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 |