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 |