SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs528851687 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18505362 | GTAGGCTCAAGTGAT[C/T]CTTCCACCTCACCCT | 7251 |
rs528867754 | snp | C/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18484347 | TTATTTTCTCAATGA[C/G]ACAGAGGCTATGTCC | 7251 |
rs528963769 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18504025 | CCTAGACAACATGGC[A/G]AAACCATTTCTACAA | 7251 |
rs529093347 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18482872 | TCTAAACTTATTTCC[C/T]AGTAACTGGCAACAT | 7251 |
rs529102708 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18526640 | TCGGGGCGGGGTTCT[A/G]AGGAGGTCGCTAAGG | 7251 |
rs529154247 | in-del | -/T | 0.493703 | 0.0557558 | intron-variant | TSG101 | GRCh38.p7 | 11:18484935 | ACCTTAATTGCCGCC[-/T]TTTTTTTTTTTTTTT | 7251 |
rs529194571 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18489698 | GTGGTCATGAACTTT[G/T]GAGTGGCAACAGCCC | 7251 |
rs529231484 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18490425 | TCAGTAGAGTTTAGA[A/G]TCTCATAGTAAAAGA | 7251 |
rs529238673 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18507253 | CCTTCTTCGGTCCAA[A/G]GTTAACTTCTTAGAA | 7251 |
rs529258298 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18520160 | ATGTGATCTTTCATG[A/G]CTAAATTATTTCACT | 7251 |
rs529341622 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18483603 | TTTCTCTCAAGTCTC[A/G]GATATGTCTTTATCA | 7251 |
rs529346210 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18512900 | GCCTGGCTAATTTTT[A/G]TATTTTTAGTAGAAA | 7251 |
rs529401201 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18526958 | ACCACTTCCGCTTCC[A/G]CTACGTCACTTCCGG | 7251 |
rs529458107 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18507230 | AATTTAGAGGAAGGT[A/T]ATTCTGGCCTTCTTC | 7251 |
rs529496181 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18500037 | AAGTCTCTGGTGTCT[A/G]TCATTCTACTGTCTA | 7251 |
rs529540187 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TSG101 | GRCh38.p7 | 11:18506647 | GTGAGCCGAGATTGC[A/G]CCACTGTACTCCAGC | 7251 |
rs529567508 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | TSG101 | GRCh38.p7 | 11:18504910 | ATCTAAAATGAATAA[A/C]CTGCTTATATATTAC | 7251 |
rs529621846 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18500503 | TTTTTTTATTTTTTG[C/T]CTTTTTAATAATGGC | 7251 |
rs529668252 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18523111 | GTTGCCCAGGCTGGT[A/C]TGGAACTCCTGGCCT | 7251 |
rs529736446 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18516025 | AGTAGGTTTAATTTG[A/G]TTATAACTCTTTGGC | 7251 |
rs529817988 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18510181 | ATCCCAGCACTTTGG[A/G]AGGCCAAGGTGGGTG | 7251 |
rs529827959 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18522437 | CCTCTCTTTTCTTCA[C/T]ATCCACAGCAAATCT | 7251 |
rs529876208 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18500567 | GGTTTTTATCTGCAT[C/T]TTCCTGATGATGAGT | 7251 |
rs529942010 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18523317 | TTCCCCATTTCTTCC[C/T]TGCTTTATTTTCTCT | 7251 |
rs529982523 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18509804 | GAAAATTTCATTTAA[C/T]TAATTTATTTTAATA | 7251 |
rs530048566 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18488711 | ACCCCTGCCCATATA[A/C]AGCATTAAAAAGTGA | 7251 |
rs530061409 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18524062 | CTCCCAAAGTATTGG[A/G]ATTACAGGCATGAGC | 7251 |
rs530121838 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | TSG101 | GRCh38.p7 | 11:18480356 | ACATTCAGCACAAAA[A/T]GTTTACAGAGGATAG | 7251 |
rs530122862 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18496061 | AATTCACAACATATG[C/G]AAGTGTCACTGAGTG | 7251 |
rs530269344 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TSG101 | GRCh38.p7 | 11:18518210 | GAGATGAGAAGGAAT[C/T]GTGTCCTAGGTTTGG | 7251 |
rs530295255 | in-del | -/TATT | 0.00119737 | 0.0244387 | intron-variant | TSG101 | GRCh38.p7 | 11:18499305 | ATATTTATATTTATA[-/TATT]TATTTATATATATTT | 7251 |
rs530329472 | snp | A/C | | | intron-variant | TSG101 | GRCh38.p7 | 11:18524054 | ATCTCTACCTCCCAA[A/C]GTATTGGGATTACAG | 7251 |
rs530341509 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18524771 | AGAGGTATAAAATAT[C/T]TTCTGAACATGCCTT | 7251 |
rs530357454 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18510843 | GGGAGGATCACCTGA[A/G]CCAGGAAGGTTGAGG | 7251 |
rs530391085 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | TSG101 | GRCh38.p7 | 11:18488491 | TGGGAGACCTGGTGA[-/G]GGGCACTAAAAAGCA | 7251 |
rs530436914 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18483768 | AGATGCCTATAATTT[C/T]CTGAACTCCTACTAT | 7251 |
rs530453210 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18527018 | CGTGTGGGATTGAGA[C/G]GGGCCTGGTGGGGTG | 7251 |
rs530507413 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18499204 | TTTTTTAAATATATA[C/T]ATATAAAATATATAT | 7251 |
rs530659771 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18513747 | TTAGCTAAGGCCCTT[A/T]GCCCAGATTCTCAGC | 7251 |
rs530833239 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18484627 | ACAAAAAAGAATGAC[A/G]TCCAAAAAATTCAAC | 7251 |
rs530886370 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18507398 | ATGAGAAGTCCTATA[C/T]AAAACTTACATTATC | 7251 |
rs530980013 | snp | A/C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18510446 | AACAAAAAAATTATA[A/C/T]GTAGATTCTAGCTTA | 7251 |
rs531013363 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18514177 | CTTCTCTACAGAATC[C/T]TGGCCATACATGTCT | 7251 |
rs531015970 | in-del | -/CAAA | 0.00119737 | 0.0244387 | intron-variant | TSG101 | GRCh38.p7 | 11:18484311 | TCCCTATTCATAGCC[-/CAAA]CAATTAGCTACAATT | 7251 |
rs531059451 | snp | A/C/G/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18488840 | GTCAAAAAGGATGAT[A/C/G/T]GGGGGCCGGGCGCAG | 7251 |
rs531117344 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TSG101 | GRCh38.p7 | 11:18506446 | ACCTGTAATCCCAGC[A/G]CTTTGGGAGTCTGAG | 7251 |
rs531135598 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18485540 | AGAAGTCCTTAGAAT[A/G/T]TGCTTTTTTGGAAAC | 7251 |
rs531157089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18481303 | CAATCAGTGATCTCA[A/G]TTTAGGTGGTATGAC | 7251 |
rs531220912 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18501087 | TGCTGGGATTACAGA[C/T]GTGAGCCACTGCATC | 7251 |
rs531327708 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18517467 | CCCATAGAGGAAAGG[C/T]TGTAATGTGCAGTAC | 7251 |
rs531455826 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TSG101 | GRCh38.p7 | 11:18510313 | ATGGTCCCAGTTACT[C/T]AGGAGGCTGAGGCAA | 7251 |
rs531508960 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18497376 | GATATCCTAAATTAT[C/G]ATAAAATAATTTGCC | 7251 |
rs531621056 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18496809 | AAAAAACAAGGATAG[C/T]GCCAGGTGTGGTGGC | 7251 |
rs531650058 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18519206 | GACGAGGTTTCACCA[C/T]ATTGCCCAGGCTGGT | 7251 |
rs531692868 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18526517 | AAGAGAGGAGGGCGG[A/G]TGGGCGGCAGGTGTC | 7251 |
rs531756086 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18505976 | GCATGTGCCACCATG[C/T]CTGGCTAATTTTGTA | 7251 |
rs532073247 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18485375 | TTTATTAGTTTAATA[A/G]CCTATTTTCTGAAGG | 7251 |
rs532142344 | snp | A/G | | | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18527848 | AATGAGAACAAGGCC[A/G]TAGTATTGATTCCCT | 7251 |
rs532166009 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18515927 | GGAAGTTTTAAGAAA[C/G]CTGAAAATGTTAGGT | 7251 |
rs532218738 | snp | G/T | 8.35848e-05 | 0.00646416 | intron-variant | TSG101 | GRCh38.p7 | 11:18509702 | AAGTCAGCTACAGAG[G/T]TGCTTTTCAGTAAAA | 7251 |
rs532222895 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18501399 | TATATGTTCTTGGCA[A/C]CTTTGCTGAAAATCA | 7251 |
rs532234217 | snp | G/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18497252 | GTTTCTGCTTTCCTT[G/T]AAGTCTAAAGTTCAA | 7251 |
rs532306401 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18517524 | TGTGTAATGTTTGGG[C/T]CTACAATGGACTGCA | 7251 |
rs532351763 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18525498 | TTGCAGTGAGCCAAG[A/G]TCGTGCCACTGCACT | 7251 |
rs532510638 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18495318 | AAGGTCAAACTGTGT[A/G]TATGTTAAAGGCCTA | 7251 |
rs532548889 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18487168 | CCTAATGTTAAATGA[C/T]GAGTTAGTAGGTGCA | 7251 |
rs532562928 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18524038 | TCAAGTGGATTCTCC[C/T]ATCTCTACCTCCCAA | 7251 |
rs532730954 | snp | G/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18513299 | CAGAGTATCTCATCT[G/T]TTCTTTTCTTTTTTG | 7251 |
rs532795806 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18490597 | AAAAATACCTAAAAT[A/G]ATCTCCTTTCATTTT | 7251 |
rs532846837 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18505878 | GGTGGAGTGTAATGG[C/T]GCGATCTCGGCTCAC | 7251 |
rs532890942 | snp | A/T | 0.000399281 | 0.0141238 | downstream-variant-500B | TSG101 | GRCh38.p7 | 11:18480212 | GAATAATACTAAATT[A/T]CAACTTAAGATGGAT | 7251 |
rs532977274 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18526979 | TCACTTCCGGGCCGC[A/C]GTCCTGCGGGCAAGG | 7251 |
rs532981218 | in-del | -/AGG | 0.00119737 | 0.0244387 | intron-variant | TSG101 | GRCh38.p7 | 11:18516847 | TCGGAAGGCTGAGGC[-/AGG]AGAATTGCTTGAACC | 7251 |
rs533012325 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18520416 | TTTTTGTAAAGACAG[A/G]GTCTTGCTATGTTGC | 7251 |
rs533250129 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18491051 | CACTCCTCTGGCAGC[A/G]GTGGCGGTGCCTGCC | 7251 |
rs533259502 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TSG101 | GRCh38.p7 | 11:18483023 | ACAGAAAGGGACCTG[C/T]GTGCGTGTGTGTGTG | 7251 |
rs533297380 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TSG101 | GRCh38.p7 | 11:18483664 | AAACAAAATGGTCTA[A/G]ATATTATACCCCTCC | 7251 |
rs533327856 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18513606 | TCCCCAGAGCTACTC[A/G]CTTCTTTATGGCTTT | 7251 |
rs533538601 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18500648 | TAAGAAATGTCTATT[C/T]ATGTTCTTTGCCCAC | 7251 |
rs533598726 | snp | G/T | 0.000424481 | 0.0145623 | intron-variant | TSG101 | GRCh38.p7 | 11:18502438 | TTTTCACAACAGGGA[G/T]TTAGACTTTGCTTAT | 7251 |
rs533614147 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18507523 | AGGTTAAAACCCAGC[A/T]AGCTTAAAGAATACT | 7251 |
rs533620479 | snp | A/C | | | intron-variant | TSG101 | GRCh38.p7 | 11:18503451 | GATCTCAGCTCACTG[A/C]AAGCTCCACTTCCTG | 7251 |
rs533683319 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | TSG101 | GRCh38.p7 | 11:18487381 | TTGGTTTCCATTTTT[G/T]GCAGGGAGGGGAAAA | 7251 |
rs533707950 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18487434 | CACAACAAATTCAAA[A/G]GATTAGAAAAAATGT | 7251 |
rs533730272 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18509934 | TTGTTCTTCATTTGA[C/T]TCCACAGAACTAACA | 7251 |
rs533739865 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18501704 | AGACTGCTTTGGGTA[A/G]TATAGTCATTTTTAC | 7251 |
rs533745621 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18488035 | TTTTTCTTTTTTGCT[A/G]TACTATTTTCACAAC | 7251 |
rs533830181 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18495583 | GAAACTGATTAAGAT[A/G]GGTATAGTCAGTTTA | 7251 |
rs533897575 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18509227 | TTCAAGTTATATGTG[C/T]TTCCAAGCTGATCAA | 7251 |
rs533920376 | snp | G/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18495636 | GAAAAAGAATCTTTG[G/T]GTTAAGTTTCAATGC | 7251 |
rs533927840 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18516859 | GGCAGGAGAATTGCT[G/T]GAACCCAGGAGGCAG | 7251 |
rs533989975 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18518631 | CATTAAATAACATTT[C/T]CCTCATCTATAAAAT | 7251 |
rs534023435 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | TSG101 | GRCh38.p7 | 11:18480393 | CATTAATAAAAGCCA[G/T]TCTTTACCAAAAGAA | 7251 |
rs534088689 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18504350 | CTTGTCCTCAACTAA[A/G]TTTTATATATGACTT | 7251 |
rs534269518 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18523637 | CTTCCCGAGTAGCTG[C/G]GATTACAGGCGTGCG | 7251 |
rs534405220 | snp | A/C/T | 3.29453e-05 | 0.00405854 | missense | TSG101 | GRCh38.p7 | 11:18483952 | GTTCGTTTCAAGGCA[A/C/T]TGAGCTCTGCCTGGG | 7251 |
rs534424635 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18519791 | ATCAGTAAATATCTA[C/T]AGTCTCAAGTCATGT | 7251 |
rs534477913 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18499785 | TTTGTTACCTGCACG[A/G]AATGTAATGTTCAAG | 7251 |
rs534503801 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18486696 | TAGTTCAACCATTGT[A/G]GAAGTCAGTGTGGCG | 7251 |
rs534532846 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18503493 | TTCTCCTGCCACAGC[C/G]TCCTGAGTAGCTGGG | 7251 |
rs534675707 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18490832 | GCAACAGAGAGCAGA[C/T]TTCTCTCTTCGTTGG | 7251 |
rs534711060 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | TSG101 | GRCh38.p7 | 11:18520158 | CAATGTGATCTTTCA[C/T]GACTAAATTATTTCA | 7251 |
rs534775278 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18507487 | CAAACAAAACAAAAG[C/T]TTAGAAATACTAGGG | 7251 |
rs534787431 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18500790 | TTACTTTGTTGACTA[C/T]CTCCTTTGTTGTGCA | 7251 |
rs534797180 | in-del | -/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18515081 | ATACTCAATTAACTG[-/T]TTTTTTCCCTCTGTT | 7251 |
rs534863721 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18500231 | CCATTCATCTGCTGA[C/T]AAATATTTAGGTTCA | 7251 |
rs534985783 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TSG101 | GRCh38.p7 | 11:18485091 | AGCAAACTTCCTGAA[G/T]GGCCTTGTGAATTAC | 7251 |
rs535022948 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18485606 | AGGTAATTATTAAAA[C/T]TGTTTATAAATATAT | 7251 |
rs535229520 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18514523 | CCCATTTCTTTTAGT[C/T]AGCCTTTTCTAATTT | 7251 |
rs535269629 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18515221 | ATTCTATAGCAGTTA[C/T]AGAATAGTGTAAATA | 7251 |
rs535299374 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18528789 | GATCCTCCTGCCTCA[C/G]CCTCCCATGTATATT | 7251 |
rs535335259 | snp | C/T | 6.64231e-05 | 0.00576256 | missense | TSG101 | GRCh38.p7 | 11:18481866 | TGTTTTTATCAACCT[C/T]GGCCTGAAAACAGAA | 7251 |
rs535435084 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | TSG101 | GRCh38.p7 | 11:18505661 | CAGACTGATTTCATT[G/T]TTAATTTAATTTAGT | 7251 |
rs535448086 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18488994 | GTGGTGCGTGCCTGT[A/G]GTCCCAGCTACTTGG | 7251 |
rs535592213 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18511701 | AGTGGCTTTTATTAT[C/T]TCACGAAGCTATGCA | 7251 |
rs535643888 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18517846 | GTTATTTTACTTACT[A/G]TTGACGAATGTAAGC | 7251 |
rs535673831 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18511145 | GGCTAACCATCTTCA[C/T]AGAAACTACTTTTTA | 7251 |
rs535675359 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18483132 | TAGTAAGTCTCACAA[G/T]ATCTGATGGGTTTAT | 7251 |
rs535722035 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18501618 | TTGGTTCCATATACA[C/T]TTTATGATAGCTTTT | 7251 |
rs535759636 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18525073 | CCCGCCATCATGCCC[A/G]GCTAATTTTTGTATT | 7251 |
rs535887047 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18500948 | AGCTGGGATTACAGG[A/G]GTGTACCACCACGCC | 7251 |
rs536005857 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18494423 | GACAGGAAGCCAAAT[C/G]AATCAGCTTCTCCTA | 7251 |
rs536027440 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18499773 | ACCATGTGATATTTT[G/T]TTACCTGCACGGAAT | 7251 |
rs536117502 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18501604 | ATTTGGCTTCTTTTT[C/T]GGTTCCATATACATT | 7251 |
rs536119923 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TSG101 | GRCh38.p7 | 11:18493701 | CGAGAACATATGAGG[A/G]TTATTTTTCTTTCAT | 7251 |
rs536124493 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18498698 | TAGGTCAGAGACATA[A/T]ATTTGAGAACTGGGG | 7251 |
rs536176269 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18525249 | CTATCAATTTAAAGA[C/T]CAAAAATGTCATGGA | 7251 |
rs536234943 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18523534 | TTGAGATGGATTCTC[A/G]CTTTGTCACCCAGGC | 7251 |
rs536244990 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18495719 | CCTTCATTATTCACC[A/G]ACTACCACCTCCTCA | 7251 |
rs536359660 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18514491 | AGTATTCTGAAAATT[A/G]CAAAGCTCTACAGAA | 7251 |
rs536369381 | snp | C/T | 3.40426e-05 | 0.00412554 | missense, utr-variant-5-prime | TSG101 | GRCh38.p7 | 11:18516156 | CCCTGGAACTGCCAT[C/T]GTTAAAAACTGAAAG | 7251 |
rs536397568 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18510409 | CTAGGCGACAGAGCA[A/G]GACTCTGTCTCAAAA | 7251 |
rs536695592 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18492590 | CCAAGACTTTCCAGC[C/T]AAAGTCATTAACCCT | 7251 |
rs536736315 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18482369 | TGGTGTCACTTTCCT[A/G]AATTCTAAAAATTGG | 7251 |
rs536807993 | snp | A/G | 9.26055e-05 | 0.00680398 | missense | TSG101 | GRCh38.p7 | 11:18502561 | CACCAGGTGGGTAAG[A/G]ACAGCCTGGGTAACC | 7251 |
rs536891862 | snp | C/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18482456 | ACAAATCACTTTCCA[C/G]AAAGCCCTCAACCTT | 7251 |
rs536959086 | snp | C/T | | | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18527410 | ATGATTTTTTTTAAG[C/T]TTAAAGACCTTCATA | 7251 |
rs537002372 | in-del | -/ATAAAATAAAATAAA | | | intron-variant | TSG101 | GRCh38.p7 | 11:18496496 | ATAAAATAAAATAAA[-/ATAAAATAAAATAAA]TCTACAGAGTGAAAC | 7251 |
rs537138294 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18490770 | TTCTGCTCAATGCTG[A/G]AGAAGACATGCCAGG | 7251 |
rs537193710 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18506262 | TGACAGTGATCTCAA[C/T]TGGTTTTTGATCTTG | 7251 |
rs537206137 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18513030 | ACCCCACCCAGCCTC[A/T]AGGACAGATTTTTAT | 7251 |
rs537224997 | snp | C/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18518538 | AAAACTCCAAGCGTT[C/G]TCTTGCCTTACAACT | 7251 |
rs537273387 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18513888 | GAGAACAGCCTCACC[A/G]ACATGGTGAAACCCC | 7251 |
rs537407025 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18491431 | AGACCCAAGGCTCAG[A/G]TGAGCTACCTTGGTG | 7251 |
rs537487561 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18505634 | TATCATTGACTTTCT[A/G]GCGTGTGTTAACAGA | 7251 |
rs537491729 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18496219 | CTGTAATCCCAGCAC[C/T]TTGGGAGGCCGAGGC | 7251 |
rs537541451 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18510414 | CGACAGAGCAAGACT[C/T]TGTCTCAAAACAAAC | 7251 |
rs537737670 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18485006 | TGCAGTCGCATGATC[C/T]CGGCTCACTGCAACC | 7251 |
rs537743930 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18527992 | TATTGTTTTTCTTTT[C/T]CTTTTTCTTTTTTTT | 7251 |
rs537889119 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18504506 | TTTTGTTTCTAGTCT[C/T]TTCAGTAATCCATGC | 7251 |
rs537895146 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18487496 | AAAACACCTTAACAC[A/C]AGGAAGAAAAAACAT | 7251 |
rs537917105 | snp | C/T | 5.51902e-05 | 0.00525281 | missense | TSG101 | GRCh38.p7 | 11:18502489 | AAGGGTACTTACCAA[C/T]AGTGGTCACAGGAGG | 7251 |
rs537972887 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18517809 | TCACTACAAAATGCA[C/T]GACTGTACATTCTTG | 7251 |
rs538067411 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18525024 | CAAGCGATTCTCCCA[C/T]CTCAGCCTCCCGAGT | 7251 |
rs538127769 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18497010 | GCAGTAGAACTGCTT[C/G]AACCTGAGAGGTGGA | 7251 |
rs538288505 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18514437 | GAATCCTGCCTATTT[C/T]AAAAAGGTTCAACTA | 7251 |
rs538569883 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18500264 | CCATATCTTAGCTAG[C/T]ATGAATACTGTTGCT | 7251 |
rs538692527 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18515602 | CAGGCTCTGTGCCAC[A/G]TCCTTTACATTCATT | 7251 |
rs538803338 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18491975 | GGACAGAATTTAGAC[C/T]GAATAAAAATCTCTA | 7251 |
rs538876859 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18493656 | TAATCCCACACAGTA[C/G]CTTACTGACCATCTA | 7251 |
rs539060992 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18515151 | CACTTCCTCTGTGAT[C/T]TTCCCATGTGGCCTT | 7251 |
rs539109983 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18485841 | GCTGAGGCAGATGGG[A/G]TGGGTCCCCGGTGAA | 7251 |
rs539148208 | in-del | -/TCAC | | | downstream-variant-500B | LDHAL6A, TSG101 | GRCh38.p7 | 11:18479895 | AACTTGGCTACAGAA[-/TCAC]TCACCATGAAGACGA | 7251 |
rs539150249 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18511091 | GTACTTCATTCATAA[A/G]TTCACTGAGTTCTGA | 7251 |
rs539188980 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TSG101 | GRCh38.p7 | 11:18509357 | ACCTACAAATGGAAG[C/T]CCAAATGCCAGTCTT | 7251 |
rs539280176 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18509983 | ACTGTACAATGTATT[A/T]TAAGTATACTGGTAC | 7251 |
rs539324029 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18525822 | TTATTTGGTCTTCAA[G/T]CAAGAACTATGGGGG | 7251 |
rs539356147 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | TSG101 | GRCh38.p7 | 11:18498535 | GGATGACTCCAAAGA[A/G]TATAGAGTAGGTAAC | 7251 |
rs539390178 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18489868 | TACAATGGAATTGTA[A/T]TTCAATGATTCTGGT | 7251 |
rs539412472 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18481458 | TCAGACCAATCCTCA[A/G]TACTCTGTAGGTAAA | 7251 |
rs539449163 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18482238 | AATGGGCACCTGCCA[C/T]AGGAGAGTAACTTTC | 7251 |
rs539496794 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18490834 | AACAGAGAGCAGATT[C/T]CTCTCTTCGTTGGAG | 7251 |
rs539568384 | in-del | -/TC | 0.00795532 | 0.062565 | intron-variant | TSG101 | GRCh38.p7 | 11:18516372 | TTTTTTTTTTCAGAG[-/TC]TCATCCTGTTGCCCA | 7251 |
rs539638637 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18511782 | CCCTGTACTCATTAG[C/T]AGTCACTTCCCGTTT | 7251 |
rs539654574 | snp | A/T | 0 | 0 | intron-variant | TSG101 | GRCh38.p7 | 11:18484881 | GACTTTTAATTATGT[A/T]TGATTATAAAATACT | 7251 |
rs539677004 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TSG101 | GRCh38.p7 | 11:18512273 | TAGCCAGGTGTGGTG[A/G]TGGGCGCCTGTAATC | 7251 |
rs539804206 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18493974 | ACACTCAGAAAAATG[C/T]GCTTTACTTGAGCTC | 7251 |
rs539860792 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18506646 | AGTGAGCCGAGATTG[C/T]GCCACTGTACTCCAG | 7251 |
rs539871763 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TSG101 | GRCh38.p7 | 11:18499538 | GCCTCAGCTTCTTGA[A/G]TAGCTAGGATTACAG | 7251 |
rs539960712 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18493013 | GAAATTTGAATATTC[A/T]CTATACCTGCTATAA | 7251 |
rs539963480 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18506187 | GTTTCTTTCAATCTA[C/T]AGAAAAGCAGCTCCT | 7251 |
rs539973651 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | TSG101 | GRCh38.p7 | 11:18501032 | AGGCTGGTCTTGAAC[G/T]CCTCACCTCAAATGA | 7251 |
rs540023147 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18514973 | CATTCCTATTTCCCC[A/C]AGCAGAATTTATTTC | 7251 |
rs540024211 | snp | A/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18505193 | AAGAAGACTTAGTAG[A/T]GTTAAATTTTCCTTG | 7251 |
rs540034940 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18522959 | CAGTGGTGTGATCAC[A/C]GCTCACTGCAACCTC | 7251 |
rs540085448 | in-del | -/A | 0.268724 | 0.249298 | intron-variant | TSG101 | GRCh38.p7 | 11:18497550 | AATCATCTAAGCTAT[-/A]AAAAAAATGCTTCGT | 7251 |
rs540112449 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TSG101 | GRCh38.p7 | 11:18491344 | GCTCAACCTCTGGAG[A/G]AGCTGGAGACTAAAG | 7251 |
rs540119464 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18486548 | GCCATCAGAGAAATG[A/C]AAATCAAAACCACAA | 7251 |
rs540270614 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18500067 | ACCTCCAAGAGATCA[A/G]GTTTTTTGGCTCCCA | 7251 |
rs540280946 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | TSG101 | GRCh38.p7 | 11:18520478 | AATCCTCCTGCCTCA[C/G]GCTCCCAAAGTGTTG | 7251 |
rs540298388 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18515910 | TTCATATATCTTGGT[A/G]AGGAAGTTTTAAGAA | 7251 |
rs540337051 | snp | C/T | 9.89283e-05 | 0.00703238 | synonymous-codon | TSG101 | GRCh38.p7 | 11:18509570 | CGTTGCCTGGTATGG[C/T]GGATAGGATGCCGAA | 7251 |
rs540425274 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18516258 | TAAAATTCATCATTA[A/T]CCTTGAAAGGGGCTG | 7251 |
rs540483942 | in-del | -/AAAG | 0.0023933 | 0.0345097 | intron-variant | TSG101 | GRCh38.p7 | 11:18508832 | GTTAATTATAATCTT[-/AAAG]AAAATTTACCAAAAA | 7251 |
rs540538492 | snp | C/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18514229 | AAAGCCTTCCAACAG[C/G]TGTTGTTTGTATTTT | 7251 |
rs540594083 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18495855 | CGTGAACCTGGAGGG[C/T]GGAGCTTGCAGTGAG | 7251 |
rs540624027 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18512555 | TCTATTGTCTTTTTT[C/T]CCTCTTGGTTCTCTT | 7251 |
rs540698875 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18518931 | CTACAGACAACACTT[G/T]GGGAAATGGACTAAA | 7251 |
rs540701846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18498300 | CACTTGAAGGTTTTG[A/G]GCAGAGGAGTGATAC | 7251 |
rs540789971 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18487728 | AACCTCAAAGTATAG[A/G]AATCTGCTATAATTC | 7251 |
rs540996156 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | TSG101 | GRCh38.p7 | 11:18501988 | AGGTAGTGGGAGATA[C/G]GCATAGGTGAAGGCT | 7251 |
rs541053927 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18506419 | ATACATAGGCTGGGC[A/C]TGGTGGCTCACACCT | 7251 |
rs541057665 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18485034 | ACCTCTGCCTCCTGA[A/G]TTCAAGCGATTCTCC | 7251 |
rs541125760 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18526963 | TTCCGCTTCCACTAC[A/G]TCACTTCCGGGCCGC | 7251 |
rs541172063 | snp | A/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18515213 | ATTTTATAATTCTAT[A/T]GCAGTTACAGAATAG | 7251 |
rs541295426 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18511654 | ATATAATTCACATCC[C/T]ATAAACTTTCTCCTT | 7251 |
rs541337125 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TSG101 | GRCh38.p7 | 11:18499080 | TTTAAGAGAAAAACG[A/G]AGAAGAGGTACTGAA | 7251 |
rs541340890 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18483535 | TTTTGCCTCCCACCA[C/T]GATTCTGAGGTCTCC | 7251 |
rs541371624 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18505326 | CAGTGGTGCAATTAC[A/G]GCTCATTGCATCCTC | 7251 |
rs541520444 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18484282 | ATTACTATTAATCCA[C/T]GTTAAACCCAGTTTC | 7251 |
rs541625001 | snp | C/T | | | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18528632 | CTTGACCTCAGGTGA[C/T]CCACCCGCCTCAGCC | 7251 |
rs541691217 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18503594 | AGCCAGGATGGTCTC[A/C]ATCTCCTGACCTCGT | 7251 |
rs541715027 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18513578 | GTCCTGGGATCACAG[C/T]CATGAGCCACCATCC | 7251 |
rs541779517 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | TSG101 | GRCh38.p7 | 11:18497103 | CAAAAACAACAACAA[A/C]AAAAAAAACAAGGAT | 7251 |
rs541831529 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18523888 | CTTGAACTCCTGGGC[C/T]TAAGTGATCCTCCTG | 7251 |
rs541918180 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18492947 | GTGGAAGATTCTCAT[C/T]TACTTTGTGAACACT | 7251 |
rs541941128 | snp | A/C | 0.163892 | 0.234703 | intron-variant | TSG101 | GRCh38.p7 | 11:18496500 | AATAAAATAAAATAA[A/C]ATAAAATAAATCTAC | 7251 |
rs542004602 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TSG101 | GRCh38.p7 | 11:18518301 | TTGCTTCCCACCTCT[C/T]TTCACCAGTTTCCTA | 7251 |
rs542117457 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TSG101 | GRCh38.p7 | 11:18510250 | ACATGGCAAAATCCC[A/G]TCTCTACTAAAAACA | 7251 |
rs542154663 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18517221 | GGGTCTAAGTTGTCC[A/G]GGCTGGACTTGAACT | 7251 |
rs542160255 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | TSG101 | GRCh38.p7 | 11:18506225 | ATTTTTATTTTAAAG[-/A]GGAAAGAAATGGGTT | 7251 |
rs542173261 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18492286 | GTCTATAATTAAGCA[A/T]TCAATCACATGCAAC | 7251 |
rs542180081 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TSG101 | GRCh38.p7 | 11:18496391 | AGATTACAGTGAGCC[A/G]AGATCATGCCACTGC | 7251 |
rs542206755 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18525267 | AAAATGTCATGGAGG[A/C]CAGGTGTGGTGGCTC | 7251 |
rs542330410 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18500016 | TCCCACCCACACACC[A/G]TTCTTAAGTCTCTGG | 7251 |
rs542377833 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18482531 | ATAAATTCTCCCTCA[A/T]GGGGATGAAAATGGA | 7251 |
rs542394458 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18526282 | ATTTCACCTGGGGCA[G/T]TAAGGGACTGGTATT | 7251 |
rs542398044 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18521454 | GCTCACTTCAGCCTC[A/G]ACCTCCTGGACTCAA | 7251 |
rs542467694 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18494329 | TGAATCAGAATCAAA[A/C/G]TAATTCCATTAAAAT | 7251 |
rs542497583 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TSG101 | GRCh38.p7 | 11:18521731 | ACCCAGGCTGGAGTG[C/T]GGTGGTGTGATCTCA | 7251 |
rs542683518 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18509439 | TCCACTAGCTTGATA[A/C]ACTAAAAAGCAAAGA | 7251 |
rs542723300 | snp | C/G | 0.000798403 | 0.0199641 | synonymous-codon | TSG101 | GRCh38.p7 | 11:18514783 | AACAAAACAGATAGG[C/G]GGATTATATGGGTAT | 7251 |
rs542824056 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | TSG101 | GRCh38.p7 | 11:18497975 | ACATAACAGAAAAAT[-/A]AAACTTCACAAGATT | 7251 |
rs542846980 | in-del | -/CAGT | | | intron-variant | TSG101 | GRCh38.p7 | 11:18512683 | CCTGTGGCAGGCAGA[-/CAGT]CAGGATCAGGGACTG | 7251 |
rs542887303 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18485218 | AAGTTTAATGCTCTC[A/G]AACATCAGATCCCAT | 7251 |
rs542967561 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18501986 | GCAGGTAGTGGGAGA[C/T]AGGCATAGGTGAAGG | 7251 |
rs543005724 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18508836 | ATTATAATCTTAAAG[A/G]AAATTTACCAAAAAA | 7251 |
rs543039254 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18511247 | TTCAGTCTCCCAAGT[A/G]GTCAGGATTACAGGA | 7251 |
rs543078305 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18501205 | CTAGGCCAATGTCCC[A/G]AAGGGTTTCCCCTAT | 7251 |
rs543078945 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18525180 | TCCCAAAGTGCTAGG[A/G]TTACAGGCGTAAGCC | 7251 |
rs543172360 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18522350 | ATTTACTTCTCCAGT[G/T]TCTTCCATATGTGTA | 7251 |
rs543197894 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18494879 | AGTCAAGAAAAACTT[C/G]TCATGTTTACTAGCT | 7251 |
rs543288572 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TSG101 | GRCh38.p7 | 11:18500154 | TGTTGCTACAATGAC[A/G]TTTTCATTCTTTTTA | 7251 |
rs543294601 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18490363 | TCAGTGTATCCAATT[C/G]AGTAATTGCTTCATC | 7251 |
rs543311074 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18507043 | CAGTTAAAAAATCCA[A/G]ATCTCAGCACCAAAA | 7251 |
rs543394330 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18518771 | CAATATATTCTTGCT[C/T]GTCTCGGTGATACAC | 7251 |
rs543466048 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18511342 | AAAGAACCAAACTCA[C/T]CTCATTTGTTCAATT | 7251 |
rs543471630 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18505319 | TGGAGTACAGTGGTG[C/T]AATTACGGCTCATTG | 7251 |
rs543506105 | snp | C/T | 0.000230605 | 0.0107354 | missense | TSG101 | GRCh38.p7 | 11:18483886 | ACTTCTTGATCTAAA[C/T]GGGTAACCATCTCTT | 7251 |
rs543597392 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18498265 | GAACTTTGGACTGAA[A/C]TCTGAGTGAAACAGG | 7251 |
rs543680427 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18498997 | ATCCATTGGATGTAA[C/T]CTCAAAAAGTTATTG | 7251 |
rs543758568 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | TSG101 | GRCh38.p7 | 11:18505787 | ATCTGAACCATTAAT[G/T]GATTCCTGCAATGTA | 7251 |
rs543761860 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18512797 | CAGTGGTGCGATCTC[A/G]GCTCACTGCAACCTC | 7251 |
rs543763192 | in-del | -/A | 0.377977 | 0.21476 | intron-variant | TSG101 | GRCh38.p7 | 11:18492765 | ATCGAACTACTTTGT[-/A]AAAAAAAAAAAAAGG | 7251 |
rs543766067 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18483481 | AGCCTGAGCGCAAGA[A/G]TGAAACTCTCAAAAA | 7251 |
rs543815401 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18526939 | AGGAAGTCGGCACCA[C/T]TACACCACTTCCGCT | 7251 |
rs543925378 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18526044 | ACATAACAAAAGCCA[C/T]TCCACTCTGGTGTGA | 7251 |
rs543949659 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18494745 | TGCACACAAGCAAGC[A/G]TGCACTAGTAAACCC | 7251 |
rs543985933 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18513416 | TCCTTTCACCTTAGC[C/T]TCCTGAGTAGCTGGG | 7251 |
rs544069421 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18516469 | CCTGCCTCAGCATCC[C/T]GAGTAGTTGGGATTA | 7251 |
rs544088438 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B | LDHAL6A, TSG101 | GRCh38.p7 | 11:18480019 | ACTCTGCTCCTTTTT[A/G]ATGAAAACACTTATG | 7251 |
rs544151902 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18495934 | GTCTCAAAAAAAAAA[A/C]AAAAGTACTCTACAG | 7251 |
rs544152033 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TSG101 | GRCh38.p7 | 11:18503518 | GCTGGGACTATAGGT[A/G]CCCGCCACCACACCC | 7251 |
rs544189420 | in-del | -/TT | | | intron-variant | TSG101 | GRCh38.p7 | 11:18484937 | CTTAATTGCCGCCTT[-/TT]TTTTTTTTTTTTTTT | 7251 |
rs544250997 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18497429 | GTACTCTTGAAAATG[C/T]AGAGTAAAATATTAG | 7251 |
rs544271656 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TSG101 | GRCh38.p7 | 11:18486026 | TGCCTTTTCCAATAC[C/T]ACCTATGGCCTGCCC | 7251 |
rs544313333 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18502734 | TATTCAAGTAAAGCT[C/T]TATGGAAATTGTATT | 7251 |
rs544374913 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18524661 | AGATATTGAGTCAAG[A/G]ACCAAAAGGCAGGTA | 7251 |
rs544378863 | snp | C/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18494272 | CATAAGCACAAAAGC[C/G]AATAAATCTGAAGGA | 7251 |
rs544390409 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18522491 | CCTTCAAAATACATC[C/T]GGAATCTCCACAGCT | 7251 |
rs544443449 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18480829 | CAGGGAAAGCATTAC[A/G]TTGCAGGATCTGGCT | 7251 |
rs544483134 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18522997 | TGGGCTCAAGTGATC[C/T]TCCCATCTCAGCCTC | 7251 |
rs544522225 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18523778 | AAGTGCTGAGATTAC[A/G]GGCATGAGCCATTGC | 7251 |
rs544555884 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18488633 | ACAGAGCTCTGGTGC[C/T]AGAAGTTCTTCTCAA | 7251 |
rs544602133 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18507029 | ACAGCAAAATTTCAC[A/G]GTTAAAAAATCCAAA | 7251 |
rs544631174 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18499173 | GGCAGGAAAAGTGGA[A/G]TAGAGAAGAGGATTC | 7251 |
rs544709795 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18510571 | AGATTTTCTCTCAAA[C/T]ACCTATTGAGCACTG | 7251 |
rs544711281 | snp | C/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18521020 | TGGGTGACAGAGCTA[C/G]ACTCCGTCTTGGAAA | 7251 |
rs544784980 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18527436 | TCATACTATACGTTG[A/G]CAAGGGTAAAGTGTA | 7251 |
rs544923622 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18485136 | TACCTGTTAGATGAT[A/C]CTGCTTTTTACCAAA | 7251 |
rs545023838 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18499943 | AAACATTAGAACTTA[C/T]TCCTTCTATCTAACT | 7251 |
rs545065392 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18528239 | ACCAGGAGTCCCTTT[A/G]ATTAGAGCAACTGTA | 7251 |
rs545067862 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18521945 | AGCCTCCCACAGTGT[C/T]GGGATTACAGGCATG | 7251 |
rs545311100 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18491957 | TTAGCTGTTCAGTCA[C/T]CTGGACAGAATTTAG | 7251 |
rs545406207 | snp | A/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18511024 | TTCAAAATGGCTTAT[A/T]TGATTATTCTTCTTT | 7251 |
rs545445703 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TSG101 | GRCh38.p7 | 11:18507797 | ACTCAAAGAAATTTA[A/G]GAAAAAAAAAATGTT | 7251 |
rs545458163 | snp | A/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18486874 | GAACCAACCCAAATG[A/T]CCAACAATGATAGAC | 7251 |
rs545465717 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18517410 | ACATAGTTTGTATTG[G/T]ACAGCTATTATTTCT | 7251 |
rs545501748 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18512548 | TCCCGTTTCTATTGT[C/T]TTTTTTTCCTCTTGG | 7251 |
rs545565846 | snp | A/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18480831 | GGGAAAGCATTACAT[A/T]GCAGGATCTGGCTCA | 7251 |
rs545569941 | in-del | -/A | 0.0248432 | 0.108648 | intron-variant | TSG101 | GRCh38.p7 | 11:18506689 | GCAAGACTCCATCTC[-/A]AAAAAAAATAAATAA | 7251 |
rs545570848 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18501055 | TCAAATGATTCGCCC[G/T]CCTTGGCTTCCCAAA | 7251 |
rs545624897 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18524437 | ACCTTCACCCTAGCT[A/T]TGTGTTCAGGGTCCT | 7251 |
rs545705242 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18503508 | CTCCTGAGTAGCTGG[G/T]ACTATAGGTGCCCGC | 7251 |
rs545713781 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | TSG101 | GRCh38.p7 | 11:18504544 | CTGTAAAGAAATGTC[A/C]ATCCTACTGAAATTT | 7251 |
rs545714707 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18497175 | ATAACAGCCCAAATC[G/T]TGACCATTGATATAC | 7251 |
rs545840664 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18482625 | GGGCTGACTTACACA[C/T]GGACTGTCCAAGGCA | 7251 |
rs546019608 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18504982 | TCTAATCTCTGCTTA[C/T]CTATCCAAAGTGACA | 7251 |
rs546050809 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18517995 | CATGAAACTATACAA[C/G]ACTTTATAATGGAGT | 7251 |
rs546056453 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18505753 | TAAGTAAATATCATG[C/T]GACAAGTTTGACCCC | 7251 |
rs546092639 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18510794 | GTACATGGTGGCATG[C/T]GCCTGTGGTCACAAC | 7251 |
rs546127685 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18511222 | GACTTGAACTCAACA[A/G]TCTTCCTGCTTCAGT | 7251 |
rs546183285 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18519100 | CTGCCTCCTGGACTG[C/T]CTCCTGGACTCAAGC | 7251 |
rs546303744 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18498122 | CAGCAAATTGGTAAG[C/G]ATAGGCCTGGCTGAT | 7251 |
rs546349890 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18498846 | TGCAGAGGAGACTAA[A/G]TATGAATACCCATGA | 7251 |
rs546369505 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18520014 | CACCATAATCAACTT[C/G]AGAACATTTTCACCA | 7251 |
rs546481671 | snp | C/G/T | 0.000399281 | 0.0141238 | utr-variant-5-prime | TSG101 | GRCh38.p7 | 11:18526882 | TGGGCTGCCCCAGAC[C/G/T]GTCCCACACAATCGC | 7251 |
rs546545786 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TSG101 | GRCh38.p7 | 11:18512449 | TGTCCTCTATTTTCT[C/T]GAATGCACTGATCAC | 7251 |
rs546660051 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18509003 | ATAATATATTCCAAT[G/T]AGGGGAGAAGCAACA | 7251 |
rs546670793 | snp | C/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18491722 | AGTGTCAGAAGTGCA[C/G]GTGGTTTTGTGAACT | 7251 |
rs546684437 | snp | A/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18524897 | TATGAATATACATAC[A/T]TTAAGGAATAAATCT | 7251 |
rs546733552 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18494569 | ATTATTGCTTTGGCA[A/G]AAAAGGATTTAACAT | 7251 |
rs546843426 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18513058 | TATAAGGCTCATTCT[A/G]CCTCTAAGTTCTCCC | 7251 |
rs546859483 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18523197 | CCATGTCAAGCACAC[A/G]GTTTCTTTACCTCTC | 7251 |
rs547044098 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18500834 | TTTGAGACAAGGTCT[C/T]GCTCTGTTGCCCAGG | 7251 |
rs547053061 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18486260 | CGGGTAAGCCAGACT[C/T]GGCCCAAGTGGGCCG | 7251 |
rs547082781 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18493529 | CCTCACCCTTAATCA[A/G]CAAAAGTAAACTACC | 7251 |
rs547151505 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18504152 | GCTACAGTAGCTGAG[A/T]TTATGCCACTGCACT | 7251 |
rs547284243 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18485764 | CAGTGCTGAAAAGTC[A/G]TTAATAGAGTAAAAT | 7251 |
rs547449618 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18489701 | GTCATGAACTTTTGA[A/G]TGGCAACAGCCCAAA | 7251 |
rs547476968 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18505406 | GACTACAGGTTCACA[C/T]CACCATGCCTGGCTA | 7251 |
rs547794149 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18512912 | TTTATATTTTTAGTA[A/G]AAATGGGATTTCACC | 7251 |
rs547870724 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18519402 | ACAGTTTTATTAGGC[A/G]GTGGTGCAATCCCAC | 7251 |
rs547957822 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18512263 | ATACAAAAATTAGCC[A/G]GGTGTGGTGGTGGGC | 7251 |
rs547975105 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18495432 | ACCACTGCTGAGACT[A/G]GAGTAAGGAATCACC | 7251 |
rs548015713 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TSG101 | GRCh38.p7 | 11:18487267 | TAAAGTATAATAAAA[A/G]AAAAAAAGAAAAAAA | 7251 |
rs548015800 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18496076 | GAAGTGTCACTGAGT[A/G]GAACACCATTCTCTT | 7251 |
rs548081765 | snp | A/G | 0.00159405 | 0.0281866 | intron-variant | TSG101 | GRCh38.p7 | 11:18499354 | TGTATATTTATATAT[A/G]TTTATATATAAATAT | 7251 |
rs548090851 | in-del | -/T | 0.0894459 | 0.191631 | intron-variant | TSG101 | GRCh38.p7 | 11:18495466 | CCTTTTAACTTCCTC[-/T]TTTTTTTACCAGGGG | 7251 |
rs548156330 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18509177 | TACAACACTGATTTT[A/G]TAGTTGCAAAGAGAA | 7251 |
rs548198918 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18524074 | TGGGATTACAGGCAT[A/G]AGCCACCACACCAGG | 7251 |
rs548222255 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18497804 | CATTTCATTATATTG[C/T]AGTTACATTAATGAC | 7251 |
rs548246404 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | TSG101 | GRCh38.p7 | 11:18480379 | GAGGATAGAAAGTGC[A/G]TTAATAAAAGCCAGT | 7251 |
rs548352518 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18523148 | GATCCTCTAGCTTCC[A/G]CCTCCCAAAATGTTT | 7251 |
rs548354365 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18515154 | TTCCTCTGTGATCTT[C/T]CCATGTGGCCTTGTT | 7251 |
rs548355708 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18510871 | AGGCTGCAGTATGAC[A/T]GCGCCACTGCACTCC | 7251 |
rs548464231 | in-del | -/AA | 0.00755907 | 0.0610114 | intron-variant | TSG101 | GRCh38.p7 | 11:18497103 | AAAAACAACAACAAC[-/AA]AAAAAAAACAAGGAT | 7251 |
rs548710574 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18489638 | CCACAAAGAATTTAA[A/G]TTTCAGGATTCGAGT | 7251 |
rs548746825 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TSG101 | GRCh38.p7 | 11:18484632 | AAAGAATGACATCCA[A/C]AAAATTCAACAGCTG | 7251 |
rs549036962 | snp | C/T | 1.66713e-05 | 0.0028871 | synonymous-codon | TSG101 | GRCh38.p7 | 11:18514711 | ATAAGGAAGATATAT[C/T]TTCCCATTTGCATCA | 7251 |
rs549079787 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | TSG101 | GRCh38.p7 | 11:18518684 | GTTTCGCAAAATGTG[-/T]TCCTGAAAATATAAA | 7251 |
rs549265894 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18486119 | CTTTGGGTAGGGGAA[C/T]CACCCCTGCATCCCC | 7251 |
rs549339186 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18508632 | TAATCCTAAAATCAA[A/G]CTTATTCTGGGAAGG | 7251 |
rs549384486 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18507863 | AGCACTTTGGGAGGC[C/T]GAGGCAGATCACTTG | 7251 |
rs549427750 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18507409 | TATACAAAACTTACA[C/T]TATCCAGACTGTTAA | 7251 |
rs549430744 | snp | A/C/G | 0.00159649 | 0.0282165 | intron-variant | TSG101 | GRCh38.p7 | 11:18493418 | AGAGTATTTACAAAC[A/C/G]ATCACTACTTCCTGG | 7251 |
rs549446112 | snp | C/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18489100 | AGCCTGACAACACAG[C/G]AAGACTCCATCTCAA | 7251 |
rs549507084 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TSG101 | GRCh38.p7 | 11:18500186 | GGCTGAACAGTATTC[C/T]ACTGTGTACACATAC | 7251 |
rs549550403 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18481592 | AGTGCCTCTACAACC[C/T]AAGTTAAAAAATCTT | 7251 |
rs549575904 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18510337 | GAGGCAAGAGAATTG[C/T]TTAAACCCCAGAGGC | 7251 |
rs549670677 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18485590 | GCTGCAATGTAGAAG[A/G]AGGTAATTATTAAAA | 7251 |
rs549794191 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18503952 | ATCACACCTGTAATC[C/G]TAGCACTTTGGGAGG | 7251 |
rs549850574 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18510827 | CTCAGGAGGCTGCAG[C/T]GGGAGGATCACCTGA | 7251 |
rs549906613 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18503105 | TGTCATTCATGTATT[C/T]GTATCAAAGTCAGAG | 7251 |
rs549932740 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18505904 | CTCACTGCAACCTCT[A/G]CCTCCTGGGTTCAAG | 7251 |
rs549977011 | snp | C/T | | | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18527289 | TCTGTCACTGACTTG[C/T]TCTTGTGATAATGGT | 7251 |
rs549990717 | snp | A/T | 0.0142736 | 0.0832652 | intron-variant | TSG101 | GRCh38.p7 | 11:18499211 | AATATATATATATAA[A/T]ATATATATATTTATA | 7251 |
rs549992625 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18490788 | AAGACATGCCAGGAA[A/G]GCAGCGGGCACCAAC | 7251 |
rs550038349 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18501088 | GCTGGGATTACAGAC[A/G]TGAGCCACTGCATCT | 7251 |
rs550098219 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18506555 | AATTAGCCGGGAATG[C/G]TGGCACAGCCTGTAG | 7251 |
rs550145994 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18503859 | TTTAGCTATAATTAT[C/T]AATTCTATGACATTT | 7251 |
rs550185318 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18519295 | AGAAATGAGCCACCA[C/G]ATCCAGGTACAGTAT | 7251 |
rs550293610 | snp | A/C/G/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18491296 | AACAGTGTGATTTAT[A/C/G/T]GGGGGGTCTGGGCCA | 7251 |
rs550346321 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18518419 | AATGGACAAGCAGCA[G/T]CATGGGTTTTCCCTC | 7251 |
rs550346566 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18526635 | GCGCCTCGGGGCGGG[G/T]TTCTGAGGAGGTCGC | 7251 |
rs550354340 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18501486 | GTTTCTGTTTTTATA[C/G]CAATACCATGCTGTT | 7251 |
rs550355804 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18525041 | TCAGCCTCCCGAGTA[A/G]GCTGGGATTACAGGC | 7251 |
rs550367637 | snp | G/T | | | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18528219 | GTTCTTAAAGCCACG[G/T]CTTAACCAGGAGTCC | 7251 |
rs550391029 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18502249 | TGTTTGGCTCACAAA[C/T]AAAACTATGTGATCA | 7251 |
rs550414924 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18512179 | GGAGGCTGAGGCGGA[C/T]GGATCACCTGAAGTC | 7251 |
rs550453564 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18505998 | AATTTTGTATTTTTA[G/T]TAGAGATGGGGTTTC | 7251 |
rs550462805 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18509072 | CATGAATTGGCTGTA[C/T]GAAAGAGAAGAAAGC | 7251 |
rs550496389 | snp | C/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18494793 | TGGGTGCCATATCCT[C/G]AAAGTACAGTTTCTG | 7251 |
rs550563772 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | TSG101 | GRCh38.p7 | 11:18515059 | TATACTTGCTTTATA[C/G]AATGCTGATACTCAA | 7251 |
rs550633329 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18520687 | CCTTTAGTATAGTTT[C/T]ATAGATATATGTTTC | 7251 |
rs550655446 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18487198 | AGCACAACAACATGG[A/C]ACATGTATACATATG | 7251 |
rs550671617 | in-del | -/TTTC | 0.00398564 | 0.0444627 | intron-variant | TSG101 | GRCh38.p7 | 11:18509465 | AAAGAAGTCATTATT[-/TTTC]TTTATTTTTTTACAA | 7251 |
rs550722246 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18526373 | AGAAAGGCTAAGACT[A/G]GAGGATCCCTAGATT | 7251 |
rs550725078 | in-del | -/C | 0.0023933 | 0.0345097 | intron-variant | TSG101 | GRCh38.p7 | 11:18482818 | GTCCTTTTAAGTCTG[-/C]TCCTAAGATGTGCAG | 7251 |
rs550739407 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18509799 | ATCATGAAAATTTCA[A/T]TTAATTAATTTATTT | 7251 |
rs550813818 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18495332 | TATATGTTAAAGGCC[G/T]AAAGCCTAGGATTCA | 7251 |
rs550818430 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18488465 | TGAGAGTTGAGCTGG[A/G]TAAGTGCACTTGGGA | 7251 |
rs550834347 | snp | C/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18481180 | TTAAGCTTGAGACAA[C/G]TTTCATACAAGAGGG | 7251 |
rs550873239 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18516759 | CTAGCCTGACCAACA[C/T]GGAGAAACCCCATCT | 7251 |
rs550925551 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18492255 | TTCTCCCATAGATTA[C/T]GTACCTAAATGATAT | 7251 |
rs551081546 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18514418 | AATGCACTTCCCACT[A/G]TGTGAATCCTGCCTA | 7251 |
rs551128882 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18491056 | CTCTGGCAGCGGTGG[C/T]GGTGCCTGCCGTGGC | 7251 |
rs551215432 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18526699 | GAAGCTTGCTTGGCT[A/G]GGCCGGGACGGACTC | 7251 |
rs551301593 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18526993 | CCGTCCTGCGGGCAA[G/T]GGTGGACACCGTGTG | 7251 |
rs551470418 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18498413 | AATCTTGTGGAAGGC[C/T]TTTGAAGTAAATTAG | 7251 |
rs551529954 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18520469 | ACCTCAAGCAATCCT[C/T]CTGCCTCAGGCTCCC | 7251 |
rs551589816 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TSG101 | GRCh38.p7 | 11:18513699 | TTTTCAGCCCTCTGA[C/G]ACTGCTAGAGACTCT | 7251 |
rs551640071 | snp | A/T | 0.000531133 | 0.0162876 | intron-variant | TSG101 | GRCh38.p7 | 11:18516058 | CATATTTATTATGTA[A/T]TCAAAATGCATCTAT | 7251 |
rs551727994 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18485385 | TAATAACCTATTTTC[C/T]GAAGGAAAGGTCTCT | 7251 |
rs551787979 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18507324 | CTTTTATAACTATGT[G/T]GGCCAATTAGCACAG | 7251 |
rs551826569 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18500148 | CATCCATGTTGCTAC[A/C]ATGACGTTTTCATTC | 7251 |
rs551904396 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | TSG101 | GRCh38.p7 | 11:18488111 | TTAGGCAGAATACTG[C/G]TTAAGGAAAAACAAA | 7251 |
rs551913636 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18502984 | GGGGATATTTAACCC[A/G]AAAACACTTGTCTTT | 7251 |
rs551921240 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18481096 | TTATCCCTAAAACCA[C/T]GTTCTCCATGACCCA | 7251 |
rs551964355 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18487427 | GGTCTCTCACAACAA[A/G]TTCAAAGGATTAGAA | 7251 |
rs551990459 | snp | C/T | 0.00398564 | 0.0444627 | utr-variant-3-prime | TSG101 | GRCh38.p7 | 11:18480461 | TTGAATGATAAACTG[C/T]AATAACTTATTCTGG | 7251 |
rs552065525 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18492555 | CAAATGCTACCATAA[C/T]ACCACCAAATAAGTC | 7251 |
rs552114558 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18482002 | AGAATAATGTTTCAA[A/G]TAACACCCTGGTCAA | 7251 |
rs552145390 | snp | A/C | | | intron-variant | TSG101 | GRCh38.p7 | 11:18498481 | GATCAGATTCTAGAT[A/C]TATTTTGAAGACAAG | 7251 |
rs552193139 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18510278 | ACACAAAAATTAGCC[A/G]GGTGTGGTGATGTGC | 7251 |
rs552269247 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18517759 | CACTCAATGATGAAA[C/T]TGCCAAATAATGCAT | 7251 |
rs552345358 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18512172 | CACTTTGGGAGGCTG[A/G]GGCGGACGGATCACC | 7251 |
rs552346597 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18496606 | GCACGGGTGGATCAC[C/T]TGAATCTAGGAGTTC | 7251 |
rs552380424 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TSG101 | GRCh38.p7 | 11:18505935 | CAATTCTCCTACCTC[A/G]GCCTCCCAAAGAGCT | 7251 |
rs552432739 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18524816 | TGGCAGGTTTCTCTA[C/G]GGAAGCTTAGGAAAC | 7251 |
rs552510427 | in-del | -/T | | | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18527574 | TTTTACCTGGTGCTG[-/T]TATTTGTGTACCTGT | 7251 |
rs552529980 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18513191 | GACTGCTGAAAACTT[G/T]GCTGATTTTCAGAGG | 7251 |
rs552536614 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18526681 | GGCTTCCGGCCCGTC[G/T]GGGAAGCTTGCTTGG | 7251 |
rs552691998 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18512576 | TGGTTCTCTTTCTTG[A/G]TGTACTTGATAAATA | 7251 |
rs552749706 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18527135 | AAACTCTGGTTCAGG[A/T]TAAGATTAGCAGGTA | 7251 |
rs552971839 | snp | C/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18492298 | GCATTCAATCACATG[C/G]AACAGTGGTGGTATT | 7251 |
rs553107604 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18528865 | TTTGTAAAGATGAGG[A/T]CTTACTTTGTTGCCC | 7251 |
rs553129553 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18513847 | TAGAAGGCCGAGATG[A/G]GTGGATCACTTGAGG | 7251 |
rs553152622 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18520798 | AGCATTTTGGGAGGC[C/T]GAGGCAGGCGGATCA | 7251 |
rs553191932 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18491843 | CTTCAAATGAGGCCA[C/T]ATAAAAAGGCAACAC | 7251 |
rs553201268 | in-del | -/AT | 0.0023933 | 0.0345097 | intron-variant | TSG101 | GRCh38.p7 | 11:18507608 | AAGAGGCTAATCAAC[-/AT]AGAGGAAGAAAAAGA | 7251 |
rs553217207 | snp | C/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18510734 | TGTAATCCAGCTTGA[C/G]CTCAGGAGTTTGAGA | 7251 |
rs553234931 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18499845 | AGTATTTATCATTTC[C/T]ATGTGGTAGGAACAT | 7251 |
rs553349531 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18521339 | CAAGCTGATTCAGCA[A/G]TATTTGACCAAACTG | 7251 |
rs553403652 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18485627 | ATAAATATATGAGCG[C/T]TCTCCAAAATAAATG | 7251 |
rs553461849 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18528095 | CCGCCTCTGTTTTTC[A/G]GCTCCTTAGTTAAGC | 7251 |
rs553476738 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18507994 | AGCGACTTGGGAGGC[C/T]GAGGCTCGAGAATCA | 7251 |
rs553516072 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TSG101 | GRCh38.p7 | 11:18485125 | GGTCTTCTAATTACC[C/T]GTTAGATGATCCTGC | 7251 |
rs553579709 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18508403 | TTTCATCATGTTGGC[C/T]AAGCTGGTCTTGAAC | 7251 |
rs553712006 | in-del | -/T | 0.499396 | 0.0173617 | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18527999 | TTCTTTTTCTTTTTC[-/T]TTTTTTTTTTTTTTT | 7251 |
rs553746232 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18514545 | TTCTAATTTACCCTC[A/C]ACTCAGTGATTAGTC | 7251 |
rs553764244 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18481342 | ACCAATGGAAATCTG[A/G]TCGTACCTCCTGATC | 7251 |
rs553801178 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18489029 | CTGAGACAGGAGAAT[C/T]GCTGGAACCCGGGAG | 7251 |
rs553945192 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18483175 | CTTTTGCTTCCTCCT[C/T]ATTTCCTCTTGCCAC | 7251 |
rs554018616 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18490215 | TGACATTGAACAGAT[C/T]ACAAAGCACAAGAAA | 7251 |
rs554030397 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18511175 | ACACCCCTCCTCCCC[A/C]CAGACAAGGTCTTGC | 7251 |
rs554055324 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18482548 | GGGATGAAAATGGAG[A/C]GTGAAATTGGCACTT | 7251 |
rs554055475 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18490826 | TTGTAGGCAACAGAG[A/G]GCAGATTTCTCTCTT | 7251 |
rs554195977 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18499824 | TTTAGGGTATCCATC[A/G]CCTTGAGTATTTATC | 7251 |
rs554251371 | snp | G/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18491600 | TAATCTGTATCTTTT[G/T]CCATAAGTCATAACT | 7251 |
rs554254953 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18500960 | AGGGGTGTACCACCA[A/C]GCCCAGATTTTTGCA | 7251 |
rs554275077 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18498777 | GAGTGAGGATAGAGA[A/G]TGCCAAGGAGACTAA | 7251 |
rs554362451 | snp | A/C/G | 0.000798403 | 0.0199641 | utr-variant-5-prime | TSG101 | GRCh38.p7 | 11:18526870 | GTCAGCCGCTGCTGG[A/C/G]CTGCCCCAGACCGTC | 7251 |
rs554413011 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18525946 | CCATTCTTGCTTTGA[C/T]AAAACTATCCCAAGC | 7251 |
rs554417068 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18493858 | AGTCCTTTTTATTTA[C/T]AGTGTATGAATATGT | 7251 |
rs554449954 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18494446 | TTCTCCTACCTTTCC[C/T]TTACTAACAAAATAA | 7251 |
rs554451817 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18485951 | GAGAACTTCTATTCC[G/T]GTTTGCCCACCCTTT | 7251 |
rs554485270 | in-del | -/ATA | | | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18528375 | TATATATATATATAT[-/ATA]TTTTTTTTTTTTTTT | 7251 |
rs554606191 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18521732 | CCCAGGCTGGAGTGC[A/G]GTGGTGTGATCTCAG | 7251 |
rs554637928 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18522831 | GCATGACAAACTTCT[C/G]TCTATGAGTCTTTGC | 7251 |
rs554982070 | in-del | -/TAAAT | 0.00279162 | 0.0372561 | intron-variant | TSG101 | GRCh38.p7 | 11:18520162 | GTGATCTTTCATGAC[-/TAAAT]TATTTCACTTAGCAT | 7251 |
rs555066489 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B | LDHAL6A, TSG101 | GRCh38.p7 | 11:18479828 | AGAACATTCTATTCT[C/G]GATGAGCTCTGCAGG | 7251 |
rs555072483 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18489516 | ATTATTGAAGCACAA[A/G]TTGCAAATTGGTAAC | 7251 |
rs555075746 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TSG101 | GRCh38.p7 | 11:18518874 | GCTCAAGCTTAACTA[C/T]AGAATTCTGCCTCTA | 7251 |
rs555078037 | snp | A/C | 0.0263992 | 0.111815 | missense, utr-variant-5-prime | TSG101 | GRCh38.p7 | 11:18526809 | AGCTGGCTCTCCGAC[A/C]CCGCCATGACGGCCG | 7251 |
rs555131718 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18503281 | TAAATTTGCATTTTG[A/G]AAGACACTCAACTAT | 7251 |
rs555254188 | snp | A/T | 1.64838e-05 | 0.00287083 | synonymous-codon | TSG101 | GRCh38.p7 | 11:18506874 | GGGATTGGGAGGGTA[A/T]CCGGATGGGTATGGA | 7251 |
rs555287518 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18510413 | GCGACAGAGCAAGAC[A/T]CTGTCTCAAAACAAA | 7251 |
rs555290513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18518754 | CTTTAGGATGTATTA[C/T]ACAATATATTCTTGC | 7251 |
rs555359826 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18509364 | AATGGAAGCCCAAAT[A/G]CCAGTCTTTGGTGGG | 7251 |
rs555421966 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TSG101 | GRCh38.p7 | 11:18500942 | CCAAGTAGCTGGGAT[C/T]ACAGGGGTGTACCAC | 7251 |
rs555583738 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18499043 | TTTAGCAAAATGGTA[C/T]GAGAAAAAGTCCAAA | 7251 |
rs555599388 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18512479 | CAACCATTTTTAAGT[C/T]TGTGTCTGATAACCA | 7251 |
rs555728694 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18484277 | AAGAGATTACTATTA[A/G]TCCATGTTAAACCCA | 7251 |
rs555878232 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18487518 | AAAAAACATTAGATC[C/G]TTTCTGTAACCATTA | 7251 |
rs555916899 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B | LDHAL6A, TSG101 | GRCh38.p7 | 11:18480047 | ATGGTTCAGTGAGGC[C/G]TAGAAAGGAAACAAA | 7251 |
rs555971842 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18528571 | AATTTTTTGTATTTT[C/T]AGTAGAGACAGGATT | 7251 |
rs556016528 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18513909 | GTGAAACCCCACCTC[A/T]ACTAAATACTAAAAT | 7251 |
rs556109070 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18516982 | TCAAACAATACCATA[C/T]TAAATGTTAACCTAC | 7251 |
rs556127098 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18521305 | CTTTGTCTTACTTCA[C/T]CTGTCAGCAGTATTT | 7251 |
rs556344037 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18510577 | TCTCTCAAATACCTA[C/T]TGAGCACTGGCCAGG | 7251 |
rs556410696 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18497033 | GAGGTGGAGGTTGCA[A/G]TGAGCCAAGATCGCG | 7251 |
rs556439464 | snp | A/G | 2.26063e-05 | 0.00336194 | utr-variant-3-prime | TSG101 | GRCh38.p7 | 11:18480516 | AGAATACTTTAAGAA[A/G]AGCTCAACCTCCAGC | 7251 |
rs556448247 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18497857 | ACCACACCACTGGAA[C/T]CTGAATAGTGTGTAT | 7251 |
rs556490422 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18496167 | ATTCAGATTACACCA[C/T]AAAATTAAAATCCAG | 7251 |
rs556532519 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18524237 | ACTAATCTGGTATAA[A/T]TATATCTGTTAATTG | 7251 |
rs556580737 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18517813 | TACAAAATGCACGAC[A/T]GTACATTCTTGACCT | 7251 |
rs556586158 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18489297 | GTTATTTCACAGGTG[A/C]AACCACAGGGCACTG | 7251 |
rs556590825 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TSG101 | GRCh38.p7 | 11:18499447 | ATGGAGTCCCACTCT[A/G]TTGCCCAGGCTGGAG | 7251 |
rs556748225 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18482391 | AAAAATTGGCTACTT[C/G/T]GAGGCTCATTTTACA | 7251 |
rs556803121 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18500272 | TAGCTAGTATGAATA[C/T]TGTTGCTATAAATAT | 7251 |
rs556868022 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18493668 | GTAGCTTACTGACCA[A/T]CTATTTAGAAACTAG | 7251 |
rs556906574 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18485878 | CCTTCAAGCCAAAAA[C/T]AGCCTGAAGGCTGAA | 7251 |
rs556960300 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18522653 | CTGAAACACAGCAAC[A/G]GCTTTTCATCATACT | 7251 |
rs557227673 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18492833 | GAAAAACCCAGAGTT[C/T]TTCAAAGAAGTAAAA | 7251 |
rs557265284 | snp | A/C | | | intron-variant | TSG101 | GRCh38.p7 | 11:18489084 | CATGCCACTGCACTC[A/C]AGCCTGACAACACAG | 7251 |
rs557400367 | snp | C/G/T | 0.000399281 | 0.0141238 | downstream-variant-500B | LDHAL6A, TSG101 | GRCh38.p7 | 11:18479911 | CACTCACCATGAAGA[C/G/T]GAAACTTTAAATGAC | 7251 |
rs557474771 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18514055 | GTGCCACTGCCCTCC[A/G]GCCTGGGCAACAGAG | 7251 |
rs557539547 | snp | A/C | | | intron-variant | TSG101 | GRCh38.p7 | 11:18511099 | TTCATAAGTTCACTG[A/C]GTTCTGAAGAATTAC | 7251 |
rs557545244 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18482555 | AAATGGAGCGTGAAA[C/T]TGGCACTTCAATTAT | 7251 |
rs557573001 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18501958 | GTAACAGGGAGAAGG[A/C]AGATATGGTGGTGCA | 7251 |
rs557594283 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18525177 | GCCTCCCAAAGTGCT[A/G]GGATTACAGGCGTAA | 7251 |
rs557607314 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18516580 | CGAACTCCTAACCTC[A/G]TTATCCACCTGCCTT | 7251 |
rs557618944 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18498553 | TAGAGTAGGTAACAA[C/T]GGAGATGGGGCAGGT | 7251 |
rs557749852 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18526024 | TTTTGGAAAATTACA[A/G]CAAAACATAACAAAA | 7251 |
rs557759391 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18483428 | TTGAACCTGGAGGGT[A/G]GAGGTTGCAGTGAGC | 7251 |
rs557835620 | in-del | -/AATAAAGT | 0.0115144 | 0.0749975 | intron-variant | TSG101 | GRCh38.p7 | 11:18519837 | TTGAATCAGGATCCA[-/AATAAAGT]AATAAAGTCCACACA | 7251 |
rs557893519 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18491412 | AAGTCCTGATAAAAA[C/T]TCTAGACCCAAGGCT | 7251 |
rs557939554 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18498124 | GCAAATTGGTAAGGA[C/T]AGGCCTGGCTGATCC | 7251 |
rs558124733 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TSG101 | GRCh38.p7 | 11:18490851 | TCTCTTCGTTGGAGT[A/G]TTCATGCCTCGTTCT | 7251 |
rs558237201 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18498971 | GGACAAGTAAGATGA[G/T]AATAGTAACTATCCA | 7251 |
rs558259066 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18494694 | GTTATTCCCAAAGGA[A/G]GTCTGTGAAAGGTGT | 7251 |
rs558281305 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B | LDHAL6A, TSG101 | GRCh38.p7 | 11:18479944 | TAAAAGCAGGGAGGC[A/C]ATGGTACACTATCTT | 7251 |
rs558396743 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18527940 | AAGCATCATTATAAA[C/T]TGTTGCTAACACGCA | 7251 |
rs558442475 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | TSG101 | GRCh38.p7 | 11:18487462 | TGTAAAATGCAATAT[A/C]ATTTGAGAAAACTTT | 7251 |
rs558456192 | snp | A/C | | | intron-variant | TSG101 | GRCh38.p7 | 11:18501948 | CCAACTTATGGTAAC[A/C]GGGAGAAGGCAGATA | 7251 |
rs558488414 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime | TSG101 | GRCh38.p7 | 11:18526883 | GGGCTGCCCCAGACC[A/G]TCCCACACAATCGCA | 7251 |
rs558515559 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18527307 | TTGTGATAATGGTAG[C/G]CTAGTGCATTTCTAG | 7251 |
rs558526788 | snp | C/T | | | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18527973 | AATAAAGGCTATTAA[C/T]AGGTATTGTTTTTCT | 7251 |
rs558551047 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TSG101 | GRCh38.p7 | 11:18495615 | GTTTTGCTCCTACAG[C/T]AACAGGAAAAAGAAT | 7251 |
rs558584711 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18501050 | TCACCTCAAATGATT[C/T]GCCCGCCTTGGCTTC | 7251 |
rs558594180 | snp | A/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18521134 | AGCACAATATATCTG[A/T]GTATCTCTGTGATAT | 7251 |
rs558595809 | snp | C/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18493535 | CCTTAATCAGCAAAA[C/G]TAAACTACCTGCCCA | 7251 |
rs558655148 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18495718 | TCCTTCATTATTCAC[C/T]GACTACCACCTCCTC | 7251 |
rs558733441 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18516456 | TTCAAGCGATTCTCC[C/T]GCCTCAGCATCCCGA | 7251 |
rs558789187 | snp | A/C/G/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18503500 | GCCACAGCCTCCTGA[A/C/G/T]TAGCTGGGACTATAG | 7251 |
rs558964048 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TSG101 | GRCh38.p7 | 11:18524162 | AAACTATGTAAAAAT[A/G]TAAGTGGCTGTATGT | 7251 |
rs558987656 | snp | A/C | 0.188946 | 0.24243 | intron-variant | TSG101 | GRCh38.p7 | 11:18496475 | AATAAAATAAAATAA[A/C]ATAAAATAAAATAAA | 7251 |
rs559051317 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18516885 | GGCAGAGGTTGCAGT[C/G]AGCCGAGACTGTGCC | 7251 |
rs559096063 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18496969 | GGTGGTACGCTCCTC[C/T]AATCCCAGCTACTTG | 7251 |
rs559276792 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TSG101 | GRCh38.p7 | 11:18498315 | AGCAGAGGAGTGATA[C/T]AATTTATTTATATTT | 7251 |
rs559351120 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18499128 | CTTCAAGGAGTTATT[C/T]AGAGAAGAATGAAGA | 7251 |
rs559361674 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | TSG101 | GRCh38.p7 | 11:18506405 | TTAAAAAAAAAAAAA[-/T]ACATAGGCTGGGCAT | 7251 |
rs559401155 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18502935 | GGGAAAATGATACTA[C/T]TTAATTTGTACCTGT | 7251 |
rs559502048 | snp | G/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18526972 | CACTACGTCACTTCC[G/T]GGCCGCCGTCCTGCG | 7251 |
rs559521433 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | TSG101 | GRCh38.p7 | 11:18502057 | AGTTGAAGAAAATTA[-/T]ATTTCAGGTAACGCT | 7251 |
rs559576999 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18515576 | CTTTTAACTGTCTGC[C/T]TATTATATTCCAGGC | 7251 |
rs559652153 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18490558 | ACACAGTGGTTTGTT[C/T]GTTGTCTCCAGATGC | 7251 |
rs559921000 | snp | A/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18503210 | CCCTGACAAATGGTC[A/T]TCTTTCTCTATTTAA | 7251 |
rs560063953 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18485083 | AGCTGGGAAGCAAAC[C/T]TCCTGAAGGGCCTTG | 7251 |
rs560131776 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18523496 | CAATCTTTATTTTAT[C/T]ATTTTTATTTATTTA | 7251 |
rs560207499 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18516520 | TGACTAATTTTTTGT[A/G]TCTTTAGTAGAGATG | 7251 |
rs560224593 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18523889 | TTGAACTCCTGGGCT[G/T]AAGTGATCCTCCTGC | 7251 |
rs560227549 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18502828 | CACCCTCATAGCAGC[A/G]GAAATGTAACTAGAG | 7251 |
rs560332329 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18511436 | TGATATCTACTTTTC[C/T]AATATTTTTCTTGTG | 7251 |
rs560413024 | in-del | -/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18506388 | TATAATACTCTCTTC[-/T]TTTAAAAAAAAAAAA | 7251 |
rs560429963 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18497104 | AAAAACAACAACAAC[A/C]AAAAAAACAAGGATA | 7251 |
rs560442010 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18510258 | AAATCCCATCTCTAC[C/T]AAAAACACAAAAATT | 7251 |
rs560443379 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18518334 | GTTTTCAAAGCCTTG[C/G]AAGCAAATGAAATTT | 7251 |
rs560475878 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18510687 | ATAATTTTAAAAATT[C/G]TAGGTCTATTCCAGT | 7251 |
rs560599971 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18496506 | ATAAAATAAAATAAA[A/C]TAAATCTACAGAGTG | 7251 |
rs560611894 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18500034 | CTTAAGTCTCTGGTG[C/T]CTATCATTCTACTGT | 7251 |
rs560649807 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18526346 | AGGCCACACTCTCTG[A/C]GGGTCGGCAAAAGAA | 7251 |
rs560695982 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18492296 | AAGCATTCAATCACA[C/T]GCAACAGTGGTGGTA | 7251 |
rs560723842 | in-del | -/ACAC | | | intron-variant | TSG101 | GRCh38.p7 | 11:18494479 | ATCATTTGTTAACTT[-/ACAC]AATAGCTTTTTTAAA | 7251 |
rs560858042 | in-del | -/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18487870 | AGCTTTTGGTAGATC[-/T]TTTTTTTTTGTATTT | 7251 |
rs560946458 | in-del | -/TCGG | 0.00358779 | 0.0422022 | intron-variant | TSG101 | GRCh38.p7 | 11:18516658 | ATTTAAAAATCACCA[-/TCGG]CCAGGCGCGGTGGTT | 7251 |
rs560996814 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TSG101 | GRCh38.p7 | 11:18485221 | TTTAATGCTCTCGAA[C/T]ATCAGATCCCATCTT | 7251 |
rs561149318 | snp | A/C | | | intron-variant | TSG101 | GRCh38.p7 | 11:18514204 | GTCTTGATTGCCTAA[A/C]CAGCTTTCCAAAGCC | 7251 |
rs561204948 | snp | G/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18484796 | TTCTAATATAAGTTT[G/T]GGTATTCTTTATGAC | 7251 |
rs561259412 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TSG101 | GRCh38.p7 | 11:18508856 | TTACCAAAAAAAAAA[A/G]AGTCACAGCTCAAAA | 7251 |
rs561329926 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18523247 | TTTTTTCAGAAAGAC[C/T]TCTCTTTACTATCAG | 7251 |
rs561405819 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TSG101 | GRCh38.p7 | 11:18511006 | CTGTGCTAGACAAAG[C/T]TGTTCAAAATGGCTT | 7251 |
rs561442416 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18518195 | GAAATAAGGTAGGCT[C/G]AGATGAGAAGGAATC | 7251 |
rs561453713 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18486840 | TTATTGCAGCACTGT[A/T]CACAATAGCAAAGAC | 7251 |
rs561663696 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18512966 | CTTCTGGCCTCAAGT[A/G]ATCCTCCCGCCTCAG | 7251 |
rs561674384 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18484200 | GAAAGAAAAAAATTA[C/T]GTTACCAGTTTCATG | 7251 |
rs561791279 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18505823 | AAGATAGGTTGTGGG[A/G]TTTTGTTTGTTTGAG | 7251 |
rs561847751 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18490378 | CAGTAATTGCTTCAT[C/G]AAATACTGTTTTTGC | 7251 |
rs561853531 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18511260 | GTAGTCAGGATTACA[G/T]GATTAGGATTGGCAC | 7251 |
rs562007131 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18498267 | ACTTTGGACTGAACT[C/G]TGAGTGAAACAGGAA | 7251 |
rs562031544 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18526957 | CACCACTTCCGCTTC[C/T]ACTACGTCACTTCCG | 7251 |
rs562049838 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18483565 | CCCAGCCATGTGGAA[C/T]TGTAAGTCCAATTAA | 7251 |
rs562134363 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18490903 | GCCATATCATCATAG[C/T]GCTCAGCCTGCTCAG | 7251 |
rs562167439 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18507187 | AAGTTCTCAAGAAGT[C/T]TATTACCTAAGAGCA | 7251 |
rs562177501 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18504825 | CAATTGTTCAGTAGC[C/T]TTGTAATTTCAAGGC | 7251 |
rs562182474 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TSG101 | GRCh38.p7 | 11:18482796 | TTGGAAACAATAAAA[C/T]AGTACTGTCCTTTTA | 7251 |
rs562276394 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TSG101 | GRCh38.p7 | 11:18513483 | AAATATTTTTTTATA[A/G]AGATGGGGTTCTCAC | 7251 |
rs562362283 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18520807 | GGAGGCCGAGGCAGG[C/T]GGATCACGAGGTCAG | 7251 |
rs562399479 | in-del | -/GTT | 0.0023933 | 0.0345097 | downstream-variant-500B | LDHAL6A, TSG101 | GRCh38.p7 | 11:18479975 | CCCTTTAATCCTAAA[-/GTT]GTTATCAGGTATATA | 7251 |
rs562401374 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18512838 | GTTCAAGCGATTCTC[C/T]TGCCTCAGCCTCCGG | 7251 |
rs562412305 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18486056 | CTTCCCCTATTCTGA[A/G]CCTGTAAGAAGCCGC | 7251 |
rs562477812 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18523057 | ACGCCTGGCTAATTT[C/T]TTTATATTTTTAGTA | 7251 |
rs562540702 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18494790 | CCTTGGGTGCCATAT[A/C]CTGAAAGTACAGTTT | 7251 |
rs562610313 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18486770 | ATCCCATTACTGGGT[A/T]TATACCCAAAGGATT | 7251 |
rs562639966 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18516022 | GAAAGTAGGTTTAAT[A/T]TGGTTATAACTCTTT | 7251 |
rs562686230 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18495984 | ATTCTGGCACAAGCA[C/T]AGCTGACAGTACATC | 7251 |
rs562686325 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18503526 | TATAGGTGCCCGCCA[A/C]CACACCCGGCTAATT | 7251 |
rs562723869 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18487957 | TTTTCCTGATTATTC[A/T]GTGTAAGGTGAAACT | 7251 |
rs562726835 | in-del | -/A | 0.411578 | 0.190768 | intron-variant | TSG101 | GRCh38.p7 | 11:18526137 | CTTTTTTAAAAATTG[-/A]AAAAAAAAAACACTA | 7251 |
rs562727129 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18510165 | GTGGTTCACACCTGT[A/C]ATCCCAGCACTTTGG | 7251 |
rs562768569 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18523791 | ACAGGCATGAGCCAT[C/T]GCACCTGGCCAATTT | 7251 |
rs562838141 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18516489 | AGTTGGGATTACAGG[C/T]ACGTGCCACCACACC | 7251 |
rs562895177 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18523652 | GGATTACAGGCGTGC[A/G]CCACCATGTCTGGCT | 7251 |
rs563003135 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18506502 | TTGAGACCAGCCTGG[C/T]CAACATGGTGAAATC | 7251 |
rs563083866 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18507046 | TTAAAAAATCCAAAT[C/T]TCAGCACCAAAACAA | 7251 |
rs563089139 | snp | A/T | 0.0154538 | 0.0865337 | intron-variant | TSG101 | GRCh38.p7 | 11:18499194 | AAGAGGATTCTTTTT[A/T]AAATATATATATATA | 7251 |
rs563237417 | in-del | -/CT | | | intron-variant | TSG101 | GRCh38.p7 | 11:18521670 | GCACCTGGCCCCTTC[-/CT]TTTTTTTTTTTTTTT | 7251 |
rs563243903 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18494286 | CCAATAAATCTGAAG[A/G]AGAGTTAAAATTCTA | 7251 |
rs563275044 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TSG101 | GRCh38.p7 | 11:18491083 | TGGCTGCAGCGACGG[C/T]AGCAGCAGCTCCTGT | 7251 |
rs563298939 | in-del | -/A | 0.324731 | 0.238569 | intron-variant | TSG101 | GRCh38.p7 | 11:18508094 | CGAGACTCTGTCTCA[-/A]AAAAAAAAAAAAAGT | 7251 |
rs563403648 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TSG101 | GRCh38.p7 | 11:18492104 | ATGATATGATGACTA[C/T]TGAAGATTTCATTAA | 7251 |
rs563441765 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TSG101 | GRCh38.p7 | 11:18484507 | TAGAGGCCAGTGAGA[A/G]GACTGAGAATGGGCA | 7251 |
rs563490529 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18485156 | TTTTTACCAAAACCA[C/T]CAACAAACTCTGTCA | 7251 |
rs563567439 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18483754 | ATTCAAATGTTTAAA[A/G]ATGCCTATAATTTTC | 7251 |
rs563613141 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18512604 | ATATAAATTGTATGC[C/T]AGACATTGTGAAAAA | 7251 |
rs563692886 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TSG101 | GRCh38.p7 | 11:18507819 | AAAAATGTTGCAGGC[C/T]GGCCGCGGTGGCTCA | 7251 |
rs563712747 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18494111 | ATTTACATAAAAATT[A/C]AAGTTTTCAAAAGTG | 7251 |
rs563758187 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18481214 | GAAAGGGCAGCCTGA[C/T]ACTTTGATGTGGGAA | 7251 |
rs563868959 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18506309 | TTTGTATATCTAGTA[C/T]AGATAGCTGAAATAT | 7251 |
rs563931231 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18500715 | TACCTTGTATATTTA[C/T]TAGTTCCTTGTCAGA | 7251 |
rs563967340 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18508557 | GTCAACAGAATTTAA[A/T]AAGATAAAAACAAAT | 7251 |
rs563985497 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | TSG101 | GRCh38.p7 | 11:18521492 | TCCCACCACCGCCTC[C/T]CAAGTAGCTGGGACT | 7251 |
rs564020993 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18503534 | CCCGCCACCACACCC[A/G]GCTAATTTTTTGTAT | 7251 |
rs564053217 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18493096 | CTGACCTTTTTACTC[A/G]AGCAGAGTCAGATTT | 7251 |
rs564131243 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18482669 | TGAGAAAGCTTAAAG[A/G]GCTGAAGGTTGCATA | 7251 |
rs564234303 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18517422 | TTGGACAGCTATTAT[G/T]TCTAACAATAATTTG | 7251 |
rs564246044 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18482014 | CAAATAACACCCTGG[G/T]CAAAGGTAGAGGAAA | 7251 |
rs564265411 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18496639 | GGCCAGCCTGGGCAA[C/T]ACAAAAATTAGCCGG | 7251 |
rs564360864 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18505964 | CTGGGATTACAGGCA[C/T]GTGCCACCATGCCTG | 7251 |
rs564413972 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18505085 | TCAAGATCCTAGATA[C/T]TATATATGTACATAT | 7251 |
rs564427109 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18490310 | CACTGTCCCAAGTAA[C/T]TGCATGATCAGAGTG | 7251 |
rs564484647 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | TSG101 | GRCh38.p7 | 11:18526508 | ACTCAGTGGAAGAGA[A/G]GAGGGCGGGTGGGCG | 7251 |
rs564528659 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18486008 | TTTTAACCAATCAAA[C/T]GTTGCCTTTTCCAAT | 7251 |
rs564546749 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18512655 | ATCTTCTTCCAGCAA[C/G]GGTTCACCCTATCCT | 7251 |
rs564641185 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18485343 | GAATCTGCTCTCTCT[C/T]AACAGTTATCACTAT | 7251 |
rs564793005 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18493052 | AGAAGAGTTTTTGGC[A/T]AACTGCCATACCCCA | 7251 |
rs564835678 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18512175 | TTTGGGAGGCTGAGG[C/T]GGACGGATCACCTGA | 7251 |
rs564954600 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18494735 | CACCCAAACCTGCAC[A/G]CAAGCAAGCGTGCAC | 7251 |
rs564975514 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18522271 | CAATTTGACATTTCC[C/T]TTGGATATCTAATAA | 7251 |
rs565021350 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18522266 | ATTACCAATTTGACA[C/T]TTCCCTTGGATATCT | 7251 |
rs565077435 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TSG101 | GRCh38.p7 | 11:18525477 | CTTGAACCTGGGAGG[C/T]GGAGATTGCAGTGAG | 7251 |
rs565079770 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18502054 | TTTAGTTGAAGAAAA[G/T]TATATTTCAGGTAAC | 7251 |
rs565212545 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18522962 | TGGTGTGATCACAGC[A/T]CACTGCAACCTCAAA | 7251 |
rs565221666 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18514277 | ATTTTTCATAGGAAC[A/G]TTAATCTGTCACAGT | 7251 |
rs565349325 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TSG101 | GRCh38.p7 | 11:18524037 | CTCAAGTGGATTCTC[C/T]CATCTCTACCTCCCA | 7251 |
rs565431962 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18508448 | GATCCACCCCCACCT[C/T]GGCCTCCCAAAGTGC | 7251 |
rs565469845 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | TSG101 | GRCh38.p7 | 11:18480207 | CTGTAGAATAATACT[A/G]AATTTCAACTTAAGA | 7251 |
rs565505968 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18480776 | GAATACCTCATTATA[C/T]GTGGCTTTTAAGCTG | 7251 |
rs565541016 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18495868 | GGCGGAGCTTGCAGT[A/G]AGCTGAGATTGCATC | 7251 |
rs565544093 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18487129 | TGTTGTGGGGTGGGG[A/G]GAGGGATAGCATTAG | 7251 |
rs565600989 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | TSG101 | GRCh38.p7 | 11:18492732 | GACTTCACTGTGAAG[C/T]ATATCTAAACTTTAA | 7251 |
rs565656619 | in-del | -/C | 0.00318978 | 0.0398085 | intron-variant | TSG101 | GRCh38.p7 | 11:18499655 | TGACCTCGCAATCTG[-/C]CCGCCTTGGCCTCCC | 7251 |
rs565700470 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18526653 | CTGAGGAGGTCGCTA[A/C]GGACTGCACCGGGGC | 7251 |
rs565720051 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TSG101 | GRCh38.p7 | 11:18496947 | AATATAAAAATTAGC[C/T]GGGTGTGGTGGTACG | 7251 |
rs565736818 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18519412 | TAGGCGGTGGTGCAA[C/T]CCCACAATTGAAAAA | 7251 |
rs565820029 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TSG101 | GRCh38.p7 | 11:18489030 | TGAGACAGGAGAATC[A/G]CTGGAACCCGGGAGG | 7251 |
rs565982025 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18482972 | TGATAAGGTTTGGCT[A/G]TGTCCCCACCCAAAT | 7251 |
rs565992389 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18510044 | CAATATTATTAAAGG[C/T]CATTAAAAGACATCA | 7251 |
rs566082827 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18498889 | ATAAAATGAGCATGG[G/T]GTTTTGGAAAACAAG | 7251 |
rs566097400 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18506695 | ACTCCATCTCAAAAA[A/C]AATAAATAAATAAAT | 7251 |
rs566167038 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18512264 | TACAAAAATTAGCCA[A/G]GTGTGGTGGTGGGCG | 7251 |
rs566207925 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18506132 | CCACACCCGGCCTTA[C/T]TGCTAGAATTTTAAG | 7251 |
rs566235808 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18501922 | TCAGCTTTAGATAGA[A/G]GCAAAGATAACCAAC | 7251 |
rs566293393 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18505081 | ACTTTCAAGATCCTA[A/G]ATATTATATATGTAC | 7251 |
rs566308909 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18496080 | TGTCACTGAGTGGAA[C/T]ACCATTCTCTTCTGG | 7251 |
rs566312043 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18527203 | GGGAAGAAGTACGAA[A/G]GGCTTGCCAGTGAGC | 7251 |
rs566475630 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18509198 | GCAAAGAGAAAGGAG[A/T]GGTCAGACTACCTTT | 7251 |
rs566479480 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18509854 | ATGATGTGCAGCAAG[G/T]TTCTTGCTTCAAGTA | 7251 |
rs566529284 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18516834 | TAATCCCAGCTACTC[A/G]GAAGGCTGAGGCAGG | 7251 |
rs566565047 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18515186 | TCCTCTGTAATCTCA[C/T]AGCACTTTTTCATTT | 7251 |
rs566603263 | snp | A/G | 0.000913533 | 0.0213526 | intron-variant | TSG101 | GRCh38.p7 | 11:18516168 | CATCGTTAAAAACTG[A/G]AAGGAAAGAACAATG | 7251 |
rs566709402 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18502429 | GAAATGTGCTTTTCA[C/T]AACAGGGAGTTAGAC | 7251 |
rs566811497 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18510439 | ACAAACAAACAAAAA[A/C]ATTATACGTAGATTC | 7251 |
rs566813175 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18517717 | CTAGGTGTGTAGTAG[G/T]ATATACCATCTAGGT | 7251 |
rs566822832 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18524078 | ATTACAGGCATGAGC[C/T]ACCACACCAGGCCCA | 7251 |
rs566848407 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18510872 | GGCTGCAGTATGACT[A/G]CGCCACTGCACTCCA | 7251 |
rs566929482 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18520660 | CACAGTTTGGAATGT[C/G]TTAATTGTATCCCTT | 7251 |
rs566984340 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18491192 | TACCCAGAGAGGCCA[A/C]GCCTTTGCCCTTGGC | 7251 |
rs567067329 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18481931 | ACTTGTCAGACACCT[A/G]CAACACTTCACAGGA | 7251 |
rs567117996 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18527034 | GGGCCTGGTGGGGTG[A/G]GTTCCAACCAACCCG | 7251 |
rs567214131 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18520999 | TCGTGCCCTTGCACT[C/T]CAGCCTGGGTGACAG | 7251 |
rs567222771 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18521437 | GCAGTGGTATGATCA[C/T]GGCTCACTTCAGCCT | 7251 |
rs567229710 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TSG101 | GRCh38.p7 | 11:18488573 | TTTTTTGATTCAGAT[C/T]CTGGTATGACTAAAG | 7251 |
rs567299163 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon | TSG101 | GRCh38.p7 | 11:18483951 | TGTTCGTTTCAAGGC[A/G]TTGAGCTCTGCCTGG | 7251 |
rs567687376 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18490821 | TGTTCTTGTAGGCAA[A/C]AGAGAGCAGATTTCT | 7251 |
rs567798750 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18492650 | CGCTTGGCCTATAAA[A/G]GTCACAGTTCACCTG | 7251 |
rs567839199 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18510597 | CACTGGCCAGGGGTG[A/G]TGGCTTACACCTGTA | 7251 |
rs567863982 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18522517 | CAGCTACAGTCCTGG[C/T]CTAAGCCACCAGCAC | 7251 |
rs568058620 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18510838 | GCAGCGGGAGGATCA[C/T]CTGAGCCAGGAAGGT | 7251 |
rs568086964 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18496812 | AAACAAGGATAGCGC[C/G]AGGTGTGGTGGCTCA | 7251 |
rs568159778 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18503118 | TTCGTATCAAAGTCA[C/G]AGGAACTTTCCTTAG | 7251 |
rs568229076 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18525060 | GGGATTACAGGCACC[C/T]GCCATCATGCCCGGC | 7251 |
rs568361541 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18502305 | ATTTATTTTCATGCC[C/T]TGGTAGAAGGTTCAT | 7251 |
rs568450647 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18498580 | AGGTGTTAGGAAGAT[A/T]GAGAATTCGGTTTTG | 7251 |
rs568517023 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18501243 | TCTAGTAGTTTTATA[A/G]CTTTGGGTCTTACAT | 7251 |
rs568569988 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18511656 | ATAATTCACATCCCA[A/T]AAACTTTCTCCTTTT | 7251 |
rs568574652 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18499572 | TGCGCCACCACGCCC[A/G]GCTAATTTTTTTGTA | 7251 |
rs568731081 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | TSG101 | GRCh38.p7 | 11:18502294 | GAGTTAATCAGATTT[A/C]TTTTCATGCCCTGGT | 7251 |
rs568771668 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18508225 | ATATTTGATATCTTT[C/T]TTTTTTTTTTTTTTG | 7251 |
rs568955480 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18523508 | TATTATTTTTATTTA[G/T]TTATTTGTTTTTGAG | 7251 |
rs569172041 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18494944 | CTTATTTTTCTTCAC[C/T]TTTTCCTTTCTTTAT | 7251 |
rs569189565 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18524052 | CCATCTCTACCTCCC[A/G]AAGTATTGGGATTAC | 7251 |
rs569324276 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18510020 | AGGGATGAATATGAG[C/G]AACAGTCACAATATT | 7251 |
rs569357571 | snp | A/G | 0.000179509 | 0.00947219 | intron-variant | TSG101 | GRCh38.p7 | 11:18526725 | GACTCGACAGGGCGC[A/G]GAAGGGAGCGGTGGG | 7251 |
rs569379589 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TSG101 | GRCh38.p7 | 11:18487212 | GCACATGTATACATA[C/T]GTAACTAACCTGCAT | 7251 |
rs569404332 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18516781 | ACCCCATCTCTACTA[A/G]AAATACAAAATTAGC | 7251 |
rs569531892 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18483082 | ACGCAGGGGTGGTAA[C/T]TGAATCATGGGAGCC | 7251 |
rs569812774 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18482322 | TCACAAAGTATCACA[C/T]GCAGGTGCTGGTTGT | 7251 |
rs569882301 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18517305 | AAAAAAGAAAAGTTC[A/G]TAGCCAAATATAAAC | 7251 |
rs569900920 | snp | G/T | | | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18527115 | CAAGACTGTTCCGAG[G/T]GTCGAAACTCTGGTT | 7251 |
rs569991954 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18513286 | AGGTGGGAAAATTCA[A/G]AGTATCTCATCTTTT | 7251 |
rs570084379 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18500153 | ATGTTGCTACAATGA[C/T]GTTTTCATTCTTTTT | 7251 |
rs570157863 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18506740 | AATAAACCAAGTTTT[A/G]TCTTCCACTAAATTG | 7251 |
rs570196577 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18499574 | CGCCACCACGCCCGG[C/T]TAATTTTTTTGTATT | 7251 |
rs570212264 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18492568 | AATACCACCAAATAA[A/G]TCCTTGCCAAGACTT | 7251 |
rs570219433 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18527945 | TCATTATAAACTGTT[A/G]CTAACACGCACAAAT | 7251 |
rs570236009 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | TSG101 | GRCh38.p7 | 11:18487546 | TTAAAATTTTTTTTC[A/T]AGTAGAGAGGTAGTC | 7251 |
rs570298549 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18484927 | GTATATTTAACCTTA[A/T]TTGCCGCCTTTTTTT | 7251 |
rs570310461 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18521171 | CCACTGATGCTCAAC[A/G]TCTAGAGACCTGGTC | 7251 |
rs570325253 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18505499 | GGCTCAAGCAATCCC[C/T]ACCTCGGCCTCCCAA | 7251 |
rs570373935 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18495630 | TAACAGGAAAAAGAA[A/T]CTTTGTGTTAAGTTT | 7251 |
rs570523002 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18510932 | AAAAACAAAAACAAA[A/T]CCCAACAACAACGAC | 7251 |
rs570532741 | in-del | -/T | 0.39527 | 0.203462 | intron-variant | TSG101 | GRCh38.p7 | 11:18500810 | TTGTTGTGCAGAAGC[-/T]TTTTTTTTTTTGAGA | 7251 |
rs570559187 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18509968 | ATTTATTTTATTGCC[A/G]CTGTACAATGTATTA | 7251 |
rs570580274 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18481134 | GCAGTAGCCAAACTT[C/T]GCTTACTAGATTTTC | 7251 |
rs570589186 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18510280 | ACAAAAATTAGCCGG[A/G]TGTGGTGATGTGCGT | 7251 |
rs570595360 | snp | A/T | 5.68629e-05 | 0.00533181 | intron-variant | TSG101 | GRCh38.p7 | 11:18502482 | AGTTTTCAAGGGTAC[A/T]TACCAACAGTGGTCA | 7251 |
rs570602574 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18524168 | TGTAAAAATATAAGT[A/G/T]GCTGTATGTATGAAA | 7251 |
rs570734158 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18497720 | ACCAAAATAAGAGAG[C/G]TTCACCAGATTTAGT | 7251 |
rs570767797 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18518384 | ATTCAGTTCCTTGCT[G/T]TCAGAGCTAAGGGAC | 7251 |
rs570799864 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18517797 | ACCATATCTCTATCA[C/T]TACAAAATGCACGAC | 7251 |
rs570912838 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18513808 | GGCTGGGCATGGTGG[C/T]TTATGCCTGTAATCC | 7251 |
rs570942854 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18524844 | AACTTAATTAGGGTA[C/G/T]AAAAAATAAGCTAAT | 7251 |
rs570975798 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18484811 | GGGTATTCTTTATGA[C/T]TATCAGTGTTCTTCA | 7251 |
rs571198507 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18507542 | TTAAAGAATACTTTA[C/T]ACATTCTTTAAAGAG | 7251 |
rs571236694 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18508150 | GAAAAGGTTACCTTT[G/T]TCATAGCGGTCACTC | 7251 |
rs571274404 | in-del | -/ATATATA | | | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18528369 | TATATATATATATAT[-/ATATATA]TATTTTTTTTTTTTT | 7251 |
rs571309053 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TSG101 | GRCh38.p7 | 11:18513832 | GTAATCCCAGCACTT[C/T]AGAAGGCCGAGATGG | 7251 |
rs571343446 | snp | C/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18481094 | TATTATCCCTAAAAC[C/G]ATGTTCTCCATGACC | 7251 |
rs571369292 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TSG101 | GRCh38.p7 | 11:18500861 | CAGGGTGGAGTGCAG[C/T]GGTGCGATCTCAGCT | 7251 |
rs571561159 | snp | C/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18515094 | CTGTTTTTTCCCTCT[C/G]TTTATTATGAATGGT | 7251 |
rs571590778 | snp | A/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18486048 | GGCCTGCCCTTCCCC[A/T]ATTCTGAGCCTGTAA | 7251 |
rs571606918 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18493632 | ACACAGCAAACTATG[G/T]AGCCCAAGTAATCCC | 7251 |
rs571670844 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18501373 | ATTTATGAACAATGT[C/G]TTTTTCCCAATATAT | 7251 |
rs571720733 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18515317 | TCTTTGTAGCCACAG[C/T]TCCTATCCTTATTGC | 7251 |
rs571786857 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18523299 | CATTTCCACACCCTA[A/G]CATTCCCCATTTCTT | 7251 |
rs571812460 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18485669 | TTAAACCAAATGAAA[G/T]AACTCATCAATATCT | 7251 |
rs572118675 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18517243 | ACTTGAACTCCTGGA[C/T]TCAAATGGTCTCCTG | 7251 |
rs572126200 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18490229 | TTACAAAGCACAAGA[A/C]ACATTACTTCTCTCC | 7251 |
rs572212441 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18480730 | GATGGGATCTAAGAA[C/T]CCTAACTCATGACCT | 7251 |
rs572272208 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18511757 | ATATTTTCATCATCC[A/G]AAAAAGAAACCCTGT | 7251 |
rs572359174 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18482558 | TGGAGCGTGAAATTG[A/G]CACTTCAATTATGCT | 7251 |
rs572448057 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18483242 | GCTCACTCCTGTAAT[A/C]CCAACACTTTGGGAG | 7251 |
rs572477198 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18498076 | GTTGAGTGTGTGGGT[A/G]GGGGGTTGGAGGGGG | 7251 |
rs572509665 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime | TSG101 | GRCh38.p7 | 11:18526875 | CCGCTGCTGGGCTGC[C/T]CCAGACCGTCCCACA | 7251 |
rs572519372 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18493938 | TCCAAAGAAATTAGG[A/G]GGCCTCAATTTATCT | 7251 |
rs572721097 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18526387 | TGGAGGATCCCTAGA[G/T]TGGGACAGGAGTAGA | 7251 |
rs572772830 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18499945 | ACATTAGAACTTATT[C/T]CTTCTATCTAACTGT | 7251 |
rs572865100 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18516408 | GGAGTGCAATGGCGC[A/G]ATTTTGGCTCGCTGC | 7251 |
rs572865417 | snp | C/T | 0.000165906 | 0.00910635 | intron-variant | TSG101 | GRCh38.p7 | 11:18509515 | TTGTTTATATGAGTT[C/T]TAAAGTAAAATCTCA | 7251 |
rs572882177 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18508330 | CCTCCCGAGTAGCTG[A/G]GACTACAGGCATGCA | 7251 |
rs572903815 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18510051 | ATTAAAGGCCATTAA[A/G]AGACATCAATGATAT | 7251 |
rs572909483 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18525539 | TGACAGAGCAAGACT[C/T]TAAAAAAAAAAAAAA | 7251 |
rs572979113 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18515882 | TCCTCTGGTGAACTT[A/C]GGCACTTATTTGTTC | 7251 |
rs573032089 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18522906 | CCAGGTTTGTTTTTT[A/T]CTTGACAGGATCTTG | 7251 |
rs573072777 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18514225 | TTCCAAAGCCTTCCA[A/G]CAGGTGTTGTTTGTA | 7251 |
rs573146366 | snp | A/C | | | intron-variant | TSG101 | GRCh38.p7 | 11:18493384 | AACACTTAAGACACC[A/C]GGTTTCATTTATCTC | 7251 |
rs573235463 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18523553 | TGTCACCCAGGCTGG[A/G]GTGCAGTGGCGTGAT | 7251 |
rs573270311 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18519747 | CCATAATACTATTAT[C/T]ACACTAAAATAATCA | 7251 |
rs573492732 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18487602 | AAATTCCAGGCTCAA[C/G]CTATCCTCCTTCCTC | 7251 |
rs573512068 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18495840 | GAGGCAGGAGAATGG[C/T]GTGAACCTGGAGGGC | 7251 |
rs573679185 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18501204 | CCTAGGCCAATGTCC[C/T]GAAGGGTTTCCCCTA | 7251 |
rs573737618 | snp | C/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18519150 | CCTGGGTAGCTGGGA[C/G]TACAGGAGCACCAGG | 7251 |
rs573872668 | snp | A/G | 3.54246e-05 | 0.00420845 | synonymous-codon | TSG101 | GRCh38.p7 | 11:18480567 | GAGGTCACTGAGACC[A/G]GCAGTCTTTCTTGCT | 7251 |
rs573896652 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18490975 | CCCGTGGGAGGGCTG[A/C]AGGGGACGAGGATGC | 7251 |
rs574008498 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18499056 | TATGAGAAAAAGTCC[A/G]AAAGGAGGTTTAAGA | 7251 |
rs574017632 | snp | C/T | 0.00279162 | 0.0372561 | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18528031 | GAGTCACTCTCACTC[C/T]ATCGCCCAGGCTGGA | 7251 |
rs574058730 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18485062 | TCCTGCCTCAGCCTC[C/T]CGAGTAGCTGGGAAG | 7251 |
rs574088604 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18484281 | GATTACTATTAATCC[A/G]TGTTAAACCCAGTTT | 7251 |
rs574119953 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18520874 | CATCTCTACTAAAAA[C/T]ACAAAAATTATCTGG | 7251 |
rs574248428 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18513982 | TACTCAGTAGGTTGA[C/G]TCTACCAAGCTGAAT | 7251 |
rs574290706 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18514518 | AGAAACCCATTTCTT[C/T]TAGTCAGCCTTTTCT | 7251 |
rs574322061 | snp | C/T | 0.00279162 | 0.0372561 | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18528617 | GGCTGGTCTGGAACT[C/T]TTGACCTCAGGTGAT | 7251 |
rs574364357 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18521308 | TGTCTTACTTCACCT[A/G]TCAGCAGTATTTGAC | 7251 |
rs574373649 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TSG101 | GRCh38.p7 | 11:18488250 | ATTTTTGTTTTTTTT[C/T]TTTTTTTGGTTTGTT | 7251 |
rs574397405 | snp | G/T | 0.00119737 | 0.0244387 | downstream-variant-500B | LDHAL6A, TSG101 | GRCh38.p7 | 11:18480068 | AGGAAACAAATTTAG[G/T]AGGGTTGGTAGGAGA | 7251 |
rs574460728 | in-del | -/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18488041 | TTTTTTGCTATACTA[-/T]TTTCACAACCACAGG | 7251 |
rs574650845 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | TSG101 | GRCh38.p7 | 11:18517171 | GGACTACAGGCGTGC[A/C]CTACCATGCCCAGCT | 7251 |
rs574733330 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18526277 | TATGTATTTCACCTG[A/G]GGCAGTAAGGGACTG | 7251 |
rs574743460 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18489385 | GACTATATGCCTACA[C/T]CACCATGCCTGACTC | 7251 |
rs574743601 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18497885 | TATCAATGAGAAAAA[C/T]GGTGGAAATAACCCT | 7251 |
rs574800373 | in-del | -/AA | | | intron-variant | TSG101 | GRCh38.p7 | 11:18495937 | TCAAAAAAAAAAAAA[-/AA]GTACTCTACAGAGAT | 7251 |
rs574829567 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18490118 | CCATGAACCATTTTT[C/G]CTAGGCTGAGGCTGT | 7251 |
rs574866227 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18500015 | ATCCCACCCACACAC[C/T]GTTCTTAAGTCTCTG | 7251 |
rs574894917 | in-del | -/A | 0.00057654 | 0.0169687 | intron-variant | TSG101 | GRCh38.p7 | 11:18484076 | CCTACTGGGACCTGC[-/A]AGGAAACAGAGGCAA | 7251 |
rs574905162 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18500300 | TATGGGAGTACAGGT[A/G]TTCCTTTAATATACT | 7251 |
rs574957954 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TSG101 | GRCh38.p7 | 11:18482472 | AAAGCCCTCAACCTT[C/T]TAAGAATTCTTTACT | 7251 |
rs575052021 | snp | A/G | 0.0023933 | 0.0345097 | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18528416 | TTTTTTTGAGACAGA[A/G]TTTTGCTCTTGCTTC | 7251 |
rs575066007 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18521602 | TCAAACTCCTGGAAG[C/T]GATCCTCTCAACTCA | 7251 |
rs575115914 | snp | C/G | 3.29544e-05 | 0.00405908 | missense | TSG101 | GRCh38.p7 | 11:18481658 | TCCAGGTCTATCACG[C/G]CCCTTCTCAAGGCTT | 7251 |
rs575202797 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18522708 | AATGGCCTGCAAGGC[C/T]CTCCAAACCTCCCAT | 7251 |
rs575419990 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18485894 | AGCCTGAAGGCTGAA[A/G]GATTGGACTGCTGGT | 7251 |
rs575446268 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18492892 | TGAACCATGCCACTT[G/T]AAGATAATGTTTATG | 7251 |
rs575485370 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18485179 | CTCTGTCAACAAACT[C/G]TAAGCCATTCTAAAC | 7251 |
rs575546587 | snp | A/C | | | intron-variant | TSG101 | GRCh38.p7 | 11:18515611 | TGCCACGTCCTTTAC[A/C]TTCATTATCTAATAA | 7251 |
rs575553472 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18508694 | TCTTTCTGTTAAATT[C/T]CCATTCAGCTTATAA | 7251 |
rs575591105 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18526197 | CTCAAAGCAAATAAA[A/T]ACGCGTTATAAGAAG | 7251 |
rs575731016 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18482241 | GGGCACCTGCCATAG[A/G]AGAGTAACTTTCCTC | 7251 |
rs575751366 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18525178 | CCTCCCAAAGTGCTA[A/G]GATTACAGGCGTAAG | 7251 |
rs575869364 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | TSG101 | GRCh38.p7 | 11:18521582 | CTATGTTGCCCAAGC[G/T]GTTCTCAAACTCCTG | 7251 |
rs575878264 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18509405 | TGCAGATGTGGGGCC[G/T]CAGAATACTTCCAAA | 7251 |
rs575920219 | snp | C/G | 3.61291e-05 | 0.00425009 | missense | TSG101 | GRCh38.p7 | 11:18502552 | GATATGGACCACCAG[C/G]TGGGTAAGGACAGCC | 7251 |
rs575920520 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18494850 | CCAGAGGGAAGAACA[A/G]CATTGGATAAGACAG | 7251 |
rs576011578 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TSG101 | GRCh38.p7 | 11:18483793 | TACTATGCCCACAAC[A/G]TCCAGGGAACATATA | 7251 |
rs576033344 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18511237 | ATCTTCCTGCTTCAG[C/T]CTCCCAAGTAGTCAG | 7251 |
rs576164724 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18481553 | ACTACAAAGAAACTC[C/T]CTTGGTTTGTGGTTT | 7251 |
rs576180247 | snp | C/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18499632 | TGGCCAGGCTGGTCT[C/G]CAACTCCTGACCTCG | 7251 |
rs576277438 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18506728 | ATAAATTCCAGGAAT[A/G]AACCAAGTTTTATCT | 7251 |
rs576278198 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18505774 | GTTTGACCCCATTAT[C/G]TGAACCATTAATTGA | 7251 |
rs576315425 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18498155 | ATGCACAGAAATAGG[A/C]CGTGGACAAATCCTA | 7251 |
rs576380350 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18483474 | TCACTCCAGCCTGAG[C/T]GCAAGAGTGAAACTC | 7251 |
rs576529783 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18504439 | AGACAAAAAAAAAAG[A/C]AAGCATTTTTGTTCC | 7251 |
rs576605128 | snp | C/T | 0 | 0 | intron-variant | TSG101 | GRCh38.p7 | 11:18513407 | CTCAAGTGATCCTTT[C/T]ACCTTAGCCTCCTGA | 7251 |
rs576610290 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18498992 | TAACTATCCATTGGA[C/T]GTAACCTCAAAAAGT | 7251 |
rs576668153 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18520750 | TGATTACAAAATTTC[C/T]GGCCAGGCGTGGTGG | 7251 |
rs576695006 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18520122 | GAATTTACTTTGTCT[C/G]TACAGATTTGCTTAT | 7251 |
rs576771638 | snp | A/T | 0.00279162 | 0.0372561 | downstream-variant-500B | LDHAL6A, TSG101 | GRCh38.p7 | 11:18479972 | CTTTCCCTTTAATCC[A/T]AAAGTTATCAGGTAT | 7251 |
rs576795806 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18502698 | AGTTGATGAATTTAT[A/C]GTCTTGGAGCTGCAA | 7251 |
rs576861436 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18493976 | ACTCAGAAAAATGCG[C/G]TTTACTTGAGCTCTA | 7251 |
rs576880886 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18525832 | TTCAATCAAGAACTA[C/T]GGGGGCGATTTAACT | 7251 |
rs576881168 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18500094 | CCCACATGAGAACAT[C/T]TGATATTTGTCTTTC | 7251 |
rs576948633 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18502109 | AAAACTACTGGTCTT[C/T]AATCATTTGTCTGAT | 7251 |
rs576998535 | in-del | -/AC | | | intron-variant | TSG101 | GRCh38.p7 | 11:18490659 | CAAGATATTTGTCCA[-/AC]AGCTCCAGAACGTCA | 7251 |
rs577007608 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18501721 | ATAGTCATTTTTACA[A/G]TATTAATTCTTCATG | 7251 |
rs577012454 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18516458 | CAAGCGATTCTCCTG[C/T]CTCAGCATCCCGAGT | 7251 |
rs577058283 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18493798 | AGGAGTTCTGATCTG[C/T]GCTATTAAGTGCAAA | 7251 |
rs577084514 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18522975 | GCTCACTGCAACCTC[A/G]AACTCCTGGGCTCAA | 7251 |
rs577095749 | in-del | -/TTTG | 0.00119737 | 0.0244387 | intron-variant | TSG101 | GRCh38.p7 | 11:18505825 | GATAGGTTGTGGGGT[-/TTTG]TTTGTTTGAGAGAGA | 7251 |
rs577189587 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18506458 | AGCGCTTTGGGAGTC[C/T]GAGGCAGGCAGATCA | 7251 |
rs577189989 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18513218 | GAGGCGTTCTGCTTA[G/T]TTTTTTTTTTAGCAT | 7251 |
rs577227670 | snp | C/T | 1.65603e-05 | 0.00287747 | intron-variant | TSG101 | GRCh38.p7 | 11:18506959 | ATTGTAAAAATAATA[C/T]ACAAGGCCTGAATAT | 7251 |
rs577303935 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TSG101 | GRCh38.p7 | 11:18512621 | GACATTGTGAAAAAT[C/T]ATAGAGAGTCTATAT | 7251 |
rs577342188 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18518970 | AACATCCCCTCCTAG[A/G]TTTAAATTTGCATAG | 7251 |
rs577477504 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18516289 | ACCTGTCAATGTATC[A/G]TCCATCCTGTCCAAT | 7251 |
rs577499239 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18496972 | GGTACGCTCCTCTAA[C/T]CCCAGCTACTTGGGA | 7251 |
rs577703512 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | TSG101 | GRCh38.p7 | 11:18520945 | CTGAGGCAGGAGAAT[C/T]GCTTGAACCCAGGAG | 7251 |
rs577737294 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18528193 | TTTAAAAGCAAGAAG[A/G]TTTTCAAACTGTTCT | 7251 |
rs577892708 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TSG101 | GRCh38.p7 | 11:18491877 | TTTCCACACTCACTG[A/C]ACATACAGATTAAAA | 7251 |
rs577897587 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18500251 | ATTTAGGTTCACTCC[A/G]TATCTTAGCTAGTAT | 7251 |
rs577921284 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18521347 | TTCAGCAATATTTGA[C/T]CAAACTGATTCCTTT | 7251 |
rs577931344 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18484289 | TTAATCCATGTTAAA[C/G]CCAGTTTCCCTATTC | 7251 |
rs577997978 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18486796 | GGATTATAAATCATG[C/T]TGCTATAAAGACACA | 7251 |
rs578006383 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TSG101 | GRCh38.p7 | 11:18521911 | TTGAATTTCTAGACT[C/G]AAGCAATCTGTCCAC | 7251 |
rs578097164 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18513952 | TATTTGGTGGTGGGC[A/G]CCTGTAATCCCATCT | 7251 |
rs578187330 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TSG101 | GRCh38.p7 | 11:18514588 | TTATCTATCCTACCT[C/G]GAATCCTCCTTGAGT | 7251 |
rs578222470 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TSG101 | GRCh38.p7 | 11:18501054 | CTCAAATGATTCGCC[C/T]GCCTTGGCTTCCCAA | 7251 |
rs745389269 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18492248 | AAAATCCTTCTCCCA[C/T]AGATTACGTACCTAA | 7251 |
rs745404071 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18490794 | TGCCAGGAAAGCAGC[A/G]GGCACCAACCATGTT | 7251 |
rs745447761 | snp | C/T | 2.53669e-05 | 0.00356129 | utr-variant-5-prime | TSG101 | GRCh38.p7 | 11:18526867 | AGGGTCAGCCGCTGC[C/T]GGGCTGCCCCAGACC | 7251 |
rs745549992 | snp | C/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18493386 | CACTTAAGACACCCG[C/G]TTTCATTTATCTCCT | 7251 |
rs745612838 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18498579 | CAGGTGTTAGGAAGA[C/T]TGAGAATTCGGTTTT | 7251 |
rs745675142 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18483208 | CCATGTAAGAAGTGC[C/T]TTTTGGCTGGGCACA | 7251 |
rs745808574 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18519193 | ATTTTTTTGTTGAGA[C/T]GAGGTTTCACCATAT | 7251 |
rs745901608 | snp | A/C | 2.23591e-05 | 0.00334351 | intron-variant | TSG101 | GRCh38.p7 | 11:18502437 | CTTTTCACAACAGGG[A/C]GTTAGACTTTGCTTA | 7251 |
rs745921247 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18490422 | TTTTCAGTAGAGTTT[A/G]GAATCTCATAGTAAA | 7251 |
rs745930489 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18523140 | CTCAATGTGATCCTC[C/T]AGCTTCCGCCTCCCA | 7251 |
rs745966913 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18524325 | CTCAAGGGAAAAAAA[A/G]ACCTTTTATAATAAA | 7251 |
rs745969355 | in-del | -/GAG | | | intron-variant | TSG101 | GRCh38.p7 | 11:18499130 | TCAAGGAGTTATTCA[-/GAG]AAGAATGAAGACATC | 7251 |
rs745985397 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18524516 | GAAGCCCTTCTTTAG[A/G]AGGAAGGAGCCCCAC | 7251 |
rs745995737 | in-del | -/TAGAG | | | intron-variant | TSG101 | GRCh38.p7 | 11:18482057 | CTATGCTGAGTGAAA[-/TAGAG]TAATGATGGAGATAT | 7251 |
rs745995790 | snp | A/G | 0.00029092 | 0.0120572 | synonymous-codon | TSG101 | GRCh38.p7 | 11:18502538 | ACTTGTTGTGGCAGG[A/G]TATGGACCACCAGGT | 7251 |
rs746074800 | in-del | -/TTG | 1.74293e-05 | 0.00295201 | cds-indel | TSG101 | GRCh38.p7 | 11:18502525 | AAGGGTACTGAGAAC[-/TTG]TTGTGGCAGGATATG | 7251 |
rs746102679 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18497734 | GCTTCACCAGATTTA[A/G]TGTGCTTTGCTTATG | 7251 |
rs746152524 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18521706 | TTTTTTGAGACAGCA[C/T]GTGGCTGTCACCCAG | 7251 |
rs746256097 | in-del | -/AGAT | | | intron-variant | TSG101 | GRCh38.p7 | 11:18481005 | CCCCACAGTGAGAGG[-/AGAT]AGATAGGCAAGATCA | 7251 |
rs746276174 | snp | A/C | 1.64974e-05 | 0.00287201 | synonymous-codon | TSG101 | GRCh38.p7 | 11:18514768 | TGAACTAGTAGGCTT[A/C]ACAAAACAGATAGGG | 7251 |
rs746281892 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18503870 | TTATCAATTCTATGA[C/T]ATTTGCCTTTTACAA | 7251 |
rs746396658 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18505713 | GATAATAAAGGTTGA[C/T]AGTACAGGTAGTCTA | 7251 |
rs746414859 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18489881 | TATTTCAATGATTCT[A/G]GTATCAGATTAAACT | 7251 |
rs746415929 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18509742 | TTAGCCATTTCTCAT[C/T]GGTTTTCAACTCAGC | 7251 |
rs746424622 | snp | G/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18488969 | AAAATACAAAAATTA[G/T]CTGGGCGTGGTGGTG | 7251 |
rs746530412 | snp | C/G | | | utr-variant-3-prime | TSG101 | GRCh38.p7 | 11:18480460 | CTTGAATGATAAACT[C/G]CAATAACTTATTCTG | 7251 |
rs746585841 | snp | A/G | 1.66319e-05 | 0.00288369 | intron-variant | TSG101 | GRCh38.p7 | 11:18509502 | TTTCTGTTCTCTTTT[A/G]TTTATATGAGTTTTA | 7251 |
rs746619849 | snp | G/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18481181 | TAAGCTTGAGACAAC[G/T]TTCATACAAGAGGGC | 7251 |
rs746661550 | snp | A/C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18490956 | TCACTTTTATCCAGT[A/C/T]GTTCCCGTGGGAGGG | 7251 |
rs746810752 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18519265 | CACCTCAGCCTCCCA[A/G]AGTGCTGGGATTACA | 7251 |
rs746850073 | snp | C/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18520322 | TCGAACTCCTGGGCT[C/G]AAGTGATTCTCCTGC | 7251 |
rs746865458 | snp | C/T | 3.303e-05 | 0.00406373 | intron-variant | TSG101 | GRCh38.p7 | 11:18519487 | AGTAAACTCAAAGTA[C/T]AGAAATTGCTATTTT | 7251 |
rs746926397 | snp | A/G | 1.64885e-05 | 0.00287123 | missense | TSG101 | GRCh38.p7 | 11:18509556 | CTATTTGGTGGCCCC[A/G]TTGCCTGGTATGGCG | 7251 |
rs746942523 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18508158 | TACCTTTGTCATAGC[A/G]GTCACTCGCTATATT | 7251 |
rs747133057 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18513611 | AGAGCTACTCACTTC[C/T]TTATGGCTTTTCTCC | 7251 |
rs747265809 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18500448 | TCCCACCAACATTGT[A/G]TAAGTTCCCTTTTCT | 7251 |
rs747269742 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18505505 | AGCAATCCCTACCTC[A/G]GCCTCCCAAAGTGCT | 7251 |
rs747273263 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18495787 | GGTTGAAGATGTCTA[C/T]AGCACTCTGATAAAA | 7251 |
rs747334087 | snp | C/T | 1.73851e-05 | 0.00294826 | intron-variant | TSG101 | GRCh38.p7 | 11:18516076 | AAAATGCATCTATGC[C/T]GGAAACCTAATAAGA | 7251 |
rs747361251 | snp | A/G | 1.65479e-05 | 0.0028764 | missense | TSG101 | GRCh38.p7 | 11:18481850 | TTTTTCAAAAGTTCT[A/G]TGTTTTTATCAACCT | 7251 |
rs747386031 | snp | A/G | 1.65081e-05 | 0.00287293 | intron-variant | TSG101 | GRCh38.p7 | 11:18483850 | ATCCAAAAATTTTAA[A/G]TCTTTAATGAGTCAC | 7251 |
rs747475709 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18491439 | GGCTCAGGTGAGCTA[C/T]CTTGGTGGGTAATAC | 7251 |
rs747540375 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18512342 | GAGTCCAGTCTGCTA[C/T]TAAACCCATCTACTG | 7251 |
rs747567241 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18524781 | AATATCTTCTGAACA[C/T]GCCTTGCCTTTGTCT | 7251 |
rs747701338 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18482021 | CACCCTGGTCAAAGG[C/T]AGAGGAAAAGATGTG | 7251 |
rs747713262 | snp | A/C | 1.80211e-05 | 0.0030017 | intron-variant | TSG101 | GRCh38.p7 | 11:18514631 | CAGATGCTAGTGAGC[A/C]AAATATATAAAACAT | 7251 |
rs747744055 | snp | C/T | 5.22662e-05 | 0.00511179 | missense | TSG101 | GRCh38.p7 | 11:18480616 | AGCTGGAACTGTTTA[C/T]GGGACAGAAGACGTA | 7251 |
rs747817408 | snp | A/G/T | 9.96834e-05 | 0.00705923 | intron-variant | TSG101 | GRCh38.p7 | 11:18509508 | TTCTCTTTTGTTTAT[A/G/T]TGAGTTTTAAAGTAA | 7251 |
rs747839812 | in-del | -/T/TT | | | intron-variant | TSG101 | GRCh38.p7 | 11:18484938 | TTAATTGCCGCCTTT[-/T/TT]TTTTTTTTTTTTTTT | 7251 |
rs747855448 | in-del | -/CA | | | intron-variant | TSG101 | GRCh38.p7 | 11:18507026 | TACACAGCAAAATTT[-/CA]CAGTTAAAAAATCCA | 7251 |
rs747860057 | snp | G/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18504052 | ACAAAAATAGAAAAA[G/T]TAGCTAGGTGTAGGG | 7251 |
rs747986378 | snp | G/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18509977 | ATTGCCACTGTACAA[G/T]GTATTATAAGTATAC | 7251 |
rs748015976 | snp | C/T | 2.21285e-05 | 0.00332623 | intron-variant | TSG101 | GRCh38.p7 | 11:18502449 | GGGAGTTAGACTTTG[C/T]TTATATGGTGAAACA | 7251 |
rs748035043 | snp | A/G | 4.08363e-05 | 0.00451846 | intron-variant | TSG101 | GRCh38.p7 | 11:18526762 | CTGGGAGGCGAGCGC[A/G]TCGCAGCCTCACCTT | 7251 |
rs748064953 | snp | C/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18495614 | TGTTTTGCTCCTACA[C/G]TAACAGGAAAAAGAA | 7251 |
rs748095407 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18516965 | CAAACAAAAAAACAC[C/T]ATCAAACAATACCAT | 7251 |
rs748115125 | snp | G/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18510538 | ACAAAGAGATTCCTA[G/T]TTTTTCATAAGTTAC | 7251 |
rs748148906 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18519384 | CTAATTTGCTACCCT[C/T]CAACAGTTTTATTAG | 7251 |
rs748238421 | snp | C/T | 1.70406e-05 | 0.0029189 | intron-variant | TSG101 | GRCh38.p7 | 11:18516092 | GGAAACCTAATAAGA[C/T]ATTTACCTCTATAAG | 7251 |
rs748253363 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18485417 | TAATCCTTATTATGC[A/G]GCCTAAATACTAAAT | 7251 |
rs748294050 | snp | A/C | | | intron-variant | TSG101 | GRCh38.p7 | 11:18501904 | TAAGGTCTAGTGGAG[A/C]AATCAGCTTTAGATA | 7251 |
rs748343434 | snp | A/C | | | intron-variant | TSG101 | GRCh38.p7 | 11:18487534 | TTTCTGTAACCATTA[A/C]AATTTTTTTTCTAGT | 7251 |
rs748380833 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18520605 | GCTCCTTAGAATTTA[C/T]TTCTTAAAGAAATTT | 7251 |
rs748451122 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18491821 | ATTTGTAGAATAAGT[C/T]GGTCTACTTCAAATG | 7251 |
rs748464901 | snp | A/G | 1.64741e-05 | 0.00286998 | synonymous-codon | TSG101 | GRCh38.p7 | 11:18484041 | AGAGGCTCGGATGGT[A/G]TCCTCGCTGATTGTG | 7251 |
rs748582786 | snp | C/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18526391 | GGATCCCTAGATTGG[C/G]ACAGGAGTAGAGGAT | 7251 |
rs748609198 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18493145 | ATTCCAGATTAGCAG[C/T]TGAAGAGCTAACAGA | 7251 |
rs748697084 | snp | C/T | 1.85623e-05 | 0.00304645 | intron-variant | TSG101 | GRCh38.p7 | 11:18516209 | GAGCATTTTTTAAGA[C/T]ACTCCCATAAGTTAT | 7251 |
rs748779660 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18483064 | GGGGTGGGGAGGGAT[A/G]GCACGCAGGGGTGGT | 7251 |
rs748782362 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18485737 | ACTGCTTTGAAGGCA[C/T]GTGGTTGGAAACAGT | 7251 |
rs748798929 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18517790 | TTCTCAGACCATATC[C/T]CTATCACTACAAAAT | 7251 |
rs748856068 | snp | A/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18518824 | TCTGATAAATCTTCA[A/T]GCAATGAAACTCAAT | 7251 |
rs748960336 | snp | C/T | 1.80081e-05 | 0.00300062 | intron-variant | TSG101 | GRCh38.p7 | 11:18514637 | CTAGTGAGCAAAATA[C/T]ATAAAACATAACTAA | 7251 |
rs748962764 | in-del | -/CT | | | intron-variant | TSG101 | GRCh38.p7 | 11:18496918 | CAACATGGTAAAACC[-/CT]GTCTCTACTAAAAAT | 7251 |
rs748998964 | snp | G/T | 1.86932e-05 | 0.00305716 | synonymous-codon | TSG101 | GRCh38.p7 | 11:18502565 | AGGTGGGTAAGGACA[G/T]CCTGGGTAACCACTA | 7251 |
rs749001591 | in-del | -/CT | | | intron-variant | TSG101 | GRCh38.p7 | 11:18521669 | GCACCTGGCCCCTTC[-/CT]CTTTTTTTTTTTTTT | 7251 |
rs749045561 | snp | C/T | 2.46953e-05 | 0.00351384 | utr-variant-5-prime | TSG101 | GRCh38.p7 | 11:18526861 | AGGCAGAGGGTCAGC[C/T]GCTGCTGGGCTGCCC | 7251 |
rs749136024 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18497477 | TCAAAAATCATAAAC[A/G]TGAGATCTGATTCCA | 7251 |
rs749162548 | snp | G/T | 1.64868e-05 | 0.00287109 | missense | TSG101 | GRCh38.p7 | 11:18506864 | TTCATTACCTGGGAT[G/T]GGGAGGGTATCCGGA | 7251 |
rs749165140 | snp | C/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18521415 | ACTCTGTCGCTCAGG[C/G]TACAGTGCAGTGGTA | 7251 |
rs749187334 | snp | C/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18482098 | GTGACAGCACTTTCA[C/G]TGACAGTAACAAGCT | 7251 |
rs749242335 | snp | C/T | 1.92806e-05 | 0.00310483 | synonymous-codon, utr-variant-5-prime | TSG101 | GRCh38.p7 | 11:18526787 | CACCTTGGACACCAT[C/T]TTCTTGAGCTGGCTC | 7251 |
rs749258953 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18498519 | CCTGATGAGGAGTCA[A/G]GGATGACTCCAAAGA | 7251 |
rs749384315 | snp | A/G | 0.000115313 | 0.0075923 | synonymous-codon | TSG101 | GRCh38.p7 | 11:18484047 | TCGGATGGTGTCCTC[A/G]CTGATTGTGCCATCC | 7251 |
rs749432847 | in-del | -/CCTGGCATG | 1.64838e-05 | 0.00287083 | cds-indel | TSG101 | GRCh38.p7 | 11:18506899 | TATGGAGAGATTCCA[-/CCTGGCATG]CCTGGCATGTAGGAA | 7251 |
rs749544931 | snp | A/G | 1.68235e-05 | 0.00290026 | missense | TSG101 | GRCh38.p7 | 11:18516114 | CTCTATAAGGCACAG[A/G]GATTGTTCCAGTGAG | 7251 |
rs749646873 | snp | C/G/T | | | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18527532 | ATTTCTCCTCTGTAC[C/G/T]CACCCATAAATGATA | 7251 |
rs749666716 | snp | G/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18481054 | CTCCAGCTACAGCTG[G/T]ATCAGATATCCCAAG | 7251 |
rs749699791 | snp | C/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18515052 | CTAAACTTATACTTG[C/G]TTTATACAATGCTGA | 7251 |
rs749801746 | snp | C/T | 1.65381e-05 | 0.00287555 | intron-variant | TSG101 | GRCh38.p7 | 11:18484107 | AAAACACTTGCTTAC[C/T]TCCCAAGTTCCTTCT | 7251 |
rs749828035 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18502309 | ATTTTCATGCCCTGG[C/T]AGAAGGTTCATTTAT | 7251 |
rs749854247 | snp | C/T | 3.51692e-05 | 0.00419325 | intron-variant | TSG101 | GRCh38.p7 | 11:18516182 | GAAAGGAAAGAACAA[C/T]GATTTAATCATGAGC | 7251 |
rs749957134 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18518444 | TCCCTCGGCCCTGGC[A/G]TATTATTTTCAAGGA | 7251 |
rs750027663 | in-del | -/TT | 1.99058e-05 | 0.00315476 | intron-variant | TSG101 | GRCh38.p7 | 11:18480653 | GGGAGGGGAGAAAAG[-/TT]TGAATAGTTTAGAAT | 7251 |
rs750114893 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18516510 | CCACCACACCTGACT[A/G]ATTTTTTGTATCTTT | 7251 |
rs750219847 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18486948 | CAGCCATAAAAAATG[A/G]TGAGTTCATGTCCTT | 7251 |
rs750291650 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18514483 | TGAATATAAGTATTC[C/T]GAAAATTACAAAGCT | 7251 |
rs750342978 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18501374 | TTTATGAACAATGTC[C/T]TTTTCCCAATATATG | 7251 |
rs750445986 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18506084 | CCTGCATCGGCCTCC[A/G]AAAGTGCTGGGTAAG | 7251 |
rs750491486 | snp | A/G | 4.25297e-05 | 0.00461118 | intron-variant | TSG101 | GRCh38.p7 | 11:18526750 | GGTGGGCGCGCCCTG[A/G]GAGGCGAGCGCGTCG | 7251 |
rs750581146 | snp | A/C | 2.31398e-05 | 0.00340138 | utr-variant-5-prime | TSG101 | GRCh38.p7 | 11:18526850 | CCCTTCCCCGCAGGC[A/C]GAGGGTCAGCCGCTG | 7251 |
rs750598030 | snp | A/T | 1.64738e-05 | 0.00286995 | synonymous-codon | TSG101 | GRCh38.p7 | 11:18481747 | CTGTTTGTATAAGGG[A/T]GCTGTGGGAATGATA | 7251 |
rs750618050 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18484535 | GCAGTTTCCCTAAAC[A/G]AATGTACAGGTTAAT | 7251 |
rs750699953 | snp | C/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18526096 | ATATAAATAAATCAT[C/G]GCTTTAAAATACAAA | 7251 |
rs750759202 | snp | A/C/T | 8.24591e-05 | 0.00642056 | missense | TSG101 | GRCh38.p7 | 11:18506915 | CTGGCATGCCTGGCA[A/C/T]GTAGGAAGCTAAAAA | 7251 |
rs750837281 | snp | G/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18517554 | ACATAAGAACACTGG[G/T]CCCATAAGATTATAA | 7251 |
rs750843962 | in-del | -/TA | | | intron-variant | TSG101 | GRCh38.p7 | 11:18517939 | GGGCTTTGTTTACTC[-/TA]AAAGTATTTGTTAAC | 7251 |
rs750849381 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18512161 | TGTAATCCCAGCACT[C/T]TGGGAGGCTGAGGCG | 7251 |
rs750887742 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18482753 | AAAGTTCCCTGAACA[C/T]ACTTTTAAAAAATGG | 7251 |
rs750906139 | snp | A/G | | | synonymous-codon | TSG101 | GRCh38.p7 | 11:18484029 | CGCAGAGATGAGAGA[A/G]GCTCGGATGGTGTCC | 7251 |
rs750963017 | snp | C/T | 1.65509e-05 | 0.00287666 | intron-variant | TSG101 | GRCh38.p7 | 11:18506832 | AATTTGTAATACAAT[C/T]ATTCAAAAGAACGTT | 7251 |
rs751002366 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18522127 | AAGTCCTTGGTCTTC[C/T]TCTCTATCTAAACTC | 7251 |
rs751016678 | snp | C/G | 1.64863e-05 | 0.00287104 | intron-variant | TSG101 | GRCh38.p7 | 11:18484087 | CCTGCAGGAAACAGA[C/G]GCAAAAAACACTTGC | 7251 |
rs751124048 | snp | A/C | | | intron-variant | TSG101 | GRCh38.p7 | 11:18523930 | CAAGTAGCTAGGACT[A/C]CAGGTGCAAGCCACG | 7251 |
rs751139551 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18497049 | TGAGCCAAGATCGCG[C/T]CACTGCACTCCAGCC | 7251 |
rs751177005 | in-del | -/A | | | intron-variant | TSG101 | GRCh38.p7 | 11:18489113 | GCAAGACTCCATCTC[-/A]AAAAAAAAAAAAGGA | 7251 |
rs751209663 | snp | C/T | 3.29462e-05 | 0.00405857 | synonymous-codon | TSG101 | GRCh38.p7 | 11:18484014 | CAGTTTGTCACTGAC[C/T]GCAGAGATGAGAGAG | 7251 |
rs751288739 | in-del | -/AGTC | 3.82183e-05 | 0.00437123 | utr-variant-3-prime | TSG101 | GRCh38.p7 | 11:18480543 | AGCTGGTATCAGAGA[-/AGTC]AGTCAGTAGAGGTCA | 7251 |
rs751320673 | snp | C/G | 1.66991e-05 | 0.00288951 | intron-variant | TSG101 | GRCh38.p7 | 11:18509697 | AATTCAAGTCAGCTA[C/G]AGAGTTGCTTTTCAG | 7251 |
rs751354236 | snp | A/G | 6.79544e-05 | 0.0058286 | synonymous-codon | TSG101 | GRCh38.p7 | 11:18514690 | TACGTGTTTCCATTC[A/G]TGTAGATAAGGAAGA | 7251 |
rs751400127 | snp | A/G | 1.69332e-05 | 0.0029097 | intron-variant | TSG101 | GRCh38.p7 | 11:18481603 | AACCCAAGTTAAAAA[A/G]TCTTGGAACGTAAAA | 7251 |
rs751548169 | snp | C/T | 6.6072e-05 | 0.00574732 | intron-variant | TSG101 | GRCh38.p7 | 11:18506844 | AATTATTCAAAAGAA[C/T]GTTTTTCATTACCTG | 7251 |
rs751568422 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18508031 | CCTGGGAGGCAGAGG[C/T]TGCAGTCAGCCCAGA | 7251 |
rs751586696 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18492875 | CAAAGTTCAAAATTC[A/G]ATGAACCATGCCACT | 7251 |
rs751703632 | snp | A/G | 1.65375e-05 | 0.0028755 | intron-variant | TSG101 | GRCh38.p7 | 11:18506944 | AACAATTTTTTTCAC[A/G]TTGTAAAAATAATAT | 7251 |
rs751707270 | snp | A/G | | | downstream-variant-500B | LDHAL6A, TSG101 | GRCh38.p7 | 11:18480070 | GAAACAAATTTAGTA[A/G]GGTTGGTAGGAGAGC | 7251 |
rs751707483 | snp | G/T | | | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18527322 | GCTAGTGCATTTCTA[G/T]CTCAGGCGCAAATTT | 7251 |
rs751727469 | snp | A/C | | | intron-variant | TSG101 | GRCh38.p7 | 11:18480731 | ATGGGATCTAAGAAC[A/C]CTAACTCATGACCTG | 7251 |
rs751738658 | snp | A/C | 2.34272e-05 | 0.00342243 | utr-variant-5-prime | TSG101 | GRCh38.p7 | 11:18526852 | CTTCCCCGCAGGCAG[A/C]GGGTCAGCCGCTGCT | 7251 |
rs751757244 | snp | C/T | | | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18528638 | CTCAGGTGATCCACC[C/T]GCCTCAGCCTGCCAG | 7251 |
rs751840349 | in-del | -/TGCACT | | | intron-variant | TSG101 | GRCh38.p7 | 11:18510382 | CTGAGATCACACCAC[-/TGCACT]TGCACTCCATCCTAG | 7251 |
rs751883516 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18518559 | CCTTACAACTTTGTC[C/T]CAATAGAAAGTAGAG | 7251 |
rs751912774 | snp | C/G | 0.000179517 | 0.0094724 | utr-variant-3-prime | TSG101 | GRCh38.p7 | 11:18480518 | AATACTTTAAGAAGA[C/G]CTCAACCTCCAGCTG | 7251 |
rs751924467 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18484166 | GGGGCAATATGAACC[A/G]ACACTTTCAAAATGT | 7251 |
rs751970821 | snp | A/T | 1.80991e-05 | 0.00300819 | intron-variant | TSG101 | GRCh38.p7 | 11:18516198 | GATTTAATCATGAGC[A/T]TTTTTTAAGATACTC | 7251 |
rs751999580 | in-del | -/ATGTGTGGAC | 1.64762e-05 | 0.00287016 | intron-variant | TSG101 | GRCh38.p7 | 11:18519647 | TTTAAAACCAATGCA[-/ATGTGTGGAC]TATATTTTACAGCTG | 7251 |
rs752017729 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18506338 | ATTAAATGGAATGCT[A/G]GTTATAATGAATTCA | 7251 |
rs752246042 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18482955 | TTCCTAGGGCAAAGG[C/T]GTGATAAGGTTTGGC | 7251 |
rs752339080 | snp | G/T | 1.93706e-05 | 0.00311206 | intron-variant | TSG101 | GRCh38.p7 | 11:18502478 | CACAAGTTTTCAAGG[G/T]TACTTACCAACAGTG | 7251 |
rs752367546 | snp | A/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18499862 | TGTGGTAGGAACATT[A/T]TAAGTCTTCTAGCTA | 7251 |
rs752473271 | snp | A/C | 3.34403e-05 | 0.00408889 | intron-variant | TSG101 | GRCh38.p7 | 11:18481887 | GAAAACAGAACAGTC[A/C]AAGCATTAATAACTG | 7251 |
rs752481637 | snp | C/T | 1.64751e-05 | 0.00287007 | missense | TSG101 | GRCh38.p7 | 11:18481764 | CTGTGGGAATGATAA[C/T]TTCATCGATATCATT | 7251 |
rs752488949 | snp | G/T | 3.39087e-05 | 0.00411742 | intron-variant | TSG101 | GRCh38.p7 | 11:18514874 | ACTTCAGTTACTCTA[G/T]TTTTATTATTTTTAA | 7251 |
rs752533478 | snp | C/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18522340 | TTCTCCCCAAATTTA[C/G]TTCTCCAGTGTCTTC | 7251 |
rs752540202 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18489882 | ATTTCAATGATTCTG[A/G]TATCAGATTAAACTT | 7251 |
rs752665775 | in-del | -/AAAT | | | intron-variant | TSG101 | GRCh38.p7 | 11:18480693 | TTAGGCCCAGGCATA[-/AAAT]AAATAGACAATTTGT | 7251 |
rs752693750 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18480898 | CACTCAAGCAAGAGA[C/T]TGTACAGAAAAAGAG | 7251 |
rs752705127 | snp | A/G | | | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18528701 | CCAGCCCATTTATAT[A/G]TTTTTGTTGCCCAGG | 7251 |
rs752737012 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18508722 | TAAACCAAGATGTTC[C/T]TCAGGAAAGAATGGA | 7251 |
rs752769993 | snp | A/G | 3.30006e-05 | 0.00406192 | synonymous-codon | TSG101 | GRCh38.p7 | 11:18509543 | TCAATTCTACTTACT[A/G]TTTGGTGGCCCCGTT | 7251 |
rs752776208 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18496569 | CTAGTGCAGTGACTC[A/G]CATCTGTAATCCGGG | 7251 |
rs752861793 | snp | C/T | 5.59196e-05 | 0.0052874 | missense | TSG101 | GRCh38.p7 | 11:18480550 | TATCAGAGAAGTCAG[C/T]AGAGGTCACTGAGAC | 7251 |
rs752863632 | snp | C/G | 1.66043e-05 | 0.00288129 | intron-variant | TSG101 | GRCh38.p7 | 11:18506969 | TAATATACAAGGCCT[C/G]AATATGTAGGCTACT | 7251 |
rs752899235 | in-del | -/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18500808 | CTTTGTTGTGCAGAA[-/G]GCTTTTTTTTTTTGA | 7251 |
rs752917475 | in-del | -/AA | | | intron-variant | TSG101 | GRCh38.p7 | 11:18494079 | ATAAACACACACCAC[-/AA]AAAAAGTTTAAATTC | 7251 |
rs752932400 | snp | G/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18503330 | CGAATATTTGAGAAC[G/T]TCTAACATTTTTCCC | 7251 |
rs753107558 | snp | G/T | 1.6516e-05 | 0.00287362 | intron-variant | TSG101 | GRCh38.p7 | 11:18484099 | AGAGGCAAAAAACAC[G/T]TGCTTACTTCCCAAG | 7251 |
rs753152219 | snp | G/T | 2.22249e-05 | 0.00333346 | intron-variant | TSG101 | GRCh38.p7 | 11:18526726 | ACTCGACAGGGCGCG[G/T]AAGGGAGCGGTGGGC | 7251 |
rs753165905 | snp | A/G | | | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18527359 | ACTCTAAAGTCATAC[A/G]CTTGCCTTAGATGAT | 7251 |
rs753173566 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18509358 | CCTACAAATGGAAGC[C/T]CAAATGCCAGTCTTT | 7251 |
rs753206887 | in-del | -/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18490625 | TTTCAAATAGAAAAT[-/G]GTTGTATAGAATTGA | 7251 |
rs753270092 | in-del | -/TTATTT | 1.65048e-05 | 0.00287265 | intron-variant | TSG101 | GRCh38.p7 | 11:18514880 | GTTACTCTATTTTTA[-/TTATTT]TTAAATTGAAGAATG | 7251 |
rs753337572 | snp | A/G | 1.71672e-05 | 0.00292973 | intron-variant | TSG101 | GRCh38.p7 | 11:18514893 | TATTATTTTTAAATT[A/G]AAGAATGGTTAAAGG | 7251 |
rs753347606 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18484399 | AAATAACCAACAAAT[A/G]GCACAATAATTTCCA | 7251 |
rs753354951 | snp | C/T | 1.65408e-05 | 0.00287578 | missense | TSG101 | GRCh38.p7 | 11:18514728 | TCCCATTTGCATCAA[C/T]ATGCTTTCCTGTTTT | 7251 |
rs753437335 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18485839 | ATGCTGAGGCAGATG[A/G]GGTGGGTCCCCGGTG | 7251 |
rs753456557 | in-del | -/GAA | 1.65854e-05 | 0.00287966 | intron-variant | TSG101 | GRCh38.p7 | 11:18481620 | CTTGGAACGTAAAAT[-/GAA]GAAATACCTTCAGGA | 7251 |
rs753460455 | in-del | -/AAAT | | | utr-variant-3-prime | TSG101 | GRCh38.p7 | 11:18480415 | CCAAAAGAAAACAGA[-/AAAT]ATATTATTGATTCAA | 7251 |
rs753471837 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18501777 | TGTCTCAATTGGACT[C/T]TTTAAGGCTTTTTTA | 7251 |
rs753573983 | snp | A/C | | | intron-variant | TSG101 | GRCh38.p7 | 11:18519963 | TTAAAGAGTATAGTT[A/C]AATGGTTTTTAGTAC | 7251 |
rs753626745 | snp | C/T | 1.64727e-05 | 0.00286986 | missense | TSG101 | GRCh38.p7 | 11:18483986 | GATCCATTTCCTCCT[C/T]CATCCGCCATCTCAG | 7251 |
rs753705491 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18499784 | TTTTGTTACCTGCAC[A/G]GAATGTAATGTTCAA | 7251 |
rs753718195 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18525712 | CTATAACTAAGGATA[A/G]CAAGTTTATCAAAAC | 7251 |
rs753854040 | snp | C/G | 1.70965e-05 | 0.00292369 | intron-variant | TSG101 | GRCh38.p7 | 11:18481582 | TTGCAAGGTCAGTGC[C/G]TCTACAACCCAAGTT | 7251 |
rs753856455 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18523525 | TATTTGTTTTTGAGA[C/T]GGATTCTCGCTTTGT | 7251 |
rs753923576 | snp | A/G/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18482547 | GGGGATGAAAATGGA[A/G/T]CGTGAAATTGGCACT | 7251 |
rs754010710 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18505040 | TGAAATTAAGACAAC[C/T]CAGAAATGAAGTGTT | 7251 |
rs754026084 | snp | G/T | 1.64857e-05 | 0.00287099 | missense, utr-variant-5-prime | TSG101 | GRCh38.p7 | 11:18519599 | GTTAGGTCTCTGTAT[G/T]TGTACTGAAAAGCAA | 7251 |
rs754053197 | snp | C/T | 1.65353e-05 | 0.00287531 | missense | TSG101 | GRCh38.p7 | 11:18509647 | TGACCTGAATAAGCC[C/T]CAACAAGTCTGACTG | 7251 |
rs754197792 | snp | G/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18510190 | CTTTGGGAGGCCAAG[G/T]TGGGTGGACTGCTTG | 7251 |
rs754250254 | snp | C/T | 6.59163e-05 | 0.00574054 | missense | TSG101 | GRCh38.p7 | 11:18481785 | CGATATCATTGTTTT[C/T]AGACTGATTTTCCAT | 7251 |
rs754275688 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18493194 | AGCAAAACTTCCTTT[A/G]AATGTCAGGTAGGAT | 7251 |
rs754399845 | snp | A/G | 2.20548e-05 | 0.00332068 | intron-variant | TSG101 | GRCh38.p7 | 11:18526735 | GGCGCGGAAGGGAGC[A/G]GTGGGCGCGCCCTGG | 7251 |
rs754409831 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18496190 | AAATCCAGGCTGGGT[A/G]AGGTGGCTTATGCCT | 7251 |
rs754430771 | in-del | -/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18518929 | GTCTACAGACAACAC[-/T]TTGGGAAATGGACTA | 7251 |
rs754466530 | in-del | -/A | 1.64727e-05 | 0.00286986 | intron-variant | TSG101 | GRCh38.p7 | 11:18516172 | TTAAAAACTGAAAGG[-/A]AAAGAACAATGATTT | 7251 |
rs754511886 | snp | A/C | | | intron-variant | TSG101 | GRCh38.p7 | 11:18484133 | CTTCTATTTGTCTCA[A/C]AGGAACCTTCAGAAA | 7251 |
rs754558645 | snp | A/G | 1.64735e-05 | 0.00286993 | missense | TSG101 | GRCh38.p7 | 11:18484015 | AGTTTGTCACTGACC[A/G]CAGAGATGAGAGAGG | 7251 |
rs754562641 | snp | A/G | 1.64866e-05 | 0.00287106 | synonymous-codon, utr-variant-5-prime | TSG101 | GRCh38.p7 | 11:18519541 | ATCCAAAACAGGTTT[A/G]AGATCTTTGTATAGA | 7251 |
rs754597991 | snp | C/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18498299 | TCACTTGAAGGTTTT[C/G]AGCAGAGGAGTGATA | 7251 |
rs754650570 | snp | A/C/G | 4.95441e-05 | 0.00497694 | intron-variant | TSG101 | GRCh38.p7 | 11:18484098 | CAGAGGCAAAAAACA[A/C/G]TTGCTTACTTCCCAA | 7251 |
rs754731711 | in-del | -/AAG | 4.60236e-05 | 0.00479684 | utr-variant-3-prime, cds-indel | TSG101 | GRCh38.p7 | 11:18480511 | AGAGAAGAATACTTT[-/AAG]AAGAGCTCAACCTCC | 7251 |
rs754737344 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18482007 | AATGTTTCAAATAAC[A/G]CCCTGGTCAAAGGTA | 7251 |
rs754804545 | snp | A/C | | | intron-variant | TSG101 | GRCh38.p7 | 11:18503258 | ATATAATTTATAAAT[A/C]GGAGTCCTAAATTTG | 7251 |
rs754848981 | snp | C/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18521470 | ACCTCCTGGACTCAA[C/G]TGATACTCCCACCAC | 7251 |
rs754887074 | snp | C/T | 1.64887e-05 | 0.00287125 | missense | TSG101 | GRCh38.p7 | 11:18509557 | TATTTGGTGGCCCCG[C/T]TGCCTGGTATGGCGG | 7251 |
rs754936195 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18509919 | AAAATTCATAGAGTT[C/T]TGTTCTTCATTTGAC | 7251 |
rs754986671 | snp | A/T | | | downstream-variant-500B | LDHAL6A, TSG101 | GRCh38.p7 | 11:18480077 | ATTTAGTAGGGTTGG[A/T]AGGAGAGCATCTCCT | 7251 |
rs754986920 | snp | C/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18503326 | AACTCGAATATTTGA[C/G]AACTTCTAACATTTT | 7251 |
rs754993333 | snp | G/T | 1.65512e-05 | 0.00287669 | intron-variant | TSG101 | GRCh38.p7 | 11:18506954 | TTCACATTGTAAAAA[G/T]AATATACAAGGCCTG | 7251 |
rs755104810 | in-del | -/AAG | | | intron-variant | TSG101 | GRCh38.p7 | 11:18492803 | ACTAAGATCTGAAAT[-/AAG]AAAGTAAAAAAAGAA | 7251 |
rs755111364 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18506068 | GACCTCAGGTGATCC[A/G]CCTGCATCGGCCTCC | 7251 |
rs755172396 | snp | A/G | 2.35098e-05 | 0.00342846 | utr-variant-5-prime | TSG101 | GRCh38.p7 | 11:18526854 | TCCCCGCAGGCAGAG[A/G]GTCAGCCGCTGCTGG | 7251 |
rs755229303 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18515601 | CCAGGCTCTGTGCCA[C/T]GTCCTTTACATTCAT | 7251 |
rs755262285 | snp | A/G | 3.30327e-05 | 0.0040639 | intron-variant | TSG101 | GRCh38.p7 | 11:18506845 | ATTATTCAAAAGAAC[A/G]TTTTTCATTACCTGG | 7251 |
rs755275239 | snp | A/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18506363 | AATTCAGCCAAGGGG[A/T]AAAATATTTTATAAT | 7251 |
rs755326157 | snp | C/T | 1.8105e-05 | 0.00300868 | intron-variant | TSG101 | GRCh38.p7 | 11:18516200 | TTTAATCATGAGCAT[C/T]TTTTAAGATACTCCC | 7251 |
rs755333531 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18488383 | AGACTGATAGGCCTA[C/T]TATCAATTCTCTCCA | 7251 |
rs755448791 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18491638 | TAATAGCTTTCAGTG[A/G]GCTTTTAAAGTCCTT | 7251 |
rs755468599 | snp | C/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18507342 | CCAATTAGCACAGCT[C/G]ATTTTGTTGGTTTAA | 7251 |
rs755519757 | snp | G/T | 1.73411e-05 | 0.00294453 | intron-variant | TSG101 | GRCh38.p7 | 11:18516078 | AATGCATCTATGCTG[G/T]AAACCTAATAAGACA | 7251 |
rs755563843 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18526364 | GTCGGCAAAAGAAAG[A/G]CTAAGACTGGAGGAT | 7251 |
rs755603734 | snp | C/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18498434 | AGTAAATTAGATGAG[C/G]CATAATGGTGACTTG | 7251 |
rs755649588 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18512652 | ATTATCTTCTTCCAG[C/T]AAGGGTTCACCCTAT | 7251 |
rs755651526 | snp | A/G | 5.74718e-05 | 0.00536028 | intron-variant | TSG101 | GRCh38.p7 | 11:18502480 | CAAGTTTTCAAGGGT[A/G]CTTACCAACAGTGGT | 7251 |
rs755676325 | snp | A/G | 1.80211e-05 | 0.0030017 | intron-variant | TSG101 | GRCh38.p7 | 11:18514632 | AGATGCTAGTGAGCA[A/G]AATATATAAAACATA | 7251 |
rs755685722 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18482999 | AAATCTCAACTTGAA[C/T]TGTATCTCACAGAAA | 7251 |
rs755728026 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18499896 | TGAAATAGACAATAC[A/G]TTGTTAACTATAGTC | 7251 |
rs755776317 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18484173 | TATGAACCGACACTT[C/T]CAAAATGTGAGGAAA | 7251 |
rs755792993 | snp | G/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18499628 | ATGTTGGCCAGGCTG[G/T]TCTCCAACTCCTGAC | 7251 |
rs755845440 | in-del | -/TAGTT | 2.03602e-05 | 0.00319056 | intron-variant | TSG101 | GRCh38.p7 | 11:18480658 | GGAGAAAAGTTTGAA[-/TAGTT]TAGTTTAGAATGGCT | 7251 |
rs755906872 | snp | A/C | | | intron-variant | TSG101 | GRCh38.p7 | 11:18522463 | AATCTGTCAAAATAT[A/C]CTGTTAGCTTTGCCT | 7251 |
rs755954629 | snp | C/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18524312 | AGCTAAGATAATGCT[C/G]AAGGGAAAAAAAGAC | 7251 |
rs755992594 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18510580 | CTCAAATACCTATTG[A/G]GCACTGGCCAGGGGT | 7251 |
rs756015224 | snp | A/G | 1.64901e-05 | 0.00287137 | synonymous-codon | TSG101 | GRCh38.p7 | 11:18481639 | AAATACCTTCAGGAA[A/G]ACATCCAGGTCTATC | 7251 |
rs756034420 | snp | C/T | 1.64754e-05 | 0.00287009 | missense | TSG101 | GRCh38.p7 | 11:18481767 | TGGGAATGATAACTT[C/T]ATCGATATCATTGTT | 7251 |
rs756047536 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18511606 | TCCTTAACTAAATCA[C/T]AGCCTCATGTAAGCC | 7251 |
rs756055031 | snp | C/G | 1.65765e-05 | 0.00287888 | missense | TSG101 | GRCh38.p7 | 11:18514721 | TATATCTTCCCATTT[C/G]CATCAACATGCTTTC | 7251 |
rs756122505 | snp | C/G/T | 0.000106556 | 0.00729847 | missense | TSG101 | GRCh38.p7 | 11:18480566 | AGAGGTCACTGAGAC[C/G/T]GGCAGTCTTTCTTGC | 7251 |
rs756122723 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18515959 | TTACTGCCAAATGAA[C/T]TTCAATTTGAATAGA | 7251 |
rs756177151 | in-del | -/GTTA | | | intron-variant | TSG101 | GRCh38.p7 | 11:18508817 | AGATAAACAAGTTTG[-/GTTA]ATTATAATCTTAAAG | 7251 |
rs756197093 | in-del | -/A | | | intron-variant | TSG101 | GRCh38.p7 | 11:18485186 | AACAAACTCTAAGCC[-/A]TTCTAAACTAACAAA | 7251 |
rs756358482 | snp | C/T | 1.64985e-05 | 0.0028721 | missense | TSG101 | GRCh38.p7 | 11:18509544 | CAATTCTACTTACTA[C/T]TTGGTGGCCCCGTTG | 7251 |
rs756367549 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18504821 | CTAGCAATTGTTCAG[C/T]AGCCTTGTAATTTCA | 7251 |
rs756484096 | snp | A/C | 1.65299e-05 | 0.00287483 | intron-variant | TSG101 | GRCh38.p7 | 11:18484105 | AAAAAACACTTGCTT[A/C]CTTCCCAAGTTCCTT | 7251 |
rs756523473 | snp | G/T | 7.5838e-05 | 0.00615737 | intron-variant | TSG101 | GRCh38.p7 | 11:18516212 | CATTTTTTAAGATAC[G/T]CCCATAAGTTATTCT | 7251 |
rs756528609 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18509388 | TGGTGGGAATCTGTA[C/T]ATGCAGATGTGGGGC | 7251 |
rs756554622 | snp | A/G | | | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18527368 | TCATACACTTGCCTT[A/G]GATGATGCCCAGTGG | 7251 |
rs756608375 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18495015 | ACACATCATTCAGCT[A/G]CAGCATTTTCAGGGT | 7251 |
rs756608826 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18490725 | CATGCTACTCTCTCC[C/T]CATCTGCTGCTGTTT | 7251 |
rs756622322 | in-del | -/A | | | intron-variant | TSG101 | GRCh38.p7 | 11:18525541 | ACAGAGCAAGACTCT[-/A]AAAAAAAAAAAAAAA | 7251 |
rs756680638 | snp | C/T | 4.94556e-05 | 0.00497246 | missense, utr-variant-5-prime | TSG101 | GRCh38.p7 | 11:18519578 | ACATTGACAGTTTCA[C/T]GTACAGTTAGGTCTC | 7251 |
rs756685421 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18514589 | TATCTATCCTACCTC[A/G]AATCCTCCTTGAGTG | 7251 |
rs756695536 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18484405 | CCAACAAATGGCACA[A/G]TAATTTCCACTAAGG | 7251 |
rs756707264 | snp | A/C | | | intron-variant | TSG101 | GRCh38.p7 | 11:18514970 | CCCCATTCCTATTTC[A/C]CCCAGCAGAATTTAT | 7251 |
rs756777495 | snp | C/T | 1.7758e-05 | 0.00297972 | intron-variant | TSG101 | GRCh38.p7 | 11:18516049 | CTTTGGCAACATATT[C/T]ATTATGTATTCAAAA | 7251 |
rs756790887 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18485852 | TGGGGTGGGTCCCCG[A/G]TGAAACGCCACCTTC | 7251 |
rs756815708 | in-del | -/CTGA | | | intron-variant | TSG101 | GRCh38.p7 | 11:18516504 | CACGTGCCACCACAC[-/CTGA]CTAATTTTTTGTATC | 7251 |
rs756896777 | snp | A/G | 1.6537e-05 | 0.00287545 | synonymous-codon | TSG101 | GRCh38.p7 | 11:18514729 | CCCATTTGCATCAAC[A/G]TGCTTTCCTGTTTTA | 7251 |
rs756914586 | snp | A/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18520056 | AAATCCATACCCTTT[A/T]GCAATCACCCCCCAT | 7251 |
rs757048905 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18511842 | TAATCTACTTTCCAT[C/T]TCTATAGATTTGCTT | 7251 |
rs757097362 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18513183 | CAACCTAAGACTGCT[A/G]AAAACTTGGCTGATT | 7251 |
rs757102616 | in-del | -/ACGGATCACCTGAGGGCA | | | intron-variant | TSG101 | GRCh38.p7 | 11:18516714 | GAGAGGCCGAGGCAG[-/ACGGATCACCTGAGGGCA]GTGGATCACCTGAGG | 7251 |
rs757190197 | snp | C/T | 1.68852e-05 | 0.00290557 | intron-variant | TSG101 | GRCh38.p7 | 11:18481913 | AACTGTACATAATTA[C/T]CCACTTGTCAGACAC | 7251 |
rs757230650 | snp | A/G | 5.11143e-05 | 0.00505515 | utr-variant-5-prime | TSG101 | GRCh38.p7 | 11:18526862 | GGCAGAGGGTCAGCC[A/G]CTGCTGGGCTGCCCC | 7251 |
rs757262824 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18505151 | CTGCATTTATCCATG[A/G]GGATTATGACTGGGT | 7251 |
rs757401618 | snp | C/T | 1.74133e-05 | 0.00295065 | synonymous-codon | TSG101 | GRCh38.p7 | 11:18480576 | GAGACCGGCAGTCTT[C/T]CTTGCTTTTTGCATT | 7251 |
rs757406470 | snp | C/T | 1.64988e-05 | 0.00287213 | intron-variant | TSG101 | GRCh38.p7 | 11:18519618 | ACTGAAAAGCAAAAT[C/T]GCATAAGAATTTAGT | 7251 |
rs757432492 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18506054 | ACTCCTGACCTCAGG[A/G]CCTCAGGTGATCCGC | 7251 |
rs757435695 | snp | C/T | 1.65425e-05 | 0.00287593 | synonymous-codon | TSG101 | GRCh38.p7 | 11:18509651 | CTGAATAAGCCCCAA[C/T]AAGTCTGACTGTGGC | 7251 |
rs757495838 | snp | C/T | 1.70834e-05 | 0.00292257 | intron-variant | TSG101 | GRCh38.p7 | 11:18481584 | GCAAGGTCAGTGCCT[C/T]TACAACCCAAGTTAA | 7251 |
rs757556844 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18491272 | TTCTTTATCTACACC[A/G]GACAGTCTAACAGTG | 7251 |
rs757559053 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18524485 | TCAGACCACACCAGC[C/T]GAAAGGAAAACATTT | 7251 |
rs757581820 | in-del | -/TTCT | 4.97236e-05 | 0.00498591 | intron-variant | TSG101 | GRCh38.p7 | 11:18484119 | TACTTCCCAAGTTCC[-/TTCT]ATTTGTCTCACAGGA | 7251 |
rs757635777 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18481082 | AAGGGTGGCTGCTAT[C/T]ATCCCTAAAACCATG | 7251 |
rs757646599 | snp | C/T | 3.31411e-05 | 0.00407056 | intron-variant | TSG101 | GRCh38.p7 | 11:18484115 | TGCTTACTTCCCAAG[C/T]TCCTTCTATTTGTCT | 7251 |
rs757661362 | in-del | -/TT | | | intron-variant | TSG101 | GRCh38.p7 | 11:18504491 | TACTGAACACAGTAC[-/TT]TTGTTTCTAGTCTCT | 7251 |
rs757684589 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18496869 | GTTGAGGCAGGTGGT[A/G]AGGTCAGGAGTTGCA | 7251 |
rs757776357 | in-del | -/GT | | | intron-variant | TSG101 | GRCh38.p7 | 11:18483031 | GACCTGTGTGCGTGT[-/GT]GTGTGTGTGTGTAGC | 7251 |
rs757779563 | snp | A/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18518463 | TATTTTCAAGGAGAC[A/T]GGGTTGAAGAAATTA | 7251 |
rs757780860 | snp | A/G | 2.18448e-05 | 0.00330483 | intron-variant | TSG101 | GRCh38.p7 | 11:18526740 | GGAAGGGAGCGGTGG[A/G]CGCGCCCTGGGAGGC | 7251 |
rs757817001 | in-del | -/C | 4.33294e-05 | 0.00465434 | intron-variant | TSG101 | GRCh38.p7 | 11:18526744 | GGAGCGGTGGGCGCG[-/C]CCCTGGGAGGCGAGC | 7251 |
rs757827562 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18517455 | ATTAACACTATACCC[A/G]TAGAGGAAAGGTTGT | 7251 |
rs757851574 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18503824 | TGGTTAGTTAGACAA[C/T]AAATCTCAATTAATC | 7251 |
rs757859462 | snp | A/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18488448 | TCTCGTTAAAACACA[A/T]CTGAGAGTTGAGCTG | 7251 |
rs757862023 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18490862 | GAGTATTCATGCCTC[A/G]TTCTGTGACTGCCTT | 7251 |
rs757962331 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18493245 | TTAGGAAATAAGATA[C/T]AATTTTTCTAGTATT | 7251 |
rs757988983 | snp | C/T | 0.000123303 | 0.00785089 | intron-variant | TSG101 | GRCh38.p7 | 11:18516067 | TATGTATTCAAAATG[C/T]ATCTATGCTGGAAAC | 7251 |
rs757993824 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18510294 | GGTGTGGTGATGTGC[A/G]TCTATGGTCCCAGTT | 7251 |
rs758020478 | snp | A/G | 1.65559e-05 | 0.00287709 | intron-variant | TSG101 | GRCh38.p7 | 11:18483823 | AGAACACTCTGCCAT[A/G]GCTACAATTCAATCC | 7251 |
rs758020891 | snp | C/G | | | missense | TSG101 | GRCh38.p7 | 11:18509636 | TACCACAATCATGAC[C/G]TGAATAAGCCCCAAC | 7251 |
rs758080689 | snp | G/T | 1.77118e-05 | 0.00297583 | intron-variant | TSG101 | GRCh38.p7 | 11:18516187 | GAAAGAACAATGATT[G/T]AATCATGAGCATTTT | 7251 |
rs758130251 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18495365 | GCTATAAATCAACTA[C/T]AATCATCTATATAGC | 7251 |
rs758174886 | snp | C/T | 3.29799e-05 | 0.00406065 | missense | TSG101 | GRCh38.p7 | 11:18509553 | TTACTATTTGGTGGC[C/T]CCGTTGCCTGGTATG | 7251 |
rs758190694 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18500295 | ATAAATATGGGAGTA[C/T]AGGTATTCCTTTAAT | 7251 |
rs758323726 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18484755 | AAATAAACATCCTCT[A/G]GATATTTTCTTCAAA | 7251 |
rs758326897 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18486073 | CTGTAAGAAGCCGCA[A/G]GACTCAGCCACTTAG | 7251 |
rs758406330 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18524442 | CACCCTAGCTATGTG[C/T]TCAGGGTCCTGGCTA | 7251 |
rs758476122 | in-del | -/TAAC | | | intron-variant | TSG101 | GRCh38.p7 | 11:18481896 | CAGTCCAAGCATTAA[-/TAAC]TAACTGTACATAATT | 7251 |
rs758539266 | snp | A/C | | | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18526975 | TACGTCACTTCCGGG[A/C]CGCCGTCCTGCGGGC | 7251 |
rs758539923 | snp | A/G | 1.77963e-05 | 0.00298292 | missense | TSG101 | GRCh38.p7 | 11:18502540 | TTGTTGTGGCAGGAT[A/G]TGGACCACCAGGTGG | 7251 |
rs758563026 | in-del | -/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18500487 | CAATAACATTTGTTA[-/T]TTTTTTTATTTTTTG | 7251 |
rs758585840 | snp | C/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18524518 | AGCCCTTCTTTAGGA[C/G]GAAGGAGCCCCACAA | 7251 |
rs758638735 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18526209 | AAATACGCGTTATAA[A/G]AAGCATACACTTAAA | 7251 |
rs758655954 | in-del | -/AA | | | intron-variant | TSG101 | GRCh38.p7 | 11:18495923 | GTGAGACTCCGTCTC[-/AA]AAAAAAAAAAAAAAA | 7251 |
rs758660462 | snp | A/C | | | intron-variant | TSG101 | GRCh38.p7 | 11:18517555 | CATAAGAACACTGGT[A/C]CCATAAGATTATAAT | 7251 |
rs758685351 | in-del | -/CTGC | | | intron-variant | TSG101 | GRCh38.p7 | 11:18502026 | AAAGAAATTCTCTCA[-/CTGC]CTTAGTTTTTTTAGT | 7251 |
rs758688206 | snp | A/G | 6.32424e-05 | 0.00562292 | intron-variant | TSG101 | GRCh38.p7 | 11:18526753 | GGGCGCGCCCTGGGA[A/G]GCGAGCGCGTCGCAG | 7251 |
rs758769890 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18482860 | GGCTTAGAACTCTCT[A/G]AACTTATTTCCTAGT | 7251 |
rs758771462 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18512167 | CCCAGCACTTTGGGA[A/G]GCTGAGGCGGACGGA | 7251 |
rs758803525 | in-del | -/TGTT | 1.64732e-05 | 0.0028699 | frameshift-variant | TSG101 | GRCh38.p7 | 11:18481733 | TACAGATTCAGGATC[-/TGTT]TGTATAAGGGAGCTG | 7251 |
rs758854845 | snp | A/C | | | intron-variant | TSG101 | GRCh38.p7 | 11:18505360 | CTGTAGGCTCAAGTG[A/C]TCCTTCCACCTCACC | 7251 |
rs758888331 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18518401 | CAGAGCTAAGGGACT[C/T]ACAATGGACAAGCAG | 7251 |
rs758890817 | in-del | -/TATAT | | | intron-variant | TSG101 | GRCh38.p7 | 11:18484707 | TCCCTTCCTAATCAG[-/TATAT]TATATCATTTCCATG | 7251 |
rs758892704 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18513839 | CAGCACTTTAGAAGG[C/T]CGAGATGGGTGGATC | 7251 |
rs758909236 | snp | C/T | 1.6543e-05 | 0.00287597 | intron-variant | TSG101 | GRCh38.p7 | 11:18506834 | TTTGTAATACAATTA[C/T]TCAAAAGAACGTTTT | 7251 |
rs758942038 | snp | A/G | 2.03275e-05 | 0.003188 | missense, utr-variant-5-prime | TSG101 | GRCh38.p7 | 11:18526812 | TGGCTCTCCGACACC[A/G]CCATGACGGCCGCCT | 7251 |
rs759020495 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18523994 | CAGAGTCTAGCTATG[C/T]TGCCCAGGCTGATCC | 7251 |
rs759022526 | snp | C/T | 4.03902e-05 | 0.00449371 | intron-variant | TSG101 | GRCh38.p7 | 11:18502471 | GGTGAAACACAAGTT[C/T]TCAAGGGTACTTACC | 7251 |
rs759070458 | snp | A/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18511551 | TGTGGGGATGGCCAC[A/T]GAGACCACATGCTTT | 7251 |
rs759073245 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18522324 | AACTGAACTCCTCAT[C/T]TTCTCCCCAAATTTA | 7251 |
rs759103049 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18499079 | GTTTAAGAGAAAAAC[A/G]GAGAAGAGGTACTGA | 7251 |
rs759110432 | snp | A/G | 1.8851e-05 | 0.00307004 | missense | TSG101 | GRCh38.p7 | 11:18502569 | GGGTAAGGACAGCCT[A/G]GGTAACCACTAAAGA | 7251 |
rs759147421 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18525445 | CAGCTACTTGGGAGG[C/T]TAAGGCAGGAGAATC | 7251 |
rs759212682 | snp | C/T | 1.65806e-05 | 0.00287924 | intron-variant | TSG101 | GRCh38.p7 | 11:18519650 | TAAAACCAATGCATA[C/T]ATTTTACAGCTGGAT | 7251 |
rs759274118 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18511391 | GATGACAATTAATAA[C/T]ATTTCTCAAAGCTTT | 7251 |
rs759318487 | snp | C/T | 3.39305e-05 | 0.00411875 | intron-variant | TSG101 | GRCh38.p7 | 11:18514872 | AAACTTCAGTTACTC[C/T]ATTTTTATTATTTTT | 7251 |
rs759319077 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18482164 | AGCCATCAGACAAGA[C/T]ACTTTCCAGCAGAAG | 7251 |
rs759357018 | snp | A/C | 1.68386e-05 | 0.00290155 | synonymous-codon | TSG101 | GRCh38.p7 | 11:18514699 | CCATTCATGTAGATA[A/C]GGAAGATATATCTTC | 7251 |
rs759413781 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18517867 | GAATGTAAGCTATAC[C/T]GCAATGTATTCTGAT | 7251 |
rs759416085 | in-del | -/GGT | | | intron-variant | TSG101 | GRCh38.p7 | 11:18483073 | GGGATGGCACGCAGG[-/GGT]GGTGGTAATTGAATC | 7251 |
rs759611597 | snp | G/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18509473 | CATTATTTTTCTTTA[G/T]TTTTTTACAAAGGTT | 7251 |
rs759670197 | in-del | -/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18520183 | ATTTCACTTAGCATG[-/T]TTTTGAGATTATCCA | 7251 |
rs759722609 | snp | A/C | | | intron-variant | TSG101 | GRCh38.p7 | 11:18494610 | AAACTCTCAGCATTT[A/C]AATTTCACTCATGAC | 7251 |
rs759795711 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18492273 | ACCTAAATGATATGT[C/T]TATAATTAAGCATTC | 7251 |
rs759799363 | snp | A/C/G | 0.000296557 | 0.0121735 | synonymous-codon | TSG101 | GRCh38.p7 | 11:18481657 | ATCCAGGTCTATCAC[A/C/G]CCCCTTCTCAAGGCT | 7251 |
rs759851267 | snp | A/G | 1.64743e-05 | 0.00287 | missense | TSG101 | GRCh38.p7 | 11:18484054 | GTGTCCTCGCTGATT[A/G]TGCCATCCCTACTGG | 7251 |
rs760078502 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18520820 | GGCGGATCACGAGGT[C/T]AGGAGTTCGAGACCA | 7251 |
rs760083082 | snp | C/T | | | utr-variant-5-prime | TSG101 | GRCh38.p7 | 11:18526886 | CTGCCCCAGACCGTC[C/T]CACACAATCGCACAC | 7251 |
rs760124493 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18516608 | CTTGGCCTCCCAAAG[C/T]GCTGGGATTACAGGT | 7251 |
rs760127148 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18521796 | ATCCTCCCATCTCAG[C/T]CTTCCAAGTAGCTGG | 7251 |
rs760134500 | in-del | -/AAA | | | intron-variant | TSG101 | GRCh38.p7 | 11:18483492 | AAGAGTGAAACTCTC[-/AAA]AAAAAAAAAAAAAAA | 7251 |
rs760139840 | snp | C/T | 2.20738e-05 | 0.00332211 | utr-variant-3-prime | TSG101 | GRCh38.p7 | 11:18480521 | ACTTTAAGAAGAGCT[C/T]AACCTCCAGCTGGTA | 7251 |
rs760158993 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18513035 | ACCCAGCCTCAAGGA[C/T]AGATTTTTATAAGGC | 7251 |
rs760211131 | snp | C/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18501699 | TCTACAGACTGCTTT[C/G]GGTAATATAGTCATT | 7251 |
rs760296077 | in-del | -/A | | | downstream-variant-500B | TSG101 | GRCh38.p7 | 11:18480108 | GGACCTTTCACAGAT[-/A]AAGTTACTCAAATGC | 7251 |
rs760337120 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18501048 | CCTCACCTCAAATGA[C/T]TCGCCCGCCTTGGCT | 7251 |
rs760377157 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18505913 | ACCTCTGCCTCCTGG[A/G]TTCAAGCAATTCTCC | 7251 |
rs760396916 | snp | C/T | 2.47204e-05 | 0.00351562 | intron-variant | TSG101 | GRCh38.p7 | 11:18502600 | CAAGAACAAAAAACA[C/T]TTAACATTTAAGATG | 7251 |
rs760399464 | in-del | -/G | 1.80279e-05 | 0.00300227 | intron-variant | TSG101 | GRCh38.p7 | 11:18514629 | AGCAGATGCTAGTGA[-/G]CAAAATATATAAAAC | 7251 |
rs760521615 | snp | C/T | 1.69838e-05 | 0.00291404 | missense, utr-variant-5-prime | TSG101 | GRCh38.p7 | 11:18516153 | GTTCCCTGGAACTGC[C/T]ATCGTTAAAAACTGA | 7251 |
rs760523726 | snp | A/G | 3.34582e-05 | 0.00408999 | intron-variant | TSG101 | GRCh38.p7 | 11:18481889 | AAACAGAACAGTCCA[A/G]GCATTAATAACTGTA | 7251 |
rs760656065 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18513238 | TTTTTTAGCATCTTA[C/T]CTTTGAAGCTCAGGA | 7251 |
rs760664470 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18525634 | TTTCAAAAAGTGATA[C/T]ATAAAAGTTACAACA | 7251 |
rs760720427 | in-del | -/A | | | intron-variant | TSG101 | GRCh38.p7 | 11:18508623 | AGAAATAGTAATCCT[-/A]AAAATCAAGCTTATT | 7251 |
rs760721135 | snp | A/C | 1.65326e-05 | 0.00287507 | synonymous-codon | TSG101 | GRCh38.p7 | 11:18509645 | CATGACCTGAATAAG[A/C]CCCAACAAGTCTGAC | 7251 |
rs760721944 | snp | C/T | 1.6947e-05 | 0.00291088 | intron-variant | TSG101 | GRCh38.p7 | 11:18514876 | TTCAGTTACTCTATT[C/T]TTATTATTTTTAAAT | 7251 |
rs760815669 | snp | A/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18517949 | TACTCTAAAAGTATT[A/T]GTTAACAATGATTTA | 7251 |
rs760829074 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18482345 | CTGGTTGTAGGCTCT[A/G]AGTTGTATTGGTGTC | 7251 |
rs760846282 | snp | A/C | | | intron-variant | TSG101 | GRCh38.p7 | 11:18483408 | GGCTGAGTCAGGAGA[A/C]TCGCTTGAACCTGGA | 7251 |
rs760904772 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18517255 | GGACTCAAATGGTCT[C/T]CTGGCCTCAGCCTCC | 7251 |
rs760932042 | snp | A/G | 4.45087e-05 | 0.00471724 | intron-variant | TSG101 | GRCh38.p7 | 11:18526729 | CGACAGGGCGCGGAA[A/G]GGAGCGGTGGGCGCG | 7251 |
rs760980448 | in-del | -/AGG | | | downstream-variant-500B | LDHAL6A, TSG101 | GRCh38.p7 | 11:18480078 | TTTAGTAGGGTTGGT[-/AGG]AGAGCATCTCCTTGG | 7251 |
rs761051037 | snp | G/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18523436 | GTTTCTTTGTCTGAT[G/T]GTTCACTGTTGCATC | 7251 |
rs761098088 | snp | A/G | 1.64735e-05 | 0.00286993 | synonymous-codon | TSG101 | GRCh38.p7 | 11:18481693 | CAAGTAAAAGATAGT[A/G]TCTTCAATAGCGTTT | 7251 |
rs761098846 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18521853 | GGCTAATTTTTGTAT[A/G]TTTTTGATAGAGCTG | 7251 |
rs761227615 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18510150 | TTCTAGCCAAGTGAG[A/G]TGGTTCACACCTGTA | 7251 |
rs761270028 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18502871 | CAATCCAACAGCATC[A/G]GAAGCAACAAGTAAT | 7251 |
rs761366222 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18504925 | CCTGCTTATATATTA[C/T]TACCAAAGGAATCTT | 7251 |
rs761501844 | snp | A/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18488271 | TTGGTTTGTTTTAAA[A/T]CAGTGCATGAGGTTT | 7251 |
rs761590019 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18508498 | CCCGGCCAAATATTT[C/T]GTATTTCAAACTTAA | 7251 |
rs761650823 | in-del | -/TT | 1.73607e-05 | 0.00294619 | frameshift-variant | TSG101 | GRCh38.p7 | 11:18480612 | CCTCAGCTGGAACTG[-/TT]TACGGGACAGAAGAC | 7251 |
rs761716911 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18493863 | TTTTTATTTATAGTG[C/T]ATGAATATGTAAGCT | 7251 |
rs761782313 | in-del | -/AAA | | | intron-variant | TSG101 | GRCh38.p7 | 11:18497104 | AAAAACAACAACAAC[-/AAA]AAAAACAAGGATAAA | 7251 |
rs761797649 | snp | A/C | | | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18527002 | GGGCAAGGGTGGACA[A/C]CGTGTGGGATTGAGA | 7251 |
rs761806798 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18489567 | GAAAAGGGGATTTAG[C/T]CAGGTGTGTTATATG | 7251 |
rs761815110 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18514310 | CACTATCAGACACAT[A/G]AACAGAAGTTCCCTA | 7251 |
rs761833641 | snp | A/G | 1.6504e-05 | 0.00287258 | intron-variant | TSG101 | GRCh38.p7 | 11:18519495 | CAAAGTATAGAAATT[A/G]CTATTTTTACTGCAT | 7251 |
rs761844917 | in-del | -/C | 1.65444e-05 | 0.00287609 | intron-variant | TSG101 | GRCh38.p7 | 11:18509527 | GTTTTAAAGTAAAAT[-/C]TCAATTCTACTTACT | 7251 |
rs761853544 | snp | C/T | 1.64735e-05 | 0.00286993 | missense | TSG101 | GRCh38.p7 | 11:18481739 | TTCAGGATCTGTTTG[C/T]ATAAGGGAGCTGTGG | 7251 |
rs761859795 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18518217 | GAAGGAATCGTGTCC[C/T]AGGTTTGGAAGAGGA | 7251 |
rs761923334 | snp | A/G | 1.65622e-05 | 0.00287764 | intron-variant | TSG101 | GRCh38.p7 | 11:18514844 | TTGTATGTATTACCT[A/G]AAAAAGAAATAGAAA | 7251 |
rs761999962 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18515134 | AATAGTGGCTCAAAT[A/G]TCACTTCCTCTGTGA | 7251 |
rs762037508 | snp | A/C | | | intron-variant | TSG101 | GRCh38.p7 | 11:18507184 | TTAAAGTTCTCAAGA[A/C]GTCTATTACCTAAGA | 7251 |
rs762059198 | snp | C/T | 0.000357551 | 0.0133659 | intron-variant | TSG101 | GRCh38.p7 | 11:18502627 | GATGACCCAACCTTA[C/T]AGTATTTTGAAGAAC | 7251 |
rs762153923 | in-del | -/CAT | | | intron-variant | TSG101 | GRCh38.p7 | 11:18517355 | TTCTCATACCACACA[-/CAT]TTTTCTATCTATAAT | 7251 |
rs762308659 | snp | G/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18498102 | GGGGGGATTGGTGGT[G/T]GTGGCAGCAAATTGG | 7251 |
rs762363527 | snp | A/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18504344 | TTATAACTTGTCCTC[A/T]ACTAAGTTTTATATA | 7251 |
rs762394157 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18489524 | AGCACAAGTTGCAAA[C/T]TGGTAACAAAGTGAA | 7251 |
rs762439860 | snp | C/T | 2.20787e-05 | 0.00332248 | utr-variant-5-prime | TSG101 | GRCh38.p7 | 11:18526840 | CCTGGCGACTCCCTT[C/T]CCCGCAGGCAGAGGG | 7251 |
rs762636458 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18481278 | TAACAGATAAAAAAT[A/G]GAGGTGGCACAATCA | 7251 |
rs762666488 | snp | A/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18495761 | AGTTTTCAAAACACT[A/T]TGTAAACTGAGGTTG | 7251 |
rs762669001 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18523647 | AGCTGGGATTACAGG[C/T]GTGCGCCACCATGTC | 7251 |
rs762700904 | snp | C/G | 1.78217e-05 | 0.00298505 | missense | TSG101 | GRCh38.p7 | 11:18480628 | TTACGGGACAGAAGA[C/G]GTACATGCTGGGAGG | 7251 |
rs762822847 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18481442 | ACTTCTCTTCCCCTG[C/T]TCAGACCAATCCTCA | 7251 |
rs762942545 | snp | C/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18515303 | ACATCCTTTATTCAT[C/G]TTTGTAGCCACAGCT | 7251 |
rs762961723 | snp | G/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18502977 | AACCTTTGGGGATAT[G/T]TAACCCGAAAACACT | 7251 |
rs763059585 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18508734 | TTCCTCAGGAAAGAA[C/T]GGATTAAAAAGGAAA | 7251 |
rs763082836 | snp | A/C | | | intron-variant | TSG101 | GRCh38.p7 | 11:18489711 | TTTGAGTGGCAACAG[A/C]CCAAACAGGTCAAGT | 7251 |
rs763099765 | snp | G/T | 1.66715e-05 | 0.00288712 | intron-variant | TSG101 | GRCh38.p7 | 11:18481879 | CTCGGCCTGAAAACA[G/T]AACAGTCCAAGCATT | 7251 |
rs763182535 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18494008 | AAAGTTTCTATCAAC[A/G]CAATCAATAAGAAAA | 7251 |
rs763239468 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18516225 | ACTCCCATAAGTTAT[C/T]CTTTCAGAAAGACTG | 7251 |
rs763337724 | snp | A/G | | | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18527190 | CTAGTGCCGGAGAGG[A/G]AAGAAGTACGAAGGG | 7251 |
rs763367848 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18499761 | ATTTACGTGGGTACC[A/G]TGTGATATTTTGTTA | 7251 |
rs763370355 | snp | A/C | | | intron-variant | TSG101 | GRCh38.p7 | 11:18519729 | TGAAAGAACCTAAAA[A/C]ACCCATAATACTATT | 7251 |
rs763381077 | snp | A/G | 1.65974e-05 | 0.0028807 | intron-variant | TSG101 | GRCh38.p7 | 11:18509512 | CTTTTGTTTATATGA[A/G]TTTTAAAGTAAAATC | 7251 |
rs763471256 | snp | A/C | 2.31908e-05 | 0.00340512 | utr-variant-3-prime | TSG101 | GRCh38.p7 | 11:18480507 | AGGAAGAGAAGAATA[A/C]TTTAAGAAGAGCTCA | 7251 |
rs763612554 | snp | A/C | 8.42637e-05 | 0.00649036 | intron-variant | TSG101 | GRCh38.p7 | 11:18502611 | AACATTTAACATTTA[A/C]GATGACCCAACCTTA | 7251 |
rs763619685 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18499946 | CATTAGAACTTATTC[C/T]TTCTATCTAACTGTA | 7251 |
rs763638354 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18504568 | GAAATTTCTAAATCC[A/G]CCTTTCTGAAAACTG | 7251 |
rs763663682 | snp | A/C | | | intron-variant | TSG101 | GRCh38.p7 | 11:18485807 | GGATTTCATTAACAG[A/C]AACAGGAGGCAGCCA | 7251 |
rs763672520 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18501051 | CACCTCAAATGATTC[A/G]CCCGCCTTGGCTTCC | 7251 |
rs763878103 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18519934 | ATAATTCACATACCA[C/T]ATAATTCACACATTT | 7251 |
rs763925768 | snp | C/T | | | intron-variant, utr-variant-5-prime | TSG101 | GRCh38.p7 | 11:18525700 | CCCATATGTCTTCTA[C/T]AACTAAGGATAACAA | 7251 |
rs763982196 | snp | A/G | 3.29451e-05 | 0.00405851 | missense | TSG101 | GRCh38.p7 | 11:18483971 | GCTCTGCCTGGGCAC[A/G]ATCCATTTCCTCCTT | 7251 |
rs764076215 | in-del | -/TTT | | | intron-variant | TSG101 | GRCh38.p7 | 11:18484936 | ACCTTAATTGCCGCC[-/TTT]TTTTTTTTTTTTTTT | 7251 |
rs764088575 | snp | A/G | 1.70883e-05 | 0.00292299 | intron-variant | TSG101 | GRCh38.p7 | 11:18514888 | ATTTTTATTATTTTT[A/G]AATTGAAGAATGGTT | 7251 |
rs764128152 | in-del | -/AG | 1.96358e-05 | 0.00313329 | utr-variant-3-prime | TSG101 | GRCh38.p7 | 11:18480539 | CCTCCAGCTGGTATC[-/AG]AGAAGTCAGTAGAGG | 7251 |
rs764132199 | snp | A/G | | | utr-variant-5-prime | TSG101 | GRCh38.p7 | 11:18526890 | CCCAGACCGTCCCAC[A/G]CAATCGCACACCCCC | 7251 |
rs764176027 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18517381 | CTATAATTTATGTCT[A/G]TAATTAATATGGCAC | 7251 |
rs764184672 | snp | A/G | 1.67784e-05 | 0.00289636 | intron-variant | TSG101 | GRCh38.p7 | 11:18481896 | ACAGTCCAAGCATTA[A/G]TAACTGTACATAATT | 7251 |
rs764218151 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18511611 | AACTAAATCATAGCC[C/T]CATGTAAGCCTCATG | 7251 |
rs764269969 | snp | G/T | 1.64925e-05 | 0.00287158 | missense | TSG101 | GRCh38.p7 | 11:18509548 | TCTACTTACTATTTG[G/T]TGGCCCCGTTGCCTG | 7251 |
rs764300635 | snp | A/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18517989 | CAGCCACATGAAACT[A/T]TACAAGACTTTATAA | 7251 |
rs764355865 | snp | C/T | 1.65359e-05 | 0.00287536 | missense | TSG101 | GRCh38.p7 | 11:18509646 | ATGACCTGAATAAGC[C/T]CCAACAAGTCTGACT | 7251 |
rs764428601 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18505929 | TTCAAGCAATTCTCC[C/T]ACCTCAGCCTCCCAA | 7251 |
rs764538057 | snp | C/T | 1.64735e-05 | 0.00286993 | missense | TSG101 | GRCh38.p7 | 11:18481704 | TAGTGTCTTCAATAG[C/T]GTTTTCTTCTGCATA | 7251 |
rs764630541 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18496760 | GACAGCACTGCTGCA[C/T]TCCAGCCTGAGCAAG | 7251 |
rs764687924 | in-del | -/CAG | 4.94548e-05 | 0.00497242 | cds-indel | TSG101 | GRCh38.p7 | 11:18519582 | TGACAGTTTCACGTA[-/CAG]TTAGGTCTCTGTATT | 7251 |
rs764727874 | snp | A/G | 4.4195e-05 | 0.00470059 | intron-variant | TSG101 | GRCh38.p7 | 11:18526731 | ACAGGGCGCGGAAGG[A/G]AGCGGTGGGCGCGCC | 7251 |
rs764756879 | snp | A/C | | | intron-variant | TSG101 | GRCh38.p7 | 11:18498038 | CAACAGCAAACTTCT[A/C]TATACCAAGCACTCT | 7251 |
rs764766346 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18485897 | CTGAAGGCTGAAAGA[C/T]TGGACTGCTGGTCCC | 7251 |
rs764774617 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18518434 | GCATGGGTTTTCCCT[C/T]GGCCCTGGCATATTA | 7251 |
rs764815398 | snp | C/T | 1.75032e-05 | 0.00295826 | intron-variant | TSG101 | GRCh38.p7 | 11:18516179 | ACTGAAAGGAAAGAA[C/T]AATGATTTAATCATG | 7251 |
rs764835670 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18502904 | GTGAGAGAACTTTTC[C/T]GATTTCTCAGTCTGT | 7251 |
rs764856545 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18488445 | GGGTCTCGTTAAAAC[A/G]CATCTGAGAGTTGAG | 7251 |
rs764908768 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18493872 | ATAGTGTATGAATAT[A/G]TAAGCTTCTAATACT | 7251 |
rs764927163 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18502123 | TCAATCATTTGTCTG[A/G]TTTGACCTGCTCATA | 7251 |
rs765026617 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18509458 | AAAAAGCAAAGAAGT[C/T]ATTATTTTTCTTTAT | 7251 |
rs765046110 | snp | C/T | 1.65031e-05 | 0.00287251 | intron-variant | TSG101 | GRCh38.p7 | 11:18519496 | AAAGTATAGAAATTG[C/T]TATTTTTACTGCATA | 7251 |
rs765064874 | snp | C/T | | | synonymous-codon | TSG101 | GRCh38.p7 | 11:18480582 | GGCAGTCTTTCTTGC[C/T]TTTTGCATTAGTGCC | 7251 |
rs765082886 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18514349 | CTTGACAGAAATGCT[C/T]TGAGTAATCAGATTT | 7251 |
rs765138138 | snp | C/G | 1.64818e-05 | 0.00287065 | intron-variant | TSG101 | GRCh38.p7 | 11:18484076 | CCCTACTGGGACCTG[C/G]AGGAAACAGAGGCAA | 7251 |
rs765168236 | in-del | -/A | | | intron-variant | TSG101 | GRCh38.p7 | 11:18514086 | TAAAACTCTGTCTCC[-/A]AAAAAAAAAAAAGGA | 7251 |
rs765179537 | snp | C/T | 1.64727e-05 | 0.00286986 | synonymous-codon | TSG101 | GRCh38.p7 | 11:18483999 | CTTCATCCGCCATCT[C/T]AGTTTGTCACTGACC | 7251 |
rs765269806 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18515199 | CATAGCACTTTTTCA[C/T]TTTATAATTCTATAG | 7251 |
rs765321516 | snp | C/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18519388 | TTTGCTACCCTCCAA[C/G]AGTTTTATTAGGCGG | 7251 |
rs765347416 | snp | C/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18487866 | AGGAAGCTTTTGGTA[C/G]ATCTTTTTTTTTTGT | 7251 |
rs765407538 | snp | C/T | 5.12055e-05 | 0.00505965 | intron-variant | TSG101 | GRCh38.p7 | 11:18481585 | CAAGGTCAGTGCCTC[C/T]ACAACCCAAGTTAAA | 7251 |
rs765496019 | snp | C/T | 1.64738e-05 | 0.00286995 | synonymous-codon | TSG101 | GRCh38.p7 | 11:18481741 | CAGGATCTGTTTGTA[C/T]AAGGGAGCTGTGGGA | 7251 |
rs765507693 | snp | C/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18511989 | ATTCATACATTCTTA[C/G]AGTTTTGTCAAGGTA | 7251 |
rs765553606 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18492674 | TCACCTGAGGAAGTT[A/G]CAAACACCAAGATTA | 7251 |
rs765702652 | snp | A/C | 1.64879e-05 | 0.00287118 | missense | TSG101 | GRCh38.p7 | 11:18506908 | ATTCCACCTGGCATG[A/C]CTGGCATGTAGGAAG | 7251 |
rs765727428 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18498157 | GCACAGAAATAGGCC[A/G]TGGACAAATCCTAAG | 7251 |
rs765775714 | snp | C/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18518299 | TGTTGCTTCCCACCT[C/G]TCTTCACCAGTTTCC | 7251 |
rs765807675 | in-del | -/AA | | | intron-variant | TSG101 | GRCh38.p7 | 11:18498494 | ATATATTTTGAAGAC[-/AA]GAGGATTTCCTGATG | 7251 |
rs765809194 | snp | A/G | 6.82664e-05 | 0.00584196 | utr-variant-5-prime | TSG101 | GRCh38.p7 | 11:18526847 | ACTCCCTTCCCCGCA[A/G]GCAGAGGGTCAGCCG | 7251 |
rs765827382 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18482575 | ACTTCAATTATGCTG[A/G]TGCTTCCACTTTATC | 7251 |
rs765904783 | snp | A/G | 0.000111597 | 0.007469 | intron-variant | TSG101 | GRCh38.p7 | 11:18502628 | ATGACCCAACCTTAT[A/G]GTATTTTGAAGAACC | 7251 |
rs765985048 | snp | C/T | 1.78784e-05 | 0.00298979 | intron-variant | TSG101 | GRCh38.p7 | 11:18516193 | ACAATGATTTAATCA[C/T]GAGCATTTTTTAAGA | 7251 |
rs766081128 | snp | A/G | 1.64914e-05 | 0.00287149 | intron-variant | TSG101 | GRCh38.p7 | 11:18519511 | CTATTTTTACTGCAT[A/G]AACTCACCATATGAA | 7251 |
rs766096868 | in-del | -/AGAAAT | 1.6591e-05 | 0.00288015 | intron-variant | TSG101 | GRCh38.p7 | 11:18514849 | TGTATTACCTGAAAA[-/AGAAAT]AGAAACTTCAGTTAC | 7251 |
rs766102615 | snp | A/G | 4.9826e-05 | 0.00499104 | intron-variant | TSG101 | GRCh38.p7 | 11:18509671 | CTGACTGTGGCTACA[A/G]AATGAAAAAAAATTC | 7251 |
rs766117798 | snp | G/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18481470 | TCAGTACTCTGTAGG[G/T]AAAAAGATGGTGCAA | 7251 |
rs766299107 | snp | G/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18515435 | TCCAAAAACAAAATG[G/T]TCTCTCATTAAGCTA | 7251 |
rs766350434 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18503149 | AGGTATTCTACTCCA[A/G]TCACCTTTCCAACAA | 7251 |
rs766474590 | snp | A/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18492741 | GTGAAGTATATCTAA[A/T]CTTTAAAAAATCGAA | 7251 |
rs766479880 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18504402 | TGGTACTTCTCTTAT[A/G]TATCAGTATAAAAGC | 7251 |
rs766581720 | snp | A/T | 3.33622e-05 | 0.00408412 | intron-variant | TSG101 | GRCh38.p7 | 11:18481881 | CGGCCTGAAAACAGA[A/T]CAGTCCAAGCATTAA | 7251 |
rs766595126 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18480711 | ATAGACAATTTGTAA[C/T]CTAGATGGGATCTAA | 7251 |
rs766692591 | snp | A/T | | | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18527256 | GGGAGGGCACTGCAC[A/T]GGCGGTCAGAGAACT | 7251 |
rs766745878 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18514600 | CCTCGAATCCTCCTT[A/G]AGTGCTAAAAGAAAG | 7251 |
rs766763861 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18513860 | TGGGTGGATCACTTG[A/G]GGTCAGGAGTTCGAG | 7251 |
rs766861182 | in-del | -/AAG | | | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18528187 | ATGTCTTTTAAAAGC[-/AAG]AAGGTTTTCAAACTG | 7251 |
rs766890688 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18485642 | CTCTCCAAAATAAAT[A/G]GTATGGTGGTATTAA | 7251 |
rs766900773 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18519854 | ATAAAGTCCACACAT[C/T]GCATTGGTTAAAACG | 7251 |
rs766957180 | snp | A/G | 1.65002e-05 | 0.00287225 | synonymous-codon | TSG101 | GRCh38.p7 | 11:18506922 | GCCTGGCATGTAGGA[A/G]GCTAAAAACAATTTT | 7251 |
rs766961767 | snp | G/T | 1.65952e-05 | 0.00288051 | intron-variant | TSG101 | GRCh38.p7 | 11:18509513 | TTTTGTTTATATGAG[G/T]TTTAAAGTAAAATCT | 7251 |
rs767032606 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18511552 | GTGGGGATGGCCACT[A/G]AGACCACATGCTTTC | 7251 |
rs767085790 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18512875 | TGGGATTATAGACAT[A/G]TGCCATCATGCCTGG | 7251 |
rs767127783 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18498309 | GTTTTGAGCAGAGGA[A/G]TGATACAATTTATTT | 7251 |
rs767212352 | snp | C/G | 1.95904e-05 | 0.00312966 | intron-variant | TSG101 | GRCh38.p7 | 11:18502476 | AACACAAGTTTTCAA[C/G]GGTACTTACCAACAG | 7251 |
rs767238843 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18483545 | CACCATGATTCTGAG[A/G]TCTCCCCAGCCATGT | 7251 |
rs767278501 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18522360 | CCAGTGTCTTCCATA[C/T]GTGTATACATACATA | 7251 |
rs767364164 | in-del | -/A | 3.32668e-05 | 0.00407827 | intron-variant | TSG101 | GRCh38.p7 | 11:18509676 | TGTGGCTACAAAATG[-/A]AAAAAAATTCAAGTC | 7251 |
rs767449913 | in-del | -/G | 1.85036e-05 | 0.00304162 | intron-variant | TSG101 | GRCh38.p7 | 11:18480638 | GAAGACGTACATGCT[-/G]GGAGGGGAGAAAAGT | 7251 |
rs767572469 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18491052 | ACTCCTCTGGCAGCG[A/G]TGGCGGTGCCTGCCG | 7251 |
rs767623706 | snp | C/T | 1.67279e-05 | 0.002892 | missense | TSG101 | GRCh38.p7 | 11:18514706 | TGTAGATAAGGAAGA[C/T]ATATCTTCCCATTTG | 7251 |
rs767709099 | snp | A/C/T | 1.64738e-05 | 0.00286995 | missense | TSG101 | GRCh38.p7 | 11:18481749 | GTTTGTATAAGGGAG[A/C/T]TGTGGGAATGATAAC | 7251 |
rs767826745 | snp | A/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18517112 | AGGCTATCCTCAAAC[A/T]CTAGGCTCAAGCAAT | 7251 |
rs767870730 | snp | C/G | 1.91977e-05 | 0.00309814 | utr-variant-3-prime | TSG101 | GRCh38.p7 | 11:18480542 | CCAGCTGGTATCAGA[C/G]AAGTCAGTAGAGGTC | 7251 |
rs767941675 | snp | C/T | 3.29717e-05 | 0.00406015 | synonymous-codon, utr-variant-5-prime | TSG101 | GRCh38.p7 | 11:18519553 | TTTGAGATCTTTGTA[C/T]AGAGTAATAACATTG | 7251 |
rs767960651 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18510078 | ATATCTTGGAAATAC[A/G]TGTTCTTAAAATTAA | 7251 |
rs768025271 | snp | A/G | 3.30202e-05 | 0.00406313 | missense | TSG101 | GRCh38.p7 | 11:18509628 | TCTCCAAATACCACA[A/G]TCATGACCTGAATAA | 7251 |
rs768068077 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18509234 | TATATGTGCTTCCAA[A/G]CTGATCAAATAAGGC | 7251 |
rs768117587 | snp | G/T | 2.03867e-05 | 0.00319264 | intron-variant | TSG101 | GRCh38.p7 | 11:18480656 | AGGGGAGAAAAGTTT[G/T]AATAGTTTAGAATGG | 7251 |
rs768123462 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18494739 | CAAACCTGCACACAA[A/G]CAAGCGTGCACTAGT | 7251 |
rs768347742 | in-del | -/A | | | intron-variant | TSG101 | GRCh38.p7 | 11:18507264 | CAAGGTTAACTTCTT[-/A]AGAAAGTAACTTCTT | 7251 |
rs768357416 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18502649 | TTGAAGAACCCCATT[C/T]AGGAAGTTAAGCTTG | 7251 |
rs768367402 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18507116 | ACATGAATTACAATA[C/T]TTATGACAATCCCTA | 7251 |
rs768401560 | snp | C/T | 1.64871e-05 | 0.00287111 | missense | TSG101 | GRCh38.p7 | 11:18506900 | ATGGAGAGATTCCAC[C/T]TGGCATGCCTGGCAT | 7251 |
rs768422162 | in-del | -/TTTTTC | | | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18528399 | TTTTTTTTTTTTTTT[-/TTTTTC]TTTTTTTTGAGACAG | 7251 |
rs768576175 | snp | A/G | 1.65119e-05 | 0.00287327 | intron-variant | TSG101 | GRCh38.p7 | 11:18519489 | TAAACTCAAAGTATA[A/G]AAATTGCTATTTTTA | 7251 |
rs768640946 | in-del | -/GA | 1.66407e-05 | 0.00288446 | intron-variant | TSG101 | GRCh38.p7 | 11:18509491 | TTTACAAAGGTTTCT[-/GA]GTTCTCTTTTGTTTA | 7251 |
rs768673433 | snp | C/T | 1.72868e-05 | 0.00293992 | missense | TSG101 | GRCh38.p7 | 11:18480596 | CTTTTTGCATTAGTG[C/T]CCTCAGCTGGAACTG | 7251 |
rs768706156 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18493771 | GAACATTTCAGACAA[C/T]TGTATGAGCAAAGGA | 7251 |
rs768709579 | in-del | -/C | | | intron-variant | TSG101 | GRCh38.p7 | 11:18524024 | CTGAACTCCTGGCCT[-/C]AAGTGGATTCTCCCA | 7251 |
rs768820730 | snp | G/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18520190 | TTAGCATGTTTTTGA[G/T]ATTATCCACGTTGTA | 7251 |
rs768823715 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18513667 | TTACTTTGGTAGACA[A/G]AACAGCAACTTTTGT | 7251 |
rs768825685 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18498954 | GTCAAATGCTGCTGA[C/T]AGGACAAGTAAGATG | 7251 |
rs768889703 | snp | C/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18500672 | TGCCCACTTTTTAAT[C/G]GTTTGTTTTACTGTT | 7251 |
rs768919903 | snp | C/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18519307 | CCACATCCAGGTACA[C/G]TATTTTTTTTTAACA | 7251 |
rs768950374 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18500564 | TGTGGTTTTTATCTG[C/T]ATTTTCCTGATGATG | 7251 |
rs768961232 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18490936 | AGTTGGCTTTCTGTA[C/T]CAGCTCACTTTTATC | 7251 |
rs768993969 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18521871 | TTTGATAGAGCTGGA[C/T]TTTAGCATGTTGCCC | 7251 |
rs768999803 | snp | A/T | 3.29554e-05 | 0.00405914 | intron-variant | TSG101 | GRCh38.p7 | 11:18483867 | CTTTAATGAGTCACT[A/T]ACTACTTCTTGATCT | 7251 |
rs769010834 | in-del | -/C | | | intron-variant | TSG101 | GRCh38.p7 | 11:18482629 | TGACTTACACACGGA[-/C]TGTCCAAGGCATAGC | 7251 |
rs769047043 | snp | C/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18525282 | CCAGGTGTGGTGGCT[C/G]ACGCCTGTATTCCCA | 7251 |
rs769174649 | snp | A/G | 1.74369e-05 | 0.00295265 | missense | TSG101 | GRCh38.p7 | 11:18480617 | GCTGGAACTGTTTAC[A/G]GGACAGAAGACGTAC | 7251 |
rs769272555 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18504100 | CAGCTACTTGGGAGG[C/T]TGAAGTTGAAAGATC | 7251 |
rs769346706 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18512437 | AATTTACCATCTTGT[C/T]CTCTATTTTCTTGAA | 7251 |
rs769379132 | in-del | -/TT | | | intron-variant | TSG101 | GRCh38.p7 | 11:18489639 | CACAAAGAATTTAAA[-/TT]TCAGGATTCGAGTTT | 7251 |
rs769475110 | snp | C/T | 2.00713e-05 | 0.00316784 | intron-variant | TSG101 | GRCh38.p7 | 11:18526766 | GAGGCGAGCGCGTCG[C/T]AGCCTCACCTTGGAC | 7251 |
rs769527586 | snp | A/G | 2.34134e-05 | 0.00342143 | utr-variant-3-prime | TSG101 | GRCh38.p7 | 11:18480497 | TACTGATAAAAGGAA[A/G]AGAAGAATACTTTAA | 7251 |
rs769627822 | snp | A/C | 2.19541e-05 | 0.00331309 | intron-variant | TSG101 | GRCh38.p7 | 11:18502452 | AGTTAGACTTTGCTT[A/C]TATGGTGAAACACAA | 7251 |
rs769702284 | in-del | -/A | 2.33866e-05 | 0.00341947 | utr-variant-3-prime | TSG101 | GRCh38.p7 | 11:18480500 | TGATAAAAGGAAGAG[-/A]AGAATACTTTAAGAA | 7251 |
rs769724035 | snp | C/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18497414 | TATATGCCTAAGACA[C/G]TACTCTTGAAAATGT | 7251 |
rs769821075 | snp | A/G | 4.96011e-05 | 0.00497977 | intron-variant | TSG101 | GRCh38.p7 | 11:18519643 | TTTAGTTTAAAACCA[A/G]TGCATATATTTTACA | 7251 |
rs769837610 | snp | A/C | | | intron-variant | TSG101 | GRCh38.p7 | 11:18481383 | CAGAAGAGTTACACT[A/C]ATCTTAATGCTGCCT | 7251 |
rs769853184 | snp | G/T | | | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18528123 | AGCATACAGCTCCAG[G/T]CAAACCAAACTAGAG | 7251 |
rs769915141 | snp | G/T | 3.40269e-05 | 0.0041246 | intron-variant | TSG101 | GRCh38.p7 | 11:18516094 | AAACCTAATAAGACA[G/T]TTACCTCTATAAGGC | 7251 |
rs769947435 | snp | A/C | | | intron-variant | TSG101 | GRCh38.p7 | 11:18485489 | AACAGAATTGGTTAT[A/C]TTCTAGGAGTCCTAG | 7251 |
rs769963004 | snp | G/T | 1.67259e-05 | 0.00289183 | intron-variant | TSG101 | GRCh38.p7 | 11:18514862 | AAAGAAATAGAAACT[G/T]CAGTTACTCTATTTT | 7251 |
rs769997893 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18500835 | TTGAGACAAGGTCTC[A/G]CTCTGTTGCCCAGGG | 7251 |
rs770037088 | in-del | -/TCTT | | | intron-variant | TSG101 | GRCh38.p7 | 11:18517000 | AATGTTAACCTACTG[-/TCTT]TCTATTTTAGAGATG | 7251 |
rs770113786 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18487550 | AATTTTTTTTCTAGT[A/G]GAGAGGTAGTCTCAC | 7251 |
rs770117300 | in-del | -/AACATTT | 2.25818e-05 | 0.00336012 | intron-variant | TSG101 | GRCh38.p7 | 11:18502596 | AAGACAAGAACAAAA[-/AACATTT]AACATTTAAGATGAC | 7251 |
rs770133899 | snp | A/G | | | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18527659 | TTGCACAATGCAAGG[A/G]TAGGTACTTCCATCT | 7251 |
rs770165929 | snp | A/G | | | downstream-variant-500B | TSG101 | GRCh38.p7 | 11:18480161 | TTTAGATTTCTATTT[A/G]GTATATCCCCATGTT | 7251 |
rs770175515 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18526557 | CCGCTCCACGCCTTT[A/G]TTGACTGTCGCCGTC | 7251 |
rs770225755 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18512635 | TTATAGAGAGTCTAT[A/G]TATTATCTTCTTCCA | 7251 |
rs770229047 | snp | A/G | 1.64735e-05 | 0.00286993 | missense | TSG101 | GRCh38.p7 | 11:18483887 | CTTCTTGATCTAAAC[A/G]GGTAACCATCTCTTC | 7251 |
rs770241615 | snp | C/T | 1.64741e-05 | 0.00286998 | missense | TSG101 | GRCh38.p7 | 11:18484043 | AGGCTCGGATGGTGT[C/T]CTCGCTGATTGTGCC | 7251 |
rs770403788 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18486131 | GAACCACCCCTGCAT[C/T]CCCTCTCCAGTGAAA | 7251 |
rs770531038 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18505663 | GACTGATTTCATTGT[C/T]AATTTAATTTAGTTA | 7251 |
rs770564885 | snp | A/T | 1.80023e-05 | 0.00300014 | intron-variant | TSG101 | GRCh38.p7 | 11:18514638 | TAGTGAGCAAAATAT[A/T]TAAAACATAACTAAT | 7251 |
rs770655318 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18506553 | AAAATTAGCCGGGAA[C/T]GGTGGCACAGCCTGT | 7251 |
rs770655752 | snp | A/G | 1.7929e-05 | 0.00299403 | missense | TSG101 | GRCh38.p7 | 11:18480629 | TACGGGACAGAAGAC[A/G]TACATGCTGGGAGGG | 7251 |
rs770687792 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18491822 | TTTGTAGAATAAGTC[A/G]GTCTACTTCAAATGA | 7251 |
rs770741984 | in-del | -/GTGA | | | intron-variant | TSG101 | GRCh38.p7 | 11:18520704 | TAGATATATGTTTCT[-/GTGA]GTTAGTTGGATCTAG | 7251 |
rs770747339 | snp | C/T | 1.64792e-05 | 0.00287042 | missense | TSG101 | GRCh38.p7 | 11:18481656 | CATCCAGGTCTATCA[C/T]GCCCCTTCTCAAGGC | 7251 |
rs770811104 | snp | C/T | 1.96458e-05 | 0.00313409 | missense, utr-variant-5-prime | TSG101 | GRCh38.p7 | 11:18526801 | TTTTCTTGAGCTGGC[C/T]CTCCGACACCGCCAT | 7251 |
rs770829710 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18482123 | CAAGCTTGTCACCTG[C/T]CAGCGACAAATGATA | 7251 |
rs770854787 | in-del | -/CAT | | | intron-variant | TSG101 | GRCh38.p7 | 11:18519775 | TCACTATTTTCTTAA[-/CAT]CAGTAAATATCTATA | 7251 |
rs770897314 | snp | C/T | 5.63989e-05 | 0.00531002 | missense | TSG101 | GRCh38.p7 | 11:18502567 | GTGGGTAAGGACAGC[C/T]TGGGTAACCACTAAA | 7251 |
rs770917761 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18483069 | GGGGAGGGATGGCAC[A/G]CAGGGGTGGTAATTG | 7251 |
rs770990559 | in-del | -/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18495668 | TACTACCAGTTAGGT[-/T]TTTTTTTTTTTTTTT | 7251 |
rs770999761 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18522722 | CCCTCCAAACCTCCC[A/G]TACCATTGATGCTGT | 7251 |
rs771039043 | snp | C/G/T | 3.2948e-05 | 0.00405871 | missense | TSG101 | GRCh38.p7 | 11:18484052 | TGGTGTCCTCGCTGA[C/G/T]TGTGCCATCCCTACT | 7251 |
rs771046061 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18517851 | TTTACTTACTGTTGA[C/T]GAATGTAAGCTATAC | 7251 |
rs771072042 | snp | A/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18521737 | GCTGGAGTGCGGTGG[A/T]GTGATCTCAGTTCAC | 7251 |
rs771123315 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18510010 | GTACAAATTTAGGGA[C/T]GAATATGAGCAACAG | 7251 |
rs771199277 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18494437 | TGAATCAGCTTCTCC[C/T]ACCTTTCCTTTACTA | 7251 |
rs771200455 | snp | A/G | 3.29794e-05 | 0.00406061 | missense | TSG101 | GRCh38.p7 | 11:18509584 | GCGGATAGGATGCCG[A/G]AATAGGACGAGAGAA | 7251 |
rs771220949 | snp | C/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18517344 | TCAATCTGTATTTCT[C/G]ATACCACACACATTT | 7251 |
rs771235956 | snp | A/T | 1.69527e-05 | 0.00291137 | missense, utr-variant-5-prime | TSG101 | GRCh38.p7 | 11:18516150 | TTAGTTCCCTGGAAC[A/T]GCCATCGTTAAAAAC | 7251 |
rs771288368 | snp | A/C | | | intron-variant | TSG101 | GRCh38.p7 | 11:18502319 | CCTGGTAGAAGGTTC[A/C]TTTATATGTTAAGTC | 7251 |
rs771325715 | snp | C/G | 0.000132227 | 0.00812995 | intron-variant | TSG101 | GRCh38.p7 | 11:18519471 | AATCATTAACAAAGA[C/G]AGTAAACTCAAAGTA | 7251 |
rs771361657 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18503607 | TCAATCTCCTGACCT[C/T]GTGATTCACCCGCCT | 7251 |
rs771380141 | in-del | -/CTTT | | | intron-variant | TSG101 | GRCh38.p7 | 11:18494950 | TTTCTTCACCTTTTC[-/CTTT]CTTTATCTAAATATT | 7251 |
rs771430984 | snp | C/T | 3.29484e-05 | 0.00405871 | missense | TSG101 | GRCh38.p7 | 11:18484033 | GAGATGAGAGAGGCT[C/T]GGATGGTGTCCTCGC | 7251 |
rs771571606 | snp | A/G | 1.89306e-05 | 0.00307652 | missense | TSG101 | GRCh38.p7 | 11:18502570 | GGTAAGGACAGCCTG[A/G]GTAACCACTAAAGAC | 7251 |
rs771695222 | snp | C/T | 3.29679e-05 | 0.00405991 | missense | TSG101 | GRCh38.p7 | 11:18481796 | TTTTCAGACTGATTT[C/T]CCATTTTTTCCAGAG | 7251 |
rs771699792 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18526006 | CTCAATCATTTTACA[C/T]AGTTTTGGAAAATTA | 7251 |
rs771713264 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18483311 | ACGAGCCTGGCCAAC[A/G]TGGTGATACCCCGTC | 7251 |
rs771746194 | in-del | -/CTA | | | intron-variant | TSG101 | GRCh38.p7 | 11:18514323 | ATAAACAGAAGTTCC[-/CTA]CTATTATTCTTGACA | 7251 |
rs771788689 | snp | C/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18517873 | AAGCTATACCGCAAT[C/G]TATTCTGATTTTGTG | 7251 |
rs771813710 | snp | C/T | 2.03143e-05 | 0.00318696 | missense, utr-variant-5-prime | TSG101 | GRCh38.p7 | 11:18526813 | GGCTCTCCGACACCG[C/T]CATGACGGCCGCCTG | 7251 |
rs771827788 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18514861 | AAAAGAAATAGAAAC[C/T]TCAGTTACTCTATTT | 7251 |
rs771947853 | snp | A/T | 1.64827e-05 | 0.00287073 | synonymous-codon | TSG101 | GRCh38.p7 | 11:18506880 | GGGAGGGTATCCGGA[A/T]GGGTATGGAGAGATT | 7251 |
rs772037584 | snp | A/G | 1.66443e-05 | 0.00288477 | intron-variant | TSG101 | GRCh38.p7 | 11:18506975 | ACAAGGCCTGAATAT[A/G]TAGGCTACTGAATAA | 7251 |
rs772210798 | in-del | -/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18498074 | TGTTGAGTGTGTGGG[-/T]TGGGGGGTTGGAGGG | 7251 |
rs772313173 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18510760 | TGAGACCAGCCTGGT[C/T]TCTACAAAAAAATTA | 7251 |
rs772361480 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18494654 | AGGATTGGAAGAAAA[C/T]GCTACTTATCCTGAA | 7251 |
rs772370384 | snp | C/T | 1.64746e-05 | 0.00287002 | missense | TSG101 | GRCh38.p7 | 11:18484060 | TCGCTGATTGTGCCA[C/T]CCCTACTGGGACCTG | 7251 |
rs772378150 | in-del | -/A | | | intron-variant | TSG101 | GRCh38.p7 | 11:18483494 | GAGTGAAACTCTCAA[-/A]AAAAAAAAAAAAAAA | 7251 |
rs772390530 | in-del | -/A | | | intron-variant | TSG101 | GRCh38.p7 | 11:18524466 | TGGCTAACAATTCTT[-/A]ACATCAGACCACACC | 7251 |
rs772396968 | snp | A/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18503881 | ATGACATTTGCCTTT[A/T]ACAAGCGCATTAAAA | 7251 |
rs772477933 | snp | C/T | 1.64963e-05 | 0.00287192 | missense | TSG101 | GRCh38.p7 | 11:18514796 | GGGGGATTATATGGG[C/T]ATGTGTCCAGTAGCC | 7251 |
rs772499923 | in-del | -/A | | | intron-variant | TSG101 | GRCh38.p7 | 11:18481270 | AGAAAATTAACAGAT[-/A]AAAAAATGGAGGTGG | 7251 |
rs772503508 | snp | C/T | 1.79583e-05 | 0.00299647 | intron-variant | TSG101 | GRCh38.p7 | 11:18514646 | AAAATATATAAAACA[C/T]AACTAATTCACAGAA | 7251 |
rs772724231 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18505603 | TACACATTTAAAACA[C/T]GGGTTAGTAATTATT | 7251 |
rs772728812 | snp | G/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18510034 | GCAACAGTCACAATA[G/T]TATTAAAGGCCATTA | 7251 |
rs772782527 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18504115 | CTGAAGTTGAAAGAT[C/T]ACCTGAGCCCAGGAG | 7251 |
rs772821009 | snp | C/T | 3.30055e-05 | 0.00406222 | intron-variant | TSG101 | GRCh38.p7 | 11:18519497 | AAGTATAGAAATTGC[C/T]ATTTTTACTGCATAA | 7251 |
rs772947525 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18510002 | GTATACTGGTACAAA[C/T]TTAGGGATGAATATG | 7251 |
rs772949509 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18493924 | TATGGAGCTTTTCTT[C/T]CAAAGAAATTAGGGG | 7251 |
rs772958760 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18481431 | GCCACCAGCCCACTT[C/T]TCTTCCCCTGCTCAG | 7251 |
rs772980303 | snp | C/T | 1.64904e-05 | 0.00287139 | synonymous-codon | TSG101 | GRCh38.p7 | 11:18509582 | TGGCGGATAGGATGC[C/T]GAAATAGGACGAGAG | 7251 |
rs773002388 | snp | A/C | | | intron-variant | TSG101 | GRCh38.p7 | 11:18495739 | CCACCTCCTCATTCC[A/C]CTAGTTAGTTTTCAA | 7251 |
rs773068192 | snp | A/G | 1.74506e-05 | 0.00295381 | synonymous-codon | TSG101 | GRCh38.p7 | 11:18480618 | CTGGAACTGTTTACG[A/G]GACAGAAGACGTACA | 7251 |
rs773085686 | snp | A/C | 3.29484e-05 | 0.00405871 | missense | TSG101 | GRCh38.p7 | 11:18502564 | CAGGTGGGTAAGGAC[A/C]GCCTGGGTAACCACT | 7251 |
rs773101737 | snp | A/G | 8.45273e-05 | 0.0065005 | synonymous-codon | TSG101 | GRCh38.p7 | 11:18516103 | AAGACATTTACCTCT[A/G]TAAGGCACAGGGATT | 7251 |
rs773188200 | snp | A/C | 1.64795e-05 | 0.00287045 | intron-variant | TSG101 | GRCh38.p7 | 11:18484081 | CTGGGACCTGCAGGA[A/C]ACAGAGGCAAAAAAC | 7251 |
rs773201186 | in-del | -/AC | 1.66902e-05 | 0.00288874 | intron-variant | TSG101 | GRCh38.p7 | 11:18509696 | AAATTCAAGTCAGCT[-/AC]AGAGTTGCTTTTCAG | 7251 |
rs773248292 | snp | A/C | | | intron-variant | TSG101 | GRCh38.p7 | 11:18491347 | CAACCTCTGGAGGAG[A/C]TGGAGACTAAAGGTC | 7251 |
rs773337182 | in-del | CTTAAAGTATAATA/GTATAAT | | | intron-variant | TSG101 | GRCh38.p7 | 11:18487250 | ACATGTACCCTAAAA[CTTAAAGTATAATA/GTATAAT]AAAAAAAAAAAGAAA | 7251 |
rs773398802 | snp | A/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18512654 | TATCTTCTTCCAGCA[A/T]GGGTTCACCCTATCC | 7251 |
rs773401383 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18508717 | GCTTATAAACCAAGA[C/T]GTTCCTCAGGAAAGA | 7251 |
rs773406361 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18517129 | TAGGCTCAAGCAATC[C/T]TCCCACCTCAGCCTT | 7251 |
rs773408053 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18489710 | TTTTGAGTGGCAACA[A/G]CCCAAACAGGTCAAG | 7251 |
rs773451505 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18499752 | TTTGTACATATTTAC[A/G]TGGGTACCATGTGAT | 7251 |
rs773474656 | snp | C/T | 6.72111e-05 | 0.00579664 | intron-variant | TSG101 | GRCh38.p7 | 11:18514867 | AATAGAAACTTCAGT[C/T]ACTCTATTTTTATTA | 7251 |
rs773479672 | snp | C/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18487551 | ATTTTTTTTCTAGTA[C/G]AGAGGTAGTCTCACT | 7251 |
rs773639061 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18515536 | TTAGCATTATCACCA[A/G]CATCACAACCATAAA | 7251 |
rs773747582 | snp | A/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18509509 | TCTCTTTTGTTTATA[A/T]GAGTTTTAAAGTAAA | 7251 |
rs773830585 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18501071 | CCTTGGCTTCCCAAA[A/G]TGCTGGGATTACAGA | 7251 |
rs773888055 | snp | A/G | 1.98699e-05 | 0.00315191 | missense, utr-variant-5-prime | TSG101 | GRCh38.p7 | 11:18526806 | TTGAGCTGGCTCTCC[A/G]ACACCGCCATGACGG | 7251 |
rs773957626 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18525204 | GTAAGCCACTGCGCC[C/T]AGCCCAAGGACTAAA | 7251 |
rs773973424 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18490985 | GGCTGCAGGGGACGA[A/G]GATGCTTCTGAGCAA | 7251 |
rs774013068 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18483296 | GATCAGGAGTTCGGG[A/G]CGAGCCTGGCCAACA | 7251 |
rs774158635 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18497692 | ACTATTCCTATTTTA[C/T]TGATAATGCTGAACC | 7251 |
rs774185883 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18482127 | CTTGTCACCTGTCAG[C/T]GACAAATGATACTGC | 7251 |
rs774244680 | snp | A/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18521777 | CACCTCCCAGGCTCA[A/T]GCAATCCTCCCATCT | 7251 |
rs774255664 | snp | G/T | 5.66374e-05 | 0.00532123 | synonymous-codon | TSG101 | GRCh38.p7 | 11:18502568 | TGGGTAAGGACAGCC[G/T]GGGTAACCACTAAAG | 7251 |
rs774295879 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18510019 | TAGGGATGAATATGA[A/G]CAACAGTCACAATAT | 7251 |
rs774350575 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18516980 | TATCAAACAATACCA[C/T]ACTAAATGTTAACCT | 7251 |
rs774365586 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18517575 | AAGATTATAATACTG[C/T]ATTTTTACTGTAACT | 7251 |
rs774389242 | in-del | -/G | 1.6608e-05 | 0.00288162 | intron-variant | TSG101 | GRCh38.p7 | 11:18509510 | CTCTTTTGTTTATAT[-/G]AGTTTTAAAGTAAAA | 7251 |
rs774405694 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18517853 | TACTTACTGTTGACG[A/G]ATGTAAGCTATACCG | 7251 |
rs774492945 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18492127 | TTCATTAAGTCCCCA[A/G]TTTATAGTAAGGCTG | 7251 |
rs774539027 | snp | A/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18495775 | TATGTAAACTGAGGT[A/T]GAAGATGTCTATAGC | 7251 |
rs774640455 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18485686 | ACTCATCAATATCTC[C/T]ACCTGAAAATCAGAA | 7251 |
rs774700223 | snp | A/G | 1.65206e-05 | 0.00287403 | intron-variant | TSG101 | GRCh38.p7 | 11:18519475 | ATTAACAAAGAGAGT[A/G]AACTCAAAGTATAGA | 7251 |
rs774704848 | snp | A/C | | | intron-variant | TSG101 | GRCh38.p7 | 11:18502345 | AAGTCATTTACTTCA[A/C]GTTTAAGATTATAGT | 7251 |
rs774713830 | snp | G/T | 1.65935e-05 | 0.00288036 | intron-variant | TSG101 | GRCh38.p7 | 11:18509514 | TTTGTTTATATGAGT[G/T]TTAAAGTAAAATCTC | 7251 |
rs774717362 | snp | A/G | 1.64898e-05 | 0.00287135 | synonymous-codon | TSG101 | GRCh38.p7 | 11:18509585 | CGGATAGGATGCCGA[A/G]ATAGGACGAGAGAAG | 7251 |
rs774860587 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18487786 | GCTCATGCTTCAGTG[A/G]GCATACATCCTCCTT | 7251 |
rs774889307 | snp | A/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18520711 | ATGTTTCTGTGAGTT[A/T]GTTGGATCTAGAGGT | 7251 |
rs774998108 | snp | C/T | 2.06234e-05 | 0.00321112 | utr-variant-5-prime | TSG101 | GRCh38.p7 | 11:18526819 | CCGACACCGCCATGA[C/T]GGCCGCCTGGCGACT | 7251 |
rs775072725 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18488944 | ACATGGTGAAAACCC[A/G]TCTCTACTAAAAATA | 7251 |
rs775095576 | snp | A/G | 1.64836e-05 | 0.0028708 | missense | TSG101 | GRCh38.p7 | 11:18506891 | CGGATGGGTATGGAG[A/G]GATTCCACCTGGCAT | 7251 |
rs775106765 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18492261 | CATAGATTACGTACC[C/T]AAATGATATGTCTAT | 7251 |
rs775115121 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18501503 | AATACCATGCTGTTT[C/T]GGTTACTATAACCTT | 7251 |
rs775155802 | snp | G/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18493659 | TCCCACACAGTAGCT[G/T]ACTGACCATCTATTT | 7251 |
rs775214935 | snp | A/C | | | utr-variant-3-prime | TSG101 | GRCh38.p7 | 11:18480352 | CCCAACATTCAGCAC[A/C]AAAAGTTTACAGAGG | 7251 |
rs775216508 | snp | G/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18519210 | AGGTTTCACCATATT[G/T]CCCAGGCTGGTCTCA | 7251 |
rs775233982 | snp | A/C | | | intron-variant | TSG101 | GRCh38.p7 | 11:18487425 | TTGGTCTCTCACAAC[A/C]AATTCAAAGGATTAG | 7251 |
rs775300460 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18517907 | TTTAAAAAAGAAAAC[C/T]ACCTTATATAAATTT | 7251 |
rs775323182 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18514960 | TCCGCATCCCCCCCA[C/T]TCCTATTTCCCCCAG | 7251 |
rs775352703 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18526088 | AAGTAATTATATAAA[C/T]AAATCATGGCTTTAA | 7251 |
rs775377326 | in-del | -/AGTT | | | downstream-variant-500B | TSG101 | GRCh38.p7 | 11:18480109 | GACCTTTCACAGATA[-/AGTT]AGTTACTCAAATGCT | 7251 |
rs775397230 | in-del | -/ATGACCCAACCTTATAGT | 2.82354e-05 | 0.00375725 | intron-variant | TSG101 | GRCh38.p7 | 11:18502613 | CATTTAACATTTAAG[-/ATGACCCAACCTTATAGT]ATTTTGAAGAACCCC | 7251 |
rs775461153 | snp | C/G | 3.39299e-05 | 0.00411872 | synonymous-codon, utr-variant-5-prime | TSG101 | GRCh38.p7 | 11:18516151 | TAGTTCCCTGGAACT[C/G]CCATCGTTAAAAACT | 7251 |
rs775515758 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18482191 | GAAGGTTCCTTTACA[C/T]AGAAAATCATAAGAG | 7251 |
rs775586204 | snp | C/T | 1.65214e-05 | 0.0028741 | missense | TSG101 | GRCh38.p7 | 11:18509635 | ATACCACAATCATGA[C/T]CTGAATAAGCCCCAA | 7251 |
rs775651298 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18521750 | GGTGTGATCTCAGTT[C/T]ACTGCAACCTCCACC | 7251 |
rs775663302 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18510862 | GGAAGGTTGAGGCTG[C/T]AGTATGACTGCGCCA | 7251 |
rs775738164 | snp | C/T | 3.30956e-05 | 0.00406776 | missense | TSG101 | GRCh38.p7 | 11:18481849 | CTTTTTCAAAAGTTC[C/T]ATGTTTTTATCAACC | 7251 |
rs775768792 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18498664 | TGGATATAACAATCT[C/T]GAGTTCAGGAGAGAG | 7251 |
rs775793081 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18497433 | TCTTGAAAATGTAGA[A/G]TAAAATATTAGTTGA | 7251 |
rs775811742 | snp | A/C | | | intron-variant | TSG101 | GRCh38.p7 | 11:18483323 | AACATGGTGATACCC[A/C]GTCTCTACTAAAAAA | 7251 |
rs775854339 | snp | A/T | 1.64738e-05 | 0.00286995 | missense | TSG101 | GRCh38.p7 | 11:18481685 | GCTTCTCCCAAGTAA[A/T]AGATAGTGTCTTCAA | 7251 |
rs776055819 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18521828 | ACTACAGGTATGCGC[C/T]ACAGTGTTTGGCTAA | 7251 |
rs776110715 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18523354 | CTTATCACTTTCCAA[C/T]GTACTTCTTGATGTA | 7251 |
rs776136819 | snp | A/T | 3.29734e-05 | 0.00406025 | synonymous-codon | TSG101 | GRCh38.p7 | 11:18506901 | TGGAGAGATTCCACC[A/T]GGCATGCCTGGCATG | 7251 |
rs776142421 | snp | A/T | 0.000216092 | 0.0103923 | intron-variant | TSG101 | GRCh38.p7 | 11:18509506 | TGTTCTCTTTTGTTT[A/T]TATGAGTTTTAAAGT | 7251 |
rs776152778 | snp | C/T | | | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18527862 | CGTAGTATTGATTCC[C/T]TTCAAAGTTGGCGTC | 7251 |
rs776263228 | in-del | -/TTTTT | | | intron-variant | TSG101 | GRCh38.p7 | 11:18512723 | TGAAGGACAGACAGA[-/TTTTT]TTTTTTTTTTTTTTT | 7251 |
rs776273259 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18515109 | GTTTATTATGAATGG[C/T]TGACTTATTAATAGT | 7251 |
rs776289556 | in-del | -/ATGTA | | | intron-variant | TSG101 | GRCh38.p7 | 11:18483817 | CATATAGAACACTCT[-/ATGTA]GCCATGGCTACAATT | 7251 |
rs776295144 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18508484 | TTACAGCTACCACAC[C/T]CGGCCAAATATTTCG | 7251 |
rs776418762 | snp | C/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18493839 | CCATTACATGGCTTA[C/G]AAAAGTCCTTTTTAT | 7251 |
rs776440091 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18507143 | CCTACCAAAAGAACT[A/G]GCAAACAGGTCAACC | 7251 |
rs776456329 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18491077 | CTGCCGTGGCTGCAG[C/T]GACGGTAGCAGCAGC | 7251 |
rs776724004 | snp | C/T | 1.65504e-05 | 0.00287662 | missense | TSG101 | GRCh38.p7 | 11:18514839 | GAATATTGTATGTAT[C/T]ACCTGAAAAAGAAAT | 7251 |
rs776726144 | snp | A/G | 8.23649e-05 | 0.00641683 | synonymous-codon | TSG101 | GRCh38.p7 | 11:18481705 | AGTGTCTTCAATAGC[A/G]TTTTCTTCTGCATAC | 7251 |
rs776795572 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18500722 | TATATTTATTAGTTC[C/T]TTGTCAGATGGGTAC | 7251 |
rs776909432 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18483671 | ATGGTCTAAATATTA[C/T]ACCCCTCCCAATCTA | 7251 |
rs776928089 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18485255 | TCTACCATTAAATTA[C/T]GGTGAAACCTAATCT | 7251 |
rs776959882 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18497872 | CCTGAATAGTGTGTA[C/T]CAATGAGAAAAACGG | 7251 |
rs777087366 | snp | G/T | 2.18926e-05 | 0.00330845 | utr-variant-5-prime | TSG101 | GRCh38.p7 | 11:18526838 | CGCCTGGCGACTCCC[G/T]TCCCCGCAGGCAGAG | 7251 |
rs777104841 | snp | C/T | 0.000281875 | 0.0118684 | missense | TSG101 | GRCh38.p7 | 11:18481859 | AGTTCTATGTTTTTA[C/T]CAACCTCGGCCTGAA | 7251 |
rs777118504 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18525014 | CTCCCAGGTTCAAGC[A/G]ATTCTCCCATCTCAG | 7251 |
rs777192981 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18483000 | AATCTCAACTTGAAT[C/T]GTATCTCACAGAAAG | 7251 |
rs777204012 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18511295 | TTTAATACTCCTGAC[A/G]GAAGAGTTCAGTGGC | 7251 |
rs777259903 | snp | G/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18521962 | GGATTACAGGCATGA[G/T]CCATCATGCCCAGCT | 7251 |
rs777272403 | in-del | -/TCC | | | intron-variant | TSG101 | GRCh38.p7 | 11:18487794 | TTCAGTGAGCATACA[-/TCC]TCCTTTTCCATTGCT | 7251 |
rs777299370 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18488312 | TTTCAGCAGATGGAC[A/G]AACAGATGGACTCTA | 7251 |
rs777350440 | snp | C/T | 1.8012e-05 | 0.00300095 | intron-variant | TSG101 | GRCh38.p7 | 11:18514635 | TGCTAGTGAGCAAAA[C/T]ATATAAAACATAACT | 7251 |
rs777391333 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18522514 | CCACAGCTACAGTCC[C/T]GGTCTAAGCCACCAG | 7251 |
rs777408196 | in-del | -/AC | | | intron-variant | TSG101 | GRCh38.p7 | 11:18520634 | TTGTTCATTTGTCCT[-/AC]AGAGGCTCTCACAGT | 7251 |
rs777445106 | snp | A/G | 3.31203e-05 | 0.00406928 | synonymous-codon | TSG101 | GRCh38.p7 | 11:18514723 | TATCTTCCCATTTGC[A/G]TCAACATGCTTTCCT | 7251 |
rs777473309 | snp | A/C | | | intron-variant | TSG101 | GRCh38.p7 | 11:18484187 | TTCAAAATGTGAGGA[A/C]AGAAAAAAATTATGT | 7251 |
rs777480451 | snp | C/G | 1.99142e-05 | 0.00315542 | intron-variant | TSG101 | GRCh38.p7 | 11:18526768 | GGCGAGCGCGTCGCA[C/G]CCTCACCTTGGACAC | 7251 |
rs777553986 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18510593 | TGAGCACTGGCCAGG[A/G]GTGGTGGCTTACACC | 7251 |
rs777570600 | snp | C/G | 4.88102e-05 | 0.00493991 | utr-variant-5-prime | TSG101 | GRCh38.p7 | 11:18526859 | GCAGGCAGAGGGTCA[C/G]CCGCTGCTGGGCTGC | 7251 |
rs777680591 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18511705 | GCTTTTATTATTTCA[C/T]GAAGCTATGCAACCA | 7251 |
rs777697603 | snp | A/G | | | downstream-variant-500B | TSG101 | GRCh38.p7 | 11:18480307 | CCAATAAAGGAGAGA[A/G]AAATTATGCAACAAA | 7251 |
rs777733628 | snp | C/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18498455 | TGGTGACTTGGATCA[C/G]CACTGGATATGATCA | 7251 |
rs777817226 | snp | A/C/G | 0.000132014 | 0.00812349 | intron-variant | TSG101 | GRCh38.p7 | 11:18519621 | GAAAAGCAAAATCGC[A/C/G]TAAGAATTTAGTTTA | 7251 |
rs777821093 | snp | A/G | 1.64754e-05 | 0.00287009 | synonymous-codon | TSG101 | GRCh38.p7 | 11:18481768 | GGGAATGATAACTTC[A/G]TCGATATCATTGTTT | 7251 |
rs777862200 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18521277 | CCACATGATATGTAA[C/T]GACCAATTCTACCTT | 7251 |
rs777871849 | snp | A/C | | | intron-variant | TSG101 | GRCh38.p7 | 11:18516089 | GCTGGAAACCTAATA[A/C]GACATTTACCTCTAT | 7251 |
rs777877433 | snp | A/C | | | intron-variant | TSG101 | GRCh38.p7 | 11:18490111 | GTTTATCCCATGAAC[A/C]ATTTTTGCTAGGCTG | 7251 |
rs777936476 | snp | C/T | 7.63665e-05 | 0.00617879 | intron-variant | TSG101 | GRCh38.p7 | 11:18516214 | TTTTTTAAGATACTC[C/T]CATAAGTTATTCTTT | 7251 |
rs777999758 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18506598 | GGGAGGCTGAGGCAG[A/G]AGAATCACTTGAACT | 7251 |
rs778069833 | snp | C/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18488843 | AAAAAGGATGATGGG[C/G]GGCCGGGCGCAGTGG | 7251 |
rs778125887 | snp | C/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18514993 | GAATTTATTTCCTGA[C/G]GGCAATAGCAAAGTC | 7251 |
rs778182585 | in-del | -/A | | | intron-variant | TSG101 | GRCh38.p7 | 11:18487502 | CTTAACACAAGGAAG[-/A]AAAAAACATTAGATC | 7251 |
rs778293241 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18520131 | TTGTCTCTACAGATT[C/T]GCTTATTCATACAAT | 7251 |
rs778297333 | snp | C/T | 1.6914e-05 | 0.00290805 | intron-variant | TSG101 | GRCh38.p7 | 11:18481915 | CTGTACATAATTATC[C/T]ACTTGTCAGACACCT | 7251 |
rs778320305 | snp | C/T | 4.94222e-05 | 0.00497078 | missense | TSG101 | GRCh38.p7 | 11:18484046 | CTCGGATGGTGTCCT[C/T]GCTGATTGTGCCATC | 7251 |
rs778361050 | snp | C/T | 6.64011e-05 | 0.00576161 | synonymous-codon | TSG101 | GRCh38.p7 | 11:18481864 | TATGTTTTTATCAAC[C/T]TCGGCCTGAAAACAG | 7251 |
rs778397984 | in-del | -/CAG | 6.66045e-05 | 0.00577043 | intron-variant | TSG101 | GRCh38.p7 | 11:18481877 | ACCTCGGCCTGAAAA[-/CAG]AACAGTCCAAGCATT | 7251 |
rs778442237 | snp | G/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18490756 | CTCATTCCTCTGTTT[G/T]CTGCTCAATGCTGGA | 7251 |
rs778464227 | in-del | -/A | | | intron-variant | TSG101 | GRCh38.p7 | 11:18525540 | ACAGAGCAAGACTCT[-/A]AAAAAAAAAAAAAAA | 7251 |
rs778495564 | snp | A/G | 1.64732e-05 | 0.0028699 | intron-variant | TSG101 | GRCh38.p7 | 11:18516050 | TTTGGCAACATATTT[A/G]TTATGTATTCAAAAT | 7251 |
rs778525159 | snp | C/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18519164 | ACTACAGGAGCACCA[C/G]GCCAACTTTAAGTAT | 7251 |
rs778546539 | in-del | -/CTT | | | intron-variant | TSG101 | GRCh38.p7 | 11:18514597 | CTACCTCGAATCCTC[-/CTT]GAGTGCTAAAAGAAA | 7251 |
rs778574428 | snp | C/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18506570 | GTGGCACAGCCTGTA[C/G]TCCCAACTGCTAGGG | 7251 |
rs778604781 | snp | A/G | 1.64985e-05 | 0.0028721 | synonymous-codon | TSG101 | GRCh38.p7 | 11:18514759 | AATAGTCATTGAACT[A/G]GTAGGCTTAACAAAA | 7251 |
rs778609527 | snp | C/T | 8.24151e-05 | 0.00641878 | missense | TSG101 | GRCh38.p7 | 11:18506876 | GATTGGGAGGGTATC[C/T]GGATGGGTATGGAGA | 7251 |
rs778639673 | in-del | -/AGA | | | intron-variant | TSG101 | GRCh38.p7 | 11:18513833 | TAATCCCAGCACTTT[-/AGA]AGGCCGAGATGGGTG | 7251 |
rs778697243 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18507663 | ACAAAAAAAAATAGT[A/G]AAGAATCTGCTCTAG | 7251 |
rs778722101 | in-del | -/TTGATGAAAG | | | | | GRCh38.p7 | 11:18480015 | GCCACTCTGCTCCTT[-/TTGATGAAAG]TTTGATGAAAACACT | 7251 |
rs778770714 | snp | C/T | 0.000378922 | 0.0137593 | missense | TSG101 | GRCh38.p7 | 11:18481778 | ACTTCATCGATATCA[C/T]TGTTTTCAGACTGAT | 7251 |
rs778782562 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18513207 | GCTGATTTTCAGAGG[C/T]GTTCTGCTTAGTTTT | 7251 |
rs778805703 | snp | C/G | 1.65696e-05 | 0.00287828 | utr-variant-5-prime | TSG101 | GRCh38.p7 | 11:18526865 | AGAGGGTCAGCCGCT[C/G]CTGGGCTGCCCCAGA | 7251 |
rs778842777 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18484470 | GCTTCGCTGCTAAGC[C/T]GAAGGAGACAAGTGC | 7251 |
rs778907106 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18500113 | TATTTGTCTTTCTGC[A/G]CCTAGTTTATTTCCA | 7251 |
rs779009016 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18484460 | CCAACATCAGGCTTC[A/G]CTGCTAAGCTGAAGG | 7251 |
rs779078517 | in-del | -/AA | | | intron-variant | TSG101 | GRCh38.p7 | 11:18483493 | AGAGTGAAACTCTCA[-/AA]AAAAAAAAAAAAAAA | 7251 |
rs779097175 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18490365 | AGTGTATCCAATTCA[A/G]TAATTGCTTCATCAA | 7251 |
rs779155033 | snp | G/T | 1.6569e-05 | 0.00287824 | intron-variant | TSG101 | GRCh38.p7 | 11:18484116 | GCTTACTTCCCAAGT[G/T]CCTTCTATTTGTCTC | 7251 |
rs779155131 | snp | C/T | 4.2789e-05 | 0.00462522 | intron-variant | TSG101 | GRCh38.p7 | 11:18526748 | GCGGTGGGCGCGCCC[C/T]GGGAGGCGAGCGCGT | 7251 |
rs779172877 | snp | A/T | 1.80013e-05 | 0.00300006 | intron-variant | TSG101 | GRCh38.p7 | 11:18514639 | AGTGAGCAAAATATA[A/T]AAAACATAACTAATT | 7251 |
rs779203861 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18522953 | GGAGTACAGTGGTGT[A/G]ATCACAGCTCACTGC | 7251 |
rs779255342 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18524499 | CTGAAAGGAAAACAT[C/T]TGAAGCCCTTCTTTA | 7251 |
rs779339518 | in-del | -/A | | | intron-variant | TSG101 | GRCh38.p7 | 11:18519323 | ATTTTTTTTTAACAT[-/A]AAAAAACTAAAACTA | 7251 |
rs779382800 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18503828 | TAGTTAGACAATAAA[C/T]CTCAATTAATCCTAT | 7251 |
rs779415450 | snp | A/C/T | 1.65663e-05 | 0.002878 | intron-variant | TSG101 | GRCh38.p7 | 11:18509521 | ATATGAGTTTTAAAG[A/C/T]AAAATCTCAATTCTA | 7251 |
rs779416737 | in-del | -/TAGTT | 2.03602e-05 | 0.00319056 | intron-variant | TSG101 | GRCh38.p7 | 11:18480659 | GGAGAAAAGTTTGAA[-/TAGTT]TAGAATGGCTTTGAT | 7251 |
rs779460696 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18481897 | CAGTCCAAGCATTAA[C/T]AACTGTACATAATTA | 7251 |
rs779524671 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18516613 | CCTCCCAAAGTGCTG[A/G]GATTACAGGTGTGAG | 7251 |
rs779537489 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18493301 | GGACCCAAAAATTCA[C/T]TGAATAATTTATGCA | 7251 |
rs779635168 | snp | A/G | 1.64732e-05 | 0.0028699 | synonymous-codon | TSG101 | GRCh38.p7 | 11:18484011 | TCTCAGTTTGTCACT[A/G]ACCGCAGAGATGAGA | 7251 |
rs779683847 | in-del | -/ATA | | | intron-variant | TSG101 | GRCh38.p7 | 11:18511739 | CCACCATCTAATTCC[-/ATA]ATATTTTCATCATCC | 7251 |
rs779729131 | snp | A/C | 1.65252e-05 | 0.00287443 | intron-variant | TSG101 | GRCh38.p7 | 11:18483842 | ACAATTCAATCCAAA[A/C]ATTTTAAGTCTTTAA | 7251 |
rs779832206 | snp | C/T | 6.65181e-05 | 0.00576668 | intron-variant | TSG101 | GRCh38.p7 | 11:18509501 | GTTTCTGTTCTCTTT[C/T]GTTTATATGAGTTTT | 7251 |
rs779840627 | snp | C/T | 1.73625e-05 | 0.00294634 | synonymous-codon | TSG101 | GRCh38.p7 | 11:18480579 | ACCGGCAGTCTTTCT[C/T]GCTTTTTGCATTAGT | 7251 |
rs779849437 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18495369 | TAAATCAACTACAAT[C/T]ATCTATATAGCTTTT | 7251 |
rs779921208 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18501655 | TCTATGGAAACTGAC[A/G]TTGGTATTTCGACAC | 7251 |
rs779995064 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18502759 | TGTATTAATGACACT[A/G]CATTTACTCTTAAAT | 7251 |
rs780015826 | in-del | -/TCA | | | intron-variant | TSG101 | GRCh38.p7 | 11:18486521 | CACATGAAAAAATGC[-/TCA]TCATCACTGGCCATC | 7251 |
rs780108253 | snp | C/T | 4.94662e-05 | 0.00497299 | synonymous-codon | TSG101 | GRCh38.p7 | 11:18509555 | ACTATTTGGTGGCCC[C/T]GTTGCCTGGTATGGC | 7251 |
rs780284160 | in-del | -/C | | | intron-variant | TSG101 | GRCh38.p7 | 11:18482564 | GTGAAATTGGCACTT[-/C]AATTATGCTGATGCT | 7251 |
rs780409438 | snp | G/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18505491 | AACTTCTGGGCTCAA[G/T]CAATCCCTACCTCGG | 7251 |
rs780419931 | snp | A/G | 1.74509e-05 | 0.00295384 | intron-variant | TSG101 | GRCh38.p7 | 11:18516074 | TCAAAATGCATCTAT[A/G]CTGGAAACCTAATAA | 7251 |
rs780420727 | snp | G/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18506170 | TGTATAATTTGAAAG[G/T]AGTTTCTTTCAATCT | 7251 |
rs780423447 | snp | A/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18517566 | TGGTCCCATAAGATT[A/T]TAATACTGTATTTTT | 7251 |
rs780472893 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18490899 | TACAGCCATATCATC[A/G]TAGCGCTCAGCCTGC | 7251 |
rs780491720 | snp | C/G | 1.78446e-05 | 0.00298697 | missense | TSG101 | GRCh38.p7 | 11:18502543 | TTGTGGCAGGATATG[C/G]ACCACCAGGTGGGTA | 7251 |
rs780563069 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18485007 | GCAGTCGCATGATCT[C/T]GGCTCACTGCAACCT | 7251 |
rs780588202 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18497186 | AATCGTGACCATTGA[C/T]ATACTGAGAAAATGT | 7251 |
rs780590429 | snp | C/T | 3.29717e-05 | 0.00406015 | synonymous-codon | TSG101 | GRCh38.p7 | 11:18509567 | CCCCGTTGCCTGGTA[C/T]GGCGGATAGGATGCC | 7251 |
rs780618313 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18488075 | GCTTGCTAGACAATA[C/T]AACCATCACAGAAGA | 7251 |
rs780663739 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18494058 | GCAGGTTTACACTTC[C/T]TGAAAATAAACACAC | 7251 |
rs780704928 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18482012 | TTCAAATAACACCCT[A/G]GTCAAAGGTAGAGGA | 7251 |
rs780913947 | snp | C/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18482900 | CATCAAGCACTCAAA[C/G]AGTCCTCCTTTGGGT | 7251 |
rs780964498 | snp | A/C | 1.74117e-05 | 0.00295052 | synonymous-codon | TSG101 | GRCh38.p7 | 11:18480615 | CAGCTGGAACTGTTT[A/C]CGGGACAGAAGACGT | 7251 |
rs781042940 | in-del | -/CTC | | | intron-variant | TSG101 | GRCh38.p7 | 11:18522316 | ATGACCAAAACTGAA[-/CTC]CTCATCTTCTCCCCA | 7251 |
rs781092260 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18509963 | CAAAAATTTATTTTA[C/T]TGCCACTGTACAATG | 7251 |
rs781147397 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18510494 | GTACAAAGGGGTGAA[C/T]TGTTAAAGGATCTTT | 7251 |
rs781157078 | snp | A/G | 1.68007e-05 | 0.00289828 | intron-variant | TSG101 | GRCh38.p7 | 11:18509712 | CAGAGTTGCTTTTCA[A/G]TAAAAAGAAAAAGGT | 7251 |
rs781176735 | snp | C/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18488649 | AGAAGTTCTTCTCAA[C/G]TCTTTAAAGCCAGGC | 7251 |
rs781229080 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18495608 | AGTTTATGTTTTGCT[C/T]CTACAGTAACAGGAA | 7251 |
rs781525384 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18526383 | AGACTGGAGGATCCC[C/T]AGATTGGGACAGGAG | 7251 |
rs781530949 | in-del | -/CC | 4.40393e-05 | 0.0046923 | utr-variant-5-prime | TSG101 | GRCh38.p7 | 11:18526839 | CCTGGCGACTCCCTT[-/CC]CCCCGCAGGCAGAGG | 7251 |
rs781547485 | in-del | -/TT | 2.22601e-05 | 0.0033361 | intron-variant | TSG101 | GRCh38.p7 | 11:18502445 | AACAGGGAGTTAGAC[-/TT]TGCTTATATGGTGAA | 7251 |
rs781556890 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18501845 | GAACAAAACTTGAGA[A/G]GAAGGAACTGCTGAA | 7251 |
rs781611786 | snp | C/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18503293 | TTGGAAGACACTCAA[C/G]TATTTGGAGACTCCT | 7251 |
rs781651256 | snp | A/G | 0.000394149 | 0.0140328 | intron-variant | TSG101 | GRCh38.p7 | 11:18516086 | TATGCTGGAAACCTA[A/G]TAAGACATTTACCTC | 7251 |
rs781656034 | snp | A/T | 1.82623e-05 | 0.00302173 | intron-variant | TSG101 | GRCh38.p7 | 11:18516204 | ATCATGAGCATTTTT[A/T]AAGATACTCCCATAA | 7251 |
rs781660147 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18491788 | TCTTACCTAATCAAG[A/G]ACTTGCTCTTCATGG | 7251 |
rs781677043 | snp | C/T | | | downstream-variant-500B | LDHAL6A, TSG101 | GRCh38.p7 | 11:18480097 | GAGCATCTCCTTGGA[C/T]CTTTCACAGATAAGT | 7251 |
rs781714141 | snp | G/T | 1.64743e-05 | 0.00287 | missense | TSG101 | GRCh38.p7 | 11:18483878 | CACTTACTACTTCTT[G/T]ATCTAAACGGGTAAC | 7251 |
rs796083115 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18483293 | TGAGATCAGGAGTTC[A/G]GGACGAGCCTGGCCA | 7251 |
rs796127311 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18506403 | TTTTAAAAAAAAAAA[A/G]ATACATAGGCTGGGC | 7251 |
rs796297526 | in-del | -/A | | | intron-variant | TSG101 | GRCh38.p7 | 11:18507658 | AACTGACAAAAAAAA[-/A]TAGTAAAGAATCTGC | 7251 |
rs796437167 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18500168 | CGTTTTCATTCTTTT[C/T]ATGGCTGAACAGTAT | 7251 |
rs796595822 | in-del | -/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18493935 | CTTCCAAAGAAATTA[-/G]GGGGGCCTCAATTTA | 7251 |
rs796652907 | snp | A/G | | | intron-variant | TSG101 | GRCh38.p7 | 11:18503106 | GTCATTCATGTATTC[A/G]TATCAAAGTCAGAGG | 7251 |
rs796717054 | in-del | -/A | | | intron-variant | TSG101 | GRCh38.p7 | 11:18508857 | TACCAAAAAAAAAAA[-/A]GTCACAGCTCAAAAC | 7251 |
rs796750031 | snp | C/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18521745 | GCGGTGGTGTGATCT[C/T]AGTTCACTGCAACCT | 7251 |
rs796764027 | snp | C/G | | | upstream-variant-2KB | TSG101 | GRCh38.p7 | 11:18528489 | TCTGCCTCCCGGGTT[C/G]AAGCGATTCTCCTGC | 7251 |
rs796846048 | in-del | -/GT | | | intron-variant | TSG101 | GRCh38.p7 | 11:18483028 | AAGGGACCTGTGTGC[-/GT]GTGTGTGTGTGTGTA | 7251 |
rs796886962 | snp | A/T | | | intron-variant | TSG101 | GRCh38.p7 | 11:18499404 | TATATATATATATAT[A/T]TTTTTTTTTTTTTTT | 7251 |