SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs4829 | snp | A/G | 0.485255 | 0.0845871 | intron-variant, utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | COX11, TOM1L1 | GRCh38.p7 | 17:54961954 | AAAAAGTATTAAATT[A/G]TTTTAATAGTGATTT | 10040 |
rs7643 | snp | C/T | 0.488302 | 0.0755777 | intron-variant, utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | COX11, TOM1L1 | GRCh38.p7 | 17:54962122 | ATAATTACTTTGAAA[C/T]TGTAGTATCATAAAA | 10040 |
rs1046935 | snp | A/G | 0 | 0 | intron-variant, utr-variant-3-prime | TOM1L1, COX11 | GRCh38.p7 | 17:54956720 | Tggtggctcatgcct[A/G]taatcccagcacttt | 10040 |
rs1057980 | snp | C/T | 0.371987 | 0.218218 | intron-variant, utr-variant-3-prime, nc-transcript-variant | COX11, TOM1L1 | GRCh38.p7 | 17:54961422 | TCTGTTGAAATCTCA[C/T]GCTGTTGTCAGGAAT | 10040 |
rs1138696 | snp | A/G | | | intron-variant | TOM1L1 | GRCh38.p7 | 17:54938400 | tcaggaggctgaggc[A/G]gaagaatcacttgaa | 10040 |
rs1802212 | snp | G/T | 0.327912 | 0.237549 | missense, utr-variant-3-prime, nc-transcript-variant | COX11, TOM1L1 | GRCh38.p7 | 17:54961293 | CAAAGCTGCACAGAG[G/T]CTACGTTTTAGAGAG | 10040 |
rs1962045 | snp | C/T | 0.325563 | 0.238307 | intron-variant | TOM1L1 | GRCh38.p7 | 17:54918789 | ttgtctactgtattt[C/T]tcctcttggagatgc | 10040 |
rs2024465 | snp | C/T | 0.387263 | 0.208947 | intron-variant, utr-variant-3-prime | TOM1L1, COX11 | GRCh38.p7 | 17:54957291 | TAGGAGTCCACTATG[C/T]ATTTTTTCCTAACTC | 10040 |
rs2111095 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant, utr-variant-3-prime | TOM1L1, COX11 | GRCh38.p7 | 17:54955090 | GTCTCTGCACACAGT[C/T]TGAGGGGCTTCCAAA | 10040 |
rs2111096 | snp | C/T | 0.488545 | 0.074807 | intron-variant, utr-variant-3-prime | TOM1L1, COX11 | GRCh38.p7 | 17:54958667 | cccaggaggtagagg[C/T]tgcagtgagctgaga | 10040 |
rs2287136 | snp | A/G | 0.387263 | 0.208947 | downstream-variant-500B, intron-variant | COX11, TOM1L1 | GRCh38.p7 | 17:54960721 | TTAAATTTTCTAAGG[A/G]CCATCTGAGTCTGAC | 10040 |
rs2332305 | snp | A/T | 0.304937 | 0.243889 | intron-variant | TOM1L1 | GRCh38.p7 | 17:54901313 | CCCGTTTTACAGATC[A/T]GAAGAGGAGGCTCTG | 10040 |
rs2332312 | snp | A/G | 0.369142 | 0.219784 | intron-variant | TOM1L1 | GRCh38.p7 | 17:54919068 | CTGGACTTAGTTTAT[A/G]TATAAAATGAAGAGC | 10040 |
rs2332313 | snp | G/T | 0.48692 | 0.0798058 | intron-variant | TOM1L1 | GRCh38.p7 | 17:54941464 | TAGGTCAGTATCTTC[G/T]GTTGGCTACCTCTTG | 10040 |
rs2332314 | snp | G/T | 0.491316 | 0.0653198 | intron-variant, utr-variant-3-prime | TOM1L1, COX11 | GRCh38.p7 | 17:54955646 | AGCATCCTTGTCTTT[G/T]TGTTGGGGATTCCCC | 10040 |
rs2541234 | snp | C/T | 0.0244538 | 0.107838 | intron-variant, utr-variant-3-prime | TOM1L1, COX11 | GRCh38.p7 | 17:54954869 | ttcccatttaccatg[C/T]ttcttgcaaaaaaag | 10040 |
rs2541238 | snp | A/G | 0.0260105 | 0.111035 | intron-variant, utr-variant-3-prime | TOM1L1, COX11 | GRCh38.p7 | 17:54957634 | TTGAAAGTCCCATGA[A/G]ATTCAGGGACTTCCC | 10040 |
rs2541246 | snp | G/T | 0.0256215 | 0.110247 | intron-variant | TOM1L1, COX11 | GRCh38.p7 | 17:54952582 | aaTATGGCTGctgat[G/T]aaaagtgtggaacca | 10040 |
rs2877634 | snp | A/G | 0.426047 | 0.177503 | intron-variant | TOM1L1 | GRCh38.p7 | 17:54910184 | GTGAGggccaggtgc[A/G]gtggttcatgcctgt | 10040 |
rs2877635 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TOM1L1 | GRCh38.p7 | 17:54902638 | CTAAACTTTGGGGTT[C/T]CCCCAAGCAAGTCCT | 10040 |
rs2877636 | snp | C/T | 0.373397 | 0.217424 | intron-variant | TOM1L1 | GRCh38.p7 | 17:54928682 | TACTATCTGGAGCTT[C/T]AAGAACAACACTGTT | 10040 |
rs2877637 | snp | A/G | 0.387453 | 0.208822 | intron-variant | TOM1L1 | GRCh38.p7 | 17:54930791 | aggttgtggtgagcc[A/G]agatcatgccactgc | 10040 |
rs2877638 | snp | C/T | 0.484561 | 0.0864924 | intron-variant | TOM1L1 | GRCh38.p7 | 17:54941463 | TTAGGTCAGTATCTT[C/T]TGTTGGCTACCTCTT | 10040 |
rs2908862 | snp | C/G | 0.101301 | 0.200969 | intron-variant | TOM1L1 | GRCh38.p7 | 17:54946668 | gagtgagaatgagaa[C/G]ccttctcctagagct | 10040 |
rs2934933 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | TOM1L1 | GRCh38.p7 | 17:54905999 | agatggtgagagccc[A/G]tctctacaaaatgtt | 10040 |
rs2934935 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | TOM1L1 | GRCh38.p7 | 17:54915985 | TACATCCTGATTTCA[A/G]TTGATTTCTAAACTT | 10040 |
rs2934936 | snp | C/T | 0 | 0 | intron-variant | TOM1L1 | GRCh38.p7 | 17:54926252 | ATTTTCTTTAGTTTT[C/T]TGAAGTGGAACGTGA | 10040 |
rs2958909 | snp | A/T | 0 | 0 | intron-variant | TOM1L1 | GRCh38.p7 | 17:54924593 | ggtgaataaatggtg[A/T]tgtgataggacggtg | 10040 |
rs2958910 | snp | C/G | 0.172674 | 0.237741 | intron-variant | TOM1L1 | GRCh38.p7 | 17:54921706 | tctccctctgttacc[C/G]aggctggagtgcagt | 10040 |
rs2958911 | snp | G/T | 0.0248432 | 0.108648 | intron-variant | TOM1L1 | GRCh38.p7 | 17:54920800 | TCTAACTGCAGAGAT[G/T]CCTAGATTCTTTTGG | 10040 |
rs2958912 | snp | A/C | 0.388398 | 0.208197 | intron-variant | TOM1L1 | GRCh38.p7 | 17:54919989 | AATAAATAAATAAAT[A/C]AATCAATAAAAAACC | 10040 |
rs2958913 | snp | C/G | 0.366266 | 0.221319 | upstream-variant-2KB | TOM1L1 | GRCh38.p7 | 17:54899581 | AACATTTAATTATCT[C/G]TAACTCAATTATTTA | 10040 |
rs2958947 | snp | C/T | 0.163564 | 0.234582 | intron-variant | TOM1L1 | GRCh38.p7 | 17:54942935 | CTTCTAGaaagatga[C/T]atattgtataattct | 10040 |
rs3053508 | snp | A/G | 0.48 | 0.0979796 | intron-variant, utr-variant-3-prime | TOM1L1, COX11 | GRCh38.p7 | 17:54958748 | AAAAAAAAAAAAAAA[A/G]GGGGTTGTTGGTAGC | 10040 |
rs3078042 | in-del | -/GTTAA | 0 | 0 | intron-variant | TOM1L1 | GRCh38.p7 | 17:54936875 | ACTTAATGTTATTAA[-/GTTAA]CGTTAATGTTAAACT | 10040 |
rs3087650 | snp | C/T | 0.257176 | 0.249897 | intron-variant, nc-transcript-variant, utr-variant-3-prime | TOM1L1, COX11 | GRCh38.p7 | 17:54951967 | GAAGTTACAGAAGAA[C/T]GCTTTCTGATCCTGG | 10040 |
rs3214380 | in-del | -/T | 0.488545 | 0.074807 | intron-variant, utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | COX11, TOM1L1 | GRCh38.p7 | 17:54961965 | AAAACAATTTAATAC[-/T]TTTTTTTTTTAACAA | 10040 |
rs3834969 | in-del | -/T | 0.395333 | 0.203417 | intron-variant | TOM1L1 | GRCh38.p7 | 17:54914768 | GGAAAAGACATCAAT[-/T]AAATGCAATGATTGT | 10040 |
rs4239188 | snp | A/G | 0.311369 | 0.242351 | intron-variant | TOM1L1 | GRCh38.p7 | 17:54932713 | GGCGTGAGCCACCGC[A/G]CCTGGCCACCATGCT | 10040 |
rs4372751 | snp | A/G | 0.413416 | 0.189196 | intron-variant | TOM1L1 | GRCh38.p7 | 17:54909364 | GGGGTGTCATCATAG[A/G]GTGGGGTAGTCACCT | 10040 |
rs4465655 | snp | C/T | 0.0707826 | 0.174302 | intron-variant | TOM1L1 | GRCh38.p7 | 17:54917278 | TATGGAACTTTAAGA[C/T]GATGAAACTTCCAGT | 10040 |
rs4468693 | snp | C/T | 0.030665 | 0.119967 | intron-variant, nc-transcript-variant, utr-variant-3-prime | TOM1L1, COX11 | GRCh38.p7 | 17:54952015 | CACTGTATCCAGAGA[C/T]GTTAGAGGAGTGAAA | 10040 |
rs4573987 | snp | C/T | 0.312104 | 0.242163 | intron-variant | TOM1L1 | GRCh38.p7 | 17:54924365 | gctcactgcaacctc[C/T]gcctcccatgttcaa | 10040 |
rs4793782 | snp | C/T | 0.387642 | 0.208697 | intron-variant | TOM1L1 | GRCh38.p7 | 17:54947981 | tccactctcaacctg[C/T]ccttcctgcagactt | 10040 |
rs4793783 | snp | C/T | 0.488666 | 0.0744214 | intron-variant | TOM1L1 | GRCh38.p7 | 17:54948119 | aaatatgtcaattat[C/T]cagccacttctcacc | 10040 |
rs4793784 | snp | A/G | 0.485392 | 0.0842056 | downstream-variant-500B, intron-variant | COX11, TOM1L1 | GRCh38.p7 | 17:54961069 | CAATGAACTATCAAA[A/G]CTTATTTATTCCCCT | 10040 |
rs4794547 | snp | A/G | 0.499902 | 0.00698814 | intron-variant | TOM1L1 | GRCh38.p7 | 17:54933811 | taggcgtgagctacc[A/G]cacctggccatccac | 10040 |
rs4794548 | snp | C/G | 0.261884 | 0.249717 | utr-variant-3-prime, intron-variant | TOM1L1 | GRCh38.p7 | 17:54937594 | TAAGGGAGTATCTCT[C/G]ATGCAAGCGGAGAAA | 10040 |
rs5821076 | in-del | -/AA | 0.384017 | 0.211044 | intron-variant | TOM1L1 | GRCh38.p7 | 17:54924750 | ATGTAATCATTCAGT[-/AA]AAACAGGCTTAATGA | 10040 |
rs5821077 | in-del | -/TTAAG | 0.5 | 0 | intron-variant | TOM1L1 | GRCh38.p7 | 17:54936871 | AATAACTTAATGTTA[-/TTAAG]ATTAACGTTAATGTT | 10040 |
rs5821078 | in-del | -/T/TT/TTT | 0.422884 | 0.202686 | intron-variant | TOM1L1 | GRCh38.p7 | 17:54937081 | CTTTTTTTTTTTTTT[-/T/TT/TTT]GCTTTGTTTTCAGAC | 10040 |
rs5821080 | in-del | -/T/TT/TTT | 0.4582 | 0.138394 | intron-variant | TOM1L1 | GRCh38.p7 | 17:54942263 | CCACACCCATCTAAT[-/T/TT/TTT]TTTTTTTTTTTTTTG | 10040 |
rs6504945 | snp | A/G | 0.498034 | 0.0312882 | intron-variant | TOM1L1 | GRCh38.p7 | 17:54922595 | tgagaccctgtctca[A/G]tttaaaaattaaaaa | 10040 |
rs6504946 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | TOM1L1 | GRCh38.p7 | 17:54926765 | AGCATCTTTGAGTCC[A/G]TCTCCCTTTCTTTGC | 10040 |
rs6504947 | snp | A/T | 0.484279 | 0.0872533 | intron-variant | TOM1L1 | GRCh38.p7 | 17:54926783 | TCCCTTTCTTTGCAG[A/T]TGAGGCTGCATATGC | 10040 |
rs7207696 | snp | A/C | 0.164799 | 0.235034 | intron-variant, downstream-variant-500B | TOM1L1, COX11 | GRCh38.p7 | 17:54953223 | GTCTCCACAAACAAA[A/C]AAAAAAATCAGCCAG | 10040 |
rs7207810 | snp | G/T | 0 | 0 | intron-variant | TOM1L1 | GRCh38.p7 | 17:54928786 | GCAAGTCTAAAATCA[G/T]AAAGTCTATCATCTG | 10040 |
rs7208123 | snp | A/G | 0.316243 | 0.241064 | intron-variant | TOM1L1 | GRCh38.p7 | 17:54928978 | ATTGTTTGAGATTCT[A/G]AATGGTTTCATGAAG | 10040 |
rs7209926 | snp | A/G | 0.382666 | 0.211895 | intron-variant | TOM1L1 | GRCh38.p7 | 17:54928963 | GCAGTCTTGTAATAG[A/G]TTGTTTGAGATTCTG | 10040 |
rs7213644 | snp | C/T | 0.497749 | 0.0334707 | intron-variant | TOM1L1 | GRCh38.p7 | 17:54921479 | gcgtggtggctcaca[C/T]ctgtaatcccagcac | 10040 |
rs7214573 | snp | C/T | 0.257732 | 0.24988 | intron-variant | TOM1L1 | GRCh38.p7 | 17:54929293 | TTGGAGTGCTTGTTT[C/T]AAAAAAATGTAGATT | 10040 |
rs7216138 | snp | A/G | 0.366266 | 0.221319 | intron-variant | TOM1L1 | GRCh38.p7 | 17:54918303 | AAAACAAACAAAACA[A/G]CTAGAGGTCATTTCT | 10040 |
rs7217666 | snp | A/G | 0.398894 | 0.200825 | intron-variant | TOM1L1, COX11 | GRCh38.p7 | 17:54960226 | AAAAATTAGCTGGGC[A/G]TGGTTGTGTGTCCCT | 10040 |
rs7220030 | snp | A/C | 0.0729998 | 0.176553 | intron-variant | TOM1L1 | GRCh38.p7 | 17:54942791 | gatacagaatagttc[A/C]gtcactcagcaaaac | 10040 |
rs7222416 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | TOM1L1 | GRCh38.p7 | 17:54911760 | GGTTTCTTCTCCCTC[C/T]GCTTGCCTTTGCAGA | 10040 |
rs7222890 | snp | A/T | 0.407845 | 0.193868 | intron-variant | TOM1L1 | GRCh38.p7 | 17:54911699 | TAGGCCTTTTCTATA[A/T]CATGCCTGAAATAGT | 10040 |
rs7224639 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | TOM1L1 | GRCh38.p7 | 17:54923521 | gtgtctGtattatag[C/T]tttttattttttaaa | 10040 |
rs7224810 | snp | C/T | 0.160938 | 0.233598 | intron-variant | TOM1L1 | GRCh38.p7 | 17:54923631 | gctcactgcaacctc[C/T]gcctcctggatttga | 10040 |
rs7224947 | snp | C/T | 0.385741 | 0.209939 | intron-variant | TOM1L1 | GRCh38.p7 | 17:54923686 | gagtagctgagacta[C/T]aggtgcctgccacca | 10040 |
rs7501447 | snp | A/C/G | 0.00119737 | 0.0244387 | intron-variant | TOM1L1 | GRCh38.p7 | 17:54904287 | aggcaggagaatggc[A/C/G]tgagcctgggaggtg | 10040 |
rs7503269 | snp | C/T | 0.499961 | 0.0043928 | intron-variant | TOM1L1 | GRCh38.p7 | 17:54942351 | tgacctacggtgatc[C/T]gcccacctcggcttc | 10040 |
rs8065212 | snp | C/T | 0.360632 | 0.224189 | intron-variant | TOM1L1 | GRCh38.p7 | 17:54946879 | acctttaagtgacat[C/T]cagtggagagacaga | 10040 |
rs8065361 | snp | A/T | 0.382666 | 0.211895 | intron-variant | TOM1L1 | GRCh38.p7 | 17:54931492 | AGTGAATTAAGAGAA[A/T]CCATGAAATAAAGCC | 10040 |
rs8066588 | snp | C/T | 0.257176 | 0.249897 | intron-variant | TOM1L1 | GRCh38.p7 | 17:54948328 | catttgctcaaaacc[C/T]acctgtgattttctt | 10040 |
rs8066744 | snp | A/T | 0.389527 | 0.207442 | intron-variant, downstream-variant-500B, utr-variant-3-prime | TOM1L1, COX11 | GRCh38.p7 | 17:54956484 | ctaatttttttgtat[A/T]tttagtagagacagg | 10040 |
rs8066750 | snp | C/T | 0.389527 | 0.207442 | intron-variant, downstream-variant-500B, utr-variant-3-prime | TOM1L1, COX11 | GRCh38.p7 | 17:54956293 | gagactattggggtg[C/T]gctaccatgcctggc | 10040 |
rs8066833 | snp | A/G | 0.257176 | 0.249897 | intron-variant | TOM1L1 | GRCh38.p7 | 17:54948114 | ttttaaaatatgtca[A/G]ttattcagccacttc | 10040 |
rs8067139 | snp | A/C | 0.34437 | 0.231505 | upstream-variant-2KB | TOM1L1 | GRCh38.p7 | 17:54898958 | CCAGGCATTGCTGAG[A/C]TAGAACACAGGTAGC | 10040 |
rs8067361 | snp | A/G | 0.0422008 | 0.138995 | intron-variant | TOM1L1 | GRCh38.p7 | 17:54925496 | gacagtggatctgga[A/G]ggccaaggaaagttc | 10040 |
rs8068364 | snp | A/T | 0.021333 | 0.101051 | intron-variant | TOM1L1, COX11 | GRCh38.p7 | 17:54952500 | tgcagtgagcccaga[A/T]cgtgccccactgcat | 10040 |
rs8069447 | snp | G/T | 0.499908 | 0.00678851 | intron-variant | TOM1L1 | GRCh38.p7 | 17:54931512 | GAAATAAAGCCAGTA[G/T]TTATGggccaagaat | 10040 |
rs8070668 | snp | A/G | 0.41408 | 0.188621 | intron-variant | TOM1L1 | GRCh38.p7 | 17:54914275 | AGCTGTGGCTTAAAA[A/G]GACTTGACATGAATT | 10040 |
rs8071572 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | TOM1L1 | GRCh38.p7 | 17:54922621 | aaaaaagaaaaattt[A/C]tttaagaaaattata | 10040 |
rs8072502 | snp | A/C | 0.0513262 | 0.151752 | intron-variant | TOM1L1 | GRCh38.p7 | 17:54922854 | ctctatttaattcca[A/C]tacattttcattacc | 10040 |
rs8073158 | snp | A/C | 0.257732 | 0.24988 | intron-variant | TOM1L1 | GRCh38.p7 | 17:54951254 | aagagatgcacaggg[A/C]gaggcatgcggaaaa | 10040 |
rs8076984 | snp | C/T | 0.257176 | 0.249897 | intron-variant, utr-variant-3-prime | TOM1L1, COX11 | GRCh38.p7 | 17:54958067 | tttggaaatgagtat[C/T]gtaggcccaaggaac | 10040 |
rs8078896 | snp | A/G | 0.391769 | 0.205917 | intron-variant | TOM1L1, COX11 | GRCh38.p7 | 17:54952329 | gaggccaaggcgcgc[A/G]gatcaccctgaattc | 10040 |
rs9303360 | snp | C/T | 0.498437 | 0.0279115 | intron-variant | TOM1L1 | GRCh38.p7 | 17:54924095 | actagacctctctag[C/T]ctggccacagagccc | 10040 |
rs9889234 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | TOM1L1 | GRCh38.p7 | 17:54921201 | ctttagatcttattt[C/G]gttttgagcctttga | 10040 |
rs9889559 | snp | C/T | 0.377187 | 0.215229 | intron-variant | TOM1L1 | GRCh38.p7 | 17:54906361 | GTAGTCCCAGCTACT[C/T]GGGAGTCTGAGACAG | 10040 |
rs9889882 | snp | C/T | 0.0388213 | 0.133804 | intron-variant | TOM1L1 | GRCh38.p7 | 17:54930064 | AAATCTCTCTCCTTT[C/T]TTTGACAGAAACTCT | 10040 |
rs9891704 | snp | A/G | 0.383246 | 0.211531 | intron-variant | TOM1L1 | GRCh38.p7 | 17:54933394 | TTACTAAtgtgaacc[A/G]aaagtatctgagaca | 10040 |
rs9893378 | snp | A/C | 0.115438 | 0.210697 | intron-variant | TOM1L1 | GRCh38.p7 | 17:54934090 | cacttctacataagc[A/C]gtagggcagaggaag | 10040 |
rs9895901 | snp | A/G | 0.35809 | 0.225425 | intron-variant | TOM1L1 | GRCh38.p7 | 17:54907524 | TACTGTGTTTCCTTT[A/G]TGTCTTTAGTTTCTT | 10040 |
rs9897646 | snp | C/G | 0.314301 | 0.241589 | intron-variant | TOM1L1 | GRCh38.p7 | 17:54907990 | CTCCTTGAGGAAGTT[C/G]GGCTATTCCAGAGTG | 10040 |
rs9897844 | snp | A/T | 0 | 0 | intron-variant | TOM1L1, COX11 | GRCh38.p7 | 17:54960502 | TACAGTGCTGGCAGT[A/T]AAAAACCAAAATAGC | 10040 |
rs9899412 | snp | A/C | 0.292008 | 0.246445 | intron-variant | TOM1L1 | GRCh38.p7 | 17:54925922 | AAAAAACAACAACAA[A/C]AAAAAAAGCAGCCTG | 10040 |
rs9899545 | snp | C/T | 0.314544 | 0.241524 | intron-variant | TOM1L1 | GRCh38.p7 | 17:54909484 | GAGAAAACTGTCAAC[C/T]ACCTCTTTTTCTTCC | 10040 |
rs9899602 | snp | C/T | 0.314544 | 0.241524 | intron-variant | TOM1L1 | GRCh38.p7 | 17:54909547 | CATCACATTCACTCC[C/T]GCTAGGAAGTTCTCC | 10040 |
rs9900816 | snp | A/C/G | 0.397179 | 0.214867 | intron-variant | TOM1L1 | GRCh38.p7 | 17:54934696 | GAATATAAGAAGCTA[A/C/G]TGCTATAACTAGATG | 10040 |