| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs778826807 | snp | A/G | 1.67916e-05 | 0.0028975 | upstream-variant-2KB, utr-variant-3-prime, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571515 | CCCAAGCCCATAAAT[A/G]GGAAGGGAGACATGG | 26168 |
| rs778849909 | snp | G/T | 2.4412e-05 | 0.00349362 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563645 | GTTTTGACTCCCCCC[G/T]GGGGCCACCTCCACC | 26168 |
| rs778876982 | snp | A/G | 1.66051e-05 | 0.00288137 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564724 | GCATCCTCATCAGCA[A/G]TGTGTGCAGCATCGG | 26168 |
| rs778939371 | in-del | -/TCTC | 1.64741e-05 | 0.00286998 | intron-variant, upstream-variant-2KB | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560709 | ACTGCGAATCTACTT[-/TCTC]TCTTTTCTCAGGTGT | 26168 |
| rs778983939 | snp | A/G | 1.67027e-05 | 0.00288982 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565018 | CTCAGCACTGATGAG[A/G]TAGTAGAGAAGCTGG | 26168 |
| rs779222477 | snp | A/G | 1.64944e-05 | 0.00287175 | missense, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560381 | TGACTTTCACCATGG[A/G]TCAGGTGGTGTCTCG | 26168 |
| rs779223275 | snp | A/G | 1.67742e-05 | 0.002896 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570308 | ACCTTCATGGCAAAA[A/G]GCAAGACTTCTGTTT | 26168 |
| rs779253454 | snp | C/G | 1.65803e-05 | 0.00287922 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571387 | GTACTGCAAGCATCT[C/G]GCCCTGTCTCAGCCA | 26168 |
| rs779255160 | snp | C/T | | | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564684 | GGGCCAGAAGGGGAG[C/T]GCAGCTTGGCACCCC | 26168 |
| rs779337220 | snp | A/G | | | utr-variant-3-prime, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7561058 | CGAATTCTTGCGTGT[A/G]TGTAGATGAGGGGCG | 26168 |
| rs779352900 | snp | C/G | 1.66095e-05 | 0.00288175 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565782 | AGGCCCAACCAGATA[C/G]GTCAGTACCCAGAGG | 26168 |
| rs779370040 | snp | C/T | 0.000439883 | 0.0148239 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564420 | ATGAGTAGGAACTCT[C/T]TCTCCATCCCTGTAG | 26168 |
| rs779454601 | snp | C/T | 6.62526e-05 | 0.00575516 | intron-variant, upstream-variant-2KB | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560207 | TCACAGAGGGCCTCT[C/T]TGGCCCCCTACTGAG | 26168 |
| rs779561054 | snp | C/G | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7569866 | CTGCGTGTTTACTTT[C/G]TGCTGTGTCTTGTTC | 26168 |
| rs779566322 | snp | C/G | 1.67086e-05 | 0.00289033 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570333 | CTGTTTGTTGTACCT[C/G]ACCTGTGGCACTATC | 26168 |
| rs779742286 | snp | A/G | 1.68892e-05 | 0.00290591 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564904 | CTCTCTCCCTTCTCC[A/G]ACTCCTAGAGGAGAG | 26168 |
| rs779794205 | snp | C/T | 5.82004e-05 | 0.00539415 | utr-variant-5-prime, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563070 | TTGTTTTTCAGGGTA[C/T]TGGAAGATGAAAGAG | 26168 |
| rs779820379 | in-del | -/G | 3.33161e-05 | 0.00408129 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565121 | GGGCCTTGGGGATGT[-/G]GAGAGAATACTGCTG | 26168 |
| rs779874368 | snp | A/G | 1.67251e-05 | 0.00289176 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564829 | AAGCCGGCCAGCACA[A/G]CCCCCTGCGAGAGGA | 26168 |
| rs779875397 | in-del | -/GAGGAGGAAGAAGAGGAG | 9.44867e-05 | 0.00687273 | cds-indel, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563305 | GCCTCAGCAAGTGAA[-/GAGGAGGAAGAAGAGGAG]GAGGAGGAGGATGAA | 26168 |
| rs779979317 | snp | G/T | 1.84514e-05 | 0.00303733 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565413 | GCTGCATCATCTTTT[G/T]TGTGACTCCACCCTT | 26168 |
| rs779990913 | snp | A/C | 4.9643e-05 | 0.00498187 | intron-variant, upstream-variant-2KB | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560171 | CTGTATAGCCAGGTA[A/C]CCCCAGCCACACTCT | 26168 |
| rs780022906 | snp | A/G | 3.30387e-05 | 0.00406427 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560951 | GAGGCGTCTTCCTGG[A/G]TTTGGCTCCCCGTTC | 26168 |
| rs780025968 | snp | G/T | 0.000120257 | 0.00775334 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563456 | GCTCACAGCGCCGCC[G/T]CCGAGCCATGAGAGC | 26168 |
| rs780108548 | snp | A/G | 1.77228e-05 | 0.00297676 | upstream-variant-2KB, synonymous-codon, nc-transcript-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7570927 | CTGTGGTGCTTTTGT[A/G]TTGCAGGTAAGCAGA | 26168 |
| rs780232663 | snp | A/G | | | downstream-variant-500B, upstream-variant-2KB, intron-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7561954 | CACCGCTGCCGGTGG[A/G]CCCGGGGCTCGCGGG | 26168 |
| rs780265522 | snp | A/C | 1.64836e-05 | 0.0028708 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560409 | TCGAGAAGGCCAAGG[A/C]AGGCAGGAGACTCTA | 26168 |
| rs780380946 | snp | C/T | 3.62812e-05 | 0.00425902 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564612 | TGCCCATTCCATTTC[C/T]CCTGCCCTATAGGCC | 26168 |
| rs780386453 | snp | C/T | 1.81807e-05 | 0.00301496 | synonymous-codon, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565059 | CCAGCAGGAGTTTTC[C/T]ACCCCTTCCAGGTGA | 26168 |
| rs780439404 | snp | C/T | | | upstream-variant-2KB, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7572235 | AACCAGGATTCATGA[C/T]AGTACCCCAAAGCCC | 26168 |
| rs780468794 | snp | G/T | 0.000133253 | 0.00816143 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564452 | ATCTCTTGGACATGT[G/T]TATCTCATGCTTATG | 26168 |
| rs780486028 | snp | A/T | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7568710 | CCTGTGCATCTTTTC[A/T]TCTGTACTCTTTGTA | 26168 |
| rs780504843 | snp | G/T | 1.65452e-05 | 0.00287616 | intron-variant, upstream-variant-2KB | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560498 | GCGCAGGTGAGAGCC[G/T]TGTGGGCAGCCGAAA | 26168 |
| rs780577374 | snp | C/T | 3.38868e-05 | 0.0041161 | upstream-variant-2KB, utr-variant-3-prime, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571526 | AAATGGGAAGGGAGA[C/T]ATGGGAGTCCCTTCC | 26168 |
| rs780667152 | in-del | -/GAGGAG | | | cds-indel, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563317 | GAAGAGGAGGAAGAA[-/GAGGAG]GAGGAGGAGGATGAA | 26168 |
| rs780876033 | snp | C/T | | | upstream-variant-2KB, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571005 | CGGGAGGCTGTTATG[C/T]ATCCCCTCATTTGGC | 26168 |
| rs780880722 | snp | C/T | 4.39126e-05 | 0.00468555 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563194 | CCCCCACCTCCCAAA[C/T]CCCGACTCAAGTCAG | 26168 |
| rs780942865 | snp | C/G | 4.99621e-05 | 0.00499786 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565003 | GGCAGCCTCATACCC[C/G]TCAGCACTGATGAGG | 26168 |
| rs781040998 | snp | C/G | 3.36327e-05 | 0.00410063 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564933 | AGTCTGGAGGCCTCA[C/G]CCCCTCCTCTCTCCC | 26168 |
| rs781041027 | in-del | -/TCTGCAGTTTTAAG | 1.66454e-05 | 0.00288486 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565802 | GTACCCAGAGGAACT[-/TCTGCAGTTTTAAG]CAGCTTTTTAAGCTC | 26168 |
| rs781117484 | snp | C/T | 2.06545e-05 | 0.00321354 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563657 | CCCGGGGGCCACCTC[C/T]ACCCCGGCTGGGTCT | 26168 |
| rs781229346 | snp | C/T | | | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564983 | ACGAATTCCTTCAAA[C/T]GTATGGCAGCCTCAT | 26168 |
| rs781373129 | snp | A/G | 1.77593e-05 | 0.00297982 | synonymous-codon, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7563757 | GGAAGATGGACTCAG[A/G]TGGACTCCAAAGTCT | 26168 |
| rs781493025 | snp | A/G | 0.000216096 | 0.0103924 | missense, nc-transcript-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7564685 | GGCCAGAAGGGGAGC[A/G]CAGCTTGGCACCCCC | 26168 |
| rs781499429 | snp | A/G | 3.35948e-05 | 0.00409833 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565601 | AGGTGAGAAAGGGTA[A/G]AGAAACAGGCCTGAG | 26168 |
| rs781524997 | snp | C/T | 3.29478e-05 | 0.00405867 | intron-variant, upstream-variant-2KB | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560704 | GCTTCACTGCGAATC[C/T]ACTTTCTCTCTTTTC | 26168 |
| rs781619220 | snp | A/G | 1.65531e-05 | 0.00287686 | intron-variant, upstream-variant-2KB | TNFSF13, SENP3, TNFSF12-TNFSF13, SENP3-EIF4A1 | GRCh38.p7 | 17:7560504 | GTGAGAGCCGTGTGG[A/G]CAGCCGAAAGCAGGA | 26168 |
| rs781708600 | snp | A/G | 1.79348e-05 | 0.00299451 | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7565430 | GTGACTCCACCCTTG[A/G]CCTACTCAGGAAGGG | 26168 |
| rs796154996 | snp | G/T | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7562923 | GACCGCGTTAACCGG[G/T]AAGATCTTAAGTTAG | 26168 |
| rs796248539 | snp | C/T | | | upstream-variant-2KB, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7572271 | AGTTTTCTTCCATCC[C/T]TCCACCATCCAGCCA | 26168 |
| rs796480584 | snp | C/T | | | intron-variant | SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7569914 | GTCACTAGTTTAATC[C/T]TCATATCAAATGGAT | 26168 |
| rs796734412 | in-del | -/A | | | upstream-variant-2KB, utr-variant-3-prime, intron-variant | EIF4A1, SENP3, SENP3-EIF4A1 | GRCh38.p7 | 17:7571841 | TCTTCAAACTTTTAT[-/A]TATATATATATATAT | 26168 |