SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6607 | snp | A/G | 0.00279162 | 0.0372561 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560941 | TGCAGGAACAGAGGC[A/G]TCTTCCTGGGTTTGG | 26168 |
rs6608 | snp | C/T | 0.235273 | 0.249566 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7561096 | GGCGCCAGGCATTGT[C/T]CAGACCTGGTCGGGG | 26168 |
rs1133249 | snp | A/C/T | 0.38821 | 0.208322 | upstream-variant-2KB, utr-variant-3-prime, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571841 | TCTTCAAACTTTTAT[A/C/T]TATATATATATATAT | 26168 |
rs1133250 | snp | A/C | 0 | 0 | upstream-variant-2KB, utr-variant-3-prime, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571926 | aaataaataAATGCC[A/C]CGGTCCTGCTCTGGT | 26168 |
rs1140986 | snp | A/T | 0 | 0 | upstream-variant-2KB, utr-variant-3-prime, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571910 | ATATATATATATATA[A/T]AAATATATAAATGCC | 26168 |
rs1140987 | snp | A/T | | | upstream-variant-2KB, utr-variant-3-prime, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571916 | atatatatataaata[A/T]ataAATGCCACGGTC | 26168 |
rs4542712 | snp | C/T | 0.272511 | 0.248984 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7566010 | GGGATGGGTTCCTAT[C/T]GTAACTATTGTAAAA | 26168 |
rs4602096 | snp | A/C | 0.485118 | 0.0849685 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570139 | CCATCATGGGTTCTC[A/C]AGTGTTCGTTCTGAT | 26168 |
rs4624241 | snp | C/T | 0.0433465 | 0.140692 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7569245 | aaaaaattagccggg[C/T]gaggtggcacgtgtc | 26168 |
rs4968212 | snp | C/T | 0.444489 | 0.157079 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564899 | CTAGCCTCTCTCCCT[C/T]CTCCGACTCCTAGAG | 26168 |
rs4968213 | snp | C/T | 0.246765 | 0.249979 | upstream-variant-2KB, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570959 | GATGGGGCCACCTCC[C/T]CTAGCTCTGAAGTCA | 26168 |
rs6503039 | snp | A/G | 0.236724 | 0.249647 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7566743 | ggccgaggcaggcag[A/G]cagacagattgaggc | 26168 |
rs7220171 | snp | C/G | 0.0337553 | 0.125452 | upstream-variant-2KB, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7572113 | CCCAAACAAATCCCC[C/G]AGATGGGAGCAGAGA | 26168 |
rs7503669 | snp | C/T | 0 | 0 | missense, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560142 | TCCGAATCCAGGATG[C/T]TGGAGTTTATCTGCT | 26168 |
rs8068222 | snp | G/T | 0.396364 | 0.202676 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565371 | AATTTGTATTCCAGG[G/T]AGTAGTAGGTATTTC | 26168 |
rs9908405 | snp | A/C | 0.23846 | 0.249734 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564144 | CGTGTATACATCTCC[A/C]GAGGGTACCATTCCC | 26168 |
rs9913914 | snp | A/G | 0.236434 | 0.249632 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565192 | AGAGCTGAAGGGGAG[A/G]ACTCTGCAGGCAGGT | 26168 |
rs9972914 | snp | A/T | 0.00975586 | 0.0691575 | upstream-variant-2KB, missense, nc-transcript-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570744 | GATTTCCACCAGGGC[A/T]GGAAAGGTTACTTCA | 26168 |
rs10438740 | snp | A/G | 0.494815 | 0.0506538 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7569566 | GCCCTCCCATTCAAA[A/G]GCCAGGAAATTTCTA | 26168 |
rs10468481 | snp | A/G | 0.395635 | 0.2032 | upstream-variant-2KB, utr-variant-3-prime, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571674 | TCTGATGTGCAGGGG[A/G]TGGCTACAGAAAAGC | 26168 |
rs11078697 | snp | C/T | 0.115788 | 0.21092 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565912 | TATTAATTTCAAATC[C/T]GTAATCTTGGGCTCT | 26168 |
rs11552709 | snp | C/G | 0 | 0 | missense, upstream-variant-2KB, intron-variant, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560822 | ACCTTCCTGGGGTTT[C/G]TGAAACTGTGATTGT | 26168 |
rs11654859 | snp | C/T | 0.267841 | 0.249363 | downstream-variant-500B, utr-variant-5-prime, nc-transcript-variant, intron-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7562022 | CGGTGGCGCTGGTGG[C/T]GGCGGTGGCGGAGGT | 26168 |
rs11656383 | snp | C/G | | | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563417 | AGCGGCCCCGCCCTT[C/G]CCGCCCCACTCATCG | 26168 |
rs11658232 | snp | A/G | 0 | 0 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570232 | CTTGCCCACAATCTA[A/G]GCCTTGGGTCTTCTG | 26168 |
rs11658330 | snp | A/G | 0.00865784 | 0.0652224 | synonymous-codon, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570493 | CCGCCGCTGCCCTAA[A/G]GTTTGAGGGGGTAGG | 26168 |
rs11870250 | snp | G/T | 0.067446 | 0.170804 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7568465 | gctgggcgtggtggc[G/T]tgcgcctgtagtccc | 26168 |
rs12452635 | snp | A/T | | | upstream-variant-2KB, utr-variant-3-prime, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571912 | ATATATATATATAAA[A/T]ATATATAAATGCCAC | 26168 |
rs12452997 | snp | C/G | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7569358 | ccactgcactccagt[C/G]tgggcaacagagcaa | 26168 |
rs12939472 | snp | C/T | 0.400682 | 0.199487 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7569415 | ATTTGTTTTTTCCTC[C/T]GCAGGTTGGATGTGG | 26168 |
rs12941164 | snp | A/T | | | upstream-variant-2KB, utr-variant-3-prime, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571878 | atatatatatatata[A/T]atatatatatatata | 26168 |
rs12941193 | snp | A/T | 0 | 0 | upstream-variant-2KB, utr-variant-3-prime, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571918 | ATATATAAAAATATA[A/T]AAATGCCACGGTCCT | 26168 |
rs12942617 | snp | C/G | 0.0338808 | 0.12567 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565698 | CTCCATGGCAAGCTG[C/G]CTCCCATCTTCTCCC | 26168 |
rs28625968 | snp | C/T | 0.372189 | 0.218105 | upstream-variant-2KB, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571221 | AAGTAAGAACACTAG[C/T]TTTAGAGTCAGGCTG | 26168 |
rs28655557 | snp | A/G | 0.234982 | 0.249549 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7567937 | GGAACAGAGCACAGT[A/G]GTCCAGGTGAGAAAC | 26168 |
rs34012149 | in-del | -/G | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7562898 | CACAGACCCTGAAGG[-/G]CCCCTTGTGGACCGC | 26168 |
rs34349099 | in-del | -/A/AA | 0 | 0 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7566684 | AAAAAAAAAAAAAAA[-/A/AA]GCCTGGTTTGTTGAC | 26168 |
rs34362644 | in-del | -/C | | | frameshift-variant, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560771 | GTGTCATAATTCCCC[-/C]GGGCAAGGGCGAAAC | 26168 |
rs34391610 | in-del | -/C | | | intron-variant, upstream-variant-2KB | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560179 | CAGGTAACCCCAGCC[-/C]ACACTCTGAGCTTCA | 26168 |
rs34434164 | in-del | -/G | | | upstream-variant-2KB, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7572184 | ATCCGAGAGGGAAGC[-/G]TGGGGAACTGGACAC | 26168 |
rs34467278 | snp | A/T | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7569345 | AGGCAAGATCACGCC[A/T]CTGCACTCCAGTCTG | 26168 |
rs34476700 | in-del | -/G | | | frameshift-variant, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560092 | GCAACCAGCTCTTAG[-/G]CGTGGGAGAGGCCTA | 26168 |
rs34655408 | in-del | -/G | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7566599 | GAACCCGGGAGGCGG[-/G]AGGTTGCAGCGAGTC | 26168 |
rs34758149 | in-del | -/C | | | upstream-variant-2KB, intron-variant, nc-transcript-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7572333 | TGATTCCTTCATCCC[-/C]TGGCACACGTCCAGG | 26168 |
rs34995901 | snp | A/G | 1.66543e-05 | 0.00288563 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564804 | CGGCTTTCTCCCCAG[A/G]CCTCTCTGCCTCTTC | 26168 |
rs35320998 | in-del | -/T | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564610 | ATGCCCATTCCATTT[-/T]CCCCTGCCCTATAGG | 26168 |
rs35424738 | in-del | -/C | | | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7561033 | TTGCTTCTGTTCCCC[-/C]ATGGAGCTCCGAATT | 26168 |
rs35596387 | snp | A/G | 0.074116 | 0.177665 | synonymous-codon, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564960 | GAATTCGTCCAAGAT[A/G]CCTGGTGGAAAGGGA | 26168 |
rs35746763 | in-del | -/G | | | upstream-variant-2KB, utr-variant-3-prime, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571622 | AAATGTTTCAATTTC[-/G]TGTATTTTTTTTTCT | 26168 |
rs35994480 | in-del | -/A | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565852 | CTCTTTCATTTTACA[-/A]CAGAGAGGGTCTCTG | 26168 |
rs55738870 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563921 | AAGAGTGCCGGCTCC[A/G]GAAGAGCTGCGAAAT | 26168 |
rs56136712 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7562706 | CCACGGTTATCATGT[A/C]CCTGAGGAAAGAAAC | 26168 |
rs56327661 | snp | C/T | | | upstream-variant-2KB, utr-variant-3-prime, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571846 | AAACTTTTATATATA[C/T]ATATATATATATATA | 26168 |
rs58131929 | in-del | -/T | | | upstream-variant-2KB, utr-variant-3-prime, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571918 | ATATATAAAAATATA[-/T]AAATGCCACGGTCCT | 26168 |
rs58682397 | in-del | -/T | | | upstream-variant-2KB, utr-variant-3-prime, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571916 | ATATATATAAAAATA[-/T]ATAAATGCCACGGTC | 26168 |
rs58805209 | in-del | -/A | | | upstream-variant-2KB, utr-variant-3-prime, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571843 | TTCAAACTTTTATAT[-/A]TATATATATATATAT | 26168 |
rs58840546 | in-del | -/ACA | | | intron-variant, upstream-variant-2KB | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560330 | ATCCTGTTTTCTTCA[-/ACA]TCTCCCTTCCCTGCC | 26168 |
rs60236248 | snp | C/T | 0.00165016 | 0.0286768 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564403 | TTTCTTTCTTCCTGT[C/T]TATGAGTAGGAACTC | 26168 |
rs60385651 | in-del | -/ATATAAAT | | | upstream-variant-2KB, utr-variant-3-prime, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571915 | TATATATATAAAAAT[-/ATATAAAT]GCCACGGTCCTGCTC | 26168 |
rs60828368 | in-del | -/AAAAAAA/AAAAAAAAAAAAA | 0 | 0 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7569398 | CAAAAAAAAAAAAAA[-/AAAAAAA/AAAAAAAAAAAAA]GATTTGTTTTTTCCT | 26168 |
rs61729121 | snp | C/G | 0.21875 | 0.248039 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564816 | AGGCCTGGGGAGAAA[C/G]CCGGCCAGCACAGCC | 26168 |
rs61760045 | snp | C/T | 0.00014843 | 0.00861354 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560448 | TATAAGAAGTATGCC[C/T]TCCCACCCGGACCGG | 26168 |
rs62059807 | snp | A/G | | | downstream-variant-500B, upstream-variant-2KB, intron-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7561799 | CACGCGCGGCCGGGC[A/G]GCGGATGTGCGCAGG | 26168 |
rs62059821 | snp | A/G | 0.0479149 | 0.147179 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7566274 | TGAACCCGTGAGGCG[A/G]AGGTTGCGGTGAGTC | 26168 |
rs62059822 | snp | A/G | 0.132409 | 0.220618 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7567242 | AACGTGAGGCTGGGC[A/G]CAGTGGCTCACGCCT | 26168 |
rs66817720 | in-del | -/A/AA | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7566669 | GCCCTGCCTCAAATA[-/A/AA]AAAAAAAAAAAAAAG | 26168 |
rs72154130 | in-del | -/CAA | 0.159664 | 0.233108 | intron-variant, upstream-variant-2KB | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560328 | CCATCCTGTTTTCTT[-/CAA]CATCTCCCTTCCCTG | 26168 |
rs72479718 | snp | C/T | 0.176861 | 0.239062 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7566528 | AAAGTTAGCTGGGCA[C/T]AGTGGCGGGTACCTG | 26168 |
rs72827565 | snp | A/G | 0.132409 | 0.220618 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7566290 | AGGTTGCGGTGAGTC[A/G]AGATCCACGCCATTG | 26168 |
rs74875436 | snp | C/T | 0.0704125 | 0.17392 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560902 | GAGACAGCCAAGAGC[C/T]GAGTATATAAAGGAG | 26168 |
rs76586164 | snp | A/G | 0.5 | 0 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7566970 | TAAACTCCGTACCAA[A/G]GGGTTATGATGGGGT | 26168 |
rs76849317 | snp | C/T | 0.0333238 | 0.124705 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563957 | CATTAAGCCCCACTT[C/T]GAGCAGAAAGTAAGC | 26168 |
rs77529322 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570037 | TAAATGGAGGAGCTG[C/T]ATTTGAATTCTGGCA | 26168 |
rs78153201 | snp | A/C | 0.000146883 | 0.00856855 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570477 | CGCAGCGTACCCTAA[A/C]CCGCCGCTGCCCTAA | 26168 |
rs78370612 | snp | C/T | 0.5 | 0 | downstream-variant-500B, upstream-variant-2KB, intron-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7561615 | TACCCCGGCTCCATT[C/T]CCCCCACTGCCTCGC | 26168 |
rs78439383 | snp | G/T | 0.0271762 | 0.113356 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7568616 | AAAACCCGAGAGGAG[G/T]AGTTTGGAGACATTC | 26168 |
rs78496193 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560573 | TAGGAGGGAGGTTGG[A/T]AACCTAAACAGAGGC | 26168 |
rs79377982 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565202 | GGGAGGACTCTGCAG[A/G]CAGGTGCCAAATCCT | 26168 |
rs80239205 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7567230 | TCAACACAGAGTAAC[A/G]TGAGGCTGGGCGCAG | 26168 |
rs111451688 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560295 | AGCGCTCCTGAGGCC[C/T]CCCAGAACTGAGCCA | 26168 |
rs111727030 | snp | C/G | | | splice-acceptor-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570355 | GGCACTATCTCTTTA[C/G]GTGGACATCTTCAAT | 26168 |
rs112246784 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560277 | CTTCTTTCTTCCCTC[A/G]TTAGCGCTCCTGAGG | 26168 |
rs113468868 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7567127 | ATTAAACGTCTCTTG[C/T]GTGTGTAGGCACTAA | 26168 |
rs113967036 | snp | C/T | 0.5 | 0 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7569113 | TTTTTTTGCCGGGCG[C/T]GGTGGCTCACGCCTG | 26168 |
rs114692970 | snp | C/T | 0.0168055 | 0.0901129 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7562646 | TAGAGAACTGTCTCC[C/T]ATTCCAGTCCAGTTT | 26168 |
rs116784454 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7567090 | GCCCTTTCCCTGACC[A/G]TGTTCATTCAGTCTT | 26168 |
rs138292852 | snp | C/T | 0.0189856 | 0.0955633 | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7561301 | CGTCCTTCTCTCCAT[C/T]TATCGGACCCCAGTT | 26168 |
rs139198089 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7566795 | GGCAACATAGTGAGA[C/G]CCTGTCTCTACCAAA | 26168 |
rs139268356 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7567292 | GAGGCCAACACGGGC[A/G]GATCACCTGAGGTCA | 26168 |
rs139278317 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7569483 | TTTTGGCCTATGTAA[C/T]GGGAAAAGTGGGAGA | 26168 |
rs139298099 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7568377 | CTGAGGCAGATGGAT[C/T]GCAAGGTCAAGAGAT | 26168 |
rs139336280 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-3-prime, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571724 | CAGGGGAGTGTGGCC[C/G]TGTGGCCTGGGTGGA | 26168 |
rs139689726 | snp | G/T | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570824 | GGTAGAAGGCAGAAA[G/T]TGAAGTCCTACCCCT | 26168 |
rs139748549 | snp | C/T | 1.65007e-05 | 0.00287229 | missense, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560456 | GTATGCCCTCCCACC[C/T]GGACCGGGCCTACAA | 26168 |
rs139860832 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564055 | GTCTTGAGCGCAGAT[C/G]AGAAAGGGAGATGTG | 26168 |
rs140764161 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7568649 | GATAGCTGAAGGCAT[A/G]GAGGCTCCCACAGGA | 26168 |
rs140832981 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7562590 | GCATCTGCACTTGAG[A/T]TGACCGCAGCCTTCC | 26168 |
rs140868033 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564093 | AAAATCCTGTCCACA[C/G]GAAATCCCTTGTCGG | 26168 |
rs141602266 | snp | A/T | 3.30071e-05 | 0.00406232 | missense, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560459 | TGCCCTCCCACCCGG[A/T]CCGGGCCTACAACAG | 26168 |
rs141869920 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570305 | AGAACCTTCATGGCA[A/G]AAGGCAAGACTTCTG | 26168 |