SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs8420 | snp | C/T | 0 | 0 | utr-variant-3-prime | SUMO2 | GRCh38.p7 | 17:75168223 | CTACCGTATAGTTTT[C/T]TCTATTCTATCATTT | 6613 |
rs13692 | snp | A/C/G | | | utr-variant-3-prime | SUMO2 | GRCh38.p7 | 17:75168048 | GCCACTAATGGAGAA[A/C/G]GGGGGTATTTTCACA | 6613 |
rs752824 | snp | A/T | 0 | 0 | intron-variant | SUMO2 | GRCh38.p7 | 17:75173660 | gcaaaaccctctctt[A/T]acaaaaaaatacaaa | 6613 |
rs899323 | snp | G/T | 0.0333695 | 0.124785 | intron-variant | SUMO2 | GRCh38.p7 | 17:75173799 | ATACTTCCAGTTTTG[G/T]CCTAGCAGGGTGGCT | 6613 |
rs899324 | snp | C/T | 0.0364509 | 0.129988 | intron-variant | SUMO2 | GRCh38.p7 | 17:75173477 | AAAAAAAAAAAAAAA[C/T]GACTTCCAGTCTTGT | 6613 |
rs1471453 | snp | G/T | 0.0329836 | 0.124112 | intron-variant | SUMO2 | GRCh38.p7 | 17:75181349 | CTGCAGGATTTTTCC[G/T]CTTTCACATTGATTT | 6613 |
rs2035252 | snp | A/G | 0.0429648 | 0.14013 | intron-variant | SUMO2 | GRCh38.p7 | 17:75171819 | AGTATCTATTGTGCT[A/G]TACTCTCAGTTATTA | 6613 |
rs2035253 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | SUMO2 | GRCh38.p7 | 17:75171498 | gagacggagttttgc[C/T]ctgtctcccagactg | 6613 |
rs2127081 | snp | C/T | 0 | 0 | downstream-variant-500B | SUMO2 | GRCh38.p7 | 17:75167682 | CTATTTATGTTTTTT[C/T]TAAGCCTCAATTTTC | 6613 |
rs2127082 | snp | A/G | 0.419296 | 0.183954 | intron-variant | SUMO2 | GRCh38.p7 | 17:75176431 | GCGGGGTTTCACCAT[A/G]TTGGCCAGGCTGATC | 6613 |
rs3205678 | snp | A/C | | | utr-variant-3-prime | SUMO2 | GRCh38.p7 | 17:75167983 | AGTTATTTTGCTCTC[A/C]CTGTTTTAACAAAAA | 6613 |
rs3940906 | snp | C/T | 0.0876345 | 0.190099 | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75183414 | GGAAGCAGGTTGAGA[C/T]TGACTGAGAGGAAGT | 6613 |
rs7213926 | snp | A/G | 0.0607341 | 0.163335 | intron-variant | SUMO2 | GRCh38.p7 | 17:75181697 | TTAAAGGAAACACAC[A/G]AACAAAAAAAACAAT | 6613 |
rs7218706 | snp | C/T | 0.499437 | 0.0167637 | intron-variant | SUMO2 | GRCh38.p7 | 17:75175355 | agacagagtcttgct[C/T]tgtcactcaggctgg | 6613 |
rs7225227 | snp | A/G | 0.182296 | 0.240658 | intron-variant | SUMO2 | GRCh38.p7 | 17:75180133 | atcacttgaggtcag[A/G]agttgaggtcaggtc | 6613 |
rs9904412 | snp | C/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75177826 | ggtaaaaccccgttt[C/T]tacgaaaaataaatt | 6613 |
rs9912562 | snp | A/G | 0 | 0 | intron-variant | SUMO2 | GRCh38.p7 | 17:75172346 | tttttttttttttga[A/G]acaggggctgttacc | 6613 |
rs9913676 | snp | A/G | 0.499995 | 0.00159744 | intron-variant | SUMO2 | GRCh38.p7 | 17:75170617 | CAAAAAACCCACGGC[A/G]ggcgtggtggctcac | 6613 |
rs10401019 | snp | C/T | 0.499987 | 0.00259581 | intron-variant | SUMO2 | GRCh38.p7 | 17:75182216 | TCGGGCCCCTGAGGC[C/T]ATTAAAGTGGGAAAT | 6613 |
rs10401035 | snp | A/T | 0.0926964 | 0.194308 | intron-variant | SUMO2 | GRCh38.p7 | 17:75181601 | ACAAAACAATAAATC[A/T]ACAGCCTGCCATTCA | 6613 |
rs11548468 | snp | A/C/T | 0.00019821 | 0.00995316 | utr-variant-5-prime | SUMO2 | GRCh38.p7 | 17:75182883 | TCGTTTGGTGCGGAC[A/C/T]TGGTACCTCTTTTGT | 6613 |
rs11657010 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | SUMO2 | GRCh38.p7 | 17:75178367 | aaaaatacaaaaatt[A/G]gctgggcacggtggc | 6613 |
rs11870102 | snp | A/T | 0.375 | 0.216506 | intron-variant | SUMO2 | GRCh38.p7 | 17:75180393 | TGAGACTCCCAGCTT[A/T]aaaaaaaaaaaaaaa | 6613 |
rs12940697 | snp | C/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75180052 | CCTATTTAGAACAAT[C/T]TGAAGGggccaggca | 6613 |
rs12941564 | snp | C/G | 0.414245 | 0.188477 | intron-variant | SUMO2 | GRCh38.p7 | 17:75180386 | AATAGAGTGAGACTC[C/G]CAGCTTaaaaaaaaa | 6613 |
rs12946898 | snp | C/T | 0.401924 | 0.198543 | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75184601 | gcacctcagacccag[C/T]aactctcaactaaaa | 6613 |
rs13343264 | snp | G/T | 0.0926964 | 0.194308 | intron-variant | SUMO2 | GRCh38.p7 | 17:75179866 | ggattttgccatggt[G/T]gccaggctgatgtca | 6613 |
rs16967636 | snp | A/G | 0.0919752 | 0.193722 | intron-variant | SUMO2 | GRCh38.p7 | 17:75171759 | ATAGCAGATAATCCC[A/G]TTTTAGTGGTGGGTA | 6613 |
rs17850328 | snp | C/T | 1.66366e-05 | 0.0028841 | missense | SUMO2 | GRCh38.p7 | 17:75181164 | TCAAATTAATATGAT[C/T]GTTGTTCTCAGTCTT | 6613 |
rs28391127 | snp | C/T | 0.0926964 | 0.194308 | intron-variant | SUMO2 | GRCh38.p7 | 17:75177240 | AGGCTAGGTGGCAGG[C/T]GCTGTAATCCCAGTT | 6613 |
rs28437274 | snp | A/C | 0.0926964 | 0.194308 | intron-variant | SUMO2 | GRCh38.p7 | 17:75175200 | GTTGGCCAGGCTGGT[A/C]TCGAACTCCTAACCT | 6613 |
rs28759168 | snp | C/T | 0.0876345 | 0.190099 | intron-variant | SUMO2 | GRCh38.p7 | 17:75177080 | CCCAGCTACTCCAGC[C/T]GGAGGTTGAGGGGGG | 6613 |
rs33971007 | in-del | -/C/CTT/CTTT/CTTTT/T | 0 | 0 | intron-variant | SUMO2 | GRCh38.p7 | 17:75172327 | ACTGTACCCAGACTT[-/C/CTT/CTTT/CTTTT/T]TTTTTTTTTTTTTTT | 6613 |
rs34017557 | in-del | -/T/TC/TCTC/TTT | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75172326 | TACTGTACCCAGACT[-/T/TC/TCTC/TTT]CTTTTTTTTTTTTTT | 6613 |
rs34125225 | in-del | -/A | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75170964 | GAAAATATCTTTAAG[-/A]ATACAGTAGATACAG | 6613 |
rs34245817 | in-del | -/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75173479 | AAGACTGGAAGTCGT[-/T]TTTTTTTTTTTTTGA | 6613 |
rs34254735 | in-del | -/A | 0.498392 | 0.028309 | intron-variant | SUMO2 | GRCh38.p7 | 17:75169849 | GTGAGACTTGGTCTC[-/A]AAAAAAAAAAAAAAG | 6613 |
rs34641551 | in-del | -/A | 0.374 | 0.217081 | utr-variant-3-prime | SUMO2 | GRCh38.p7 | 17:75168131 | TAAAAAAAAAAAAAA[-/A]TGCAATATGCTTGTG | 6613 |
rs34969900 | in-del | -/GTT | 0.471673 | 0.115589 | intron-variant | SUMO2 | GRCh38.p7 | 17:75181907 | TCGACCCAACCTAAA[-/GTT]GTCCAAAATCGAGTG | 6613 |
rs35271045 | snp | C/T | 0.441021 | 0.161279 | intron-variant | SUMO2 | GRCh38.p7 | 17:75179199 | CAATTCATAAGTTCA[C/T]GTAGGGTGATTTCAG | 6613 |
rs35302801 | in-del | -/T | 0.107694 | 0.205546 | intron-variant | SUMO2 | GRCh38.p7 | 17:75171067 | CTGTAAGGGGCAGTT[-/T]AAAAAAAAAAAAAAG | 6613 |
rs35348154 | in-del | -/A | 0.488965 | 0.0734569 | intron-variant | SUMO2 | GRCh38.p7 | 17:75179528 | GCGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 6613 |
rs35389462 | in-del | -/A | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75168835 | TCTCAAACTCCTGAG[-/A]CTCAAGTGATCTGCC | 6613 |
rs35509383 | in-del | -/A | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75172121 | CTTTCCCCCGCCCAG[-/A]ATTCTCCTGGCTCAA | 6613 |
rs55817377 | in-del | -/A | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75177186 | CAAAAAAAAAAAAAA[-/A]TTAATTAATTAAATA | 6613 |
rs55895120 | snp | A/G | | | synonymous-codon | SUMO2 | GRCh38.p7 | 17:75168345 | GTTCCCTTTTCAGTA[A/G]ACACCTCCCGTCTGC | 6613 |
rs56156468 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | SUMO2 | GRCh38.p7 | 17:75172111 | CTGTCTGACACCTTT[C/T]CCCCGCCCAGATTCT | 6613 |
rs56225637 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | SUMO2 | GRCh38.p7 | 17:75173745 | GCGTCACAGTGCTGG[C/T]ATTACAAGCACTTTG | 6613 |
rs56335300 | in-del | -/GA | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75173492 | TTTTTTTTTTTTTTT[-/GA]GAGAGAGGGCCTCAC | 6613 |
rs56705892 | snp | C/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75180097 | TGTAATCCCAGCACT[C/T]TGAGAGGCCAAGGTG | 6613 |
rs56739230 | snp | G/T | 0.5 | 0.000399361 | intron-variant | SUMO2 | GRCh38.p7 | 17:75180740 | AAATAATAAAAGACT[G/T]ATAAGTAATTTTACC | 6613 |
rs57535130 | snp | A/C | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75174364 | ACACTGTACTCAAGC[A/C]TGGGCGATGGAGTGA | 6613 |
rs57566541 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SUMO2 | GRCh38.p7 | 17:75179961 | AAAGGAAGTTTTTAT[C/T]TTCACTGATCTTTCA | 6613 |
rs58402695 | in-del | -/A/AAAA | 0 | 0 | intron-variant | SUMO2 | GRCh38.p7 | 17:75180421 | AAAAAAAAAAAAAAA[-/A/AAAA]CGACTTCTTGGTTTG | 6613 |
rs58684188 | in-del | -/AAAA | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75180418 | AAAAAAAAAAAAAAA[-/AAAA]CGACTTCTTGGTTTG | 6613 |
rs59220364 | snp | C/T | 0.109461 | 0.206758 | intron-variant | SUMO2 | GRCh38.p7 | 17:75180895 | TCCTAAGGGTTTTCA[C/T]GAGCTATCAATATAC | 6613 |
rs59613076 | in-del | -/A/AAAAAAA | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75178011 | AAAAAAAAAAAAAAA[-/A/AAAAAAA]GAATCGCCCAGTGGC | 6613 |
rs60507027 | snp | A/G | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75178528 | AAAAAAAAAAAAAAA[A/G]AAAAGAATACTGTTC | 6613 |
rs60542675 | snp | C/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75171164 | GATGGAGTTTCGCTG[C/T]TGTTGCCCAGGGTGG | 6613 |
rs61579555 | in-del | -/AA | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75179545 | AAAAAAAAAAAAAAA[-/AA]GGTATCTTTATAAGG | 6613 |
rs62085030 | snp | G/T | 0.0134861 | 0.0810011 | downstream-variant-500B | SUMO2 | GRCh38.p7 | 17:75167644 | GCTTTATTTCCTTCT[G/T]GAAATGTTACTTCTA | 6613 |
rs62085031 | snp | G/T | 0.5 | 0 | intron-variant | SUMO2 | GRCh38.p7 | 17:75171816 | TTCTAATAACTGAGA[G/T]TACAGCACAATAGAT | 6613 |
rs62085032 | snp | C/T | 0.309894 | 0.242719 | intron-variant | SUMO2 | GRCh38.p7 | 17:75176259 | TAGCCAGGATGGTCT[C/T]AATTTCCTGACCTCG | 6613 |
rs71159444 | in-del | -/T | 0 | 0 | intron-variant | SUMO2 | GRCh38.p7 | 17:75169863 | CCGCCCCCCCCCACC[-/T]TTTTTTTTTTTTTTG | 6613 |
rs71159445 | in-del | -/TTGT/TTTG | 0 | 0 | intron-variant | SUMO2 | GRCh38.p7 | 17:75177837 | CGTGCTCGGCTAATT[-/TTGT/TTTG]TATTTTTCGTAGAAA | 6613 |
rs71361663 | in-del | -/T | 0.5 | 0 | intron-variant | SUMO2 | GRCh38.p7 | 17:75172343 | TTTTTTTTTTTTTTT[-/T]GAGACAGGGGCTGTT | 6613 |
rs71361664 | in-del | -/TGT | 0.5 | 0 | intron-variant | SUMO2 | GRCh38.p7 | 17:75181909 | GACCCAACCTAAAGT[-/TGT]CCAAAATCGAGTGCA | 6613 |
rs71796908 | in-del | -/CAGT | 0.046775 | 0.145601 | intron-variant | SUMO2 | GRCh38.p7 | 17:75170977 | AAGATACAGTAGATA[-/CAGT]GTTAGGCTAAAAACA | 6613 |
rs73352427 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SUMO2 | GRCh38.p7 | 17:75174323 | TTAAGCATGGCAGGC[A/G]AGGGCTGCCATGACC | 6613 |
rs73995797 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | SUMO2 | GRCh38.p7 | 17:75173826 | GTATTTAATGGAACT[C/T]TGAAAGGGTAAAAAG | 6613 |
rs73995798 | snp | G/T | 0.0166325 | 0.0896639 | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75184044 | CTTTATTATTTCCTT[G/T]TGTCCCTGAATTTTC | 6613 |
rs74254449 | snp | A/T | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75171070 | CTGTAAGGGGCAGTT[A/T]AAAAAAAAAAAAAGT | 6613 |
rs74326862 | snp | G/T | 0.5 | 0 | intron-variant | SUMO2 | GRCh38.p7 | 17:75168624 | TTTTTGTTTTTTTTT[G/T]GAGACAGGATTTCTG | 6613 |
rs74976467 | snp | G/T | 0.5 | 0 | intron-variant | SUMO2 | GRCh38.p7 | 17:75173478 | CAAGACTGGAAGTCA[G/T]TTTTTTTTTTTTTTG | 6613 |
rs75175871 | snp | G/T | 0.5 | 0 | intron-variant | SUMO2 | GRCh38.p7 | 17:75173491 | CATTTTTTTTTTTTT[G/T]TGAGAGAGGGCCTCA | 6613 |
rs75176740 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | SUMO2 | GRCh38.p7 | 17:75176593 | AGCACTCCAGCCTGG[A/G]TGACAGACCAGATTC | 6613 |
rs75264446 | in-del | -/AA | | | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75184094 | TAGAAAAAAAAAAAA[-/AA]GCTCCCAATTCTATG | 6613 |
rs75369313 | snp | C/T | 0 | 0 | intron-variant | SUMO2 | GRCh38.p7 | 17:75176185 | GGGCATGGTGGCACG[C/T]GCCTGTAACCCCAGC | 6613 |
rs75642533 | snp | G/T | 0.0501905 | 0.150254 | intron-variant | SUMO2 | GRCh38.p7 | 17:75181714 | ACAAAAAAAACAATC[G/T]AAGAATATCCCGATT | 6613 |
rs75991532 | snp | A/G | | | intron-variant | SUMO2 | GRCh38.p7 | 17:75169068 | TACAAAAAAAAAAAG[A/G]AAAAAAAAAAAAAAT | 6613 |
rs76153429 | snp | G/T | 0 | 0 | intron-variant | SUMO2 | GRCh38.p7 | 17:75173479 | AAGACTGGAAGTCAT[G/T]TTTTTTTTTTTTTGA | 6613 |
rs76340926 | snp | G/T | 0.5 | 0 | intron-variant | SUMO2 | GRCh38.p7 | 17:75168625 | TTTTGTTTTTTTTTT[G/T]AGACAGGATTTCTGT | 6613 |
rs76359910 | snp | A/C/G | 0 | 0 | intron-variant | SUMO2 | GRCh38.p7 | 17:75176150 | CAAGAGGCTGAGGCA[A/C/G]GAGAATCACTTGAAC | 6613 |
rs77301277 | snp | C/T | 0 | 0 | intron-variant | SUMO2 | GRCh38.p7 | 17:75172328 | ACTGTACCCAGACTT[C/T]TTTTTTTTTTTTTTT | 6613 |
rs77515216 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75184095 | AGAAAAAAAAAAAAA[A/G]GCTCCCAATTCTATG | 6613 |
rs79205959 | snp | A/C/G/T | 0.00636936 | 0.0560724 | intron-variant | SUMO2 | GRCh38.p7 | 17:75176132 | GAATCACTTGAACCC[A/C/G/T]GGAGGTGGAGGTTGC | 6613 |
rs79249555 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SUMO2 | GRCh38.p7 | 17:75171546 | AAAAAAGCTGGGGAG[A/G]CAGGAGGCCTGCTAA | 6613 |
rs79489412 | snp | A/T | 0 | 0 | intron-variant | SUMO2 | GRCh38.p7 | 17:75169082 | GGAAAAAAAAAAAAA[A/T]TTAGCCAGCCATGGT | 6613 |
rs79661503 | snp | A/T | 0.5 | 0 | intron-variant | SUMO2 | GRCh38.p7 | 17:75168770 | ACCATGCCCAGCTAA[A/T]TTTTTTGTATTTTTA | 6613 |
rs79694832 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | SUMO2 | GRCh38.p7 | 17:75171583 | TTAATTTATCACAAT[C/T]CTGCTATCTAACAAA | 6613 |
rs79815344 | snp | A/G/T | 0.0268644 | 0.113242 | intron-variant | SUMO2 | GRCh38.p7 | 17:75177968 | CACTCCAGTCTGACC[A/G/T]ACAAAGCGAGACTCC | 6613 |
rs80028650 | snp | C/T | 0.5 | 0 | intron-variant | SUMO2 | GRCh38.p7 | 17:75170403 | GGTGAAACCCTGTTT[C/T]TACCAAAAATACAAA | 6613 |
rs80110636 | snp | A/T | 0.5 | 0 | intron-variant | SUMO2 | GRCh38.p7 | 17:75168768 | CCACCATGCCCAGCT[A/T]ATTTTTTTGTATTTT | 6613 |
rs80223643 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SUMO2 | GRCh38.p7 | 17:75170682 | AGTGAAACCCCGTCT[C/T]TACTAAAAATACAAA | 6613 |
rs80236856 | snp | A/C | 0.5 | 0 | intron-variant | SUMO2 | GRCh38.p7 | 17:75178511 | AGTGCGAGACTCTCA[A/C]AAAAAAAAAAAAAAA | 6613 |
rs80271291 | snp | A/T | 0.5 | 0 | intron-variant | SUMO2 | GRCh38.p7 | 17:75169084 | AAAAAAAAAAAAAAT[A/T]AGCCAGCCATGGTGA | 6613 |
rs111392577 | snp | C/T | 0.039522 | 0.134904 | upstream-variant-2KB | SUMO2 | GRCh38.p7 | 17:75183516 | GCTCAGTCGCCCAGG[C/T]TGGAGTGCAGTGGCA | 6613 |
rs111427495 | snp | C/T | 0.0523666 | 0.153105 | utr-variant-5-prime | SUMO2 | GRCh38.p7 | 17:75182862 | AGTCTCCTCAGCTGC[C/T]GCTTCACAAAAGAGG | 6613 |
rs111503956 | in-del | -/ACAA | 0.0356815 | 0.128715 | intron-variant | SUMO2 | GRCh38.p7 | 17:75177836 | GTTTCTACGAAAAAT[-/ACAA]TAAATTAGCCGAGCA | 6613 |
rs111658496 | snp | A/C | 0.5 | 0 | intron-variant | SUMO2 | GRCh38.p7 | 17:75174566 | AATTAAAAATAAATG[A/C]ATAAAAACCATTGGC | 6613 |