| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs779262624 | snp | C/T | | | intron-variant | TRIM59 | GRCh38.p7 | 3:160441256 | TATAAGGGCAGGAAT[C/T]GTGTCTAAACAATGG | 286827 |
| rs779270292 | snp | A/G | | | downstream-variant-500B | SMC4, TRIM59 | GRCh38.p7 | 3:160435314 | TTGCCATGTTGGCCA[A/G]GCTGGTCTCAAACTC | 286827 |
| rs779357981 | in-del | -/C | | | upstream-variant-2KB | TRIM59 | GRCh38.p7 | 3:160451134 | ATTCCTCCCAAGGCT[-/C]GGAATAAAGTTCCAA | 286827 |
| rs779629743 | snp | C/T | 1.65321e-05 | 0.00287502 | missense | TRIM59 | GRCh38.p7 | 3:160438450 | AATTTAAGTGGAGAC[C/T]CTTCTTGTAAAGATA | 286827 |
| rs779778804 | snp | C/T | 7.13891e-05 | 0.00597406 | missense | TRIM59 | GRCh38.p7 | 3:160438019 | TCAACAAATAGAAAA[C/T]GTGACACAGTATATT | 286827 |
| rs780054570 | in-del | -/C | 1.80439e-05 | 0.0030036 | frameshift-variant | TRIM59 | GRCh38.p7 | 3:160439094 | TCCAAACAATTTCTA[-/C]CAAAATGTATGAGAG | 286827 |
| rs780094886 | snp | A/C | 1.6476e-05 | 0.00287014 | missense | TRIM59 | GRCh38.p7 | 3:160438738 | TCAGTCAACTGTTCA[A/C]GCAGTTTTTGAGGAG | 286827 |
| rs780099101 | snp | A/C | 1.81949e-05 | 0.00301614 | missense | TRIM59 | GRCh38.p7 | 3:160439129 | GCAGTACACGAGGAT[A/C]TTCAAAAATACTATA | 286827 |
| rs780104727 | snp | A/T | | | intron-variant | TRIM59 | GRCh38.p7 | 3:160442026 | AGAAAAACAAATGTG[A/T]TTTTCAGAGTATTTC | 286827 |
| rs780117475 | snp | C/G | | | upstream-variant-2KB | TRIM59 | GRCh38.p7 | 3:160450713 | TCAGCTTTATCTCAA[C/G]ACATCACCGCTTCCC | 286827 |
| rs780152672 | snp | C/T | 0.00016621 | 0.00911467 | splice-acceptor-variant | TRIM59 | GRCh38.p7 | 3:160448797 | CTTTTATTCTTATTC[C/T]AAAATTAAAATAATG | 286827 |
| rs780205071 | snp | G/T | | | upstream-variant-2KB | TRIM59 | GRCh38.p7 | 3:160449918 | CAAGGCATCGGCCAA[G/T]GGGAACTATTGCTGG | 286827 |
| rs780333273 | snp | A/G | 3.29554e-05 | 0.00405914 | synonymous-codon | TRIM59 | GRCh38.p7 | 3:160438827 | ACCTATGGTAAGGCA[A/G]TGACCACAAACTAAT | 286827 |
| rs780378470 | snp | C/T | | | intron-variant | TRIM59 | GRCh38.p7 | 3:160440904 | ACAAGAGCGAAACTC[C/T]GTCTCAAAAAAAATA | 286827 |
| rs780423842 | snp | C/T | | | intron-variant | TRIM59 | GRCh38.p7 | 3:160447678 | TCTAAACATGAACAG[C/T]TGTAAAACGTTCATT | 286827 |
| rs780825484 | in-del | -/TCTTTGTTGATCTCGTGGTTTGGGGGCTGAATACACTCTTC | 1.86555e-05 | 0.00305408 | utr-variant-5-prime | TRIM59 | GRCh38.p7 | 3:160439184 | TCAAAATTGTGCATT[lengthTooLong]TCCTGTCAAGAGAAA | 286827 |
| rs780886275 | snp | A/G | 0.000160552 | 0.00895826 | intron-variant | TRIM59 | GRCh38.p7 | 3:160449661 | GACTGTGCTACAGGA[A/G]AAGAAAAAGGACTCA | 286827 |
| rs781169587 | snp | C/T | | | intron-variant | TRIM59 | GRCh38.p7 | 3:160448381 | TACATGAATGCATAG[C/T]GAAAAAGTATCCAGG | 286827 |
| rs781222206 | snp | A/G | 1.71041e-05 | 0.00292434 | synonymous-codon | TRIM59 | GRCh38.p7 | 3:160438044 | TATATTCTTTACCTT[A/G]TGCAGACTGTTAGAT | 286827 |
| rs781295047 | snp | A/C | 1.66765e-05 | 0.00288756 | missense | TRIM59 | GRCh38.p7 | 3:160438196 | CTACAACAATGTTTA[A/C]AATTTTTAAAAATTC | 286827 |
| rs781355477 | snp | A/G | 1.64988e-05 | 0.00287213 | missense | TRIM59 | GRCh38.p7 | 3:160438975 | ACAGGTAAAGATTCA[A/G]TGCCAGTTGGAGCAA | 286827 |
| rs781369671 | snp | C/T | | | missense | TRIM59 | GRCh38.p7 | 3:160438832 | TGGTAAGGCAATGAC[C/T]ACAAACTAATTTTTT | 286827 |
| rs781405258 | snp | C/T | | | missense | TRIM59 | GRCh38.p7 | 3:160438904 | CAGGGCAGGTGACAA[C/T]ATCTGGATGGTCTTC | 286827 |
| rs781442999 | snp | C/T | | | utr-variant-3-prime | TRIM59 | GRCh38.p7 | 3:160436729 | TGTGAACCCGGGAGG[C/T]GGGGCTTGCAATGAG | 286827 |
| rs781560403 | snp | A/C | 3.30595e-05 | 0.00406554 | missense | TRIM59 | GRCh38.p7 | 3:160438460 | GAGACTCTTCTTGTA[A/C]AGATATTGTCAGTGC | 286827 |
| rs781605237 | snp | A/G | | | intron-variant | TRIM59 | GRCh38.p7 | 3:160445974 | TTAACACACATGCCT[A/G]ATGTTTTTATGCTTT | 286827 |
| rs781652228 | snp | G/T | 1.65762e-05 | 0.00287886 | missense | TRIM59 | GRCh38.p7 | 3:160438550 | CTTGATTAATTAGAT[G/T]GCCAACATCACAGAG | 286827 |
| rs796291674 | multinucleotide-polymorphism | CT/GA | | | utr-variant-3-prime | TRIM59 | GRCh38.p7 | 3:160435585 | TTTACATACATCAAC[CT/GA]TTGCAATCTTCCTGC | 286827 |
| rs796341469 | snp | C/T | | | intron-variant | TRIM59 | GRCh38.p7 | 3:160443041 | GGAGGATCACTTGAG[C/T]CCAAGAAGTTGAGGC | 286827 |
| rs796396681 | in-del | -/AG | | | intron-variant | TRIM59 | GRCh38.p7 | 3:160443662 | TTTTTTTTTTGAAAC[-/AG]AGTCTCGCTCTGTCG | 286827 |
| rs796471427 | snp | C/T | | | utr-variant-3-prime | TRIM59 | GRCh38.p7 | 3:160437268 | CAGAGGCGGGAGGAT[C/T]GATTGAGCCTGGGTG | 286827 |
| rs796734933 | snp | A/G | | | intron-variant | TRIM59 | GRCh38.p7 | 3:160441913 | AGTAAAGAAGATGAC[A/G]TTCACTGCAGATAAA | 286827 |
| rs796971812 | in-del | GT/TTCTCAGC | | | utr-variant-3-prime | TRIM59 | GRCh38.p7 | 3:160436194 | AGTGTTAAGACTTAT[GT/TTCTCAGC]GGTAAGAGTTTTAGA | 286827 |