SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs8018 | snp | C/T | 0.0150087 | 0.0853176 | synonymous-codon | TSG101 | GRCh38.p7 | 11:18481759 | TATCGATGAAGTTAT[C/T]ATTCCCACAGCTCCC | 7251 |
rs15387 | snp | A/T | 0 | 0 | utr-variant-3-prime | TSG101 | GRCh38.p7 | 11:18480490 | ATTCTTCTCTTCCTT[A/T]TATCAGTAGGTGCCC | 7251 |
rs171496 | snp | A/G | 0 | 0 | intron-variant | TSG101 | GRCh38.p7 | 11:18521609 | ggaaggctgagttga[A/G]aggatcacttccagg | 7251 |
rs181714 | snp | C/T | 0 | 0 | intron-variant | TSG101 | GRCh38.p7 | 11:18517200 | acttagaccccattt[C/T]taaaaaaaaaaaaag | 7251 |
rs193329 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18521586 | cttccaggagtttga[A/G]aacagcttgggcaac | 7251 |
rs243826 | snp | G/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18521652 | AGGggccaggtgcag[G/T]ggttcatacctgtaa | 7251 |
rs868069 | snp | A/G | 0.499 | 0.0223418 | intron-variant | TSG101 | GRCh38.p7 | 11:18495474 | ACTTCCTCTTTTTTT[A/G]CCAGGGGCAGGGGTG | 7251 |
rs1395319 | snp | G/T | 0.499 | 0.0223418 | intron-variant | TSG101 | GRCh38.p7 | 11:18526636 | CGCCTCGGGGCGGGG[G/T]TCTGAGGAGGTCGCT | 7251 |
rs1395320 | snp | C/G | 0.498927 | 0.0231381 | intron-variant | TSG101 | GRCh38.p7 | 11:18526648 | GGGTTCTGAGGAGGT[C/G]GCTAAGGACTGCACC | 7251 |
rs1804795 | snp | A/G | 0 | 0 | missense | TSG101 | GRCh38.p7 | 11:18480599 | AAACAGTTCCAGCTG[A/G]GGGCACTAATGCAAA | 7251 |
rs1848047 | snp | A/C | 0 | 0 | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18528057 | ctggagtgcagtagc[A/C]ccatctcggctcact | 7251 |
rs1857908 | snp | C/T | 0.0205511 | 0.0992634 | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18527027 | TTGAGAGGGGCCTGG[C/T]GGGGTGGGTTCCAAC | 7251 |
rs1857909 | snp | A/G | 0.185155 | 0.241444 | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18527334 | CTAGCTCAGGCGCAA[A/G]TTTCTCCCGACTCTA | 7251 |
rs1973412 | snp | A/G | 0.18325 | 0.240924 | intron-variant | TSG101 | GRCh38.p7 | 11:18513796 | taagccaccatgccc[A/G]gccTACTTACTTATT | 7251 |
rs2088181 | snp | A/G | 0.48 | 0.0979796 | intron-variant | TSG101 | GRCh38.p7 | 11:18521670 | aaaaaaaaaaaaaaa[A/G]gaaggggccaggtgc | 7251 |
rs2088182 | snp | G/T | 0.139564 | 0.224285 | intron-variant | TSG101 | GRCh38.p7 | 11:18521513 | GGTGTGATGGTGCAT[G/T]CCTGTAGTCCCAGCT | 7251 |
rs2088183 | snp | C/T | 0.340333 | 0.233109 | intron-variant | TSG101 | GRCh38.p7 | 11:18521487 | cagctacttgggagg[C/T]ggtggtgggagtatc | 7251 |
rs2088184 | snp | G/T | 0.340108 | 0.233197 | intron-variant | TSG101 | GRCh38.p7 | 11:18522306 | GAGGAGTTCAGTTTT[G/T]GTCATGTTCAATTTG | 7251 |
rs2132302 | snp | C/T | 0.37778 | 0.214877 | intron-variant | TSG101 | GRCh38.p7 | 11:18495370 | AAAAAGCTATATAGA[C/T]GATTGTAGTTGATTT | 7251 |
rs2174614 | snp | A/G | 0 | 0 | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18528189 | GTCTTTTAAAAGCAA[A/G]AAGGTTTTCAAACTG | 7251 |
rs2279900 | snp | C/T | 0.344193 | 0.231576 | intron-variant | TSG101 | GRCh38.p7 | 11:18481612 | TAAAAAATCTTGGAA[C/T]GTAAAATGAAGAAAT | 7251 |
rs2279901 | snp | A/G | 0.105282 | 0.203854 | synonymous-codon | TSG101 | GRCh38.p7 | 11:18484005 | CCGCCATCTCAGTTT[A/G]TCACTGACCGCAGAG | 7251 |
rs2279902 | snp | A/G | 0.264575 | 0.249575 | intron-variant | TSG101 | GRCh38.p7 | 11:18484085 | GACCTGCAGGAAACA[A/G]AGGCAAAAAACACTT | 7251 |
rs2291751 | snp | A/G | 0.271432 | 0.24908 | downstream-variant-500B | TSG101 | GRCh38.p7 | 11:18480107 | TTGGACCTTTCACAG[A/G]TAAGTTACTCAAATG | 7251 |
rs2291752 | snp | C/T | 0.369958 | 0.21934 | downstream-variant-500B | TSG101 | GRCh38.p7 | 11:18480181 | ATCCCCATGTTAATT[C/T]ACTTTATATGCTGTA | 7251 |
rs2291753 | snp | A/C | 0.154661 | 0.231107 | downstream-variant-500B | TSG101 | GRCh38.p7 | 11:18480287 | TCATGGATCTTTCCT[A/C]AAGTCCAATAAAGGA | 7251 |
rs2291754 | snp | C/T | 0.0232847 | 0.105357 | utr-variant-3-prime | TSG101 | GRCh38.p7 | 11:18480471 | AACTGCAATAACTTA[C/T]TCTGGGCACCTACTG | 7251 |
rs2292176 | snp | G/T | 0.339429 | 0.233457 | intron-variant | TSG101 | GRCh38.p7 | 11:18509481 | AGAACAGAAACCTTT[G/T]TAAAAAAATAAAGAA | 7251 |
rs2292177 | snp | C/T | 0 | 0 | intron-variant | TSG101 | GRCh38.p7 | 11:18526697 | GGGAAGCTTGCTTGG[C/T]TGGGCCGGGACGGAC | 7251 |
rs2292178 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime | TSG101 | GRCh38.p7 | 11:18526904 | CACAATCGCACACCC[C/G]CAACCCGGCCTCAAA | 7251 |
rs2292179 | snp | A/G | 0.27008 | 0.249192 | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18526999 | TGCGGGCAAGGGTGG[A/G]CACCGTGTGGGATTG | 7251 |
rs2643866 | snp | A/G | 0.39527 | 0.203462 | intron-variant | TSG101 | GRCh38.p7 | 11:18510909 | TTGTTTTTTTGAAAC[A/G]GGGTCTCACTCTAAC | 7251 |
rs2643867 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TSG101 | GRCh38.p7 | 11:18510634 | ttgatcctcctgcct[C/T]ggcctcccaaagtgc | 7251 |
rs2643868 | snp | A/G | 0.182933 | 0.240836 | intron-variant | TSG101 | GRCh38.p7 | 11:18505846 | TGGGCGACAGAGCAA[A/G]ACTCTCTCTCAAACA | 7251 |
rs2643869 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | TSG101 | GRCh38.p7 | 11:18497532 | GCTTAGATGATTTCC[A/G]TATATCCAAAGAATA | 7251 |
rs2643870 | snp | A/G | 0.433963 | 0.169285 | intron-variant | TSG101 | GRCh38.p7 | 11:18483623 | TTAGTTCGTTTTCAC[A/G]CTGCTGATAAAGACA | 7251 |
rs2658547 | snp | C/T | 0.18325 | 0.240924 | intron-variant | TSG101 | GRCh38.p7 | 11:18507268 | AATAAAGAAGTTACT[C/T]TCTAAGAAGTTAACC | 7251 |
rs2658552 | snp | A/G | 0.395087 | 0.203592 | intron-variant | TSG101 | GRCh38.p7 | 11:18502661 | ACAACCATATGTCAA[A/G]CTTAACTTCCTGAAT | 7251 |
rs2658554 | snp | A/G | 0.480302 | 0.0972668 | intron-variant | TSG101 | GRCh38.p7 | 11:18491419 | TCACCTGAGCCTTGG[A/G]TCTAGAGTTTTTATC | 7251 |
rs2658555 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | TSG101 | GRCh38.p7 | 11:18489459 | AGCTAAAGAAAAGCC[A/G]TGTGTTTTATGAATG | 7251 |
rs2658556 | snp | A/T | 0.0205511 | 0.0992634 | intron-variant | TSG101 | GRCh38.p7 | 11:18481187 | TTTCAAGCCCTCTTG[A/T]ATGAAAGTTGTCTCA | 7251 |
rs2658564 | snp | A/G | 0.480931 | 0.0957637 | intron-variant | TSG101 | GRCh38.p7 | 11:18510127 | GGCTAGAATCTACCT[A/G]TAATTTCAGAGTTCA | 7251 |
rs2658567 | snp | C/G | 0.4021 | 0.198407 | intron-variant | TSG101 | GRCh38.p7 | 11:18509008 | GAGAGTGTTGCTTCT[C/G]CCCTAATTGGAATAT | 7251 |
rs2698565 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | TSG101 | GRCh38.p7 | 11:18502745 | GCAGTGTCATTAATA[A/C]AATTTCCATAGAGCT | 7251 |
rs2698567 | snp | C/G | 0.481396 | 0.0946345 | intron-variant | TSG101 | GRCh38.p7 | 11:18488946 | ATGGTGAAAACCCAT[C/G]TCTACTAAAAATACA | 7251 |
rs2896534 | snp | A/C | 0.5 | 0 | intron-variant | TSG101 | GRCh38.p7 | 11:18521734 | aactgagatcacacc[A/C]ccgcactccagcctg | 7251 |
rs3781640 | snp | A/G | 0.268995 | 0.249277 | intron-variant | TSG101 | GRCh38.p7 | 11:18482190 | AGAAGGTTCCTTTAC[A/G]TAGAAAATCATAAGA | 7251 |
rs3802965 | snp | C/G | 0.345482 | 0.231048 | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18527772 | AAAATTTTACAATAC[C/G]TTGAATGACACTGTG | 7251 |
rs3802966 | snp | C/G | 0.345704 | 0.230956 | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18527416 | GTATAGTATGAAGGT[C/G]TTTAAGCTTAAAAAA | 7251 |
rs3925781 | snp | G/T | 0.498832 | 0.0241331 | intron-variant | TSG101 | GRCh38.p7 | 11:18502943 | GATACTATTTAATTT[G/T]TACCTGTGGCTTATT | 7251 |
rs3958123 | snp | A/G | | | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18528244 | GAGTCCCTTTAATTA[A/G]AGCAACTGTACCTTT | 7251 |
rs4298881 | snp | C/T | 0.498813 | 0.0243321 | intron-variant | TSG101 | GRCh38.p7 | 11:18507245 | AATTCTGGCCTTCTT[C/T]GGTCCAAGGTTAACT | 7251 |
rs4388870 | snp | C/G | 0.0174175 | 0.0916809 | intron-variant | TSG101 | GRCh38.p7 | 11:18520900 | tctgggcgtggtggt[C/G]cgcacctataatccc | 7251 |
rs4390325 | snp | A/C | 0.340333 | 0.233109 | intron-variant | TSG101 | GRCh38.p7 | 11:18521323 | GTCAGCAGTATTTGA[A/C]CAAGCTGATTCAGCA | 7251 |
rs4483571 | snp | A/G | 0 | 0 | intron-variant | TSG101 | GRCh38.p7 | 11:18521553 | TTTAAATTTTTCATA[A/G]AGACAGGATCTCACT | 7251 |
rs4635056 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | TSG101 | GRCh38.p7 | 11:18525502 | AGTGAGCCAAGATCG[C/T]GCCACTGCACTCCAG | 7251 |
rs4636650 | snp | C/T | 0.318656 | 0.240388 | intron-variant | TSG101 | GRCh38.p7 | 11:18520887 | aatacaaaaattatc[C/T]gggcgtggtggtccg | 7251 |
rs4757669 | snp | C/T | 0.339429 | 0.233457 | intron-variant | TSG101 | GRCh38.p7 | 11:18501716 | GTAATATAGTCATTT[C/T]TACAATATTAATTCT | 7251 |
rs6486430 | snp | A/G | 0.481396 | 0.0946345 | intron-variant | TSG101 | GRCh38.p7 | 11:18488226 | TTTTTGTTCAGTTAG[A/G]AAGGAGGGATTTTTG | 7251 |
rs6486431 | snp | A/G | 0.340333 | 0.233109 | intron-variant | TSG101 | GRCh38.p7 | 11:18520680 | TTGTATCCCTTTAGT[A/G]TAGTTTCATAGATAT | 7251 |
rs7107677 | snp | C/G | 0.195214 | 0.243923 | intron-variant | TSG101 | GRCh38.p7 | 11:18513073 | ACCTCTAAGTTCTCC[C/G]TCCTAAGATGTGTTC | 7251 |
rs7110705 | snp | C/G/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18488861 | ccgggcgcagtggct[C/G/T]acacctgcaattcca | 7251 |
rs7113379 | snp | A/G | 0 | 0 | intron-variant | TSG101 | GRCh38.p7 | 11:18489402 | accatgcctgacTCA[A/G]AAGATTATTCTTAAA | 7251 |
rs7127716 | snp | C/T | 0.0603597 | 0.1629 | intron-variant | TSG101 | GRCh38.p7 | 11:18500655 | tgtctattcatgttc[C/T]ttgcccactttttaa | 7251 |
rs7129164 | snp | C/T | 0.393803 | 0.204501 | intron-variant | TSG101 | GRCh38.p7 | 11:18518667 | GGACAGTCCAGAGTA[C/T]AGTTTCGCAAAATGT | 7251 |
rs7928872 | snp | A/G | 0.499846 | 0.00878459 | intron-variant | TSG101 | GRCh38.p7 | 11:18516254 | TGGTTAAAATTCATC[A/G]TTATCCTTGAAAGGG | 7251 |
rs7931630 | snp | A/G | 0.499017 | 0.0221427 | intron-variant | TSG101 | GRCh38.p7 | 11:18525785 | TGCTTTATTTTGAAA[A/G]CTGTCATTTTCTCCT | 7251 |
rs7934817 | snp | C/T | 0.49889 | 0.0235361 | intron-variant | TSG101 | GRCh38.p7 | 11:18516493 | gggattacaggcacg[C/T]gccaccacacctgac | 7251 |
rs7942548 | snp | C/T | 0.499846 | 0.00878459 | intron-variant | TSG101 | GRCh38.p7 | 11:18516253 | CTGGTTAAAATTCAT[C/T]ATTATCCTTGAAAGG | 7251 |
rs9633899 | snp | C/T | 0.378568 | 0.214407 | intron-variant | TSG101 | GRCh38.p7 | 11:18525097 | TTGTATTTTAGGAGA[C/T]GGGGTTTCACCATGT | 7251 |
rs10444226 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | TSG101 | GRCh38.p7 | 11:18523437 | TTTCTTTGTCTGATT[A/G]TTCACTGTTGCATCC | 7251 |
rs10444251 | snp | A/C | 0.0207302 | 0.0996762 | intron-variant | TSG101 | GRCh38.p7 | 11:18502616 | TTAACATTTAAGATG[A/C]CCCAACCTTATAGTA | 7251 |
rs10500836 | snp | C/T | 0.498813 | 0.0243321 | intron-variant | TSG101 | GRCh38.p7 | 11:18507561 | GTTCTTTGGCATTCA[C/T]GTTCTCTTTAAAGAA | 7251 |
rs10639268 | in-del | -/AAT | 0.420096 | 0.183214 | intron-variant | TSG101 | GRCh38.p7 | 11:18510944 | AAACCCAACAACAAC[-/AAT]GACAACAAAAAACAA | 7251 |
rs10766483 | snp | C/T | 0.499437 | 0.0167637 | intron-variant | TSG101 | GRCh38.p7 | 11:18496199 | CTGGGTGAGGTGGCT[C/T]ATGCCTGTAATCCCA | 7251 |
rs10766484 | snp | C/T | 0.499017 | 0.0221427 | intron-variant | TSG101 | GRCh38.p7 | 11:18518383 | AATTCAGTTCCTTGC[C/T]TTCAGAGCTAAGGGA | 7251 |
rs10832938 | snp | A/G | 0.381697 | 0.212499 | intron-variant | TSG101 | GRCh38.p7 | 11:18483128 | GTGATAGTAAGTCTC[A/G]CAAGATCTGATGGGT | 7251 |
rs10832939 | snp | C/T | 0.339656 | 0.233371 | intron-variant | TSG101 | GRCh38.p7 | 11:18508500 | CGGCCAAATATTTCG[C/T]ATTTCAAACTTAAGC | 7251 |
rs11024674 | snp | C/T | 0.39009 | 0.207062 | intron-variant | TSG101 | GRCh38.p7 | 11:18486311 | cagcaggtagcatgg[C/T]tgagggaggcccagg | 7251 |
rs11024675 | snp | G/T | 0.378174 | 0.214642 | intron-variant | TSG101 | GRCh38.p7 | 11:18486635 | aggtgctggagagga[G/T]gtggagaaataggaa | 7251 |
rs11024676 | snp | C/T | 0.384017 | 0.211044 | intron-variant | TSG101 | GRCh38.p7 | 11:18486654 | gagaaataggaacac[C/T]tttacactgttggtg | 7251 |
rs11024677 | snp | A/C | 0.271702 | 0.249056 | intron-variant | TSG101 | GRCh38.p7 | 11:18487487 | AACTTTACTAAAACA[A/C]CTTAACACAAGGAAG | 7251 |
rs11024678 | snp | G/T | 0.378174 | 0.214642 | intron-variant | TSG101 | GRCh38.p7 | 11:18488242 | AAGGAGGGATTTTTG[G/T]TTTTTTTCTTTTTTT | 7251 |
rs11024679 | snp | C/T | 0.378765 | 0.214288 | intron-variant | TSG101 | GRCh38.p7 | 11:18488474 | AGCTGGATAAGTGCA[C/T]TTGGGAGACCTGGTG | 7251 |
rs11024682 | snp | C/T | 0.0410537 | 0.137264 | intron-variant | TSG101 | GRCh38.p7 | 11:18493674 | TACTGACCATCTATT[C/T]AGAAACTAGACCGAG | 7251 |
rs11024683 | snp | A/G | 0.378962 | 0.21417 | intron-variant | TSG101 | GRCh38.p7 | 11:18495770 | AACACTATGTAAACT[A/G]AGGTTGAAGATGTCT | 7251 |
rs11024685 | snp | C/T | 0.384017 | 0.211044 | intron-variant | TSG101 | GRCh38.p7 | 11:18498062 | GCACTCTTCTGGATG[C/T]TGAGTGTGTGGGTGG | 7251 |
rs11024686 | snp | A/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18499279 | TTTATATATATTTAT[A/T]TATATCATATATATT | 7251 |
rs11024688 | snp | C/T | 0.269267 | 0.249256 | intron-variant | TSG101 | GRCh38.p7 | 11:18500244 | GATAAATATTTAGGT[C/T]CACTCCATATCTTAG | 7251 |
rs11024689 | snp | G/T | 0.377385 | 0.215112 | intron-variant | TSG101 | GRCh38.p7 | 11:18500591 | GATGAGTGATATTGA[G/T]CATTTTTTCATATAC | 7251 |
rs11024690 | snp | C/T | 0.498832 | 0.0241331 | intron-variant | TSG101 | GRCh38.p7 | 11:18503461 | CACTGCAAGCTCCAC[C/T]TCCTGGGTTCACGCC | 7251 |
rs11024691 | snp | A/G | 0.339203 | 0.233544 | intron-variant | TSG101 | GRCh38.p7 | 11:18504700 | TCTTCTAAGCCTACA[A/G]ATATTAACTTCAGAG | 7251 |
rs11024692 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | TSG101 | GRCh38.p7 | 11:18510444 | caaacaaaaaaaTTA[C/T]ACGTAGATTCTAGCT | 7251 |
rs11024693 | snp | A/G | 0.273049 | 0.248935 | intron-variant | TSG101 | GRCh38.p7 | 11:18512975 | TCAAGTGATCCTCCC[A/G]CCTCAGCCTCCCAAA | 7251 |
rs11024694 | snp | A/G | 0.40157 | 0.198813 | intron-variant | TSG101 | GRCh38.p7 | 11:18513349 | TGTCCAGGCTGGAGG[A/G]CAGTGATGCAATCAT | 7251 |
rs11024695 | snp | A/T | 0.376394 | 0.215696 | intron-variant | TSG101 | GRCh38.p7 | 11:18519202 | TTGAGACGAGGTTTC[A/T]CCATATTGCCCAGGC | 7251 |
rs11024696 | snp | C/G | 0.378372 | 0.214524 | intron-variant | TSG101 | GRCh38.p7 | 11:18520991 | AGCCGAGATCGTGCC[C/G]TTGCACTCCAGCCTG | 7251 |
rs11024697 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18521389 | TTTTTTTTTTTTTGA[A/G]ATAGGGTCTCACTCT | 7251 |
rs11024698 | snp | A/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18521391 | TTTTTTTTTTTGAGA[A/T]AGGGTCTCACTCTGT | 7251 |
rs11024699 | snp | A/T | 0.499265 | 0.0191552 | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18528019 | TTTTTTTTTTTTGAG[A/T]CACTCTCACTCCATC | 7251 |
rs11024700 | snp | A/G/T | | | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18528379 | tatatatatatatat[A/G/T]ttttttttttttttt | 7251 |
rs11542667 | snp | C/T | 0 | 0 | missense | TSG101 | GRCh38.p7 | 11:18480554 | GCCGGTCTCAGTGAC[C/T]TCTACTGACTTCTCT | 7251 |
rs11542668 | snp | A/G | | | utr-variant-3-prime | TSG101 | GRCh38.p7 | 11:18480406 | CAGTCTTTACCAAAA[A/G]AAAACAGAAAATATA | 7251 |
rs11556821 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18490685 | AGGCAGAACTGCAGG[A/G]CATCTGCAATGATGT | 7251 |
rs11600246 | snp | C/T | 0.341909 | 0.232492 | intron-variant | TSG101 | GRCh38.p7 | 11:18514163 | CTCTTTGCTGTTTTC[C/T]TCTCTACAGAATCTT | 7251 |
rs11603992 | snp | C/T | 0.339429 | 0.233457 | intron-variant | TSG101 | GRCh38.p7 | 11:18510399 | GCACTCCATCCTAGG[C/T]GACAGAGCAAGACTC | 7251 |
rs11606375 | snp | C/T | 0.339656 | 0.233371 | intron-variant | TSG101 | GRCh38.p7 | 11:18514104 | AAAAAAAAAAGGAAT[C/T]AGTAAGTACCCTGGG | 7251 |
rs11821116 | snp | A/G | 0.00938946 | 0.0678717 | intron-variant | TSG101 | GRCh38.p7 | 11:18505440 | ttaattttttttgta[A/G]aaatgaggtctacta | 7251 |
rs12222210 | snp | C/T | 0.390464 | 0.206809 | intron-variant | TSG101 | GRCh38.p7 | 11:18491025 | TGAGGTGACCACTTC[C/T]TTCCCAAGCCCACTC | 7251 |
rs12225463 | snp | A/C | 0.38555 | 0.210062 | intron-variant | TSG101 | GRCh38.p7 | 11:18488914 | GTGGATCATGAGGTC[A/C]AGAGATCGAGATCAA | 7251 |
rs12271838 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18526577 | CTGTCGCCGTCCCCC[A/G]CCCTCCCAGCTCCCG | 7251 |
rs12283473 | snp | C/T | 0.183568 | 0.241012 | intron-variant | TSG101 | GRCh38.p7 | 11:18516716 | agaggccgaggcagg[C/T]ggatcacctgaggtc | 7251 |
rs12287214 | snp | C/T | 0 | 0 | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18528086 | ctgcaacctccgcct[C/T]TGTTTTTCAGCTCCT | 7251 |
rs12287275 | snp | C/T | 0.00472811 | 0.0483911 | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18528207 | GGTTTTCAAACTGTT[C/T]TTAAAGCCACGGCTT | 7251 |
rs12419063 | snp | C/T | 0.498832 | 0.0241331 | intron-variant | TSG101 | GRCh38.p7 | 11:18503771 | GTGTTTCCCTTACAA[C/T]GAAGAAGAAAATTAG | 7251 |
rs12419375 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | TSG101 | GRCh38.p7 | 11:18509939 | CTTCATTTGACTCCA[A/C/T]AGAACTAACAAAAAT | 7251 |
rs12419592 | snp | C/T | 0.376592 | 0.215579 | intron-variant | TSG101 | GRCh38.p7 | 11:18517231 | TGTCCGGGCTGGACT[C/T]GAACTCCTGGACTCA | 7251 |
rs12421394 | snp | A/T | 0.271972 | 0.249033 | intron-variant | TSG101 | GRCh38.p7 | 11:18508473 | AAGTGCTGGGGTTAC[A/T]GCTACCACACCCGGC | 7251 |
rs12574333 | snp | G/T | 0.34877 | 0.229661 | intron-variant | TSG101 | GRCh38.p7 | 11:18514668 | TTCACAGAACACTAT[G/T]AATACTTACGTGTTT | 7251 |
rs12576836 | snp | A/G | 0 | 0 | intron-variant | TSG101 | GRCh38.p7 | 11:18482851 | CTTTATCATGGCTTA[A/G]AACTCTCTAAACTTA | 7251 |
rs12577132 | snp | A/C | 0.150667 | 0.229419 | intron-variant | TSG101 | GRCh38.p7 | 11:18514283 | CATAGGAACATTAAT[A/C]TGTCACAGTTACACT | 7251 |
rs12577874 | snp | C/G | 0.379158 | 0.214052 | intron-variant | TSG101 | GRCh38.p7 | 11:18497220 | TGTGGACTCTAATAT[C/G]TAAATGATACTTTTA | 7251 |
rs12785895 | snp | C/T | 0.0501905 | 0.150254 | intron-variant | TSG101 | GRCh38.p7 | 11:18489268 | tctccctacgttgtc[C/T]aggctggagtgcggt | 7251 |
rs12787005 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18483624 | gtctttatcagcagt[A/G]tgaaaacgaactaat | 7251 |
rs12787707 | snp | C/T | 0.00475057 | 0.0485048 | intron-variant | TSG101 | GRCh38.p7 | 11:18492606 | AAAGTCATTAACCCT[C/T]AAAATAAGAACCAAG | 7251 |
rs12801920 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18528483 | gcaacctctgcctcc[C/T]gggttcaagcgattc | 7251 |
rs12803110 | snp | A/T | | | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18528380 | atatatatatatatt[A/T]ttttttttttttttt | 7251 |
rs12808078 | snp | G/T | 0 | 0 | intron-variant | TSG101 | GRCh38.p7 | 11:18485258 | ACCATTAAATTATGG[G/T]GAAACCTAATCTTTG | 7251 |
rs16914838 | snp | A/G | 0.379354 | 0.213933 | intron-variant | TSG101 | GRCh38.p7 | 11:18489650 | TAAATTTCAGGATTC[A/G]AGTTTCTTCAGAGGA | 7251 |
rs16935476 | snp | C/T | 0.424037 | 0.179474 | intron-variant | TSG101 | GRCh38.p7 | 11:18488446 | GGTCTCGTTAAAACA[C/T]ATCTGAGAGTTGAGC | 7251 |
rs16935479 | snp | A/C | 0.0505692 | 0.150756 | intron-variant | TSG101 | GRCh38.p7 | 11:18488497 | ACCTGGTGAGGGGCA[A/C]TAAAAAGCATGATCA | 7251 |
rs16935482 | snp | A/G | 0.339203 | 0.233544 | intron-variant | TSG101 | GRCh38.p7 | 11:18503888 | TTGCCTTTTACAAGC[A/G]CATTAAAATTACTGA | 7251 |
rs16935488 | snp | A/G | 0.339203 | 0.233544 | intron-variant | TSG101 | GRCh38.p7 | 11:18507789 | AATTTAAAACTCAAA[A/G]AAATTTAGGAAAAAA | 7251 |
rs16935495 | snp | A/T | 0.0170251 | 0.090679 | intron-variant | TSG101 | GRCh38.p7 | 11:18510031 | TGAGCAACAGTCACA[A/T]TATTATTAAAGGCCA | 7251 |
rs16935504 | snp | A/C | 0.384017 | 0.211044 | intron-variant | TSG101 | GRCh38.p7 | 11:18513784 | TCCTTCATCAAGAAT[A/C]AGTAAGTAGGCTGGG | 7251 |
rs16935515 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | TSG101 | GRCh38.p7 | 11:18520508 | GGGATTTACAGGCAC[A/G]TATGGCCCACTTCTT | 7251 |
rs17492613 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | TSG101 | GRCh38.p7 | 11:18485132 | TAATTACCTGTTAGA[C/T]GATCCTGCTTTTTAC | 7251 |
rs17849606 | snp | A/G | | | missense | TSG101 | GRCh38.p7 | 11:18481686 | CTTCTCCCAAGTAAA[A/G]GATAGTGTCTTCAAT | 7251 |
rs28499082 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18525622 | ATATACCGTTTTTTT[C/T]AAAAAGTGATATATA | 7251 |
rs34063850 | snp | G/T | 0.00998959 | 0.0699643 | intron-variant | TSG101 | GRCh38.p7 | 11:18484199 | ATGAAACTGGTAACA[G/T]AATTTTTTTCTTTCC | 7251 |
rs34117046 | in-del | -/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18499194 | AAGAGGATTCTTTTT[-/T]AAATATATATATATA | 7251 |
rs34126789 | snp | G/T | 0.5 | 0 | intron-variant | TSG101 | GRCh38.p7 | 11:18500551 | GATTATATTTCTTTG[G/T]GGTTTTTATCTGCAT | 7251 |
rs34150212 | snp | A/G | 0.16618 | 0.23553 | intron-variant | TSG101 | GRCh38.p7 | 11:18515062 | TAATTGAGTATCAGC[A/G]TTGTATAAAGCAAGT | 7251 |
rs34165683 | in-del | -/A | 0.5 | 0 | intron-variant | TSG101 | GRCh38.p7 | 11:18526138 | AATTGAAAAAAAAAA[-/A]CACTAGTCTTGAGCC | 7251 |
rs34169487 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TSG101 | GRCh38.p7 | 11:18514498 | AATGGGTTTCTGTAG[A/G]GCTTTGTAATTTTCA | 7251 |
rs34178768 | snp | A/G | 0.0622301 | 0.165053 | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18527094 | AACAGTCTTGCCCAC[A/G]TCTTTGGGACCCGAT | 7251 |
rs34260314 | snp | C/G | 0.0142736 | 0.0832652 | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18527233 | GCCCTCCCACTTGAT[C/G]AATCAGTCATTAAGG | 7251 |
rs34361410 | snp | A/G | 0.0142736 | 0.0832652 | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18527338 | ACTTTAGAGTCGGGA[A/G]AAAYTTGCGCCTGAG | 7251 |
rs34377889 | in-del | -/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18480955 | CAGCCATTCATGTGG[-/G]TTGTACCACTTCTGA | 7251 |
rs34385327 | snp | A/G | 0.00388348 | 0.0438937 | missense | TSG101 | GRCh38.p7 | 11:18506904 | CTACATGCCAGGCAT[A/G]CCAGGTGGAATCTCT | 7251 |
rs34435519 | in-del | -/T/TT | 0.5 | 0 | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18528015 | TTTTTTTTTTTTTTT[-/T/TT]GAGTCACTCTCACTC | 7251 |
rs34457574 | snp | G/T | 0.499017 | 0.0221427 | intron-variant | TSG101 | GRCh38.p7 | 11:18519027 | TTTTTTTGAGACAGG[G/T]TCTTGCTCTGTTGCC | 7251 |
rs34532219 | snp | A/C | 0.0119091 | 0.0762411 | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18527845 | GAATCAATACTACGG[A/C]CTTSTTCTCATTAGG | 7251 |
rs34597429 | in-del | -/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18502414 | CAAAATTCACAAGTG[-/G]AAATGTGCTTTTCAC | 7251 |
rs34670032 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | TSG101 | GRCh38.p7 | 11:18495250 | GGTATTGGCTTTAAC[C/T]GGGAATAAACACCTA | 7251 |
rs34707820 | in-del | -/T | | | frameshift-variant | TSG101 | GRCh38.p7 | 11:18483961 | AGGCATTGAGCTCTG[-/T]CCTGGGCACGATCCA | 7251 |
rs34715514 | in-del | -/C | | | downstream-variant-500B | TSG101 | GRCh38.p7 | 11:18480285 | TTCATGGATCTTTCC[-/C]TAAAGTCCAATAAAG | 7251 |
rs34756064 | in-del | -/C | | | intron-variant | TSG101 | GRCh38.p7 | 11:18485827 | GGAGGCAGCCAAATG[-/C]TGAGGCAGATGGGGT | 7251 |
rs34787404 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | TSG101 | GRCh38.p7 | 11:18480787 | TTTATAATATGCAGC[A/T]TAAAAGCCACATATA | 7251 |
rs34804659 | in-del | -/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18483153 | TGGGTTTATCAGGGG[-/G]TTCCAGCTTTTGCTT | 7251 |
rs34890142 | in-del | -/AAT | | | intron-variant | TSG101 | GRCh38.p7 | 11:18510945 | AACCCAACAACAACG[-/AAT]ACAACAAAAAACAAC | 7251 |
rs34926761 | in-del | -/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18487974 | GTAAGGTGAAACTGG[-/G]AACTGTTTAAAAGAC | 7251 |
rs34996730 | in-del | -/A | 0.499382 | 0.017561 | intron-variant | TSG101 | GRCh38.p7 | 11:18496004 | GACAGTACATCCTCC[-/A]AAGGGAGGGGCCAAT | 7251 |
rs35067149 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18527841 | CAATACTACGGMCTT[C/G]TTCTCATTAGGGCTG | 7251 |
rs35176471 | in-del | -/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18517732 | ATATACCATCTAGGT[-/G]TTGTCTAAGTACACT | 7251 |
rs35188373 | snp | C/T | 0.00998959 | 0.0699643 | intron-variant | TSG101 | GRCh38.p7 | 11:18481294 | CCTAAATTGAGATCA[C/T]TGATTGTGCCACCTC | 7251 |
rs35188857 | snp | A/G | 0.00989172 | 0.0696277 | intron-variant | TSG101 | GRCh38.p7 | 11:18514576 | TTCGAGGTAGGATAG[A/G]TAAGTTCAGATAATG | 7251 |
rs35209297 | snp | A/C | 0.00998959 | 0.0699643 | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18527870 | TTCACTTAGACGCCA[A/C]CTTTGAAGGGAATCA | 7251 |
rs35221637 | snp | G/T | 0.5 | 0 | intron-variant | TSG101 | GRCh38.p7 | 11:18500554 | TATATTTCTTTGTGG[G/T]TTTTATCTGCATTTT | 7251 |
rs35224427 | in-del | -/A | 0.375 | 0.216506 | intron-variant | TSG101 | GRCh38.p7 | 11:18497111 | ACAACAACAAAAAAA[-/A]CAAGGATAAATAACC | 7251 |
rs35325862 | in-del | -/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18519663 | TATATTTTACAGCTG[-/G]ATGAATTTTCTTAAA | 7251 |
rs35338224 | in-del | -/C | | | intron-variant | TSG101 | GRCh38.p7 | 11:18482746 | ATTGAGAAAGTTCCC[-/C]TGAACATACTTTTAA | 7251 |
rs35376013 | snp | C/T | 0.00398564 | 0.0444627 | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18527756 | TTGAATGACACTGTG[C/T]TTACAAAACTGACGG | 7251 |
rs35471524 | in-del | -/A | 0 | 0 | intron-variant | TSG101 | GRCh38.p7 | 11:18483511 | AAAAAAAAAAAAAAA[-/A]GGAGTGCCTTTTGCC | 7251 |
rs35570386 | snp | C/T | 0.00998959 | 0.0699643 | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18527001 | CTCAATCCCACACGG[C/T]GYCCACCCTTGCCCG | 7251 |
rs35604713 | snp | C/G/T | 0.0150663 | 0.0855261 | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18527364 | TGGGCATCATCTAAG[C/G/T]CAAGTGTATGACTTT | 7251 |
rs35616300 | in-del | -/G | | | frameshift-variant | TSG101 | GRCh38.p7 | 11:18514754 | TTTTAATAGTCATTG[-/G]AACTAGTAGGCTTAA | 7251 |
rs35642875 | in-del | -/T | 0.350327 | 0.228986 | intron-variant | TSG101 | GRCh38.p7 | 11:18524912 | ATTAAGGAATAAATC[-/T]TTTTTTTTTTTTTTT | 7251 |
rs35643065 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TSG101 | GRCh38.p7 | 11:18519741 | TTTTAGTGTGATAAT[A/G]GTATTATGGGTTTTT | 7251 |
rs35699673 | snp | A/G | 0.0111196 | 0.0737302 | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18527549 | TAAAATACGGCCTGT[A/G]TTATCATTTATGGGT | 7251 |
rs35734910 | in-del | -/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18504451 | AGAAAGCATTTTTGT[-/G]TCCTAGTGGACACAT | 7251 |
rs35811211 | in-del | -/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18523508 | ATTATTTTTATTTAT[-/G]TTATTTGTTTTTGAG | 7251 |
rs35811728 | in-del | -/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18500275 | TAGTATGAATACTGT[-/G]TGCTATAAATATGGG | 7251 |
rs35817606 | snp | C/T | 0.00563802 | 0.0527941 | synonymous-codon | TSG101 | GRCh38.p7 | 11:18506877 | CTCTCCATACCCATC[C/T]GGATACCCTCCCAAT | 7251 |
rs35831615 | snp | C/G | 0.00998959 | 0.0699643 | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18527802 | TAATTGAAACTGTCA[C/G]ACATCATCAAACTCA | 7251 |
rs35840325 | in-del | -/A | | | intron-variant | TSG101 | GRCh38.p7 | 11:18516933 | GGCAACAAGAGCAAA[-/A]CTCCACTGCAAACAA | 7251 |
rs35887178 | snp | A/T | 0.0123036 | 0.0774623 | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18528463 | TAGTGTGATCTTGGC[A/T]CACTGCAACCTCTGC | 7251 |
rs35901786 | in-del | -/C | | | intron-variant | TSG101 | GRCh38.p7 | 11:18484415 | GCACAATAATTTCCA[-/C]TAAGGAAAAACATTT | 7251 |
rs35958204 | in-del | -/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18495683 | TTTTTTTTTTTTTTT[-/T]GCTACATGAATTGGT | 7251 |
rs36092798 | in-del | -/AA | | | intron-variant | TSG101 | GRCh38.p7 | 11:18495938 | AAAAAAAAAAAAAAA[-/AA]GTACTCTACAGAGAT | 7251 |
rs55923115 | in-del | -/A | 0.237593 | 0.249692 | intron-variant | TSG101 | GRCh38.p7 | 11:18508846 | TAAAGAAAATTTACC[-/A]AAAAAAAAAAAGTCA | 7251 |
rs55926604 | in-del | -/A | 0.498871 | 0.0237351 | intron-variant | TSG101 | GRCh38.p7 | 11:18507650 | TTGAGCTTAACTGAC[-/A]AAAAAAAATAGTAAA | 7251 |
rs55964013 | snp | C/T | 0.378372 | 0.214524 | intron-variant | TSG101 | GRCh38.p7 | 11:18522243 | GAACTCCAGAAAACA[C/T]ATATACAATTACCAA | 7251 |
rs56097703 | snp | C/T | 0.378372 | 0.214524 | intron-variant | TSG101 | GRCh38.p7 | 11:18517591 | ATTTTTACTGTAACT[C/T]TTCTACGGTTAGATA | 7251 |
rs56138729 | snp | C/G | 0.338976 | 0.23363 | intron-variant | TSG101 | GRCh38.p7 | 11:18507443 | CTAGTCTAGGTGACA[C/G]AGTGAGACCCTATCT | 7251 |
rs56151849 | snp | A/T | 0.378372 | 0.214524 | intron-variant | TSG101 | GRCh38.p7 | 11:18520699 | TTTCATAGATATATG[A/T]TTCTGTGAGTTAGTT | 7251 |
rs56333121 | snp | A/G | 0.498794 | 0.0245311 | intron-variant | TSG101 | GRCh38.p7 | 11:18507869 | TTGGGAGGCCGAGGC[A/G]GATCACTTGAGGTCA | 7251 |
rs56382668 | snp | A/C | 0.0322114 | 0.122752 | intron-variant | TSG101 | GRCh38.p7 | 11:18494035 | AAAAAATTTAAAGAA[A/C]GCTATCAGCAGGTTT | 7251 |
rs56991251 | snp | A/T | 0.338976 | 0.23363 | intron-variant | TSG101 | GRCh38.p7 | 11:18497154 | TCTCATGGCCTCAGT[A/T]ACAGAATAACAGCCC | 7251 |
rs57567646 | snp | A/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18499402 | TATATATATATATAT[A/T]TTTTTTTTTTTTTTT | 7251 |
rs57640464 | in-del | -/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18484936 | CCTTAATTGCCGCCT[-/T]TTTTTTTTTTTTTTT | 7251 |
rs57943351 | in-del | -/A | | | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18528373 | TATATATATATATAT[-/A]TATATTTTTTTTTTT | 7251 |
rs58515919 | snp | C/G | 0.155325 | 0.23138 | intron-variant | TSG101 | GRCh38.p7 | 11:18516268 | CATTATCCTTGAAAG[C/G]GGCTGACCTGTCAAT | 7251 |
rs58876868 | snp | A/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18499400 | TATATATATATATAT[A/T]TATTTTTTTTTTTTT | 7251 |
rs59032896 | snp | A/G | 0.380529 | 0.213219 | intron-variant | TSG101 | GRCh38.p7 | 11:18516419 | GCGCGATTTTGGCTC[A/G]CTGCAACCTCCACCT | 7251 |
rs59738510 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18509310 | ACTTTCTCCTCCATT[G/T]TGGAATCCAGCACAA | 7251 |
rs60389211 | in-del | -/A | 0 | 0 | intron-variant | TSG101 | GRCh38.p7 | 11:18492766 | GTAAAAAAAAAAAAA[-/A]GGAATTATAACTAAG | 7251 |
rs61603313 | in-del | -/GT | | | intron-variant | TSG101 | GRCh38.p7 | 11:18483043 | TGTGTGTGTGTGTGT[-/GT]AGCAGGGGGTGGGGA | 7251 |
rs61884673 | snp | C/T | 0.271972 | 0.249033 | intron-variant | TSG101 | GRCh38.p7 | 11:18505870 | TCGCCCAGGGTGGAG[C/T]GTAATGGCGCGATCT | 7251 |
rs61884675 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | TSG101 | GRCh38.p7 | 11:18513391 | GCCTCGAATTCCCAG[A/G]CTCAAGTGATCCTTT | 7251 |
rs61884676 | snp | A/C | | | intron-variant | TSG101 | GRCh38.p7 | 11:18513742 | GCCTCTTAGCTAAGG[A/C]CCTTTGCCCAGATTC | 7251 |
rs61884677 | snp | C/T | 0.377187 | 0.215229 | intron-variant | TSG101 | GRCh38.p7 | 11:18514021 | CCTGGGAGGTGGAGG[C/T]TGTAAGTGAGCTGAG | 7251 |
rs61884681 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18521031 | GCTAGACTCCGTCTT[A/G]GAAAAAAAAAAAAAA | 7251 |
rs61886142 | snp | A/G | 0.5 | 0 | intron-variant | TSG101 | GRCh38.p7 | 11:18483511 | AAAAAAAAAAAAAAA[A/G]GGAGTGCCTTTTGCC | 7251 |
rs61886143 | snp | A/G | 0.5 | 0 | intron-variant | TSG101 | GRCh38.p7 | 11:18483513 | AAAAAAAAAAAAAAG[A/G]AGTGCCTTTTGCCTC | 7251 |
rs71050605 | in-del | -/TTTAT | 0 | 0 | intron-variant | TSG101 | GRCh38.p7 | 11:18496510 | GTTTCACTCTGTAGA[-/TTTAT]TTTATTTTATTTTAT | 7251 |
rs71050606 | in-del | -/AAAAAAAAAAAAAAAAAATATATATATATATATATATATAT | 0 | 0 | intron-variant | TSG101 | GRCh38.p7 | 11:18499403 | AAAAAAAAAAAAAAA[lengthTooLong]ATATATATATATATA | 7251 |
rs71313424 | in-del | -/A | | | intron-variant | TSG101 | GRCh38.p7 | 11:18516363 | GATGAGACTCTGAAA[-/A]AAAAAAACAAAAAAG | 7251 |
rs71457900 | in-del | -/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18500811 | AAGCTTTTTTTTTTT[-/T]GAGACAAGGTCTCGC | 7251 |
rs71457901 | in-del | -/C | 0.5 | 0 | intron-variant | TSG101 | GRCh38.p7 | 11:18504228 | AAAAAAAAGCTAGCC[-/C]TAGGACACTGGAGCA | 7251 |
rs71457902 | in-del | -/C | 0.5 | 0 | intron-variant | TSG101 | GRCh38.p7 | 11:18512154 | TCACACCTGTAATCC[-/C]AGCACTTTGGGAGGC | 7251 |
rs71486868 | snp | A/C/G | 0.5 | 0 | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18528576 | TTTGTATTTTTAGTA[A/C/G]AGACAGGATTTCACT | 7251 |
rs72031390 | in-del | -/TGGA | 0.161924 | 0.233971 | intron-variant | TSG101 | GRCh38.p7 | 11:18519661 | CATATATTTTACAGC[-/TGGA]TGAATTTTCTTAAAA | 7251 |
rs72871713 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | TSG101 | GRCh38.p7 | 11:18492934 | GAAAAAAGATTTGGT[A/G]GAAGATTCTCATCTA | 7251 |
rs72871724 | snp | C/T | 0.130008 | 0.219321 | intron-variant | TSG101 | GRCh38.p7 | 11:18500442 | TTACATTCCCACCAA[C/T]ATTGTATAAGTTCCC | 7251 |
rs72871727 | snp | A/G | 0.161924 | 0.233971 | intron-variant | TSG101 | GRCh38.p7 | 11:18500769 | CCCACTCAACAGGTC[A/G]TCTCTTTACTTTGTT | 7251 |
rs72871737 | snp | A/G | 0.377385 | 0.215112 | intron-variant | TSG101 | GRCh38.p7 | 11:18506077 | TGATCCGCCTGCATC[A/G]GCCTCCGAAAGTGCT | 7251 |
rs72871738 | snp | A/T | 0.316968 | 0.240864 | intron-variant | TSG101 | GRCh38.p7 | 11:18506698 | CCATCTCAAAAAAAA[A/T]AAATAAATAAATAAA | 7251 |
rs72871768 | snp | A/C | 0.163236 | 0.234461 | intron-variant | TSG101 | GRCh38.p7 | 11:18522565 | GCAACAGCCTCCTTA[A/C]GTGTCTCTGCCTCCA | 7251 |
rs72871772 | snp | A/G | 0.163892 | 0.234703 | intron-variant | TSG101 | GRCh38.p7 | 11:18526254 | GAAAATCCCTGAAAT[A/G]GTAATGGTATGTATT | 7251 |
rs73422519 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | TSG101 | GRCh38.p7 | 11:18521422 | CGCTCAGGCTACAGT[A/G]CAGTGGTATGATCAT | 7251 |
rs74331446 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | TSG101 | GRCh38.p7 | 11:18482677 | CTTAAAGAGCTGAAG[A/G]TTGCATATGCTATGT | 7251 |
rs74344015 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | TSG101 | GRCh38.p7 | 11:18526472 | AAACGAAAAACTACA[C/T]TGCCCCACAGACAGC | 7251 |
rs74391442 | snp | C/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18501674 | GTATTTCGACACAGA[C/G]TGCACTGAATCTACA | 7251 |
rs74579352 | snp | G/T | 0.5 | 0 | intron-variant | TSG101 | GRCh38.p7 | 11:18500485 | CCTCAATAACATTTG[G/T]TATTTTTTTATTTTT | 7251 |
rs74654089 | snp | A/G | 0.5 | 0 | intron-variant | TSG101 | GRCh38.p7 | 11:18521034 | AGACTCCGTCTTGGA[A/G]AAAAAAAAAAAAAAT | 7251 |
rs74679449 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18498538 | TGACTCCAAAGAGTA[C/T]AGAGTAGGTAACAAT | 7251 |
rs74756946 | snp | A/G | 0.152667 | 0.230274 | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18528684 | GGCGTAAGCCACTGC[A/G]CCCAGCCCATTTATA | 7251 |
rs74815351 | snp | G/T | | | missense | TSG101 | GRCh38.p7 | 11:18480555 | GAGAAGTCAGTAGAG[G/T]TCACTGAGACCGGCA | 7251 |
rs74894912 | in-del | -/GTGT | 0 | 0 | intron-variant | TSG101 | GRCh38.p7 | 11:18483028 | AAGGGACCTGTGTGC[-/GTGT]GTGTGTGTGTGTAGC | 7251 |
rs74961207 | snp | C/T | 0.5 | 0 | intron-variant | TSG101 | GRCh38.p7 | 11:18501577 | GAATAGCCAAAGCAA[C/T]CTTGAACAAAAAGAA | 7251 |
rs74985475 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | TSG101 | GRCh38.p7 | 11:18520692 | AGTATAGTTTCATAG[A/G]TATATGTTTCTGTGA | 7251 |
rs75046764 | in-del | -/A | 0.172028 | 0.23753 | intron-variant | TSG101 | GRCh38.p7 | 11:18504428 | AAAGCAAAATCAGAC[-/A]AAAAAAAAAGAAAGC | 7251 |
rs75707896 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | TSG101 | GRCh38.p7 | 11:18485325 | ACGTCAGCACAACAA[C/T]TAGAATCTGCTCTCT | 7251 |
rs75785184 | snp | G/T | 0 | 0 | intron-variant | TSG101 | GRCh38.p7 | 11:18484952 | TTTTTTTTTTTTTTT[G/T]TTTTGAGATGGAGTC | 7251 |
rs75901341 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18510803 | GGCATGCGCCTGTGG[C/T]CACAACTACTCAGGA | 7251 |
rs76204461 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | TSG101 | GRCh38.p7 | 11:18493515 | GATAATTTTTCTGAC[C/T]TCACCCTTAATCAGC | 7251 |
rs76262127 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TSG101 | GRCh38.p7 | 11:18505574 | GAGTACTCCTAGATT[A/G]CCACTGAAACAAGTA | 7251 |
rs76304734 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | TSG101 | GRCh38.p7 | 11:18483054 | TGTGTAGCAGGGGGT[A/G]GGGAGGGATGGCACG | 7251 |
rs76309188 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | TSG101 | GRCh38.p7 | 11:18492806 | AAGATCTGAAATAAG[A/G]AAGTAAAAAAAGAAA | 7251 |
rs76331117 | snp | C/T | 0.5 | 0 | intron-variant | TSG101 | GRCh38.p7 | 11:18517186 | ACTACCATGCCCAGC[C/T]TTTTTTTTTTTTAGA | 7251 |
rs76619483 | snp | A/G | 0 | 0 | intron-variant | TSG101 | GRCh38.p7 | 11:18501598 | CAAAAAAAAAAAAAA[A/G]AAAAGCCAGAATAGC | 7251 |
rs76763128 | snp | A/T | 0.5 | 0 | intron-variant | TSG101 | GRCh38.p7 | 11:18525538 | GTGACAGAGCAAGAC[A/T]CTAAAAAAAAAAAAA | 7251 |
rs76797067 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | TSG101 | GRCh38.p7 | 11:18499158 | ACATCCAATAGTGGT[A/G]GCAGGAAAAGTGGAA | 7251 |
rs76807978 | snp | A/T | 0.5 | 0 | intron-variant | TSG101 | GRCh38.p7 | 11:18519310 | CATCCAGGTACAGTA[A/T]TTTTTTTTAACATAA | 7251 |
rs76824155 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18514478 | AATATTGAATATAAG[C/T]ATTCTGAAAATTACA | 7251 |
rs76982783 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | TSG101 | GRCh38.p7 | 11:18497636 | CTACAAATCAAAAGG[A/G]TTATACTATTATTTC | 7251 |
rs77038933 | snp | A/T | 0.5 | 0 | intron-variant | TSG101 | GRCh38.p7 | 11:18487263 | AACTTAAAGTATAAT[A/T]AAAAAAAAAAAGAAA | 7251 |
rs77157134 | snp | A/T | 0.156319 | 0.231784 | intron-variant | TSG101 | GRCh38.p7 | 11:18491242 | GCCCTCAGAACTTCC[A/T]GACTAATTAGAGTGT | 7251 |
rs77182799 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18510944 | AAAACCCAACAACAA[C/T]GACAACAAAAAACAA | 7251 |
rs77340091 | snp | A/T | 0.5 | 0 | intron-variant | TSG101 | GRCh38.p7 | 11:18492782 | AAAAAAAAAAAAGGA[A/T]TTATAACTAAGATCT | 7251 |
rs77363968 | snp | A/G | 0.021333 | 0.101051 | intron-variant | TSG101 | GRCh38.p7 | 11:18512176 | TTGGGAGGCTGAGGC[A/G]GACGGATCACCTGAA | 7251 |
rs77370735 | snp | A/C | 0.185788 | 0.241613 | intron-variant | TSG101 | GRCh38.p7 | 11:18496455 | TCAAAAATAAAATAA[A/C]ATAAAATAAAATAAA | 7251 |
rs77385773 | snp | A/T | 0.5 | 0 | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18527398 | GTCCTCTAATTAATG[A/T]TTTTTTTTAAGCTTA | 7251 |
rs77467392 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | TSG101 | GRCh38.p7 | 11:18519907 | ACTCACCATTAATAG[C/T]TTTTTAAAGATATAA | 7251 |
rs77519950 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | TSG101 | GRCh38.p7 | 11:18494140 | TGAAGGTAAGTAGGT[A/G]TAAGTCTTGCTAAAA | 7251 |
rs77589309 | snp | A/C | 0.5 | 0 | intron-variant | TSG101 | GRCh38.p7 | 11:18505397 | TGGTGGTGCAGCACC[A/C]GTGGTCTCAGCTACT | 7251 |
rs77666126 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | TSG101 | GRCh38.p7 | 11:18518673 | TCCAGAGTATAGTTT[C/T]GCAAAATGTGTTCCT | 7251 |
rs77666705 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | TSG101 | GRCh38.p7 | 11:18481285 | TAAAAAATGGAGGTG[A/G]CACAATCAGTGATCT | 7251 |
rs77948394 | snp | C/T | 0.00399292 | 0.044503 | intron-variant | TSG101 | GRCh38.p7 | 11:18484106 | AAAAACACTTGCTTA[C/T]TTCCCAAGTTCCTTC | 7251 |
rs77951303 | snp | C/T | 0.151334 | 0.229706 | intron-variant | TSG101 | GRCh38.p7 | 11:18485600 | AGAAGAAGGTAATTA[C/T]TAAAATTGTTTATAA | 7251 |
rs77974643 | in-del | -/GA | 0.378765 | 0.214288 | intron-variant | TSG101 | GRCh38.p7 | 11:18490071 | TTATGTGACCAATCT[-/GA]GTTTTAGAATACAAA | 7251 |
rs77982047 | in-del | -/AA | | | intron-variant | TSG101 | GRCh38.p7 | 11:18508856 | TTACCAAAAAAAAAA[-/AA]GTCACAGCTCAAAAC | 7251 |
rs78251685 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | TSG101 | GRCh38.p7 | 11:18484185 | CTTTCAAAATGTGAG[C/G]AAAGAAAAAAATTAT | 7251 |
rs78303038 | snp | C/T | | | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18527774 | CAGTGTCATTCAAGG[C/T]ATTGTAAAATTTTGA | 7251 |
rs78316363 | snp | A/G | 0.0603597 | 0.1629 | intron-variant | TSG101 | GRCh38.p7 | 11:18508988 | ATAGAGATAACAGAG[A/G]TAATATATTCCAATT | 7251 |
rs78338086 | in-del | -/AG | | | intron-variant | TSG101 | GRCh38.p7 | 11:18490072 | TATGTGACCAATCTG[-/AG]TTTTAGAATACAAAC | 7251 |
rs78382297 | snp | A/T | 0.5 | 0 | intron-variant | TSG101 | GRCh38.p7 | 11:18487262 | AAACTTAAAGTATAA[A/T]AAAAAAAAAAAAGAA | 7251 |
rs78423047 | snp | A/T | 0.5 | 0 | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18527399 | TCCTCTAATTAATGA[A/T]TTTTTTTAAGCTTAA | 7251 |
rs78512795 | snp | C/T | 0.5 | 0 | intron-variant | TSG101 | GRCh38.p7 | 11:18504603 | AAACTGCTCTTTTTT[C/T]CTGGAGTTTCTCCCA | 7251 |
rs78712880 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | TSG101 | GRCh38.p7 | 11:18487939 | ACTTTTGAAGTTTTA[C/T]ACTTTTCCTGATTAT | 7251 |
rs78762001 | snp | C/T | 0.0364509 | 0.129988 | intron-variant | TSG101 | GRCh38.p7 | 11:18512042 | CTTTTACACTAAATT[C/T]TTTGAAGAAAAAAAT | 7251 |
rs78766998 | snp | C/T | 0.0494327 | 0.149241 | intron-variant | TSG101 | GRCh38.p7 | 11:18495134 | TTTCTGATCCTTGTT[C/T]ATTTGATTTTTAGGA | 7251 |
rs79078017 | snp | C/T | 0.0306994 | 0.120242 | intron-variant | TSG101 | GRCh38.p7 | 11:18488015 | CTAGTACATCAGTAA[C/T]AGGATTTTTCTTTTT | 7251 |
rs79325235 | in-del | -/TTTG | | | intron-variant | TSG101 | GRCh38.p7 | 11:18484954 | TTTTTTTTTTTTTTT[-/TTTG]AGATGGAGTCTCACT | 7251 |
rs79344880 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | TSG101 | GRCh38.p7 | 11:18493074 | CATACCCCAAGTCCC[C/T]AACACACTGACCTTT | 7251 |
rs79403725 | snp | C/T | 0.154329 | 0.23097 | intron-variant | TSG101 | GRCh38.p7 | 11:18490900 | ACAGCCATATCATCA[C/T]AGCGCTCAGCCTGCT | 7251 |
rs79408094 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | TSG101 | GRCh38.p7 | 11:18513563 | CCTCAGCTTTCCAAA[A/G]TCCTGGGATCACAGC | 7251 |
rs79687295 | snp | A/G | 0.0528381 | 0.153711 | intron-variant | TSG101 | GRCh38.p7 | 11:18491121 | TATTTTTAAAGTTCA[A/G]GCAAAATAAGGCAAA | 7251 |
rs79752716 | in-del | -/TTT | 0.27008 | 0.249192 | intron-variant | TSG101 | GRCh38.p7 | 11:18505261 | CAGTATATGCCAATC[-/TTT]TTTTTTTTTTTGAGA | 7251 |
rs79855193 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | TSG101 | GRCh38.p7 | 11:18490878 | TTCTGTGACTGCCTT[C/T]GTGACTACAGCCATA | 7251 |
rs80140828 | snp | A/C | 0.148661 | 0.22854 | intron-variant | TSG101 | GRCh38.p7 | 11:18500600 | TATTGAGCATTTTTT[A/C]ATATACCTGTTGGCC | 7251 |
rs80198231 | snp | C/T | | | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18527999 | TTTCTTTTTCTTTTT[C/T]TTTTTTTTTTTTTTT | 7251 |
rs80237693 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TSG101 | GRCh38.p7 | 11:18507166 | GGTCAACCTGGTCAG[C/T]TTTTAAAGTTCTCAA | 7251 |
rs80254500 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | TSG101 | GRCh38.p7 | 11:18516236 | TTATTCTTTCAGAAA[C/G]ACTGGTTAAAATTCA | 7251 |
rs80291312 | snp | A/C | 0.203267 | 0.245593 | intron-variant | TSG101 | GRCh38.p7 | 11:18496450 | CTGTCTCAAAAATAA[A/C]ATAAAATAAAATAAA | 7251 |
rs80292142 | snp | C/T | | | missense | TSG101 | GRCh38.p7 | 11:18480556 | AGAAGTCAGTAGAGG[C/T]CACTGAGACCGGCAG | 7251 |
rs111252813 | snp | A/C | 0.5 | 0 | utr-variant-5-prime | TSG101 | GRCh38.p7 | 11:18526913 | ACACCCCCAACCCGG[A/C]CTCAAACAACAGGAA | 7251 |
rs111295172 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18484909 | ACTACGTGAGGACGT[C/G/T]AAGTATATTTAACCT | 7251 |
rs111493786 | snp | C/T | 0.5 | 0 | intron-variant | TSG101 | GRCh38.p7 | 11:18483708 | AATGCCAAACATAGG[C/T]TCCACTGTAAACAAA | 7251 |
rs111544807 | snp | C/G | 0.5 | 0 | intron-variant | TSG101 | GRCh38.p7 | 11:18489079 | GAGATCATGCCACTG[C/G]ACTCCAGCCTGACAA | 7251 |
rs111596294 | in-del | -/C | 0.5 | 0 | intron-variant | TSG101 | GRCh38.p7 | 11:18523795 | GCATGAGCCATTGCA[-/C]CTGGCCAATTTTGTT | 7251 |
rs111632548 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | TSG101 | GRCh38.p7 | 11:18516504 | CACGTGCCACCACAC[C/T]TGACTAATTTTTTGT | 7251 |
rs111664985 | snp | C/T | 0.444444 | 0.157135 | intron-variant | TSG101 | GRCh38.p7 | 11:18515872 | AACATTAAACTCCTC[C/T]GGTGAACTTAGGCAC | 7251 |
rs111714699 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18498533 | AAGGATGACTCCAAA[A/G]AGTATAGAGTAGGTA | 7251 |
rs111740586 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TSG101 | GRCh38.p7 | 11:18507263 | TCCAAGGTTAACTTC[C/T]TAGAAAGTAACTTCT | 7251 |
rs111746229 | snp | A/G | 0.5 | 0 | intron-variant | TSG101 | GRCh38.p7 | 11:18489137 | AAAAGGATGGTGGGA[A/G]AGAATGTTTTGATTT | 7251 |
rs111910766 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18500353 | TACCCAGCAGTGGGA[C/T]TGCTGAACTGTCTGG | 7251 |
rs112268279 | snp | A/G | 0.5 | 0 | intron-variant | TSG101 | GRCh38.p7 | 11:18495841 | AGGCAGGAGAATGGC[A/G]TGAACCTGGAGGGCG | 7251 |
rs112359274 | snp | G/T | 0.5 | 0 | intron-variant | TSG101 | GRCh38.p7 | 11:18502889 | AGCAACAAGTAATTT[G/T]TGAGAGAACTTTTCC | 7251 |
rs112480739 | in-del | -/A | 0.40733 | 0.194287 | intron-variant | TSG101 | GRCh38.p7 | 11:18487263 | AACTTAAAGTATAAT[-/A]AAAAAAAAAAAGAAA | 7251 |
rs112743513 | snp | C/T | 0.5 | 0 | utr-variant-3-prime | TSG101 | GRCh38.p7 | 11:18480485 | ATTCTGGGCACCTAC[C/T]GATAAAAGGAAGAGA | 7251 |
rs112790714 | snp | A/G | 0 | 0 | intron-variant | TSG101 | GRCh38.p7 | 11:18521099 | ATCACTTCATAGAGG[A/G]TAACGTTTTTTCATC | 7251 |
rs112813339 | snp | C/T | 0 | 0 | intron-variant | TSG101 | GRCh38.p7 | 11:18485625 | TTATAAATATATGAG[C/T]GCTCTCCAAAATAAA | 7251 |
rs112913390 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18501068 | CCGCCTTGGCTTCCC[A/T]AAGTGCTGGGATTAC | 7251 |
rs112916947 | snp | A/T | 0.0759472 | 0.179459 | intron-variant | TSG101 | GRCh38.p7 | 11:18523641 | CCGAGTAGCTGGGAT[A/T]ACAGGCGTGCGCCAC | 7251 |
rs112960903 | in-del | -/A | 0.270621 | 0.249148 | intron-variant | TSG101 | GRCh38.p7 | 11:18510765 | CAGCCTGGTCTCTAC[-/A]AAAAAAATTAACTGT | 7251 |
rs113003134 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TSG101 | GRCh38.p7 | 11:18511756 | AATATTTTCATCATC[C/T]GAAAAAGAAACCCTG | 7251 |
rs113009086 | in-del | -/C | 0.00398564 | 0.0444627 | intron-variant | TSG101 | GRCh38.p7 | 11:18526049 | ACAAAAGCCATTCCA[-/C]TCTGGTGTGAGGTGC | 7251 |
rs113136633 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | TSG101 | GRCh38.p7 | 11:18500087 | TTTGGCTCCCACATG[A/G]GAACATTTGATATTT | 7251 |
rs113172823 | snp | C/T | 0 | 0 | intron-variant | TSG101 | GRCh38.p7 | 11:18506409 | AAAAAAAAAAATACA[C/T]AGGCTGGGCATGGTG | 7251 |
rs113489427 | in-del | -/T | 0.5 | 0 | intron-variant | TSG101 | GRCh38.p7 | 11:18489228 | CAGAACATCATTCTA[-/T]TTTTTTTTTTTTTTG | 7251 |
rs113581499 | in-del | -/A | 0.489024 | 0.0732638 | intron-variant | TSG101 | GRCh38.p7 | 11:18506392 | ATACTCTCTTCTTTT[-/A]AAAAAAAAAAAATAC | 7251 |
rs113618844 | snp | A/G | 0.5 | 0 | intron-variant | TSG101 | GRCh38.p7 | 11:18481577 | GTGGTTTGCAAGGTC[A/G]GTGCCTCTACAACCC | 7251 |
rs113754265 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TSG101 | GRCh38.p7 | 11:18510265 | ATCTCTACTAAAAAC[A/G]CAAAAATTAGCCGGG | 7251 |
rs113836914 | snp | C/T | 0 | 0 | intron-variant | TSG101 | GRCh38.p7 | 11:18511969 | GTAGTATGAATCAAT[C/T]CTTCATTCATACATT | 7251 |
rs113853985 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | TSG101 | GRCh38.p7 | 11:18501576 | GTTCTTTTAGTTCAA[C/G]ATCACTTTGGCTATT | 7251 |
rs113901829 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | TSG101 | GRCh38.p7 | 11:18511560 | GGCCACTGAGACCAC[A/G]TGCTTTCTCAATTTT | 7251 |
rs113923850 | snp | C/T | 0.5 | 0 | intron-variant | TSG101 | GRCh38.p7 | 11:18483027 | AAAGGGACCTGTGTG[C/T]GTGTGTGTGTGTGTG | 7251 |
rs113933142 | snp | A/C | 0.275732 | 0.248672 | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18528415 | TTTTTTTTGAGACAG[A/C]GTTTTGCTCTTGCTT | 7251 |
rs114011995 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | TSG101 | GRCh38.p7 | 11:18516903 | CCGAGACTGTGCCCA[C/T]TGCACTTTAGTCTGG | 7251 |
rs114250357 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | TSG101 | GRCh38.p7 | 11:18480904 | AGCAAGAGATTGTAC[A/G]GAAAAAGAGTCCTCT | 7251 |
rs114371448 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | TSG101 | GRCh38.p7 | 11:18496886 | GGTCAGGAGTTGCAG[C/T]TGGAGATCAGCCTGG | 7251 |
rs114436060 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TSG101 | GRCh38.p7 | 11:18481507 | ACATCTCATTTAGTG[C/T]TTTTTGGGAAGATAA | 7251 |
rs114438044 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | TSG101 | GRCh38.p7 | 11:18515683 | AAAGATATCCATATA[C/T]AACATGTAACAAAAC | 7251 |
rs114658042 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | TSG101 | GRCh38.p7 | 11:18524792 | AACATGCCTTGCCTT[C/T]GTCTTTGATGGCAGG | 7251 |
rs114748773 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | TSG101 | GRCh38.p7 | 11:18500961 | GGGGTGTACCACCAC[A/G]CCCAGATTTTTGCAT | 7251 |
rs114966126 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | TSG101 | GRCh38.p7 | 11:18482128 | TTGTCACCTGTCAGC[A/G]ACAAATGATACTGCA | 7251 |
rs115340105 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | TSG101 | GRCh38.p7 | 11:18514116 | AATCAGTAAGTACCC[C/T]GGGGGAAAAGTTATT | 7251 |
rs115356918 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | TSG101 | GRCh38.p7 | 11:18486335 | GCCCAGGCAGGGTGT[C/T]GCTCGTCAGAGGTCC | 7251 |
rs115554728 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | TSG101 | GRCh38.p7 | 11:18515009 | GGCAATAGCAAAGTC[A/G]GTAATCTTAAATTTT | 7251 |
rs115752480 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | TSG101 | GRCh38.p7 | 11:18516334 | TGTTGATTCACTCAA[C/T]GTCATTGATCAGCTC | 7251 |
rs116075732 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18489865 | CTTTACAATGGAATT[G/T]TATTTCAATGATTCT | 7251 |
rs116091566 | snp | A/G | 0.0364509 | 0.129988 | intron-variant | TSG101 | GRCh38.p7 | 11:18489403 | CCATGCCTGACTCAG[A/G]AGATTATTCTTAAAG | 7251 |
rs116220140 | snp | A/G | 0.00597247 | 0.0543191 | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18528676 | GGATTACAGGCGTAA[A/G]CCACTGCGCCCAGCC | 7251 |
rs116419506 | snp | G/T | 0.0387552 | 0.1337 | intron-variant | TSG101 | GRCh38.p7 | 11:18504197 | AGAGTGAAGCCCCCA[G/T]CTCAAAAAAAAAAAA | 7251 |
rs116534112 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | TSG101 | GRCh38.p7 | 11:18523931 | AAGTAGCTAGGACTA[C/T]AGGTGCAAGCCACGA | 7251 |
rs116696596 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TSG101 | GRCh38.p7 | 11:18518611 | CTCTACAGAATTAAA[A/G]ACCACATTAAATAAC | 7251 |
rs116733625 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | TSG101 | GRCh38.p7 | 11:18496855 | CAGCACTTTGGTGGG[A/T]TGAGGCAGGTGGTGA | 7251 |
rs116918649 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18508213 | TGAGACTAGGAAATA[C/T]TTGATATCTTTTTTT | 7251 |
rs116926675 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TSG101 | GRCh38.p7 | 11:18522712 | GCCTGCAAGGCCCTC[C/T]AAACCTCCCATACCA | 7251 |
rs116936242 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | TSG101 | GRCh38.p7 | 11:18491824 | TGTAGAATAAGTCGG[C/T]CTACTTCAAATGAGG | 7251 |
rs117255412 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18521069 | TTTTATATTTTTCTC[C/T]TCTTCTCTGGTAAGA | 7251 |
rs117754928 | snp | A/G | 0.0387552 | 0.1337 | intron-variant | TSG101 | GRCh38.p7 | 11:18488802 | AAATTTAGAGAGGAG[A/G]GAAGGGAAAACCAAA | 7251 |
rs117777271 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | TSG101 | GRCh38.p7 | 11:18511793 | TTAGTAGTCACTTCC[C/T]GTTTCCCTTTCCCCA | 7251 |
rs117777920 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TSG101 | GRCh38.p7 | 11:18524540 | GCCCCACAACTGCTT[C/T]TATTACTTTACTTCC | 7251 |
rs117808690 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TSG101 | GRCh38.p7 | 11:18480949 | TTATATCCAGCCATT[A/C]ATGTGGTTGTACCAC | 7251 |
rs117892915 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TSG101 | GRCh38.p7 | 11:18494297 | GAAGGAGAGTTAAAA[C/T]TCTATTCTTAAAAAA | 7251 |
rs117920272 | snp | A/T | 0.0271762 | 0.113356 | intron-variant | TSG101 | GRCh38.p7 | 11:18515298 | GAGGTACATCCTTTA[A/T]TCATCTTTGTAGCCA | 7251 |
rs118090642 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TSG101 | GRCh38.p7 | 11:18518535 | AGGAAAACTCCAAGC[A/G]TTGTCTTGCCTTACA | 7251 |
rs137874721 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | TSG101 | GRCh38.p7 | 11:18521826 | GGACTACAGGTATGC[A/G]CCACAGTGTTTGGCT | 7251 |
rs137915611 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18482676 | GCTTAAAGAGCTGAA[A/G]GTTGCATATGCTATG | 7251 |
rs137990012 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18525247 | TGCTATCAATTTAAA[C/G]ATCAAAAATGTCATG | 7251 |
rs138153893 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | TSG101 | GRCh38.p7 | 11:18510633 | AGCACTTTGGGAGGC[C/T]AAGGCAGGAGGATCA | 7251 |
rs138164057 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18493003 | CATCTTAGAAGAAAT[C/T]TGAATATTCTCTATA | 7251 |
rs138320197 | in-del | -/G | 0.0729998 | 0.176553 | intron-variant | TSG101 | GRCh38.p7 | 11:18491295 | AACAGTGTGATTTAT[-/G]GGGGGGGTCTGGGCC | 7251 |
rs138407352 | in-del | -/TCAAG | | | intron-variant | TSG101 | GRCh38.p7 | 11:18488645 | TGCTAGAAGTTCTTC[-/TCAAG]TCTTTAAAGCCAGGC | 7251 |
rs138461059 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18482025 | CTGGTCAAAGGTAGA[A/G]GAAAAGATGTGATCT | 7251 |
rs138571842 | snp | A/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18494017 | ATCAACACAATCAAT[A/T]AGAAAAAATTTAAAG | 7251 |
rs138669929 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | TSG101 | GRCh38.p7 | 11:18522104 | CCAATTATTATTGAG[C/T]ACAGGCTAAGTCCTT | 7251 |
rs138767140 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | TSG101 | GRCh38.p7 | 11:18521408 | GGGTCTCACTCTGTC[A/G]CTCAGGCTACAGTGC | 7251 |
rs138779299 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TSG101 | GRCh38.p7 | 11:18524689 | GTAGGATGCCCTCTC[C/T]CACCTCTTCCCTACC | 7251 |
rs138878060 | snp | C/T | 0.000148848 | 0.00862564 | synonymous-codon | TSG101 | GRCh38.p7 | 11:18514834 | TATTGGAATATTGTA[C/T]GTATTACCTGAAAAA | 7251 |
rs138878379 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | TSG101 | GRCh38.p7 | 11:18518492 | TATGTTAGGATTTGG[C/T]AGGGACAGAAAAGAC | 7251 |
rs139037267 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TSG101 | GRCh38.p7 | 11:18511352 | ACTCACCTCATTTGT[C/T]CAATTTTGACCTAAC | 7251 |
rs139038527 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | TSG101 | GRCh38.p7 | 11:18512287 | GGTGGGCGCCTGTAA[A/T]CCCAGCTACTCAGGA | 7251 |
rs139041895 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | TSG101 | GRCh38.p7 | 11:18500787 | TCTTTACTTTGTTGA[C/G]TATCTCCTTTGTTGT | 7251 |
rs139185746 | snp | A/G | 0.0391387 | 0.134304 | intron-variant | TSG101 | GRCh38.p7 | 11:18505857 | GAGTTTTGCTCTGTC[A/G]CCCAGGGTGGAGTGT | 7251 |
rs139230835 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TSG101 | GRCh38.p7 | 11:18497936 | ATTTACATCAGACCT[C/T]AGGATGGTTACAAGT | 7251 |
rs139235624 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TSG101 | GRCh38.p7 | 11:18490053 | TTCAGAATGCCGTGG[C/T]ATTTATGTGACCAAT | 7251 |
rs139311488 | snp | A/C | 0.0364509 | 0.129988 | intron-variant | TSG101 | GRCh38.p7 | 11:18489427 | CTTAAAGGTATTATC[A/C]AGGAAACAGATAAGG | 7251 |
rs139372554 | in-del | -/ATAAA | | | intron-variant | TSG101 | GRCh38.p7 | 11:18496461 | TAAAATAAAATAAAA[-/ATAAA]TAAAATAAAATAAAA | 7251 |
rs139478645 | snp | A/G | 0.000214163 | 0.0103458 | synonymous-codon | TSG101 | GRCh38.p7 | 11:18481771 | AATGATAACTTCATC[A/G]ATATCATTGTTTTCA | 7251 |
rs139534572 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18507766 | TTGAATACTGCACTT[C/G]CAATGTCAATTTAAA | 7251 |
rs139640907 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TSG101 | GRCh38.p7 | 11:18522566 | CAACAGCCTCCTTAC[A/G]TGTCTCTGCCTCCAT | 7251 |
rs139774651 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | TSG101 | GRCh38.p7 | 11:18485977 | CCTTTCCCATTGATT[C/G]TTCCTCAATAATGCC | 7251 |
rs139838559 | snp | C/G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18527922 | CTAACTGAAAGCATG[C/G/T]GGAAGCATCATTATA | 7251 |
rs139863450 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TSG101 | GRCh38.p7 | 11:18503164 | ATCACCTTTCCAACA[A/G]TCTCTTATCTACACA | 7251 |
rs139900570 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | TSG101 | GRCh38.p7 | 11:18520256 | GGAGACAGGGTCTCG[C/T]TCTGTCGCCCAGGAT | 7251 |
rs140091544 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | TSG101 | GRCh38.p7 | 11:18516802 | CAAAATTAGCTGGGC[A/G]TGGTGGCACATGCCT | 7251 |
rs140101726 | snp | G/T | 0.000230593 | 0.0107351 | missense | TSG101 | GRCh38.p7 | 11:18483930 | ACCCTTTTTCAGGTC[G/T]TCTTCTGTTCGTTTC | 7251 |
rs140111803 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18502827 | TCACCCTCATAGCAG[C/T]GGAAATGTAACTAGA | 7251 |
rs140156278 | snp | A/G | 6.59576e-05 | 0.00574234 | missense | TSG101 | GRCh38.p7 | 11:18509583 | GGCGGATAGGATGCC[A/G]AAATAGGACGAGAGA | 7251 |
rs140204844 | in-del | -/AATT | 0.161596 | 0.233848 | intron-variant | TSG101 | GRCh38.p7 | 11:18511966 | GTGGTAGTATGAATC[-/AATT]CTTCATTCATACATT | 7251 |
rs140210743 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | TSG101 | GRCh38.p7 | 11:18492372 | GAGTCTTTTTATAGT[G/T]AGTGAATTTTTCACA | 7251 |
rs140265012 | snp | A/G | 0.0051083 | 0.0502798 | intron-variant | TSG101 | GRCh38.p7 | 11:18516216 | TTTTAAGATACTCCC[A/G]TAAGTTATTCTTTCA | 7251 |
rs140407671 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TSG101 | GRCh38.p7 | 11:18504640 | ATACCTTTGCAAAGA[C/T]AATGTGATCACATTG | 7251 |
rs140466640 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18517830 | TACATTCTTGACCTT[C/T]GTTATTTTACTTACT | 7251 |
rs140531532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18495809 | CTGATAAAAGGACTC[C/T]ACATAGATCAAGGCT | 7251 |
rs140599537 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | TSG101 | GRCh38.p7 | 11:18481167 | CTGTACAACAGCATT[A/T]AGCTTGAGACAACTT | 7251 |
rs140642135 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | TSG101 | GRCh38.p7 | 11:18512504 | TAACCAAGTTACCTG[C/T]GTGTTTGTGGGGGTG | 7251 |
rs140653653 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18524195 | GAAACATCTAAAGTG[C/G]GAAGTTGTTTCTGTA | 7251 |
rs140681190 | snp | A/G/T | 0.0111196 | 0.0737302 | intron-variant | TSG101 | GRCh38.p7 | 11:18497078 | CCTTGGCGACAGAGC[A/G/T]AGTCTGTCTCAAAAA | 7251 |
rs140728711 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | TSG101 | GRCh38.p7 | 11:18513840 | AGCACTTTAGAAGGC[C/T]GAGATGGGTGGATCA | 7251 |
rs141054027 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TSG101 | GRCh38.p7 | 11:18494957 | ACCTTTTCCTTTCTT[C/T]ATCTAAATATTCAGT | 7251 |
rs141090789 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TSG101 | GRCh38.p7 | 11:18518165 | AAATACCATTGTACA[C/T]ATAGTATGCAGACAG | 7251 |
rs141211086 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18512180 | GAGGCTGAGGCGGAC[A/G]GATCACCTGAAGTCA | 7251 |
rs141214424 | in-del | -/AAT | | | intron-variant | TSG101 | GRCh38.p7 | 11:18510942 | CAAAACCCAACAACA[-/AAT]ACGACAACAAAAAAC | 7251 |
rs141329144 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TSG101 | GRCh38.p7 | 11:18484798 | CTAATATAAGTTTGG[A/G]TATTCTTTATGACTA | 7251 |
rs141441464 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | TSG101 | GRCh38.p7 | 11:18500867 | GGAGTGCAGTGGTGC[A/G]ATCTCAGCTCACTGC | 7251 |
rs141676413 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | TSG101 | GRCh38.p7 | 11:18488847 | AGGATGATGGGGGGC[C/T]GGGCGCAGTGGCTCA | 7251 |
rs141702484 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | TSG101 | GRCh38.p7 | 11:18521082 | TCCTCTTCTCTGGTA[A/C]GATCACTTCATAGAG | 7251 |
rs141775107 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | TSG101 | GRCh38.p7 | 11:18520107 | ATCCTAGACAACCAC[A/G]AATTTACTTTGTCTC | 7251 |
rs141793878 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | TSG101 | GRCh38.p7 | 11:18522328 | GAACTCCTCATCTTC[C/T]CCCCAAATTTACTTC | 7251 |
rs141831498 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant | TSG101 | GRCh38.p7 | 11:18525047 | TCCCGAGTAGGCTGG[G/T]ATTACAGGCACCCGC | 7251 |
rs141870865 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | TSG101 | GRCh38.p7 | 11:18488966 | CTAAAAATACAAAAA[C/T]TAGCTGGGCGTGGTG | 7251 |
rs142125204 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TSG101 | GRCh38.p7 | 11:18505708 | AAATGGATAATAAAG[A/G]TTGATAGTACAGGTA | 7251 |
rs142193389 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18507609 | AGAGGCTAATCAACA[C/T]AGAGGAAGAAAAAGA | 7251 |
rs142228434 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TSG101 | GRCh38.p7 | 11:18511474 | GTAAATTTATATACT[A/G]AGACTCGGGGTGTTA | 7251 |
rs142267119 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | TSG101 | GRCh38.p7 | 11:18509802 | ATGAAAATTTCATTT[A/C]ATTAATTTATTTTAA | 7251 |
rs142324138 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | TSG101 | GRCh38.p7 | 11:18490000 | TTAAAAAAAATTAAA[C/G]ACACAGTAATCCTGT | 7251 |
rs142440412 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TSG101 | GRCh38.p7 | 11:18521030 | AGCTAGACTCCGTCT[C/T]GGAAAAAAAAAAAAA | 7251 |
rs142496923 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18487529 | GATCGTTTCTGTAAC[C/T]ATTAAAATTTTTTTT | 7251 |
rs142613047 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18489578 | TTAGTCAGGTGTGTT[A/G]TATGAGCACTTGGAC | 7251 |
rs142634651 | snp | A/C | 0.0170251 | 0.090679 | intron-variant | TSG101 | GRCh38.p7 | 11:18490505 | TTCTTCTTTCTTACT[A/C]ATTTCAAATGCTTCC | 7251 |
rs142649282 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | TSG101 | GRCh38.p7 | 11:18493131 | AGTGCCCTTCTACAA[C/T]TCCAGATTAGCAGTT | 7251 |
rs142658759 | snp | C/T | 1.64882e-05 | 0.00287121 | missense | TSG101 | GRCh38.p7 | 11:18506863 | TTTCATTACCTGGGA[C/T]TGGGAGGGTATCCGG | 7251 |
rs142724008 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TSG101 | GRCh38.p7 | 11:18519314 | CAGGTACAGTATTTT[C/T]TTTTAACATAAAAAA | 7251 |
rs142763573 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18482034 | GGTAGAGGAAAAGAT[G/T]TGATCTACTATGCTG | 7251 |
rs142800175 | snp | C/T | 8.27547e-05 | 0.00643199 | missense | TSG101 | GRCh38.p7 | 11:18481851 | TTTTCAAAAGTTCTA[C/T]GTTTTTATCAACCTC | 7251 |
rs142873250 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TSG101 | GRCh38.p7 | 11:18513044 | CAAGGACAGATTTTT[A/G]TAAGGCTCATTCTAC | 7251 |
rs142946177 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | TSG101 | GRCh38.p7 | 11:18497653 | TATACTATTATTTCA[A/G]TGAGAAACAGGGTGA | 7251 |
rs143062912 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | TSG101 | GRCh38.p7 | 11:18492240 | CAGGAAGGAAAATCC[C/T]TCTCCCATAGATTAC | 7251 |
rs143338814 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18514928 | GAGGTTTAGTCTAGA[C/T]ACAATTTATACATAT | 7251 |
rs143349224 | in-del | -/AAAC | 0.077417 | 0.180873 | intron-variant | TSG101 | GRCh38.p7 | 11:18508806 | TTTGTCTTGTAAGAT[-/AAAC]AAGTTTGGTTAATTA | 7251 |
rs143396051 | snp | A/G | 0.00318978 | 0.0398085 | downstream-variant-500B | TSG101 | GRCh38.p7 | 11:18480301 | TAAAGTCCAATAAAG[A/G]AGAGAAAAATTATGC | 7251 |
rs143502397 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TSG101 | GRCh38.p7 | 11:18515501 | TGAAAGACAGGCTAA[C/T]AGAGATCAATTATCT | 7251 |
rs143543783 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TSG101 | GRCh38.p7 | 11:18518674 | CCAGAGTATAGTTTC[A/G]CAAAATGTGTTCCTG | 7251 |
rs143568794 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TSG101 | GRCh38.p7 | 11:18499907 | ATACATTGTTAACTA[C/T]AGTCACCCTACTCTG | 7251 |
rs143627574 | in-del | -/A | | | intron-variant | TSG101 | GRCh38.p7 | 11:18497551 | AATCATCTAAGCTAT[-/A]AAAAAAATGCTTCGT | 7251 |
rs143665489 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | TSG101 | GRCh38.p7 | 11:18517597 | ACTGTAACTTTTCTA[C/T]GGTTAGATACATAAA | 7251 |
rs143673185 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TSG101 | GRCh38.p7 | 11:18506193 | TTCAATCTACAGAAA[A/G]GCAGCTCCTGGGCTG | 7251 |
rs143818714 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | TSG101 | GRCh38.p7 | 11:18518037 | TTGATAAATGTATTT[A/G]TTCTTTTATATGCAG | 7251 |
rs143870465 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18484165 | GGGGGCAATATGAAC[C/T]GACACTTTCAAAATG | 7251 |
rs143904115 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18496648 | GGGCAATACAAAAAT[C/T]AGCCGGGCATGGTGG | 7251 |
rs143924160 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TSG101 | GRCh38.p7 | 11:18500220 | ATTGTCTTTATCCAT[C/T]CATCTGCTGATAAAT | 7251 |
rs144017737 | in-del | -/AAAG | 0.00953873 | 0.0683987 | intron-variant | TSG101 | GRCh38.p7 | 11:18514612 | CCTCCTTGAGTGCTA[-/AAAG]AAAGCAGATGCTAGT | 7251 |
rs144047883 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18503026 | TTCCTCTTTTGATAA[C/T]ATTCGTACCAAACTC | 7251 |
rs144099782 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | TSG101 | GRCh38.p7 | 11:18522073 | GTCTCTTTGCTGGTT[C/T]GTTCTCTTATCCTAA | 7251 |
rs144263540 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | TSG101 | GRCh38.p7 | 11:18525522 | CTGCACTCCAGCCTG[A/G]GTGACAGAGCAAGAC | 7251 |
rs144308424 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18485312 | CATAATTCCCAAAAC[A/G]TCAGCACAACAACTA | 7251 |
rs144437860 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | TSG101 | GRCh38.p7 | 11:18519413 | AGGCGGTGGTGCAAT[A/C]CCACAATTGAAAAAT | 7251 |
rs144449859 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18510004 | ATACTGGTACAAATT[C/T]AGGGATGAATATGAG | 7251 |
rs144452331 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18509028 | GCAACACTCTCTCCA[C/T]GCTCCCACCACTCCA | 7251 |
rs144489961 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | TSG101 | GRCh38.p7 | 11:18512682 | TCCTGTGGCAGGCAG[A/G]CAGTCAGGATCAGGG | 7251 |
rs144601860 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TSG101 | GRCh38.p7 | 11:18524439 | CTTCACCCTAGCTAT[A/G]TGTTCAGGGTCCTGG | 7251 |
rs144710363 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18494398 | GTTAGAGGTATTCTA[C/T]AGGAATAACGACAGG | 7251 |
rs144816008 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | TSG101 | GRCh38.p7 | 11:18497431 | ACTCTTGAAAATGTA[C/G]AGTAAAATATTAGTT | 7251 |
rs144863512 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18490814 | CCAACCATGTTCTTG[C/T]AGGCAACAGAGAGCA | 7251 |
rs144902515 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | TSG101 | GRCh38.p7 | 11:18495417 | CAAAAGAGAACTTTC[A/G]CCACTGCTGAGACTG | 7251 |
rs144985550 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | TSG101 | GRCh38.p7 | 11:18511123 | GAATTACTCAATCAC[C/G]TTGATAGGCTAACCA | 7251 |
rs145018841 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | TSG101 | GRCh38.p7 | 11:18513593 | CCATGAGCCACCATC[C/G]CCAGAGCTACTCACT | 7251 |
rs145175849 | snp | A/G | 0.0383715 | 0.133092 | intron-variant | TSG101 | GRCh38.p7 | 11:18520939 | AGGAGGCTGAGGCAG[A/G]AGAATCGCTTGAACC | 7251 |
rs145241217 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TSG101 | GRCh38.p7 | 11:18492715 | TATCTCTATCACACA[C/T]AGACTTCACTGTGAA | 7251 |
rs145300932 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | TSG101 | GRCh38.p7 | 11:18509268 | TCTGCAGCATGCATA[A/G]TTTTAAAAATTCTAG | 7251 |
rs145391976 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18494488 | TAACTTACACAATAG[A/C]TTTTTTAAAAGCTTT | 7251 |
rs145539122 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | TSG101 | GRCh38.p7 | 11:18495917 | CAACAGAGTGAGACT[C/T]CGTCTCAAAAAAAAA | 7251 |
rs145573466 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | TSG101 | GRCh38.p7 | 11:18512942 | CATGTTGGCCAGGCT[C/T]GTCTCAAACTTCTGG | 7251 |
rs145594121 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | TSG101 | GRCh38.p7 | 11:18523686 | TTTGTATTTTTAGTA[C/G]AGATGGGGTTTCACC | 7251 |
rs145671308 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TSG101 | GRCh38.p7 | 11:18490205 | GGGTACAGAGTGACA[C/T]TGAACAGATTACAAA | 7251 |
rs145672358 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TSG101 | GRCh38.p7 | 11:18498790 | GAGTGCCAAGGAGAC[C/T]AAGCCAGGGTCACAC | 7251 |
rs145701738 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18486022 | ATGTTGCCTTTTCCA[A/G]TACTACCTATGGCCT | 7251 |
rs145804577 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18491133 | TCAAGCAAAATAAGG[C/G]AAAATGCCTTACAGC | 7251 |
rs145828306 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | TSG101 | GRCh38.p7 | 11:18518876 | TCAAGCTTAACTATA[C/G]AATTCTGCCTCTACC | 7251 |
rs145861165 | snp | C/T | 0.029116 | 0.117091 | intron-variant | TSG101 | GRCh38.p7 | 11:18513884 | GTTCGAGAACAGCCT[C/T]ACCAACATGGTGAAA | 7251 |
rs145885289 | snp | A/G | 1.64852e-05 | 0.00287094 | missense, utr-variant-5-prime | TSG101 | GRCh38.p7 | 11:18519579 | CATTGACAGTTTCAC[A/G]TACAGTTAGGTCTCT | 7251 |
rs145953069 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TSG101 | GRCh38.p7 | 11:18505737 | TAGTCTATGAACTGA[A/G]TAAGTAAATATCATG | 7251 |
rs145997806 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TSG101 | GRCh38.p7 | 11:18489579 | TAGTCAGGTGTGTTA[C/T]ATGAGCACTTGGACT | 7251 |
rs146084845 | snp | C/T | 6.58892e-05 | 0.00573936 | synonymous-codon | TSG101 | GRCh38.p7 | 11:18483900 | ACGGGTAACCATCTC[C/T]TCCAGTTTCTGGTGA | 7251 |
rs146129590 | snp | C/G | 1.74494e-05 | 0.00295371 | stop-gained | TSG101 | GRCh38.p7 | 11:18502514 | AGGAGGCTGAGAAGG[C/G]TACTGAGAACTTGTT | 7251 |
rs146141513 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18507074 | CAAAACAAATACCTC[A/T]CCCTTTCATAATCCT | 7251 |
rs146216750 | in-del | -/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18516356 | ATCAGCTCTTTTTTG[-/T]TTTTTTTTTTCAGAG | 7251 |
rs146239899 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | TSG101 | GRCh38.p7 | 11:18522535 | AAGCCACCAGCACCT[C/G]TCACCTAGATTACTG | 7251 |
rs146250235 | snp | A/C | 0.0360663 | 0.129354 | intron-variant | TSG101 | GRCh38.p7 | 11:18525185 | AAGTGCTAGGATTAC[A/C]GGCGTAAGCCACTGC | 7251 |
rs146250716 | snp | A/G | 0.0325976 | 0.123435 | intron-variant | TSG101 | GRCh38.p7 | 11:18485008 | CAGTCGCATGATCTC[A/G]GCTCACTGCAACCTC | 7251 |
rs146261234 | snp | C/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18489280 | GTCCAGGCTGGAGTG[C/G]GGTTATTTCACAGGT | 7251 |
rs146361555 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | TSG101 | GRCh38.p7 | 11:18507715 | TGACTGAGTACAAAA[C/T]TGAATTGCAACAGTA | 7251 |
rs146428478 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | TSG101 | GRCh38.p7 | 11:18498389 | GGGGGACAAGGAAAG[A/C]AGCAGAGAAATCTTG | 7251 |
rs146440252 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TSG101 | GRCh38.p7 | 11:18503031 | CTTTTGATAACATTC[A/G]TACCAAACTCATCTT | 7251 |
rs146564031 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18485486 | ATCAACAGAATTGGT[G/T]ATCTTCTAGGAGTCC | 7251 |
rs146665093 | in-del | -/CT | 0.00993419 | 0.0697739 | intron-variant | TSG101 | GRCh38.p7 | 11:18504596 | AACTGGGATAAACTG[-/CT]CTTTTTTTCTGGAGT | 7251 |
rs146780518 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18513751 | CTAAGGCCCTTTGCC[A/C]AGATTCTCAGCCCTT | 7251 |
rs146791462 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | TSG101 | GRCh38.p7 | 11:18517618 | GATACATAAATACCA[C/T]TGTGTTACAACTGCC | 7251 |
rs146802409 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | TSG101 | GRCh38.p7 | 11:18520743 | ATTTTCATGATTACA[A/G]AATTTCCGGCCAGGC | 7251 |
rs146948085 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18482187 | AGCAGAAGGTTCCTT[G/T]ACATAGAAAATCATA | 7251 |
rs146957725 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | TSG101 | GRCh38.p7 | 11:18487766 | GTAACAGGAGTGGTG[A/G]CCCAGCTCATGCTTC | 7251 |
rs147087579 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | TSG101 | GRCh38.p7 | 11:18521248 | AAATTGTTCATTAAG[G/T]TCACCAATAACTGCC | 7251 |
rs147097471 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18481396 | CTCATCTTAATGCTG[C/T]CTGTGGGCAGAGAAC | 7251 |
rs147107179 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TSG101 | GRCh38.p7 | 11:18486336 | CCCAGGCAGGGTGTC[A/G]CTCGTCAGAGGTCCC | 7251 |
rs147136541 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18512335 | TTCTACTGAGTCCAG[C/T]CTGCTACTAAACCCA | 7251 |
rs147146705 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18515926 | AGGAAGTTTTAAGAA[A/G]GCTGAAAATGTTAGG | 7251 |
rs147242778 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TSG101 | GRCh38.p7 | 11:18494744 | CTGCACACAAGCAAG[C/T]GTGCACTAGTAAACC | 7251 |
rs147252436 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | TSG101 | GRCh38.p7 | 11:18496810 | AAAAACAAGGATAGC[A/G]CCAGGTGTGGTGGCT | 7251 |
rs147398375 | in-del | -/TTAA | 0.00557542 | 0.0525036 | downstream-variant-500B | TSG101 | GRCh38.p7 | 11:18480174 | TGGTATATCCCCATG[-/TTAA]TTAATTCACTTTATA | 7251 |
rs147441714 | in-del | -/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18495473 | CCTTTTAACTTCCTC[-/T]TTTTTTTACCAGGGG | 7251 |
rs147713562 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | TSG101 | GRCh38.p7 | 11:18523812 | TGGCCAATTTTGTTA[C/T]AGTTTAAAATGTTTA | 7251 |
rs147723427 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TSG101 | GRCh38.p7 | 11:18486385 | AGAAGAAAATCCTGC[A/G]TCATCAACACTATCA | 7251 |
rs147733177 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TSG101 | GRCh38.p7 | 11:18490360 | CATTCAGTGTATCCA[A/G]TTCAGTAATTGCTTC | 7251 |
rs147795922 | snp | A/G | 6.59533e-05 | 0.00574215 | missense | TSG101 | GRCh38.p7 | 11:18509571 | GTTGCCTGGTATGGC[A/G]GATAGGATGCCGAAA | 7251 |
rs147933496 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | TSG101 | GRCh38.p7 | 11:18521075 | ATTTTTCTCCTCTTC[C/T]CTGGTAAGATCACTT | 7251 |
rs147969671 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | TSG101 | GRCh38.p7 | 11:18523537 | AGATGGATTCTCGCT[C/T]TGTCACCCAGGCTGG | 7251 |
rs147983858 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | TSG101 | GRCh38.p7 | 11:18524129 | AGCAGTGACTGTGCC[C/T]CTAGAAATGCTGTAG | 7251 |
rs148017410 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TSG101 | GRCh38.p7 | 11:18515349 | TTATGAATAGCAGGT[A/G]CTATGTGAAATCAAT | 7251 |
rs148019791 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | TSG101 | GRCh38.p7 | 11:18488496 | GACCTGGTGAGGGGC[A/T]CTAAAAAGCATGATC | 7251 |
rs148079655 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | TSG101 | GRCh38.p7 | 11:18506408 | AAAAAAAAAAAATAC[A/G]TAGGCTGGGCATGGT | 7251 |
rs148132622 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TSG101 | GRCh38.p7 | 11:18511868 | TGCTTTCCTAAATGT[C/T]TCATATAAATGAAAT | 7251 |
rs148196789 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TSG101 | GRCh38.p7 | 11:18492363 | AAAACTTAAGAGTCT[C/T]TTTATAGTTAGTGAA | 7251 |
rs148238384 | in-del | -/A | | | intron-variant | TSG101 | GRCh38.p7 | 11:18521033 | TAGACTCCGTCTTGG[-/A]AAAAAAAAAAAAAAA | 7251 |
rs148392973 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18509094 | GAAGAAAGCTAAGAG[A/C/G]TAGATGTCCAATTGT | 7251 |
rs148455832 | snp | A/G | 1.77764e-05 | 0.00298125 | missense | TSG101 | GRCh38.p7 | 11:18502503 | ACAGTGGTCACAGGA[A/G]GCTGAGAAGGGTACT | 7251 |
rs148508762 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | TSG101 | GRCh38.p7 | 11:18494457 | TTCCTTTACTAACAA[A/G]ATAAAAATCATTTGT | 7251 |
rs148585509 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | TSG101 | GRCh38.p7 | 11:18497509 | ATATACCATTTTCCA[A/C]ACATTTCTATTCTTT | 7251 |
rs148701007 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | TSG101 | GRCh38.p7 | 11:18484712 | TCCTAATCAGTATAT[C/T]ATATCATTTCCATGC | 7251 |
rs148753162 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | TSG101 | GRCh38.p7 | 11:18489873 | TGGAATTGTATTTCA[A/G]TGATTCTGGTATCAG | 7251 |
rs148855953 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | TSG101 | GRCh38.p7 | 11:18524011 | GCCCAGGCTGATCCT[C/G]AACTCCTGGCCTCAA | 7251 |
rs148951774 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18506083 | GCCTGCATCGGCCTC[C/T]GAAAGTGCTGGGTAA | 7251 |
rs148985120 | snp | C/T | 0.00115333 | 0.0239861 | missense, utr-variant-5-prime | TSG101 | GRCh38.p7 | 11:18519566 | TATAGAGTAATAACA[C/T]TGACAGTTTCACGTA | 7251 |
rs149014446 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | TSG101 | GRCh38.p7 | 11:18486166 | TTTCATCAGTCAATA[A/G]AACTCCCTGTCTTGC | 7251 |
rs149065967 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | TSG101 | GRCh38.p7 | 11:18491625 | ATAACTGTGAGTATA[A/C]TAGCTTTCAGTGAGC | 7251 |
rs149126329 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | TSG101 | GRCh38.p7 | 11:18511062 | TAATCTATTTTGTGT[A/G]TATCTCATCTCACGT | 7251 |
rs149444993 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18483104 | ATGGGAGCCGGTCTT[C/T]CTATTCTCGTGATAG | 7251 |
rs149540489 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | TSG101 | GRCh38.p7 | 11:18522016 | TCATTTGATTTCCAG[A/G]ACATCAACTGTTCTC | 7251 |
rs149635436 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18502070 | TATATTTCAGGTAAC[A/G]CTAATAAGCAAACAC | 7251 |
rs149694224 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18495828 | TAGATCAAGGCTGAG[A/G]CAGGAGAATGGCGTG | 7251 |
rs149716557 | snp | C/T | 1.64727e-05 | 0.00286986 | missense | TSG101 | GRCh38.p7 | 11:18483991 | ATTTCCTCCTTCATC[C/T]GCCATCTCAGTTTGT | 7251 |
rs149783061 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | TSG101 | GRCh38.p7 | 11:18486006 | CCTTTTAACCAATCA[A/C]ATGTTGCCTTTTCCA | 7251 |
rs149852719 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18523461 | TGCATCCCTAGAACC[C/T]AAAACAGTGAGGGAC | 7251 |
rs149858470 | in-del | -/G | 0.0252325 | 0.109451 | intron-variant | TSG101 | GRCh38.p7 | 11:18524376 | TGGCCAGAGTACCAT[-/G]ATGTGTGTGGAGAGC | 7251 |
rs149905626 | snp | C/T | 0.00279162 | 0.0372561 | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18528081 | GCTCACTGCAACCTC[C/T]GCCTCTGTTTTTCAG | 7251 |
rs149942126 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18516670 | CCATCGGCCAGGCGC[A/G]GTGGTTCGCGCCTGT | 7251 |
rs150096505 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TSG101 | GRCh38.p7 | 11:18488896 | TTTGGGAGGCCAAGG[C/T]GGGTGGATCATGAGG | 7251 |
rs150253115 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | TSG101 | GRCh38.p7 | 11:18518398 | TTTCAGAGCTAAGGG[A/T]CTCACAATGGACAAG | 7251 |
rs150304165 | snp | G/T | 0.0138799 | 0.0821421 | intron-variant | TSG101 | GRCh38.p7 | 11:18521584 | ATGTTGCCCAAGCTG[G/T]TCTCAAACTCCTGGA | 7251 |
rs150324655 | snp | C/T | 0.000153988 | 0.00877327 | synonymous-codon | TSG101 | GRCh38.p7 | 11:18514804 | ATATGGGTATGTGTC[C/T]AGTAGCCATAGGCAT | 7251 |
rs150368112 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant | TSG101 | GRCh38.p7 | 11:18505448 | TTTTGTAGAAATGAG[G/T]TCTACTATGTTGCCC | 7251 |
rs150420218 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TSG101 | GRCh38.p7 | 11:18510447 | ACAAAAAAATTATAC[A/G]TAGATTCTAGCTTAG | 7251 |
rs150568158 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | TSG101 | GRCh38.p7 | 11:18520139 | ACAGATTTGCTTATT[C/G]ATACAATGTGATCTT | 7251 |
rs150570292 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TSG101 | GRCh38.p7 | 11:18493975 | CACTCAGAAAAATGC[A/G]CTTTACTTGAGCTCT | 7251 |
rs150619777 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | TSG101 | GRCh38.p7 | 11:18523177 | TTGGATTTCAGGTGT[A/G]AGCCCCATGTCAAGC | 7251 |
rs150733917 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | TSG101 | GRCh38.p7 | 11:18512202 | CTGAAGTCAAGAGTT[C/T]GAGACCAGACTGGCC | 7251 |
rs150822663 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18501219 | CGAAGGGTTTCCCCT[A/G]TGTATTCTTCTAGTA | 7251 |
rs150830557 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TSG101 | GRCh38.p7 | 11:18490049 | AAACTTCAGAATGCC[A/G]TGGCATTTATGTGAC | 7251 |
rs151086393 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TSG101 | GRCh38.p7 | 11:18497824 | ACATTAATGACAAAT[A/G]CATTTTAATAAATCA | 7251 |
rs151128443 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18518098 | TTTTCTCCCCACTGA[A/T]GCCATTTAAAAACTA | 7251 |
rs151138951 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TSG101 | GRCh38.p7 | 11:18503662 | CAGCTGTGAGCCACC[A/G]CACCCAGCCCTAACT | 7251 |
rs151152617 | in-del | -/ACAGA | 0.0162398 | 0.0886349 | intron-variant | TSG101 | GRCh38.p7 | 11:18484599 | CCCTTTACCAACAGG[-/ACAGA]ACAGATGAACAAAAA | 7251 |
rs151305204 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TSG101 | GRCh38.p7 | 11:18495698 | TGCTACATGAATTGG[C/T]TTGTTCCTTCATTAT | 7251 |
rs151338708 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | TSG101 | GRCh38.p7 | 11:18481009 | CACAGTGAGAGGAGA[C/T]AGGCAAGATCAGCAC | 7251 |
rs180892481 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18490672 | CAACAGCTCCAGAAC[A/G]TCATTGCAGATGTCC | 7251 |
rs180954360 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18511627 | CATGTAAGCCTCATG[C/T]ATGTAGGTGAAATAT | 7251 |
rs181164169 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18486065 | TTCTGAGCCTGTAAG[A/C]AGCCGCAGGACTCAG | 7251 |
rs181168498 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TSG101 | GRCh38.p7 | 11:18496188 | TAAAATCCAGGCTGG[A/G]TGAGGTGGCTTATGC | 7251 |
rs181180564 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TSG101 | GRCh38.p7 | 11:18507824 | TGTTGCAGGCCGGCC[A/G]CGGTGGCTCACGCCT | 7251 |
rs181189753 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18528639 | TCAGGTGATCCACCC[A/G]CCTCAGCCTGCCAGA | 7251 |
rs181384951 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18489618 | TGTCATAAGCCAGTT[A/T]TCTGCCACAAAGAAT | 7251 |
rs181400376 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18511176 | CACCCCTCCTCCCCC[C/T]AGACAAGGTCTTGCC | 7251 |
rs181435365 | snp | G/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18504593 | AAACTGGGATAAACT[G/T]CTCTTTTTTTCTGGA | 7251 |
rs181585541 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | TSG101 | GRCh38.p7 | 11:18524049 | CTCCCATCTCTACCT[C/T]CCAAAGTATTGGGAT | 7251 |
rs181587604 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TSG101 | GRCh38.p7 | 11:18517909 | TAAAAAAGAAAACCA[C/T]CTTATATAAATTTGG | 7251 |
rs181613597 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18483701 | AAGACCAAATGCCAA[A/G]CATAGGCTCCACTGT | 7251 |
rs181747016 | snp | C/T | | | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18528422 | TGAGACAGAGTTTTG[C/T]TCTTGCTTCCCAGGC | 7251 |
rs181761280 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | TSG101 | GRCh38.p7 | 11:18499619 | GGTTTCACCATGTTG[A/G]CCAGGCTGGTCTCCA | 7251 |
rs181804386 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18491300 | GTGTGATTTATGGGG[A/G]GGTCTGGGCCATGCA | 7251 |
rs181805863 | snp | A/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18522309 | ATTGAACATGACCAA[A/T]ACTGAACTCCTCATC | 7251 |
rs181820245 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18511819 | CCCCACAGCCCTTTA[C/G]CAACCACTAATCTAC | 7251 |
rs182001993 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | TSG101 | GRCh38.p7 | 11:18497401 | TTTGCCTCTAGCCTA[A/T]ATGCCTAAGACAGTA | 7251 |
rs182008078 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TSG101 | GRCh38.p7 | 11:18507381 | AGAGACTTCAAACTA[C/T]TATGAGAAGTCCTAT | 7251 |
rs182009878 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | TSG101 | GRCh38.p7 | 11:18516940 | AGAGCAAAACTCCAC[C/T]GCAAACAAACAAACA | 7251 |
rs182096698 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18520299 | CACAATCACAGCTCA[C/T]TGTAACCTCGAACTC | 7251 |
rs182100172 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18501250 | GTTTTATAGCTTTGG[A/G]TCTTACATTAAGTCT | 7251 |
rs182277127 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18503812 | TTACTGGCCACCTGG[A/T]TAGTTAGACAATAAA | 7251 |
rs182315606 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TSG101 | GRCh38.p7 | 11:18508075 | CTCCGGCCTGGGCAA[C/T]AGAGCGAGACTCTGT | 7251 |
rs182341805 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18524399 | TGGAGAGCCTACAAT[C/T]AGATAAAGAGAAAAC | 7251 |
rs182344743 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18505332 | TGCAATTACGGCTCA[A/T]TGCATCCTCGATCTG | 7251 |
rs182465381 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | TSG101 | GRCh38.p7 | 11:18487767 | TAACAGGAGTGGTGG[C/T]CCAGCTCATGCTTCA | 7251 |
rs182478912 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TSG101 | GRCh38.p7 | 11:18509143 | AATGTGAACGCTTCA[A/G]TTGACCTTAATCCTT | 7251 |
rs182589185 | snp | C/T | 0 | 0 | intron-variant | TSG101 | GRCh38.p7 | 11:18486440 | CTGCCCAACCAGCCA[C/T]CATAATTCAGGGCTA | 7251 |
rs182592783 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18528759 | CACTGCAGCCTCGAC[C/T]TCCCTGGCTCAAGTG | 7251 |
rs182636396 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18493091 | ACACACTGACCTTTT[C/T]ACTCAAGCAGAGTCA | 7251 |
rs182701502 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18512039 | TTCCTTTTACACTAA[A/G]TTCTTTGAAGAAAAA | 7251 |
rs182710475 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | TSG101 | GRCh38.p7 | 11:18492617 | CCCTCAAAATAAGAA[C/G]CAAGCCGAGGCAGCA | 7251 |
rs182719830 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18481037 | CACATGACCTGACCA[A/G]GCTCCAGCTACAGCT | 7251 |
rs182919767 | snp | A/G | 0.000528218 | 0.0162429 | intron-variant | TSG101 | GRCh38.p7 | 11:18519632 | TCGCATAAGAATTTA[A/G]TTTAAAACCAATGCA | 7251 |
rs182936127 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18513010 | TGAGACTACAGGTGT[A/G]AGCCACCCCACCCAG | 7251 |
rs182948570 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TSG101 | GRCh38.p7 | 11:18508305 | CAGCTCACTGCAACA[C/T]CTGCCTCAGCCTCCC | 7251 |
rs183187732 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18500587 | TGATGATGAGTGATA[C/T]TGAGCATTTTTTCAT | 7251 |
rs183245871 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18506254 | TTGAGTAATGACAGT[A/G/T]ATCTCAATTGGTTTT | 7251 |
rs183479922 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18525732 | TTTATCAAAACAAAA[C/T]CAAGAAGCCTAAAAT | 7251 |
rs183489412 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18521842 | CCACAGTGTTTGGCT[A/G]ATTTTTGTATATTTT | 7251 |
rs183492421 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18502807 | TGGTCCCAGTTATAT[A/G]AGAGTCACCCTCATA | 7251 |
rs183524432 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18501770 | ATTTGTTTGTCTCAA[C/T]TGGACTCTTTAAGGC | 7251 |
rs183686733 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TSG101 | GRCh38.p7 | 11:18482269 | CTCAGTCTATGAAGA[A/G]GATTCAATGCATAGA | 7251 |
rs183703869 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | TSG101 | GRCh38.p7 | 11:18506493 | GTCAGGAGTTTGAGA[A/C]CAGCCTGGCCAACAT | 7251 |
rs183719191 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | TSG101 | GRCh38.p7 | 11:18526235 | TTAAAAGTAGTTACT[C/G]TTAGAAAATCCCTGA | 7251 |
rs183764822 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18520886 | AAATACAAAAATTAT[A/C]TGGGCGTGGTGGTCC | 7251 |
rs183785098 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | TSG101 | GRCh38.p7 | 11:18480391 | TGCATTAATAAAAGC[C/T]AGTCTTTACCAAAAG | 7251 |
rs183815295 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | TSG101 | GRCh38.p7 | 11:18525160 | GTGATCCACCCGCCT[C/T]GGCCTCCCAAAGTGC | 7251 |
rs183987094 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18505659 | AACAGACTGATTTCA[C/T]TGTTAATTTAATTTA | 7251 |
rs184138203 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18510071 | ATCAATGATATCTTG[A/G]AAATACGTGTTCTTA | 7251 |
rs184149059 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | TSG101 | GRCh38.p7 | 11:18511415 | AAGCTTTCTGTGAAA[A/C]CTTGCTGATATCTAC | 7251 |
rs184270706 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18488276 | TTGTTTTAAATCAGT[A/G]CATGAGGTTTTCTTT | 7251 |
rs184370690 | snp | C/G | 0.000376773 | 0.0137202 | intron-variant | TSG101 | GRCh38.p7 | 11:18514649 | ATATATAAAACATAA[C/G]TAATTCACAGAACAC | 7251 |
rs184402584 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18507764 | TCTTGAATACTGCAC[G/T]TCCAATGTCAATTTA | 7251 |
rs184454604 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TSG101 | GRCh38.p7 | 11:18496572 | GTGCAGTGACTCACA[C/T]CTGTAATCCGGGAGG | 7251 |
rs184604944 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18515986 | TAGAAGTTAAAATCT[A/G]TATCAGCATCAAAGC | 7251 |
rs184622124 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TSG101 | GRCh38.p7 | 11:18489035 | CAGGAGAATCGCTGG[A/G]ACCCGGGAGGCGGAG | 7251 |
rs184638056 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | TSG101 | GRCh38.p7 | 11:18510810 | GCCTGTGGTCACAAC[G/T]ACTCAGGAGGCTGCA | 7251 |
rs184711462 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | TSG101 | GRCh38.p7 | 11:18521496 | ACCACCGCCTCCCAA[A/G]TAGCTGGGACTACAG | 7251 |
rs184748275 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18490281 | TTCCTGGTTTTCCGA[C/T]GTCCACAGAGTAACA | 7251 |
rs184840893 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18502372 | TAGTACATTATTATA[A/G]GTTTTCCTCTAAGAA | 7251 |
rs184856305 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TSG101 | GRCh38.p7 | 11:18494407 | ATTCTATAGGAATAA[C/T]GACAGGAAGCCAAAT | 7251 |
rs184869475 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | TSG101 | GRCh38.p7 | 11:18513795 | GAATAAGTAAGTAGG[C/T]TGGGCATGGTGGCTT | 7251 |
rs185115277 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18495829 | AGATCAAGGCTGAGG[C/T]AGGAGAATGGCGTGA | 7251 |
rs185199773 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18505351 | ATCCTCGATCTGTAG[A/G]CTCAAGTGATCCTTC | 7251 |
rs185209789 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18524772 | GAGGTATAAAATATC[G/T]TCTGAACATGCCTTG | 7251 |
rs185423348 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18486290 | GAATGGGAGGGCTGT[C/T]TCTGGCAGCAGGTAG | 7251 |
rs185439546 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | TSG101 | GRCh38.p7 | 11:18507891 | TTGAGGTCAGGAGTT[C/T]GAGACCAGCCTGGCC | 7251 |
rs185458657 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18528643 | GTGATCCACCCGCCT[C/G]AGCCTGCCAGAATGT | 7251 |
rs185527919 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | TSG101 | GRCh38.p7 | 11:18483292 | CTGAGATCAGGAGTT[C/T]GGGACGAGCCTGGCC | 7251 |
rs185534348 | snp | A/C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18527432 | ACCTTCATACTATAC[A/C/G]TTGGCAAGGGTAAAG | 7251 |
rs185651056 | snp | A/T | 0.0154538 | 0.0865337 | intron-variant | TSG101 | GRCh38.p7 | 11:18506702 | CTCAAAAAAAATAAA[A/T]AAATAAATAAATAAA | 7251 |
rs185713209 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18504659 | GTGATCACATTGCTG[A/C]ATTTTTTTGTAACTT | 7251 |
rs185939494 | snp | A/C | 0.0160683 | 0.0881813 | intron-variant | TSG101 | GRCh38.p7 | 11:18484083 | GGGACCTGCAGGAAA[A/C]AGAGGCAAAAAACAC | 7251 |
rs185942313 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TSG101 | GRCh38.p7 | 11:18490995 | GACGAGGATGCTTCT[C/G]AGCAAAGCTCCAAGT | 7251 |
rs185991714 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18491523 | TCCACTGGGAGAAGA[A/C]AACTAGAAGCTTTGC | 7251 |
rs186004228 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18511852 | TCCATCTCTATAGAT[C/T]TGCTTTCCTAAATGT | 7251 |
rs186091291 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18500759 | AATATTTTCTCCCAC[A/T]CAACAGGTCGTCTCT | 7251 |
rs186250887 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18517721 | GTGTGTAGTAGGATA[C/T]ACCATCTAGGTTTGT | 7251 |
rs186254470 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18498290 | AACAGGAAATCACTT[G/T]AAGGTTTTGAGCAGA | 7251 |
rs186348102 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18524351 | ATAAACACATAAAAC[A/G]TAAGGCAGGTGGCCA | 7251 |
rs186606933 | snp | C/G/T | 0.00350069 | 0.0416911 | utr-variant-5-prime | TSG101 | GRCh38.p7 | 11:18526820 | CGACACCGCCATGAC[C/G/T]GCCGCCTGGCGACTC | 7251 |
rs186633313 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18519047 | GCTCTGTTGCCCAGG[C/T]TGGAGTGCAGTGGCC | 7251 |
rs186798909 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18509800 | TCATGAAAATTTCAT[C/T]TAATTAATTTATTTT | 7251 |
rs186842439 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18499783 | ATTTTGTTACCTGCA[C/T]GGAATGTAATGTTCA | 7251 |
rs186894811 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18503998 | CACTTGAGTCCAGGA[A/G]TTCAAGGCAAGCCTA | 7251 |
rs187042442 | snp | C/T | 3.41664e-05 | 0.00413304 | intron-variant | TSG101 | GRCh38.p7 | 11:18481579 | GGTTTGCAAGGTCAG[C/T]GCCTCTACAACCCAA | 7251 |
rs187048826 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18525733 | TTATCAAAACAAAAC[C/G]AAGAAGCCTAAAATA | 7251 |
rs187059253 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18506300 | TTTAAGAAATTTGTA[C/T]ATCTAGTATAGATAG | 7251 |
rs187112271 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18522470 | CAAAATATCCTGTTA[G/T]CTTTGCCTTCAAAAT | 7251 |
rs187188272 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TSG101 | GRCh38.p7 | 11:18486465 | GGGCTAAGCCCCTTC[A/G]GCAGTTAAATTCTTT | 7251 |
rs187269467 | snp | A/C/G/T | 0.00398731 | 0.0445001 | intron-variant | TSG101 | GRCh38.p7 | 11:18487125 | GACCTGTTGTGGGGT[A/C/G/T]GGGGGAGGGATAGCA | 7251 |
rs187282339 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18508396 | GATGGGGTTTCATCA[C/T]GTTGGCCAAGCTGGT | 7251 |
rs187388203 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18508166 | TCATAGCGGTCACTC[A/G]CTATATTATCTGAGC | 7251 |
rs187526217 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18513043 | TCAAGGACAGATTTT[C/T]ATAAGGCTCATTCTA | 7251 |
rs187669434 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TSG101 | GRCh38.p7 | 11:18514309 | ACACTATCAGACACA[C/T]AAACAGAAGTTCCCT | 7251 |
rs187672095 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TSG101 | GRCh38.p7 | 11:18494422 | CGACAGGAAGCCAAA[C/T]GAATCAGCTTCTCCT | 7251 |
rs187763538 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TSG101 | GRCh38.p7 | 11:18494246 | AAAGATGAAAGATGC[C/T]ACCTGGTAGGCATAA | 7251 |
rs187922698 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TSG101 | GRCh38.p7 | 11:18520659 | TCACAGTTTGGAATG[C/T]GTTAATTGTATCCCT | 7251 |
rs187930234 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18501695 | TGAATCTACAGACTG[C/T]TTTGGGTAATATAGT | 7251 |
rs188000269 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TSG101 | GRCh38.p7 | 11:18492623 | AAATAAGAACCAAGC[C/T]GAGGCAGCAGTCGCT | 7251 |
rs188039912 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | TSG101 | GRCh38.p7 | 11:18488031 | AGGATTTTTCTTTTT[G/T]GCTATACTATTTTCA | 7251 |
rs188072488 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | TSG101 | GRCh38.p7 | 11:18506548 | ATACAAAAATTAGCC[A/G]GGAATGGTGGCACAG | 7251 |
rs188081269 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18497400 | ATTTGCCTCTAGCCT[A/G]TATGCCTAAGACAGT | 7251 |
rs188278099 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18512274 | AGCCAGGTGTGGTGG[C/T]GGGCGCCTGTAATCC | 7251 |
rs188301659 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18520986 | CAGTGAGCCGAGATC[A/G]TGCCCTTGCACTCCA | 7251 |
rs188328054 | snp | A/G | 4.36424e-05 | 0.00467111 | intron-variant | TSG101 | GRCh38.p7 | 11:18502456 | AGACTTTGCTTATAT[A/G]GTGAAACACAAGTTT | 7251 |
rs188526667 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18505759 | AATATCATGCGACAA[A/G]TTTGACCCCATTATC | 7251 |
rs188564918 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | TSG101 | GRCh38.p7 | 11:18501928 | TTAGATAGAAGCAAA[A/G]ATAACCAACTTATGG | 7251 |
rs188741673 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TSG101 | GRCh38.p7 | 11:18485913 | TGGACTGCTGGTCCC[A/G]GATGAAACCCCTGAC | 7251 |
rs188757943 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | TSG101 | GRCh38.p7 | 11:18507771 | TACTGCACTTCCAAT[A/G]TCAATTTAAAACTCA | 7251 |
rs188819326 | snp | A/G | 0.00112146 | 0.0236532 | intron-variant | TSG101 | GRCh38.p7 | 11:18480683 | ATGGCTTTGATTTAG[A/G]CCCAGGCATAAAATA | 7251 |
rs188819972 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | TSG101 | GRCh38.p7 | 11:18488655 | TCTTCTCAAGTCTTT[A/T]AAGCCAGGCTTGCTC | 7251 |
rs188829580 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18525284 | AGGTGTGGTGGCTCA[C/T]GCCTGTATTCCCATC | 7251 |
rs188989078 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18489095 | ACTCCAGCCTGACAA[C/G]ACAGCAAGACTCCAT | 7251 |
rs189002634 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18510873 | GCTGCAGTATGACTG[C/T]GCCACTGCACTCCAG | 7251 |
rs189075088 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18482353 | AGGCTCTGAGTTGTA[C/T]TGGTGTCACTTTCCT | 7251 |
rs189113196 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18516407 | TGGAGTGCAATGGCG[C/T]GATTTTGGCTCGCTG | 7251 |
rs189115888 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18510161 | TGAGGTGGTTCACAC[A/C]TGTAATCCCAGCACT | 7251 |
rs189149775 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | TSG101 | GRCh38.p7 | 11:18517868 | AATGTAAGCTATACC[A/G]CAATGTATTCTGATT | 7251 |
rs189156054 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | TSG101 | GRCh38.p7 | 11:18499280 | TTATATATATTTATA[C/T]ATATCATATATATTT | 7251 |
rs189375519 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18511478 | ATTTATATACTGAGA[C/T]TCGGGGTGTTATAAG | 7251 |
rs189394988 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18503030 | TCTTTTGATAACATT[C/T]GTACCAAACTCATCT | 7251 |
rs189405483 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18522124 | GCTAAGTCCTTGGTC[G/T]TCTTCTCTATCTAAA | 7251 |
rs189641224 | snp | G/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18495989 | GGCACAAGCACAGCT[G/T]ACAGTACATCCTCCA | 7251 |
rs189644428 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18521557 | AATTTTTCATAAAGA[A/C]AGGATCTCACTATGT | 7251 |
rs189665361 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18490671 | CCAACAGCTCCAGAA[C/T]GTCATTGCAGATGTC | 7251 |
rs189811785 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TSG101 | GRCh38.p7 | 11:18500873 | CAGTGGTGCGATCTC[A/G]GCTCACTGCAACCTC | 7251 |
rs189820164 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18528705 | CCCATTTATATATTT[C/T]TGTTGCCCAGGTCAT | 7251 |
rs189824193 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TSG101 | GRCh38.p7 | 11:18520263 | GGGTCTCGCTCTGTC[A/G]CCCAGGATGAAGTAG | 7251 |
rs189916119 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | TSG101 | GRCh38.p7 | 11:18515085 | CTCAATTAACTGTTT[G/T]TTCCCTCTGTTTATT | 7251 |
rs189946379 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18522583 | GTCTCTGCCTCCATC[A/G]TTAACCCCCTACAGT | 7251 |
rs190076717 | snp | A/C | 0.0252325 | 0.109451 | intron-variant | TSG101 | GRCh38.p7 | 11:18524374 | GGTGGCCAGAGTACC[A/C]TGATGTGTGTGGAGA | 7251 |
rs190082969 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18505122 | TTACCTATGACATGT[A/G]TTCAGAAATCTGGCT | 7251 |
rs190177164 | snp | C/T | 3.29739e-05 | 0.00406028 | missense | TSG101 | GRCh38.p7 | 11:18506899 | TATGGAGAGATTCCA[C/T]CTGGCATGCCTGGCA | 7251 |
rs190180218 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TSG101 | GRCh38.p7 | 11:18504491 | TACTGAACACAGTAC[C/T]TTTGTTTCTAGTCTC | 7251 |
rs190204760 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18487555 | TTTTTCTAGTAGAGA[C/G]GTAGTCTCACTATGT | 7251 |
rs190218976 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18508799 | CATATAATTTGTCTT[A/G]TAAGATAAACAAGTT | 7251 |
rs190435521 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18527665 | AATGCAAGGGTAGGT[A/C]CTTCCATCTTAATTG | 7251 |
rs190451355 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | TSG101 | GRCh38.p7 | 11:18492358 | TAATGAAAACTTAAG[A/C]GTCTTTTTATAGTTA | 7251 |
rs190468166 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18511891 | AATGAAATCATACAA[C/T]ATATGGCCTTTTGTG | 7251 |
rs190743664 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18486339 | AGGCAGGGTGTCGCT[C/T]GTCAGAGGTCCCTGG | 7251 |
rs190988204 | snp | G/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18507923 | ACATGGTGAAACCCC[G/T]ACTCTACTAAAAATA | 7251 |
rs191040754 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TSG101 | GRCh38.p7 | 11:18512627 | GTGAAAAATTATAGA[A/G]AGTCTATATATTATC | 7251 |
rs191153569 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TSG101 | GRCh38.p7 | 11:18525140 | TCTTGAACTCGTGAC[C/T]TCAGGTGATCCACCC | 7251 |
rs191271623 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18492754 | AAACTTTAAAAAATC[A/G]AACTACTTTGTAAAA | 7251 |
rs191275932 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18499996 | ACCTTTCTTCATAAG[C/T]CCTATCCCACCCACA | 7251 |
rs191298190 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18521762 | GTTCACTGCAACCTC[C/T]ACCTCCCAGGCTCAA | 7251 |
rs191532682 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18482115 | GACAGTAACAAGCTT[A/G]TCACCTGTCAGCGAC | 7251 |
rs191533868 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TSG101 | GRCh38.p7 | 11:18519401 | AACAGTTTTATTAGG[C/T]GGTGGTGCAATCCCA | 7251 |
rs191547175 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18506436 | GGTGGCTCACACCTG[C/T]AATCCCAGCGCTTTG | 7251 |
rs191562222 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TSG101 | GRCh38.p7 | 11:18525812 | TCCTTAGAGATTATT[C/T]GGTCTTCAATCAAGA | 7251 |
rs191831264 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TSG101 | GRCh38.p7 | 11:18508284 | TGGAGTGCAGTAATG[C/T]GATCTCAGCTCACTG | 7251 |
rs192029336 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18491263 | ATTAGAGTGTTCTTT[A/G]TCTACACCAGACAGT | 7251 |
rs192047329 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18505637 | CATTGACTTTCTAGC[A/G]TGTGTTAACAGACTG | 7251 |
rs192156287 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18514473 | AACAAAATATTGAAT[A/G]TAAGTATTCTGAAAA | 7251 |
rs192167589 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18494971 | TTATCTAAATATTCA[C/G/T]TATGGACTAAAGAGT | 7251 |
rs192317073 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18488167 | AAACAGGCTTAGCTC[C/T]ACATTCACTACTGCA | 7251 |
rs192387191 | snp | C/T | | | downstream-variant-500B | TSG101 | GRCh38.p7 | 11:18480275 | CTTACTAAGGTTTCA[C/T]GGATCTTTCCTAAAG | 7251 |
rs192392281 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18511794 | TAGTAGTCACTTCCC[A/G]TTTCCCTTTCCCCAC | 7251 |
rs192401771 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18501756 | TGAAATGTCTTTCCA[C/T]TTGTTTGTCTCAATT | 7251 |
rs192410624 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | TSG101 | GRCh38.p7 | 11:18488976 | AAAAATTAGCTGGGC[A/G]TGGTGGTGCGTGCCT | 7251 |
rs192413985 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18520805 | TGGGAGGCCGAGGCA[A/G]GCGGATCACGAGGTC | 7251 |
rs192606103 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18494363 | CGTTTTGTGAAAAGA[A/C]TAATTTAAGAATCTA | 7251 |
rs192617900 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18515647 | CACTTCCCCCAAGTT[A/G]GGTACTATTATCCAA | 7251 |
rs192620210 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18513715 | ACTGCTAGAGACTCT[A/G]CAGGTTTCTCTGCCT | 7251 |
rs192708913 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18509846 | TTTTAAACATGATGT[A/G]CAGCAAGGTTCTTGC | 7251 |
rs192769778 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18501965 | GGAGAAGGCAGATAT[A/G]GTGGTGCAGGTAGTG | 7251 |
rs192895620 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18480953 | ATCCAGCCATTCATG[C/T]GGTTGTACCACTTCT | 7251 |
rs192896861 | snp | G/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18525630 | TTTTTTTCAAAAAGT[G/T]ATATATAAAAGTTAC | 7251 |
rs193042712 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | TSG101 | GRCh38.p7 | 11:18510162 | GAGGTGGTTCACACC[A/T]GTAATCCCAGCACTT | 7251 |
rs193122648 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TSG101 | GRCh38.p7 | 11:18506099 | GAAAGTGCTGGGTAA[G/T]ATTACAGGTGTGAGC | 7251 |
rs193136665 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | TSG101 | GRCh38.p7 | 11:18506694 | GACTCCATCTCAAAA[A/T]AAATAAATAAATAAA | 7251 |
rs193290295 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18483098 | TGAATCATGGGAGCC[A/G]GTCTTTCTATTCTCG | 7251 |
rs193293134 | snp | C/T | 0.00478085 | 0.0486577 | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18527342 | GGCGCAAATTTCTCC[C/T]GACTCTAAAGTCATA | 7251 |
rs199584605 | in-del | -/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18496007 | AGTACATCCTCCAAA[-/G]GGAGGGGCCAATTAG | 7251 |
rs199585213 | in-del | -/ATATATA | | | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18528371 | TATATATATATATAT[-/ATATATA]TTTTTTTTTTTTTTT | 7251 |
rs199602141 | snp | A/G | 4.99322e-05 | 0.00499636 | intron-variant | TSG101 | GRCh38.p7 | 11:18481613 | AAAAAATCTTGGAAC[A/G]TAAAATGAAGAAATA | 7251 |
rs199628620 | snp | A/C | 0.202651 | 0.245475 | intron-variant | TSG101 | GRCh38.p7 | 11:18496480 | AATAAAATAAAATAA[A/C]ATAAAATAAAATAAA | 7251 |
rs199648260 | in-del | -/TACTT | 0.000162259 | 0.00900572 | utr-variant-3-prime | TSG101 | GRCh38.p7 | 11:18480505 | AAAGGAAGAGAAGAA[-/TACTT]TAAGAAGAGCTCAAC | 7251 |
rs199657458 | in-del | -/CTGTAC | 0.0364509 | 0.129988 | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18528250 | CTTTAATTAGAGCAA[-/CTGTAC]CTTTGTGAGTTGGAG | 7251 |
rs199665217 | snp | A/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18490072 | TATGTGACCAATCTG[A/T]GTTTTAGAATACAAA | 7251 |
rs199716284 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18526137 | GCTTTTTTAAAAATT[A/G]AAAAAAAAAACACTA | 7251 |
rs199742708 | snp | A/C | 0.187053 | 0.241946 | intron-variant | TSG101 | GRCh38.p7 | 11:18496460 | AATAAAATAAAATAA[A/C]ATAAAATAAAATAAA | 7251 |
rs199766860 | snp | C/T | 0.000165055 | 0.00908296 | intron-variant | TSG101 | GRCh38.p7 | 11:18519493 | CTCAAAGTATAGAAA[C/T]TGCTATTTTTACTGC | 7251 |
rs199800915 | snp | A/G | 0.00520983 | 0.0507718 | intron-variant | TSG101 | GRCh38.p7 | 11:18480660 | GAGAAAAGTTTGAAT[A/G]GTTTAGAATGGCTTT | 7251 |
rs199809899 | in-del | -/ATATATATA | | | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18528369 | TATATATATATATAT[-/ATATATATA]TTTTTTTTTTTTTTT | 7251 |
rs199827125 | in-del | -/G | 0.00597247 | 0.0543191 | intron-variant | TSG101 | GRCh38.p7 | 11:18487633 | GCCTCCTGGAGTGCT[-/G]GGGATTACAGGCATG | 7251 |
rs199925543 | snp | A/G | 0.00199806 | 0.0315443 | synonymous-codon, utr-variant-5-prime | TSG101 | GRCh38.p7 | 11:18519577 | AACATTGACAGTTTC[A/G]CGTACAGTTAGGTCT | 7251 |
rs199998388 | snp | A/G | | | synonymous-codon | TSG101 | GRCh38.p7 | 11:18502577 | ACAGCCTGGGTAACC[A/G]CTAAAGACAAGAACA | 7251 |
rs200034601 | in-del | -/GAGGC | 0.0260105 | 0.111035 | intron-variant | TSG101 | GRCh38.p7 | 11:18483522 | AAAAGGAGTGCCTTT[-/GAGGC]TGCCTCCCACCATGA | 7251 |
rs200065106 | in-del | -/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18506698 | CCATCTCAAAAAAAA[-/T]AAATAAATAAATAAA | 7251 |
rs200072277 | in-del | -/GTATAAT | | | intron-variant | TSG101 | GRCh38.p7 | 11:18487256 | ACCCTAAAACTTAAA[-/GTATAAT]AAAAAAAAAAAAGAA | 7251 |
rs200075333 | snp | A/C | | | intron-variant | TSG101 | GRCh38.p7 | 11:18482230 | TCCCAACAAATGGGC[A/C]CCTGCCATAGGAGAG | 7251 |
rs200088808 | in-del | -/C | 0.341685 | 0.232581 | intron-variant | TSG101 | GRCh38.p7 | 11:18521669 | TGCACCTGGCCCCTT[-/C]CTTTTTTTTTTTTTT | 7251 |
rs200093000 | snp | A/C | | | intron-variant | TSG101 | GRCh38.p7 | 11:18508846 | TAAAGAAAATTTACC[A/C]AAAAAAAAAAAGTCA | 7251 |
rs200106661 | in-del | -/CAA | | | intron-variant | TSG101 | GRCh38.p7 | 11:18510934 | AACAAAAACAAAACC[-/CAA]CAACAACAACGACAA | 7251 |
rs200125110 | snp | C/T | 0.000263531 | 0.0114759 | synonymous-codon | TSG101 | GRCh38.p7 | 11:18483963 | GGCATTGAGCTCTGC[C/T]TGGGCACGATCCATT | 7251 |
rs200182464 | snp | A/C | 0.190833 | 0.242898 | intron-variant | TSG101 | GRCh38.p7 | 11:18496495 | AATAAAATAAAATAA[A/C]ATAAAATAAAATAAA | 7251 |
rs200200355 | snp | G/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18510701 | TCTAGGTCTATTCCA[G/T]TACTTTCCCCTCCAT | 7251 |
rs200225514 | in-del | -/T | 0.0142736 | 0.0832652 | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18527410 | TGATTTTTTTTAAGC[-/T]TTAAAGACCTTCATA | 7251 |
rs200277353 | snp | A/G | 1.79522e-05 | 0.00299596 | intron-variant | TSG101 | GRCh38.p7 | 11:18514648 | AATATATAAAACATA[A/G]CTAATTCACAGAACA | 7251 |
rs200289940 | in-del | -/TATATA | 0.236434 | 0.249632 | intron-variant | TSG101 | GRCh38.p7 | 11:18499301 | ATATATATTTATATT[-/TATATA]TTTATTTATATATAT | 7251 |
rs200338928 | snp | A/T | 0.0704125 | 0.17392 | intron-variant | TSG101 | GRCh38.p7 | 11:18487252 | ATGTACCCTAAAACT[A/T]AAAGTATAATAAAAA | 7251 |
rs200476543 | snp | A/C | 0.381503 | 0.21262 | intron-variant | TSG101 | GRCh38.p7 | 11:18486764 | CCAGCCATCCCATTA[A/C]TGGGTATATACCCAA | 7251 |
rs200530920 | snp | A/G | 0.000104363 | 0.00722294 | intron-variant | TSG101 | GRCh38.p7 | 11:18526756 | CGCGCCCTGGGAGGC[A/G]AGCGCGTCGCAGCCT | 7251 |
rs200617283 | snp | A/C | 0.201727 | 0.245295 | intron-variant | TSG101 | GRCh38.p7 | 11:18496485 | AATAAAATAAAATAA[A/C]ATAAAATAAAATAAA | 7251 |
rs200618111 | in-del | -/AAC | 0.00597247 | 0.0543191 | intron-variant | TSG101 | GRCh38.p7 | 11:18497092 | CGAGTCTGTCTCAAA[-/AAC]AACAACAACAAAAAA | 7251 |
rs200656803 | in-del | -/A | | | intron-variant | TSG101 | GRCh38.p7 | 11:18508107 | CAAAAAAAAAAAAAA[-/A]GTTGCTTAGGAGACT | 7251 |
rs200739579 | in-del | -/A | 0.0138799 | 0.0821421 | intron-variant | TSG101 | GRCh38.p7 | 11:18509461 | AGCAAAGAAGTCATT[-/A]ATTTTTCTTTATTTT | 7251 |
rs200775736 | snp | A/C | 0.202343 | 0.245416 | intron-variant | TSG101 | GRCh38.p7 | 11:18496465 | AATAAAATAAAATAA[A/C]ATAAAATAAAATAAA | 7251 |
rs200777114 | in-del | -/TATATATAT | | | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18528370 | ATATATATATATATA[-/TATATATAT]TTTTTTTTTTTTTTT | 7251 |
rs200880173 | snp | A/C/G | 0.0011847 | 0.0243098 | utr-variant-5-prime | TSG101 | GRCh38.p7 | 11:18526851 | CCTTCCCCGCAGGCA[A/C/G]AGGGTCAGCCGCTGC | 7251 |
rs200933195 | snp | A/G | 0.000399281 | 0.0141238 | missense | TSG101 | GRCh38.p7 | 11:18502573 | AAGGACAGCCTGGGT[A/G]ACCACTAAAGACAAG | 7251 |
rs201011900 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18502624 | TAAGATGACCCAACC[G/T]TATAGTATTTTGAAG | 7251 |
rs201013126 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18521033 | TAGACTCCGTCTTGG[A/G]AAAAAAAAAAAAAAA | 7251 |
rs201089472 | snp | A/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18510773 | GTCTCTACAAAAAAA[A/T]TAACTGTACATGGTG | 7251 |
rs201168438 | snp | G/T | | | downstream-variant-500B | LDHAL6A, TSG101 | GRCh38.p7 | 11:18479997 | AGGTATATAGTTTGG[G/T]CCTGCCACTCTGCTC | 7251 |
rs201202252 | snp | A/C/G | 0.000515176 | 0.0160415 | missense, synonymous-codon | TSG101 | GRCh38.p7 | 11:18514678 | ACTATGAATACTTAC[A/C/G]TGTTTCCATTCATGT | 7251 |
rs201238071 | snp | A/G | 0.00199806 | 0.0315442 | intron-variant | TSG101 | GRCh38.p7 | 11:18509722 | TTTCAGTAAAAAGAA[A/G]AAGGTTAGCCATTTC | 7251 |
rs201256675 | snp | A/C | 0.201727 | 0.245295 | intron-variant | TSG101 | GRCh38.p7 | 11:18496470 | AATAAAATAAAATAA[A/C]ATAAAATAAAATAAA | 7251 |
rs201285696 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18496006 | CAGTACATCCTCCAA[A/G]GGGAGGGGCCAATTA | 7251 |
rs201368614 | in-del | -/A | | | intron-variant | TSG101 | GRCh38.p7 | 11:18489114 | CTCAAAAAAAAAAAA[-/A]GGATGGTGGGAAAGA | 7251 |
rs201372216 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant | TSG101 | GRCh38.p7 | 11:18499306 | TATTTATATTTATAT[A/T]TTTATTTATATATAT | 7251 |
rs201423201 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18524551 | GCTTCTATTACTTTA[C/T]TTCCTATTCTTACCT | 7251 |
rs201441420 | snp | A/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18487253 | TGTACCCTAAAACTT[A/T]AAGTATAATAAAAAA | 7251 |
rs201480350 | in-del | -/AAAATAAAAT | 0.239037 | 0.24976 | intron-variant | TSG101 | GRCh38.p7 | 11:18496443 | CGAAACTCTGTCTCA[-/AAAATAAAAT]AAAATAAAATAAAAT | 7251 |
rs201511968 | in-del | -/ACTGT | | | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18528249 | CCTTTAATTAGAGCA[-/ACTGT]ACCTTTGTGAGTTGG | 7251 |
rs201530764 | in-del | -/T | 0.374149 | 0.216995 | intron-variant | TSG101 | GRCh38.p7 | 11:18499354 | TATTTATATATGTTT[-/T]ATATATAAATATGTT | 7251 |
rs201652670 | in-del | -/TT | | | intron-variant | TSG101 | GRCh38.p7 | 11:18495667 | ATACTACCAGTTAGG[-/TT]TTTTTTTTTTTTTTT | 7251 |
rs201817783 | in-del | -/A | | | intron-variant | TSG101 | GRCh38.p7 | 11:18506690 | CCATCTCAAAAAAAA[-/A]TAAATAAATAAATAA | 7251 |
rs201826521 | snp | C/T | 4.94254e-05 | 0.00497094 | missense | TSG101 | GRCh38.p7 | 11:18481770 | GAATGATAACTTCAT[C/T]GATATCATTGTTTTC | 7251 |
rs201829233 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18480661 | AGAAAAGTTTGAATA[A/G]TTTAGAATGGCTTTG | 7251 |
rs201837337 | in-del | -/CT | | | intron-variant | TSG101 | GRCh38.p7 | 11:18490069 | ATTTATGTGACCAAT[-/CT]GAGTTTTAGAATACA | 7251 |
rs201944274 | in-del | -/TATATATATATTTTTTTTTTTT | | | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18528368 | ATATATATATATATA[-/TATATATATATTTTTTTTTTTT]TTTTTTTTTTTTTTT | 7251 |
rs201946532 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18502597 | AGACAAGAACAAAAA[A/G]CATTTAACATTTAAG | 7251 |
rs201946715 | in-del | -/A | | | intron-variant | TSG101 | GRCh38.p7 | 11:18487274 | AATAAAAAAAAAAAA[-/A]GAAAAAAAAATTTCT | 7251 |
rs201987070 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18510945 | AAACCCAACAACAAC[C/T]ACAACAAAAAACAAC | 7251 |
rs201989230 | snp | A/G/T | 0.00789851 | 0.0623455 | missense, synonymous-codon | TSG101 | GRCh38.p7 | 11:18514806 | ATGGGTATGTGTCCA[A/G/T]TAGCCATAGGCATAT | 7251 |
rs202019084 | snp | A/C | 0.198014 | 0.244535 | intron-variant | TSG101 | GRCh38.p7 | 11:18496490 | AATAAAATAAAATAA[A/C]ATAAAATAAAATAAA | 7251 |
rs202060916 | snp | G/T | 0.03789 | 0.132323 | stop-gained | TSG101 | GRCh38.p7 | 11:18502571 | GTAAGGACAGCCTGG[G/T]TAACCACTAAAGACA | 7251 |
rs202090861 | in-del | -/CA | | | intron-variant | TSG101 | GRCh38.p7 | 11:18523192 | AAGCCCCATGTCAAG[-/CA]CACAGTTTCTTTACC | 7251 |
rs202121568 | snp | A/C | | | intron-variant | TSG101 | GRCh38.p7 | 11:18484155 | CTTCAGAAAAGGGGG[A/C]AATATGAACCGACAC | 7251 |
rs202129487 | in-del | -/CTT | | | intron-variant | TSG101 | GRCh38.p7 | 11:18521670 | GCACCTGGCCCCTTC[-/CTT]TTTTTTTTTTTTTTT | 7251 |
rs202156088 | snp | C/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18487250 | ACATGTACCCTAAAA[C/G]TTAAAGTATAATAAA | 7251 |
rs367565092 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18521416 | CTCTGTCGCTCAGGC[C/T]ACAGTGCAGTGGTAT | 7251 |
rs367580544 | snp | C/T | 8.27698e-05 | 0.00643258 | intron-variant | TSG101 | GRCh38.p7 | 11:18483822 | TAGAACACTCTGCCA[C/T]GGCTACAATTCAATC | 7251 |
rs367590449 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18492753 | TAAACTTTAAAAAAT[C/T]GAACTACTTTGTAAA | 7251 |
rs367599062 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18508080 | GCCTGGGCAACAGAG[C/T]GAGACTCTGTCTCAA | 7251 |
rs367779669 | snp | A/C | 5.20323e-05 | 0.00510034 | missense | TSG101 | GRCh38.p7 | 11:18480581 | CGGCAGTCTTTCTTG[A/C]TTTTTGCATTAGTGC | 7251 |
rs367793516 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18523271 | CTATCAGATATAAAA[C/T]GGTGACTCATCCCAT | 7251 |
rs368007421 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TSG101 | GRCh38.p7 | 11:18505624 | AGTAATTATTTATCA[C/T]TGACTTTCTAGCGTG | 7251 |
rs368097803 | in-del | -/AATTA | | | intron-variant | TSG101 | GRCh38.p7 | 11:18520164 | GATCTTTCATGACTA[-/AATTA]TTTCACTTAGCATGT | 7251 |
rs368222298 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18500048 | GTCTATCATTCTACT[C/G]TCTACCTCCAAGAGA | 7251 |
rs368311931 | in-del | -/A | | | intron-variant | TSG101 | GRCh38.p7 | 11:18503061 | TAGTTTAAAAAAAAA[-/A]CCTTTTTTCTCACTT | 7251 |
rs368421543 | snp | C/G | 0.000153988 | 0.00877327 | intron-variant | TSG101 | GRCh38.p7 | 11:18519478 | AACAAAGAGAGTAAA[C/G]TCAAAGTATAGAAAT | 7251 |
rs368443850 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18498216 | AAAAGTAATGGGGAA[A/G]AGGGCAGGATCATGT | 7251 |
rs368528074 | in-del | -/A | | | intron-variant | TSG101 | GRCh38.p7 | 11:18497978 | TAACAGAAAAATAAA[-/A]CTTCACAAGATTCTA | 7251 |
rs368590616 | snp | C/T | 3.30087e-05 | 0.00406242 | synonymous-codon | TSG101 | GRCh38.p7 | 11:18481633 | ATGAAGAAATACCTT[C/T]AGGAAGACATCCAGG | 7251 |
rs368619928 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18500112 | ATATTTGTCTTTCTG[C/T]GCCTAGTTTATTTCC | 7251 |
rs368620147 | snp | A/G | 3.30017e-05 | 0.00406199 | intron-variant | TSG101 | GRCh38.p7 | 11:18519619 | CTGAAAAGCAAAATC[A/G]CATAAGAATTTAGTT | 7251 |
rs368678350 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18503034 | TTGATAACATTCGTA[C/T]CAAACTCATCTTTAG | 7251 |
rs368764998 | in-del | -/TTCTC | 0.00199481 | 0.0315187 | intron-variant | TSG101 | GRCh38.p7 | 11:18488291 | GCATGAGGTTTTCTT[-/TTCTC]ATTTCAGCAGATGGA | 7251 |
rs368824082 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18498588 | GGAAGATTGAGAATT[C/T]GGTTTTGGTTGAGTT | 7251 |
rs368828756 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18510166 | TGGTTCACACCTGTA[A/G]TCCCAGCACTTTGGG | 7251 |
rs368862110 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | TSG101 | GRCh38.p7 | 11:18480764 | AACCTTTGGAATGAA[C/T]ACCTCATTATATGTG | 7251 |
rs368907086 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18519869 | TATAAATTATTGAGA[C/T]GTTTTAACCAATGCA | 7251 |
rs369012514 | snp | G/T | 1.65575e-05 | 0.00287724 | intron-variant | TSG101 | GRCh38.p7 | 11:18519648 | TTTAAAACCAATGCA[G/T]ATATTTTACAGCTGG | 7251 |
rs369033981 | snp | C/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18482715 | TAGCTCTTTAGCCAA[C/G]CAAGTATCTCTGGAT | 7251 |
rs369066821 | snp | A/G | 8.26631e-05 | 0.00642843 | intron-variant | TSG101 | GRCh38.p7 | 11:18506838 | TAATACAATTATTCA[A/G]AAGAACGTTTTTCAT | 7251 |
rs369079090 | snp | A/G | 0.000107681 | 0.00733681 | intron-variant | TSG101 | GRCh38.p7 | 11:18502459 | CTTTGCTTATATGGT[A/G]AAACACAAGTTTTCA | 7251 |
rs369120319 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TSG101 | GRCh38.p7 | 11:18484283 | TTACTATTAATCCAT[C/G]TTAAACCCAGTTTCC | 7251 |
rs369178192 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18515036 | TTTTACTCAGTCTTC[C/T]CTAAACTTATACTTG | 7251 |
rs369241530 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18506060 | GACCTCAGGACCTCA[A/G]GTGATCCGCCTGCAT | 7251 |
rs369246064 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18507568 | AAGAGAACGTGAATG[A/C]CAAAGAACTAAGATC | 7251 |
rs369361191 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18525610 | CTATGTAAAACAATA[C/T]ACCGTTTTTTTCAAA | 7251 |
rs369366617 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18511484 | ATACTGAGACTCGGG[A/G]TGTTATAAGCACAGT | 7251 |
rs369390481 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18504264 | TCCTTCTGAGTTTAT[C/T]GTCAATAATCCTTTT | 7251 |
rs369400607 | in-del | -/ACCC | | | intron-variant | TSG101 | GRCh38.p7 | 11:18490885 | CTGCCTTCGTGACTA[-/ACCC]CAGCCATATCATCAT | 7251 |
rs369434068 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18484968 | TTTTGAGATGGAGTC[C/T]CACTCTGTCACCCAG | 7251 |
rs369480079 | in-del | -/T | 0.499722 | 0.0117779 | intron-variant | TSG101 | GRCh38.p7 | 11:18495667 | ATACTACCAGTTAGG[-/T]TTTTTTTTTTTTTTT | 7251 |
rs369667198 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18510473 | CTTAGAAATTGCTAG[A/G]TTGTAGTACAAAGGG | 7251 |
rs369716520 | in-del | -/TT | 0.00557542 | 0.0525036 | intron-variant | TSG101 | GRCh38.p7 | 11:18490832 | GCAACAGAGAGCAGA[-/TT]TCTCTCTTCGTTGGA | 7251 |
rs369754521 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TSG101 | GRCh38.p7 | 11:18514405 | TACTATTTTTTAAAA[C/T]GCACTTCCCACTATG | 7251 |
rs369795840 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18509100 | AGCTAAGAGCTAGAT[A/G]TCCAATTGTGTATAC | 7251 |
rs369798357 | snp | A/G | 3.3222e-05 | 0.00407553 | synonymous-codon | TSG101 | GRCh38.p7 | 11:18481867 | GTTTTTATCAACCTC[A/G]GCCTGAAAACAGAAC | 7251 |
rs370013076 | snp | A/G | 0.000195981 | 0.00989706 | intron-variant | TSG101 | GRCh38.p7 | 11:18526723 | CGGACTCGACAGGGC[A/G]CGGAAGGGAGCGGTG | 7251 |
rs370047965 | in-del | -/GAAA | | | intron-variant | TSG101 | GRCh38.p7 | 11:18508835 | AATTATAATCTTAAA[-/GAAA]ATTTACCAAAAAAAA | 7251 |
rs370083418 | snp | A/G | 1.79638e-05 | 0.00299693 | intron-variant | TSG101 | GRCh38.p7 | 11:18514645 | CAAAATATATAAAAC[A/G]TAACTAATTCACAGA | 7251 |
rs370128455 | snp | A/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18499788 | GTTACCTGCACGGAA[A/T]GTAATGTTCAAGTGA | 7251 |
rs370131570 | snp | A/G | 1.78115e-05 | 0.0029842 | intron-variant | TSG101 | GRCh38.p7 | 11:18514659 | CATAACTAATTCACA[A/G]AACACTATGAATACT | 7251 |
rs370396669 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18512068 | AAAATTAATATCTAT[A/G]TTAATATCTACTTCC | 7251 |
rs370434012 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18507367 | GTTTAAAGACTTCAA[A/G]AGACTTCAAACTACT | 7251 |
rs370452981 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18489293 | TGCGGTTATTTCACA[A/G]GTGCAACCACAGGGC | 7251 |
rs370646135 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18507825 | GTTGCAGGCCGGCCG[C/T]GGTGGCTCACGCCTG | 7251 |
rs370671181 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | TSG101 | GRCh38.p7 | 11:18482937 | ATCCTTTGCCTAAAA[C/T]ATTTCCTAGGGCAAA | 7251 |
rs370693801 | snp | A/C | | | intron-variant | TSG101 | GRCh38.p7 | 11:18499913 | TGTTAACTATAGTCA[A/C]CCTACTCTGCTATCA | 7251 |
rs370790655 | snp | A/C | | | intron-variant | TSG101 | GRCh38.p7 | 11:18494989 | TGGACTAAAGAGTGG[A/C]AACTACAGAAACACA | 7251 |
rs370791508 | snp | A/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18497347 | AAAGGGTAGAAAAAC[A/T]ATATATATTAAAGGA | 7251 |
rs370924761 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18521026 | ACAGAGCTAGACTCC[A/G]TCTTGGAAAAAAAAA | 7251 |
rs370929926 | snp | A/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18499398 | TATATATATATATAT[A/T]TATATTTTTTTTTTT | 7251 |
rs371008075 | snp | A/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18510981 | AAATATCTACCAACC[A/T]CTAATTAAGCTGTGC | 7251 |
rs371335978 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18514456 | AAGGTTCAACTAAAG[C/G]CAACAAAATATTGAA | 7251 |
rs371341854 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18484436 | AAAAACATTTGGTGC[A/C]GGCCAAGTCCAACAT | 7251 |
rs371349445 | snp | C/T | 1.66205e-05 | 0.00288271 | intron-variant | TSG101 | GRCh38.p7 | 11:18509505 | CTGTTCTCTTTTGTT[C/T]ATATGAGTTTTAAAG | 7251 |
rs371428124 | snp | C/G | 0.000153988 | 0.00877327 | synonymous-codon | TSG101 | GRCh38.p7 | 11:18481720 | GTTTTCTTCTGCATA[C/G]AGATTCAGGATCTGT | 7251 |
rs371490370 | snp | A/C/G | 0.000153214 | 0.00875131 | intron-variant | TSG101 | GRCh38.p7 | 11:18480645 | TACATGCTGGGAGGG[A/C/G]AGAAAAGTTTGAATA | 7251 |
rs371949495 | snp | A/G | 1.6473e-05 | 0.00286988 | synonymous-codon | TSG101 | GRCh38.p7 | 11:18484001 | TCATCCGCCATCTCA[A/G]TTTGTCACTGACCGC | 7251 |
rs371965876 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18489426 | TCTTAAAGGTATTAT[C/T]CAGGAAACAGATAAG | 7251 |
rs371975065 | snp | A/G/T | 3.3127e-05 | 0.00406972 | intron-variant | TSG101 | GRCh38.p7 | 11:18519649 | TTAAAACCAATGCAT[A/G/T]TATTTTACAGCTGGA | 7251 |
rs372134787 | snp | C/T | 1.64933e-05 | 0.00287165 | intron-variant | TSG101 | GRCh38.p7 | 11:18519506 | AATTGCTATTTTTAC[C/T]GCATAAACTCACCAT | 7251 |
rs372157242 | snp | A/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18488548 | AGAAGTCAGGGATAT[A/T]TAAAAATACTTTTTT | 7251 |
rs372169828 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18484426 | TCCACTAAGGAAAAA[C/T]ATTTGGTGCAGGCCA | 7251 |
rs372194451 | snp | G/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18518457 | GCATATTATTTTCAA[G/T]GAGACAGGGTTGAAG | 7251 |
rs372205892 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18505886 | GTAATGGCGCGATCT[C/T]GGCTCACTGCAACCT | 7251 |
rs372258462 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | LDHAL6A, TSG101 | GRCh38.p7 | 11:18479898 | TTGGCTACAGAATCA[C/T]TCACCATGAAGACGA | 7251 |
rs372332720 | in-del | -/A | 0.00279162 | 0.0372561 | intron-variant | TSG101 | GRCh38.p7 | 11:18495418 | AAAGAGAACTTTCAC[-/A]CACTGCTGAGACTGG | 7251 |
rs372393626 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18503502 | CACAGCCTCCTGAGT[A/G]GCTGGGACTATAGGT | 7251 |
rs372538273 | multinucleotide-polymorphism | AAAA/TCTC | | | intron-variant | TSG101 | GRCh38.p7 | 11:18483492 | AAGAGTGAAACTCTC[AAAA/TCTC]AAAAAAAAAAAAAAA | 7251 |
rs372599419 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18502623 | TTAAGATGACCCAAC[C/T]TTATAGTATTTTGAA | 7251 |
rs372741718 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18511480 | TTATATACTGAGACT[C/T]GGGGTGTTATAAGCA | 7251 |
rs372796420 | snp | A/C | 4.95864e-05 | 0.00497903 | intron-variant | TSG101 | GRCh38.p7 | 11:18519641 | AATTTAGTTTAAAAC[A/C]AATGCATATATTTTA | 7251 |
rs372922556 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18494778 | ATGGGCTGGGTGCCT[C/T]GGGTGCCATATCCTG | 7251 |
rs372956858 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18498899 | CATGGTGTTTTGGAA[A/C]ACAAGAGGAAAGTGT | 7251 |
rs373035474 | snp | A/C | | | intron-variant | TSG101 | GRCh38.p7 | 11:18484701 | CAAATGTCCCTTCCT[A/C]ATCAGTATATTATAT | 7251 |
rs373068204 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18509204 | AGAAAGGAGAGGTCA[A/G]ACTACCTTTCAAGTT | 7251 |
rs373155651 | in-del | -/ACAA | | | intron-variant | TSG101 | GRCh38.p7 | 11:18508808 | TGTCTTGTAAGATAA[-/ACAA]GTTTGGTTAATTATA | 7251 |
rs373365304 | in-del | -/TTTAT | 0.0023933 | 0.0345097 | intron-variant | TSG101 | GRCh38.p7 | 11:18509808 | ATTTCATTTAATTAA[-/TTTAT]TTTAATAGAGTTAAG | 7251 |
rs373365500 | snp | C/G | 2.22804e-05 | 0.00333762 | intron-variant | TSG101 | GRCh38.p7 | 11:18502442 | CACAACAGGGAGTTA[C/G]ACTTTGCTTATATGG | 7251 |
rs373588196 | snp | C/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18507722 | GTACAAAATTGAATT[C/G]CAACAGTAACAATAG | 7251 |
rs373646158 | snp | A/G | 1.69568e-05 | 0.00291172 | intron-variant | TSG101 | GRCh38.p7 | 11:18514873 | AACTTCAGTTACTCT[A/G]TTTTTATTATTTTTA | 7251 |
rs373805758 | in-del | -/TT | | | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18528000 | TCTTTTTCTTTTTCT[-/TT]TTTTTTTTTTTTTTT | 7251 |
rs373888257 | snp | C/T | 1.64925e-05 | 0.00287158 | synonymous-codon | TSG101 | GRCh38.p7 | 11:18509549 | CTACTTACTATTTGG[C/T]GGCCCCGTTGCCTGG | 7251 |
rs373949414 | snp | G/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18526599 | CAGCTCCCGTACGGG[G/T]ATTCCCGCACCAGGC | 7251 |
rs374013951 | snp | A/G | 6.81849e-05 | 0.00583848 | synonymous-codon, utr-variant-5-prime | TSG101 | GRCh38.p7 | 11:18516157 | CCTGGAACTGCCATC[A/G]TTAAAAACTGAAAGG | 7251 |
rs374123987 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18490891 | TTCGTGACTACAGCC[A/G]TATCATCATAGCGCT | 7251 |
rs374170086 | snp | A/C/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | TSG101 | GRCh38.p7 | 11:18480504 | AAAAGGAAGAGAAGA[A/C/G]TACTTTAAGAAGAGC | 7251 |
rs374235181 | in-del | -/AAACTT | 0.150333 | 0.229274 | intron-variant | TSG101 | GRCh38.p7 | 11:18487247 | TGCACATGTACCCTA[-/AAACTT]AAAGTATAATAAAAA | 7251 |
rs374249578 | in-del | -/GATG | | | intron-variant | TSG101 | GRCh38.p7 | 11:18519663 | TATATTTTACAGCTG[-/GATG]AATTTTCTTAAAATC | 7251 |
rs374335811 | in-del | -/A | | | intron-variant | TSG101 | GRCh38.p7 | 11:18504437 | CAGACAAAAAAAAAA[-/A]GAAAGCATTTTTGTT | 7251 |
rs374339797 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18502618 | AACATTTAAGATGAC[C/T]CAACCTTATAGTATT | 7251 |
rs374348628 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18489098 | CCAGCCTGACAACAC[A/G]GCAAGACTCCATCTC | 7251 |
rs374348782 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18499559 | AGGATTACAGGCGTG[C/T]GCCACCACGCCCGGC | 7251 |
rs374382093 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TSG101 | GRCh38.p7 | 11:18511232 | CAACAATCTTCCTGC[C/T]TCAGTCTCCCAAGTA | 7251 |
rs374480564 | in-del | -/AAGTC | | | intron-variant | TSG101 | GRCh38.p7 | 11:18488647 | CTAGAAGTTCTTCTC[-/AAGTC]TTTAAAGCCAGGCTT | 7251 |
rs374553035 | snp | C/T | 0.000153988 | 0.00877327 | intron-variant | TSG101 | GRCh38.p7 | 11:18509535 | GTAAAATCTCAATTC[C/T]ACTTACTATTTGGTG | 7251 |
rs374567342 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18507780 | TCCAATGTCAATTTA[A/C]AACTCAAAGAAATTT | 7251 |
rs374585159 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18502003 | GGCATAGGTGAAGGC[C/T]GGAGTCTAAAGAAAT | 7251 |
rs374612103 | snp | A/G | 0.000638258 | 0.0178528 | intron-variant | TSG101 | GRCh38.p7 | 11:18481902 | CAAGCATTAATAACT[A/G]TACATAATTATCCAC | 7251 |
rs374661300 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18512998 | CTCCCAAAGTGCTGA[C/G]ACTACAGGTGTGAGC | 7251 |
rs374696854 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18520106 | CATCCTAGACAACCA[C/T]GAATTTACTTTGTCT | 7251 |
rs374828812 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18516813 | GGGCGTGGTGGCACA[C/T]GCCTGTAATCCCAGC | 7251 |
rs374831105 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18498665 | GGATATAACAATCTC[A/G]AGTTCAGGAGAGAGG | 7251 |
rs374840188 | snp | A/C | | | intron-variant | TSG101 | GRCh38.p7 | 11:18506569 | GGTGGCACAGCCTGT[A/C]GTCCCAACTGCTAGG | 7251 |
rs374861582 | in-del | -/C | | | intron-variant | TSG101 | GRCh38.p7 | 11:18499657 | ACCTCGCAATCTGCC[-/C]GCCTTGGCCTCCCAA | 7251 |
rs374865209 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18505544 | TTTTAAGTTAGCCCA[C/T]AGACCACCTTTGGAG | 7251 |
rs375058356 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18526384 | GACTGGAGGATCCCT[A/G]GATTGGGACAGGAGT | 7251 |
rs375284013 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18520768 | CCAGGCGTGGTGGCT[C/T]ACACTTGTAATCCTA | 7251 |
rs375314866 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18500301 | ATGGGAGTACAGGTA[C/T]TCCTTTAATATACTG | 7251 |
rs375320955 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18523611 | AGGTTCAGGCAATTC[C/T]CCTTTCTCAGCTTCC | 7251 |
rs375410450 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18506036 | TGGCCAGGCTGGTCT[C/T]GAACTCCTGACCTCA | 7251 |
rs375609448 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18501295 | GTTGATTTTTGTATG[C/T]GGTACAAGATAGGGG | 7251 |
rs375612358 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18497530 | TCTATTCTTTGGATA[C/T]ATGGAAATCATCTAA | 7251 |
rs375701084 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18510859 | CCAGGAAGGTTGAGG[C/T]TGCAGTATGACTGCG | 7251 |
rs375711754 | snp | C/G/T | 9.88728e-05 | 0.00703041 | missense | TSG101 | GRCh38.p7 | 11:18481653 | AGACATCCAGGTCTA[C/G/T]CACGCCCCTTCTCAA | 7251 |
rs375904335 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18514257 | TTTCTCTTGCTTTTC[C/T]AGTTATTTTTCATAG | 7251 |
rs375985920 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18502268 | ACTATGTGATCAAAA[A/G]AAAGATTGATGAGTT | 7251 |
rs375989010 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18496948 | ATATAAAAATTAGCC[A/G]GGTGTGGTGGTACGC | 7251 |
rs376026501 | snp | C/G | 1.64909e-05 | 0.00287144 | intron-variant | TSG101 | GRCh38.p7 | 11:18519514 | TTTTTACTGCATAAA[C/G]TCACCATATGAATCC | 7251 |
rs376351223 | snp | C/G/T | 4.94273e-05 | 0.00497108 | missense | TSG101 | GRCh38.p7 | 11:18484066 | ATTGTGCCATCCCTA[C/G/T]TGGGACCTGCAGGAA | 7251 |
rs376420770 | in-del | -/A | 0.43758 | 0.165269 | intron-variant | TSG101 | GRCh38.p7 | 11:18508094 | GCGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAGT | 7251 |
rs376447756 | snp | A/G | 1.65378e-05 | 0.00287552 | intron-variant | TSG101 | GRCh38.p7 | 11:18519645 | TAGTTTAAAACCAAT[A/G]CATATATTTTACAGC | 7251 |
rs376545696 | snp | C/T | 1.64917e-05 | 0.00287151 | missense | TSG101 | GRCh38.p7 | 11:18509592 | GATGCCGAAATAGGA[C/T]GAGAGAAGACTGGAG | 7251 |
rs376581909 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18493436 | CACTACTTCCTGGAA[C/T]TCAAATGAAGCTATT | 7251 |
rs376689067 | snp | A/C | | | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18527050 | GTTCCAACCAACCCG[A/C]CCCTCGAGTGCCGGA | 7251 |
rs376697972 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18507002 | ATAAGATATACATCA[C/T]ACTGTCAATACACAG | 7251 |
rs376769044 | snp | C/T | 0.000148306 | 0.00860993 | synonymous-codon | TSG101 | GRCh38.p7 | 11:18481654 | GACATCCAGGTCTAT[C/T]ACGCCCCTTCTCAAG | 7251 |
rs376772296 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18493076 | TACCCCAAGTCCCCA[A/G]CACACTGACCTTTTT | 7251 |
rs376794585 | snp | A/C/T | 6.54348e-05 | 0.0057196 | intron-variant | TSG101 | GRCh38.p7 | 11:18502455 | TAGACTTTGCTTATA[A/C/T]GGTGAAACACAAGTT | 7251 |
rs376880681 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18503501 | CCACAGCCTCCTGAG[C/T]AGCTGGGACTATAGG | 7251 |
rs376909322 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18481380 | GCACAGAAGAGTTAC[A/G]CTCATCTTAATGCTG | 7251 |
rs376919001 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TSG101 | GRCh38.p7 | 11:18514111 | AAAGGAATCAGTAAG[C/T]ACCCTGGGGGAAAAG | 7251 |
rs376934219 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18487340 | ATACTACCATAATTA[C/T]CATAATTCAATCTCC | 7251 |
rs377045407 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TSG101 | GRCh38.p7 | 11:18502303 | AGATTTATTTTCATG[A/C]CCTGGTAGAAGGTTC | 7251 |
rs377145114 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18481097 | TATCCCTAAAACCAT[A/G]TTCTCCATGACCCAA | 7251 |
rs377156997 | snp | C/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18524228 | AGAAGAAGGACTAAT[C/G]TGGTATAAATATATC | 7251 |
rs377236746 | in-del | -/TA | | | intron-variant | TSG101 | GRCh38.p7 | 11:18507609 | AGAGGCTAATCAACA[-/TA]GAGGAAGAAAAAGAG | 7251 |
rs377266259 | snp | A/C/G/T | 0.000182959 | 0.00956312 | intron-variant | TSG101 | GRCh38.p7 | 11:18506974 | TACAAGGCCTGAATA[A/C/G/T]GTAGGCTACTGAATA | 7251 |
rs377309935 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18484997 | AGGCTGGAGTGCAGT[C/T]GCATGATCTCGGCTC | 7251 |
rs377404452 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18504523 | TCAGTAATCCATGCT[A/G]TAATGCTGTAAAGAA | 7251 |
rs377464243 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18486828 | GCACACATATGTTTA[C/T]TGCAGCACTGTTCAC | 7251 |
rs377685617 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18486974 | TCCTTTGTAGGGACA[C/T]GGATGAAGCTGGAAA | 7251 |
rs386751178 | in-del | ACTTCTG/GTGATCCTCAAGTGATCCTCCC | | | intron-variant | TSG101 | GRCh38.p7 | 11:18512950 | CCAGGCTCGTCTCAA[ACTTCTG/GTGATCCTCAAGTGATCCTCCC]GCCTCAAGTGATCCT | 7251 |
rs386751179 | multinucleotide-polymorphism | CA/TG | | | intron-variant | TSG101 | GRCh38.p7 | 11:18516253 | CTGGTTAAAATTCAT[CA/TG]TTATCCTTGAAAGGG | 7251 |
rs386751180 | in-del | ATG/CT | | | intron-variant | TSG101 | GRCh38.p7 | 11:18524374 | GGTGGCCAGAGTACC[ATG/CT]ATGTGTGTGGAGAGC | 7251 |
rs397736013 | in-del | -/T | 0 | 0 | intron-variant | TSG101 | GRCh38.p7 | 11:18484956 | TTTTTTTTTTTTTTT[-/T]GAGATGGAGTCTCAC | 7251 |
rs397795617 | in-del | -/A | 0.5 | 0 | intron-variant | TSG101 | GRCh38.p7 | 11:18526147 | AATTGAAAAAAAAAA[-/A]CACTAGTCTTGAGCC | 7251 |
rs397847883 | in-del | -/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18508239 | TTTTTTTTTTTTTTT[-/T]GATACAGAGTCTTGC | 7251 |
rs397848238 | in-del | -/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18503390 | TTTTTTTTTTTTTTT[-/T]GAGACGGAGTCTCGC | 7251 |
rs397849106 | in-del | -/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18524928 | TTTTTTTTTTTTTTT[-/T]GAGATGGAGTCTTGC | 7251 |
rs397849444 | in-del | -/A | | | intron-variant | TSG101 | GRCh38.p7 | 11:18496006 | CAGTACATCCTCCAA[-/A]GGGAGGGGCCAATTA | 7251 |
rs397953814 | in-del | -/A | | | intron-variant | TSG101 | GRCh38.p7 | 11:18492778 | GTAAAAAAAAAAAAA[-/A]GGAATTATAACTAAG | 7251 |
rs398040250 | in-del | -/A | 0.5 | 0 | intron-variant | TSG101 | GRCh38.p7 | 11:18516366 | CAGGATGAGACTCTG[-/A]AAAAAAAAAACAAAA | 7251 |
rs398045025 | in-del | -/T | 0.5 | 0 | intron-variant | TSG101 | GRCh38.p7 | 11:18500821 | AAGCTTTTTTTTTTT[-/T]GAGACAAGGTCTCGC | 7251 |
rs398055035 | in-del | -/GTGT | | | intron-variant | TSG101 | GRCh38.p7 | 11:18483040 | TGCGTGTGTGTGTGT[-/GTGT]AGCAGGGGGTGGGGA | 7251 |
rs398055036 | in-del | -/AA | | | intron-variant | TSG101 | GRCh38.p7 | 11:18492777 | TTGTAAAAAAAAAAA[-/AA]GGAATTATAACTAAG | 7251 |
rs398055037 | in-del | -/TTT | | | intron-variant | TSG101 | GRCh38.p7 | 11:18505272 | AATCTTTTTTTTTTT[-/TTT]GAGACAGGTTCTCAC | 7251 |
rs398075754 | in-del | -/A | | | intron-variant | TSG101 | GRCh38.p7 | 11:18496005 | ACAGTACATCCTCCA[-/A]AGGGAGGGGCCAATT | 7251 |
rs398075755 | in-del | -/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18500820 | GAAGCTTTTTTTTTT[-/T]TGAGACAAGGTCTCG | 7251 |
rs398075756 | in-del | -/A | | | intron-variant | TSG101 | GRCh38.p7 | 11:18504436 | ATCAGACAAAAAAAA[-/A]AGAAAGCATTTTTGT | 7251 |
rs398097392 | in-del | -/A | | | intron-variant | TSG101 | GRCh38.p7 | 11:18504437 | TCAGACAAAAAAAAA[-/A]GAAAGCATTTTTGTT | 7251 |
rs527242670 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18516555 | TTCACCATGTTGGCT[A/G]GGCTGGTCTCGAACT | 7251 |
rs527334817 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | TSG101 | GRCh38.p7 | 11:18480197 | ACTTTATATGCTGTA[A/G]AATAATACTAAATTT | 7251 |
rs527452270 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | TSG101 | GRCh38.p7 | 11:18496135 | TTGAACATCTGGTAA[A/C]TTTTAAATCTTTCTT | 7251 |
rs527467206 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18503672 | CCACCGCACCCAGCC[C/G]TAACTATTCTTAATT | 7251 |
rs527569060 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18510757 | GTTTGAGACCAGCCT[A/G]GTCTCTACAAAAAAA | 7251 |
rs527664837 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18523634 | CAGCTTCCCGAGTAG[C/T]TGGGATTACAGGCGT | 7251 |
rs527684014 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18524797 | GCCTTGCCTTTGTCT[C/T]TGATGGCAGGTTTCT | 7251 |
rs527719825 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18525373 | AACATGGTGAAATCC[C/T]GTCTCTACTAAAAAT | 7251 |
rs527728732 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18498335 | TATTTATATTTTATT[A/G]GGATCACTCTAGCTG | 7251 |
rs527929375 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18512135 | TGAGGCGAGGCACAA[C/T]GGCTCACACCTGTAA | 7251 |
rs528001350 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18518372 | CTCAGCTACAAAATT[C/T]AGTTCCTTGCTTTCA | 7251 |
rs528063749 | in-del | -/ATT | 0.00398564 | 0.0444627 | intron-variant | TSG101 | GRCh38.p7 | 11:18494514 | GCTTTCAAATCTATC[-/ATT]ATTGCTTTGAATTTC | 7251 |
rs528072988 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18527814 | TGTGTGACAGTTTCA[A/T]TTATTTTAGTACAGC | 7251 |
rs528090981 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | TSG101 | GRCh38.p7 | 11:18482200 | TTACATAGAAAATCA[-/T]TAAGAGGTTTTTCTT | 7251 |
rs528126038 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18528492 | GCCTCCCGGGTTCAA[A/G]CGATTCTCCTGCCTA | 7251 |
rs528165733 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18492353 | AGAACTAATGAAAAC[G/T]TAAGAGTCTTTTTAT | 7251 |
rs528182307 | in-del | -/A | | | intron-variant | TSG101 | GRCh38.p7 | 11:18491486 | CATACTGTTACTGGG[-/A]AAAGTCAGCACTGCC | 7251 |
rs528201368 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18484787 | AGGTCCCCTTTCTAA[C/T]ATAAGTTTGGGTATT | 7251 |
rs528201626 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18520404 | AATTTATTTTTATTT[C/T]TGTAAAGACAGGGTC | 7251 |
rs528224930 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18522153 | AACTCATTCCTTTGA[C/T]CTCCCTCATGGTTGA | 7251 |
rs528225006 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18514295 | AATCTGTCACAGTTA[C/T]ACTATCAGACACATA | 7251 |
rs528297285 | in-del | -/T | 0.25801 | 0.249872 | intron-variant | TSG101 | GRCh38.p7 | 11:18508222 | GAAATATTTGATATC[-/T]TTTTTTTTTTTTTTT | 7251 |
rs528309943 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18514961 | CCGCATCCCCCCCAT[G/T]CCTATTTCCCCCAGC | 7251 |
rs528442108 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | TSG101 | GRCh38.p7 | 11:18480203 | TATGCTGTAGAATAA[C/T]ACTAAATTTCAACTT | 7251 |
rs528453440 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18501249 | AGTTTTATAGCTTTG[C/G]GTCTTACATTAAGTC | 7251 |
rs528479944 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18501997 | GAGATAGGCATAGGT[A/G]AAGGCTGGAGTCTAA | 7251 |
rs528516070 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TSG101 | GRCh38.p7 | 11:18524396 | GTGTGGAGAGCCTAC[A/C]ATCAGATAAAGAGAA | 7251 |
rs528578594 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18511603 | AATTCCTTAACTAAA[C/T]CATAGCCTCATGTAA | 7251 |
rs528721792 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18523182 | TTTCAGGTGTAAGCC[C/T]CATGTCAAGCACACA | 7251 |
rs528787742 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18486217 | ATCCCCATTCTTTGT[G/T]GGCACAGGACAAGAA | 7251 |