SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs770610547 | snp | C/G | | | intron-variant | TRIM60 | GRCh38.p7 | 4:165033182 | CGACAGAGTGAGATC[C/G]TGTCTCAAAAAGTAA | 166655 |
rs770637035 | snp | C/T | 1.6473e-05 | 0.00286988 | synonymous-codon | TRIM60 | GRCh38.p7 | 4:165040189 | CTTCTGTCGCTCCTG[C/T]CTCAGTGTATCCTGG | 166655 |
rs770793679 | snp | A/C | | | | | GRCh38.p7 | 4:165027439 | GCGGTAAGCTGTGAT[A/C]GCGCCATTGCACTCC | 166655 |
rs770947431 | snp | A/C | 0.000148798 | 0.00862421 | synonymous-codon | TRIM60 | GRCh38.p7 | 4:165040942 | CTTGGACAGAATTAT[A/C]AAGCCATTTCAAGTA | 166655 |
rs770987704 | snp | C/T | | | | | GRCh38.p7 | 4:165024241 | TAAGTACTTACTCTG[C/T]ATTGGCTCACTAATC | 166655 |
rs770995556 | snp | A/G | 1.8627e-05 | 0.00305175 | intron-variant | TRIM60 | GRCh38.p7 | 4:165040025 | CTCTACGGAGGCAGG[A/G]CTGATCAAAGGGAGG | 166655 |
rs771013356 | in-del | -/CTT | 3.29641e-05 | 0.00405968 | cds-indel | TRIM60 | GRCh38.p7 | 4:165040994 | ACAGCACATCCTCAA[-/CTT]CTTGTCTCTGAGGAT | 166655 |
rs771077642 | snp | C/T | | | intron-variant | TRIM60 | GRCh38.p7 | 4:165037937 | TCCCTATGAATAAGG[C/T]AGACTAAGTACCTAC | 166655 |
rs771106385 | snp | A/C | 1.66374e-05 | 0.00288417 | missense | TRIM60 | GRCh38.p7 | 4:165040602 | TGAAAAAGAAGGTAG[A/C]ATATAAGAGGGAAGA | 166655 |
rs771303652 | in-del | -/TAAG | | | intron-variant | TRIM60 | GRCh38.p7 | 4:165036291 | CAAACTCAGAGAAAT[-/TAAG]TTAGTTGATCAATGA | 166655 |
rs771321532 | snp | A/T | 1.65985e-05 | 0.00288079 | missense | TRIM60 | GRCh38.p7 | 4:165040722 | TTTTAGCAAAACTAA[A/T]TGAAAACCTTGTAGA | 166655 |
rs771327740 | in-del | -/TCA | | | | | GRCh38.p7 | 4:165024965 | TCTCCATCTCTGACC[-/TCA]TCATGATCTGCCCGC | 166655 |
rs771471935 | snp | C/G | 1.64746e-05 | 0.00287002 | missense | TRIM60 | GRCh38.p7 | 4:165040269 | CATACAAGAGCTTCA[C/G]GAGGAACCCCCAGCT | 166655 |
rs771599222 | snp | C/T | 1.80932e-05 | 0.0030077 | missense | TRIM60 | GRCh38.p7 | 4:165041466 | CTCTTAAAATCTGCT[C/T]AGTATCAGATTCTGA | 166655 |
rs771680403 | snp | A/G | | | upstream-variant-2KB | TRIM60 | GRCh38.p7 | 4:165031606 | ATCGCTTGAGCCCAT[A/G]AGTTCGAGACCAGCC | 166655 |
rs771691096 | snp | C/T | 1.65392e-05 | 0.00287564 | missense | TRIM60 | GRCh38.p7 | 4:165040427 | ATCTTATGTACACAG[C/T]GCAGTTTCTCCACTA | 166655 |
rs771789881 | in-del | -/CATTTGTTATGAC | 0.000230669 | 0.0107369 | frameshift-variant | TRIM60 | GRCh38.p7 | 4:165041047 | AAGAAAAAAACGAAA[-/CATTTGTTATGAC]CCAAGGAGATTTTAT | 166655 |
rs771839443 | snp | C/T | 1.6486e-05 | 0.00287102 | synonymous-codon | TRIM60 | GRCh38.p7 | 4:165040967 | CAAGTAGATGTGATT[C/T]TAGATCTCAACACAG | 166655 |
rs772047800 | snp | G/T | 1.6473e-05 | 0.00286988 | missense | TRIM60 | GRCh38.p7 | 4:165041139 | ACTGGGAAGTAGAAG[G/T]GGGAAACAAACCTAA | 166655 |
rs772068077 | snp | A/G | | | | | GRCh38.p7 | 4:165026137 | CAACCTCCGCCTCCC[A/G]GGTTCAAGCGATTCT | 166655 |
rs772481373 | snp | C/T | | | upstream-variant-2KB | TRIM60 | GRCh38.p7 | 4:165031839 | TGTGATTTAAATGAC[C/T]CACTGAAGCCATCAG | 166655 |
rs772503443 | snp | C/G | 8.30061e-05 | 0.00644175 | missense | TRIM60 | GRCh38.p7 | 4:165041395 | TCTCTATACTTTTAA[C/G]GATTGTTTCACAGAA | 166655 |
rs772548550 | in-del | -/A | | | intron-variant | TRIM60 | GRCh38.p7 | 4:165035396 | ATAGTGAAAGGATAC[-/A]AAGCAAAATCAGCAA | 166655 |
rs772711694 | snp | C/T | 0.000121793 | 0.00780268 | intron-variant | TRIM60 | GRCh38.p7 | 4:165040064 | TGCATTACCTTTGTT[C/T]GCAGCTCGATGGAGT | 166655 |
rs772788059 | snp | C/G | | | intron-variant | TRIM60 | GRCh38.p7 | 4:165032155 | GCAGTAGGGCCTGGC[C/G]GGAGGCTTACTTAAC | 166655 |
rs772879913 | snp | C/T | | | upstream-variant-2KB | TRIM60 | GRCh38.p7 | 4:165031103 | GTAGTCCTAGCCACT[C/T]GGGGGGCTGAGGCAG | 166655 |
rs772964136 | snp | C/T | 1.64735e-05 | 0.00286993 | missense | TRIM60 | GRCh38.p7 | 4:165041265 | AGAGTGGTTATGTTG[C/T]GTCAGGTCCTAAGAC | 166655 |
rs772971594 | snp | C/T | 1.64732e-05 | 0.0028699 | synonymous-codon | TRIM60 | GRCh38.p7 | 4:165040174 | CAACTGTGGGCACAA[C/T]TTCTGTCGCTCCTGC | 166655 |
rs773046596 | snp | C/T | | | intron-variant | TRIM60 | GRCh38.p7 | 4:165037259 | AGTGATTTAGTATCA[C/T]ACCAGTAGTCACACC | 166655 |
rs773097439 | snp | G/T | | | intron-variant | TRIM60 | GRCh38.p7 | 4:165035262 | TAGAGATGAGGTCTT[G/T]CTCTGTTGCCCAGAC | 166655 |
rs773200467 | snp | C/T | 1.6557e-05 | 0.00287719 | missense | TRIM60 | GRCh38.p7 | 4:165040755 | TTTCAGATTATGTTT[C/T]CACATTAAAACATCT | 166655 |
rs773474719 | snp | C/T | 4.24674e-05 | 0.00460781 | utr-variant-3-prime | TRIM60 | GRCh38.p7 | 4:165041519 | GTCTGTTTCAGTTTT[C/T]GTAGGTAACTTAGCC | 166655 |
rs773476295 | snp | A/G | 1.66366e-05 | 0.0028841 | missense | TRIM60 | GRCh38.p7 | 4:165040598 | GAGCTGAAAAAGAAG[A/G]TAGAATATAAGAGGG | 166655 |
rs773504018 | snp | A/C | 1.65605e-05 | 0.0028775 | missense | TRIM60 | GRCh38.p7 | 4:165040473 | ACATTTGCCCTATTA[A/C]GAAAGCTGCCTCTTA | 166655 |
rs773650153 | snp | C/T | | | | | GRCh38.p7 | 4:165029601 | GGGACCACAAGTAAA[C/T]TGGCGTGAAGCTCCT | 166655 |
rs773852714 | snp | A/G | 1.64735e-05 | 0.00286993 | missense | TRIM60 | GRCh38.p7 | 4:165041282 | TCAGGTCCTAAGACA[A/G]CCCAGCTTCTGCCAG | 166655 |
rs773855109 | snp | C/T | | | | | GRCh38.p7 | 4:165029450 | ATGTAAGGATAAATA[C/T]GAATATAGATTTTTT | 166655 |
rs774016319 | snp | A/T | | | | | GRCh38.p7 | 4:165029289 | ATTTAAAAGTCAAAC[A/T]AATCAAATACAAAAT | 166655 |
rs774029116 | snp | G/T | 1.64727e-05 | 0.00286986 | missense | TRIM60 | GRCh38.p7 | 4:165040195 | TCGCTCCTGCCTCAG[G/T]GTATCCTGGAAGGAT | 166655 |
rs774123163 | snp | C/T | 1.64743e-05 | 0.00287 | missense | TRIM60 | GRCh38.p7 | 4:165040253 | TGCCGTTTTTGCTTT[C/T]CATACAAGAGCTTCA | 166655 |
rs774237296 | snp | A/C | 1.64895e-05 | 0.00287132 | missense | TRIM60 | GRCh38.p7 | 4:165040953 | TTATCAAGCCATTTC[A/C]AGTAGATGTGATTCT | 166655 |
rs774339090 | in-del | -/A | | | | | GRCh38.p7 | 4:165023961 | GTGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 166655 |
rs774401793 | snp | C/T | | | | | GRCh38.p7 | 4:165024824 | TCCGCTTCCCGGATT[C/T]ACGCCATTCTCCATT | 166655 |
rs774771215 | in-del | -/AC | | | | | GRCh38.p7 | 4:165024132 | CAAGACCCTGTCTCT[-/AC]ACACACACACACACA | 166655 |
rs774893907 | snp | C/G | 1.65405e-05 | 0.00287576 | missense | TRIM60 | GRCh38.p7 | 4:165040429 | CTTATGTACACAGTG[C/G]AGTTTCTCCACTAAA | 166655 |
rs774995561 | in-del | -/T | 1.80517e-05 | 0.00300425 | intron-variant | TRIM60 | GRCh38.p7 | 4:165040049 | AGGGAGGTTACCTTA[-/T]GCATTACCTTTGTTC | 166655 |
rs775059303 | in-del | -/C | 1.64779e-05 | 0.00287031 | frameshift-variant | TRIM60 | GRCh38.p7 | 4:165041059 | AAACATTTGTTATGA[-/C]CCAAGGAGATTTTAT | 166655 |
rs775161100 | in-del | -/CTC | | | | | GRCh38.p7 | 4:165027060 | GATGACTCCTCAATT[-/CTC]CTTCTTCTTCCTGAA | 166655 |
rs775207569 | snp | A/G | 1.64849e-05 | 0.00287092 | missense | TRIM60 | GRCh38.p7 | 4:165040970 | GTAGATGTGATTCTA[A/G]ATCTCAACACAGCAC | 166655 |
rs775486322 | in-del | -/AC | | | intron-variant | TRIM60 | GRCh38.p7 | 4:165037784 | CTCTTTTAATTTTGA[-/AC]AGTTTCCCAACCTAA | 166655 |
rs775543878 | snp | A/G | | | intron-variant | TRIM60 | GRCh38.p7 | 4:165035397 | TAGTGAAAGGATACA[A/G]AGCAAAATCAGCAAA | 166655 |
rs775706864 | snp | C/T | | | missense | TRIM60 | GRCh38.p7 | 4:165040581 | AAGGCAGCAAATCAG[C/T]GGAGCTGAAAAAGAA | 166655 |
rs775734767 | snp | C/G/T | 1.65789e-05 | 0.0028791 | missense | TRIM60 | GRCh38.p7 | 4:165040740 | AAAACCTTGTAGAAC[C/G/T]TTCAGATTATGTTTC | 166655 |
rs775738567 | snp | C/T | 1.64741e-05 | 0.00286998 | missense | TRIM60 | GRCh38.p7 | 4:165041301 | AGCTTCTGCCAGTAG[C/T]AAAACCCAGTAAAAT | 166655 |
rs776060811 | snp | A/G | 1.66098e-05 | 0.00288177 | missense | TRIM60 | GRCh38.p7 | 4:165041396 | CTCTATACTTTTAAC[A/G]ATTGTTTCACAGAAG | 166655 |
rs776145138 | snp | C/T | 1.64746e-05 | 0.00287002 | synonymous-codon | TRIM60 | GRCh38.p7 | 4:165041077 | AAGGAGATTTTATGT[C/T]TGCCCTGCTGTCCTA | 166655 |
rs776230575 | in-del | -/G | 1.65064e-05 | 0.00287279 | frameshift-variant | TRIM60 | GRCh38.p7 | 4:165041373 | ATAATATGAATGATA[-/G]GTCTATTCTCTATAC | 166655 |
rs776319593 | snp | G/T | | | | | GRCh38.p7 | 4:165026405 | ACTTACAATGTGCTC[G/T]TTTCTCAAGAAATAC | 166655 |
rs776421248 | snp | A/G | | | intron-variant | TRIM60 | GRCh38.p7 | 4:165036833 | TTGCAGTGAGCCGAG[A/G]TCGTGCCATCGCATT | 166655 |
rs776427598 | snp | A/G | | | | | GRCh38.p7 | 4:165027442 | GTAAGCTGTGATCGC[A/G]CCATTGCACTCCAGC | 166655 |
rs776438394 | snp | A/G | | | downstream-variant-500B | TRIM60 | GRCh38.p7 | 4:165042151 | TCTTTTCATTTTGGG[A/G]TGCCATCAACCCAAA | 166655 |
rs776518188 | snp | A/G | 1.64996e-05 | 0.0028722 | missense | TRIM60 | GRCh38.p7 | 4:165040844 | AAGAGTATGCACCAC[A/G]AGTATCAAAACCTAA | 166655 |
rs776652511 | snp | A/G | | | intron-variant | TRIM60 | GRCh38.p7 | 4:165034061 | TCTGGAAGATGGGTT[A/G]GGGGAAGCTGGAGTG | 166655 |
rs776796805 | in-del | -/TTTTG | | | intron-variant | TRIM60 | GRCh38.p7 | 4:165037321 | AAATCATTATACTTT[-/TTTTG]TTTTGTTTTGTTTTG | 166655 |
rs776799467 | snp | C/T | 1.65015e-05 | 0.00287237 | synonymous-codon | TRIM60 | GRCh38.p7 | 4:165040933 | ATATTCTGGCTTGGA[C/T]AGAATTATCAAGCCA | 166655 |
rs777004830 | snp | A/G | 2.03759e-05 | 0.00319179 | utr-variant-3-prime | TRIM60 | GRCh38.p7 | 4:165041504 | GGAACTGGTAAATGG[A/G]TCTGTTTCAGTTTTT | 166655 |
rs777006576 | snp | C/G | 0.000131822 | 0.00811748 | missense | TRIM60 | GRCh38.p7 | 4:165040296 | AGCTCCGTAATTTGA[C/G]TGAAATTGCTAAACA | 166655 |
rs777096413 | snp | C/T | 3.31131e-05 | 0.00406884 | synonymous-codon | TRIM60 | GRCh38.p7 | 4:165040465 | GAAGCACTACATTTG[C/T]CCTATTAAGAAAGCT | 166655 |
rs777624782 | snp | C/T | 1.65302e-05 | 0.00287486 | synonymous-codon | TRIM60 | GRCh38.p7 | 4:165041380 | GAATGATAGGTCTAT[C/T]CTCTATACTTTTAAC | 166655 |
rs777633071 | snp | A/C | | | intron-variant | TRIM60 | GRCh38.p7 | 4:165033117 | ATCGCTTGAGCCTGG[A/C]GGCAGAGGTTGCAGT | 166655 |
rs777711092 | snp | C/T | 1.64746e-05 | 0.00287002 | missense | TRIM60 | GRCh38.p7 | 4:165040241 | CCCTGTCCTGTCTGC[C/T]GTTTTTGCTTTCCAT | 166655 |
rs777713015 | snp | A/G | 1.75656e-05 | 0.00296353 | missense | TRIM60 | GRCh38.p7 | 4:165041447 | ACTGGAACAGATTCC[A/G]AACCTCTTAAAATCT | 166655 |
rs777734899 | in-del | -/TATCATAA | 1.65097e-05 | 0.00287308 | frameshift-variant | TRIM60 | GRCh38.p7 | 4:165040919 | GTCTTCCTCCTCAAT[-/TATCATAA]ATTCTGGCTTGGACA | 166655 |
rs777803054 | snp | A/C | 1.65241e-05 | 0.00287433 | synonymous-codon | TRIM60 | GRCh38.p7 | 4:165040390 | CCAGTTTCTGACCCT[A/C]TTCTGTGTTAAAGAT | 166655 |
rs778209744 | snp | G/T | 6.60164e-05 | 0.0057449 | missense | TRIM60 | GRCh38.p7 | 4:165040797 | TAGAGGGCAAGTCTG[G/T]GCAGTCAAACCTGGA | 166655 |
rs778239651 | snp | C/T | | | intron-variant | TRIM60 | GRCh38.p7 | 4:165033411 | CGTGAACTGTACTCT[C/T]CAGTGTCCTTAACCA | 166655 |
rs778253842 | snp | A/T | | | | | GRCh38.p7 | 4:165025437 | TTATTTGAAACAGCG[A/T]CTCACTCTGTCACCC | 166655 |
rs778315956 | snp | C/T | 3.31697e-05 | 0.00407231 | synonymous-codon | TRIM60 | GRCh38.p7 | 4:165041392 | TATTCTCTATACTTT[C/T]AACGATTGTTTCACA | 166655 |
rs778318300 | snp | A/G | 3.32099e-05 | 0.00407478 | missense | TRIM60 | GRCh38.p7 | 4:165040712 | GAGATGAACATTTTA[A/G]CAAAACTAAATGAAA | 166655 |
rs778327047 | in-del | -/AG | | | intron-variant | TRIM60 | GRCh38.p7 | 4:165036283 | AATAGAAACAAACTC[-/AG]AGAAATTAAGTTAGT | 166655 |
rs778604867 | snp | A/G | 1.78356e-05 | 0.00298622 | missense | TRIM60 | GRCh38.p7 | 4:165041459 | TCCGAACCTCTTAAA[A/G]TCTGCTCAGTATCAG | 166655 |
rs778606590 | snp | C/T | | | utr-variant-5-prime | TRIM60 | GRCh38.p7 | 4:165032026 | CCAAGGCGCCCAGGG[C/T]TGTGTGAGGGTTTCC | 166655 |
rs778772934 | snp | C/G | 1.65307e-05 | 0.0028749 | missense | TRIM60 | GRCh38.p7 | 4:165040406 | TTCTGTGTTAAAGAT[C/G]TAGAGATCTTATGTA | 166655 |
rs778809439 | in-del | -/A | | | frameshift-variant | TRIM60 | GRCh38.p7 | 4:165041034 | TGTGCGATATGAAAG[-/A]AAAAAAACGAAACAT | 166655 |
rs778858382 | snp | A/G | 1.66059e-05 | 0.00288144 | missense | TRIM60 | GRCh38.p7 | 4:165040533 | AGCCCTTGAGGAATA[A/G]TATAGAACGAGTTGA | 166655 |
rs778877732 | snp | A/C | 1.64784e-05 | 0.00287035 | missense | TRIM60 | GRCh38.p7 | 4:165041041 | ATATGAAAGAAAAAA[A/C]CGAAACATTTGTTAT | 166655 |
rs778962990 | snp | A/G | 6.65104e-05 | 0.00576635 | missense | TRIM60 | GRCh38.p7 | 4:165040574 | ATTCTGCAAGGCAGC[A/G]AATCAGTGGAGCTGA | 166655 |
rs778969341 | snp | A/G | 1.6504e-05 | 0.00287258 | missense | TRIM60 | GRCh38.p7 | 4:165040119 | AAGAGGAGTCTAGCT[A/G]TCCCATCTGTCTGGA | 166655 |
rs779073214 | snp | A/G | | | upstream-variant-2KB | TRIM60 | GRCh38.p7 | 4:165031128 | AGGCAGGAGAACAGC[A/G]TGAACCCGGGAGGCA | 166655 |
rs779268700 | snp | A/C | 1.65138e-05 | 0.00287343 | missense | TRIM60 | GRCh38.p7 | 4:165040907 | AAATATGGTTTCAGT[A/C]TTCCTCCTCAATATT | 166655 |
rs779367996 | snp | C/T | 1.64982e-05 | 0.00287208 | stop-gained | TRIM60 | GRCh38.p7 | 4:165040823 | CTGGAATTACTGACA[C/T]AAGCTAAGAGTATGC | 166655 |
rs779477208 | in-del | -/T | | | intron-variant | TRIM60 | GRCh38.p7 | 4:165033838 | AAAAATTACAAAAAG[-/T]GGGAAAGGGGTGGTT | 166655 |
rs779482704 | snp | A/G | 1.82241e-05 | 0.00301856 | synonymous-codon | TRIM60 | GRCh38.p7 | 4:165041470 | TAAAATCTGCTCAGT[A/G]TCAGATTCTGAAAGA | 166655 |
rs779689110 | in-del | -/AC | | | | | GRCh38.p7 | 4:165024133 | AGACCCTGTCTCTAC[-/AC]ACACACACACACACA | 166655 |
rs779737750 | snp | C/G/T | 3.32542e-05 | 0.00407752 | synonymous-codon | TRIM60 | GRCh38.p7 | 4:165040564 | AAAAGTGATAATTCT[C/G/T]CAAGGCAGCAAATCA | 166655 |
rs779934987 | snp | A/G | 3.29451e-05 | 0.00405851 | missense | TRIM60 | GRCh38.p7 | 4:165041147 | GTAGAAGTGGGAAAC[A/G]AACCTAAATGGATAT | 166655 |
rs780026570 | snp | G/T | 1.84548e-05 | 0.00303761 | intron-variant | TRIM60 | GRCh38.p7 | 4:165040037 | AGGACTGATCAAAGG[G/T]AGGTTACCTTATGCA | 166655 |
rs780098349 | snp | C/T | 8.23621e-05 | 0.00641672 | missense | TRIM60 | GRCh38.p7 | 4:165041226 | CAGTTCTGGGCGGAT[C/T]CTGGGCAATTGGGCG | 166655 |
rs780219096 | in-del | -/A | | | intron-variant | TRIM60 | GRCh38.p7 | 4:165038640 | GAAAGACCCTGTCTC[-/A]AAAAAAAAAAAAAAA | 166655 |
rs780234367 | snp | A/C | | | utr-variant-3-prime | TRIM60 | GRCh38.p7 | 4:165041587 | ACCACTGAAAACCAG[A/C]GTCGATTTTTCTCCT | 166655 |
rs780313105 | snp | A/G | | | upstream-variant-2KB | TRIM60 | GRCh38.p7 | 4:165030784 | TATTTTTAGAGAGAC[A/G]GGGTTTTGCCACTTT | 166655 |
rs780400002 | snp | A/G | | | | | GRCh38.p7 | 4:165028034 | GGCCAAAGCAGGCGA[A/G]TCACCTGAGGTTGGG | 166655 |
rs780428573 | snp | C/G | | | | | GRCh38.p7 | 4:165027128 | CTCAAGACACCCAAA[C/G]TGAGGATAGTATCAA | 166655 |
rs780483733 | snp | A/C | 1.65157e-05 | 0.0028736 | missense | TRIM60 | GRCh38.p7 | 4:165040911 | ATGGTTTCAGTCTTC[A/C]TCCTCAATATTCTGG | 166655 |
rs780526481 | snp | A/G | 4.25885e-05 | 0.00461437 | utr-variant-3-prime | TRIM60 | GRCh38.p7 | 4:165041520 | TCTGTTTCAGTTTTT[A/G]TAGGTAACTTAGCCA | 166655 |
rs780573718 | snp | C/T | 1.64817e-05 | 0.00287064 | missense | TRIM60 | GRCh38.p7 | 4:165041019 | CTGAGGATAGAAAAG[C/T]TGTGCGATATGAAAG | 166655 |
rs780640325 | in-del | -/AATT | | | upstream-variant-2KB | TRIM60 | GRCh38.p7 | 4:165031060 | CTAAAAAATAGAAAA[-/AATT]AGCTGGGCGTGGTGT | 166655 |
rs780678846 | snp | C/T | | | intron-variant | TRIM60 | GRCh38.p7 | 4:165035094 | TTTTTTTGAGGTATC[C/T]CTCTCTGTCACCCAG | 166655 |
rs780681540 | snp | A/T | 1.6617e-05 | 0.00288239 | missense | TRIM60 | GRCh38.p7 | 4:165040692 | TTAGGCAGATACAAG[A/T]TGAAGAGATGAACAT | 166655 |
rs780804486 | snp | A/G | | | intron-variant | TRIM60 | GRCh38.p7 | 4:165034730 | TTATGATTGAAAAAT[A/G]TTATAATTTTTAAGA | 166655 |
rs780972538 | snp | A/G | 3.29484e-05 | 0.00405871 | missense | TRIM60 | GRCh38.p7 | 4:165040164 | CAGTGACCATCAACT[A/G]TGGGCACAACTTCTG | 166655 |
rs781054453 | snp | A/T | | | | | GRCh38.p7 | 4:165028632 | GCAACCCCAAATTTA[A/T]TAATAGATTTAGGCA | 166655 |
rs781170081 | snp | A/C | 1.64909e-05 | 0.00287144 | missense | TRIM60 | GRCh38.p7 | 4:165041358 | GTGATCTTTCCTTTT[A/C]TAATATGAATGATAG | 166655 |
rs781196343 | snp | A/G | | | | | GRCh38.p7 | 4:165024620 | GAGTTCACCACCACA[A/G]TTGTCTTGGAAACTT | 166655 |
rs781259882 | snp | C/G | 9.8837e-05 | 0.00702914 | synonymous-codon | TRIM60 | GRCh38.p7 | 4:165040228 | AGATGATACCTTTCC[C/G]TGTCCTGTCTGCCGT | 166655 |
rs781278256 | snp | C/T | | | intron-variant | TRIM60 | GRCh38.p7 | 4:165037970 | CCAGTCTATCTCATT[C/T]ACCAGCTAAGGCCAA | 166655 |
rs781285876 | in-del | -/ACA | 1.65311e-05 | 0.00287494 | cds-indel | TRIM60 | GRCh38.p7 | 4:165040898 | GATTAACAAAATATG[-/ACA]GTTTCAGTCTTCCTC | 166655 |
rs781583585 | snp | C/T | | | | | GRCh38.p7 | 4:165026967 | AGGCTGCAAAGGCCA[C/T]TGTGCCATGAGAGTT | 166655 |
rs781753402 | snp | C/T | | | intron-variant | TRIM60 | GRCh38.p7 | 4:165033286 | TGAGAGTAGGGAATC[C/T]ACTGCAGGTTTGATT | 166655 |
rs796085450 | snp | A/G | | | intron-variant | TRIM60 | GRCh38.p7 | 4:165039295 | ATATAATCCTAGAGT[A/G]AAATTTTGAGAATGT | 166655 |
rs796127120 | snp | G/T | | | intron-variant | TRIM60 | GRCh38.p7 | 4:165038667 | AAAAAAAAGCCTGCT[G/T]TTTTTCCCAGCACTG | 166655 |
rs796231000 | in-del | -/T | | | intron-variant | TRIM60 | GRCh38.p7 | 4:165034157 | TTAAATGAAATACAC[-/T]TTTTTTTTTTTTTTA | 166655 |
rs796373110 | snp | A/G | | | intron-variant | TRIM60 | GRCh38.p7 | 4:165036580 | AGAAGAAAAGATGGT[A/G]TGCTTAGGCCGGGCG | 166655 |
rs796684921 | snp | C/T | | | | | GRCh38.p7 | 4:165024955 | AGCTAGGATGGTCTC[C/T]ATCTCTGACCTCATG | 166655 |
rs796992020 | in-del | AA/TAC | | | | | GRCh38.p7 | 4:165028100 | GTCTCTACTAAAAAT[AA/TAC]AAAAAAAAAAGACAA | 166655 |