SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs914 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime | TRIM37 | GRCh38.p7 | 17:58998352 | TGTCTCTCACATGTA[C/T]ATTTAATTATTCATG | 4591 |
rs972849 | snp | A/T | 0.428635 | 0.174898 | intron-variant | TRIM37 | GRCh38.p7 | 17:59062943 | TGAAGCATTAATTAA[A/T]TTTGGGAGACTTGGT | 4591 |
rs1182112 | snp | C/T | 0 | 0 | intron-variant | TRIM37 | GRCh38.p7 | 17:58992456 | cacaatcttggttca[C/T]ggcaacctccacctc | 4591 |
rs1509345 | snp | C/T | 0 | 0 | intron-variant | TRIM37 | GRCh38.p7 | 17:59003261 | GAATTTTGTCTGTTT[C/T]TACTGGGCTCTGAAG | 4591 |
rs1509346 | snp | C/T | 0.0109286 | 0.0731087 | intron-variant | TRIM37 | GRCh38.p7 | 17:59003444 | TCTGGAAGGAAGGTT[C/T]TAGGTACAATGGAGC | 4591 |
rs1967414 | snp | A/G | 0.414905 | 0.187899 | intron-variant | TRIM37 | GRCh38.p7 | 17:59034509 | ggattacaggcatgc[A/G]gcaccatgcctggct | 4591 |
rs1967415 | snp | A/C | 0.474903 | 0.109173 | intron-variant | TRIM37 | GRCh38.p7 | 17:59035763 | caaaaaaacaaaaaa[A/C]caaaaaaACAAAAAA | 4591 |
rs2108434 | snp | A/G | 0.00333889 | 0.0407222 | intron-variant | TRIM37 | GRCh38.p7 | 17:59020327 | atgaaataaatctaa[A/G]aacttggtctttgag | 4591 |
rs2108435 | snp | C/T | 0.463989 | 0.129263 | intron-variant | TRIM37 | GRCh38.p7 | 17:59024772 | AGAAGCCATCCTCCC[C/T]CATCAGCATCCCAAA | 4591 |
rs2136372 | snp | A/C/G | 1.79142e-05 | 0.00299279 | intron-variant | TRIM37 | GRCh38.p7 | 17:59049127 | AAAAGCCATGATGCT[A/C/G]CTGTTTTTTTTTAAT | 4591 |
rs2136373 | snp | A/C | 0.0104709 | 0.0715948 | missense, nc-transcript-variant | TRIM37 | GRCh38.p7 | 17:59049193 | ATGATAATCTTCATT[A/C]TGAATCTTCTCCTCA | 4591 |
rs2158966 | snp | A/G | 0.474723 | 0.109542 | intron-variant | TRIM37 | GRCh38.p7 | 17:59020029 | tgaggtcaggagttc[A/G]agaccagcctggcca | 4591 |
rs2333409 | snp | C/T | 0.339656 | 0.233371 | intron-variant | TRIM37 | GRCh38.p7 | 17:59061773 | CAGCCTTCATTGTCT[C/T]GTTGGGGGAACAGAT | 4591 |
rs2333410 | snp | C/T | 0.485118 | 0.0849685 | intron-variant | TRIM37 | GRCh38.p7 | 17:59059768 | CTAACAAAAGTGAGA[C/T]CTGAAAGGATCAAAT | 4591 |
rs2877926 | snp | C/T | 0.464309 | 0.12873 | intron-variant | TRIM37 | GRCh38.p7 | 17:59061932 | ATTCATTGATATCTA[C/T]TGAGTGATTATCATG | 4591 |
rs3217009 | in-del | -/GCAGCAGCAGCAGCA/GCAGCAGCAGCAGCACCA | | | intron-variant | TRIM37 | GRCh38.p7 | 17:59012229 | CCAGCAGCAGCAGCA[lengthTooLong]CCACCACCACCACCA | 4591 |
rs3809722 | snp | A/C | 0.0629771 | 0.165899 | intron-variant, utr-variant-3-prime, nc-transcript-variant | TRIM37, PPM1E | GRCh38.p7 | 17:58984772 | TTCAAAATAGAAGAT[A/C]AAATGCTGCTTTAAG | 4591 |
rs3809723 | snp | A/C | 0.465473 | 0.126772 | intron-variant, utr-variant-3-prime, nc-transcript-variant | TRIM37, PPM1E | GRCh38.p7 | 17:58984617 | GGGCATTTGTCCTTT[A/C]ACATCACGTGATTTT | 4591 |
rs3809724 | snp | C/T | 0.227664 | 0.249 | intron-variant, utr-variant-3-prime, nc-transcript-variant | TRIM37, PPM1E | GRCh38.p7 | 17:58983877 | ACTTCAGTTGGTGAC[C/T]TGAAGTTTGTTTCCC | 4591 |
rs3826353 | snp | A/G | 0.481627 | 0.0940692 | intron-variant, downstream-variant-500B | TRIM37 | GRCh38.p7 | 17:58997938 | GCTTTAGTATATAAG[A/G]TGGCTTGGAAACGAG | 4591 |
rs3826354 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, utr-variant-3-prime | TRIM37 | GRCh38.p7 | 17:58998416 | TAATTTCCACAAATA[C/T]ATAGCAGCTCAAACA | 4591 |
rs4598970 | snp | A/T | 0.459687 | 0.136129 | intron-variant | TRIM37 | GRCh38.p7 | 17:58999532 | ATTTTCCTTCCCAAG[A/T]CTTTAAATAATCTTA | 4591 |
rs4932690 | snp | A/G | 0.42263 | 0.180829 | intron-variant | TRIM37 | GRCh38.p7 | 17:59056587 | AGTAAAAAATTAGCC[A/G]GGCGTGGTGGCGGGC | 4591 |
rs4932691 | snp | C/T | 0.45383 | 0.144752 | intron-variant | TRIM37 | GRCh38.p7 | 17:59017256 | TCAGGTAATAAATAT[C/T]TACCCCACTAAAAGT | 4591 |
rs4932692 | snp | C/T | 0.0577344 | 0.159793 | intron-variant | TRIM37 | GRCh38.p7 | 17:59017486 | AAACTCACTATTTAG[C/T]CTGTCAGAAAAAGTT | 4591 |
rs4932693 | snp | C/T | 0.474992 | 0.108989 | intron-variant | TRIM37 | GRCh38.p7 | 17:59032966 | ATCTGTAGGCAGATA[C/T]TATGCCTATACCCCT | 4591 |
rs6416932 | snp | A/G | 0.477853 | 0.102875 | intron-variant | TRIM37 | GRCh38.p7 | 17:59071630 | GATTGTATTCTAGGT[A/G]ACAGAATACAAAACG | 4591 |
rs6416933 | snp | A/G | 0.474363 | 0.110278 | intron-variant | TRIM37 | GRCh38.p7 | 17:59075559 | ACAGAGAGAGACTCC[A/G]TCTCAAAAAAAAAAA | 4591 |
rs6503890 | snp | A/G | 0.47726 | 0.104176 | intron-variant, downstream-variant-500B | TRIM37 | GRCh38.p7 | 17:58986806 | TGAGACACCACGCCC[A/G]GCCCCATCTGTCATC | 4591 |
rs6503891 | snp | A/C | 0.463451 | 0.130149 | intron-variant | TRIM37 | GRCh38.p7 | 17:58988563 | AACAGAGACCCTCCC[A/C]AACCTAGGGACACAG | 4591 |
rs6503892 | snp | A/G | 0.463881 | 0.12944 | intron-variant | TRIM37 | GRCh38.p7 | 17:58989725 | aaatcaacccagaac[A/G]taatatacaaaagct | 4591 |
rs6503893 | snp | A/G | 0.474544 | 0.10991 | intron-variant | TRIM37 | GRCh38.p7 | 17:59072334 | tgacaggcctagcaa[A/G]ctaatataCTATCAA | 4591 |
rs6503894 | snp | A/G | 0.474903 | 0.109173 | intron-variant | TRIM37 | GRCh38.p7 | 17:59096484 | TTGAACCCAGGAGGC[A/G]GAGGTTGCAATGAGC | 4591 |
rs6503895 | snp | C/T | 0.117188 | 0.211804 | intron-variant | TRIM37 | GRCh38.p7 | 17:59096704 | TGCatTTGaaattaa[C/T]taaaaatataagtat | 4591 |
rs7207393 | snp | A/T | | | intron-variant | TRIM37 | GRCh38.p7 | 17:59092342 | aggcagaggttgcag[A/T]gagccgagatcctgc | 4591 |
rs7207551 | snp | G/T | 0.0114282 | 0.0747228 | intron-variant | TRIM37 | GRCh38.p7 | 17:59092424 | aaacaaaaaaaaCGG[G/T]TTCATAGTTCAGTAA | 4591 |
rs7207556 | snp | C/T | | | intron-variant | TRIM37 | GRCh38.p7 | 17:59048605 | ACACCtttttttttt[C/T]tttttctttgagaca | 4591 |
rs7209276 | snp | A/C | 0 | 0 | intron-variant | TRIM37 | GRCh38.p7 | 17:59096563 | TCAAAAAAAAAAAAA[A/C]AAAAAAAAAAAAACC | 4591 |
rs7213449 | snp | A/T | 0 | 0 | intron-variant | TRIM37 | GRCh38.p7 | 17:59051105 | ATTTTTTTTCTAATT[A/T]CAAATTACAAAATTA | 4591 |
rs7214335 | snp | A/G | 0.483852 | 0.0883933 | intron-variant | TRIM37 | GRCh38.p7 | 17:59081479 | ATTAAAAAGAACCAA[A/G]ATCTTTAACCACAGC | 4591 |
rs7214402 | snp | C/T | 0.429087 | 0.174436 | intron-variant | TRIM37 | GRCh38.p7 | 17:59080984 | TACAGCCTATCAAAT[C/T]TGCAAATCTTGAAAA | 4591 |
rs7214892 | snp | A/G | 0.479904 | 0.0982045 | intron-variant, synonymous-codon | TRIM37 | GRCh38.p7 | 17:58988040 | TTGCAGAGTAACCAA[A/G]TGGCACCAAATGGAG | 4591 |
rs7218103 | snp | G/T | 0.428333 | 0.175206 | intron-variant | TRIM37 | GRCh38.p7 | 17:59055649 | cttgcagtgagccga[G/T]atgtcgcctctgggc | 4591 |
rs7222388 | snp | C/T | 0.00714036 | 0.0593228 | missense, nc-transcript-variant | TRIM37 | GRCh38.p7 | 17:59015674 | AAACTGCAACCACAA[C/T]AGCATCTGAATCCAA | 4591 |
rs7224717 | snp | C/T | 0.0399052 | 0.1355 | intron-variant | TRIM37 | GRCh38.p7 | 17:59053186 | AGTTCTAATATTTTG[C/T]CATTAAAACAAAACC | 4591 |
rs7224809 | snp | A/G | 0.117886 | 0.21224 | intron-variant | TRIM37 | GRCh38.p7 | 17:59053066 | CAACTGAGCAGAGAC[A/G]ATTCACAGTCTAGGA | 4591 |
rs7226134 | snp | G/T | 0.00394476 | 0.0442359 | intron-variant | TRIM37 | GRCh38.p7 | 17:59040657 | GGATAAGATTACCCA[G/T]GATTAAAGTCAGGAG | 4591 |
rs7501698 | snp | A/C | | | intron-variant | TRIM37 | GRCh38.p7 | 17:59096562 | ctcaaaaaaaaaaaa[A/C]caaaaaaaaaaaaaC | 4591 |
rs7502088 | snp | A/G | 0 | 0 | intron-variant, utr-variant-3-prime, nc-transcript-variant | TRIM37, PPM1E | GRCh38.p7 | 17:58983722 | TAATTTAGTGGTGGT[A/G]AAAGTTCTACACTCA | 4591 |
rs7502208 | snp | A/G | 0.475525 | 0.107882 | intron-variant | TRIM37 | GRCh38.p7 | 17:59087736 | ATTTCTAAACATTCA[A/G]GGGTCCTGGAATCTC | 4591 |
rs7503179 | snp | A/T | 0.432063 | 0.171327 | intron-variant | TRIM37 | GRCh38.p7 | 17:59082629 | TAGCCTCACAAATCC[A/T]GTTGCATTCAGCTCA | 4591 |
rs7503190 | snp | A/C | 0.474992 | 0.108989 | utr-variant-5-prime, upstream-variant-2KB | TRIM37 | GRCh38.p7 | 17:59106801 | CTGACGGTGGAGTTC[A/C]GCGAAGAAGGTGCCG | 4591 |
rs7503316 | snp | C/T | 0.431325 | 0.172108 | intron-variant | TRIM37 | GRCh38.p7 | 17:59059577 | ctcaagcaatcctcc[C/T]gccttggcctcccaa | 4591 |
rs8064501 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | TRIM37 | GRCh38.p7 | 17:59021854 | ttatgcattgtaagc[A/G]tgtatcaaaatatct | 4591 |
rs8065740 | snp | C/G | 0.119281 | 0.213102 | intron-variant | TRIM37 | GRCh38.p7 | 17:59057488 | gctgggattgcaggc[C/G]tgagccaccacaccc | 4591 |
rs8067187 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | TRIM37 | GRCh38.p7 | 17:59036191 | ggcaggaggactaat[C/T]gaggccaggagttgg | 4591 |
rs8067264 | snp | C/G | 0.474903 | 0.109173 | intron-variant, upstream-variant-2KB | TRIM37 | GRCh38.p7 | 17:59105432 | AAGAAACAGTATTAT[C/G]TTTGCAAGCCTCAAT | 4591 |
rs8069033 | snp | A/T | 0.474544 | 0.10991 | intron-variant | TRIM37 | GRCh38.p7 | 17:59054220 | GTTCAGAACATATTT[A/T]AATCTTTTTTAAATA | 4591 |
rs8071291 | snp | C/T | 0.117188 | 0.211804 | intron-variant | TRIM37 | GRCh38.p7 | 17:59097325 | gaaataaaaagtatc[C/T]taattaaaaaagaag | 4591 |
rs8072712 | snp | A/T | 0.471483 | 0.115954 | intron-variant | TRIM37 | GRCh38.p7 | 17:59085103 | gccaaggcgggtgga[A/T]cacttgaagccagga | 4591 |
rs8074595 | snp | A/G | 0 | 0 | intron-variant | TRIM37 | GRCh38.p7 | 17:59034293 | TACAGTAGAGAAAGC[A/G]GTGTCTCCTGTTTCT | 4591 |
rs8077332 | snp | C/T | 0.42574 | 0.177808 | intron-variant | TRIM37 | GRCh38.p7 | 17:59027862 | ctttgccatactggt[C/T]ttccttcaatccttc | 4591 |
rs8078926 | snp | C/T | 0.426507 | 0.177046 | intron-variant | TRIM37 | GRCh38.p7 | 17:59100409 | caatggaatactact[C/T]agcaataaaaaggaa | 4591 |
rs8079298 | snp | C/T | 0.122758 | 0.215196 | intron-variant | TRIM37 | GRCh38.p7 | 17:59065296 | CCCAAACTTCCTACT[C/T]TGGAATGGATTATGG | 4591 |
rs8080071 | snp | C/T | 0.426047 | 0.177503 | intron-variant | TRIM37 | GRCh38.p7 | 17:59016464 | TTTTATGCCAAGCAT[C/T]TAAAATTAAGGAGTC | 4591 |
rs8081058 | snp | C/G | 0.343701 | 0.231776 | intron-variant | TRIM37 | GRCh38.p7 | 17:59083152 | TTAATTAAGTATTCA[C/G]AGGCTGGGCGCGGTG | 4591 |
rs8081297 | snp | C/T | 0.474363 | 0.110278 | intron-variant | TRIM37 | GRCh38.p7 | 17:58994874 | cctgcctcagcctcc[C/T]gagtagctgggatta | 4591 |
rs8081967 | snp | C/T | 0.474544 | 0.10991 | intron-variant | TRIM37 | GRCh38.p7 | 17:58995340 | agaaccatggttcct[C/T]aggaagtggttaatt | 4591 |
rs8082334 | snp | A/G | 0.343254 | 0.231956 | intron-variant | TRIM37 | GRCh38.p7 | 17:59039448 | gcctcccaggttcac[A/G]acattctcctgcctc | 4591 |
rs8082544 | snp | A/G | 0.474813 | 0.109357 | upstream-variant-2KB | TRIM37 | GRCh38.p7 | 17:59108446 | GGACTTATTGCACCA[A/G]TTCATAATAGCGAAC | 4591 |
rs8182277 | snp | C/T | 0.474992 | 0.108989 | intron-variant | TRIM37 | GRCh38.p7 | 17:59067006 | TTGCGAAAGAAATTA[C/T]TTTGCTTTTTAAATT | 4591 |
rs9889414 | snp | C/T | 0.00119737 | 0.0244387 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant, intron-variant | TRIM37, PPM1E | GRCh38.p7 | 17:58982173 | TGGAAGACACATGAG[C/T]GTCCTGCTTACATGT | 4591 |
rs9889935 | snp | A/G | 0.426813 | 0.17674 | intron-variant | TRIM37 | GRCh38.p7 | 17:59086430 | TTTTAATACAGACAG[A/G]GTTTCACCATGTTGG | 4591 |
rs9891449 | snp | A/T | 0.43221 | 0.171171 | intron-variant | TRIM37 | GRCh38.p7 | 17:59086511 | CCCAAAGTGCTGGGA[A/T]TACAAGCATGAGCCA | 4591 |
rs9892666 | snp | A/T | 0.463559 | 0.129972 | intron-variant | TRIM37 | GRCh38.p7 | 17:59098745 | AATTAacagaatacc[A/T]tatgacccagcaatt | 4591 |
rs9893447 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TRIM37 | GRCh38.p7 | 17:59063883 | TTTGggcagggcacc[A/G]tggctaatgcctata | 4591 |
rs9893979 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TRIM37 | GRCh38.p7 | 17:59012644 | gcactttgggaggcc[A/C]aggtgggtggatcac | 4591 |
rs9898048 | snp | A/G | 0.425894 | 0.177655 | intron-variant | TRIM37 | GRCh38.p7 | 17:59031182 | TCTTGCCTTAAAACT[A/G]CATCAAAATCAGAGT | 4591 |
rs9898200 | snp | A/G | 0.462909 | 0.131034 | intron-variant | TRIM37 | GRCh38.p7 | 17:59009607 | CCCGCCACCACACTC[A/G]GCTAATTTTTGTATA | 4591 |
rs9900045 | snp | C/T | 0 | 0 | intron-variant | TRIM37 | GRCh38.p7 | 17:59075328 | cagcagcttgggagg[C/T]tgaggcgggcagatc | 4591 |
rs9901188 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TRIM37 | GRCh38.p7 | 17:59065144 | ATTATTAAACTAAGT[A/G]CAAGAAATACACTTT | 4591 |
rs9903702 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | TRIM37 | GRCh38.p7 | 17:59102215 | TACTCCCAGAAACCT[C/T]AGAGTAGAGAACGAC | 4591 |
rs9904621 | snp | C/T | 0.432357 | 0.171014 | intron-variant | TRIM37 | GRCh38.p7 | 17:59072543 | GACCTCATGACCTGG[C/T]TAGTTCAAGGCCTGG | 4591 |
rs9905541 | snp | A/G | 0 | 0 | intron-variant | TRIM37 | GRCh38.p7 | 17:59002042 | GTTTTTTTTTCAGTC[A/G]CAAGAGATAACAGGA | 4591 |
rs9906355 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | TRIM37 | GRCh38.p7 | 17:59009562 | gcgattctcctgcct[C/T]agcctcccaagtaga | 4591 |
rs9906653 | snp | A/G | 0.418653 | 0.184544 | intron-variant | TRIM37 | GRCh38.p7 | 17:59056698 | TCGCGCCAGGGCGAC[A/G]GAGCGAGACTATGTC | 4591 |
rs9907031 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM37 | GRCh38.p7 | 17:59009123 | TCTTCCAAGttcttt[C/T]ttttcttttcttctt | 4591 |
rs9907756 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | TRIM37 | GRCh38.p7 | 17:59009396 | gccttcccaaagtgc[C/T]gggattacaggcatt | 4591 |
rs9907821 | snp | A/G | 0.0490535 | 0.14873 | intron-variant | TRIM37 | GRCh38.p7 | 17:59019615 | tgggaggctgaggca[A/G]gagaatggcgtgaac | 4591 |
rs9908435 | snp | C/T | | | intron-variant | TRIM37 | GRCh38.p7 | 17:59020062 | atggtgaaaccccat[C/T]tctactaaaaataca | 4591 |
rs9908437 | snp | C/T | | | intron-variant | TRIM37 | GRCh38.p7 | 17:59020064 | ggtgaaaccccatct[C/T]tactaaaaatacaaa | 4591 |
rs9908869 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM37 | GRCh38.p7 | 17:59018330 | tcttttaaaaatACA[C/T]tttaaaaaaagaata | 4591 |
rs9908946 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TRIM37 | GRCh38.p7 | 17:59036036 | TTTGTTACAAATTAC[A/G]TACCGATATTTACCA | 4591 |
rs9909268 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM37 | GRCh38.p7 | 17:59020218 | cctggtggacagagc[A/G]agactctgtctcaaa | 4591 |
rs9910352 | snp | C/T | | | intron-variant | TRIM37 | GRCh38.p7 | 17:59102703 | ATTTAACTGGGTCTT[C/T]TGCGCATGGTACAGT | 4591 |
rs9912439 | snp | G/T | | | intron-variant | TRIM37 | GRCh38.p7 | 17:59103460 | gattctcctgcctca[G/T]cctcctgagtagctg | 4591 |
rs9912716 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM37 | GRCh38.p7 | 17:59054380 | aatctcggctcactg[C/T]aacatctgcctcccg | 4591 |
rs9914789 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM37 | GRCh38.p7 | 17:59032956 | CATTACAGACATCTG[C/T]AGGCAGATATTATGC | 4591 |
rs9915076 | snp | C/T | 0 | 0 | intron-variant | TRIM37 | GRCh38.p7 | 17:59049453 | CACAGTAAAAGATGT[C/T]TCAAGTGAAAAAAAA | 4591 |
rs9915407 | snp | A/G | 0.00119737 | 0.0244387 | downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant, intron-variant | TRIM37, PPM1E | GRCh38.p7 | 17:58982247 | ATTTAGTTATATTTG[A/G]TATTTTGAAACTGTC | 4591 |