SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs7385 | snp | A/C | 0.448963 | 0.151372 | utr-variant-3-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75715878 | TTGCAACTTCTAAAC[A/C]CAAATAAAAAGAAAA | 26054 |
rs9250 | snp | A/G | 0.390868 | 0.206534 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75715572 | AAGGAACAGAACAAT[A/G]TGTCAATAGTATCTC | 26054 |
rs12302 | snp | A/G | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75715633 | TACTTTCAGAAACTA[A/G]ATGACTTTCAAATTT | 26054 |
rs276681 | snp | A/T | 0.0295035 | 0.117819 | utr-variant-3-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75715657 | CAAATTTGGGTATAG[A/T]CAATAAAGAACTGAA | 26054 |
rs276683 | snp | A/G | 0.449726 | 0.150364 | utr-variant-3-prime, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75716686 | ATAGGGATCTTGCAT[A/G]TATCTGCAGAAACTT | 26054 |
rs276684 | snp | A/G | 0.367708 | 0.220556 | utr-variant-3-prime, downstream-variant-500B | SENP6 | GRCh38.p7 | 6:75717349 | CCTACTTGTTTTTGC[A/G]TTAATTTGTAATGCT | 26054 |
rs471638 | snp | A/C | 0.449979 | 0.150028 | intron-variant | SENP6 | GRCh38.p7 | 6:75627859 | aaaccccgtctctta[A/C]taaaaatataaaaaa | 26054 |
rs472458 | snp | C/T | 0.450105 | 0.149859 | intron-variant | SENP6 | GRCh38.p7 | 6:75660870 | gctgaggtgggtgga[C/T]cacgtgaggtcagga | 26054 |
rs477976 | snp | C/T | 0.0770498 | 0.180522 | intron-variant | SENP6 | GRCh38.p7 | 6:75660269 | GTAAAATATCATTAA[C/T]GTGAAAATCAACATC | 26054 |
rs478934 | snp | C/T | 0.487113 | 0.0792303 | intron-variant | SENP6 | GRCh38.p7 | 6:75615380 | ctagcctggccaatg[C/T]tgcgaaaccccgtct | 26054 |
rs494761 | snp | A/C | 0.0425829 | 0.139564 | intron-variant | SENP6 | GRCh38.p7 | 6:75614682 | cattgatgattcatg[A/C]ctgaatcccccaatt | 26054 |
rs494940 | snp | A/G | 0.368119 | 0.220336 | intron-variant | SENP6 | GRCh38.p7 | 6:75645381 | TGATCTGCCTGCCTC[A/G]GCCTCCCAAAGTGCT | 26054 |
rs498753 | snp | A/G | 0.186737 | 0.241863 | intron-variant | SENP6 | GRCh38.p7 | 6:75636430 | AGGAAGAAAACCGAA[A/G]AACTCTCAATGACTT | 26054 |
rs499527 | snp | A/G | 0.186421 | 0.24178 | intron-variant | SENP6 | GRCh38.p7 | 6:75636378 | TTTAGTGACAGTCAT[A/G]CTGCAGTTGGAATAA | 26054 |
rs501181 | snp | G/T | 0 | 0 | intron-variant | SENP6 | GRCh38.p7 | 6:75655454 | catgttctttcacag[G/T]tagtccctacctctt | 26054 |
rs504446 | snp | A/G | 0.367708 | 0.220556 | intron-variant | SENP6 | GRCh38.p7 | 6:75617223 | CATTGAAACTTCTAT[A/G]TAAATTTAAATGTAT | 26054 |
rs507662 | snp | C/T | 0.0779399 | 0.181371 | synonymous-codon, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75659338 | ATAGGTACTACAGTG[C/T]CGTTTCTGTTGTACT | 26054 |
rs510535 | snp | C/T | 0.498434 | 0.0279367 | intron-variant | SENP6 | GRCh38.p7 | 6:75659001 | ATACTCACAATTCCC[C/T]TTTTTTTTTTTTTTT | 26054 |
rs511900 | snp | C/T | 0.186737 | 0.241863 | intron-variant | SENP6 | GRCh38.p7 | 6:75616540 | AGGCTGGTCTCGAAC[C/T]CCTGACCTTGTGATC | 26054 |
rs515538 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SENP6 | GRCh38.p7 | 6:75649185 | tgggattataggtat[A/G]tgccatcatgcccag | 26054 |
rs518622 | snp | A/G | 0.449979 | 0.150028 | intron-variant | SENP6 | GRCh38.p7 | 6:75614353 | gcttaaacctgggag[A/G]cagaggttgcagtga | 26054 |
rs518969 | snp | G/T | 0.449979 | 0.150028 | intron-variant | SENP6 | GRCh38.p7 | 6:75639390 | AAAAATATACAAATT[G/T]AAAAAAAATTTTCAA | 26054 |
rs523465 | snp | C/G | 0.367708 | 0.220556 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75620718 | GCAGTGGGGATAATT[C/G]TGATGTCTTAAGCTT | 26054 |
rs525178 | snp | A/C | 0.186737 | 0.241863 | intron-variant | SENP6 | GRCh38.p7 | 6:75630350 | Tggccgagcagctca[A/C]acctgtaatcccagc | 26054 |
rs526908 | snp | C/T | 0.0433465 | 0.140692 | intron-variant | SENP6 | GRCh38.p7 | 6:75613459 | tctgCCCTAGAGAAA[C/T]ATACATGCACAAGGA | 26054 |
rs567903 | snp | C/T | 0.367091 | 0.220884 | intron-variant | SENP6 | GRCh38.p7 | 6:75618135 | tgtctgtgtttttga[C/T]gtaagttaccaagtt | 26054 |
rs569731 | snp | C/T | 0.368119 | 0.220336 | intron-variant | SENP6 | GRCh38.p7 | 6:75647877 | GGAATATTCTAAAGC[C/T]AGCATCGTATCTCCA | 26054 |
rs570939 | snp | C/T | 0.487049 | 0.0794222 | intron-variant | SENP6 | GRCh38.p7 | 6:75657008 | CAGGATGAAATGATA[C/T]TGTTTTTTTAAATGT | 26054 |
rs572118 | snp | C/T | 0.187053 | 0.241946 | intron-variant | SENP6 | GRCh38.p7 | 6:75615974 | CTTTCTTTGGTCAAC[C/T]ATACTAGTTCCTATT | 26054 |
rs594804 | snp | C/T | 0.450105 | 0.149859 | intron-variant | SENP6 | GRCh38.p7 | 6:75654038 | CAGGGTCTCACTATG[C/T]TGGCCAGTCTGGTCT | 26054 |
rs602873 | snp | A/T | 0.367708 | 0.220556 | intron-variant | SENP6 | GRCh38.p7 | 6:75614102 | attccttatattttt[A/T]aaaaatgcataacct | 26054 |
rs603301 | snp | C/T | 0.187053 | 0.241946 | intron-variant | SENP6 | GRCh38.p7 | 6:75614009 | cctgttttcttaaaa[C/T]atgtcaaggtcaaga | 26054 |
rs613562 | snp | A/T | 0.449726 | 0.150364 | intron-variant | SENP6 | GRCh38.p7 | 6:75647941 | ATTGAAGAAATTCTC[A/T]AATCAGTTACAAAAA | 26054 |
rs614065 | snp | C/T | 0.367297 | 0.220775 | intron-variant | SENP6 | GRCh38.p7 | 6:75605917 | CCCAGTCTCCACTGA[C/T]ATCATGCTAATTGAA | 26054 |
rs618239 | snp | C/T | 0.367913 | 0.220446 | intron-variant | SENP6 | GRCh38.p7 | 6:75640322 | TAGTACCGAATCCAA[C/T]ATACCAAAATGAAGC | 26054 |
rs619786 | snp | A/G | 0.449979 | 0.150028 | intron-variant, upstream-variant-2KB | SENP6 | GRCh38.p7 | 6:75619239 | cagaggctaaaggaa[A/G]tagagaaatggagaa | 26054 |
rs619920 | snp | C/G | 0.449853 | 0.150196 | intron-variant | SENP6 | GRCh38.p7 | 6:75612584 | ctagcgttttgggtg[C/G]ctaaggcaagaggat | 26054 |
rs634862 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SENP6 | GRCh38.p7 | 6:75611540 | ATTCTGTGAGACAGA[C/T]CAATGAAATTTGAGA | 26054 |
rs646967 | snp | C/T | 0.449599 | 0.150533 | intron-variant | SENP6 | GRCh38.p7 | 6:75611130 | ACTAAATTCTGGAGA[C/T]AAGATGAAGGTACTA | 26054 |
rs655471 | snp | C/T | 0.0711525 | 0.174681 | intron-variant | SENP6 | GRCh38.p7 | 6:75623770 | TAAAGGGCCAAACCA[C/T]AGTCTTTGCAGGCCA | 26054 |
rs657638 | snp | A/T | 0.187053 | 0.241946 | intron-variant | SENP6 | GRCh38.p7 | 6:75629894 | aaaaactcactcata[A/T]ctgctgctaatcaaa | 26054 |
rs664019 | snp | C/T | 0.186737 | 0.241863 | intron-variant | SENP6 | GRCh38.p7 | 6:75609618 | TGTCATTTAAAATAC[C/T]ACATGACTGTTGAAA | 26054 |
rs671806 | snp | C/T | 0.186421 | 0.24178 | intron-variant | SENP6 | GRCh38.p7 | 6:75622429 | CTGGATGTGGTGGCA[C/T]ACACCTGTAATCCCA | 26054 |
rs672731 | snp | G/T | 0.0696718 | 0.173152 | intron-variant | SENP6 | GRCh38.p7 | 6:75628829 | gggaggctgaggcgg[G/T]aggatcgcttgagcc | 26054 |
rs675681 | snp | C/G | 0.367708 | 0.220556 | intron-variant | SENP6 | GRCh38.p7 | 6:75652600 | atccacctgcctcgg[C/G]ctcccaaagtgccag | 26054 |
rs678985 | snp | A/G | 0.187053 | 0.241946 | intron-variant | SENP6 | GRCh38.p7 | 6:75608550 | gaaggaaagaaagga[A/G]gaaagaaaggaagga | 26054 |
rs684966 | snp | A/C | | | intron-variant | SENP6 | GRCh38.p7 | 6:75658975 | gagaccttgtctccc[A/C]aaaaaaaaaaaaaaa | 26054 |
rs688398 | snp | A/G | 0.368119 | 0.220336 | intron-variant | SENP6 | GRCh38.p7 | 6:75653139 | GGAGGGTGAGGCAGG[A/G]AAATCGCTTGAACCC | 26054 |
rs696645 | snp | G/T | 0.186737 | 0.241863 | intron-variant | SENP6 | GRCh38.p7 | 6:75651450 | GCCTCGACCTCCTAG[G/T]CTTACATCATTCTCC | 26054 |
rs699169 | snp | A/G | 0.0711525 | 0.174681 | intron-variant | SENP6 | GRCh38.p7 | 6:75664155 | CTTCTAAAAAATAGA[A/G]ATTGGGCACAGTGGT | 26054 |
rs699170 | snp | A/G | 0.159292 | 0.232964 | intron-variant | SENP6 | GRCh38.p7 | 6:75664261 | TAGGACCCTGTTGCT[A/G]AAAAAAAAAAACAAT | 26054 |
rs715090 | snp | G/T | 0.301932 | 0.244547 | intron-variant | SENP6 | GRCh38.p7 | 6:75651447 | GCAGCCTCGACCTCC[G/T]AGTCTTACATCATTC | 26054 |
rs715091 | snp | A/G | 0 | 0 | intron-variant | SENP6 | GRCh38.p7 | 6:75651552 | AGATAAGGTTTCACC[A/G]TGTTGCCCAGTTTGC | 26054 |
rs766244 | snp | C/T | 0.321292 | 0.23962 | intron-variant | SENP6 | GRCh38.p7 | 6:75657485 | TTTGTGACACAGAGA[C/T]AATGATTCATACACA | 26054 |
rs775057 | snp | C/T | 0.186421 | 0.24178 | intron-variant | SENP6 | GRCh38.p7 | 6:75647145 | CTGTTGCACTTTTTG[C/T]AGTTCCCCTTCTGTG | 26054 |
rs775058 | snp | C/T | 0.187053 | 0.241946 | intron-variant | SENP6 | GRCh38.p7 | 6:75658721 | AGTAATGAGAAAAAT[C/T]TGAATTCAAACAGTA | 26054 |
rs775059 | snp | A/C | 0.367708 | 0.220556 | intron-variant | SENP6 | GRCh38.p7 | 6:75660414 | attcatatgtacatg[A/C]tgatataaatgaata | 26054 |
rs775060 | snp | A/G | 0.367913 | 0.220446 | intron-variant | SENP6 | GRCh38.p7 | 6:75663851 | CTAAAATAACATAAA[A/G]TATGCATAGCCCAAT | 26054 |
rs775061 | snp | A/T | 0.186737 | 0.241863 | intron-variant | SENP6 | GRCh38.p7 | 6:75664805 | cgcatgacttttgaa[A/T]gctttttctgtgtca | 26054 |
rs775071 | snp | A/G | 0.487177 | 0.0790385 | intron-variant | SENP6 | GRCh38.p7 | 6:75667789 | TTGGCAAACAAAATC[A/G]TTGCCTGTTAATATG | 26054 |
rs775072 | snp | A/G | 0.368119 | 0.220336 | intron-variant | SENP6 | GRCh38.p7 | 6:75668282 | GTAGCACGAGCAAAA[A/G]TAGTAAATGAAAAGA | 26054 |
rs775073 | snp | C/T | 0.186421 | 0.24178 | intron-variant | SENP6 | GRCh38.p7 | 6:75668345 | GTGTAGCAAAACACT[C/T]TAAACACAATTTGAT | 26054 |
rs775074 | snp | A/G | 0.177824 | 0.239355 | intron-variant | SENP6 | GRCh38.p7 | 6:75669989 | CCCAGGCTGGAGTGC[A/G]GTGGTGCGTTCTCAG | 26054 |
rs775075 | snp | A/C | 0.368119 | 0.220336 | intron-variant | SENP6 | GRCh38.p7 | 6:75670319 | GAGTACTATTCCTGA[A/C]TGCCATACTATTACT | 26054 |
rs775076 | snp | G/T | 0.186737 | 0.241863 | intron-variant | SENP6 | GRCh38.p7 | 6:75672852 | TTTTGTTTTGAGACA[G/T]AGTCTCACTCTGTTG | 26054 |
rs775077 | snp | A/G | 0.0429648 | 0.14013 | intron-variant | SENP6 | GRCh38.p7 | 6:75673280 | ATTCAGTTTAAATTT[A/G]GAAACTTTCACAATG | 26054 |
rs956653 | snp | G/T | 0.25912 | 0.249834 | intron-variant | SENP6 | GRCh38.p7 | 6:75663064 | TTAATTTTGAGACTT[G/T]GAGGGGATTCCTTAA | 26054 |
rs956654 | snp | A/C | 0 | 0 | intron-variant | SENP6 | GRCh38.p7 | 6:75663144 | TTAAAGTTTATGAAC[A/C]CCGTGAATGTTCAAA | 26054 |
rs985487 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75664095 | ATTAAGTGAATAATG[C/G]AAGCTACAGATAAGA | 26054 |
rs985488 | snp | A/G | 0 | 0 | intron-variant | SENP6 | GRCh38.p7 | 6:75664367 | CATGGGCCTTTTTAA[A/G]AAATCTATATACATG | 26054 |
rs986064 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SENP6 | GRCh38.p7 | 6:75660023 | tatgcttatagaatt[C/G]aattcagggtcatgt | 26054 |
rs1018103 | snp | A/C | 0.487049 | 0.0794222 | intron-variant, utr-variant-3-prime | SENP6 | GRCh38.p7 | 6:75679273 | gactataggtatatg[A/C]ctggctaatttttaa | 26054 |
rs1061347 | snp | A/G | 1.65877e-05 | 0.00287986 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75678643 | CAGTTTTTTGATGAA[A/G]AAGAAGAAACTGGAG | 26054 |
rs1061348 | snp | G/T | 0 | 0 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75678845 | CCTCCAGCTAAGGGA[G/T]GCATCTCTGTTACCA | 26054 |
rs1091353 | snp | C/T | 0.186105 | 0.241697 | intron-variant | SENP6 | GRCh38.p7 | 6:75604262 | AACTCGAATTTATCA[C/T]ACCTATACATTCAAA | 26054 |
rs1391559 | snp | G/T | 0.186737 | 0.241863 | intron-variant | SENP6 | GRCh38.p7 | 6:75677321 | AAAGGGAAATATGTT[G/T]TATTTTAATACTGTT | 26054 |
rs1498383 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | SENP6 | GRCh38.p7 | 6:75645980 | AAAGATGGCTCAGTA[C/T]ACAAGTTCAAATTGC | 26054 |
rs2133192 | snp | A/G | 0.487241 | 0.0788465 | intron-variant | SENP6 | GRCh38.p7 | 6:75696370 | TTAGATATTATGGAT[A/G]AACATCTAGGATAAA | 26054 |
rs2133193 | snp | C/T | 0.258843 | 0.249844 | intron-variant | SENP6 | GRCh38.p7 | 6:75696284 | CACATTTGGGAAACA[C/T]TATTCTAGATATTTG | 26054 |
rs2173402 | snp | C/T | 0.449979 | 0.150028 | intron-variant | SENP6 | GRCh38.p7 | 6:75694987 | cttgggaggctgagg[C/T]gggagaatcacttga | 26054 |
rs2275114 | snp | A/G | 0.0715223 | 0.175059 | intron-variant | SENP6 | GRCh38.p7 | 6:75647652 | AATGGCATACTTACA[A/G]TAAGCCTATTAAAAG | 26054 |
rs2297698 | snp | A/G | 0.0296125 | 0.118023 | intron-variant | SENP6 | GRCh38.p7 | 6:75602599 | CCCTCCCTTCTCCCC[A/G]TCAAGGGCAGAAACA | 26054 |
rs2313589 | snp | C/T | 0.293294 | 0.246223 | intron-variant | SENP6 | GRCh38.p7 | 6:75608837 | TAATAAAATAAATAA[C/T]ATCAAGTAACACGGA | 26054 |
rs2647399 | snp | C/T | 0.431916 | 0.171483 | intron-variant | SENP6 | GRCh38.p7 | 6:75680361 | CAGTTGAGCAAATGG[C/T]GCTAGAGTTTGGTTG | 26054 |
rs2647400 | snp | C/G | 0.499424 | 0.0169631 | intron-variant | SENP6 | GRCh38.p7 | 6:75642283 | ggacaaagactaata[C/G]tgaacaagtaaaaca | 26054 |
rs2647401 | snp | A/G | 0.431916 | 0.171483 | intron-variant | SENP6 | GRCh38.p7 | 6:75643336 | CATACTAAAATAACA[A/G]TGTGAAAGTAAGTTT | 26054 |
rs2647402 | snp | A/G | 0.43221 | 0.171171 | intron-variant | SENP6 | GRCh38.p7 | 6:75646013 | GAGCACTGCATTAAT[A/G]TAACAGTTTCATCAA | 26054 |
rs2647403 | snp | C/T | 0.431916 | 0.171483 | intron-variant | SENP6 | GRCh38.p7 | 6:75652330 | ATTTTTATATCCAAG[C/T]TTCTATAATCTTTTT | 26054 |
rs2647409 | snp | C/T | 0.431916 | 0.171483 | intron-variant | SENP6 | GRCh38.p7 | 6:75660751 | gttcttctgtctcag[C/T]ctcctgagtatctgg | 26054 |
rs2647412 | snp | A/G | 0.43221 | 0.171171 | downstream-variant-500B | SENP6 | GRCh38.p7 | 6:75718601 | TTTTCTTCTTCCTGA[A/G]TAGGAAATGACAAAT | 26054 |
rs2647413 | snp | C/T | 0.432357 | 0.171014 | intron-variant | SENP6 | GRCh38.p7 | 6:75695032 | aaaaatttagccggg[C/T]gtggtggcgagtgcc | 26054 |
rs2647414 | snp | A/G | 0.0696718 | 0.173152 | intron-variant | SENP6 | GRCh38.p7 | 6:75665523 | ttgtatttgactcAA[A/G]TACAATGTGAGTGGC | 26054 |
rs2647415 | snp | A/G | 0.486984 | 0.079614 | intron-variant | SENP6 | GRCh38.p7 | 6:75665605 | CAAGGTATAAGAGCA[A/G]ATTACCATCATAGTG | 26054 |
rs2647416 | snp | C/T | 0.487368 | 0.0784625 | intron-variant | SENP6 | GRCh38.p7 | 6:75665824 | CTGAGGTCGGGAGTT[C/T]GAGACCAGCCTGGCC | 26054 |
rs2647418 | snp | A/G | 0.432063 | 0.171327 | intron-variant | SENP6 | GRCh38.p7 | 6:75673147 | GCATTATTTAGAAGC[A/G]TCCATTTTATTTAAA | 26054 |
rs2647419 | snp | C/G | 0.429837 | 0.173662 | intron-variant | SENP6 | GRCh38.p7 | 6:75674208 | GTTGCTCAGGCTGGA[C/G]TTCAGTGCTGCAGTC | 26054 |
rs2748953 | snp | A/T | 0.432357 | 0.171014 | intron-variant | SENP6 | GRCh38.p7 | 6:75714658 | CACCTATGTGATCTG[A/T]CCCCCTATTTAAGCT | 26054 |
rs2756039 | snp | A/T | 0.431621 | 0.171796 | intron-variant | SENP6 | GRCh38.p7 | 6:75639389 | AAAATATACAAATTT[A/T]AAAAAAATTTTCAAA | 26054 |
rs2783350 | snp | C/G/T | 0.000531403 | 0.0162917 | missense, nc-transcript-variant | SENP6 | GRCh38.p7 | 6:75670626 | CTCCAGATGCTTTAG[C/G/T]TTTAAGCTGCCAAAG | 26054 |
rs2783351 | snp | C/T | 0.474701 | 0.109588 | intron-variant | SENP6 | GRCh38.p7 | 6:75663558 | TTGCTTATATCAATC[C/T]AGTATTTTTCAGATA | 26054 |