SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs950268 | snp | A/C | 0.0115794 | 0.0752039 | stop-gained | TRIM60 | GRCh38.p7 | 4:165040697 | CTAAAATGTTCATCT[A/C]TTCATCTTGTATCTG | 166655 |
rs2056252 | snp | C/T | 0.411746 | 0.190626 | | | GRCh38.p7 | 4:165026338 | AAAAACAAAACAGGC[C/T]TGGcgtctgtaatcc | 166655 |
rs4133108 | snp | C/G | 0.462472 | 0.13174 | upstream-variant-2KB | TRIM60 | GRCh38.p7 | 4:165031283 | TTGGTAAATGAGACA[C/G]TGAAAGAGGCTAATA | 166655 |
rs4133109 | snp | C/T | 0.0788843 | 0.182262 | upstream-variant-2KB | TRIM60 | GRCh38.p7 | 4:165031206 | tatttatttttgaga[C/T]ggagtctcgctgtgt | 166655 |
rs4690800 | snp | A/G | 0.410568 | 0.191619 | upstream-variant-2KB | TRIM60 | GRCh38.p7 | 4:165030838 | GACCTCAGCTGATCC[A/G]CCCGCCTTGGCCTCC | 166655 |
rs4691144 | snp | A/G | 0.00279162 | 0.0372561 | | | GRCh38.p7 | 4:165027895 | agcatggatacactg[A/G]atgaaggggtgattt | 166655 |
rs6536885 | snp | A/G | 0.304688 | 0.243945 | | | GRCh38.p7 | 4:165029523 | TTTTTTTTGTTTCTC[A/G]TGTTTCTGCTGACTG | 166655 |
rs6536886 | snp | A/G | 0.484701 | 0.0861117 | utr-variant-5-prime | TRIM60 | GRCh38.p7 | 4:165032103 | TGAGCCGCCGGTCCA[A/G]CTGCTCCAGGTAAGC | 166655 |
rs6847301 | snp | C/T | 0.331642 | 0.236293 | | | GRCh38.p7 | 4:165027154 | atcaaatcctatata[C/T]gcacactatgttttt | 166655 |
rs7675665 | snp | G/T | 0.269538 | 0.249235 | | | GRCh38.p7 | 4:165024793 | TGCAGTGGCGCGATC[G/T]CGGCTCACTGCAAGC | 166655 |
rs9996271 | snp | G/T | 0.00318978 | 0.0398085 | upstream-variant-2KB | TRIM60 | GRCh38.p7 | 4:165031936 | CGGCATTGAGCATGC[G/T]CAGGCCTTTCCCGCC | 166655 |
rs10000216 | snp | C/T | 0.11228 | 0.208646 | intron-variant | TRIM60 | GRCh38.p7 | 4:165033713 | ttgcaatagggagaa[C/T]tcagcatgaacagaa | 166655 |
rs10009883 | snp | A/C | 0.32768 | 0.237625 | intron-variant | TRIM60 | GRCh38.p7 | 4:165032847 | CTGGGAATCTCCCAC[A/C]GGTTTGATTTATATT | 166655 |
rs10213520 | snp | C/G | | | intron-variant | TRIM60 | GRCh38.p7 | 4:165032175 | GCTTACTTAACTGGG[C/G]AGGGGCTTCCTGAGT | 166655 |
rs10708866 | in-del | -/T | 0.427271 | 0.176281 | intron-variant | TRIM60 | GRCh38.p7 | 4:165034171 | TTAAATGAAATACAC[-/T]TTTTTTTTTTTTTTA | 166655 |
rs11300124 | in-del | -/A | 0.305186 | 0.243833 | | | GRCh38.p7 | 4:165028741 | AGAAATAGTTTCACC[-/A]AAAAAAACTGAACTC | 166655 |
rs11352653 | in-del | -/A | | | | | GRCh38.p7 | 4:165029157 | AAAAAAAAAAAAAAA[-/A]GAGATCAATTAGTAA | 166655 |
rs11932584 | snp | C/T | 0.12932 | 0.218944 | intron-variant | TRIM60 | GRCh38.p7 | 4:165036414 | CATCTTACATGTTTG[C/T]TTGTTTTTTTAAGTT | 166655 |
rs11934736 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | TRIM60 | GRCh38.p7 | 4:165033947 | gacaggggccttgtc[C/T]tcaggtatCAGAAGA | 166655 |
rs11935096 | snp | C/T | 0.0352966 | 0.128072 | | | GRCh38.p7 | 4:165024186 | aataaaaTGTTTCGA[C/T]aacatatattttgtt | 166655 |
rs12505213 | snp | A/G | 0.303187 | 0.244277 | upstream-variant-2KB | TRIM60 | GRCh38.p7 | 4:165030551 | GACTTCATCACAAGA[A/G]GGTATTTTTCTGGGA | 166655 |
rs12511557 | snp | C/T | 0.333261 | 0.235728 | intron-variant | TRIM60 | GRCh38.p7 | 4:165032472 | CAGGCTGGTGTCGAA[C/T]TTCCGACCTCAGGTG | 166655 |
rs12511595 | snp | C/G | 0.33303 | 0.235809 | intron-variant | TRIM60 | GRCh38.p7 | 4:165032554 | GTGCTCGGCCGGATT[C/G]TGTTTTCGCCGCGGA | 166655 |
rs13110286 | snp | A/G | 0.401037 | 0.199218 | intron-variant | TRIM60 | GRCh38.p7 | 4:165035251 | ATAAAATTTTGTAGA[A/G]ATGAGGTCTTGCTCT | 166655 |
rs13110766 | snp | A/G | 0.483995 | 0.0880135 | intron-variant | TRIM60 | GRCh38.p7 | 4:165035476 | ccaaaagtccgctct[A/G]cgtgatgtcacacag | 166655 |
rs13111010 | snp | A/G | 0.493837 | 0.055168 | intron-variant | TRIM60 | GRCh38.p7 | 4:165035589 | ccggaatttttattg[A/G]gaagagatcatgcag | 166655 |
rs13112943 | snp | A/G | 0.0232847 | 0.105357 | | | GRCh38.p7 | 4:165025647 | aactcctgacctcac[A/G]tgatccacccgcctc | 166655 |
rs13125623 | snp | G/T | | | intron-variant | TRIM60 | GRCh38.p7 | 4:165037539 | catgttggccaggat[G/T]gtctccgtctcttga | 166655 |
rs13133280 | snp | A/T | | | | | GRCh38.p7 | 4:165028115 | tacaaaaaAAAAAAG[A/T]CAAGCCACTTAAAAC | 166655 |
rs13133281 | snp | A/T | | | | | GRCh38.p7 | 4:165028117 | caaaaaAAAAAAGAC[A/T]AGCCACTTAAAACTT | 166655 |
rs13141887 | snp | C/T | 0.409382 | 0.192607 | | | GRCh38.p7 | 4:165029769 | TCATTAAATAAAATA[C/T]GTAATTTTTATAGGT | 166655 |
rs13152363 | snp | A/T | | | intron-variant | TRIM60 | GRCh38.p7 | 4:165037538 | ccatgttggccagga[A/T]ggtctccgtctcttg | 166655 |
rs28370983 | snp | A/C | 0.463881 | 0.12944 | | | GRCh38.p7 | 4:165028102 | TCTCTACTAAAAATA[A/C]AAAAAAAAAAAGACA | 166655 |
rs28435486 | snp | A/T | 0.463881 | 0.12944 | | | GRCh38.p7 | 4:165028100 | TGTCTCTACTAAAAA[A/T]ACAAAAAAAAAAAGA | 166655 |
rs28545643 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TRIM60 | GRCh38.p7 | 4:165038544 | TGGGCCTGGTGGCAC[A/G]AGCCTGTGGTCGTGG | 166655 |
rs34545516 | snp | A/C | | | | | GRCh38.p7 | 4:165027728 | AGCACTTTAAGGCTT[A/C]TATTTGGCATATATC | 166655 |
rs34640102 | in-del | -/C | | | | | GRCh38.p7 | 4:165027206 | AAAAATTTGGCTGGG[-/C]CGCGGTGGCTCATGC | 166655 |
rs34680036 | in-del | -/A | | | intron-variant | TRIM60 | GRCh38.p7 | 4:165038659 | AAAAAAAAAAAAAAA[-/A]GCCTGCTTTTTTTCC | 166655 |
rs34987029 | snp | A/C | | | | | GRCh38.p7 | 4:165027730 | CACTTTAAGGCTTAT[A/C]TTTGGCATATATCAA | 166655 |
rs35080277 | in-del | -/G | | | intron-variant | TRIM60 | GRCh38.p7 | 4:165033817 | TCAGTAGAGTCAGGG[-/G]AAGTGAAAAATTACA | 166655 |
rs35092752 | in-del | -/T | 0 | 0 | | | GRCh38.p7 | 4:165024692 | TTTTTTTTTTTTTTT[-/T]GAGACGGAGTGTAGC | 166655 |
rs35150831 | in-del | -/T/TT | | | intron-variant | TRIM60 | GRCh38.p7 | 4:165038378 | AATTACATTTTTTTT[-/T/TT]CCCCTCATATGTAAG | 166655 |
rs35266025 | in-del | -/AA | | | | | GRCh38.p7 | 4:165023980 | AAAAAAAAAAAAAAA[-/AA]GTGATAACTAATGTG | 166655 |
rs35391980 | in-del | -/A | | | | | GRCh38.p7 | 4:165029156 | AAAAAAAAAAAAAAA[-/A]AGAGATCAATTAGTA | 166655 |
rs35449092 | snp | C/G | 0.409382 | 0.192607 | | | GRCh38.p7 | 4:165028524 | CTGACGTGAACAGTA[C/G]TTCAGGTTTTTCAAA | 166655 |
rs35558620 | in-del | -/A | | | | | GRCh38.p7 | 4:165025128 | GTATAATTTATGCAA[-/A]GAGAAAAAGAGGATC | 166655 |
rs35680343 | snp | G/T | 0.440333 | 0.16209 | upstream-variant-2KB, utr-variant-5-prime | TRIM60 | GRCh38.p7 | 4:165031982 | AGCCAACCACCGCGC[G/T]GGTCAATTGTATGCC | 166655 |
rs35712467 | snp | A/G | | | | | GRCh38.p7 | 4:165024858 | CTTCCTCAGCCTCCA[A/G]AGTAGCTGGGACTAC | 166655 |
rs35857243 | in-del | -/T | | | frameshift-variant | TRIM60 | GRCh38.p7 | 4:165041133 | ACATTACTGGGAAGT[-/T]AGAAGTGGGAAACAA | 166655 |
rs35971522 | snp | A/T | | | intron-variant | TRIM60 | GRCh38.p7 | 4:165032678 | GAGCGTTAAGGAAGG[A/T]CCTCCCACCCTACAG | 166655 |
rs35973949 | snp | G/T | 0.359575 | 0.224707 | intron-variant | TRIM60 | GRCh38.p7 | 4:165039137 | ATAGTAGAATTTTAT[G/T]TATTTTATATATATA | 166655 |
rs35976516 | in-del | -/GATA | 0.409721 | 0.192325 | | | GRCh38.p7 | 4:165029543 | TCTGCTGACTGTAAT[-/GATA]GATATTCTGTTTACA | 166655 |
rs55667905 | snp | A/G | 0.140919 | 0.224948 | intron-variant | TRIM60 | GRCh38.p7 | 4:165035897 | CCAGCTAGTTTTTGT[A/G]TTTTTAGTAGAGACA | 166655 |
rs55862946 | snp | C/T | 0.141596 | 0.225274 | intron-variant | TRIM60 | GRCh38.p7 | 4:165035871 | GAGATTACAGGCATG[C/T]GCCACCACACCCAGC | 166655 |
rs56118433 | snp | A/G | 0.12932 | 0.218944 | intron-variant | TRIM60 | GRCh38.p7 | 4:165036165 | AGTCTTAGGCCTGCT[A/G]TGCTCATTCTTCCGC | 166655 |
rs56132390 | in-del | -/AAAAAAAAAAAAAA/AAAAAAAAAAAAAAA | 0 | 0 | | | GRCh38.p7 | 4:165028113 | ATACAAAAAAAAAAA[lengthTooLong]GACAAGCCACTTAAA | 166655 |
rs56182744 | snp | A/G | 0.140919 | 0.224948 | intron-variant | TRIM60 | GRCh38.p7 | 4:165035903 | AGTTTTTGTATTTTT[A/G]GTAGAGACAGGGTTT | 166655 |
rs56263535 | snp | G/T | | | intron-variant | TRIM60 | GRCh38.p7 | 4:165037385 | CTGGAGTGCAGTGGC[G/T]GGATCTTGGCTCACT | 166655 |
rs56273239 | snp | C/T | 0.081446 | 0.184634 | utr-variant-5-prime | TRIM60 | GRCh38.p7 | 4:165032052 | TTTCCGCTCTGCGCC[C/T]CGCGGGGTTCCATGG | 166655 |
rs57046161 | snp | C/G | 0.0829062 | 0.185956 | intron-variant | TRIM60 | GRCh38.p7 | 4:165032545 | TGAGCCACCGTGCTC[C/G]GCCGGATTCTGTTTT | 166655 |
rs58476773 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TRIM60 | GRCh38.p7 | 4:165037631 | TCCTGGGCTCAAGCA[A/G]TTTTCTTGCCTCAGC | 166655 |
rs58806777 | snp | C/T | 0.130008 | 0.219321 | intron-variant | TRIM60 | GRCh38.p7 | 4:165036178 | CTGTGCTCATTCTTC[C/T]GCACAATACCACTTG | 166655 |
rs59349426 | in-del | -/T | | | downstream-variant-500B, utr-variant-3-prime | TRIM60 | GRCh38.p7 | 4:165041760 | ATAATTTTTTTTTTT[-/T]AGTTAAGCAAATTAT | 166655 |
rs59901169 | snp | G/T | | | intron-variant | TRIM60 | GRCh38.p7 | 4:165035907 | TTTGTATTTTTAGTA[G/T]AGACAGGGTTTCATC | 166655 |
rs60082479 | in-del | -/T | | | intron-variant | TRIM60 | GRCh38.p7 | 4:165035740 | TTTCTTTTTTTTTTT[-/T]AGACAGAGTTTTGCT | 166655 |
rs60221283 | snp | C/T | 0.00159617 | 0.0282053 | synonymous-codon | TRIM60 | GRCh38.p7 | 4:165040162 | CCCAGTGACCATCAA[C/T]TGTGGGCACAACTTC | 166655 |
rs60349844 | in-del | -/T/TTTT | 0.5 | 0 | intron-variant | TRIM60 | GRCh38.p7 | 4:165036235 | CTTACATTTTTTTTT[-/T/TTTT]CATTTAATGCTTTCA | 166655 |
rs61226884 | snp | A/G | 0.138886 | 0.22395 | intron-variant | TRIM60 | GRCh38.p7 | 4:165038527 | ATATTTTAAAAATTA[A/G]CTGGGCCTGGTGGCA | 166655 |
rs61630737 | in-del | -/CAAA | | | intron-variant | TRIM60 | GRCh38.p7 | 4:165037989 | AGGCCAAAAGACAAA[-/CAAA]TACCTGAAGAAAAGA | 166655 |
rs62355806 | snp | C/T | | | | | GRCh38.p7 | 4:165029838 | ATACATATCATGCTA[C/T]TATAATACAATAAAA | 166655 |
rs66625894 | in-del | -/TTAAT | | | | | GRCh38.p7 | 4:165029432 | TCAATGTCTTTTAAT[-/TTAAT]GTAAGGATAAATACG | 166655 |
rs71602556 | in-del | -/GT | 0.5 | 0 | upstream-variant-2KB | TRIM60 | GRCh38.p7 | 4:165030272 | GCAATCCTCTCCATT[-/GT]TGGTCTTCCAAAGTG | 166655 |
rs71602557 | in-del | -/C | 0.5 | 0 | intron-variant | TRIM60 | GRCh38.p7 | 4:165033162 | CACTGCACTCCAGCC[-/C]TTGGCGACAGAGTGA | 166655 |
rs71618429 | snp | C/T | 0.5 | 0 | intron-variant | TRIM60 | GRCh38.p7 | 4:165037162 | GCCGAGACTGCACCA[C/T]TGCACTCCAGCCTGG | 166655 |
rs72393527 | in-del | -/TTTAA | 0.409382 | 0.192607 | | | GRCh38.p7 | 4:165029426 | TGCCTCTCAATGTCT[-/TTTAA]TTTAATGTAAGGATA | 166655 |
rs72697987 | snp | A/G | 0.403684 | 0.197183 | intron-variant | TRIM60 | GRCh38.p7 | 4:165032765 | TCAGGAAACTGCTAC[A/G]GATGAGAAAGTTTAG | 166655 |
rs73003896 | snp | C/T | 0.0592355 | 0.161582 | | | GRCh38.p7 | 4:165029666 | AAAAGAACTTCCTCA[C/T]TGAAGATTTAAGAGT | 166655 |
rs73005708 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | TRIM60 | GRCh38.p7 | 4:165033358 | TAAGAATCAGAGTTG[A/G]TAATTCAGTTGTGAG | 166655 |
rs73005711 | snp | C/G | 0.0865458 | 0.189163 | intron-variant | TRIM60 | GRCh38.p7 | 4:165035167 | ACTCCTGGGCTCAAG[C/G]AATCCTCTCACCCCA | 166655 |
rs73005720 | snp | A/T | 0.0349115 | 0.127424 | intron-variant | TRIM60 | GRCh38.p7 | 4:165036394 | TGTGTGATATCTGTT[A/T]ACATCATCTTACATG | 166655 |
rs73005723 | snp | G/T | 0.12932 | 0.218944 | intron-variant | TRIM60 | GRCh38.p7 | 4:165036659 | ACTGAGGCAGGCAGA[G/T]CACTTGAGGTCAGGA | 166655 |
rs73005726 | snp | C/T | 0.125874 | 0.217008 | intron-variant | TRIM60 | GRCh38.p7 | 4:165037204 | AAAACTGTCTCAAAA[C/T]GAAACAAAACAAACA | 166655 |
rs73005728 | snp | A/G | 0.093417 | 0.194889 | intron-variant | TRIM60 | GRCh38.p7 | 4:165037255 | GCTTAGTGATTTAGT[A/G]TCACACCAGTAGTCA | 166655 |
rs73005730 | snp | C/T | 0.12932 | 0.218944 | intron-variant | TRIM60 | GRCh38.p7 | 4:165037298 | TTAGGACTTTGGATA[C/T]GCCTATCAAATCATT | 166655 |
rs73005732 | snp | A/G | 0.12932 | 0.218944 | intron-variant | TRIM60 | GRCh38.p7 | 4:165037314 | GCCTATCAAATCATT[A/G]TACTTTTTTTGTTTT | 166655 |
rs73005799 | snp | C/T | 0.12932 | 0.218944 | intron-variant | TRIM60 | GRCh38.p7 | 4:165038249 | GGAAATTCAGGAAGC[C/T]TAACTTTGATGTATT | 166655 |
rs73005801 | snp | A/C | 0.12932 | 0.218944 | intron-variant | TRIM60 | GRCh38.p7 | 4:165038317 | AATTTGTCCTATACT[A/C]TCTACTTTATTGCAA | 166655 |
rs73007605 | snp | C/T | 0.093777 | 0.195178 | utr-variant-3-prime | TRIM60 | GRCh38.p7 | 4:165041666 | TATGAATATCAATTG[C/T]CAGGTGCTTTGATTT | 166655 |
rs73007606 | snp | A/T | 0.154382 | 0.230992 | downstream-variant-500B, utr-variant-3-prime | TRIM60 | GRCh38.p7 | 4:165041749 | TTCAAATTGCCTATA[A/T]TTTTTTTTTTTAGTT | 166655 |
rs73871564 | snp | A/G | 0.0573587 | 0.15934 | | | GRCh38.p7 | 4:165029548 | TGACTGTAATGATAG[A/G]TATTCTGTTTACAGA | 166655 |
rs73871565 | snp | C/T | 0.104149 | 0.203046 | intron-variant | TRIM60 | GRCh38.p7 | 4:165034110 | ATTGAGTTCCAGGAT[C/T]TATGCAGGAATGTTC | 166655 |
rs73871570 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | TRIM60 | GRCh38.p7 | 4:165042030 | TATATCACCTGCCAA[C/T]CTAGACCAACTACAC | 166655 |
rs74557337 | snp | A/G | 0.0509478 | 0.151255 | downstream-variant-500B | TRIM60 | GRCh38.p7 | 4:165042285 | AACTTGATGGTTTTG[A/G]CAAGTCTGATATCAG | 166655 |
rs74634224 | snp | G/T | | | intron-variant | TRIM60 | GRCh38.p7 | 4:165034420 | GCCTCCCAAAGTGCT[G/T]GGATTACAGGCGTGA | 166655 |
rs74673273 | snp | A/C | 0.00636936 | 0.0560724 | | | GRCh38.p7 | 4:165028373 | CTGTATTCAGCAGTC[A/C]GCCCCAGTTGAAGGT | 166655 |
rs74862056 | snp | A/G | 0.0387552 | 0.1337 | intron-variant | TRIM60 | GRCh38.p7 | 4:165034474 | ACCCTTTTTTACAGC[A/G]ATGTGGTTCTTTCTT | 166655 |
rs74866759 | snp | A/T | 0.0061835 | 0.0552586 | missense | TRIM60 | GRCh38.p7 | 4:165040737 | ATGAAAACCTTGTAG[A/T]ACTTTCAGATTATGT | 166655 |
rs75136942 | snp | A/G/T | 3.29453e-05 | 0.00405854 | missense | TRIM60 | GRCh38.p7 | 4:165040217 | TGGAAGGATCTAGAT[A/G/T]ATACCTTTCCCTGTC | 166655 |
rs75175125 | snp | A/C | 0.5 | 0 | | | GRCh38.p7 | 4:165027487 | GAGACTCAAAAAAAC[A/C]AAAAACAAAAAGAAA | 166655 |
rs75562933 | snp | C/T | 0.5 | 0 | | | GRCh38.p7 | 4:165024125 | AAGATGGCAAGACCC[C/T]GTCTCTACACACACA | 166655 |