SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs1775 | snp | G/T | 0.00491398 | 0.0493238 | intron-variant | SENP1 | GRCh38.p7 | 12:48058721 | TGTCTTCTAGAGGTA[G/T]GAAAAAATGAGAGCA | 29843 |
rs3997 | snp | C/T | 0.295599 | 0.245806 | intron-variant | SENP1 | GRCh38.p7 | 12:48087804 | CTTCTATCAACACCA[C/T]AAAGCTCAAACTTGA | 29843 |
rs726354 | snp | A/G | 0.45866 | 0.137698 | intron-variant, upstream-variant-2KB | PFKM, SENP1 | GRCh38.p7 | 12:48106551 | GTTAGTGCTTGTAGA[A/G]GTTATTGGAGATACT | 29843 |
rs767420 | snp | A/G | 0 | 0 | intron-variant | SENP1 | GRCh38.p7 | 12:48051068 | TCACTTCAGACTTAC[A/G]ATTCCAGAGGTAATC | 29843 |
rs886588 | snp | C/T | 0.294893 | 0.245936 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | SENP1 | GRCh38.p7 | 12:48083639 | ATGTCGTCGAAGTCT[C/T]TTGAGCCCCAAGAAA | 29843 |
rs886589 | snp | A/G | 0.499631 | 0.0135733 | intron-variant | SENP1 | GRCh38.p7 | 12:48083414 | AAAGAGATTAAAGAG[A/G]TGTTTTAGCAGGACT | 29843 |
rs973398 | snp | C/T | 0.329084 | 0.237162 | intron-variant | SENP1 | GRCh38.p7 | 12:48097265 | TATGTACTCAGGGTA[C/T]AGCACCACCTCTGAT | 29843 |
rs989144 | snp | A/G | 0.269538 | 0.249235 | intron-variant | SENP1 | GRCh38.p7 | 12:48090190 | TAGCATCATGTTTCT[A/G]TCCTCAAAATTATAG | 29843 |
rs1018973 | snp | C/G | 0.453087 | 0.145793 | intron-variant | SENP1 | GRCh38.p7 | 12:48047909 | TTGATACCTTCAATG[C/G]AGTGATTGATAAAAT | 29843 |
rs1476608 | snp | A/G | 0.452719 | 0.146304 | intron-variant | SENP1 | GRCh38.p7 | 12:48099948 | TATTCTAGCTCTTCT[A/G]TAGTAACAAAGGTAT | 29843 |
rs1968070 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SENP1 | GRCh38.p7 | 12:48099560 | CCAGAGTGCTGGGAT[C/T]ACAGGTGTGAGCCAC | 29843 |
rs1968071 | snp | A/G | 0.452842 | 0.146134 | intron-variant | SENP1 | GRCh38.p7 | 12:48095574 | AGTTATACCATTGAA[A/G]CTGCCTCAACAGGAA | 29843 |
rs1978161 | snp | C/T | 0.49962 | 0.0137727 | intron-variant | SENP1 | GRCh38.p7 | 12:48073938 | TGTGAGTAAACTAAA[C/T]CCACAAATAGGATAT | 29843 |
rs2051851 | snp | C/G | 0.32955 | 0.237006 | intron-variant | SENP1 | GRCh38.p7 | 12:48092157 | GATGAAAATGAGCAG[C/G]AAGGCCCAAACTTTA | 29843 |
rs2107639 | snp | A/G | 0 | 0 | intron-variant | SENP1 | GRCh38.p7 | 12:48085468 | TGGGGAGAGGCCTGA[A/G]AATGAGGGAAGGGCT | 29843 |
rs2107640 | snp | A/G | 0.499631 | 0.0135733 | intron-variant | SENP1 | GRCh38.p7 | 12:48082050 | TACAAAAAATTAGCC[A/G]GGCGTGGTGGCGGGC | 29843 |
rs2158516 | snp | A/T | 0.270892 | 0.249126 | intron-variant | SENP1 | GRCh38.p7 | 12:48097051 | GAATTATTTCATTAG[A/T]TTGTCTATGTGTTTT | 29843 |
rs2286022 | snp | C/T | 0.416382 | 0.186593 | downstream-variant-500B | SENP1 | GRCh38.p7 | 12:48042864 | CACTGCTCATATTCA[C/T]CTGCCTTCCCTAAAA | 29843 |
rs2408955 | snp | G/T | 0.411564 | 0.19078 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | PFKM, SENP1 | GRCh38.p7 | 12:48105348 | GAGAAACGAGGCATA[G/T]ATCCAGAGATCACGT | 29843 |
rs3054235 | in-del | -/AA | | | intron-variant | SENP1 | GRCh38.p7 | 12:48095558 | aaaaaaaaaaaaaaa[-/AA]TTCCTGTTGAGGCAG | 29843 |
rs3054238 | in-del | -/AA | | | intron-variant | SENP1 | GRCh38.p7 | 12:48098660 | aaaaaaaaaaaaaaa[-/AA]Gttagccagccaatg | 29843 |
rs3742074 | snp | A/G | 0.452597 | 0.146474 | intron-variant | SENP1 | GRCh38.p7 | 12:48063602 | TGGATGACCTGCATT[A/G]GAATCATCTCTCATA | 29843 |
rs3742075 | snp | G/T | 0.306927 | 0.243432 | intron-variant | SENP1 | GRCh38.p7 | 12:48063556 | GTAACTATGAGGGAG[G/T]GTGGTGGAGACAGGC | 29843 |
rs3782910 | snp | A/G | 0.269538 | 0.249235 | intron-variant | SENP1 | GRCh38.p7 | 12:48089724 | GTTTTAAATTGTCCA[A/G]TTCTGCAGATAGGGA | 29843 |
rs3782911 | snp | A/C | 0.269809 | 0.249214 | intron-variant | SENP1 | GRCh38.p7 | 12:48089709 | ATTCTGCAGATAGGG[A/C]GAGGAGGTTATAGAA | 29843 |
rs3825403 | snp | C/T | 0.47885 | 0.100637 | intron-variant | SENP1 | GRCh38.p7 | 12:48063376 | CAAATAAGTATTAGC[C/T]GACCATGTTGCAGCA | 29843 |
rs4258439 | snp | A/G | 0.478603 | 0.101197 | intron-variant | SENP1 | GRCh38.p7 | 12:48074869 | AACTAGCATGTAAAC[A/G]GAATCCTAGCTCTGC | 29843 |
rs4293182 | snp | A/C | 0.452965 | 0.145963 | intron-variant | SENP1 | GRCh38.p7 | 12:48058176 | gtctcaaactcctga[A/C]cccaagtgatccacc | 29843 |
rs4589362 | snp | C/T | 0.452719 | 0.146304 | intron-variant | SENP1 | GRCh38.p7 | 12:48084881 | GCTGAATATTCTAAA[C/T]TCAATGAAATCAACT | 29843 |
rs4760619 | snp | A/T | 0.187802 | 0.242139 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | PFKM, SENP1 | GRCh38.p7 | 12:48106148 | GCTAGGTGGCTGAAG[A/T]GGAGGGGGCTGGGGC | 29843 |
rs4760677 | snp | C/T | 0.453087 | 0.145793 | intron-variant | SENP1 | GRCh38.p7 | 12:48055380 | AGAACTGTGCAGGCT[C/T]CCCAAAGATCAGACT | 29843 |
rs4760678 | snp | C/T | 0.49962 | 0.0137727 | intron-variant | SENP1 | GRCh38.p7 | 12:48067798 | GGCAACATAGTGAGA[C/T]TCTGTCTCTTAAAAA | 29843 |
rs4760679 | snp | G/T | 0.329317 | 0.237084 | intron-variant | SENP1 | GRCh38.p7 | 12:48067852 | ATAGTGCTTGGCACA[G/T]AGTAGGCATTTAGTG | 29843 |
rs4760680 | snp | G/T | 0.269267 | 0.249256 | intron-variant | SENP1 | GRCh38.p7 | 12:48072914 | TCCCCCCACAGATAA[G/T]GGGGAACTACTGTAG | 29843 |
rs5798058 | in-del | -/A | | | intron-variant | SENP1 | GRCh38.p7 | 12:48051083 | CTGAAGTGAAAAAAA[-/A]AAAAAAAGAATGACA | 29843 |
rs5798059 | in-del | -/T | 0 | 0 | intron-variant | SENP1 | GRCh38.p7 | 12:48084467 | TTTTTTTTTTTTTTT[-/T]GAGATGGAATCTTGC | 29843 |
rs5798061 | in-del | -/AA | | | intron-variant | SENP1 | GRCh38.p7 | 12:48095536 | GGGAGACTCTGTGTC[-/AA]AAAAAAAAAAAAAAA | 29843 |
rs6580652 | snp | A/C | 0.329084 | 0.237162 | intron-variant | SENP1 | GRCh38.p7 | 12:48053322 | CTAAAAACTAAAAAC[A/C]AACAAAAAAGCCAGG | 29843 |
rs7133249 | snp | C/T | 0.452597 | 0.146474 | intron-variant | SENP1 | GRCh38.p7 | 12:48063040 | CCCAGTTTTCTTTTG[C/T]TGTAAAAATAACCTT | 29843 |
rs7138229 | snp | C/T | | | intron-variant | SENP1 | GRCh38.p7 | 12:48071902 | AGAACAGAAATAGGT[C/T]TTAGTGAAGAATTTG | 29843 |
rs7138917 | snp | A/G | 0.490453 | 0.0684267 | intron-variant | SENP1 | GRCh38.p7 | 12:48061472 | GAGTACAGTGGCTCA[A/G]TCATAGCTCACTATA | 29843 |
rs7139330 | snp | A/C | 0.32955 | 0.237006 | intron-variant | SENP1 | GRCh38.p7 | 12:48089701 | AGAATAATTTCTATA[A/C]CCTCCTCTCCCTATC | 29843 |
rs7295580 | snp | C/T | 0.324145 | 0.238752 | intron-variant | SENP1 | GRCh38.p7 | 12:48098410 | agcactttgggaggt[C/T]gaggcgggtggatca | 29843 |
rs7296913 | snp | A/G | 0.452719 | 0.146304 | intron-variant | SENP1 | GRCh38.p7 | 12:48095137 | GAGCATCCTACTAAC[A/G]TCTTTTTAGGGAGGA | 29843 |
rs7299704 | snp | C/T | 0.47885 | 0.100637 | intron-variant | SENP1 | GRCh38.p7 | 12:48050705 | CTGCCTCTAGGTTTC[C/T]GAAGGCAGCCATAAA | 29843 |
rs7299987 | snp | C/T | 0 | 0 | intron-variant | SENP1 | GRCh38.p7 | 12:48050900 | ATGATCTGCCAGTTA[C/T]TGTAAGCGAAACCTT | 29843 |
rs7303677 | snp | A/G | 0.305685 | 0.24372 | intron-variant | SENP1 | GRCh38.p7 | 12:48084756 | CCCAGCCAATTTTGA[A/G]TTTTTTCTATGTGCT | 29843 |
rs7304428 | snp | G/T | 0.478271 | 0.101943 | intron-variant | SENP1 | GRCh38.p7 | 12:48100492 | aaaaattagccggac[G/T]tggcggcgcacgcat | 29843 |
rs7312326 | snp | A/G | 0.452719 | 0.146304 | intron-variant | SENP1 | GRCh38.p7 | 12:48086860 | CCTTGCTAATATGGC[A/G]AAATGCCGTCTCTAC | 29843 |
rs7313834 | snp | A/C | | | intron-variant | SENP1 | GRCh38.p7 | 12:48069068 | taaggcacgagaatc[A/C]cttgaacccgggagg | 29843 |
rs7959755 | snp | A/T | 0.452719 | 0.146304 | intron-variant | SENP1 | GRCh38.p7 | 12:48052535 | TTATCAACCACAAAG[A/T]CCAAGAGACTAACAG | 29843 |
rs7963640 | snp | C/T | 0.283158 | 0.247791 | intron-variant | SENP1 | GRCh38.p7 | 12:48083012 | TGGGCTCAAGCAATC[C/T]TCCCACCTCAGCCTC | 29843 |
rs7963934 | snp | C/G | 0.452597 | 0.146474 | intron-variant | SENP1 | GRCh38.p7 | 12:48083303 | GATCAAAGAGAGATA[C/G]TTTGATGTATGAGAA | 29843 |
rs7967740 | snp | G/T | | | intron-variant | SENP1 | GRCh38.p7 | 12:48056389 | tatatatttaatata[G/T]tacatattacatata | 29843 |
rs7968610 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | SENP1 | GRCh38.p7 | 12:48044075 | AGATGCTAGAAAGAA[A/C]AAAAGGAATAGCAGT | 29843 |
rs7971668 | snp | C/T | 0.452719 | 0.146304 | intron-variant | SENP1 | GRCh38.p7 | 12:48075913 | TCAGTCCTAGAAATA[C/T]ATAAAAGAATATTCC | 29843 |
rs7975632 | snp | C/T | 0.294832 | 0.245947 | intron-variant | SENP1 | GRCh38.p7 | 12:48049265 | TCAACATCCAACAGA[C/T]TCATTTCTCTAAATC | 29843 |
rs7978968 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | SENP1 | GRCh38.p7 | 12:48055663 | taatccaaccggaga[C/T]gtgctataagtgtaa | 29843 |
rs9630296 | snp | C/T | 0.117188 | 0.211804 | intron-variant | SENP1 | GRCh38.p7 | 12:48061421 | AAGTTTTGTATTCTT[C/T]TGAAGACACAGAGTC | 29843 |
rs9630299 | snp | G/T | 0 | 0 | intron-variant | SENP1 | GRCh38.p7 | 12:48060257 | cctttatcatgacca[G/T]aagcaaaagtAAGTT | 29843 |
rs9971924 | snp | C/G | 0.329084 | 0.237162 | intron-variant | SENP1 | GRCh38.p7 | 12:48086049 | AGCTTAAAGGGCTTC[C/G]ACTAGCCAAATTTCT | 29843 |
rs10128967 | snp | C/T | 0.104859 | 0.203554 | intron-variant | SENP1 | GRCh38.p7 | 12:48058926 | gacaaatttgtttct[C/T]ctgcagtacttcaaa | 29843 |
rs10128968 | snp | C/T | 0.104504 | 0.2033 | intron-variant | SENP1 | GRCh38.p7 | 12:48059256 | TTAACCTGTCTGGTA[C/T]AATCCCACAGCTCAC | 29843 |
rs10161320 | snp | G/T | 0.0134861 | 0.0810011 | intron-variant | SENP1 | GRCh38.p7 | 12:48101917 | ACTTCATAAACAAGT[G/T]ACAGACTTTGTGATG | 29843 |
rs10161358 | snp | C/T | 0.329084 | 0.237162 | intron-variant | SENP1 | GRCh38.p7 | 12:48099306 | GCACTCCAGCCTGGG[C/T]GACAGAGTGAGACCC | 29843 |
rs10492080 | snp | C/T | 0.45866 | 0.137698 | intron-variant, upstream-variant-2KB | PFKM, SENP1 | GRCh38.p7 | 12:48107628 | GGTCAAAATCTTACC[C/T]GGAAAATACACGACT | 29843 |
rs10492081 | snp | C/T | 0.384593 | 0.210677 | intron-variant | SENP1 | GRCh38.p7 | 12:48081070 | TTAATTCTGTGTTCA[C/T]TGTAAGTTTGCCATT | 29843 |
rs10564674 | in-del | -/A | 0 | 0 | intron-variant | SENP1 | GRCh38.p7 | 12:48069178 | AAAAAAAAAAAAAAA[-/A]GAAAGAAAGAAAAGG | 29843 |
rs10600081 | in-del | -/AG | 0.0205511 | 0.0992634 | intron-variant | SENP1 | GRCh38.p7 | 12:48083294 | TCTAGCAAAGATCAA[-/AG]AGAGATACTTTGATG | 29843 |
rs10672694 | in-del | -/AAG | 0.453209 | 0.145623 | intron-variant | SENP1 | GRCh38.p7 | 12:48051842 | AATTCCCTTTGAAAT[-/AAG]GAGCTAAAAGTAGAT | 29843 |
rs10747528 | snp | C/T | 0.0023933 | 0.0345097 | utr-variant-3-prime, nc-transcript-variant | SENP1 | GRCh38.p7 | 12:48044625 | GCAAACCCCTGCTTT[C/T]ACGGAAAGGACTGCT | 29843 |
rs10747529 | snp | A/G | 0.478768 | 0.100824 | intron-variant | SENP1 | GRCh38.p7 | 12:48079586 | GCTAGCTAATGTTAC[A/G]TTTTAAAACCTGAAA | 29843 |
rs10875732 | snp | A/C | 0.272151 | 0.250148 | intron-variant | SENP1 | GRCh38.p7 | 12:48048322 | GTGAAGCCTTTTTCT[A/C]ATGTTCATTCTCTCC | 29843 |
rs10875733 | snp | A/C | 0.307176 | 0.243374 | intron-variant | SENP1 | GRCh38.p7 | 12:48052522 | ATTAAATTTACCCTT[A/C]TCAACCACAAAGTCC | 29843 |
rs10875735 | snp | C/T | 0.269267 | 0.249256 | intron-variant | SENP1 | GRCh38.p7 | 12:48070023 | CAATCATAGTAATGG[C/T]TACTATGGATTACTA | 29843 |
rs10875736 | snp | C/T | 0.269538 | 0.249235 | intron-variant | SENP1 | GRCh38.p7 | 12:48078583 | TGGAGTGCAGTGGCG[C/T]GATCTTGGCTCACTG | 29843 |
rs10875737 | snp | A/G | 0.269267 | 0.249256 | intron-variant | SENP1 | GRCh38.p7 | 12:48079276 | AGGCCGAGGCAGGTG[A/G]ATCATGAAGTCAGTA | 29843 |
rs10875738 | snp | A/T | 0.269538 | 0.249235 | intron-variant | SENP1 | GRCh38.p7 | 12:48079956 | CAGTTCTAAGAAAAG[A/T]ATAAAACCATCACTG | 29843 |
rs10875739 | snp | C/T | 0.478603 | 0.101197 | intron-variant | SENP1 | GRCh38.p7 | 12:48087136 | TTCCAGATGCAAAAC[C/T]AAACTAACTATAAAA | 29843 |
rs10875740 | snp | C/T | 0.269267 | 0.249256 | intron-variant | SENP1 | GRCh38.p7 | 12:48095334 | TTGAGGTTAAGAGTT[C/T]GGACCAGCCTGGCCA | 29843 |
rs10875741 | snp | A/C | 0.478188 | 0.10213 | intron-variant, missense | SENP1 | GRCh38.p7 | 12:48099139 | CCAGCCTGGGAAATA[A/C]GGCAAAATCTTGTCT | 29843 |
rs10875742 | snp | A/G | 0.454302 | 0.144085 | intron-variant | SENP1 | GRCh38.p7 | 12:48099591 | GAGGCTGAGGTGGGC[A/G]GATCACTTACTTGAG | 29843 |
rs10875743 | snp | C/T | 0.329084 | 0.237162 | upstream-variant-2KB, intron-variant | PFKM, SENP1 | GRCh38.p7 | 12:48104630 | GAGCAGCTCACTGTC[C/T]AGTAGGGAAAGCCAG | 29843 |
rs10875744 | snp | C/G | 0.478104 | 0.102316 | upstream-variant-2KB, intron-variant | PFKM, SENP1 | GRCh38.p7 | 12:48104657 | CCAGATCCATAAACA[C/G]GTACCGCAAGACAGT | 29843 |
rs11168371 | snp | A/G | 0.273318 | 0.24891 | utr-variant-3-prime, nc-transcript-variant | SENP1 | GRCh38.p7 | 12:48043903 | TGCTGGAAAGAATGC[A/G]GTACAACGGGAGAGG | 29843 |
rs11168372 | snp | C/T | 0.5 | 0 | utr-variant-3-prime, nc-transcript-variant | SENP1 | GRCh38.p7 | 12:48044361 | TTTTATACATACATA[C/T]ATATATATATATATG | 29843 |
rs11168373 | snp | C/T | 0.309401 | 0.24284 | intron-variant | SENP1 | GRCh38.p7 | 12:48047810 | GCATTAGGATAGTAA[C/T]TGCTCCCATTAGGGC | 29843 |
rs11168374 | snp | A/G | 0.269267 | 0.249256 | intron-variant | SENP1 | GRCh38.p7 | 12:48054683 | TAATCCCAGCTACTC[A/G]GGGGGCTGGGGCAGG | 29843 |
rs11168375 | snp | G/T | 0.330947 | 0.236533 | intron-variant | SENP1 | GRCh38.p7 | 12:48056420 | TAATTATTTAATATA[G/T]TACATATTACATATA | 29843 |
rs11168376 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | SENP1 | GRCh38.p7 | 12:48057671 | GCTGGAGTACAGTGG[C/T]GCGATCTCAGCTCAC | 29843 |
rs11168377 | snp | A/G | | | intron-variant | SENP1 | GRCh38.p7 | 12:48058081 | CTTCCAGGTAGCTGA[A/G]ATTACAGGCATGCAC | 29843 |
rs11168378 | snp | A/T | 0.306679 | 0.24349 | intron-variant | SENP1 | GRCh38.p7 | 12:48058298 | AAATATGTGGCTCAC[A/T]TTATATTTCTATTGG | 29843 |
rs11168380 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SENP1 | GRCh38.p7 | 12:48066634 | ctcccgcctcagcct[C/T]ccaagtagctaggat | 29843 |
rs11168381 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SENP1 | GRCh38.p7 | 12:48068042 | attttttcttttttt[A/T]atttttattttagta | 29843 |
rs11168382 | snp | A/T | | | intron-variant | SENP1 | GRCh38.p7 | 12:48068043 | ttttttctttttttt[A/T]tttttattttagtag | 29843 |
rs11168383 | snp | A/G | 0.269538 | 0.249235 | intron-variant | SENP1 | GRCh38.p7 | 12:48069085 | TTGAACCCGGGAGGC[A/G]GAGGTTGCAGTGAGC | 29843 |
rs11168384 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | SENP1 | GRCh38.p7 | 12:48071007 | gaggatcacttgagc[C/T]caggagttcaaagct | 29843 |
rs11168385 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | SENP1 | GRCh38.p7 | 12:48071408 | atcacttgaggtcag[A/G]agttcgagaccagcc | 29843 |
rs11168386 | snp | C/T | 0.269538 | 0.249235 | intron-variant | SENP1 | GRCh38.p7 | 12:48074194 | GATTTTGGAACATTT[C/T]GGACTTCATATTTTC | 29843 |
rs11168388 | snp | C/T | 0.375 | 0.216506 | intron-variant | SENP1 | GRCh38.p7 | 12:48076643 | AATATGTAGTTTTTG[C/T]TTTTTTTTTTTCTTT | 29843 |