0 | 0 | intron-variant | RAB40B | GRCh38.p7 | 17:82678880 | AGCTCCCTTTCTGCG[-/T]TTTTTTTTTTTTTTT | 10966 |
rs35878129 | snp | C/T | 0.128632 | 0.218563 | intron-variant | RAB40B | GRCh38.p7 | 17:82697755 | TTCAAGCCTCAAACT[C/T]GGGGGATCCCCGGGC | 10966 |
rs35919262 | in-del | -/T | | | utr-variant-3-prime | RAB40B | GRCh38.p7 | 17:82657324 | AATGTAGTAAATAAC[-/T]TAGCAAAAACTTTAT | 10966 |
rs35936659 | in-del | -/AG/G | 0.00636936 | 0.0560724 | intron-variant | RAB40B | GRCh38.p7 | 17:82660399 | ATGCACGCATACACA[-/AG/G]GGGCATGTACCTTCA | 10966 |
rs36021310 | in-del | -/T | | | intron-variant | RAB40B | GRCh38.p7 | 17:82685757 | CTCACATTCACCCAG[-/T]AACTTCAGAATGTGA | 10966 |
rs36041792 | snp | G/T | | | intron-variant | RAB40B | GRCh38.p7 | 17:82660466 | TGCACGCATACACAG[G/T]GCAAGTACCTGCACA | 10966 |
rs36094405 | in-del | -/T | 0.452965 | 0.145963 | intron-variant | RAB40B | GRCh38.p7 | 17:82685807 | CTCTTCTTCTTCTTC[-/T]TTTTTTTTTTTTTTG | 10966 |
rs55690940 | snp | C/T | | | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82665804 | CCCGGGAGGCGGAGG[C/T]TGCAGTGAACTGAGA | 10966 |
rs55701300 | snp | A/T | | | intron-variant | RAB40B | GRCh38.p7 | 17:82693574 | GGGACCTTTCAACAG[A/T]AATGCAAAGGATGTG | 10966 |
rs55778904 | snp | A/G | 0 | 0 | intron-variant | RAB40B | GRCh38.p7 | 17:82681033 | CTCAAAAAAAAAAAA[A/G]AAAAAAAAAAAAAAA | 10966 |
rs55831679 | snp | A/T | | | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82665704 | AAACCCCATCTCTAC[A/T]AAAAATTCAAAAATT | 10966 |
rs55869205 | snp | A/G | 0.190205 | 0.242744 | intron-variant, upstream-variant-2KB | RAB40B, MIR4525 | GRCh38.p7 | 17:82668857 | CCCAGCCATGCCTCC[A/G]CTGCAGCCGGCATCT | 10966 |
rs55957216 | snp | C/T | 0.0520825 | 0.152737 | intron-variant | RAB40B | GRCh38.p7 | 17:82660083 | TGTTGCATACACACA[C/T]GCAGGCACTCATGCA | 10966 |
rs55976121 | snp | A/G | | | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82665782 | TGAGGCAGGAGAATT[A/G]CTTGAACCCGGGAGG | 10966 |
rs55985676 | snp | A/C | | | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82671847 | CACACCCCACCCCGT[A/C]ACTCTAAAACACACA | 10966 |
rs55997823 | snp | A/G | | | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82665788 | AGGAGAATTGCTTGA[A/G]CCCGGGAGGCGGAGG | 10966 |
rs56002738 | snp | C/T | 0.234109 | 0.249494 | intron-variant | RAB40B | GRCh38.p7 | 17:82677569 | CTCCATCAGCCCTGA[C/T]GCCGCGTCTCTGTCC | 10966 |
rs56058624 | snp | C/T | 0.201418 | 0.245234 | intron-variant | RAB40B | GRCh38.p7 | 17:82659339 | CGCATAGCCGAGGTA[C/T]GCCGTGGACGCTCGT | 10966 |
rs56078747 | snp | C/G | | | intron-variant | RAB40B | GRCh38.p7 | 17:82679020 | CCCAGGTAGCTGGGA[C/G]TACAGGCACCTGCCA | 10966 |
rs56137100 | snp | C/T | 0.451732 | 0.147663 | intron-variant, upstream-variant-2KB | RAB40B, MIR4525 | GRCh38.p7 | 17:82670266 | TCTCGCTCACTGCAA[C/T]CTCCGCCCACCGGGT | 10966 |
rs56171164 | snp | C/G | | | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82665636 | CTTTGGGAGGCTGAG[C/G]CGGGTGGATCACTTG | 10966 |
rs56237834 | snp | C/G | | | intron-variant, upstream-variant-2KB | RAB40B, MIR4525 | GRCh38.p7 | 17:82670123 | ACTGCCTGAGCTTGG[C/G]TGGGTCCTCTGACTT | 10966 |
rs56324563 | snp | A/T | | | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82665711 | ATCTCTACTAAAAAT[A/T]CAAAAATTAGCCGGG | 10966 |
rs56348712 | snp | A/G | 0.0119091 | 0.0762411 | | | GRCh38.p7 | 17:82655144 | TTTCCTGAGGCTGCC[A/G]TAACAATCGCCACAA | 10966 |
rs56878377 | snp | A/C | | | intron-variant | RAB40B | GRCh38.p7 | 17:82673103 | CAGATACTTGGGAGG[A/C]TGAGGCAGGAGAATC | 10966 |
rs56933880 | snp | A/G | 0.081446 | 0.184634 | intron-variant | RAB40B | GRCh38.p7 | 17:82664195 | CGACGGTGGTGGGGG[A/G]AGGGTGCTCCCTGGG | 10966 |
rs57190418 | in-del | -/CA | 0.479583 | 0.0989539 | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82671271 | ACACACAGTCACACA[-/CA]TCCTGTACTCACTGA | 10966 |
rs57312817 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RAB40B | GRCh38.p7 | 17:82679040 | GGCACCTGCCACCAC[A/G]CCTGGCTAATTTTTT | 10966 |
rs58088509 | in-del | -/CCCTGTCCTCCAGGCGCTCAATCTCCAG | | | intron-variant, utr-variant-5-prime | RAB40B | GRCh38.p7 | 17:82696781 | GCGCTCAATCTCCAG[-/CCCTGTCCTCCAGGCGCTCAATCTCCAG]GGCAGCGCTGGCCCT | 10966 |
rs58155276 | in-del | -/A/AA | 0 | 0 | intron-variant | RAB40B | GRCh38.p7 | 17:82689981 | AAAAAAAAAAAAAAA[-/A/AA]GAAGTAGAAAACCAT | 10966 |
rs58213596 | snp | A/G | | | intron-variant | RAB40B | GRCh38.p7 | 17:82681043 | AAAAAAAAAAAAAAA[A/G]AAAAAAAGAAAGAGA | 10966 |
rs58247763 | snp | C/T | 0.0588605 | 0.161139 | intron-variant | RAB40B | GRCh38.p7 | 17:82658275 | TGCAGCAAGCCCTGC[C/T]GCGACGTCCCCTCTG | 10966 |
rs58311022 | snp | C/T | 0.243061 | 0.249904 | intron-variant | RAB40B | GRCh38.p7 | 17:82690410 | TGTGCACATGTGTTC[C/T]CAGGGAGCAGAGAGT | 10966 |
rs58514911 | snp | A/G | 0.0577344 | 0.159793 | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82671129 | CTCGGTCACTGACAC[A/G]CCCCACCCCTGTAAC | 10966 |
rs58762800 | in-del | -/CAAC | 0.0368353 | 0.130617 | intron-variant | RAB40B | GRCh38.p7 | 17:82685358 | CTGTGGCCGTGCACT[-/CAAC]TGAACGCAGATTCCT | 10966 |
rs58883418 | snp | A/G | 0.381113 | 0.21286 | intron-variant | RAB40B | GRCh38.p7 | 17:82692359 | AAGACAAACGCCCAG[A/G]AGGGAGAATCCAGGC | 10966 |
rs59071512 | snp | A/G | 0.245916 | 0.249967 | intron-variant | RAB40B | GRCh38.p7 | 17:82690402 | GCATGGAGTGTGCAC[A/G]TGTGTTCTCAGGGAG | 10966 |
rs59088511 | snp | A/C | | | intron-variant | RAB40B | GRCh38.p7 | 17:82679396 | ACGCCATTCTCCTGC[A/C]TCAGCCTCCCGAGTA | 10966 |
rs59127037 | snp | A/G | 0.0948562 | 0.196037 | upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82700114 | TTTGCAACACCTGTT[A/G]TTCATTGGTTGATTA | 10966 |
rs59139508 | snp | C/T | 0.040671 | 0.13668 | intron-variant | RAB40B | GRCh38.p7 | 17:82664183 | GGGGCGCTGTGCCGA[C/T]GGTGGTGGGGGAAGG | 10966 |
rs59235468 | snp | C/G | 0.33693 | 0.2344 | intron-variant | RAB40B | GRCh38.p7 | 17:82674166 | GCCAACATGGTCAAA[C/G]CCCAACTCTACTAAA | 10966 |
rs59717571 | snp | A/G | 0.138207 | 0.223612 | | | GRCh38.p7 | 17:82655338 | CCAAGGCCTCCGGGC[A/G]GCCCGTGCATTCGGT | 10966 |
rs59895598 | snp | G/T | 0.137867 | 0.223442 | intron-variant | RAB40B | GRCh38.p7 | 17:82692230 | CAGTGGGGCCCGCAC[G/T]GTCCGTGGGCTGAGG | 10966 |
rs59990353 | in-del | -/C | | | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82665905 | AAAAAAAAAAAAAAA[-/C]AAAAAAAAACTACAC | 10966 |
rs60103503 | snp | C/T | | | intron-variant | RAB40B | GRCh38.p7 | 17:82664161 | GGTGGTGGGAGGGTG[C/T]TCCCCGGGGGCGCTG | 10966 |
rs60183674 | in-del | -/C | | | intron-variant | RAB40B | GRCh38.p7 | 17:82695197 | TTTCTTTCTTTCTTT[-/C]TTTTTTTTTTTTCGA | 10966 |
rs60290410 | snp | G/T | 0.040671 | 0.13668 | intron-variant | RAB40B | GRCh38.p7 | 17:82664185 | GGCGCTGTGCCGACG[G/T]TGGTGGGGGAAGGGT | 10966 |
rs60358619 | snp | A/G | 0.0418186 | 0.138422 | upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82700413 | TGGGATTGCAGCACT[A/G]TTTTTTTTTAGAAGG | 10966 |
rs60428181 | snp | A/G | 0.0948562 | 0.196037 | upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82700356 | GCCAGGCTGGTCTTT[A/G]ACTCCTGACCTCAAG | 10966 |
rs60502332 | snp | A/G | | | intron-variant | RAB40B | GRCh38.p7 | 17:82683818 | TCCAAAAAAAAAAAA[A/G]AAAAAGAAAAGAAAA | 10966 |
rs60578904 | in-del | -/ATTT | | | intron-variant | RAB40B | GRCh38.p7 | 17:82676937 | TTTATTTATTTATTT[-/ATTT]TTTCTGAGACGGAGT | 10966 |
rs60867757 | snp | C/T | | | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82671511 | ACTCACTGACACACC[C/T]CACCCCTGTAACTCT | 10966 |
rs61133530 | snp | G/T | | | intron-variant | RAB40B | GRCh38.p7 | 17:82664151 | TGCCGATGGTGGTGG[G/T]GGGAGGGTGTTCCCC | 10966 |
rs61220947 | snp | C/G | 0.243061 | 0.249904 | intron-variant | RAB40B | GRCh38.p7 | 17:82690409 | GTGTGCACATGTGTT[C/G]TCAGGGAGCAGAGAG | 10966 |
rs61247912 | snp | A/G | 0.0836354 | 0.186609 | intron-variant | RAB40B | GRCh38.p7 | 17:82664410 | GATGGGTGCTCCCCG[A/G]GGCACTGTGCTGACA | 10966 |
rs61268931 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | RAB40B | GRCh38.p7 | 17:82685363 | GCCGTGCACTCAACT[A/G]AACGCAGATTCCTGG | 10966 |
rs61350339 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82671305 | TGACACACTTCACCC[C/T]GTAACTCTAACACAC | 10966 |
rs61354261 | snp | C/T | 0.159292 | 0.232964 | intron-variant | RAB40B | GRCh38.p7 | 17:82692882 | CCAGGATCACACAGC[C/T]GACAAAGGACTCACA | 10966 |
rs61519669 | snp | C/T | 0.0655868 | 0.168795 | intron-variant | RAB40B | GRCh38.p7 | 17:82694707 | GAAGGGAAGGACAAG[C/T]CTCCACATGGGGAAA | 10966 |
rs61726352 | snp | C/G | | | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82671836 | GTACTCACTGACACA[C/G]CCCACCCCGTCACTC | 10966 |
rs61726362 | snp | C/T | | | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82671838 | ACTCACTGACACACC[C/T]CACCCCGTCACTCTA | 10966 |
rs61728522 | snp | C/T | | | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82671786 | ACCCACTGACACAGC[C/T]CACCCCGTAACTCTA | 10966 |
rs61728789 | snp | A/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82671746 | CCACCCCTGTAACTC[A/T]AACACACACTCACAT | 10966 |
rs61728825 | in-del | -/TGCT | | | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82671761 | TAACACACACTCACA[-/TGCT]CCCTGTACCCACTGA | 10966 |
rs61728826 | in-del | -/A | | | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82671750 | CCCTGTAACTCTAAC[-/A]CACACTCACATGCTC | 10966 |
rs61735047 | snp | C/T | 0.0555102 | 0.157079 | missense | RAB40B | GRCh38.p7 | 17:82658041 | AAGGACTTGAGGTGG[C/T]TTCTTAAGGCAATGG | 10966 |
rs61758746 | snp | A/C/G | 3.29675e-05 | 0.00405991 | missense | RAB40B | GRCh38.p7 | 17:82658086 | TCCACCAGGTGCACC[A/C/G]GCGTGCAGGACACGA | 10966 |
rs61758747 | snp | C/T | 0.00371697 | 0.0429496 | synonymous-codon | RAB40B | GRCh38.p7 | 17:82658061 | TAAGGCAATGGGGAG[C/T]GGGAGCTTGTCCACC | 10966 |
rs62079718 | snp | C/G | 0.0551013 | 0.156571 | intron-variant | RAB40B | GRCh38.p7 | 17:82660253 | TTCATGTGTGCACAT[C/G]CATGCACATAAACAG | 10966 |
rs62079719 | snp | A/T | 0.5 | 0 | intron-variant | RAB40B | GRCh38.p7 | 17:82660526 | TCATGCACAGATGCA[A/T]ACACAGTGCACATAC | 10966 |
rs62079720 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | RAB40B | GRCh38.p7 | 17:82660532 | ACAGATGCATACACA[A/C/G]TGCACATACCTACAC | 10966 |
rs62079721 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RAB40B | GRCh38.p7 | 17:82660544 | ACAGTGCACATACCT[A/G]CACACACGTGTACAC | 10966 |
rs62079722 | snp | A/C | 0.416708 | 0.186302 | intron-variant, downstream-variant-500B | RAB40B | GRCh38.p7 | 17:82660593 | TCATGCCCAGATGCA[A/C]ACATACACTGCACAT | 10966 |
rs62079743 | snp | C/G | 0.0551013 | 0.156571 | intron-variant | RAB40B | GRCh38.p7 | 17:82663377 | GGCAGCAGTGCAGGA[C/G]GGATGCCCAAGAGGG | 10966 |
rs62079744 | snp | G/T | 0.0872718 | 0.189788 | intron-variant, upstream-variant-2KB | RAB40B, MIR4525 | GRCh38.p7 | 17:82669933 | AGCAATCCTCAAAGA[G/T]AATTTTGGAAATATT | 10966 |
rs62079746 | snp | C/T | 0.0894459 | 0.191631 | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82670828 | GTGAGGTACCGCGCC[C/T]GGCTTCCTGATGGTC | 10966 |
rs62079747 | snp | A/G | 0.0952156 | 0.196321 | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82670943 | ACGATCCACGATGTT[A/G]GACCCTGGCCCACCC | 10966 |
rs62079748 | snp | A/C | | | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82671792 | TGACACAGCTCACCC[A/C]GTAACTCTAACACAC | 10966 |
rs62079749 | snp | C/T | | | intron-variant | RAB40B | GRCh38.p7 | 17:82672210 | ACTCACTGACACACC[C/T]CACCCCTGTAACTCT | 10966 |
rs62079750 | snp | C/T | | | intron-variant | RAB40B | GRCh38.p7 | 17:82672267 | ACTCACTGACACACC[C/T]CACCCCGTAACTCTA | 10966 |
rs62079751 | snp | C/T | | | intron-variant | RAB40B | GRCh38.p7 | 17:82672273 | TGACACACCCCACCC[C/T]GTAACTCTAACACAC | 10966 |
rs62079752 | snp | C/T | 0.5 | 0 | intron-variant | RAB40B | GRCh38.p7 | 17:82672303 | CAAACTCACACGCTC[C/T]CTGTACTGACACACC | 10966 |
rs62079753 | snp | A/C | | | intron-variant | RAB40B | GRCh38.p7 | 17:82683804 | AGCAAGACCCTGTTT[A/C]CAAAAAAAAAAAAAA | 10966 |
rs62079754 | snp | A/C | 0.5 | 0 | intron-variant | RAB40B | GRCh38.p7 | 17:82683806 | CAAGACCCTGTTTCC[A/C]AAAAAAAAAAAAAAA | 10966 |
rs62636907 | snp | C/G | | | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82671784 | GTACCCACTGACACA[C/G]CTCACCCCGTAACTC | 10966 |
rs62638280 | snp | A/T | | | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82671756 | AACTCTAACACACAC[A/T]CACATGCTCCCTGTA | 10966 |
rs62638692 | snp | A/G | 0.00751647 | 0.0608419 | synonymous-codon | RAB40B | GRCh38.p7 | 17:82658013 | CCTGGCATTCAGGCC[A/G]TTGGCCATCGAGAAG | 10966 |
rs62641989 | snp | C/T | 0.357451 | 0.225731 | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82672073 | TCTAACACACACACA[C/T]GCTCCCTGTACTCAC | 10966 |
rs62641990 | snp | C/T | 0.444444 | 0.157135 | intron-variant | RAB40B | GRCh38.p7 | 17:82672185 | TAACACACACTCACA[C/T]GCTCCCTGTACTCAC | 10966 |
rs62644906 | snp | C/T | 0.498982 | 0.0225409 | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82672098 | ACTCACTGACACACC[C/T]CACCCCTGTAACTCT | 10966 |
rs66478872 | in-del | -/T | 0 | 0 | | | GRCh38.p7 | 17:82655968 | TTTTTTTTTTTTTTT[-/T]AGATGGAGTTTCACT | 10966 |
rs66693031 | snp | A/G | 0.145642 | 0.227177 | upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82699811 | CGAGGTCTGCCCTTC[A/G]CTCTGAGGGTCTCAC | 10966 |
rs66713002 | in-del | -/AC | | | intron-variant, downstream-variant-500B | RAB40B | GRCh38.p7 | 17:82660688 | CCTGCACACACATGT[-/AC]ACACACACACACACA | 10966 |
rs66722562 | in-del | -/CA | 0.5 | 0 | intron-variant, downstream-variant-500B | RAB40B | GRCh38.p7 | 17:82660705 | ACACACACACACACA[-/CA]GGCACTCATGCACAG | 10966 |
rs66904866 | snp | G/T | 0.16028 | 0.233346 | intron-variant | RAB40B | GRCh38.p7 | 17:82697018 | GCGCCTGGGGACAGG[G/T]AGAGACGCAGGCTCC | 10966 |
rs67510470 | in-del | -/CCCGCACGGTCCGTGGGCTGAGGTGACAGGCAGAGCAGTGGGGCCCGCACGGTCCGTGGGCTGAGGTGACAGGCAGAGCAGTGGGG | 0 | 0 | intron-variant | RAB40B | GRCh38.p7 | 17:82692180 | GGCAGAGCAGTGGGG[lengthTooLong]TCCACATAGTCTGTG | 10966 |
rs67994207 | in-del | -/CA | | | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82671272 | CTAACACACACAGTC[-/CA]ACACATCCTGTACTC | 10966 |
rs71168129 | in-del | -/ACACCTGCCACC | 0 | 0 | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82666044 | ACTGCACCTGCCACC[-/ACACCTGCCACC]GCACCTGCCACCGCA | 10966 |
rs71168131 | in-del | -/T | 0 | 0 | intron-variant, upstream-variant-2KB | RAB40B, MIR4525 | GRCh38.p7 | 17:82670203 | TTTTTTTTTTTTTTT[-/T]GAGACAGAGTCTCGC | 10966 |
rs71168136 | in-del | -/A/AA/G | | | intron-variant | RAB40B | GRCh38.p7 | 17:82684238 | AAAAAAAAAAAAAAA[-/A/AA/G]TTACAATGAGATACC | 10966 |
rs71370230 | snp | C/T | 0 | 0 | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82672020 | TCTAACACACACACA[C/T]GCTCCCTGTACTCAC | 10966 |
rs71376517 | snp | A/G | 0.5 | 0 | intron-variant | RAB40B | GRCh38.p7 | 17:82686247 | CTCCTAAGCAGCTGA[A/G]ATAACAGGCACCTGC | 10966 |
rs71376518 | snp | A/G | 0.5 | 0 | intron-variant | RAB40B | GRCh38.p7 | 17:82690207 | ATGTGTGTCCAGGGG[A/G]AGATCTGCAGAATTG | 10966 |
rs71376519 | snp | C/T | 0.5 | 0 | intron-variant | RAB40B | GRCh38.p7 | 17:82690232 | GAATTGGAGGGAGCA[C/T]GGAGTGTGCACACGT | 10966 |
rs71376520 | snp | A/G | 0.243061 | 0.249904 | intron-variant | RAB40B | GRCh38.p7 | 17:82690412 | TGCACATGTGTTCTC[A/G]GGGAGCAGAGAGTGT | 10966 |
rs71376521 | snp | C/T | 0.5 | 0 | intron-variant | RAB40B | GRCh38.p7 | 17:82690429 | GGAGCAGAGAGTGTG[C/T]ATGTGTGTCCAGGGG | 10966 |
rs71376523 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RAB40B | GRCh38.p7 | 17:82690431 | AGCAGAGAGTGTGTA[C/T]GTGTGTCCAGGGGAA | 10966 |
rs71376524 | snp | A/G | 0.5 | 0 | intron-variant | RAB40B | GRCh38.p7 | 17:82690443 | GTATGTGTGTCCAGG[A/G]GAAGATCTGCAGAAT | 10966 |
rs71376525 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RAB40B | GRCh38.p7 | 17:82690470 | GAATTGGAGGGAGCA[C/T]GGAGTGTGCACGTGT | 10966 |
rs71376526 | snp | C/T | 0.5 | 0 | intron-variant | RAB40B | GRCh38.p7 | 17:82690481 | AGCATGGAGTGTGCA[C/T]GTGTGTTGCCGGGGA | 10966 |
rs72051438 | in-del | -/AT | 0.319376 | 0.240181 | intron-variant | RAB40B | GRCh38.p7 | 17:82694559 | TACATACACACACAC[-/AT]ACACACACACACCTG | 10966 |
rs72634338 | snp | A/G | 0.0387552 | 0.1337 | intron-variant | RAB40B | GRCh38.p7 | 17:82694957 | TCTAGGTGATTAAGA[A/G]GGACAGCACAATGAA | 10966 |
rs72853015 | snp | A/G | 0.216349 | 0.247725 | intron-variant, utr-variant-3-prime | RAB40B | GRCh38.p7 | 17:82662161 | GACCACCCTCAGCAC[A/G]AGAGAGAAGGGCCTG | 10966 |
rs72853019 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | RAB40B | GRCh38.p7 | 17:82662863 | TGGGAGAGGGCACGC[A/G]CCAGCCCTGATGCAA | 10966 |
rs72853024 | snp | G/T | 0.326976 | 0.237854 | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82665853 | GCCTGGGCGACAGAG[G/T]GAGACTCTGTATCAA | 10966 |
rs72853027 | snp | C/T | 0.207559 | 0.246371 | intron-variant, downstream-variant-500B, utr-variant-5-prime | RAB40B, MIR4525 | GRCh38.p7 | 17:82668179 | GACAGGGTAGCTCTC[C/T]GCAGCTGGTCATCCC | 10966 |
rs72853041 | snp | C/G | | | intron-variant | RAB40B | GRCh38.p7 | 17:82679755 | AGCACAGGGCAGGGG[C/G]CAGCCTCCACCAAGC | 10966 |
rs73357156 | snp | C/T | 0.306431 | 0.243548 | intron-variant | RAB40B | GRCh38.p7 | 17:82662797 | GGCCCACTGGGCAGC[C/T]GGGGTCAGGGAGGCG | 10966 |
rs73357159 | snp | C/T | 0.302435 | 0.244439 | intron-variant | RAB40B | GRCh38.p7 | 17:82662923 | GGGCAGGCGTGGGGC[C/T]GAGTGCGGCCTTTGG | 10966 |
rs73357173 | snp | A/G | 0.277867 | 0.248442 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | RAB40B, MIR4525 | GRCh38.p7 | 17:82670096 | CATATTTGTCTTTCC[A/G]GAGATTAATCCACTG | 10966 |
rs73357180 | snp | C/T | 0.294832 | 0.245947 | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82670901 | GTTTTCATGGAGTCA[C/T]GGATGCTCACAGTCT | 10966 |
rs73357200 | snp | C/T | 0.254664 | 0.249956 | intron-variant | RAB40B | GRCh38.p7 | 17:82676080 | TTCGTCCATCTCCCC[C/T]GGGTCTCCGTTTCCC | 10966 |
rs73359105 | snp | C/G | 0.245346 | 0.249957 | intron-variant | RAB40B | GRCh38.p7 | 17:82678160 | CCATCTGTGTGTTTG[C/G]TCTTTCGTTATTTAC | 10966 |
rs73359110 | snp | C/T | 0.170733 | 0.237101 | intron-variant | RAB40B | GRCh38.p7 | 17:82683308 | TATAAAAGAAAAAAA[C/T]TGATCAACTGGATTT | 10966 |
rs73359123 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | RAB40B | GRCh38.p7 | 17:82688065 | CAATAAGCCAGACCC[A/G]GTTTCAAAAAAGACT | 10966 |
rs73359135 | snp | A/T | 0.320096 | 0.239972 | intron-variant | RAB40B | GRCh38.p7 | 17:82694535 | AGACTACATCTAAGA[A/T]AAAAAAAATACATAC | 10966 |
rs73359138 | snp | C/G | 0.160609 | 0.233472 | intron-variant | RAB40B | GRCh38.p7 | 17:82697564 | CAGGCTGGGCTCCTT[C/G]CACAGCCTCAGGGTC | 10966 |
rs73359141 | snp | A/G | 0.0352966 | 0.128072 | upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82700630 | TACCTTCTTTTGCTC[A/G]CTCCCCACCTACACA | 10966 |
rs74002924 | snp | C/T | 0.314544 | 0.241524 | intron-variant, missense | RAB40B | GRCh38.p7 | 17:82662465 | GCCGGCCTCCTGGGC[C/T]GCTGCCACCCTGAAG | 10966 |
rs74002927 | snp | G/T | 0.263998 | 0.249614 | intron-variant | RAB40B | GRCh38.p7 | 17:82664607 | TGCAGCTAACAGGAC[G/T]CTGGAAGTCTCACGT | 10966 |
rs74002940 | snp | A/G/T | 0.0123036 | 0.0774623 | intron-variant | RAB40B | GRCh38.p7 | 17:82697479 | CGGCTGCCCTCCTCC[A/G/T]CCCAGGACTCAGAGC | 10966 |
rs74193995 | snp | A/G | 0.298398 | 0.245271 | intron-variant | RAB40B | GRCh38.p7 | 17:82660448 | CACAGGCACTCATGC[A/G]GATGCACGCATACAC | 10966 |
rs74208771 | snp | A/C | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82671535 | TAACTCTAACACACA[A/C]ACTCACACGCTCCCT | 10966 |
rs74456423 | snp | C/T | | | intron-variant | RAB40B | GRCh38.p7 | 17:82673322 | ATCTAAATCTGCTCT[C/T]GGTACCTGCAAACAT | 10966 |
rs74532348 | snp | C/G | 0.0528381 | 0.153711 | intron-variant | RAB40B | GRCh38.p7 | 17:82687173 | GAACCCGTGAGTGTA[C/G]CACAGTGTTCTCTCC | 10966 |
rs74608927 | snp | A/G | 0 | 0 | intron-variant | RAB40B | GRCh38.p7 | 17:82664064 | GGTGCTGGGCAGATG[A/G]TGGTGGGGGGAGCTT | 10966 |
rs74704236 | snp | A/C | 0.0948562 | 0.196037 | upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82699796 | CAAGGGTTGCCAGGC[A/C]GAGGTCTGCCCTTCG | 10966 |
rs74812537 | snp | A/G | 0.0741063 | 0.177655 | intron-variant | RAB40B | GRCh38.p7 | 17:82692610 | GGGTGGGGGGCATCC[A/G]ACTGAAAAAAGTGTG | 10966 |
rs74815239 | snp | A/T | | | upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82699215 | CCCCCGCAGGCCGCC[A/T]CGCCGGAGGAGTCCC | 10966 |
rs74923719 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | RAB40B | GRCh38.p7 | 17:82676499 | CCACACACCAATTCC[A/G]TGGCGAGTCTCTCGG | 10966 |
rs74925893 | snp | C/T | 0.0788843 | 0.182262 | intron-variant | RAB40B | GRCh38.p7 | 17:82694866 | CAAAGATAAAGACCA[C/T]GGGCAGACATTCTCA | 10966 |
rs74940854 | snp | A/C/G | 0.158302 | 0.232576 | intron-variant | RAB40B | GRCh38.p7 | 17:82685201 | AAGCAGAGAGGAAGC[A/C/G]GGAGAGGAAAGGAAT | 10966 |
rs75177948 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RAB40B | GRCh38.p7 | 17:82688207 | TTAAACTTTCTGTAG[A/G]GACGAGGTTTCCCTA | 10966 |
rs75272178 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RAB40B | GRCh38.p7 | 17:82695086 | AGCAAGGGCTATAAA[C/T]CTGGACAATATAAAA | 10966 |
rs75436053 | snp | A/T | 0 | 0 | intron-variant | RAB40B | GRCh38.p7 | 17:82673462 | ATCCTTCCCTCTCTT[A/T]AGCTGACTCCTCTTT | 10966 |
rs75451198 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | RAB40B | GRCh38.p7 | 17:82692497 | GACAGAGTCTGACCC[A/G]GGGCACACACACAAG | 10966 |
rs75501098 | snp | C/G | 0.0130921 | 0.0798413 | intron-variant | RAB40B | GRCh38.p7 | 17:82663523 | AGCTGGCCCCAAGGT[C/G]GGGGTGCTGGGGGAG | 10966 |
rs75721851 | snp | A/G | 0.109814 | 0.206997 | intron-variant | RAB40B | GRCh38.p7 | 17:82681725 | ATGCAAGGTTGGTTC[A/G]ACCTTTGAAAATCTA | 10966 |
rs75726826 | snp | C/T | 0.0744748 | 0.178019 | intron-variant | RAB40B | GRCh38.p7 | 17:82696354 | CACAAACATTCTGTG[C/T]GTGACCCTTCTCACA | 10966 |
rs75751528 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | RAB40B | GRCh38.p7 | 17:82675719 | AGGGAGCTCTTGGAT[C/G]CTTCACTCATCCCAT | 10966 |
rs75928467 | snp | C/T | | | intron-variant | RAB40B | GRCh38.p7 | 17:82680624 | CAGTGTAGTTCATTT[C/T]ACTGTTTATGTATAT | 10966 |
rs75959248 | snp | A/G | 0.0696718 | 0.173152 | intron-variant, upstream-variant-2KB | RAB40B, MIR4525 | GRCh38.p7 | 17:82670011 | TCTATTTTCGAATGC[A/G]GAGATAACTCCAGCT | 10966 |
rs75995169 | snp | G/T | 0 | 0 | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82670550 | TTTTTTTTTTTTTTT[G/T]TTGAGACGGAGTCTT | 10966 |
rs76101796 | snp | C/T | 0.021333 | 0.101051 | intron-variant | RAB40B | GRCh38.p7 | 17:82695164 | TGGAGTGTGGAGTTA[C/T]GAACGCCCTCATCTT | 10966 |
rs76304814 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82700429 | TTTTTTTTTAGAAGG[A/G]AGGTCAGAGGAAGAA | 10966 |
rs76398290 | snp | A/T | 0 | 0 | intron-variant | RAB40B | GRCh38.p7 | 17:82674489 | ACAAAAAAAAAAAAA[A/T]TTAGCCGGGTGTGGT | 10966 |
rs76444460 | snp | A/G | 0.00199481 | 0.0315187 | utr-variant-3-prime | RAB40B | GRCh38.p7 | 17:82657316 | TAATCCCAAAATGTA[A/G]TAAATAACTAGCAAA | 10966 |
rs76555211 | snp | G/T | 0.5 | 0 | intron-variant | RAB40B | GRCh38.p7 | 17:82688650 | ACAAATAGTTTTGTT[G/T]GGGCCGGGCGTGGTG | 10966 |
rs76692969 | snp | A/G | 0.5 | 0 | intron-variant, utr-variant-3-prime | RAB40B | GRCh38.p7 | 17:82661890 | AGACTCTGTCTCAGA[A/G]AAAAAAAAAAAAAAA | 10966 |
rs76729625 | snp | C/T | 0.5 | 0 | intron-variant | RAB40B | GRCh38.p7 | 17:82672351 | ACACACACACTCACA[C/T]GCTCCCTGTACCCAC | 10966 |
rs76819354 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82666654 | ACTTCTAGCGCTTCC[A/G]GATGAGCACCAGGTC | 10966 |
rs76891339 | snp | A/G | 0.0107246 | 0.0724382 | | | GRCh38.p7 | 17:82656012 | GGGGTGCAGTGGTAC[A/G]ATCTCGGCTCACTGC | 10966 |
rs76952543 | snp | A/T | 0.0759472 | 0.179459 | intron-variant | RAB40B | GRCh38.p7 | 17:82696239 | ATTACAAAGCATTGG[A/T]CCATTGTTTTGGTTC | 10966 |
rs76988187 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | RAB40B | GRCh38.p7 | 17:82674748 | GCGTCACTCTGGCAT[C/T]GCAGGCAACGTTCGT | 10966 |
rs77000066 | in-del | -/TTT | | | intron-variant | RAB40B | GRCh38.p7 | 17:82685807 | CTCTTCTTCTTCTTC[-/TTT]TTTTTTTTTTTTGAG | 10966 |
rs77032026 | snp | G/T | 0 | 0 | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82665269 | TCTTCTTTTTTTTTT[G/T]TGAGACAGAGTTTCT | 10966 |
rs77106756 | snp | C/T | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82672032 | ACACGCTCCCTGTAC[C/T]CACTGACACACCCCA | 10966 |
rs77138975 | snp | A/C | 0.0193772 | 0.0965046 | intron-variant | RAB40B | GRCh38.p7 | 17:82697185 | CTCACCCCGTCCCCT[A/C]AGCTGAGGTGTGGCC | 10966 |
rs77352777 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB | RAB40B, MIR4525 | GRCh38.p7 | 17:82670021 | AATGCGGAGATAACT[C/T]CAGCTTTGATATGTC | 10966 |
rs77381026 | snp | C/T | | | upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82699216 | CCCCGCAGGCCGCCT[C/T]GCCGGAGGAGTCCCT | 10966 |
rs77467263 | snp | A/C | 0.0744748 | 0.178019 | intron-variant, utr-variant-5-prime | RAB40B | GRCh38.p7 | 17:82696544 | AGACCCCGAGGGCAC[A/C]GTGCAGACAAAGCCC | 10966 |
rs77471570 | snp | C/T | 0.0948562 | 0.196037 | upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82700716 | CACCCAGCAGTCCAG[C/T]AGTGTTCACGGTGGG | 10966 |
rs77819445 | snp | C/T | 0.110167 | 0.207236 | intron-variant | RAB40B | GRCh38.p7 | 17:82676674 | GCTGTGTCGCCCAGG[C/T]TGGAATGCAATGGCG | 10966 |
rs78107747 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82671147 | CCACCCCTGTAACTC[C/T]AACACACACAGTCAC | 10966 |
rs78145617 | snp | C/G | 0.077417 | 0.180873 | upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82700613 | ACCTAGTGAGGAAAG[C/G]GTACCTTCTTTTGCT | 10966 |
rs78351073 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RAB40B | GRCh38.p7 | 17:82677554 | GCCTGTGTTGTGGCT[C/T]TCCATCAGCCCTGAC | 10966 |
rs78677890 | snp | A/G | 0.221439 | 0.248363 | intron-variant, upstream-variant-2KB | RAB40B, MIR4525 | GRCh38.p7 | 17:82669855 | CAGCCGTCAGCAATG[A/G]ACACACTGAGCGTGA | 10966 |
rs78764686 | snp | A/G | 0.000197974 | 0.00994725 | synonymous-codon | RAB40B | GRCh38.p7 | 17:82658100 | CGGCGTGCAGGACAC[A/G]ACCGCCCGGCAGCAG | 10966 |
rs78892211 | snp | G/T | 0.5 | 0 | intron-variant | RAB40B | GRCh38.p7 | 17:82678895 | TTTTTTTTTTTTTTT[G/T]TTTTTGAGACGGAGT | 10966 |
rs78908709 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | RAB40B | GRCh38.p7 | 17:82678215 | TACGTTTTGGTCCAC[A/G]AGAAACTAAGAAACA | 10966 |
rs78926345 | snp | A/T | 0.0759472 | 0.179459 | intron-variant, utr-variant-5-prime | RAB40B | GRCh38.p7 | 17:82696419 | ACACTGTCAACCGTC[A/T]GCTCCCCCAAAACAC | 10966 |
rs78964815 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82671491 | CACACTCACATGCTC[C/T]CTGTACTCACTGACA | 10966 |
rs79003395 | snp | G/T | 0.0520825 | 0.152737 | intron-variant | RAB40B | GRCh38.p7 | 17:82686602 | AGAACGCCGAGGGCT[G/T]CCAGCAGCACCCCAG | 10966 |
rs79085870 | snp | A/G | 0.0707826 | 0.174302 | intron-variant | RAB40B | GRCh38.p7 | 17:82688295 | CAGGTGTGAGCCACC[A/G]TGCCTGGCCCTCATG | 10966 |
rs79143585 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | RAB40B | GRCh38.p7 | 17:82693345 | GAATTTCGCATAGAC[A/G]TATGAAAAGGTGCTC | 10966 |
rs79285929 | snp | C/G | | | intron-variant | RAB40B | GRCh38.p7 | 17:82664729 | GGGGCCCTGCCTGCG[C/G]CCTCCCGCACCCGGG | 10966 |
rs79361730 | snp | G/T | 0.5 | 0 | intron-variant | RAB40B | GRCh38.p7 | 17:82678897 | TTTTTTTTTTTTTTT[G/T]TTTGAGACGGAGTCT | 10966 |
rs79500370 | snp | A/G | 0 | 0 | intron-variant | RAB40B | GRCh38.p7 | 17:82674653 | AAAAAAAAAAAAAAA[A/G]AAAAGAAAAGAAAAG | 10966 |
rs79513727 | in-del | -/CACA | | | intron-variant, downstream-variant-500B | RAB40B | GRCh38.p7 | 17:82660703 | ACACACACACACACA[-/CACA]GGCACTCATGCACAG | 10966 |
rs79533384 | in-del | -/AAA | | | intron-variant | RAB40B | GRCh38.p7 | 17:82695557 | ATTAAAAAAAAAAAA[-/AAA]CATGGCCAGGTGCTG | 10966 |
rs79533931 | snp | C/T | | | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82671145 | CCCCACCCCTGTAAC[C/T]CCAACACACACAGTC | 10966 |
rs79607652 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | RAB40B | GRCh38.p7 | 17:82685780 | GAATGTGACCTGATT[C/T]GGAAACAGGATCTCT | 10966 |
rs79672366 | snp | C/T | 0.00105581 | 0.0229519 | synonymous-codon | RAB40B | GRCh38.p7 | 17:82658103 | CGTGCAGGACACGAC[C/T]GCCCGGCAGCAGAGG | 10966 |
rs79751177 | snp | C/G | 0.206029 | 0.246103 | intron-variant | RAB40B | GRCh38.p7 | 17:82664800 | GGCTCGCATCACCCT[C/G]GCCCAGGGGGCTCCC | 10966 |
rs79808127 | snp | C/T | 0.121022 | 0.21416 | intron-variant, downstream-variant-500B | RAB40B | GRCh38.p7 | 17:82660884 | ATACGTAAGCTTAAC[C/T]GCCTTGTCCTCCAAT | 10966 |
rs79887293 | snp | A/G | 0.5 | 0 | intron-variant | RAB40B | GRCh38.p7 | 17:82678687 | ACCGGAAAGCCAAAA[A/G]GCAGACTGGCGGTCC | 10966 |
rs79922403 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | RAB40B | GRCh38.p7 | 17:82673821 | TCTCAATTTTGGGGA[A/G]CTTTCTTGGATAATT | 10966 |
rs79948093 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | RAB40B | GRCh38.p7 | 17:82684347 | TGACGGGGATGCAAA[C/T]GGTGTGGTCAGTGTG | 10966 |
rs79957862 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | RAB40B, MIR4525 | GRCh38.p7 | 17:82669845 | CCAAGTCCTGCAGCC[A/G]TCAGCAATGAACACA | 10966 |
rs79963701 | snp | C/T | 0 | 0 | intron-variant | RAB40B | GRCh38.p7 | 17:82686106 | CGCACCCAGCCTTCT[C/T]TTTTTTTTTTTTTTT | 10966 |
rs80060027 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | RAB40B | GRCh38.p7 | 17:82689195 | CAAATGCACCCAGCG[C/T]GGAGCAGCCTGCACT | 10966 |
rs80075184 | snp | A/C | 0.0115144 | 0.0749975 | intron-variant | RAB40B | GRCh38.p7 | 17:82693772 | TTCACATAACGGGGG[A/C]CAGAGACACAGTCAC | 10966 |
rs80151141 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | RAB40B | GRCh38.p7 | 17:82673845 | GATAATTTGTTCTCT[A/C]CTTCTGGGATGTGAT | 10966 |
rs80233511 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, missense | RAB40B | GRCh38.p7 | 17:82662560 | CAGGCAGAAGACCCA[C/G]TTGTGGGCACCAGGA | 10966 |
rs80267471 | snp | C/G | 0.0142736 | 0.0832652 | intron-variant | RAB40B | GRCh38.p7 | 17:82667013 | GGGAGAAGCAGCGCC[C/G]AGGCTCGCACCAGAC | 10966 |
rs80282627 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | RAB40B | GRCh38.p7 | 17:82674826 | CGAACCCCAGAATGA[A/T]CCTAACACAGAAGAA | 10966 |
rs80301250 | snp | A/G | 0.0479149 | 0.147179 | intron-variant, upstream-variant-2KB | RAB40B, MIR4525 | GRCh38.p7 | 17:82669969 | TCCCTTGGCAGGCAC[A/G]AGGCAATGAACGAAT | 10966 |
rs80325314 | snp | A/G | 0.5 | 0 | intron-variant | RAB40B | GRCh38.p7 | 17:82674651 | TTAAAAAAAAAAAAA[A/G]AGAAAAGAAAAGAAA | 10966 |
rs80343211 | snp | C/T | 0.5 | 0 | intron-variant | RAB40B | GRCh38.p7 | 17:82672356 | CACACTCACACGCTC[C/T]CTGTACCCACTGACA | 10966 |
rs111171459 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82671543 | ACACACACACTCACA[C/T]GCTCCCTGTACTCAC | 10966 |
rs111171460 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82671548 | CACACTCACACGCTC[C/T]CTGTACTCACTGACA | 10966 |
rs111171461 | snp | C/T | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82671773 | ACATGCTCCCTGTAC[C/T]CACTGACACAGCTCA | 10966 |
rs111171462 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82671894 | ACCCACTGACACACC[C/T]CACCCCTGTAACTCT | 10966 |
rs111174345 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82671360 | CCTCACCCCTGTAAC[C/T]CTAACACACACACTC | 10966 |
rs111174349 | snp | C/T | 0 | 0 | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82671924 | TAACACACACTCACA[C/T]GCTCCCTGTACCCAC | 10966 |
rs111174351 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82672078 | CACACACACATGCTC[C/T]CTGTACTCACTGACA | 10966 |
rs111174352 | snp | C/G | 0.5 | 0 | intron-variant | RAB40B | GRCh38.p7 | 17:82672104 | TGACACACCCCACCC[C/G]TGTAACTCTAACACA | 10966 |
rs111174354 | snp | C/T | 0.5 | 0 | intron-variant | RAB40B | GRCh38.p7 | 17:82672190 | CACACTCACATGCTC[C/T]CTGTACTCACTGACA | 10966 |
rs111211192 | snp | C/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82671348 | TGTACTGACACACCT[C/G]ACCCCTGTAACTCTA | 10966 |
rs111218941 | snp | C/T | | | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82672045 | ACTCACTGACACACC[C/T]CACCCCTGTAACTCT | 10966 |
rs111219114 | snp | A/T | | | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82671495 | CTCACATGCTCCCTG[A/T]ACTCACTGACACACC | 10966 |
rs111235911 | in-del | -/ACAC | 0.5 | 0 | intron-variant, downstream-variant-500B | RAB40B | GRCh38.p7 | 17:82660688 | CCTGCACACACATGT[-/ACAC]ACACACACACACACA | 10966 |
rs111264297 | snp | C/T | 0.5 | 0 | intron-variant | RAB40B | GRCh38.p7 | 17:82673930 | CATCTCTCTCTCTTT[C/T]TCCCAGCATTCTGGG | 10966 |
rs111272491 | snp | A/G | 0.5 | 0 | intron-variant | RAB40B | GRCh38.p7 | 17:82663179 | CTGTGCAGCAGGAAG[A/G]GTCGGGGCGCTTGGG | 10966 |
rs111276855 | snp | C/T | 0.5 | 0 | | | GRCh38.p7 | 17:82656235 | ACAGGTGTGAGCCAT[C/T]ACACCCAGCTGGGTC | 10966 |
rs111294198 | snp | A/G | 0.00377437 | 0.0432775 | utr-variant-3-prime | RAB40B | GRCh38.p7 | 17:82657738 | CATCACACGGAAGGC[A/G]TCGCACACATTCGCA | 10966 |
rs111345343 | snp | C/T | 0.5 | 0 | upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82699689 | GTGTGCGTGCGCTTG[C/T]TTGTGCATCCATGCA | 10966 |
rs111359581 | snp | A/G | 0.154993 | 0.231244 | intron-variant | RAB40B | GRCh38.p7 | 17:82683819 | CCAAAAAAAAAAAAA[A/G]AAAAGAAAAGAAAAG | 10966 |
rs111361249 | snp | A/G | 0.5 | 0 | intron-variant | RAB40B | GRCh38.p7 | 17:82698154 | CGCTGCGCGCAGACT[A/G]CGGAGAAGGATGGAG | 10966 |
rs111391487 | snp | A/C | 0.0387552 | 0.1337 | intron-variant | RAB40B | GRCh38.p7 | 17:82664381 | CCGGGGGCGCTGTGC[A/C]GATGGTGGTGGGGGA | 10966 |
rs111441332 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RAB40B | GRCh38.p7 | 17:82687535 | AAGAAGTTGAGATAC[A/G]TAACCCACATAAAGT | 10966 |
rs111487914 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82671718 | TCACACACCCTGTAC[C/T]CACTGACACACCCCA | 10966 |
rs111534887 | snp | A/G | 0.5 | 0 | intron-variant | RAB40B | GRCh38.p7 | 17:82690463 | ATCTGCAGAATTGGA[A/G]GGAGCATGGAGTGTG | 10966 |
rs111549422 | snp | G/T | 0.258565 | 0.249853 | missense | RAB40B | GRCh38.p7 | 17:82657909 | TTTTTGGGGGGGCTC[G/T]GGGGGGGGCGGACGA | 10966 |
rs111580573 | snp | A/G | 0.046775 | 0.145601 | intron-variant | RAB40B | GRCh38.p7 | 17:82690337 | TGTGTGTTCCTGGGA[A/G]CAGAGAGTGTGTACG | 10966 |
rs111619662 | snp | A/C | 0.5 | 0 | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82670980 | CTGTCTCCCTTCCCC[A/C]TTTTAATCCTTTAAA | 10966 |
rs111622180 | snp | A/G | 0.079617 | 0.182947 | intron-variant, utr-variant-3-prime | RAB40B | GRCh38.p7 | 17:82661959 | CAGGGATCAGTTCCC[A/G]GAGGAGGCGGCCCTG | 10966 |
rs111664585 | snp | C/T | 0.5 | 0 | intron-variant | RAB40B | GRCh38.p7 | 17:82695518 | AATAACAAGCACCTA[C/T]AGTGTTTCTCAGCGA | 10966 |
rs111679623 | snp | C/G | 0.0948562 | 0.196037 | upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82700580 | ATGTTCCAATCAGCT[C/G]TGGGTCACATGGCTA | 10966 |
rs111724693 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant, downstream-variant-500B | RAB40B, MIR4525 | GRCh38.p7 | 17:82667761 | AGCAGCACTGAGAAC[A/G]CCCGAAGCACCCGCT | 10966 |
rs111748068 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RAB40B | GRCh38.p7 | 17:82663971 | GGGTGCTCCCCGGGG[C/T]GCTGTGCCGACGGTG | 10966 |
rs111750126 | snp | C/T | 0.5 | 0 | intron-variant | RAB40B | GRCh38.p7 | 17:82663474 | GAGCTCCCCCCATCC[C/T]AAGCCAAGAGCGGGT | 10966 |
rs111816226 | snp | A/C | 0.5 | 0 | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82671135 | CACTGACACACCCCA[A/C]CCCTGTAACTCCAAC | 10966 |
rs111832707 | snp | A/G | 0.0547245 | 0.156101 | intron-variant | RAB40B | GRCh38.p7 | 17:82692235 | GGGCCCGCACGGTCC[A/G]TGGGCTGAGGTGACA | 10966 |
rs111835757 | snp | A/G | 0.5 | 0 | intron-variant, downstream-variant-500B, utr-variant-5-prime | RAB40B, MIR4525 | GRCh38.p7 | 17:82667942 | GGCATGGGCGCTGAC[A/G]GGGCACTGATGGGGC | 10966 |
rs111909290 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40B | GRCh38.p7 | 17:82683710 | ACTGGGGAAACAGGT[A/G]GGAGGATCACTTGAG | 10966 |
rs111918589 | snp | A/G | 0.0825414 | 0.185628 | intron-variant | RAB40B | GRCh38.p7 | 17:82674246 | TCAGGAGGCTGAGGC[A/G]GGAGAGTCACTGAGG | 10966 |
rs111927417 | snp | C/T | 0.0948562 | 0.196037 | upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82699665 | CTGCTTCTATGCATG[C/T]GCTCCTATGTGTGCG | 10966 |
rs111927470 | snp | A/G | 0.0748431 | 0.178382 | intron-variant | RAB40B | GRCh38.p7 | 17:82693854 | TTGGGAGGCCGAGGC[A/G]GGCAGATCACCTTAG | 10966 |
rs111938469 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | RAB40B | GRCh38.p7 | 17:82695753 | TCTCAACTTCTTACT[A/G]TTTTTCAGAATATCT | 10966 |
rs111946258 | snp | A/G | 0.221737 | 0.248397 | | | GRCh38.p7 | 17:82656029 | TCTCGGCTCACTGCA[A/G]CCCCTGCCTCCCAGG | 10966 |
rs111968045 | snp | A/T | | | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82671812 | CTCTAACACACACAC[A/T]CACACCCTGTACTCA | 10966 |
rs111994804 | snp | A/G | 0.0788843 | 0.182262 | intron-variant | RAB40B | GRCh38.p7 | 17:82695486 | TGAGCCACTGCGCCC[A/G]GCTGCCCTCACCTTT | 10966 |
rs112010542 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | RAB40B | GRCh38.p7 | 17:82695209 | TTTCTTTTTTTTTTT[C/T]CGAGACAAAATCTCA | 10966 |
rs112012746 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RAB40B | GRCh38.p7 | 17:82680117 | GGCTGGCCCGTCCTG[C/T]TCAGACCGGAGGCCT | 10966 |
rs112014024 | snp | A/G | 0.122411 | 0.214991 | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82670574 | GAGTCTTACTCTGTC[A/G]CCCAGGCTGGAGTGC | 10966 |
rs112105623 | snp | A/C | | | intron-variant | RAB40B | GRCh38.p7 | 17:82694441 | GGAGGTTGAAGCAGG[A/C]GAATCACTTGAACCT | 10966 |
rs112153836 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | RAB40B | GRCh38.p7 | 17:82676017 | CTGGTAAAGCACAGA[C/T]GCTGCAGCCTGGGGC | 10966 |
rs112160580 | snp | C/T | 0.0539704 | 0.155153 | intron-variant | RAB40B | GRCh38.p7 | 17:82684829 | TGTCAAAACTCAAGA[C/T]GGGGCCAGGCACGGT | 10966 |
rs112179385 | snp | A/G | 0.5 | 0 | intron-variant | RAB40B | GRCh38.p7 | 17:82677625 | GAACCCTGCCTTCCC[A/G]TGTCCACCTTCCAAT | 10966 |
rs112183912 | snp | G/T | 0.00993419 | 0.0697739 | downstream-variant-500B | RAB40B | GRCh38.p7 | 17:82656932 | GGCAGGAGAATCGCT[G/T]GAACCCGGGAGGCGG | 10966 |
rs112219981 | in-del | -/A | 0.5 | 0 | intron-variant | RAB40B | GRCh38.p7 | 17:82679748 | TCACCGAGCACAGGG[-/A]CAGGGGGCAGCCTCC | 10966 |
rs112224372 | in-del | -/TA | 0.5 | 0 | intron-variant | RAB40B | GRCh38.p7 | 17:82660048 | ATGCACGCACACACA[-/TA]GTGCACGTACCTGCA | 10966 |
rs112231588 | snp | C/T | 0.0509478 | 0.151255 | intron-variant | RAB40B | GRCh38.p7 | 17:82688148 | CTTCTCTCTGCCAGC[C/T]GGGGCCCAAAACACA | 10966 |
rs112251068 | snp | A/G | 0.0528381 | 0.153711 | intron-variant | RAB40B | GRCh38.p7 | 17:82691960 | GCGTGTGTGAGGTGT[A/G]TTGCAGAACAGAAGA | 10966 |
rs112264082 | snp | A/C | 0.5 | 0 | intron-variant | RAB40B | GRCh38.p7 | 17:82676267 | TCAACAGCATCTCCC[A/C]CACACACAGTGAGGG | 10966 |
rs112303097 | snp | C/T | 0.000972145 | 0.0220256 | synonymous-codon | RAB40B | GRCh38.p7 | 17:82658085 | GTCCACCAGGTGCAC[C/T]GGCGTGCAGGACACG | 10966 |
rs112394420 | snp | A/G | 0.5 | 0 | intron-variant | RAB40B | GRCh38.p7 | 17:82686555 | GTGTGACGACAGACA[A/G]CAGGGACTGGAACGG | 10966 |
rs112519498 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40B | GRCh38.p7 | 17:82663776 | GGGCTGCCTCAACCA[C/T]GCTGCATCGGTCCCC | 10966 |
rs112584679 | snp | C/G | 0.0547245 | 0.156101 | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82665590 | TACAATTAAGGGCTG[C/G]ATGCGGTGGCTGACG | 10966 |
rs112594508 | in-del | -/GC | 0.5 | 0 | intron-variant | RAB40B | GRCh38.p7 | 17:82660040 | TGTGCACAGATGCAC[-/GC]ACACACAGTGCACGT | 10966 |
rs112673604 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RAB40B | GRCh38.p7 | 17:82673538 | TTGCACGTCTGAAAA[C/T]GTCTTTAGGCTGCCC | 10966 |
rs112781241 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-5-prime | RAB40B | GRCh38.p7 | 17:82664880 | CGCGGGGCTGTGGCC[A/G]CTGGGTGTGCCCCCG | 10966 |
rs112815054 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82666044 | ACTGCACCTGCCACC[A/G]CACCTGCCACCGCAC | 10966 |
rs112927514 | in-del | -/G | 0.5 | 0 | intron-variant | RAB40B | GRCh38.p7 | 17:82685363 | GCCGTGCACTCAACT[-/G]AACGCAGATTCCTGG | 10966 |
rs112966844 | in-del | -/TTC | 0.5 | 0 | intron-variant | RAB40B | GRCh38.p7 | 17:82679462 | ATTTTTTGTATTTTT[-/TTC]AGTAGAGACAGGGTT | 10966 |
rs112975457 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82670926 | CAGTCTGAAGTGCTG[C/T]CACGATCCACGATGT | 10966 |
rs112980143 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | RAB40B | GRCh38.p7 | 17:82692600 | TGCGGGGTGGGGGTG[A/G]GGGGCATCCGACTGA | 10966 |
rs113021661 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82671196 | GACACACCCCACCCC[C/T]GTAACTCTAACACAC | 10966 |
rs113052368 | snp | A/G | 0 | 0 | intron-variant | RAB40B | GRCh38.p7 | 17:82672299 | CACACAAACTCACAC[A/G]CTCCCTGTACTGACA | 10966 |
rs113065566 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | RAB40B | GRCh38.p7 | 17:82659860 | AACCCTCAAATGTCA[C/T]GGTGATCTGGGGACT | 10966 |
rs113068696 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | RAB40B | GRCh38.p7 | 17:82674068 | CAACCTGGCCAGGCG[C/T]GGTGGCTCGCGCCTG | 10966 |
rs113076609 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82671303 | ACTGACACACTTCAC[C/T]CCGTAACTCTAACAC | 10966 |
rs113101651 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RAB40B | GRCh38.p7 | 17:82677736 | CCCGCATCCTCTTTG[C/T]GCAGGACACTTGAAG | 10966 |
rs113111046 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RAB40B | GRCh38.p7 | 17:82674624 | AGCCTGGGCGACAGA[A/G]CAAGACTCGTCTTAA | 10966 |
rs113115085 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RAB40B | GRCh38.p7 | 17:82663966 | GCTGGGGGTGCTCCC[C/T]GGGGCGCTGTGCCGA | 10966 |
rs113212944 | snp | A/C | 0.0103295 | 0.0711199 | intron-variant | RAB40B | GRCh38.p7 | 17:82667694 | TTAGACCAAGCAACA[A/C]CAGAGCAAACTCCCC | 10966 |
rs113212961 | snp | C/T | 0.122064 | 0.214785 | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82670308 | TCGTGCCTCAGCGTC[C/T]CGTGTAGCTGGAATT | 10966 |
rs113218404 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant, synonymous-codon | RAB40B | GRCh38.p7 | 17:82662485 | CCACCCTGAAGGAGC[A/G]GAGCAGAGCCCAACC | 10966 |
rs113228947 | snp | C/G | 0.0554779 | 0.157039 | intron-variant, downstream-variant-500B | RAB40B | GRCh38.p7 | 17:82660916 | ATCCATTAAAGGATG[C/G]TAAGTTAAGCATTGT | 10966 |
rs113302493 | snp | A/G | 0.5 | 0 | intron-variant | RAB40B | GRCh38.p7 | 17:82690543 | ATCTGCAGAATTGGA[A/G]GGAGCATGGAGTGTG | 10966 |
rs113313182 | snp | C/T | | | intron-variant | RAB40B | GRCh38.p7 | 17:82682882 | GGGCACGGTGACTCA[C/T]GCCTGCAATCCCAGC | 10966 |
rs113324417 | snp | A/C | 0.5 | 0 | intron-variant | RAB40B | GRCh38.p7 | 17:82663118 | AGCGAGGGCATGGCC[A/C]CGGGGGAGTGGGGAC | 10966 |
rs113425033 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82699445 | TGTGTCCCTCTGCAG[A/G]TGTCTGCACATCTAT | 10966 |
rs113428242 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | RAB40B | GRCh38.p7 | 17:82674048 | GGACAAACTAGAAAA[C/T]GCAACAACCTGGCCA | 10966 |
rs113448856 | in-del | -/C | 0 | 0 | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82665892 | CAAGAACAACAACAA[-/C]AAAAAAAAAAAAAAA | 10966 |
rs113495099 | snp | A/C | 0.133435 | 0.221162 | intron-variant | RAB40B | GRCh38.p7 | 17:82676260 | CTCACCTTCAACAGC[A/C]TCTCCCCCACACACA | 10966 |
rs113498316 | in-del | -/AC | 0.5 | 0 | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82671910 | ACCCCTGTAACTCTA[-/AC]ACACACACTCACATG | 10966 |
rs113596735 | snp | A/G | 0.5 | 0 | | | GRCh38.p7 | 17:82654549 | CGGCAGGGTAGGGAC[A/G]GTGGTTTTATTTTTA | 10966 |
rs113616220 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RAB40B | GRCh38.p7 | 17:82691718 | GGGCAAAAGGCAGAA[A/C]ACTCAGCACTCAGAG | 10966 |
rs113622752 | snp | A/G | 0.5 | 0 | intron-variant | RAB40B | GRCh38.p7 | 17:82678379 | GAATGTTCACTGAGT[A/G]AGTCAGAAAACAGGG | 10966 |
rs113720239 | snp | C/G | 0.5 | 0 | upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82699481 | TGCGTGTGCATGTGT[C/G]CCTCTGCAGGTGTCT | 10966 |
rs113722770 | snp | G/T | 0.0158469 | 0.0875917 | intron-variant | RAB40B | GRCh38.p7 | 17:82683722 | GGTGGGAGGATCACT[G/T]GAGCCCAGTAGGTGG | 10966 |
rs113763328 | snp | C/G | 0.5 | 0 | intron-variant | RAB40B | GRCh38.p7 | 17:82694970 | GAGGGACAGCACAAT[C/G]AACAGAGACATAAAT | 10966 |
rs113821879 | snp | A/G | 0.5 | 0 | intron-variant | RAB40B | GRCh38.p7 | 17:82658219 | CACACCTGTTCTCCC[A/G]CCCTCCCAAGGCTCG | 10966 |
rs113875887 | snp | A/G | 0.5 | 0 | intron-variant | RAB40B | GRCh38.p7 | 17:82660432 | CACGTGTAAACACAC[A/G]CACAGGCACTCATGC | 10966 |
rs113925433 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | RAB40B | GRCh38.p7 | 17:82676443 | AACAGCCTCTCCCCC[C/G]CCACACAGGGCACCC | 10966 |
rs113934752 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | RAB40B | GRCh38.p7 | 17:82660844 | ACCACTCTACAGCAC[A/G]TTTTTAGACTCTCAG | 10966 |
rs113949319 | snp | C/T | 0.5 | 0 | intron-variant | RAB40B | GRCh38.p7 | 17:82695993 | TCCTGCCTCAGCCTC[C/T]CGAGTAGCTGGGATT | 10966 |
rs113984001 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82665200 | TCTTTCCACATTTCT[A/G]TTTTTTCAAGTTAAA | 10966 |
rs113985277 | snp | A/G | 0.5 | 0 | intron-variant | RAB40B | GRCh38.p7 | 17:82664012 | GGTGTTCCCGGGGGC[A/G]CTGTGCCAACGGTGG | 10966 |
rs114038357 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RAB40B | GRCh38.p7 | 17:82677538 | CCGAGGCCCAGAGGC[A/G]GCCTGTGTTGTGGCT | 10966 |
rs114060137 | snp | A/G | 1.65636e-05 | 0.00287776 | missense, downstream-variant-500B | RAB40B | GRCh38.p7 | 17:82660998 | TTACCTGTGCGCCCC[A/G]GGAGTAGGAGCGGAA | 10966 |
rs114084216 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | RAB40B | GRCh38.p7 | 17:82687926 | AAAATAAAATAATTA[A/G]CCGGGCATGGTGGCA | 10966 |
rs114094674 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | RAB40B | GRCh38.p7 | 17:82691961 | CGTGTGTGAGGTGTG[C/T]TGCAGAACAGAAGAC | 10966 |
rs114167038 | snp | G/T | 0.0271762 | 0.113356 | intron-variant | RAB40B | GRCh38.p7 | 17:82692482 | TGCCCATCCACAGAA[G/T]ACAGAGTCTGACCCG | 10966 |
rs114239805 | snp | C/G | 0.0154538 | 0.0865337 | intron-variant | RAB40B | GRCh38.p7 | 17:82679231 | CAGCAACCACCTTCT[C/G]CGGTAGCCTGAAGGA | 10966 |
rs114335069 | snp | A/G | 0.0700422 | 0.173537 | intron-variant, upstream-variant-2KB | RAB40B, MIR4525 | GRCh38.p7 | 17:82669118 | TAAGGTGAGAGGATC[A/G]CTTGAGCCCAGGAAT | 10966 |
rs114455449 | snp | C/G | 0.111224 | 0.207945 | intron-variant | RAB40B | GRCh38.p7 | 17:82694391 | AAACAAATTGGCCCA[C/G]TGTGGTGGCAGGCAC | 10966 |
rs114598293 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | RAB40B, MIR4525 | GRCh38.p7 | 17:82670010 | ATCTATTTTCGAATG[C/T]GGAGATAACTCCAGC | 10966 |
rs114668895 | snp | C/G | 0.0166325 | 0.0896639 | intron-variant | RAB40B | GRCh38.p7 | 17:82688992 | CTAATATTTTTATGC[C/G]CAAGCCCTTTGGATG | 10966 |
rs114683064 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RAB40B | GRCh38.p7 | 17:82675703 | CCTAGCTGGAGGGGC[A/G]AGGGAGCTCTTGGAT | 10966 |
rs114731697 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82665066 | CAGACGTGACGCTGC[A/G]TGGGATGCCCGCTCT | 10966 |
rs114733951 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40B | GRCh38.p7 | 17:82684697 | TCCGGGATGCAGGCA[C/T]GTTGGAGGCTGAGGA | 10966 |
rs114820721 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | RAB40B | GRCh38.p7 | 17:82691109 | TGTGTCCACGCACCG[C/T]GTAGTCTTGAGGGAG | 10966 |
rs114822108 | snp | C/G/T | 0.000148929 | 0.00862799 | missense | RAB40B | GRCh38.p7 | 17:82657906 | CAGTTTTTGGGGGGG[C/G/T]TCTGGGGGGGGCGGA | 10966 |
rs114887873 | snp | C/T | 0.00177842 | 0.0297665 | synonymous-codon | RAB40B | GRCh38.p7 | 17:82658073 | GAGCGGGAGCTTGTC[C/T]ACCAGGTGCACCGGC | 10966 |
rs114898379 | snp | G/T | 0.0329836 | 0.124112 | intron-variant | RAB40B | GRCh38.p7 | 17:82667727 | GTCAGAGGAGAGTGA[G/T]TCAGAGGACAAAAGA | 10966 |
rs114926493 | snp | C/T | 0.0248432 | 0.108648 | upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82700504 | ATTTAGTCCCCAGCC[C/T]CACCACTCTGCCAAA | 10966 |
rs115003173 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RAB40B | GRCh38.p7 | 17:82675381 | AGCCGCCTGTCTGAC[A/G]TGGTCTCCACCAAGC | 10966 |
rs115010567 | snp | A/C | 0.0111196 | 0.0737302 | | | GRCh38.p7 | 17:82654705 | TAGACGTGCACCACC[A/C]TGCCCGGCTAGTGGT | 10966 |
rs115412546 | snp | C/G | 0.0232847 | 0.105357 | upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82699650 | GTGTGTCTGCGTGTG[C/G]TGCTTCTATGCATGC | 10966 |
rs115429052 | snp | C/T | 0.0726307 | 0.176182 | intron-variant | RAB40B | GRCh38.p7 | 17:82667282 | CGAGGTGTGCAGTGG[C/T]GGTGCCACCGGTGGC | 10966 |
rs115508155 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | RAB40B | GRCh38.p7 | 17:82689662 | TCTCACAAGTGGTAC[C/T]GCAGGAGGTAAAGAA | 10966 |
rs115564695 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RAB40B | GRCh38.p7 | 17:82658912 | AATTAGGGCCCTCAT[C/T]TAATGACTGGTGTCC | 10966 |
rs115618214 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RAB40B | GRCh38.p7 | 17:82681121 | ATATCTGCTTCATAT[A/G]CATTGAACACAGTTG | 10966 |
rs115806162 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RAB40B | GRCh38.p7 | 17:82684464 | AAATAAAAACAAGTT[C/T]GCACAAAAACGAGTC | 10966 |
rs115854239 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | RAB40B | GRCh38.p7 | 17:82697495 | CCCAGGACTCAGAGC[A/G]GGTCTCTGTTGGAAG | 10966 |
rs116093146 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | RAB40B | GRCh38.p7 | 17:82663703 | CCAGGACGCTCCGAG[C/T]TCCCTGCCGGGTGCT | 10966 |
rs116276735 | snp | C/T | 0.0178098 | 0.0926698 | upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82699502 | GCAGGTGTCTGCACA[C/T]GTATGTGCGTGTGCA | 10966 |
rs116310749 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant, utr-variant-5-prime | RAB40B | GRCh38.p7 | 17:82696438 | CCCCCAAAACACGCA[C/T]AGCTCTTAAAGCGCC | 10966 |
rs116338339 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | RAB40B | GRCh38.p7 | 17:82680391 | GGGGACGGGACGGCA[A/G]TTCCCCCACGTGTGT | 10966 |
rs116494688 | snp | A/G | 0.0952156 | 0.196321 | intron-variant | RAB40B | GRCh38.p7 | 17:82695482 | GCTGTGAGCCACTGC[A/G]CCCGGCTGCCCTCAC | 10966 |
rs116520398 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | RAB40B | GRCh38.p7 | 17:82691411 | GTGCAAAAGGCCGGG[C/T]GCGGTGGCTCACGCC | 10966 |
rs116676628 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | RAB40B | GRCh38.p7 | 17:82664762 | CCTCCTGTCCTCAGC[C/T]GCCTTGGCCTCTGTG | 10966 |
rs117130969 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | RAB40B | GRCh38.p7 | 17:82689584 | AATGGCAAAACTTGA[C/T]ACAATGCAATGGTGT | 10966 |
rs117233767 | snp | A/C/T | 0.00993945 | 0.0698483 | | | GRCh38.p7 | 17:82656460 | GGCTACATCTTCATG[A/C/T]GGAATTCCTGACAGC | 10966 |
rs117287332 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RAB40B | GRCh38.p7 | 17:82694253 | GAAAAATTCAGGCCG[C/T]GCACTGTGGCTCACA | 10966 |
rs117399128 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RAB40B | GRCh38.p7 | 17:82687151 | TCAAACCAACACGAC[A/G]CAATTTGAACCCGTG | 10966 |
rs117445894 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82670977 | CCCCTGTCTCCCTTC[C/T]CCATTTTAATCCTTT | 10966 |
rs117563886 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | RAB40B | GRCh38.p7 | 17:82690270 | GGGAGCAGAGAGTGT[A/G]TTTGTGTGTCCAGGG | 10966 |
rs117628433 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | RAB40B | GRCh38.p7 | 17:82678843 | TCACATCTGACTTTA[A/G]GTGTGTGGTTTTTGT | 10966 |
rs117651631 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | RAB40B | GRCh38.p7 | 17:82688971 | TGTTTGATAAAGTCT[A/G]GATCTCTAATATTTT | 10966 |
rs117702884 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RAB40B | GRCh38.p7 | 17:82659325 | CAAACCTGACCCCAC[A/G]CATAGCCGAGGTACG | 10966 |
rs117730815 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RAB40B | GRCh38.p7 | 17:82686505 | CTTATAAGCACAGAG[A/G]GATTTGGGGACACAG | 10966 |
rs117735186 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RAB40B | GRCh38.p7 | 17:82678177 | CTTTCGTTATTTACC[A/G]TTTCTCCTTCTCTGT | 10966 |
rs117735422 | snp | G/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | RAB40B | GRCh38.p7 | 17:82657514 | AAATTCCATTGAATT[G/T]ATACTAATCACTCCA | 10966 |
rs117796022 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | RAB40B | GRCh38.p7 | 17:82695232 | AAATCTCACTCTGTC[A/G]CTGGGCTGGAGTGCA | 10966 |
rs117845191 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | RAB40B | GRCh38.p7 | 17:82682821 | CTGTGCAAAAGTAAC[G/T]AATCTCAATCTATAC | 10966 |
rs118027829 | snp | C/T | 0.0456336 | 0.143994 | intron-variant | RAB40B | GRCh38.p7 | 17:82680657 | ATGATTTTCTTTCTA[C/T]CTAGTAGTAATACCT | 10966 |
rs118045907 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RAB40B | GRCh38.p7 | 17:82696993 | GGGGGTAGGACATGC[A/G]GGGGCAGCGGCGCCT | 10966 |
rs118196936 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82671486 | GTGAGTACAGGGAGC[A/G]TGTGAGTGTGTGTTA | 10966 |
rs137868013 | snp | G/T | 0.0166325 | 0.0896639 | intron-variant | RAB40B | GRCh38.p7 | 17:82693942 | ACAAAAATTAGCCAG[G/T]CGTGGTGGCGCACAC | 10966 |
rs137963946 | snp | A/G/T | 0.00011559 | 0.00760149 | missense, synonymous-codon, utr-variant-5-prime | RAB40B | GRCh38.p7 | 17:82664522 | CTTCACCCGCCGCCC[A/G/T]TCCAGCAGGATGGTG | 10966 |
rs138049871 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, utr-variant-5-prime, utr-variant-3-prime | RAB40B | GRCh38.p7 | 17:82661215 | TCCCTGAAGGGATCC[A/G]GGTGTTGGGATGTCC | 10966 |
rs138229768 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | RAB40B, MIR4525 | GRCh38.p7 | 17:82670294 | GGTTCAAGCAATTCT[C/T]GTGCCTCAGCGTCCC | 10966 |
rs138243423 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40B | GRCh38.p7 | 17:82683946 | AAGATACTGGCCGGG[C/T]GCAGCGGCTAACGCC | 10966 |
rs138441321 | snp | G/T | | | intron-variant | RAB40B | GRCh38.p7 | 17:82682571 | GCCAACATTTAAAAG[G/T]AAAGTCAAAAGAGCA | 10966 |
rs138481009 | in-del | -/TG | | | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82671333 | CACTCACACGCTCTC[-/TG]TACTGACACACCTCA | 10966 |
rs138565228 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | RAB40B | GRCh38.p7 | 17:82696480 | GGCGTACACGTTGTT[G/T]GGTGCTTTATTCCTG | 10966 |
rs138600310 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RAB40B, MIR4525 | GRCh38.p7 | 17:82670030 | ATAACTCCAGCTTTG[A/C]TATGTCTGTCTCCAG | 10966 |
rs138620962 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RAB40B | GRCh38.p7 | 17:82675433 | ACTTGGCCCTTCTCC[C/T]GAATCTATTCTGCTC | 10966 |
rs138700632 | in-del | -/AA | | | intron-variant | RAB40B | GRCh38.p7 | 17:82672177 | GTAACTCTAACACAC[-/AA]ACTCACATGCTCCCT | 10966 |
rs138780192 | in-del | -/C | 0.00517822 | 0.0506191 | intron-variant | RAB40B | GRCh38.p7 | 17:82696113 | ACCTCAGGTGATCCG[-/C]CCCGCCTTGGCCTCC | 10966 |
rs138853791 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RAB40B | GRCh38.p7 | 17:82686852 | CTCCACGTTCCTCCC[A/G]TCCAGTGCTGGGGGG | 10966 |
rs138867801 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | RAB40B | GRCh38.p7 | 17:82675912 | GCTACGTGGGTCCTT[C/T]TCACCAGGGGGGAGA | 10966 |
rs138907807 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | RAB40B | GRCh38.p7 | 17:82690609 | GTGTCCAGGGGAAGA[G/T]CTGCAGAATTGGAGG | 10966 |
rs139073542 | in-del | -/CACT | | | intron-variant | RAB40B | GRCh38.p7 | 17:82672343 | TAACTCTAACACACA[-/CACT]CACACGCTCCCTGTA | 10966 |
rs139081573 | snp | C/T | 0.040671 | 0.13668 | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82670655 | TTCTCCTGTCTCAGC[C/T]TCCTGAGTAGCTGGG | 10966 |
rs139132148 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RAB40B | GRCh38.p7 | 17:82677391 | AAAGAGCTAAAACCA[A/G]TCACTGGTTTCTCCC | 10966 |
rs139167220 | in-del | -/CACCTGCCACCA | 0.318896 | 0.240319 | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82666033 | ATAGGCACACCACTG[-/CACCTGCCACCA]CACCTGCCACCGCAC | 10966 |
rs139196077 | snp | A/C | 0.0185938 | 0.0946107 | | | GRCh38.p7 | 17:82654920 | TAAGAATCTGTAGAT[A/C]TAAAGCAACAGGCCA | 10966 |
rs139236513 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RAB40B | GRCh38.p7 | 17:82673529 | TCTGAGACTTTGCAC[A/G]TCTGAAAATGTCTTT | 10966 |
rs139324874 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | RAB40B | GRCh38.p7 | 17:82682772 | AATAAAGAATAGTCT[C/T]TTCAACAAATGCTGC | 10966 |
rs139368876 | snp | C/T | | | intron-variant | RAB40B | GRCh38.p7 | 17:82672376 | ACCCACTGACACACC[C/T]CACCCCTGTAACTCT | 10966 |
rs139391141 | snp | C/G/T | 0.0531838 | 0.155781 | intron-variant | RAB40B | GRCh38.p7 | 17:82686403 | AGGCATGAGCCACCG[C/G/T]GCCCGGCCAAGGGTC | 10966 |
rs139396349 | snp | G/T | 0.0217236 | 0.101931 | intron-variant | RAB40B | GRCh38.p7 | 17:82685568 | GGGCAGGTCCTAGGG[G/T]CCCCTCCAGGGCCCT | 10966 |
rs139460448 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | RAB40B | GRCh38.p7 | 17:82687155 | ACCAACACGACGCAA[C/T]TTGAACCCGTGAGTG | 10966 |
rs139547175 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RAB40B | GRCh38.p7 | 17:82688997 | ATTTTTATGCCCAAG[A/C]CCTTTGGATGCTGTT | 10966 |
rs139561389 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RAB40B | GRCh38.p7 | 17:82691946 | AACCAGGGGTACCAG[C/T]GTGTGTGAGGTGTGT | 10966 |
rs139611729 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RAB40B | GRCh38.p7 | 17:82690897 | TGCCCCGGGGGAGCA[G/T]GGAGTGGGCACGCAT | 10966 |
rs139658648 | snp | C/T | | | intron-variant, utr-variant-3-prime | RAB40B | GRCh38.p7 | 17:82662366 | TCAATCTGCCAGCTT[C/T]GCAGGGAGGCCGAAG | 10966 |
rs139742092 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | RAB40B | GRCh38.p7 | 17:82667648 | CTCCACACTCTGTCC[A/G]CAGAGACTGCCCATC | 10966 |
rs139750553 | snp | C/T | 0.00279162 | 0.0372561 | upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82699586 | CTCTGCAGGTGTCTG[C/T]ACATGTATGTGCGTG | 10966 |
rs139768052 | in-del | -/GA | | | intron-variant | RAB40B | GRCh38.p7 | 17:82675070 | AAAGCACAATGACTG[-/GA]GAGAGAGAGAGAAAA | 10966 |
rs140084045 | snp | C/T | 1.64972e-05 | 0.00287199 | missense | RAB40B | GRCh38.p7 | 17:82659605 | TCCTTAATCCATCGA[C/T]CAATGCCGTCAAAAG | 10966 |
rs140218905 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RAB40B | GRCh38.p7 | 17:82681941 | GGTAAAAAACAGAAC[A/G]CTTTCCCCATGAAAA | 10966 |
rs140258794 | snp | C/G | 0.21875 | 0.248039 | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82670563 | TTTTTGAGACGGAGT[C/G]TTACTCTGTCGCCCA | 10966 |
rs140447282 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | RAB40B, MIR4525 | GRCh38.p7 | 17:82667764 | AGCACTGAGAACGCC[C/T]GAAGCACCCGCTTTG | 10966 |
rs140481976 | snp | A/G | | | intron-variant | RAB40B | GRCh38.p7 | 17:82695731 | AATAAAAAACAAAAC[A/G]TAATGATCTCAACTT | 10966 |
rs140482168 | snp | A/G | 0.0437281 | 0.141251 | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82665761 | AATCCTAGCTAGTAG[A/G]GAGGCTGAGGCAGGA | 10966 |
rs140608099 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | RAB40B | GRCh38.p7 | 17:82689480 | GGGCTGGGGTTACAG[A/C]AGTAACAGGTCAAGC | 10966 |
rs140615730 | snp | A/G | 0.0494327 | 0.149241 | intron-variant | RAB40B | GRCh38.p7 | 17:82693046 | CCCACTCTGTTGCCC[A/G]GGCTGGTGTGCAGTG | 10966 |
rs140709442 | snp | A/G | 0.00795532 | 0.062565 | intron-variant, upstream-variant-2KB | RAB40B, MIR4525 | GRCh38.p7 | 17:82668800 | AGCGGGCCGCGGCAC[A/G]CAGGGAAGGCGGAGC | 10966 |
rs140779446 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RAB40B | GRCh38.p7 | 17:82686024 | GGCCAGGCTGGTCTC[A/G]AACTGCTGAACTCGT | 10966 |
rs140801838 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RAB40B | GRCh38.p7 | 17:82673651 | CCTTTTGAGATCGGC[C/T]GTAAACTCATTCTTG | 10966 |
rs140904221 | in-del | -/T | | | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82671518 | GACACACCCCACCCC[-/T]GTAACTCTAACACAC | 10966 |
rs140987654 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RAB40B | GRCh38.p7 | 17:82696210 | TCCTCCCTCCGTGTC[A/G]AGGGAAAGCCTTTAT | 10966 |
rs141093890 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | RAB40B | GRCh38.p7 | 17:82692544 | GGTGCAGACCCAGAC[C/T]CACAGGCGGGCTCTC | 10966 |
rs141105430 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | RAB40B | GRCh38.p7 | 17:82677595 | TGTCCCTGTGGACTC[A/G]GCCTTTCCCAGTGGG | 10966 |
rs141363265 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40B | GRCh38.p7 | 17:82667348 | TTCAGGCAGGCCTGG[A/G]CGTTGCAGCAGCTCT | 10966 |
rs141454292 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | RAB40B | GRCh38.p7 | 17:82696575 | TGTCCTCCAGGCGCT[C/G]AATCTCCAGCCCTGT | 10966 |
rs141549135 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RAB40B | GRCh38.p7 | 17:82673077 | GGCATGGTGGTGGGC[A/G]CCTGTAGTCCCAGAT | 10966 |
rs141630266 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RAB40B | GRCh38.p7 | 17:82675580 | AACAACAGAAACTTG[C/T]CATCACAGTTCTGGA | 10966 |
rs141680730 | snp | C/G | | | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82671990 | TCACCCACTGACACA[C/G]CTCACCCCTGTAACT | 10966 |
rs141720210 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RAB40B | GRCh38.p7 | 17:82659454 | CCTTCCTGCTGGAGC[A/G]CCATCCGGTGCCCTG | 10966 |
rs141727310 | in-del | -/T/TTTTTTGTGGGG/TTTTTTTGT | 0.12463 | 0.221177 | upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82699968 | AGACCCCATTAGAAG[-/T/TTTTTTGTGGGG/TTTTTTTGT]TTTTTTGTGGGGGAG | 10966 |
rs141730340 | in-del | -/CCTGTGCAGCG | 0.456568 | 0.140818 | intron-variant | RAB40B | GRCh38.p7 | 17:82667437 | CCTGATCTGAGCACA[-/CCTGTGCAGCG]CCTTCCATGAGATCC | 10966 |
rs141785750 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RAB40B | GRCh38.p7 | 17:82687033 | AGTGCTGGGGGGAAG[G/T]GTGCTCAGAGGTCAA | 10966 |
rs141848764 | snp | C/G/T | 0.000164841 | 0.00907718 | missense | RAB40B | GRCh38.p7 | 17:82657916 | GGGGGCTCTGGGGGG[C/G/T]GCGGACGAGCTTCAC | 10966 |
rs141867486 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 17:82655030 | CAAACACACAGTCTT[C/T]TACTTAGTCCGGTCT | 10966 |
rs142051710 | snp | C/T | | | intron-variant, downstream-variant-500B | RAB40B | GRCh38.p7 | 17:82660713 | ACACACACAGGCACT[C/T]ATGCACAGATGCACG | 10966 |
rs142125807 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | RAB40B | GRCh38.p7 | 17:82688386 | TTGGGAGTCCGAGGC[A/G]GGTAGATCACGAGGT | 10966 |
rs142178404 | snp | A/C | 8.70853e-05 | 0.00659811 | synonymous-codon, utr-variant-5-prime | RAB40B | GRCh38.p7 | 17:82698471 | CGCCGGGTGGCCGTA[A/C]GGGGACTCGGCCGCG | 10966 |
rs142445256 | snp | A/G | 0.00034795 | 0.0131854 | synonymous-codon | RAB40B | GRCh38.p7 | 17:82658537 | ATGCCGCAGCAGCAC[A/G]ATCCTGGCCAGCTCC | 10966 |
rs142470055 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | RAB40B, MIR4525 | GRCh38.p7 | 17:82668650 | CCCAACTGTGCTCCA[C/G/T]GACTGGAGCGGGCGT | 10966 |
rs142509073 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | RAB40B | GRCh38.p7 | 17:82686270 | GCACCTGCCACCACG[C/T]CCAGCTAATTTTTGT | 10966 |
rs142637956 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | RAB40B | GRCh38.p7 | 17:82680754 | TATAATTTCTGGGCC[A/G]GGCACGGTGGCTCAC | 10966 |
rs142649681 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | RAB40B | GRCh38.p7 | 17:82682690 | AAAAATGGAACAGAA[C/T]TGAGTCTAGAAATAG | 10966 |
rs142910700 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | RAB40B | GRCh38.p7 | 17:82692385 | CAGGCCTCGCTGACC[A/G]TATCGGAGCAAAGGG | 10966 |
rs143034746 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RAB40B | GRCh38.p7 | 17:82683186 | AAAAACCCAAAATGG[A/C]CCATAGTCATAAATG | 10966 |
rs143127570 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | RAB40B | GRCh38.p7 | 17:82680242 | GGGGCCTGGGTCTCT[C/T]CTAGGTTCCCATACA | 10966 |
rs143263318 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40B | GRCh38.p7 | 17:82659919 | AACACAGGATGCAGG[A/G]GCACCGCAGTAATCG | 10966 |
rs143452492 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RAB40B | GRCh38.p7 | 17:82697512 | GTCTCTGTTGGAAGC[A/G]TGGGTTCAGCCCCGA | 10966 |
rs143505052 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RAB40B | GRCh38.p7 | 17:82684796 | CCTTGACCGTGATGG[C/T]GGTCACACCACTGTC | 10966 |
rs143541936 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RAB40B, MIR4525 | GRCh38.p7 | 17:82670270 | GCTCACTGCAACCTC[C/T]GCCCACCGGGTTCAA | 10966 |
rs143545537 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RAB40B | GRCh38.p7 | 17:82693952 | GCCAGGCGTGGTGGC[A/G]CACACCTGTAGTCCC | 10966 |
rs143563421 | in-del | -/C | 0.093777 | 0.195178 | intron-variant | RAB40B | GRCh38.p7 | 17:82698032 | CTCCCGCCCCTCCTG[-/C]CCCCGCGGCCGAACG | 10966 |
rs143626208 | snp | A/C/G | 6.6172e-05 | 0.00575174 | missense | RAB40B | GRCh38.p7 | 17:82657900 | CTGGTGCAGTTTTTG[A/C/G]GGGGGCTCTGGGGGG | 10966 |
rs143657485 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RAB40B | GRCh38.p7 | 17:82686591 | CCACAGGCCACAGAA[C/T]GCCGAGGGCTGCCAG | 10966 |
rs143725019 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82670494 | CCAGCCAAGGGCCAA[A/C]CAACTTTAAAATGTG | 10966 |
rs143790245 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RAB40B | GRCh38.p7 | 17:82682307 | TGAAATTAAATAGCA[C/T]TAGGTACAGTAGCCC | 10966 |
rs143863036 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RAB40B | GRCh38.p7 | 17:82695030 | TATTTAAATGTTGAA[C/T]TGATACTAAATCATT | 10966 |
rs143867346 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | RAB40B | GRCh38.p7 | 17:82697707 | CCGCCTTTCTTTCCC[C/T]GGAGCCGTCCACCCC | 10966 |
rs143877793 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40B | GRCh38.p7 | 17:82687987 | TGAGGTGAGAGGACT[A/G]TTTGAGCCCAGGAGG | 10966 |
rs143924663 | snp | C/G | 0.0741063 | 0.177655 | upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82699457 | CAGGTGTCTGCACAT[C/G]TATGTGTCTGCGTGT | 10966 |
rs144044653 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | RAB40B | GRCh38.p7 | 17:82684662 | GGGCTGCTGAGTGAC[C/T]GGAGCCAGGTTCAAA | 10966 |
rs144235452 | snp | G/T | 0.00318978 | 0.0398085 | upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82699617 | TGCATGTGTGCCTTT[G/T]CAGGCATCTTTGCAT | 10966 |
rs144260816 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | RAB40B, MIR4525 | GRCh38.p7 | 17:82667785 | ACCCGCTTTGCAGAC[A/G]CCACCTGCCCCGTGA | 10966 |
rs144446989 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, synonymous-codon | RAB40B | GRCh38.p7 | 17:82662503 | GCAGAGCCCAACCCC[A/G]GCCCCAGTGGGTGTG | 10966 |
rs144596040 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RAB40B | GRCh38.p7 | 17:82674761 | ATCGCAGGCAACGTT[C/T]GTATGGTTTGGAGTT | 10966 |
rs144602859 | in-del | -/GAGACAG | 0.0829062 | 0.185956 | intron-variant | RAB40B | GRCh38.p7 | 17:82696054 | TTTGTATTTATAGTA[-/GAGACAG]GGTTTCTCCATGTTG | 10966 |
rs144628884 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | RAB40B | GRCh38.p7 | 17:82677847 | CCCTGCACCTGACCC[A/G]GGGCCTCTTCTCCAT | 10966 |
rs144674283 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | RAB40B | GRCh38.p7 | 17:82676972 | TATTTTTTCTGAGAC[A/G]GAGTCTCACTCTGTC | 10966 |
rs144747452 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40B | GRCh38.p7 | 17:82680641 | CTGTTTATGTATATA[C/T]ATGATTTTCTTTCTA | 10966 |
rs144826018 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RAB40B | GRCh38.p7 | 17:82675978 | CTGAGTCTCCTGGTA[C/T]GGGACGGTGAGGACC | 10966 |
rs144871735 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | RAB40B | GRCh38.p7 | 17:82689130 | CACAGCCAGCACATA[C/G]CAGCTGATTCCACTG | 10966 |
rs144967801 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RAB40B | GRCh38.p7 | 17:82682083 | GATTAAAACCATCTC[A/G]ATTACCAGATGACAT | 10966 |
rs145027264 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RAB40B | GRCh38.p7 | 17:82692571 | TCTCAGCTGGGACAA[A/C]GGTGGCCGTGCGATG | 10966 |
rs145088675 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40B | GRCh38.p7 | 17:82659348 | GAGGTACGCCGTGGA[C/T]GCTCGTTTCGTCTGG | 10966 |
rs145108946 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | RAB40B | GRCh38.p7 | 17:82675902 | CCCTCCATCTGCTAC[A/G]TGGGTCCTTCTCACC | 10966 |
rs145147027 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82699999 | GAACAGAAGAGGGAG[C/T]GGAAGAAGAATTACA | 10966 |
rs145205570 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40B | GRCh38.p7 | 17:82690361 | GTGTACGTGTGTCCA[A/G]GGGGAGATCTGCAGA | 10966 |
rs145310413 | snp | A/G | 0.0448719 | 0.142907 | intron-variant | RAB40B | GRCh38.p7 | 17:82678348 | ATATACAAAGCTTCT[A/G]GAACAAAGCCCGTCA | 10966 |
rs145359467 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant, upstream-variant-2KB | RAB40B, MIR4525 | GRCh38.p7 | 17:82668472 | GTTCATGCCAAGGGG[C/T]GCCTGCAGGCCAGCA | 10966 |
rs145596290 | snp | C/T | 0.00150971 | 0.0274331 | intron-variant | RAB40B | GRCh38.p7 | 17:82664480 | TGCGGGACGCTCGCA[C/T]CTCCTCCAGACTCAC | 10966 |
rs145627597 | snp | A/G | 0.0777841 | 0.181223 | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82665846 | TGCTCCAGCCTGGGC[A/G]ACAGAGGGAGACTCT | 10966 |
rs145718820 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82665139 | ACGGGACTGCACACC[C/T]GTCCCAGCCACCTCT | 10966 |
rs145726258 | in-del | -/G | | | intron-variant | RAB40B | GRCh38.p7 | 17:82678697 | AAAAAGCAGACTGGC[-/G]GGTCCCCGGGGCAGA | 10966 |
rs145916099 | in-del | -/ACAC | | | intron-variant | RAB40B | GRCh38.p7 | 17:82660076 | GCACACATGTTGCAT[-/ACAC]ACACGCAGGCACTCA | 10966 |
rs145916987 | snp | G/T | 7.73694e-05 | 0.00621922 | synonymous-codon, utr-variant-5-prime | RAB40B | GRCh38.p7 | 17:82698588 | GACCGGGCTGCCCAG[G/T]GCGCTCATCGTGACG | 10966 |
rs145995032 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant, utr-variant-3-prime | RAB40B | GRCh38.p7 | 17:82661956 | CCCCAGGGATCAGTT[A/C]CCAGAGGAGGCGGCC | 10966 |
rs146119458 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | RAB40B | GRCh38.p7 | 17:82672883 | TTTTCCTTCATGTAC[A/G]AATTTTTGTTTCTAC | 10966 |
rs146232021 | in-del | -/T | | | intron-variant | RAB40B | GRCh38.p7 | 17:82672217 | GACACACCCCACCCC[-/T]GTAACTCTAACACAC | 10966 |
rs146241172 | snp | A/G | 0.0337553 | 0.125452 | intron-variant | RAB40B | GRCh38.p7 | 17:82687070 | GGAAGACTCTTGTCT[A/G]TGGGCCCCCCCACAC | 10966 |
rs146244829 | snp | A/G | 0.0131667 | 0.0800625 | utr-variant-3-prime | RAB40B | GRCh38.p7 | 17:82657772 | AGCATTCGCCGAGAG[A/G]AACCGGGATCTGAGA | 10966 |
rs146281802 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | RAB40B | GRCh38.p7 | 17:82684974 | GAAAAATTACCCGGG[C/T]GTGGTGGCAGGCGCC | 10966 |
rs146323238 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant, utr-variant-5-prime, utr-variant-3-prime | RAB40B | GRCh38.p7 | 17:82661197 | CAACAAAACTTTCCA[A/G]TGTCCCTGAAGGGAT | 10966 |
rs146448508 | in-del | -/G | 0.0341408 | 0.126114 | intron-variant | RAB40B | GRCh38.p7 | 17:82691897 | TGAACCGGGGACCCA[-/G]CTGCCAGACGGAAAT | 10966 |
rs146639483 | snp | A/G | 0.000651591 | 0.018038 | missense | RAB40B | GRCh38.p7 | 17:82658499 | GGCCTACCCTTGCTC[A/G]GCCGCCAGAGCCGGT | 10966 |
rs146649992 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RAB40B | GRCh38.p7 | 17:82677997 | CAGCCATGTCTGCCT[A/G]GAGAAATCCTCAAAC | 10966 |
rs146669446 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | RAB40B | GRCh38.p7 | 17:82681796 | CCCACATGATCTCAG[C/T]GAGGCAGCATTTGAC | 10966 |
rs146791575 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | RAB40B | GRCh38.p7 | 17:82695048 | ATACTAAATCATTGC[A/G]GGCACTACAGCCACA | 10966 |
rs146863218 | snp | A/G | 0.00159617 | 0.0282053 | | | GRCh38.p7 | 17:82654644 | AACCTCCACCTCCCA[A/G]GTCCAAGCAATTTTC | 10966 |
rs146895067 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | RAB40B | GRCh38.p7 | 17:82682726 | CACAAAAATGGCCAA[C/T]TGATGTTTGACCAAA | 10966 |
rs147057391 | in-del | -/AC | | | intron-variant | RAB40B | GRCh38.p7 | 17:82660363 | CCTGCACGCACGTGT[-/AC]ACACACACACGCACA | 10966 |
rs147082048 | snp | C/T | 0.000547968 | 0.0165434 | intron-variant | RAB40B | GRCh38.p7 | 17:82659529 | TAATTCCTGGCCTGA[C/T]GTCCTCCCAAGCCTA | 10966 |
rs147104848 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 17:82655041 | TCTTCTACTTAGTCC[A/G]GTCTGTATTAGGTTT | 10966 |
rs147136937 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | RAB40B | GRCh38.p7 | 17:82667712 | GAGCAAACTCCCCCC[A/G]TCAGAGGAGAGTGAT | 10966 |
rs147141745 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82670503 | GGCCAAACAACTTTA[A/C]AATGTGTTCATAAAT | 10966 |
rs147219869 | snp | A/C/G/T | 0.000313641 | 0.0125197 | synonymous-codon | RAB40B | GRCh38.p7 | 17:82657911 | TTTGGGGGGGCTCTG[A/C/G/T]GGGGGGCGGACGAGC | 10966 |
rs147243199 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | RAB40B | GRCh38.p7 | 17:82676585 | TTTTGAGGCTTACCC[C/T]CGCCAGTTTGACATC | 10966 |
rs147246318 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | RAB40B | GRCh38.p7 | 17:82680110 | GTCCTCGGGCTGGCC[C/T]GTCCTGCTCAGACCG | 10966 |
rs147275946 | snp | A/T | | | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82671593 | AACTCTAACACACAC[A/T]CACATGCTCCCTGTA | 10966 |
rs147338519 | in-del | -/A | | | intron-variant | RAB40B | GRCh38.p7 | 17:82673214 | TGAGACTCTTGTCTC[-/A]AAAAAAAAAATTGCC | 10966 |
rs147351276 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | RAB40B | GRCh38.p7 | 17:82691505 | AGCCTGACCAACATG[A/G]TGAAACCCCCATCTC | 10966 |
rs147542578 | in-del | -/CTTCAA | | | intron-variant | RAB40B | GRCh38.p7 | 17:82676293 | GAGGGCACCCCTCAC[-/CTTCAA]CAGCCTCTCCCTCCA | 10966 |
rs147701659 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RAB40B | GRCh38.p7 | 17:82673593 | GCATACAATTGAGGG[A/G]GAAGATGCTTTTCCC | 10966 |
rs147723915 | snp | A/G | 0.0532157 | 0.154195 | intron-variant | RAB40B | GRCh38.p7 | 17:82686204 | GAAACCTCCGCTTCC[A/G]GGGTTCAAGTGATTC | 10966 |
rs147806641 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RAB40B | GRCh38.p7 | 17:82688952 | AAAAATTTAAAAATT[A/G]TTTTGTTTGATAAAG | 10966 |
rs147917424 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40B | GRCh38.p7 | 17:82689265 | GATGAGGCAGGACTG[C/T]GGGTCTGCCTGCTCC | 10966 |
rs147969582 | snp | A/C | | | intron-variant | RAB40B | GRCh38.p7 | 17:82676469 | CACCCCCGACCTTCA[A/C]CAGCCTCTCCTCACC | 10966 |
rs148025330 | in-del | -/C | 0.0948562 | 0.196037 | upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82699928 | ACTTCATCCCCTCCA[-/C]CCTGCGTTGTGTAGG | 10966 |
rs148075506 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RAB40B | GRCh38.p7 | 17:82686598 | CCACAGAACGCCGAG[A/G]GCTGCCAGCAGCACC | 10966 |
rs148233029 | snp | A/G | 0.0744748 | 0.178019 | intron-variant | RAB40B | GRCh38.p7 | 17:82698011 | GGAGCCCCGGAGCTC[A/G]CGTCCCCTCCCGCCC | 10966 |
rs148235842 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | RAB40B | GRCh38.p7 | 17:82667057 | CCGTCGTGGAGCACA[C/T]GGCCTCTGCAGCTCT | 10966 |
rs148287585 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RAB40B | GRCh38.p7 | 17:82660009 | TACACATGGAGCTCA[C/T]GCACACACAGGCACT | 10966 |
rs148345099 | in-del | -/CAGCCTCCACCAAGCACAGGCTAGGGACAGGGGC/CC | 0.432797 | 0.170544 | intron-variant | RAB40B | GRCh38.p7 | 17:82679755 | GCACAGGGCAGGGGG[lengthTooLong]CAGCCTCCACCAAGC | 10966 |
rs148357057 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | RAB40B | GRCh38.p7 | 17:82678801 | GGTGGTGATTCAACG[C/T]CGCTTTACACCTGCA | 10966 |
rs148529691 | snp | A/C | 0.0205511 | 0.0992634 | intron-variant | RAB40B | GRCh38.p7 | 17:82680671 | ACCTAGTAGTAATAC[A/C]TATAATGATATATGT | 10966 |
rs148552010 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RAB40B | GRCh38.p7 | 17:82692338 | CTGCAACTACAGACC[A/G]AGAGGAAGACAAACG | 10966 |
rs148662088 | in-del | -/GGGG | | | upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82699976 | TTAGAAGTTTTTTGT[-/GGGG]GGGGGAGGAACAGAA | 10966 |
rs148685023 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RAB40B | GRCh38.p7 | 17:82658403 | CCTTGAGACGGGTCC[C/T]GGGAGGCAGACACTT | 10966 |
rs148761645 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | RAB40B, MIR4525 | GRCh38.p7 | 17:82668578 | AAGGGCTGGTGTGTC[C/T]GTGCTGCCCCAAGTG | 10966 |
rs148798841 | snp | C/T | | | intron-variant | RAB40B | GRCh38.p7 | 17:82694973 | GGACAGCACAATGAA[C/T]AGAGACATAAATGGT | 10966 |
rs148846473 | snp | A/G | 0.0103295 | 0.0711199 | | | GRCh38.p7 | 17:82654599 | CTGTCACTCAGGCTG[A/G]AGTGCAGTGGTGCAA | 10966 |
rs148892112 | in-del | -/A/AA | 0.0829062 | 0.185956 | intron-variant | RAB40B | GRCh38.p7 | 17:82696975 | TGCCACCGAGCGGGG[-/A/AA]AGGGGGGTAGGACAT | 10966 |
rs148904202 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | RAB40B | GRCh38.p7 | 17:82674109 | ACTTTGGGAGGCCGA[A/G]GCGGGCGGATCACCT | 10966 |
rs149006226 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RAB40B | GRCh38.p7 | 17:82686499 | AGTGTTCTTATAAGC[A/G]CAGAGAGATTTGGGG | 10966 |
rs149167180 | snp | C/T | 0.00557542 | 0.0525036 | upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82700294 | CATGTGCCACCACAC[C/T]CAGCTAATTTTTGCA | 10966 |
rs149210378 | snp | A/G | 0.00013303 | 0.00815457 | missense | RAB40B | GRCh38.p7 | 17:82658512 | TCGGCCGCCAGAGCC[A/G]GTCCATCCCATGCCG | 10966 |
rs149304874 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | RAB40B, MIR4525 | GRCh38.p7 | 17:82670247 | CTGGAGTGCAGTGAC[A/G]TGATCTCGCTCACTG | 10966 |
rs149376935 | snp | A/G | 0.00453307 | 0.0473918 | utr-variant-3-prime | RAB40B | GRCh38.p7 | 17:82657692 | TGCACATCCACGTAG[A/G]AATTCGAAGTCCGAC | 10966 |
rs149435743 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | RAB40B | GRCh38.p7 | 17:82675935 | GGGGGAGAGGTGGCA[A/G]CAGTGACGACCTGAA | 10966 |
rs149524257 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | RAB40B | GRCh38.p7 | 17:82687784 | CCTTCAAGACTTTAC[A/G]CCCCCAGCCAGGCGC | 10966 |
rs149524447 | in-del | -/G | | | frameshift-variant | RAB40B | GRCh38.p7 | 17:82658676 | ACGCCAGGTGCAGGC[-/G]GGTTCCCCACCAGGA | 10966 |
rs149575647 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | RAB40B | GRCh38.p7 | 17:82684136 | TGAGGCAGGAGAATC[A/G]CTTGAACCCGGGAGG | 10966 |
rs149682056 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | RAB40B | GRCh38.p7 | 17:82686082 | GCTGGGATTACAGGC[A/G]TGAGCCACCGCACCC | 10966 |
rs149834536 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82670880 | TCAAAACCATCTTTC[A/G]TTTCTGTTTTCATGG | 10966 |
rs149872925 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | RAB40B | GRCh38.p7 | 17:82682007 | TACCACTCCAATTCA[A/T]TATCATTTTGGAAGT | 10966 |
rs149924982 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RAB40B | GRCh38.p7 | 17:82677501 | TCTGGCCCTTCCCTG[A/T]TGTGTCCCCCTTGCC | 10966 |
rs150046812 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RAB40B | GRCh38.p7 | 17:82694325 | ACCTGAGGTTAGGGG[C/T]TCGAGACCACCCTGG | 10966 |
rs150141020 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | RAB40B | GRCh38.p7 | 17:82696356 | CAAACATTCTGTGCG[G/T]GACCCTTCTCACACA | 10966 |
rs150184240 | in-del | -/CT | 0.00835141 | 0.0640778 | | | GRCh38.p7 | 17:82655874 | CAGGGACCAGTGCTC[-/CT]CTCTCCTGTCTGGGC | 10966 |
rs150210194 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RAB40B, MIR4525 | GRCh38.p7 | 17:82669810 | ACCCTACTAAGCTCT[C/T]GGGAAGGCACCATCA | 10966 |
rs150211460 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RAB40B | GRCh38.p7 | 17:82686789 | CATTAGTCACAGCAG[C/T]CCATCCAAAAGCCAC | 10966 |
rs150336027 | snp | A/G | 4.95569e-05 | 0.00497755 | missense, utr-variant-5-prime | RAB40B | GRCh38.p7 | 17:82664515 | GCTGCAGCTTCACCC[A/G]CCGCCCGTCCAGCAG | 10966 |
rs150472881 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40B | GRCh38.p7 | 17:82689922 | CAGTGAACCGAGATC[A/G]TGCCACTGCACTCCA | 10966 |
rs150498412 | in-del | -/AG | | | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82666689 | ATTGAGAACATGGAA[-/AG]AGAGGGTTTGAGTTA | 10966 |
rs150542962 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | RAB40B | GRCh38.p7 | 17:82694006 | GAAAATCGCTTGAAC[C/T]TGGGAGGCAGAGGTT | 10966 |
rs150581754 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | RAB40B | GRCh38.p7 | 17:82690808 | TGTGCATGTGTGTTC[C/T]TGGGGAACAGAGAGT | 10966 |
rs150608118 | snp | A/G | 0.00079041 | 0.019864 | synonymous-codon | RAB40B | GRCh38.p7 | 17:82657989 | GGAGTAGGAACCGCC[A/G]TGCATCATCCTGGCA | 10966 |
rs150610160 | snp | C/G/T | 0.00279162 | 0.0372561 | | | GRCh38.p7 | 17:82656344 | TTAGTCCCTCATTTG[C/G/T]GACCCCCAGCCACAG | 10966 |
rs150617991 | in-del | -/CA | | | intron-variant, downstream-variant-500B | RAB40B | GRCh38.p7 | 17:82660624 | ACCTGCACACACGTG[-/CA]CACACACACGCACAG | 10966 |
rs150670146 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82699291 | CAGGGCCTCGTCGTT[A/G]CCCCATTTACGCGGC | 10966 |
rs150738196 | snp | A/G | 0.00795532 | 0.062565 | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82670621 | CTCATTGTAACCTCC[A/G]CCTCCCGGGTTCAAG | 10966 |
rs150790421 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | RAB40B | GRCh38.p7 | 17:82667406 | TGCAGCCATGAGCAC[A/G]TGCATGGCACACCTG | 10966 |
rs150822134 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | RAB40B | GRCh38.p7 | 17:82683943 | AATAAGATACTGGCC[A/G]GGCGCAGCGGCTAAC | 10966 |
rs150826453 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40B | GRCh38.p7 | 17:82673174 | GTGCAACTGCACTCC[A/G]GCCTGGGTGATGGAG | 10966 |
rs150990027 | in-del | -/G | | | intron-variant | RAB40B | GRCh38.p7 | 17:82675822 | TCAGCACCCGAATTT[-/G]GGGGGGGTCACAAAC | 10966 |
rs151072672 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40B | GRCh38.p7 | 17:82695860 | GCAGCTCAGGCCAAG[C/T]AGACAATAAAGCTCT | 10966 |
rs151089734 | snp | C/T | 8.26631e-05 | 0.00642843 | splice-acceptor-variant | RAB40B | GRCh38.p7 | 17:82664558 | CTTGTAGTCGATGCC[C/T]GCGGAAGGGTTAGAG | 10966 |
rs151125166 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RAB40B | GRCh38.p7 | 17:82692513 | GGGCACACACACAAG[A/G]GACAGGCGGGCCAAC | 10966 |
rs151142298 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | RAB40B | GRCh38.p7 | 17:82658835 | ACCCAGAACCTCAGC[A/G]TGGGACCTCGTTTGG | 10966 |
rs151152124 | snp | A/G | 1.68216e-05 | 0.00290009 | missense | RAB40B | GRCh38.p7 | 17:82658656 | CCGTGGGCACCTGCC[A/G]CTTGAACGCCAGGTG | 10966 |
rs151200527 | snp | A/T | 0.00318978 | 0.0398085 | upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82700475 | GGACGCTAGAAAACT[A/T]TGAGAAAGATGGCAT | 10966 |
rs151333600 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RAB40B, MIR4525 | GRCh38.p7 | 17:82668664 | ACGACTGGAGCGGGC[A/G]TGGGGAGTGAGGAGA | 10966 |
rs180743348 | snp | C/T | 0.215747 | 0.247642 | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82671221 | ACACACACTCACACG[C/T]TCCCTGTACTCACTG | 10966 |
rs180798187 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RAB40B | GRCh38.p7 | 17:82697863 | CCCTCTTCCGCACGC[G/T]AGTCACCTGTGCTCC | 10966 |
rs180842828 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RAB40B | GRCh38.p7 | 17:82673553 | TGTCTTTAGGCTGCC[C/G]TCACTCTTCCTTGTG | 10966 |
rs180845761 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RAB40B | GRCh38.p7 | 17:82682158 | ACGCATGCACACACA[C/G]ACATACACCTCTCCA | 10966 |
rs181083088 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RAB40B | GRCh38.p7 | 17:82667010 | GAGGGGAGAAGCAGC[A/G]CCGAGGCTCGCACCA | 10966 |
rs181083284 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40B | GRCh38.p7 | 17:82687247 | TTCCAGATGAATTTT[A/G]TTAATCTAAGAGAAA | 10966 |
rs181147362 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RAB40B | GRCh38.p7 | 17:82693654 | ACCACCCAAATGCCC[A/G]TCACCCGCAGGATGG | 10966 |
rs181184826 | snp | C/G/T | 0.00279242 | 0.0372774 | utr-variant-3-prime | RAB40B | GRCh38.p7 | 17:82657399 | CCTCTACATCTGCAG[C/G/T]GTTTTATAAATTGGC | 10966 |
rs181185833 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | RAB40B | GRCh38.p7 | 17:82677137 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT | 10966 |
rs181201488 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82671126 | GCTCTCGGTCACTGA[C/T]ACACCCCACCCCTGT | 10966 |
rs181217117 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40B | GRCh38.p7 | 17:82690253 | GTGCACACGTGTTCT[C/T]GGGGAGCAGAGAGTG | 10966 |
rs181464852 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82699469 | CATCTATGTGTCTGC[A/G]TGTGCATGTGTCCCT | 10966 |
rs181489078 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82666579 | AAAAATATGTTTCCC[C/T]GCCCCCATCACCCCC | 10966 |
rs181585543 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40B | GRCh38.p7 | 17:82683563 | GAGGCCGAGGTAGGA[C/T]GATCTCTTGAGCCCA | 10966 |
rs181667771 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | RAB40B | GRCh38.p7 | 17:82686436 | TTCAGATGTAATCAA[G/T]TTAAGATGAGGTCAT | 10966 |
rs181787544 | snp | C/T | | | intron-variant, upstream-variant-2KB | RAB40B, MIR4525 | GRCh38.p7 | 17:82670246 | CCTGGAGTGCAGTGA[C/T]GTGATCTCGCTCACT | 10966 |
rs181799536 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40B | GRCh38.p7 | 17:82689774 | GAGTTCAAGATCAGC[C/T]TGGCCAAGATGGTGA | 10966 |
rs181963503 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RAB40B | GRCh38.p7 | 17:82682654 | ACACAGTATGGTACT[A/G]GTATAAAAAATACTG | 10966 |
rs182077365 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | RAB40B | GRCh38.p7 | 17:82693808 | TGCACATTGGCCAGG[C/T]GCAGTGGCTCACGCC | 10966 |
rs182092233 | snp | C/T | | | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82672085 | ACATGCTCCCTGTAC[C/T]CACTGACACACCCCA | 10966 |
rs182128535 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82700080 | CCTAGAAAATGTTTA[C/T]TTTGGAATGCCAATT | 10966 |
rs182131887 | snp | A/G | | | intron-variant | RAB40B | GRCh38.p7 | 17:82663983 | GGGCGCTGTGCCGAC[A/G]GTGGTGGTGGGAGGG | 10966 |
rs182137434 | snp | C/T | | | intron-variant | RAB40B | GRCh38.p7 | 17:82684096 | TGTGGTGGCAGGCAC[C/T]TGTAATCCCAGCTAC | 10966 |
rs182261126 | snp | G/T | 0.00755907 | 0.0610114 | upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82699041 | GAGCGCCACGAACTC[G/T]CTCCCACGGTCGTCG | 10966 |
rs182269402 | snp | A/G | 8.28548e-05 | 0.00643588 | intron-variant, downstream-variant-500B | RAB40B | GRCh38.p7 | 17:82660980 | AGCTCGGGGGATGCT[A/G]TGTTACCTGTGCGCC | 10966 |
rs182402476 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RAB40B | GRCh38.p7 | 17:82686153 | TCTGTCATCCAGGCT[G/T]GAGGCTGGAGTGCAG | 10966 |
rs182666748 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | RAB40B | GRCh38.p7 | 17:82692020 | GGGCCCGCACGGTCC[A/G]TGGGCTGAGGTGACA | 10966 |
rs182701636 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | RAB40B | GRCh38.p7 | 17:82661628 | TTGGCGGCTCACACC[A/G]ATAATCCCAGCGCTT | 10966 |
rs182812865 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RAB40B | GRCh38.p7 | 17:82691542 | AAATACAAAAATTAG[C/T]CGGGCATGGTACACC | 10966 |
rs182932462 | snp | A/C | | | intron-variant | RAB40B | GRCh38.p7 | 17:82676390 | CTCACCTTCAACAGC[A/C]TCTCCTCACCCACAG | 10966 |
rs182948753 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RAB40B | GRCh38.p7 | 17:82694252 | AGAAAAATTCAGGCC[A/G]CGCACTGTGGCTCAC | 10966 |
rs182950299 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B, utr-variant-5-prime | RAB40B, MIR4525 | GRCh38.p7 | 17:82668086 | CTTTACTGAGTGTTA[G/T]AACAGCTCAGGGGAG | 10966 |
rs183109064 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | RAB40B | GRCh38.p7 | 17:82688447 | GTGAAACCCCATCTC[C/T]ATTAAAAATACCAAA | 10966 |
rs183116516 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RAB40B | GRCh38.p7 | 17:82695240 | CTCTGTCGCTGGGCT[A/G]GAGTGCAATGGTGTG | 10966 |
rs183130006 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | RAB40B | GRCh38.p7 | 17:82659191 | ACACTCATACAGTGG[C/G]CTTAGTGTCGACCAC | 10966 |
rs183173999 | snp | A/G | | | intron-variant | RAB40B | GRCh38.p7 | 17:82679408 | TGCCTCAGCCTCCCG[A/G]GTAGCTGGGACTACA | 10966 |
rs183215465 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40B | GRCh38.p7 | 17:82675189 | GAATTTCACTAACAA[A/C/T]AAACAAGAACTGGAA | 10966 |
rs183243866 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RAB40B | GRCh38.p7 | 17:82690934 | GGGGAACATCTGTCC[A/G]AGGCAAAGAGGAAGG | 10966 |
rs183268532 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RAB40B | GRCh38.p7 | 17:82674358 | AAGAAAAGACCAGGC[A/G]TGGTGGTTCACGCCT | 10966 |
rs183356858 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RAB40B | GRCh38.p7 | 17:82658772 | AGATTTTGTTGTCGT[C/T]GTAATGTGGGTGCTC | 10966 |
rs183416484 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RAB40B | GRCh38.p7 | 17:82680899 | GCTGGGCTTGGTGGC[A/G]TGCACCTGTAGTCCC | 10966 |
rs183429148 | snp | C/T | 0 | 0 | intron-variant | RAB40B | GRCh38.p7 | 17:82659551 | CCAAGCCTACAGGGA[C/T]CTTGGGCAGTGGCAT | 10966 |
rs183430725 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40B | GRCh38.p7 | 17:82695586 | GCTGTGGCTCAGGCC[C/T]ATAATCTCAGCATTT | 10966 |
rs183442142 | snp | C/T | 0.00318978 | 0.0398085 | | | GRCh38.p7 | 17:82655727 | CCTGCACGAGGCTGG[C/T]CACCCTCTCCAGACA | 10966 |
rs183577312 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RAB40B | GRCh38.p7 | 17:82679134 | GTGATCCACCTGCCT[C/T]GGCCTCCCAAAGTGC | 10966 |
rs183678596 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RAB40B | GRCh38.p7 | 17:82684307 | AAACCAAAGAATGTT[G/T]ACAACTGAAACACTC | 10966 |
rs183849600 | snp | A/G | 0 | 0 | intron-variant | RAB40B | GRCh38.p7 | 17:82685526 | ACGCTCAGATGGGGC[A/G]GGCCCCAGGCACCCG | 10966 |
rs183871494 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82665735 | AGCCGGGTGTGGTGG[C/T]GGGCTCCTGGAATCC | 10966 |
rs183904404 | snp | A/G | 4.9717e-05 | 0.00498558 | intron-variant | RAB40B | GRCh38.p7 | 17:82664576 | GGAAGGGTTAGAGAC[A/G]GCTTAGGCCTGAGGC | 10966 |
rs183971873 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40B | GRCh38.p7 | 17:82660084 | GTTGCATACACACAC[A/G]CAGGCACTCATGCAC | 10966 |
rs183977598 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RAB40B | GRCh38.p7 | 17:82689531 | GGGGAGAGGACCCTG[A/C]AGGACACAGGCGAGG | 10966 |
rs184005426 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | RAB40B, MIR4525 | GRCh38.p7 | 17:82668958 | AGTGGGGCACGCGGC[A/G]TAGCCTCCATTGCTG | 10966 |
rs184075069 | snp | A/C | 0.0103295 | 0.0711199 | intron-variant | RAB40B | GRCh38.p7 | 17:82667510 | CAGCCTGTCCCCTGC[A/C]CTCTGCTTCCTCCTC | 10966 |
rs184223014 | snp | A/G | 0.000798403 | 0.0199641 | | | GRCh38.p7 | 17:82656278 | AAGAATCTACAGATC[A/G]TCAGCAGGAACTAGG | 10966 |
rs184310043 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82665410 | GGCATGTGCCACTAG[A/G]GCCAGATAATTTTTG | 10966 |
rs184384718 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82670359 | CAAGCTAATTTGTGT[A/G]CTTTTAGTAGACACG | 10966 |
rs184396658 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RAB40B | GRCh38.p7 | 17:82690205 | GCATGTGTGTCCAGG[C/G]GAAGATCTGCAGAAT | 10966 |
rs184518656 | snp | A/T | 0.030278 | 0.119257 | intron-variant | RAB40B | GRCh38.p7 | 17:82676958 | TTTATTTATTTATTT[A/T]TTTTTTCTGAGACGG | 10966 |
rs184529176 | snp | G/T | | | downstream-variant-500B | RAB40B | GRCh38.p7 | 17:82656808 | CACCTGAGGTTAGGA[G/T]TTCAACACCAGCCTG | 10966 |
rs184535770 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RAB40B | GRCh38.p7 | 17:82692726 | TTTTAAATCTGGGAG[A/C]AGCAAAGGTTTGTTC | 10966 |
rs184565671 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RAB40B | GRCh38.p7 | 17:82681951 | AGAACGCTTTCCCCA[C/T]GAAAATGAGAAAATA | 10966 |
rs184869635 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40B | GRCh38.p7 | 17:82697530 | GGTTCAGCCCCGAGG[C/T]GCGGCAGGAAGGTGG | 10966 |
rs184889401 | snp | A/C | | | intron-variant | RAB40B | GRCh38.p7 | 17:82660425 | CTTCACACACGTGTA[A/C]ACACACGCACAGGCA | 10966 |
rs184923930 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RAB40B | GRCh38.p7 | 17:82677059 | GTTCAAGCAATTCTC[C/T]TGCCTCAGCCTCCCG | 10966 |
rs185011205 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | RAB40B | GRCh38.p7 | 17:82697928 | CGGGACCGGACCCTG[A/G]TCTCCCCTCCCCTCC | 10966 |
rs185021513 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RAB40B | GRCh38.p7 | 17:82693492 | TGAAAAATGCTTTGC[A/G]AGAATCTACTACAGG | 10966 |
rs185025217 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | RAB40B | GRCh38.p7 | 17:82657001 | CCTGGGCAACAAGAG[C/T]GAAACTCTGTCTCAA | 10966 |
rs185123175 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RAB40B | GRCh38.p7 | 17:82687543 | GAGATACGTAACCCA[A/C]ATAAAGTAAAAACAG | 10966 |
rs185231499 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | RAB40B | GRCh38.p7 | 17:82696198 | TTTTAGCCTAAATCC[G/T]CCCTCCGTGTCAAGG | 10966 |
rs185265140 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RAB40B | GRCh38.p7 | 17:82659723 | CTGTGGCCATGCACG[A/C]AAAGACATACAACTA | 10966 |
rs185380122 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | RAB40B | GRCh38.p7 | 17:82681446 | GGTAGGGAAAAAAGC[A/C]CCTCTGCTTGGATGA | 10966 |
rs185384001 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | RAB40B | GRCh38.p7 | 17:82657596 | ATCATGATAAAGTAA[C/T]ATTCAGAATTTCATG | 10966 |
rs185422566 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RAB40B | GRCh38.p7 | 17:82683929 | CAAATTAAAATTACA[A/G]TAAGATACTGGCCGG | 10966 |
rs185436938 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | RAB40B | GRCh38.p7 | 17:82661812 | GAATTGTTTGAGCCC[A/G]GCAGGCGGAGGTTGC | 10966 |
rs185437094 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82699659 | CGTGTGCTGCTTCTA[C/T]GCATGCGCTCCTATG | 10966 |
rs185500374 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82665932 | ACACTTAAAAAAAAT[A/C]TTTTTTGAGACAGGG | 10966 |
rs185534790 | snp | A/C | | | intron-variant | RAB40B | GRCh38.p7 | 17:82686194 | TCAGCTCACTGAAAC[A/C]TCCGCTTCCGGGGTT | 10966 |
rs185588396 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82666698 | ATGGAAAGAGAGGGT[G/T]TGAGTTAAGGGGCTG | 10966 |
rs185596346 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RAB40B | GRCh38.p7 | 17:82686500 | GTGTTCTTATAAGCA[A/C]AGAGAGATTTGGGGA | 10966 |
rs185811449 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RAB40B | GRCh38.p7 | 17:82689673 | GTACCGCAGGAGGTA[A/C]AGAAGTAGAAAACTG | 10966 |
rs185970919 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RAB40B | GRCh38.p7 | 17:82690649 | GTGTGCACATGTGTT[C/T]CCGGGGAGCAGAGAG | 10966 |
rs185991015 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40B | GRCh38.p7 | 17:82693660 | CAAATGCCCGTCACC[C/T]GCAGGATGGAGAATA | 10966 |
rs186000791 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RAB40B | GRCh38.p7 | 17:82667047 | ACCCTGGAGACCGTC[A/G]TGGAGCACACGGCCT | 10966 |
rs186067643 | snp | A/C/T | | | intron-variant | RAB40B | GRCh38.p7 | 17:82672142 | ACACGCTCCCTGTAC[A/C/T]CACTGACACAGCTCA | 10966 |
rs186101869 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RAB40B | GRCh38.p7 | 17:82691460 | GGAGGCCCAGGCAGG[C/T]GGATTGCCTGAGGTC | 10966 |
rs186153808 | snp | C/T | 0.0399052 | 0.1355 | intron-variant | RAB40B | GRCh38.p7 | 17:82677168 | TGGTCAGGCTGGTCT[C/T]GAACCCCTGACCTCG | 10966 |
rs186402731 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40B | GRCh38.p7 | 17:82693874 | GATCACCTTAGGCCC[A/G]GAGTTCCAGACCATC | 10966 |
rs186514517 | snp | G/T | | | intron-variant | RAB40B | GRCh38.p7 | 17:82672733 | ACCTTGGACTTCCCA[G/T]CCTCCAGAACTGTAA | 10966 |
rs186524879 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | RAB40B | GRCh38.p7 | 17:82682166 | ACACACACACATACA[C/G]CTCTCCAAAAACCAA | 10966 |
rs186528154 | snp | A/C | 0.0126979 | 0.078662 | intron-variant | RAB40B | GRCh38.p7 | 17:82676445 | CAGCCTCTCCCCCCC[A/C]ACACAGGGCACCCCC | 10966 |
rs186536046 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, downstream-variant-500B | RAB40B | GRCh38.p7 | 17:82660621 | CATACCTGCACACAC[A/G]TGCACACACACACGC | 10966 |
rs186560534 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | RAB40B | GRCh38.p7 | 17:82656705 | TGGCGCAGTGAAGTA[A/G]AGGGCTATAAGAAAT | 10966 |
rs186563568 | snp | A/G | 0.00318978 | 0.0398085 | upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82700335 | AGATGGGATTTTGCC[A/G]TGTTGGCCAGGCTGG | 10966 |
rs186567521 | snp | A/C | 0.0718919 | 0.175435 | intron-variant | RAB40B | GRCh38.p7 | 17:82664139 | CCTGGGGTGCTGTGC[A/C]GATGGTGGTGGTGGG | 10966 |
rs186568687 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RAB40B | GRCh38.p7 | 17:82684124 | TACTCGGGAGGCTGA[A/G]GCAGGAGAATCGCTT | 10966 |
rs186634489 | snp | A/G | 0.182296 | 0.240658 | intron-variant | RAB40B | GRCh38.p7 | 17:82679368 | CTCACTGCAAGCTCC[A/G]CCTCCTGGGTTCACG | 10966 |
rs186659095 | snp | A/G | | | intron-variant | RAB40B | GRCh38.p7 | 17:82680294 | TCCAGTCCTGCCCTG[A/G]CCCTGGGTCGCAGGC | 10966 |
rs186665579 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RAB40B | GRCh38.p7 | 17:82659263 | AGGCACAAGCGCCGG[A/T]CACTGCTGGTCAGCC | 10966 |
rs186666565 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | RAB40B | GRCh38.p7 | 17:82659037 | GTTGCTGGCACCGCC[G/T]AGAGCTGGGAGAGGC | 10966 |
rs186802544 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82699351 | CCTGTGTACGTGTGC[A/G]TGTGTTCGTGTGTGT | 10966 |
rs186812348 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | RAB40B | GRCh38.p7 | 17:82661506 | CAGGGAACTGCCTGG[C/T]GTGAGCTGCAGGCAG | 10966 |
rs186865528 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RAB40B | GRCh38.p7 | 17:82694895 | CAGACACAAAAAAAC[A/T]CTCAGGAAATACTCG | 10966 |
rs186999358 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RAB40B | GRCh38.p7 | 17:82682872 | GAACCCGGCCGGGCA[C/T]GGTGACTCATGCCTG | 10966 |
rs187083303 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | RAB40B | GRCh38.p7 | 17:82685360 | GTGGCCGTGCACTCA[A/G]CTGAACGCAGATTCC | 10966 |
rs187096933 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82665602 | CTGGATGCGGTGGCT[A/G]ACGCCTGTCATCCCA | 10966 |
rs187328331 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RAB40B | GRCh38.p7 | 17:82673700 | GGTTTTCCTCCTGGT[A/G]GGCATGGAGGCGCTT | 10966 |
rs187401510 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40B | GRCh38.p7 | 17:82688610 | ACAAAGCGAGACTCC[A/G]TCTCAAAAATACATA | 10966 |
rs187414865 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RAB40B, MIR4525 | GRCh38.p7 | 17:82668673 | GCGGGCGTGGGGAGT[A/G]AGGAGAGGCCAGGCA | 10966 |
rs187534686 | snp | A/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 17:82654749 | AGAGACGGGGTTTCA[A/T]CATGTTGCCCAGGCT | 10966 |
rs187604020 | snp | C/T | | | intron-variant, upstream-variant-2KB | RAB40B, MIR4525 | GRCh38.p7 | 17:82669073 | CCAGGCACGGTGGCT[C/T]ACGCCTGTAATCCCA | 10966 |
rs187610474 | snp | A/C | | | intron-variant | RAB40B | GRCh38.p7 | 17:82695272 | TCTCAGCTCACTTCA[A/C]CCTCCACCTCCTGGG | 10966 |
rs187704142 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | RAB40B | GRCh38.p7 | 17:82695857 | ACAGCAGCTCAGGCC[A/T]AGTAGACAATAAAGC | 10966 |
rs187707730 | snp | C/T | 1.6577e-05 | 0.00287893 | intron-variant | RAB40B | GRCh38.p7 | 17:82659703 | GAACACAGATGCAGG[C/T]ACAGCTGTGGCCATG | 10966 |
rs187712158 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RAB40B | GRCh38.p7 | 17:82680978 | GTGAGCTGAGATTGC[A/G]CCATTGCACTCCAGC | 10966 |
rs187748463 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40B | GRCh38.p7 | 17:82692420 | CCTGGGCACAGCTGC[C/T]TGAGCAAGGACAAGA | 10966 |
rs187905808 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RAB40B | GRCh38.p7 | 17:82691648 | TGTGGCACCATTGCA[C/T]TCCAGCCTGGGCGAC | 10966 |
rs187936822 | snp | G/T | 0.00517822 | 0.0506191 | | | GRCh38.p7 | 17:82655922 | CTGAATACAGGCTTT[G/T]CCCCTGATTCTAGGG | 10966 |
rs188043918 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RAB40B | GRCh38.p7 | 17:82689565 | GGCCGAATTGAGGGC[G/T]TCTAATGGCAAAACT | 10966 |
rs188095357 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RAB40B | GRCh38.p7 | 17:82693661 | AAATGCCCGTCACCC[G/T]CAGGATGGAGAATAA | 10966 |
rs188131429 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RAB40B | GRCh38.p7 | 17:82677359 | GTAAAAGCTCATTAC[A/G]ATGAGATTCCCCTCA | 10966 |
rs188137213 | snp | C/T | 5.20052e-05 | 0.00509901 | utr-variant-3-prime | RAB40B | GRCh38.p7 | 17:82657750 | GGCGTCGCACACATT[C/T]GCAAGCAGCATTCGC | 10966 |
rs188435370 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RAB40B | GRCh38.p7 | 17:82697722 | CGGAGCCGTCCACCC[A/C]CTCGCCGGGCGCCGG | 10966 |
rs188457336 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RAB40B | GRCh38.p7 | 17:82660334 | CTCATACACAGGGCA[C/T]GTACCTGCACGCACG | 10966 |
rs188470202 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40B | GRCh38.p7 | 17:82682013 | TCCAATTCAATATCA[C/T]TTTGGAAGTTATAAC | 10966 |
rs188676008 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RAB40B | GRCh38.p7 | 17:82684328 | TGAAACACTCACACA[C/G]TGCTGACGGGGATGC | 10966 |
rs188740559 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RAB40B | GRCh38.p7 | 17:82688130 | AGCGTCCATCAGTCC[A/G]TCCTTCTCTCTGCCA | 10966 |
rs188771682 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82670831 | AGGTACCGCGCCCGG[A/C]TTCCTGATGGTCTTT | 10966 |
rs188786756 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | RAB40B | GRCh38.p7 | 17:82690246 | ACGGAGTGTGCACAC[A/G]TGTTCTCGGGGAGCA | 10966 |
rs189006343 | snp | A/G | 0.030665 | 0.119967 | intron-variant | RAB40B | GRCh38.p7 | 17:82686092 | CAGGCGTGAGCCACC[A/G]CACCCAGCCTTCTTT | 10966 |
rs189007276 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40B | GRCh38.p7 | 17:82667528 | CTGCTTCCTCCTCCG[A/G]GCCCTGCCCCCTTCC | 10966 |
rs189109598 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40B | GRCh38.p7 | 17:82677015 | GTGCAGTGGCACGAT[C/T]TCGGCTCACCGCAAG | 10966 |
rs189121962 | snp | A/T | 0.00795532 | 0.062565 | downstream-variant-500B | RAB40B | GRCh38.p7 | 17:82656866 | TAAAAATACAAAAAT[A/T]AGCCGGGCGTGGTGG | 10966 |
rs189123849 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40B | GRCh38.p7 | 17:82692923 | ATATTTTAAACACTC[C/T]TAGCAAGCATTGAAA | 10966 |
rs189316086 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82665799 | TTGAACCCGGGAGGC[A/G]GAGGTTGCAGTGAAC | 10966 |
rs189485446 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40B | GRCh38.p7 | 17:82693544 | GTGCCTGATACCCAG[C/T]GATTCACACGCATAG | 10966 |
rs189489649 | snp | C/T | 0.0023933 | 0.0345097 | utr-variant-3-prime | RAB40B | GRCh38.p7 | 17:82657273 | AAAACTGTAGATTTA[C/T]AGAAAAATATGCATA | 10966 |
rs189540434 | snp | C/G | 0.0185938 | 0.0946107 | intron-variant | RAB40B | GRCh38.p7 | 17:82698271 | CCGCGAACCGCGCTC[C/G]TCCTCAGCCCCGCGC | 10966 |
rs189548151 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RAB40B | GRCh38.p7 | 17:82682532 | AAAATCCTAGCAGGA[C/T]TTTTCTTGGTAGAAA | 10966 |
rs189767289 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RAB40B | GRCh38.p7 | 17:82677072 | TCCTGCCTCAGCCTC[C/T]CGAGTAGCTGGGATT | 10966 |
rs189853239 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | RAB40B | GRCh38.p7 | 17:82662054 | TCCCCAGTGGGCCAG[C/G]GGCTGGCCCCGCACA | 10966 |
rs189854969 | snp | C/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82699980 | GAAGTTTTTTGTGGG[C/G]GAGGAACAGAAGAGG | 10966 |
rs189860346 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40B | GRCh38.p7 | 17:82681753 | CTATCAATGCAATTT[A/G]TCACATCAATAAATC | 10966 |
rs189861117 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | RAB40B | GRCh38.p7 | 17:82684077 | AATACAAAAATTAGC[G/T]GGGTGTGGTGGCAGG | 10966 |
rs190079906 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant, utr-variant-5-prime | RAB40B | GRCh38.p7 | 17:82696559 | AGTGCAGACAAAGCC[C/T]TGTCCTCCAGGCGCT | 10966 |
rs190115282 | snp | C/G | 0 | 0 | intron-variant | RAB40B | GRCh38.p7 | 17:82660043 | GCACAGATGCACGCA[C/G]ACACAGTGCACGTAC | 10966 |
rs190152517 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82666092 | ACCACACCTGCCACC[A/G]CACCTGCCACCACAC | 10966 |
rs190198225 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82666829 | TGTGGGATTTGCTTG[A/G]TTTATTTCATGTATA | 10966 |
rs190202333 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40B | GRCh38.p7 | 17:82686921 | ATCCAGTGCTGGGGC[A/G]AAGGGTGCTCAGAGG | 10966 |
rs190291678 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | RAB40B | GRCh38.p7 | 17:82660867 | ACTCTCAGCACCAAT[G/T]TATACGTAAGCTTAA | 10966 |
rs190309815 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RAB40B | GRCh38.p7 | 17:82689698 | AAACTGGCCGGGCAC[A/G]TGGCTCACACCTGTA | 10966 |
rs190391525 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RAB40B | GRCh38.p7 | 17:82686259 | TGAGATAACAGGCAC[A/C]TGCCACCACGCCCAG | 10966 |
rs190444894 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 17:82654848 | GAGCCACCGCGCCCT[A/G]CCAGGACAGTGGTTT | 10966 |
rs190457029 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | RAB40B | GRCh38.p7 | 17:82674593 | GCAGTGAGCCGAGAT[C/T]GCGCCACTGCACTCC | 10966 |
rs190553465 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RAB40B, MIR4525 | GRCh38.p7 | 17:82669533 | TGGTGCACACCTGTC[A/G]TCCCAGCTTCTCAGG | 10966 |
rs190603182 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | RAB40B | GRCh38.p7 | 17:82687908 | AAGACCCTCTCTCTA[C/G/T]TAAAAATAAAATAAT | 10966 |
rs190614619 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RAB40B | GRCh38.p7 | 17:82691538 | CTAAAAATACAAAAA[G/T]TAGCCGGGCATGGTA | 10966 |
rs190760742 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RAB40B | GRCh38.p7 | 17:82693938 | AAATACAAAAATTAG[C/T]CAGGCGTGGTGGCGC | 10966 |
rs190764425 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B, synonymous-codon | RAB40B, MIR4525 | GRCh38.p7 | 17:82667896 | CGAGCCCAGCAGGCA[C/T]GCTGAGTGCACCGTC | 10966 |
rs190855357 | snp | C/T | | | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82671881 | TCACACACCCTGTAC[C/T]CACTGACACACCCCA | 10966 |
rs190859127 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40B | GRCh38.p7 | 17:82667283 | GAGGTGTGCAGTGGC[A/G]GTGCCACCGGTGGCC | 10966 |
rs190951428 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RAB40B | GRCh38.p7 | 17:82673361 | TTCACTTTCTTTGGG[G/T]CATCTTTCCAGACCT | 10966 |
rs191125886 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RAB40B | GRCh38.p7 | 17:82674107 | GCACTTTGGGAGGCC[A/G]AGGCGGGCGGATCAC | 10966 |
rs191257929 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | RAB40B | GRCh38.p7 | 17:82680770 | GGCACGGTGGCTCAC[A/G]CCTTTAATCCCAGCA | 10966 |
rs191268388 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RAB40B | GRCh38.p7 | 17:82659116 | TCCAGAACCGTGAGA[G/T]AATGCATTTCTGTTG | 10966 |
rs191272414 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RAB40B | GRCh38.p7 | 17:82659295 | AGCCCGACCACAGCA[A/G]GGAGTGAAGCAGGCC | 10966 |
rs191272780 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RAB40B | GRCh38.p7 | 17:82695555 | TCATTAAAAAAAAAA[A/C]AAAACATGGCCAGGT | 10966 |
rs191385599 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RAB40B | GRCh38.p7 | 17:82682958 | GACCATCCTGGCTAA[C/T]AAGGTAAAACCCTGT | 10966 |
rs191476171 | snp | C/T | 0.160938 | 0.233598 | intron-variant | RAB40B | GRCh38.p7 | 17:82679426 | AGCTGGGACTACAGG[C/T]GCCTGCCACCACGCC | 10966 |
rs191531958 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82665723 | AATTCAAAAATTAGC[C/T]GGGTGTGGTGGCGGG | 10966 |
rs191648089 | snp | A/G | | | upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82699447 | TGTCCCTCTGCAGGT[A/G]TCTGCACATCTATGT | 10966 |
rs191666638 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime | RAB40B | GRCh38.p7 | 17:82661608 | AAACAAATGAAAGGC[A/C]GGGCTTGGCGGCTCA | 10966 |
rs191680288 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RAB40B | GRCh38.p7 | 17:82685456 | CCAAGCATGGACGAC[C/T]GGCAGAATGAGCTGT | 10966 |
rs191811184 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | RAB40B | GRCh38.p7 | 17:82688660 | TTGTTTGGGCCGGGC[A/G]TGGTGGCTCACGCCT | 10966 |
rs191833188 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant, upstream-variant-2KB | RAB40B, MIR4525 | GRCh38.p7 | 17:82668792 | CCCAGGGCAGCGGGC[C/G]GCGGCACGCAGGGAA | 10966 |
rs192012880 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RAB40B | GRCh38.p7 | 17:82690888 | GTGCACGTTTGCCCC[A/G]GGGGAGCATGGAGTG | 10966 |
rs192020829 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RAB40B | GRCh38.p7 | 17:82688210 | AACTTTCTGTAGAGA[C/T]GAGGTTTCCCTATAT | 10966 |
rs192038414 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | RAB40B | GRCh38.p7 | 17:82658362 | TACTTCTCTCAAATG[C/T]CTTGCTCTGAGAACG | 10966 |
rs192062681 | snp | A/G | | | intron-variant | RAB40B | GRCh38.p7 | 17:82693089 | CTCACTGCAACCTCC[A/G]CCTCCCGGGTTCAAG | 10966 |
rs192069708 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | RAB40B | GRCh38.p7 | 17:82677025 | ACGATCTCGGCTCAC[C/T]GCAAGCTCCACCTCC | 10966 |
rs192218361 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RAB40B | GRCh38.p7 | 17:82695912 | ACAGAATTTCGCTCT[C/T]GTTGCCCAGGCTGGA | 10966 |
rs192270000 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RAB40B | GRCh38.p7 | 17:82689596 | TGATACAATGCAATG[A/G]TGTTATTTTCAAATG | 10966 |
rs192365555 | snp | C/T | | | intron-variant | RAB40B | GRCh38.p7 | 17:82684135 | CTGAGGCAGGAGAAT[C/T]GCTTGAACCCGGGAG | 10966 |
rs192429827 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40B | GRCh38.p7 | 17:82675920 | GGTCCTTCTCACCAG[A/G]GGGGAGAGGTGGCAA | 10966 |
rs192526276 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40B | GRCh38.p7 | 17:82676689 | CTGGAATGCAATGGC[A/G]TGATCTCAACTCACT | 10966 |
rs192542275 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40B | GRCh38.p7 | 17:82692434 | CCTGAGCAAGGACAA[A/G]ATGCATCTGACTGCC | 10966 |
rs192563357 | snp | A/G | 0.00755907 | 0.0610114 | downstream-variant-500B | RAB40B | GRCh38.p7 | 17:82656791 | GGCCAAGGTGGGTGG[A/G]TCACCTGAGGTTAGG | 10966 |
rs192710688 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | RAB40B | GRCh38.p7 | 17:82697082 | CAGCTGCCAGAGACT[C/T]CCCCGCATGCTGCAG | 10966 |
rs192766413 | snp | C/T | | | intron-variant | RAB40B | GRCh38.p7 | 17:82692010 | CAGAGCAGTGGGGCC[C/T]GCACGGTCCGTGGGC | 10966 |
rs192781482 | snp | A/G | 0.0185938 | 0.0946107 | | | GRCh38.p7 | 17:82656010 | CTGGGGTGCAGTGGT[A/G]CGATCTCGGCTCACT | 10966 |
rs192886667 | snp | A/G | 0.00159617 | 0.0282053 | downstream-variant-500B | RAB40B | GRCh38.p7 | 17:82656875 | AAAAATTAGCCGGGC[A/G]TGGTGGTGCACCTCT | 10966 |
rs192897610 | snp | C/T | | | intron-variant | RAB40B | GRCh38.p7 | 17:82684474 | AAGTTCGCACAAAAA[C/T]GAGTCATAAACATGC | 10966 |
rs192934213 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RAB40B | GRCh38.p7 | 17:82681840 | TTTTCACAACAAAAG[C/T]TCTCAGCAAACTAGG | 10966 |
rs193116856 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RAB40B | GRCh38.p7 | 17:82664163 | TGGTGGGAGGGTGTT[A/C]CCCGGGGGCGCTGTG | 10966 |
rs193118509 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82665282 | TTTTGAGACAGAGTT[C/T]CTCTCTGTCGCCCTG | 10966 |
rs193184411 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RAB40B | GRCh38.p7 | 17:82659722 | GCTGTGGCCATGCAC[A/G]CAAAGACATACAACT | 10966 |
rs199534613 | snp | A/C | | | intron-variant | RAB40B | GRCh38.p7 | 17:82676298 | CACCCCTCACCTTCA[A/C]CAGCCTCTCCCTCCA | 10966 |
rs199572182 | in-del | -/TGGCCGTGCACTTA | | | intron-variant | RAB40B | GRCh38.p7 | 17:82685363 | CCGTGCACTCAACTG[-/TGGCCGTGCACTTA]AACGCAGATTCCTGG | 10966 |
rs199586588 | snp | G/T | 0.000128173 | 0.00800439 | missense, utr-variant-5-prime | RAB40B | GRCh38.p7 | 17:82698502 | CCATCCTGCAGGCTC[G/T]CCAGGATCTCGCCCT | 10966 |
rs199586923 | snp | A/G | 1.72139e-05 | 0.00293371 | intron-variant, missense, downstream-variant-500B | RAB40B | GRCh38.p7 | 17:82661066 | GAAAAGATGTTGGAG[A/G]CCATTAAGAAGAAAC | 10966 |
rs199611755 | snp | C/T | | | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82671219 | TAACACACACTCACA[C/T]GCTCCCTGTACTCAC | 10966 |
rs199642999 | snp | C/T | | | intron-variant, downstream-variant-500B | RAB40B | GRCh38.p7 | 17:82660687 | ACCTGCACACACATG[C/T]ACACACACACACACA | 10966 |
rs199644115 | snp | C/T | 0.00536575 | 0.0515178 | utr-variant-5-prime | RAB40B | GRCh38.p7 | 17:82698610 | ATCGTGACGGCCCGG[C/T]GCCCCCACCCATGCC | 10966 |
rs199695531 | snp | C/T | | | intron-variant | RAB40B | GRCh38.p7 | 17:82683083 | GGGAGATGGAGCTTG[C/T]AGTGAGCCGAGATCA | 10966 |
rs199700140 | snp | A/G | 4.9423e-05 | 0.00497082 | synonymous-codon | RAB40B | GRCh38.p7 | 17:82657977 | GCTGGTGGTGAGGGA[A/G]TAGGAACCGCCGTGC | 10966 |
rs199734002 | in-del | -/AC | 0.0356815 | 0.128715 | intron-variant | RAB40B | GRCh38.p7 | 17:82660426 | TTCACACACGTGTAA[-/AC]ACACGCACAGGCACT | 10966 |
rs199774110 | snp | A/C | | | intron-variant | RAB40B | GRCh38.p7 | 17:82676429 | CACCCCTCACCTTCA[A/C]CAGCCTCTCCCCCCC | 10966 |
rs199805662 | in-del | -/TT | | | intron-variant | RAB40B | GRCh38.p7 | 17:82679279 | TTATTATTATTATTA[-/TT]TTATTTTATTTTATT | 10966 |
rs199886901 | snp | C/T | 0.000500843 | 0.0158168 | missense | RAB40B | GRCh38.p7 | 17:82658502 | CTACCCTTGCTCGGC[C/T]GCCAGAGCCGGTCCA | 10966 |
rs199944935 | in-del | -/GCTCCCTGT | | | intron-variant | RAB40B | GRCh38.p7 | 17:82672243 | CACACACACTCACAC[-/GCTCCCTGT]ACTCACTGACACACC | 10966 |
rs199951104 | snp | A/T | 0.000399281 | 0.0141238 | missense | RAB40B | GRCh38.p7 | 17:82658685 | TGCAGGCGGTTCCCC[A/T]CCAGGATCTTGGGGA | 10966 |
rs199980695 | snp | C/T | 3.39115e-05 | 0.0041176 | intron-variant | RAB40B | GRCh38.p7 | 17:82658470 | GGCAGAGGTGGCCCC[C/T]GGAATAGCCCCTGGG | 10966 |
rs200050151 | snp | A/G | | | intron-variant | RAB40B | GRCh38.p7 | 17:82679777 | CCACCAAGCACAGGG[A/G]AGGGGCCAGCTTCCA | 10966 |
rs200128051 | snp | C/T | | | intron-variant | RAB40B | GRCh38.p7 | 17:82686352 | CCTGACCTCAAGTGA[C/T]CCACCTGCCTCGGCC | 10966 |
rs200147669 | in-del | -/G | | | intron-variant | RAB40B | GRCh38.p7 | 17:82673464 | CCTTCCCTCTCTTAA[-/G]CTGACTCCTCTTTTC | 10966 |
rs200164038 | snp | C/T | 0.000187731 | 0.0096866 | intron-variant | RAB40B | GRCh38.p7 | 17:82658443 | GCCGCTGACCCACCT[C/T]GGCATCTGGAGGGCA | 10966 |
rs200202167 | snp | C/G/T | 0.000153988 | 0.00877328 | missense | RAB40B | GRCh38.p7 | 17:82658704 | GGATCTTGGGGACTC[C/G/T]GGGGGCATGCTAGCG | 10966 |
rs200212347 | snp | A/T | | | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82672029 | CACACACGCTCCCTG[A/T]ACTCACTGACACACC | 10966 |
rs200220668 | in-del | -/GCTT | 0.0948562 | 0.196037 | upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82699683 | CCTATGTGTGCGTGC[-/GCTT]GCTTGTTTGTGCATC | 10966 |
rs200372195 | snp | C/G | | | intron-variant, upstream-variant-2KB | RAB40B | GRCh38.p7 | 17:82671574 | TGACACACCCCACCC[C/G]TGTAACTCTAACACA | 10966 |
rs200447399 | in-del | -/A | 0.0158469 | 0.0875917 | intron-variant | RAB40B | GRCh38.p7 | 17:82681890 | GATAAAGTGCATCTT[-/A]AAAAAAAGAACCTCA | 10966 |
rs200465969 | snp | G/T | 1.78892e-05 | 0.0029907 | synonymous-codon, utr-variant-5-prime | RAB40B | GRCh38.p7 | 17:82698513 | GCTCGCCAGGATCTC[G/T]CCCTTGCCCACGTCG | 10966 |
rs200488513 | snp | A/C | 0.00608168 | 0.0548074 | intron-variant | RAB40B | GRCh38.p7 | 17:82659679 | GAGAGGTCACAGGCT[A/C]AGCACGCAGAACACA | 10966 |
rs200519672 | snp | A/G | 0.000355328 | 0.0133243 | intron-variant | RAB40B | GRCh38.p7 | 17:82658176 | TTAGTGGATGTCCCC[A/G]CCTGGGCTGGGAATG | 10966 |
rs200528124 | snp | A/G | | | intron-variant, downstream-variant-500B | RAB40B | GRCh38.p7 | 17:82660684 | CGTACCTGCACACAC[A/G]TGTACACACACACAC | 10966 |
rs200530803 | snp | A/G | | | intron-variant | RAB40B | GRCh38.p7 | 17:82667447 | GCACACCTGTGCAGC[A/G]CCTTCCATGAGATCC | 10966 |