SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs2063276 | snp | A/G | 0.449373 | 0.150832 | missense | TRIM51 | GRCh38.p7 | 11:55885487 | GTCCCATCTGCATGA[A/G]CTACTTCCTAGACCC | 84767 |
rs2063277 | snp | A/C | 0.0261367 | 0.111289 | missense | TRIM51 | GRCh38.p7 | 11:55885495 | TGCATGAACTACTTC[A/C]TAGACCCAGTCACCA | 84767 |
rs3862669 | snp | A/G | 0.0543475 | 0.155628 | intron-variant | TRIM51 | GRCh38.p7 | 11:55887680 | ACATAACTTGCCCCA[A/G]TTCTCCAAAGTAGAA | 84767 |
rs3862670 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | TRIM51 | GRCh38.p7 | 11:55888456 | AGGTCCCTCCTACTT[C/T]ATCCACCAGCAACAA | 84767 |
rs4107303 | snp | A/G | 0.255782 | 0.249933 | intron-variant | TRIM51 | GRCh38.p7 | 11:55889189 | TTATTAAGCAGCTCA[A/G]TGAAAGTTCTGCAAA | 84767 |
rs4107304 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | TRIM51 | GRCh38.p7 | 11:55889206 | GAAAGTTCTGCAAAA[C/G]CAAAAAAATAAATAA | 84767 |
rs4107305 | snp | A/G | 0.434253 | 0.168969 | downstream-variant-500B | TRIM51 | GRCh38.p7 | 11:55892101 | AACCTATACTTTGAG[A/G]TAATCTTATTTGACC | 84767 |
rs4125446 | snp | A/G | 0.278133 | 0.248412 | upstream-variant-2KB | TRIM51 | GRCh38.p7 | 11:55881856 | AGTCAATATTTAGTT[A/G]TTTTTTAAAATTCAA | 84767 |
rs4341561 | snp | A/G | 0.0126979 | 0.078662 | upstream-variant-2KB | TRIM51 | GRCh38.p7 | 11:55882571 | TGGATTGTTAGTTCC[A/G]GCTTTTATTCTGTCA | 84767 |
rs4489766 | snp | A/G | 0 | 0 | intron-variant | TRIM51 | GRCh38.p7 | 11:55886830 | AGTCTAAGGACTTGA[A/G]AAGAATTCTAGAAAT | 84767 |
rs4939537 | snp | G/T | 0.440609 | 0.161766 | upstream-variant-2KB | TRIM51 | GRCh38.p7 | 11:55881495 | ATAAAATATATTCTG[G/T]TTTTTTTTCTTTATT | 84767 |
rs4939538 | snp | C/T | 0.255224 | 0.249945 | upstream-variant-2KB | TRIM51 | GRCh38.p7 | 11:55882236 | ATGGGAAACCGTTTT[C/T]TGGAGGCAGTAGTAA | 84767 |
rs7120357 | snp | C/T | 0.0158847 | 0.0876927 | intron-variant | TRIM51 | GRCh38.p7 | 11:55889923 | TGTAGATGTGATAAC[C/T]CTATCTTTCCCCTTG | 84767 |
rs7126397 | snp | A/G | 0.0158931 | 0.0877152 | intron-variant | TRIM51 | GRCh38.p7 | 11:55889918 | TTGGCTGTAGATGTG[A/G]TAACCCTATCTTTCC | 84767 |
rs7483200 | snp | A/T | 0.307763 | 0.243235 | intron-variant | TRIM51 | GRCh38.p7 | 11:55889007 | TATTACACAGGTGAG[A/T]GCACACCAAGATTTT | 84767 |
rs10897403 | snp | A/G | 0.487237 | 0.0788573 | missense | TRIM51 | GRCh38.p7 | 11:55885688 | TCCGGCAATTCCTTA[A/G]CTCTGAGGAGCAAAT | 84767 |
rs10897405 | snp | G/T | 0.0562307 | 0.157967 | intron-variant | TRIM51 | GRCh38.p7 | 11:55890258 | TTCTGGGCTCACATG[G/T]ATAGAGTTATATATT | 84767 |
rs11231429 | snp | A/G | 0.168785 | 0.236441 | upstream-variant-2KB | TRIM51 | GRCh38.p7 | 11:55882864 | GGAATTCAAGGCTGC[A/G]GTGAGCTAAGACTGT | 84767 |
rs11231443 | snp | A/T | 0.344147 | 0.231595 | intron-variant | TRIM51 | GRCh38.p7 | 11:55889844 | TAGCAAATGTGTGGG[A/T]TAAAGGGATTCTCAT | 84767 |
rs11231445 | snp | A/T | 0.0248432 | 0.108648 | intron-variant | TRIM51 | GRCh38.p7 | 11:55890555 | GTAAAAATGGAAATG[A/T]TAATTTCAGTTTAGT | 84767 |
rs12222964 | snp | C/T | 0.28052 | 0.24813 | intron-variant | TRIM51 | GRCh38.p7 | 11:55889489 | TCGGAATGTTTGAAC[C/T]GTGTAGGCCTCCAGA | 84767 |
rs12224686 | snp | C/T | 0.496778 | 0.0400063 | intron-variant | TRIM51 | GRCh38.p7 | 11:55889286 | TGAGCATCTGTATTC[C/T]TAATTTCCTTTTTAT | 84767 |
rs12279610 | snp | A/C | | | intron-variant | TRIM51 | GRCh38.p7 | 11:55890754 | AAGCTAAAATCTTCC[A/C]ATTCTTGCCAAAATT | 84767 |
rs12417534 | snp | A/G | 0.159951 | 0.233219 | upstream-variant-2KB | TRIM51 | GRCh38.p7 | 11:55881472 | AAATCATCATTCATG[A/G]TCATGGCATAAAATA | 84767 |
rs12801313 | snp | A/T | 0.255782 | 0.249933 | intron-variant | TRIM51 | GRCh38.p7 | 11:55890461 | TTGTACTTTCTTACA[A/T]TAAATATATTTTATT | 84767 |
rs12805952 | snp | G/T | | | upstream-variant-2KB | TRIM51 | GRCh38.p7 | 11:55881393 | AAAACTCATTTATTG[G/T]GTTACTATTAAAAAT | 84767 |
rs17156540 | snp | A/C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | TRIM51 | GRCh38.p7 | 11:55891705 | CCCTCTTTTTCGCAC[A/C/T]TCATCAAACAGAACA | 84767 |
rs17594658 | snp | C/T | 0.484429 | 0.0868505 | utr-variant-3-prime | TRIM51 | GRCh38.p7 | 11:55891794 | TGTTTCTATTAAATA[C/T]GGTGAAAACATTAAA | 84767 |
rs28496248 | snp | A/C | | | intron-variant | TRIM51 | GRCh38.p7 | 11:55884157 | TGTACATAACTATAA[A/C]TATATATATATATAT | 84767 |
rs28609353 | snp | C/T | | | intron-variant | TRIM51 | GRCh38.p7 | 11:55884182 | ATATATATATATATA[C/T]ACACATACCAAAAAT | 84767 |
rs34250328 | snp | C/T | 0.0412736 | 0.137598 | missense | TRIM51 | GRCh38.p7 | 11:55891417 | CTCTTTCTTCTTGGA[C/T]GTGTTAAGGAGGACA | 84767 |
rs34352908 | snp | A/C | 0.24019 | 0.249807 | upstream-variant-2KB | TRIM51 | GRCh38.p7 | 11:55882708 | CTAATTCTAATCCGG[A/C]TGGTCACTGTAACAC | 84767 |
rs34476777 | snp | G/T | 0.214541 | 0.247473 | upstream-variant-2KB | TRIM51 | GRCh38.p7 | 11:55882209 | GAGTCAATGATGAGA[G/T]TAGCTGTGGAAATGG | 84767 |
rs34568391 | in-del | -/C | 0.250732 | 0.249999 | intron-variant | TRIM51 | GRCh38.p7 | 11:55884485 | TGGAGATACCAATAT[-/C]CTGGCTGAGTTAGAA | 84767 |
rs35103991 | snp | C/T | 0.16976 | 0.236773 | intron-variant | TRIM51 | GRCh38.p7 | 11:55883475 | ACTGTCTAAACTTAC[C/T]GAATGATCTTATTTG | 84767 |
rs35149540 | snp | A/T | 0.143848 | 0.226344 | utr-variant-3-prime | TRIM51 | GRCh38.p7 | 11:55891671 | CTGTATGCTCTGGGA[A/T]CCTGTTTATCCCAGA | 84767 |
rs35527108 | in-del | -/T | | | frameshift-variant | TRIM51 | GRCh38.p7 | 11:55891175 | CAATAGTCATATCTT[-/T]CCTGTGTGGAGATTT | 84767 |
rs35687091 | in-del | -/TA | | | intron-variant | TRIM51 | GRCh38.p7 | 11:55887301 | GTATCTGGATGTTGG[-/TA]TATATATATATATAT | 84767 |
rs35692543 | in-del | -/G | | | intron-variant | TRIM51 | GRCh38.p7 | 11:55887106 | GAGAATAATCAAGCA[-/G]GGAAAGTAGAAAAGG | 84767 |
rs35822483 | snp | A/G | 0.444444 | 0.157135 | missense | TRIM51 | GRCh38.p7 | 11:55891397 | AGATAGATGGAGAGG[A/G]GGGACTCTTTCTTCT | 84767 |
rs56096512 | in-del | -/AT | | | intron-variant | TRIM51 | GRCh38.p7 | 11:55887320 | TATATATATATATAT[-/AT]GGATACATTTGAGGA | 84767 |
rs61897545 | snp | A/C | 0.0622301 | 0.165053 | upstream-variant-2KB | TRIM51 | GRCh38.p7 | 11:55881949 | TGATACAATATTCTC[A/C]TAAGGATTTCTTAAC | 84767 |
rs61897546 | snp | C/T | 0.5 | 0 | intron-variant | TRIM51 | GRCh38.p7 | 11:55884188 | ATATATATATACACA[C/T]ACCAAAAATACTTAC | 84767 |
rs61897547 | snp | C/T | | | intron-variant | TRIM51 | GRCh38.p7 | 11:55884206 | CAAAAATACTTACAA[C/T]TGTGGTACAATTGCC | 84767 |
rs61897548 | snp | A/G | 0.0618563 | 0.164627 | intron-variant | TRIM51 | GRCh38.p7 | 11:55888767 | TCACTTGTGAAGAGA[A/G]TGTCTTCAAGACTTA | 84767 |
rs61897549 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TRIM51 | GRCh38.p7 | 11:55890727 | TCCAGTTATCTAGAG[C/T]GGTGCTTGAGTAAGC | 84767 |
rs61897550 | snp | A/C | 0.117576 | 0.212054 | missense | TRIM51 | GRCh38.p7 | 11:55891274 | TTGTATGGGGGGCTC[A/C]GGCTTTCACATCTGG | 84767 |
rs66501224 | snp | C/G | 0.164873 | 0.23506 | intron-variant | TRIM51 | GRCh38.p7 | 11:55889855 | TGGGTTAAAGGGATT[C/G]TCATGAAATGTCTTT | 84767 |
rs71055549 | in-del | -/TATATATATATATATATATATATATATATACA | 0 | 0 | intron-variant | TRIM51 | GRCh38.p7 | 11:55884183 | ATATATATATATATA[lengthTooLong]CACATACCAAAAATA | 84767 |
rs74746632 | snp | C/T | 0.0611083 | 0.163768 | upstream-variant-2KB | TRIM51 | GRCh38.p7 | 11:55882185 | GGCACAGAATAAACT[C/T]GGATGGCAGAGTCAA | 84767 |
rs76226257 | snp | A/G | 0.0611083 | 0.163768 | upstream-variant-2KB | TRIM51 | GRCh38.p7 | 11:55882186 | GCACAGAATAAACTT[A/G]GATGGCAGAGTCAAT | 84767 |
rs77556048 | snp | A/T | 0.5 | 0 | intron-variant | TRIM51 | GRCh38.p7 | 11:55884166 | CTATAACTATATATA[A/T]ATATATATATATATA | 84767 |
rs78177696 | snp | A/G | 0.000166439 | 0.00912096 | missense | TRIM51 | GRCh38.p7 | 11:55891579 | ATATACACCATCCCC[A/G]ATTGCTCCTTCTCAC | 84767 |
rs78850585 | snp | A/T | 0 | 0 | intron-variant | TRIM51 | GRCh38.p7 | 11:55884917 | CTGTCTTTTTTTTTT[A/T]AATCTGGTCGGTTGG | 84767 |
rs79621993 | snp | A/C | | | intron-variant | TRIM51 | GRCh38.p7 | 11:55889212 | TCTGCAAAAGCAAAA[A/C]AATAAATAAATAAAT | 84767 |
rs111365947 | snp | A/C/G | 1.75894e-05 | 0.00296553 | intron-variant | TRIM51 | GRCh38.p7 | 11:55890070 | TTGGCAGAATTCCCA[A/C/G]AGTCTATTACTTCTT | 84767 |
rs111937228 | snp | C/T | 0.5 | 0 | intron-variant | TRIM51 | GRCh38.p7 | 11:55888887 | GTAGGAAAATAGTAT[C/T]TTCAGAAACTGTCTC | 84767 |
rs111962758 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | TRIM51 | GRCh38.p7 | 11:55882893 | GTGCCACTGCACTCC[A/G]GAGGGTGAAACTTTC | 84767 |
rs112052698 | snp | A/T | 0.0329836 | 0.124112 | intron-variant | TRIM51 | GRCh38.p7 | 11:55886584 | CCTTCTAAGGCTGAG[A/T]CAGTATGAATTTGAA | 84767 |
rs112230296 | snp | C/G | 0.5 | 0 | intron-variant | TRIM51 | GRCh38.p7 | 11:55890217 | ATTATAACATGAAGA[C/G]TACAACATAGTGAAA | 84767 |
rs112587265 | snp | G/T | 0.5 | 0 | missense | TRIM51 | GRCh38.p7 | 11:55885543 | TTTTGCCGGCCCTGT[G/T]TGTACCTCAACTGGC | 84767 |
rs113314326 | snp | G/T | 0 | 0 | missense | TRIM51 | GRCh38.p7 | 11:55885557 | TTTGTACCTCAACTG[G/T]CAAGACACGGCAGTT | 84767 |
rs113733739 | snp | C/T | | | missense | TRIM51 | GRCh38.p7 | 11:55885685 | GCCTCCGGCAATTCC[C/T]TAGCTCTGAGGAGCA | 84767 |
rs114602644 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | TRIM51 | GRCh38.p7 | 11:55889719 | TAACTAGGAGCAATA[C/T]GAAGAAAGATCCTAA | 84767 |
rs114801559 | snp | G/T | 0.0240643 | 0.107019 | intron-variant | TRIM51 | GRCh38.p7 | 11:55885075 | CATAGTCATTCAGTT[G/T]TTATTTGAAAGAGAA | 84767 |
rs114915773 | snp | C/T | 0.0054785 | 0.0520503 | intron-variant | TRIM51 | GRCh38.p7 | 11:55889891 | AAGAGTGGTGTTTTT[C/T]ATGTATTTTTTTTGG | 84767 |
rs118080224 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | TRIM51 | GRCh38.p7 | 11:55884650 | CTCCGGAAACACCTT[C/G]ACAGACTCACCCAGA | 84767 |
rs138269041 | snp | G/T | 0.00030026 | 0.0122491 | missense | TRIM51 | GRCh38.p7 | 11:55891508 | GCACAGTAGGATTAT[G/T]CCTGGATTGTGAAGG | 84767 |
rs138301526 | snp | A/G | 0.00511657 | 0.05032 | missense | TRIM51 | GRCh38.p7 | 11:55886193 | GAAATCTGAACATGG[A/G]AACCACAAGAACCAG | 84767 |
rs138472560 | snp | C/T | 0.127944 | 0.218179 | intron-variant | TRIM51 | GRCh38.p7 | 11:55883432 | TCTCTTCCTTTAAAA[C/T]AGTAAATTACAGTGA | 84767 |
rs138722707 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | TRIM51 | GRCh38.p7 | 11:55887243 | AAATGTGTATATCCT[C/T]CTGTTTGCCTTCCTC | 84767 |
rs138812218 | snp | A/G | 0.00118726 | 0.0243356 | synonymous-codon | TRIM51 | GRCh38.p7 | 11:55888040 | ACTGCAGGATTATGT[A/G]AGTTTAAGGATAGAA | 84767 |
rs138830390 | snp | A/C/T | 3.369e-05 | 0.00410416 | stop-gained, synonymous-codon | TRIM51 | GRCh38.p7 | 11:55891299 | ATCTGGCAAATATTA[A/C/T]TGGGAGGTTCATATG | 84767 |
rs139319596 | snp | A/G | 0.00148777 | 0.0272337 | synonymous-codon | TRIM51 | GRCh38.p7 | 11:55888130 | CTTGGAAAGGCTGCG[A/G]AAGGAGGGCGAGGAC | 84767 |
rs139439628 | snp | A/G | 0.00104404 | 0.0228239 | synonymous-codon | TRIM51 | GRCh38.p7 | 11:55889966 | TCTGCTGCTGCAAGT[A/G]TCTGAGCCTGTGAAT | 84767 |
rs139479732 | snp | A/T | 0.000252319 | 0.0112292 | missense | TRIM51 | GRCh38.p7 | 11:55891613 | CTCTCAGGCCTATCT[A/T]TTGCTGTAGTCACTT | 84767 |
rs139492043 | in-del | -/A | | | intron-variant | TRIM51 | GRCh38.p7 | 11:55887889 | GTACAGAAAAAAAAA[-/A]TAAAAGGGATAAAAT | 84767 |
rs139600668 | snp | A/G | 0.000167943 | 0.00916206 | synonymous-codon | TRIM51 | GRCh38.p7 | 11:55888178 | TGAAAGCAAAGCCAG[A/G]ATGGAACATTCCAGG | 84767 |
rs139646527 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | TRIM51 | GRCh38.p7 | 11:55886057 | CATTTTGGGTCCTTC[A/G]TATATCAGAGTGTGA | 84767 |
rs139676401 | snp | A/G | 0.00132365 | 0.0256919 | missense | TRIM51 | GRCh38.p7 | 11:55885676 | GAAAAGCCAGCCTCC[A/G]GCAATTCCTTAGCTC | 84767 |
rs139810817 | snp | A/G | 0.00438332 | 0.0466095 | upstream-variant-2KB | TRIM51 | GRCh38.p7 | 11:55882003 | AAAATTAGTAGGTTT[A/G]TATTAATGAGGACTT | 84767 |
rs140692052 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | TRIM51 | GRCh38.p7 | 11:55886747 | AAGTGGCGAGAAATG[C/T]ACACTTGTGTCTTGA | 84767 |
rs141124318 | snp | C/T | 0.000117977 | 0.0076795 | stop-gained | TRIM51 | GRCh38.p7 | 11:55891273 | CTTGTATGGGGGGCT[C/T]AGGCTTTCACATCTG | 84767 |
rs141358395 | snp | A/T | 0.0158469 | 0.0875917 | intron-variant | TRIM51 | GRCh38.p7 | 11:55886552 | GTTATTTGTCAGTCA[A/T]GGAAATTTCAGGTGA | 84767 |
rs141376347 | snp | C/T | 0.000133127 | 0.00815756 | synonymous-codon | TRIM51 | GRCh38.p7 | 11:55891578 | GATATACACCATCCC[C/T]AATTGCTCCTTCTCA | 84767 |
rs141475510 | snp | G/T | 0.0111196 | 0.0737302 | intron-variant | TRIM51 | GRCh38.p7 | 11:55883480 | CTAAACTTACCGAAT[G/T]ATCTTATTTGTAACT | 84767 |
rs141719000 | snp | A/C/T | 6.6183e-05 | 0.00575221 | synonymous-codon | TRIM51 | GRCh38.p7 | 11:55888139 | GCTGCGAAAGGAGGG[A/C/T]GAGGACATTTTTCAG | 84767 |
rs142801506 | snp | C/G | | | intron-variant | TRIM51 | GRCh38.p7 | 11:55885154 | GTTTCATGTCGACAT[C/G]CAGGGAGTAGGTTTT | 84767 |
rs143260124 | snp | A/G | 8.24776e-05 | 0.00642122 | synonymous-codon | TRIM51 | GRCh38.p7 | 11:55886218 | AACCAGATGCTGGAA[A/G]GTTAGTACCGTATGA | 84767 |
rs143686383 | snp | A/C | 1.72314e-05 | 0.0029352 | missense | TRIM51 | GRCh38.p7 | 11:55885601 | CTGAATGCAAGAAGA[A/C]AACGCGGCAGAGAAA | 84767 |
rs143743456 | snp | A/T | 5.06017e-05 | 0.00502974 | missense | TRIM51 | GRCh38.p7 | 11:55891250 | TCACTGGAAAATCTG[A/T]ATGTTTTCTTGTATG | 84767 |
rs143840865 | in-del | -/TATATATATA | 0.392696 | 0.205275 | intron-variant | TRIM51 | GRCh38.p7 | 11:55884158 | GTACATAACTATAAC[-/TATATATATA]TATATATATATATAT | 84767 |
rs143941463 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | TRIM51 | GRCh38.p7 | 11:55885032 | TTCTCATGTTTTGTT[A/G]CCCAATGTAGGTTTT | 84767 |
rs144249891 | snp | A/C | 0.0603597 | 0.1629 | intron-variant | TRIM51 | GRCh38.p7 | 11:55889604 | GTCTTAAAAATAACC[A/C]CACTTTTCCAGACAG | 84767 |
rs144396749 | snp | A/C | 0.0536309 | 0.154723 | missense | TRIM51 | GRCh38.p7 | 11:55886141 | GAGCTCCTAAAAAAA[A/C]TGCAGTCTTTATGGG | 84767 |
rs144632182 | in-del | -/T | 0.102741 | 0.202027 | intron-variant | TRIM51 | GRCh38.p7 | 11:55889897 | GGTGTTTTTTATGTA[-/T]TTTTTTTTGGCTGTA | 84767 |
rs145711485 | snp | A/G | 0.000270042 | 0.0116167 | synonymous-codon | TRIM51 | GRCh38.p7 | 11:55891470 | CTCCCCACTTGTGGT[A/G]CAATATGTTCCAAGA | 84767 |
rs145752663 | snp | A/G | 0.0111663 | 0.0738815 | missense | TRIM51 | GRCh38.p7 | 11:55885693 | CAATTCCTTAGCTCT[A/G]AGGAGCAAATATGTG | 84767 |
rs146275956 | snp | A/C | 0.00398564 | 0.0444627 | downstream-variant-500B | TRIM51 | GRCh38.p7 | 11:55892294 | ATACACAGTGCATTC[A/C]CACATGGATTCATGC | 84767 |
rs146327492 | snp | A/G | 4.96257e-05 | 0.004981 | missense | TRIM51 | GRCh38.p7 | 11:55888129 | ACTTGGAAAGGCTGC[A/G]AAAGGAGGGCGAGGA | 84767 |