SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs751198532 | snp | C/G | | | intron-variant, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25975684 | TTCTCTAGGTAGGGT[C/G]ATCTATATCTTTCCC | 10475 |
rs751365134 | snp | A/G | 6.61048e-05 | 0.00574874 | synonymous-codon, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25966768 | GGGAAGCCTCATTGA[A/G]GCCCTCAAAGAGACG | 10475 |
rs751491662 | snp | C/T | 1.64846e-05 | 0.0028709 | synonymous-codon, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25971952 | GGAAGAGAAGTCTTA[C/T]CTCTGGAGGCTGGAG | 10475 |
rs751581966 | snp | A/G | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25968669 | CAATTAGCAATTTGG[A/G]TCAGCTTCAAATCAC | 10475 |
rs751654734 | snp | C/T | 1.65165e-05 | 0.00287367 | missense, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25973241 | CTATGTGCAATGTTT[C/T]CAAGCTTTACTTCGA | 10475 |
rs751670571 | snp | C/T | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25971639 | TGGTCTTGCCAACAC[C/T]TTGTAACCACTATTT | 10475 |
rs751741401 | snp | A/T | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25981013 | AAAAGCTAACTGAAT[A/T]GAGTTTGAAAAAGGA | 10475 |
rs751761777 | snp | C/T | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25980035 | CTGTGTAATACAGAT[C/T]TATTGAAACTTGTTC | 10475 |
rs751810277 | snp | A/T | | | upstream-variant-2KB | TRIM38 | GRCh38.p7 | 6:25962534 | GTGGCAAAAGTAGAA[A/T]GATCTCAAATCAGAG | 10475 |
rs751872864 | in-del | -/CG | | | utr-variant-3-prime | TRIM38 | GRCh38.p7 | 6:25987211 | GTACTCCCCGCCCCC[-/CG]CGCCCGCCACACACC | 10475 |
rs751903226 | snp | A/G | 1.65422e-05 | 0.0028759 | missense, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25969409 | ACAGCAATGCGAATA[A/G]CTAAATGGAAAGTAA | 10475 |
rs751931905 | snp | A/G | | | upstream-variant-2KB | TRIM38 | GRCh38.p7 | 6:25961107 | TCCTCCCCTTTTTAG[A/G]CTATATAGGGTAGCT | 10475 |
rs751948008 | snp | C/G | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25972584 | AAGGCTGAGTGTATA[C/G]CATGATTGCTTTACC | 10475 |
rs751953044 | snp | A/T | 1.65622e-05 | 0.00287764 | intron-variant | TRIM38 | GRCh38.p7 | 6:25969310 | TAGGCTTCACTTATC[A/T]AATTTTTCCTTCAGG | 10475 |
rs752088663 | in-del | -/TGATTTACCCA | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25976990 | CCCTTCAGGCCTCTG[-/TGATTTACCCA]TGATTTACTGTGGTT | 10475 |
rs752125608 | snp | G/T | 1.64849e-05 | 0.00287092 | missense, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25971947 | CATGAGGAAGAGAAG[G/T]CTTATCTCTGGAGGC | 10475 |
rs752326019 | snp | C/G | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25964863 | TTCACCCAGGCTGGA[C/G]TGCAGTGGTGTAATC | 10475 |
rs752436872 | snp | G/T | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25964186 | CCTCTGCCAATGGGG[G/T]TAGATACTTATATAG | 10475 |
rs752474237 | snp | A/C | 8.25634e-05 | 0.00642455 | missense, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25966666 | CTTTAAAAACCCAAG[A/C]CAAAAGCAACTGAGG | 10475 |
rs752779658 | snp | A/G | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25970011 | CAATGTCCACCTCCC[A/G]GGTTCAAGCAATTCC | 10475 |
rs752805118 | snp | A/G | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25967820 | GAGGCATGAACCACT[A/G]TGCCCAGCTACTGTG | 10475 |
rs752981947 | snp | C/T | 1.65455e-05 | 0.00287619 | missense, downstream-variant-500B | TRIM38 | GRCh38.p7 | 6:25983608 | TTACTTTCCCGAAGG[C/T]TTCCTTCTCTGATAC | 10475 |
rs753001898 | snp | C/T | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25966965 | GGGAGCTTTGGTAAG[C/T]ACCAAGTCTTATCCT | 10475 |
rs753111105 | snp | G/T | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25963028 | CAGCTCTCACCTCTT[G/T]CCTGCTCTTTCTTTC | 10475 |
rs753131077 | snp | C/T | | | upstream-variant-2KB | TRIM38 | GRCh38.p7 | 6:25961822 | CCAAACTCCATGTTC[C/T]ATTGGCTATCAGGGT | 10475 |
rs753172554 | snp | A/C | 1.6477e-05 | 0.00287024 | missense, downstream-variant-500B | TRIM38 | GRCh38.p7 | 6:25983496 | TCTCCCCCAACTTCC[A/C]TTCATCTGCATGAGC | 10475 |
rs753288167 | snp | C/G | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25973879 | TGATTTTTTAAATCA[C/G]TGCTGACTATACTTT | 10475 |
rs753536986 | snp | C/T | | | utr-variant-3-prime | TRIM38 | GRCh38.p7 | 6:25985364 | CTAGAAACTCAAAGT[C/T]CTTTTCGTCTTCCTT | 10475 |
rs753625071 | snp | A/G | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25978594 | ATGGCTCCACCACCT[A/G]AGCTAAAGTGATCTT | 10475 |
rs753632464 | snp | A/C | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25979398 | GTAGTGATTTCATTT[A/C]TTTAATGTTAGGTCT | 10475 |
rs753646980 | snp | A/C/G | 0.000230796 | 0.01074 | missense, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25973175 | CTGCTTATTCTAGGA[A/C/G]TTGGGCTGTGAAGCT | 10475 |
rs753690512 | snp | A/G | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25966237 | TCTAAACAACCACTT[A/G]TAACTGCTTGCTAAT | 10475 |
rs753714052 | snp | A/G | | | intron-variant, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25975938 | CAAACTGGGATTGCC[A/G]AGGTTGTTGTTAATC | 10475 |
rs753743090 | snp | A/G | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25978386 | GATAGAGGATACTAT[A/G]TCTATATCTGTATCT | 10475 |
rs753769626 | snp | C/T | 1.75798e-05 | 0.00296472 | utr-variant-5-prime, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25966522 | CTTTTCAATAAAAGC[C/T]ATGGCCTCAACCACC | 10475 |
rs753972204 | snp | C/T | 8.27561e-05 | 0.00643205 | missense, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25966871 | TGCTGGCGCTGTGAG[C/T]GGGCACCACAGCACA | 10475 |
rs754120902 | snp | A/G | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25970133 | ATGTTGGCCAGGATG[A/G]TCTTGATCTCCTGAC | 10475 |
rs754224236 | snp | C/T | 1.64819e-05 | 0.00287066 | missense, downstream-variant-500B | TRIM38 | GRCh38.p7 | 6:25983313 | TTGGGTTGTGAAGGC[C/T]TCACCTCAGGAAGAC | 10475 |
rs754247504 | snp | C/T | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25982676 | TCTCTGCAACAAATA[C/T]GGTAATTTCCACTTT | 10475 |
rs754344997 | snp | C/T | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25964464 | CTTGTAAATGGTTCT[C/T]TTTGGAAAATGAATG | 10475 |
rs754349053 | snp | A/G | 1.64768e-05 | 0.00287021 | missense, downstream-variant-500B | TRIM38 | GRCh38.p7 | 6:25983490 | CTTACTTCTCCCCCA[A/G]CTTCCCTTCATCTGC | 10475 |
rs754386890 | in-del | -/AAAAAT | 1.65112e-05 | 0.00287321 | cds-indel, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25971892 | ACAGATTCAGAGACA[-/AAAAAT]CCGGTCTGACTTTAA | 10475 |
rs754447717 | snp | A/G | 0.000115669 | 0.00760402 | splice-acceptor-variant | TRIM38 | GRCh38.p7 | 6:25969324 | CAAATTTTTCCTTCA[A/G]GAAAAGCTCCAGAAA | 10475 |
rs754488252 | snp | A/G | | | upstream-variant-2KB | TRIM38 | GRCh38.p7 | 6:25960878 | TCCTTGCCTTCTGCT[A/G]TGGTTGTGAGGTCTC | 10475 |
rs754640210 | snp | A/G | 1.7156e-05 | 0.00292878 | intron-variant | TRIM38 | GRCh38.p7 | 6:25969451 | CATTGATCTCAAGCT[A/G]TTTTCCATTCTAGAG | 10475 |
rs754657005 | snp | A/C | | | intron-variant, downstream-variant-500B | TRIM38 | GRCh38.p7 | 6:25976844 | ACTCCTCCAAAACTC[A/C]CTGAGTCTTTACTTA | 10475 |
rs754853168 | snp | A/G | 1.72293e-05 | 0.00293503 | missense, downstream-variant-500B | TRIM38 | GRCh38.p7 | 6:25983650 | ATTTCCAGGTTTATC[A/G]ATATTCTCCTTTGTT | 10475 |
rs754894308 | snp | A/G | 1.75314e-05 | 0.00296064 | missense, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25966523 | TTTTCAATAAAAGCT[A/G]TGGCCTCAACCACCA | 10475 |
rs754962404 | snp | A/G | | | downstream-variant-500B, utr-variant-3-prime | TRIM38 | GRCh38.p7 | 6:25987639 | TGTCCCCCCACCATA[A/G]ACATCCAGCACCACA | 10475 |
rs754985805 | snp | C/T | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25973882 | TTTTTTAAATCAGTG[C/T]TGACTATACTTTCAC | 10475 |
rs754989203 | in-del | -/C | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25967551 | TTTTTTTTTTTTTTT[-/C]CTGAGGTAGGGTCTT | 10475 |
rs755063259 | snp | G/T | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25968760 | AAATCATTTTAAATT[G/T]GATTCATGATACCAT | 10475 |
rs755161078 | snp | A/G | 1.64754e-05 | 0.00287009 | intron-variant | TRIM38 | GRCh38.p7 | 6:25972125 | GTACTTGGAGTAGGG[A/G]AAAAAGGTATGTTAT | 10475 |
rs755182681 | snp | A/G | 1.64909e-05 | 0.00287144 | intron-variant | TRIM38 | GRCh38.p7 | 6:25973081 | ACTTTGAGCAGGTAA[A/G]TCCTGTTTGAATGCA | 10475 |
rs755198507 | snp | C/T | | | utr-variant-3-prime | TRIM38 | GRCh38.p7 | 6:25986779 | GGAAACTCCAGAAAA[C/T]CACAGATTCCTTCCA | 10475 |
rs755198908 | snp | A/G | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25981092 | CACCCAGAACTAGGA[A/G]CAGTTAGAGAGCCAT | 10475 |
rs755224786 | snp | G/T | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25967357 | CCATCAAAAATGTCT[G/T]CCTGGAGGTCCCTGG | 10475 |
rs755260932 | snp | C/G | 1.6483e-05 | 0.00287076 | missense, downstream-variant-500B | TRIM38 | GRCh38.p7 | 6:25983322 | GAAGGCTTCACCTCA[C/G]GAAGACGTTACTTTG | 10475 |
rs755312585 | snp | G/T | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25980170 | ATGTATTGACTATGA[G/T]ATTGCGCTTCTTAGA | 10475 |
rs755377608 | in-del | -/GG | 1.86426e-05 | 0.00305303 | intron-variant | TRIM38 | GRCh38.p7 | 6:25972133 | GTAGGGAAAAAAGGT[-/GG]ATGTTATAGTGCTAT | 10475 |
rs755460617 | in-del | -/G | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25975416 | AATGTTGGCCAGGCT[-/G]GTCTCAAACCCCTGA | 10475 |
rs755520782 | snp | C/T | 1.64768e-05 | 0.00287021 | missense, downstream-variant-500B | TRIM38 | GRCh38.p7 | 6:25983491 | TTACTTCTCCCCCAA[C/T]TTCCCTTCATCTGCA | 10475 |
rs755525397 | snp | C/T | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25971414 | TGTCCCAGTGGCTGA[C/T]TGTGTGTGTGTGTGT | 10475 |
rs755536630 | snp | A/G | 1.65559e-05 | 0.00287709 | missense, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25966872 | GCTGGCGCTGTGAGC[A/G]GGCACCACAGCACAA | 10475 |
rs755578148 | snp | A/G | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25972617 | TGTGTGATACCTGCT[A/G]CCACCATCTTAGTGG | 10475 |
rs755578856 | snp | A/T | 1.6477e-05 | 0.00287024 | missense, downstream-variant-500B | TRIM38 | GRCh38.p7 | 6:25983509 | CCCTTCATCTGCATG[A/T]GCAGCCCCTGCTTGT | 10475 |
rs755754975 | snp | A/T | 1.65485e-05 | 0.00287645 | intron-variant | TRIM38 | GRCh38.p7 | 6:25969317 | CACTTATCAAATTTT[A/T]CCTTCAGGAAAAGCT | 10475 |
rs755769073 | snp | C/T | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25966125 | TCCCGAGATTTGTAA[C/T]ACAAAGAACAATGTA | 10475 |
rs755932234 | snp | A/G/T | 9.89551e-05 | 0.0070334 | intron-variant | TRIM38 | GRCh38.p7 | 6:25973114 | AGGGGAGGGGTGTGC[A/G/T]TATATAGAAATGAAT | 10475 |
rs756017126 | snp | C/G | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25977299 | AGGAGGATCTCCTGA[C/G]CCCAGGAGTTCGAGG | 10475 |
rs756021914 | snp | G/T | 6.60491e-05 | 0.00574632 | intron-variant | TRIM38 | GRCh38.p7 | 6:25973051 | CTTTTTGTTTCTTTA[G/T]AGAATGTGAATGACA | 10475 |
rs756190343 | snp | G/T | 1.65231e-05 | 0.00287424 | synonymous-codon, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25966783 | AGCCCTCAAAGAGAC[G/T]GATCAAGAAATGTCA | 10475 |
rs756338561 | snp | A/G | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25970093 | TGGCTAATTTTTTGT[A/G]TTTTAGTAGAGACGG | 10475 |
rs756376320 | snp | C/G | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25981316 | GCCTGGTTAATCTGT[C/G]CATGTCAGCCTTCCT | 10475 |
rs756468366 | in-del | -/G | 1.66324e-05 | 0.00288374 | splice-donor-variant | TRIM38 | GRCh38.p7 | 6:25969420 | ATAACTAAATGGAAA[-/G]GTAAGAATCTGACTT | 10475 |
rs756633394 | snp | A/T | 1.65214e-05 | 0.0028741 | stop-gained, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25966699 | GGAGACATTCTGCTG[A/T]CCCCAGTGTCGGGCT | 10475 |
rs756696007 | snp | C/G | 1.74439e-05 | 0.00295325 | missense, utr-variant-3-prime, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25983184 | GTGACTCTGGATCCA[C/G]ATACAGCTCATCACG | 10475 |
rs756845686 | snp | A/T | 3.29538e-05 | 0.00405904 | missense, downstream-variant-500B | TRIM38 | GRCh38.p7 | 6:25983501 | CCCAACTTCCCTTCA[A/T]CTGCATGAGCAGCCC | 10475 |
rs756936805 | snp | C/T | 3.29739e-05 | 0.00406028 | synonymous-codon, downstream-variant-500B | TRIM38 | GRCh38.p7 | 6:25983360 | TGTTGGCGAAGGAAC[C/T]GGATGGGATTTAGGA | 10475 |
rs756941173 | snp | A/G | | | utr-variant-3-prime | TRIM38 | GRCh38.p7 | 6:25986685 | CAGTGGCTGAAACAA[A/G]TTTATTTATCTCCCA | 10475 |
rs757008571 | in-del | -/TTTG | 1.85057e-05 | 0.00304179 | intron-variant | TRIM38 | GRCh38.p7 | 6:25983138 | AGCAACAAAATTATT[-/TTTG]TTTGTTTTGTTTTGT | 10475 |
rs757029199 | snp | A/G | | | utr-variant-3-prime | TRIM38 | GRCh38.p7 | 6:25985420 | TTAAAATGCTATATA[A/G]GCCCAAGTTCTAAAT | 10475 |
rs757164858 | snp | G/T | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25966249 | CTTGTAACTGCTTGC[G/T]AATGAGGGCAACTTG | 10475 |
rs757253578 | snp | C/G | 1.65767e-05 | 0.00287891 | missense, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25972085 | TGTCAGGGCTCAGCC[C/G]AGAAATTGCTGCAGG | 10475 |
rs757271754 | snp | A/T | 1.64806e-05 | 0.00287054 | missense, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25971959 | AAGTCTTATCTCTGG[A/T]GGCTGGAGAAAGAAG | 10475 |
rs757567958 | snp | C/G | 3.29538e-05 | 0.00405904 | synonymous-codon, downstream-variant-500B | TRIM38 | GRCh38.p7 | 6:25983516 | TCTGCATGAGCAGCC[C/G]CTGCTTGTGGGAATT | 10475 |
rs757765424 | snp | C/T | 1.65567e-05 | 0.00287716 | synonymous-codon, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25973254 | TTCCAAGCTTTACTT[C/T]GATGTGAAGAAAATG | 10475 |
rs757952732 | snp | A/G | | | utr-variant-5-prime, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25963278 | AGAGGAAAACAGCCT[A/G]CCCGGTAATTGTAGT | 10475 |
rs757961451 | snp | C/T | | | intron-variant, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25975652 | TCAAGGTTTTTCCCA[C/T]CCGTCTCCAATCTGA | 10475 |
rs758236250 | snp | C/G | 1.65146e-05 | 0.0028735 | missense, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25966667 | TTTAAAAACCCAAGC[C/G]AAAAGCAACTGAGGC | 10475 |
rs758255628 | snp | A/G | 8.64431e-05 | 0.00657374 | intron-variant | TRIM38 | GRCh38.p7 | 6:25969458 | CTCAAGCTATTTTCC[A/G]TTCTAGAGCTTAGGC | 10475 |
rs758269854 | snp | C/T | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25967299 | AACAGGGAAGAAAGA[C/T]CCATCACCTTTTAGG | 10475 |
rs758339782 | snp | C/T | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25968356 | ATTGAGTTTTGTCAC[C/T]TACTAGATGGGCAAT | 10475 |
rs758432703 | snp | C/G | 1.64898e-05 | 0.00287135 | intron-variant | TRIM38 | GRCh38.p7 | 6:25973112 | GGAGGGGAGGGGTGT[C/G]CGTATATAGAAATGA | 10475 |
rs758498918 | snp | C/T | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25979950 | GTTTACATTTCCTAA[C/T]ATTTAGAATCTTTTT | 10475 |
rs758613786 | snp | A/G | 5.07644e-05 | 0.00503782 | missense, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25966538 | ATGGCCTCAACCACC[A/G]GCACCAAGAAGATGA | 10475 |
rs758632326 | snp | A/G | 1.65021e-05 | 0.00287241 | missense, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25973232 | AACTTCATACTATGT[A/G]CAATGTTTCCAAGCT | 10475 |
rs758683066 | snp | A/G | | | upstream-variant-2KB | TRIM38 | GRCh38.p7 | 6:25960985 | CAGCAGTGTGAAAAT[A/G]GACTAATACAGATAC | 10475 |
rs758718241 | snp | A/C | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25972460 | GATTTGCTTGTAGAA[A/C]CCTTGCTCCAGAGCT | 10475 |
rs758727754 | snp | C/T | 1.69686e-05 | 0.00291273 | missense, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25966908 | ACACCACAGCTCTTG[C/T]TGAAGACGTATGCCA | 10475 |
rs758770690 | snp | A/G | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25982377 | CACCTGTTTACCCTC[A/G]CGTCCTCACCACCTG | 10475 |
rs758877306 | snp | C/T | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25971161 | ATAAGTAAAAACCTC[C/T]TTTTATCCTTGTAAC | 10475 |
rs759025551 | snp | C/T | 1.65261e-05 | 0.0028745 | missense, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25966725 | GGGCTCCATTTCATA[C/T]GGATAGCCTCCGACC | 10475 |
rs759107235 | snp | G/T | 1.64972e-05 | 0.00287199 | missense, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25971909 | AAATCCGGTCTGACT[G/T]TAAGAATCTCCAGTG | 10475 |
rs759171616 | snp | C/T | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25978062 | ATATATATAGTATTC[C/T]CTCCCAGTGTCTTCA | 10475 |
rs759337307 | in-del | -/ACAA | | | downstream-variant-500B, utr-variant-3-prime | TRIM38 | GRCh38.p7 | 6:25987586 | TGCATTGTGGGAAAC[-/ACAA]ACATTTACTTCAACT | 10475 |
rs759425299 | in-del | -/C | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25975034 | TTTCTTTCTTTCTTT[-/C]CTTTTTTTTTTTTTT | 10475 |
rs759490048 | snp | C/T | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25982420 | ATCACCAATAAATAG[C/T]GTGGGCTCCCAGAGC | 10475 |
rs759490613 | snp | C/T | 1.85345e-05 | 0.00304416 | intron-variant | TRIM38 | GRCh38.p7 | 6:25983134 | TCACAGCAACAAAAT[C/T]ATTTTTGTTTGTTTT | 10475 |
rs759535896 | snp | A/G | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25970865 | ACTGCATTAATTTAG[A/G]CAGCACTAATGGAAA | 10475 |
rs759710401 | snp | A/G | 1.87016e-05 | 0.00305785 | utr-variant-3-prime, downstream-variant-500B | TRIM38 | GRCh38.p7 | 6:25983721 | CTTGGTTTAACCAGC[A/G]CAGAGAAAATAATAT | 10475 |
rs760152419 | snp | A/G | 1.77893e-05 | 0.00298234 | intron-variant | TRIM38 | GRCh38.p7 | 6:25973312 | AAAGAATTCCTGAAT[A/G]CTGTGGATAGAAGGG | 10475 |
rs760188434 | snp | G/T | | | utr-variant-3-prime | TRIM38 | GRCh38.p7 | 6:25986236 | ATGAAATTCAGACAC[G/T]TACAGAGCAGCCAGG | 10475 |
rs760306216 | snp | A/C | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25980638 | GTTGGGCAGGCTGGT[A/C]TTGAACTCCTGGCTT | 10475 |
rs760308094 | snp | C/G | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25966987 | TCTTATCCTGCTCCC[C/G]AGGAGCTGAGATGAT | 10475 |
rs760313257 | snp | A/G | 1.79358e-05 | 0.00299459 | utr-variant-5-prime, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25966516 | TTGGAGCTTTTCAAT[A/G]AAAGCTATGGCCTCA | 10475 |
rs760326581 | snp | C/T | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25979354 | CTTGATAAAGATGCA[C/T]GTTTTATTATCTGTC | 10475 |
rs760436169 | snp | C/T | 1.65023e-05 | 0.00287244 | synonymous-codon, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25966615 | AGTAAGCATCAACTG[C/T]GGACACAGCTACTGC | 10475 |
rs760453317 | in-del | -/TG | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25965200 | TTTTGTGAGGAAGCC[-/TG]CATTGCTTCTCCCAG | 10475 |
rs760527795 | snp | A/G | | | intron-variant, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25975888 | TCCATGCATCCTTAT[A/G]TCCTGGTGCTTTCAT | 10475 |
rs760674633 | snp | A/G | 1.66192e-05 | 0.00288259 | synonymous-codon, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25972090 | GGGCTCAGCCCAGAA[A/G]TTGCTGCAGGTGAGG | 10475 |
rs760879360 | snp | C/T | 9.88582e-05 | 0.00702989 | missense, downstream-variant-500B | TRIM38 | GRCh38.p7 | 6:25983484 | GTAGCACTTACTTCT[C/T]CCCCAACTTCCCTTC | 10475 |
rs760914309 | snp | C/T | 5.45113e-05 | 0.00522041 | intron-variant | TRIM38 | GRCh38.p7 | 6:25966961 | GCCCGGGAGCTTTGG[C/T]AAGTACCAAGTCTTA | 10475 |
rs760936843 | snp | G/T | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25978443 | ATATCTAATAAGATG[G/T]AATCTATATTATATA | 10475 |
rs760981124 | snp | C/T | 0.0001157 | 0.00760503 | missense, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25966862 | CAGCTCATCTGCTGG[C/T]GCTGTGAGCGGGCAC | 10475 |
rs761002626 | snp | C/T | 0.000115431 | 0.00759618 | synonymous-codon, downstream-variant-500B | TRIM38 | GRCh38.p7 | 6:25983576 | CTTTTATAACGGGAA[C/T]ACTGGCTGCCACATC | 10475 |
rs761160098 | snp | C/T | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25964305 | AATATGTATGTATAA[C/T]GTTTATACATGTATA | 10475 |
rs761268422 | snp | C/G | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25975413 | CACAATGTTGGCCAG[C/G]CTGGTCTCAAACCCC | 10475 |
rs761384233 | snp | A/T | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25968036 | ATTAAGGAAGGTGGG[A/T]CTTTGCTGTTGGCAG | 10475 |
rs761564484 | snp | A/G | 6.59946e-05 | 0.00574395 | missense, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25966838 | CACCTGTTCTGCGAA[A/G]ACGAGGGGCAGCTCA | 10475 |
rs761583136 | snp | C/T | 1.64931e-05 | 0.00287163 | intron-variant | TRIM38 | GRCh38.p7 | 6:25973154 | CTCTGAAGAAATCTC[C/T]CGCCTCTGCTTATTC | 10475 |
rs761702049 | snp | A/G | | | utr-variant-3-prime | TRIM38 | GRCh38.p7 | 6:25985970 | TAAGGAAGGCCAGAA[A/G]AAATATAAAATTGGA | 10475 |
rs761862433 | snp | C/T | | | upstream-variant-2KB | TRIM38 | GRCh38.p7 | 6:25961581 | TTCTTTCTCCTCTCT[C/T]TGTGTGCTGGTTGCC | 10475 |
rs761916936 | snp | A/G | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25973459 | TCAGTGAATGTGATG[A/G]GCATTGCATTCTGGT | 10475 |
rs762006693 | snp | A/G | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25972163 | TTAAAGGAGAATGGT[A/G]AGGAAGCATGGGAAG | 10475 |
rs762006709 | snp | A/G | | | utr-variant-3-prime | TRIM38 | GRCh38.p7 | 6:25985889 | GCTGAATAAGAAAGA[A/G]TGATAATAAAATAAA | 10475 |
rs762023081 | snp | A/G | | | utr-variant-3-prime | TRIM38 | GRCh38.p7 | 6:25984736 | ATACAAAAATTAGCC[A/G]GGCATGGTGGTAGGG | 10475 |
rs762043452 | in-del | -/TCCC | 1.65214e-05 | 0.0028741 | frameshift-variant, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25966698 | GGAGACATTCTGCTG[-/TCCC]TCCCCAGTGTCGGGC | 10475 |
rs762159536 | in-del | -/CTAA | | | downstream-variant-500B, utr-variant-3-prime | TRIM38 | GRCh38.p7 | 6:25987507 | GGATCTCAACTAAAC[-/CTAA]CTATCACCCAAAGAG | 10475 |
rs762209733 | snp | C/T | 1.66629e-05 | 0.00288638 | splice-donor-variant | TRIM38 | GRCh38.p7 | 6:25969422 | TAACTAAATGGAAAG[C/T]AAGAATCTGACTTCA | 10475 |
rs762242457 | snp | A/G | 1.64803e-05 | 0.00287052 | synonymous-codon, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25972009 | ACTGAGGGACTATGA[A/G]GCTGGTCTGGGGCTG | 10475 |
rs762249473 | snp | A/G | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25964833 | TTTTTTTTTTTTAAG[A/G]CAGATTCTCGCTCTT | 10475 |
rs762421013 | snp | A/G | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25964584 | ATAGGGGTTGGAAGG[A/G]AAAACAATTGTTCTT | 10475 |
rs762480958 | snp | C/T | | | intron-variant, downstream-variant-500B | TRIM38 | GRCh38.p7 | 6:25976566 | ATGAACCACCATCTC[C/T]GGCCTGAAGTTTATT | 10475 |
rs762533292 | snp | A/G | 1.64974e-05 | 0.00287201 | missense, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25972065 | TCCTGGAACTGGAGG[A/G]AAAATGTCAGGGCTC | 10475 |
rs762566365 | snp | G/T | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25968614 | GAGTATACTTGTTGG[G/T]TTTACAGAGGACAGG | 10475 |
rs762597398 | snp | A/G | 1.65999e-05 | 0.00288091 | intron-variant | TRIM38 | GRCh38.p7 | 6:25973014 | GCCCCATGAAATACC[A/G]ATGTTCCCATGCTCA | 10475 |
rs762657990 | snp | A/C/G | 3.92426e-05 | 0.00442942 | utr-variant-5-prime, intron-variant, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25966479 | AATTCTGGCTGCTTC[A/C/G]TCTCCATCTCTAGAG | 10475 |
rs762741075 | in-del | -/GATGATG | 1.67396e-05 | 0.00289301 | frameshift-variant, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25966549 | CACCAGCACCAAGAA[-/GATGATG]GAGGAAGCCACCTGC | 10475 |
rs762815765 | snp | A/G | 1.64991e-05 | 0.00287215 | synonymous-codon, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25966828 | AGAGCAGTTCCACCT[A/G]TTCTGCGAAGACGAG | 10475 |
rs762964839 | snp | C/T | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25982164 | GTGGCTTGGATGGAA[C/T]CCAGGGCTCAGGGCA | 10475 |
rs763049224 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB | TRIM38 | GRCh38.p7 | 6:25962704 | CTTTACCGGAGAGGC[A/G]GAGTGCAAATGATAT | 10475 |
rs763147386 | snp | A/G | 1.65531e-05 | 0.00287686 | synonymous-codon, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25971874 | TTGACTCCAGGAGAA[A/G]GTACAGATTCAGAGA | 10475 |
rs763170503 | snp | C/T | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25973634 | ACAAAGTGCTTAGCC[C/T]TGTGACTGACACATG | 10475 |
rs763330856 | snp | A/G | | | utr-variant-3-prime | TRIM38 | GRCh38.p7 | 6:25986030 | AAGAATATAAGTCCT[A/G]CTAGATAAATCATTA | 10475 |
rs763343803 | snp | C/G | | | utr-variant-3-prime | TRIM38 | GRCh38.p7 | 6:25984905 | TCACCTCTGAGAATA[C/G]GAGAAATGAAGCAAC | 10475 |
rs763785013 | snp | G/T | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25967111 | CTAGACTGTCCATCC[G/T]GACCTTCAATGGGAT | 10475 |
rs763810951 | snp | C/T | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25978200 | GGCTGAGTGGTGCAG[C/T]AGTGCGATTATGGCT | 10475 |
rs763904436 | snp | A/G | 1.65888e-05 | 0.00287996 | intron-variant | TRIM38 | GRCh38.p7 | 6:25973017 | CCATGAAATACCGAT[A/G]TTCCCATGCTCACCT | 10475 |
rs763933929 | snp | C/T | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25983096 | CATCTCAAAATAAAA[C/T]AAAATAAAATAACCT | 10475 |
rs763944825 | snp | A/G | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25979374 | TATTATCTGTCGGTA[A/G]AATTTAAAGTAGTGA | 10475 |
rs763952404 | snp | A/G | | | upstream-variant-2KB | TRIM38 | GRCh38.p7 | 6:25960781 | GTCAATAAGTTTCAT[A/G]AGACCTGATGGTTTT | 10475 |
rs764106738 | snp | A/C | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25981522 | CCATTTTTTATTTTT[A/C]AAACTGCATACTGTT | 10475 |
rs764238225 | in-del | -/T | 3.31082e-05 | 0.00406854 | frameshift-variant, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25966570 | GAGGAAGCCACCTGC[-/T]TCCATCTGCCTGAGC | 10475 |
rs764267831 | snp | G/T | 0.000346772 | 0.013163 | missense, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25966672 | AAACCCAAGCCAAAA[G/T]CAACTGAGGCAGGAG | 10475 |
rs764277576 | snp | A/G | 1.81421e-05 | 0.00301176 | intron-variant | TRIM38 | GRCh38.p7 | 6:25983155 | TGTTTGTTTTGTTTT[A/G]TTTTGCAGTTAGTGT | 10475 |
rs764431379 | snp | C/T | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25982566 | GGTGTTGGGCCTGAT[C/T]ACCCCAACAACTACC | 10475 |
rs764470286 | snp | A/G | 3.33756e-05 | 0.00408493 | missense, downstream-variant-500B | TRIM38 | GRCh38.p7 | 6:25983622 | GCTTCCTTCTCTGAT[A/G]CTCTCCGGCCCTATT | 10475 |
rs764581461 | snp | A/G | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25964328 | CATGTATACATATTT[A/G]TTTCAGAGGGGAAGG | 10475 |
rs764722089 | snp | A/G | | | utr-variant-5-prime, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25963148 | CCCATCTCCCCAGAA[A/G]AGCAGTGACCCCAGC | 10475 |
rs764746648 | snp | A/G | | | intron-variant, downstream-variant-500B | TRIM38 | GRCh38.p7 | 6:25976425 | GGCAAGCACTGCCAC[A/G]TCTGGCTAATTTTTT | 10475 |
rs764943913 | snp | G/T | | | upstream-variant-2KB | TRIM38 | GRCh38.p7 | 6:25962379 | ACTCAGATGAATTTT[G/T]TGATGCCAATGAGTC | 10475 |
rs764952584 | snp | G/T | 1.84783e-05 | 0.00303954 | intron-variant | TRIM38 | GRCh38.p7 | 6:25983141 | AACAAAATTATTTTT[G/T]TTTGTTTTGTTTTGT | 10475 |
rs764961957 | snp | A/G | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25967267 | ACAATATGTAAAGCC[A/G]TGCAGTAGGGCCTGA | 10475 |
rs764999606 | snp | A/G | 4.9458e-05 | 0.00497258 | synonymous-codon, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25971943 | CCTACATGAGGAAGA[A/G]AAGTCTTATCTCTGG | 10475 |
rs765013980 | snp | C/T | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25968154 | CCTTATTCTGTCCTC[C/T]ATGAGGCAGAGGTGG | 10475 |
rs765047550 | snp | A/G | 3.29794e-05 | 0.00406061 | missense, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25973216 | GAGGCTGTCTCCTTG[A/G]AACTTCATACTATGT | 10475 |
rs765099738 | snp | A/T | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25980697 | AAGTGCTGGGATTAC[A/T]GGCATGAGCCACCAC | 10475 |
rs765154381 | snp | A/G | 1.65108e-05 | 0.00287317 | missense, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25966658 | ACAGACTTCTTTAAA[A/G]ACCCAAGCCAAAAGC | 10475 |
rs765179018 | snp | A/G | 1.65064e-05 | 0.00287279 | missense, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25969400 | AAGCTGTCCACAGCA[A/G]TGCGAATAACTAAAT | 10475 |
rs765216291 | snp | A/G | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25978801 | CTTCCCGAGTAGCTG[A/G]GACTATTGGTGTGCA | 10475 |
rs765222265 | snp | A/G | | | upstream-variant-2KB | TRIM38 | GRCh38.p7 | 6:25961701 | TCTGTGAGCACCCAG[A/G]AGGGTGCAGTGCTGA | 10475 |
rs765402372 | snp | G/T | | | upstream-variant-2KB | TRIM38 | GRCh38.p7 | 6:25960852 | CATCCATGTAAGACC[G/T]GACTTGCTCCTCCTT | 10475 |
rs765451825 | snp | C/T | 1.6477e-05 | 0.00287024 | synonymous-codon, downstream-variant-500B | TRIM38 | GRCh38.p7 | 6:25983495 | TTCTCCCCCAACTTC[C/T]CTTCATCTGCATGAG | 10475 |
rs765807086 | snp | C/T | 1.66366e-05 | 0.0028841 | intron-variant | TRIM38 | GRCh38.p7 | 6:25969274 | ATTCCCCCTAGGTCC[C/T]TAATGAAGAGTCAAA | 10475 |
rs765864907 | snp | C/T | 3.30055e-05 | 0.00406222 | missense, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25966628 | TGTGGACACAGCTAC[C/T]GCCACTTGTGTATAA | 10475 |
rs765902547 | snp | C/T | 0.00010061 | 0.0070919 | synonymous-codon, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25966897 | GCACAAAGGGCACAC[C/T]ACAGCTCTTGTTGAA | 10475 |
rs765912458 | snp | C/T | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25978034 | TTCATAATATATATA[C/T]ACACACACACATATA | 10475 |
rs765916926 | snp | G/T | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25964595 | AAGGAAAAACAATTG[G/T]TCTTCTTGTCTAGTG | 10475 |
rs766066088 | snp | C/T | | | utr-variant-3-prime | TRIM38 | GRCh38.p7 | 6:25984250 | AGGGTTAAGACTGGC[C/T]TACAATGAGATGCTT | 10475 |
rs766133818 | snp | A/G | 3.30213e-05 | 0.00406319 | splice-acceptor-variant | TRIM38 | GRCh38.p7 | 6:25973052 | TTTTTGTTTCTTTAT[A/G]GAATGTGAATGACAC | 10475 |
rs766196745 | snp | A/T | 1.78309e-05 | 0.00298582 | utr-variant-5-prime, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25966518 | GGAGCTTTTCAATAA[A/T]AGCTATGGCCTCAAC | 10475 |
rs766286261 | snp | C/T | 1.64933e-05 | 0.00287165 | intron-variant | TRIM38 | GRCh38.p7 | 6:25973160 | AGAAATCTCTCGCCT[C/T]TGCTTATTCTAGGAG | 10475 |
rs766330926 | snp | C/T | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25963961 | AACCGACCTTATTAA[C/T]CAGTGTTGGTTGTTG | 10475 |
rs766482904 | snp | A/T | | | utr-variant-5-prime, upstream-variant-2KB | TRIM38 | GRCh38.p7 | 6:25962714 | GAGGCGGAGTGCAAA[A/T]GATATGAACAACGTC | 10475 |
rs766510524 | snp | A/G | 1.65326e-05 | 0.00287507 | missense, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25966863 | AGCTCATCTGCTGGC[A/G]CTGTGAGCGGGCACC | 10475 |
rs766559864 | snp | A/G | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25980969 | GGTAATATGAATTGA[A/G]ACCCCAAACTTCTGT | 10475 |
rs766598574 | snp | C/T | 3.29533e-05 | 0.00405901 | missense, downstream-variant-500B | TRIM38 | GRCh38.p7 | 6:25983485 | TAGCACTTACTTCTC[C/T]CCCAACTTCCCTTCA | 10475 |
rs766607446 | snp | A/G | | | upstream-variant-2KB | TRIM38 | GRCh38.p7 | 6:25961777 | CTTGCCTTTATTTTG[A/G]GTAGTTGGACCAGAG | 10475 |
rs766650813 | snp | A/C | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25973751 | TAGGTGAGTATGATA[A/C]CCTATCATTCACATA | 10475 |
rs766669435 | snp | C/T | | | utr-variant-3-prime | TRIM38 | GRCh38.p7 | 6:25986104 | TATATACTGGAATAA[C/T]TTTGAGAGTAATTTG | 10475 |
rs766784019 | snp | C/T | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25972516 | CTGTAGGAAGATAAA[C/T]ATCTGGAGCCATTAA | 10475 |
rs766793758 | snp | G/T | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25967187 | TTTGCTTTAGAACAG[G/T]TTGTTCTCAAACCAA | 10475 |
rs766872059 | snp | C/T | | | utr-variant-3-prime | TRIM38 | GRCh38.p7 | 6:25984948 | ATGTCAGAGGCATGG[C/T]TGGGCCTCCATCTCT | 10475 |
rs766930255 | in-del | -/A | 1.68394e-05 | 0.00290162 | intron-variant | TRIM38 | GRCh38.p7 | 6:25971848 | TACTTCCACCTTTTG[-/A]CCATACTTTCTTGAC | 10475 |
rs766991702 | snp | C/T | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25970976 | AGGGTAGTAGAACAG[C/T]ATTTCTCAGTTAACC | 10475 |
rs767130406 | snp | C/T | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25982146 | TAGGGCATAAAACCC[C/T]TTGTGGCTTGGATGG | 10475 |
rs767170115 | snp | A/T | 1.65217e-05 | 0.00287412 | intron-variant | TRIM38 | GRCh38.p7 | 6:25973045 | CCTTTTCTTTTTGTT[A/T]CTTTATAGAATGTGA | 10475 |
rs767201955 | snp | A/G | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25978108 | CACATACACACATAT[A/G]TTATATTCTCTCTAT | 10475 |
rs767289800 | snp | C/T | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25976993 | TTCAGGCCTCTGTGA[C/T]TTACCCATGATTTAC | 10475 |
rs767349586 | snp | C/T | 1.64781e-05 | 0.00287033 | utr-variant-5-prime, intron-variant, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25966490 | CTTCATCTCCATCTC[C/T]AGAGCCAATATTGGA | 10475 |
rs767432453 | snp | A/C | 1.6486e-05 | 0.00287102 | missense, downstream-variant-500B | TRIM38 | GRCh38.p7 | 6:25983266 | AGAATCAGGACACAT[A/C]TTCCAGGAGATTTAC | 10475 |
rs767701613 | snp | C/T | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25969990 | TGGTGCGATCTCAGC[C/T]CACTGCAATGTCCAC | 10475 |
rs767706824 | in-del | -/A | 1.65203e-05 | 0.002874 | frameshift-variant, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25966788 | TCAAAGAGACGGATC[-/A]AGAAATGTCATGTGA | 10475 |
rs767768024 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB | TRIM38 | GRCh38.p7 | 6:25962797 | CTCAGTTTAATCCGG[C/T]CTGAGTTAACTTCCT | 10475 |
rs767796287 | snp | G/T | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25975232 | CAAATTTTTTTTTGA[G/T]ATGGAGTCTCGCTGT | 10475 |
rs767903512 | snp | A/C | 1.67253e-05 | 0.00289178 | intron-variant | TRIM38 | GRCh38.p7 | 6:25969426 | TAAATGGAAAGTAAG[A/C]ATCTGACTTCATTGA | 10475 |
rs767972352 | snp | A/C | | | upstream-variant-2KB | TRIM38 | GRCh38.p7 | 6:25961821 | GCCAAACTCCATGTT[A/C]CATTGGCTATCAGGG | 10475 |
rs768111372 | snp | C/T | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25973854 | CCATTTACTGAGTTT[C/T]CTGCTCCCTTGATTT | 10475 |
rs768243892 | snp | C/T | | | intron-variant, synonymous-codon | TRIM38 | GRCh38.p7 | 6:25981880 | GAACTTTGGACAGGA[C/T]GGTAACCATATTAAC | 10475 |
rs768283590 | snp | C/G/T | 3.29632e-05 | 0.00405964 | missense, stop-gained, downstream-variant-500B | TRIM38 | GRCh38.p7 | 6:25983418 | ACTGGCATGAAGCAA[C/G/T]AGCCTCAGTCTGGAT | 10475 |
rs768398838 | snp | A/G | 1.64969e-05 | 0.00287196 | intron-variant | TRIM38 | GRCh38.p7 | 6:25973137 | AAATGAATGGAATGC[A/G]CCTCTGAAGAAATCT | 10475 |
rs768411111 | snp | A/C | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25968824 | GAACTGTTTCTAATA[A/C]CCAGCTGGCATCCTG | 10475 |
rs768562441 | snp | C/T | 3.51426e-05 | 0.00419167 | intron-variant | TRIM38 | GRCh38.p7 | 6:25966939 | GGGCTACAAGGTGAG[C/T]GTGTGGGCCCGGGAG | 10475 |
rs768580955 | snp | C/T | 1.64977e-05 | 0.00287203 | missense, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25966830 | AGCAGTTCCACCTGT[C/T]CTGCGAAGACGAGGG | 10475 |
rs768708142 | snp | A/G | 3.29533e-05 | 0.00405901 | synonymous-codon, downstream-variant-500B | TRIM38 | GRCh38.p7 | 6:25983525 | GCAGCCCCTGCTTGT[A/G]GGAATTTTTCTGGAC | 10475 |
rs768901728 | snp | A/G | | | downstream-variant-500B, utr-variant-3-prime | TRIM38 | GRCh38.p7 | 6:25987818 | AAGTTTCACTGCCCT[A/G]AAAATCCTGTGTTCT | 10475 |
rs769016986 | snp | C/T | 1.65282e-05 | 0.00287469 | missense, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25971882 | AGGAGAAGGTACAGA[C/T]TCAGAGACAAAAAAT | 10475 |
rs769081181 | snp | A/G | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25965302 | ACATGCAACTATTAA[A/G]CAATCAAAATGTGGC | 10475 |
rs769081249 | snp | A/G | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25978784 | TGATCCTCTCACCTC[A/G]GCTTCCCGAGTAGCT | 10475 |
rs769103693 | snp | C/T | 1.65252e-05 | 0.00287443 | missense, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25966709 | TGCTGTCCCCAGTGT[C/T]GGGCTCCATTTCATA | 10475 |
rs769138835 | snp | C/T | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25977854 | CACCAGAACTCTCCA[C/T]GTATATGGCAAGTTC | 10475 |
rs769170803 | snp | A/C | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25977626 | GAGCTGAGATTGTGC[A/C]ACTGCACTCCAGCTT | 10475 |
rs769398705 | snp | A/G | | | utr-variant-5-prime, intron-variant, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25966389 | GGAAGGAAAACCTTC[A/G]AGACCTATGGAAGTC | 10475 |
rs769405665 | snp | C/T | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25981969 | ATCATTATTACTACA[C/T]GTTGTTAGAAGAGCT | 10475 |
rs769453884 | snp | C/T | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25970519 | CTCTACCCTGATCTT[C/T]GTTTGTGGATGTTGC | 10475 |
rs769532244 | in-del | -/A | | | downstream-variant-500B, utr-variant-3-prime | TRIM38 | GRCh38.p7 | 6:25987680 | ATTACAATTGAACTT[-/A]ACATTGACACGTCAT | 10475 |
rs769653599 | snp | G/T | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25968527 | ATAGCACTTGGCATA[G/T]AGTAAGGACAATGTC | 10475 |
rs769693795 | snp | A/G | 4.9458e-05 | 0.00497258 | missense, downstream-variant-500B | TRIM38 | GRCh38.p7 | 6:25983376 | GGATGGGATTTAGGA[A/G]TTTGTATGGAAAATG | 10475 |
rs769720479 | in-del | -/G | 8.24083e-05 | 0.00641852 | frameshift-variant, downstream-variant-500B | TRIM38 | GRCh38.p7 | 6:25983283 | TCCAGGAGATTTACT[-/G]CCTTCCCCTGTGTCT | 10475 |
rs769732310 | snp | A/C | | | upstream-variant-2KB | TRIM38 | GRCh38.p7 | 6:25962563 | AGTCTGTGAACTGAA[A/C]CTCTGCAGGCTTCCT | 10475 |
rs769747367 | snp | A/G | 1.65285e-05 | 0.00287471 | synonymous-codon, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25966738 | TATGGATAGCCTCCG[A/G]CCCAACAAGCAGCTG | 10475 |
rs769897053 | snp | G/T | | | utr-variant-3-prime | TRIM38 | GRCh38.p7 | 6:25984860 | AAAAAAAAATTAATG[G/T]TTACTGATATTTGTT | 10475 |
rs770057928 | snp | C/G | 1.6623e-05 | 0.00288292 | intron-variant | TRIM38 | GRCh38.p7 | 6:25971863 | ACCATACTTTCTTGA[C/G]TCCAGGAGAAGGTAC | 10475 |
rs770084719 | snp | C/T | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25982923 | GAAACCCCATCTCTA[C/T]AGAAAATTTAAAAAA | 10475 |
rs770101144 | snp | G/T | | | utr-variant-3-prime | TRIM38 | GRCh38.p7 | 6:25986007 | TTGGGGTGCAGGAAA[G/T]TTATGGAAAGAATAT | 10475 |
rs770165904 | snp | G/T | 1.87545e-05 | 0.00306217 | utr-variant-3-prime, downstream-variant-500B | TRIM38 | GRCh38.p7 | 6:25983724 | GGTTTAACCAGCACA[G/T]AGAAAATAATATAAA | 10475 |
rs770168393 | snp | G/T | 1.97116e-05 | 0.00313933 | utr-variant-5-prime, intron-variant, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25966473 | GTGGAAAATTCTGGC[G/T]GCTTCATCTCCATCT | 10475 |
rs770211105 | in-del | -/TAC | | | cds-indel, downstream-variant-500B | TRIM38 | GRCh38.p7 | 6:25983594 | TGGCTGCCACATCTT[-/TAC]TTTCCCGAAGGCTTC | 10475 |
rs770238412 | snp | G/T | 1.68049e-05 | 0.00289865 | missense, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25973278 | GAAAATGTTAAGGAG[G/T]CATCAAGGTATGTTC | 10475 |
rs770296747 | snp | C/T | 1.6729e-05 | 0.00289209 | missense, utr-variant-3-prime, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25983220 | ATTCTCTCTGAGGAT[C/T]GGAGACAAGTGACTC | 10475 |
rs770323594 | snp | A/G | | | upstream-variant-2KB | TRIM38 | GRCh38.p7 | 6:25961163 | AACCACTATGGAGCT[A/G]GTGGGAATGCCTTCT | 10475 |
rs770494870 | snp | A/G | 1.65272e-05 | 0.0028746 | missense, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25966722 | GTCGGGCTCCATTTC[A/G]TATGGATAGCCTCCG | 10475 |
rs770603008 | snp | C/T | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25976976 | TGTATGTCCATTAGC[C/T]CTTCAGGCCTCTGTG | 10475 |
rs770694852 | in-del | -/TTGAG | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25973584 | ACAGCTCCTACTTCA[-/TTGAG]TTATCATCAAAATTA | 10475 |
rs770765987 | snp | C/T | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25971733 | TTGCCCTTTTGTTTC[C/T]GGCTTATTTTGCTTG | 10475 |
rs770784104 | snp | C/T | | | utr-variant-3-prime | TRIM38 | GRCh38.p7 | 6:25984175 | ATCTAAGCGGCAGTC[C/T]TGGAGGCTACCAGAC | 10475 |
rs770807000 | snp | C/T | 1.69752e-05 | 0.0029133 | intron-variant | TRIM38 | GRCh38.p7 | 6:25971839 | CATTTGGTTTACTTC[C/T]ACCTTTTGACCATAC | 10475 |
rs770946939 | snp | A/G | | | intron-variant, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25976096 | TGGTTCTTGTTTTAT[A/G]TCACAGTCCTCTCTA | 10475 |
rs771078461 | snp | C/T | 1.64936e-05 | 0.00287168 | synonymous-codon, downstream-variant-500B | TRIM38 | GRCh38.p7 | 6:25983582 | TAACGGGAATACTGG[C/T]TGCCACATCTTTACT | 10475 |
rs771256360 | snp | C/T | 0.00018134 | 0.00952036 | missense, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25969377 | TTGAAGACAGATGTA[C/T]GGAGCAGAAGCTGTC | 10475 |
rs771276197 | snp | A/C/T | 9.96999e-05 | 0.00705982 | intron-variant | TRIM38 | GRCh38.p7 | 6:25973013 | AGCCCCATGAAATAC[A/C/T]GATGTTCCCATGCTC | 10475 |
rs771705327 | snp | G/T | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25972965 | TCTCTTTACTTCTTC[G/T]GGTAAAGCAAAGAAG | 10475 |
rs771717359 | snp | C/T | 1.80647e-05 | 0.00300533 | intron-variant | TRIM38 | GRCh38.p7 | 6:25966955 | GTGTGGGCCCGGGAG[C/T]TTTGGTAAGTACCAA | 10475 |
rs771830791 | snp | A/G | 1.65042e-05 | 0.0028726 | missense, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25966596 | TGAGCCTGATGACGA[A/G]CCCAGTAAGCATCAA | 10475 |
rs771855479 | snp | A/G | | | upstream-variant-2KB | TRIM38 | GRCh38.p7 | 6:25961348 | TGCCTATTTCATCCT[A/G]TGACTTACAATGCCT | 10475 |
rs771920836 | snp | G/T | 1.7002e-05 | 0.0029156 | splice-donor-variant | TRIM38 | GRCh38.p7 | 6:25973286 | TAAGGAGTCATCAAG[G/T]TATGTTCACTAAAGA | 10475 |
rs771945158 | snp | A/T | 1.76456e-05 | 0.00297026 | missense, downstream-variant-500B | TRIM38 | GRCh38.p7 | 6:25983668 | ATTCTCCTTTGTTTC[A/T]GCCTCCCCCAGGTGA | 10475 |
rs772024879 | snp | A/G | 1.6516e-05 | 0.00287362 | missense, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25971888 | AGGTACAGATTCAGA[A/G]ACAAAAAATCCGGTC | 10475 |
rs772051229 | snp | G/T | 1.64882e-05 | 0.00287121 | missense, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25969353 | AAGCTGTGACAAAAC[G/T]GAAGCAACTTGAAGA | 10475 |
rs772152686 | snp | C/T | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25965179 | CTGAGTTCTCTCTTT[C/T]ACAGCTTTTGTGAGG | 10475 |
rs772303308 | snp | C/G | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25965729 | AAGAGATCGAGCCAA[C/G]CAACATGGTGAAACC | 10475 |
rs772545893 | snp | A/T | 1.64833e-05 | 0.00287078 | intron-variant | TRIM38 | GRCh38.p7 | 6:25972138 | GGAAAAAAGGTATGT[A/T]ATAGTGCTATTAAAG | 10475 |
rs772635730 | snp | A/G | 3.29587e-05 | 0.00405934 | missense, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25972019 | TATGAGGCTGGTCTG[A/G]GGCTGAAGAGCAATG | 10475 |
rs772648047 | snp | C/T | | | utr-variant-3-prime | TRIM38 | GRCh38.p7 | 6:25986345 | TAGCCTGGGCAAGGC[C/T]CCCATCTCTAAAAGA | 10475 |
rs772668007 | snp | C/T | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25980060 | TTGTTCAGACTGTTT[C/T]CTGCCTAGTATTTAC | 10475 |
rs772695247 | snp | A/G | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25970551 | CTTGAGCTCCTGAGT[A/G]CACTCTTACTTCCCC | 10475 |
rs772766089 | snp | A/G | 1.71425e-05 | 0.00292762 | intron-variant | TRIM38 | GRCh38.p7 | 6:25973290 | GAGTCATCAAGGTAT[A/G]TTCACTAAAGAATTC | 10475 |
rs772797726 | snp | A/C | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25974031 | ATCTATTAGTACAAA[A/C]AAATTACCATAATTT | 10475 |
rs772879397 | snp | A/T | 1.64868e-05 | 0.00287109 | synonymous-codon, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25969363 | AAAACTGAAGCAACT[A/T]GAAGACAGATGTACG | 10475 |
rs773075354 | snp | C/T | 1.81207e-05 | 0.00300999 | intron-variant | TRIM38 | GRCh38.p7 | 6:25966958 | TGGGCCCGGGAGCTT[C/T]GGTAAGTACCAAGTC | 10475 |
rs773225082 | snp | A/T | | | upstream-variant-2KB | TRIM38 | GRCh38.p7 | 6:25962605 | CTCTGTGTTGGGGTC[A/T]CATGATAGTTTACAG | 10475 |
rs773339493 | snp | C/G | | | utr-variant-3-prime | TRIM38 | GRCh38.p7 | 6:25986027 | GGAAAGAATATAAGT[C/G]CTGCTAGATAAATCA | 10475 |
rs773352350 | snp | C/T | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25975036 | TTCTTTCTTTCTTTC[C/T]TTTTTTTTTTTTTTG | 10475 |
rs773366342 | snp | A/G | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25978291 | CAGGCATGGGCCACC[A/G]CATCTGGCTGATGTT | 10475 |
rs773408033 | snp | A/G | 1.64773e-05 | 0.00287026 | missense, downstream-variant-500B | TRIM38 | GRCh38.p7 | 6:25983478 | GGCTATGTAGCACTT[A/G]CTTCTCCCCCAACTT | 10475 |
rs773455790 | snp | A/G | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25967419 | AGAGTGGTTCATCTT[A/G]GAAGTAACTCCTGAA | 10475 |
rs773528724 | snp | A/G | 1.6489e-05 | 0.00287128 | missense, downstream-variant-500B | TRIM38 | GRCh38.p7 | 6:25983571 | GTATCCTTTTATAAC[A/G]GGAATACTGGCTGCC | 10475 |
rs773552995 | snp | A/G | 1.64803e-05 | 0.00287052 | missense, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25972029 | GTCTGGGGCTGAAGA[A/G]CAATGAACTCAAGAG | 10475 |
rs773722117 | snp | C/T | | | synonymous-codon, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25966732 | ATTTCATATGGATAG[C/T]CTCCGACCCAACAAG | 10475 |
rs773747204 | snp | A/G | 2.02292e-05 | 0.00318028 | intron-variant | TRIM38 | GRCh38.p7 | 6:25972151 | GTTATAGTGCTATTA[A/G]AGGAGAATGGTAAGG | 10475 |
rs773793293 | snp | C/T | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25978046 | ATATACACACACACA[C/T]ATATATATAGTATTC | 10475 |
rs773952261 | snp | A/G | | | upstream-variant-2KB | TRIM38 | GRCh38.p7 | 6:25961273 | GGTGGGTTTTGGTCA[A/G]CTTCTTTACTGCAAC | 10475 |
rs773980755 | snp | G/T | 1.65323e-05 | 0.00287505 | intron-variant | TRIM38 | GRCh38.p7 | 6:25973042 | TCACCTTTTCTTTTT[G/T]TTTCTTTATAGAATG | 10475 |
rs774127238 | in-del | -/TATT | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25970424 | TTGCACCAATCTTTA[-/TATT]TATATAATTCACTAG | 10475 |
rs774184355 | snp | C/T | 1.64958e-05 | 0.00287187 | intron-variant | TRIM38 | GRCh38.p7 | 6:25973150 | GCACCTCTGAAGAAA[C/T]CTCTCGCCTCTGCTT | 10475 |
rs774186878 | snp | C/T | 0.000115488 | 0.00759806 | synonymous-codon, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25966834 | GTTCCACCTGTTCTG[C/T]GAAGACGAGGGGCAG | 10475 |
rs774197981 | snp | C/T | 7.16615e-05 | 0.00598545 | intron-variant | TRIM38 | GRCh38.p7 | 6:25966949 | GTGAGTGTGTGGGCC[C/T]GGGAGCTTTGGTAAG | 10475 |
rs774215183 | snp | G/T | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25969142 | TACCAACTATTCAGG[G/T]TTGCCAAGGGGATCA | 10475 |
rs774253186 | in-del | -/A | 1.65102e-05 | 0.00287312 | frameshift-variant, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25966654 | ATAACAGACTTCTTT[-/A]AAAAACCCAAGCCAA | 10475 |
rs774377118 | snp | A/G | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25983135 | CACAGCAACAAAATT[A/G]TTTTTGTTTGTTTTG | 10475 |
rs774393760 | snp | C/T | 1.64863e-05 | 0.00287104 | missense, downstream-variant-500B | TRIM38 | GRCh38.p7 | 6:25983263 | AGGAGAATCAGGACA[C/T]ATCTTCCAGGAGATT | 10475 |
rs774550296 | snp | C/T | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25975124 | TGCAAGCTCCGCCTT[C/T]CGGGTCAAGTGAAAC | 10475 |
rs774586407 | snp | C/T | | | intron-variant, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25976198 | TAACTAGAAGGTAGT[C/T]ATAGAAAGAGTCTAG | 10475 |
rs774631579 | in-del | -/T | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25973347 | TATGCAGTAACCAAG[-/T]TTACCACCTGTCCCT | 10475 |
rs774887811 | snp | C/T | | | utr-variant-5-prime, intron-variant, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25966456 | GGTGTATTTTCATCA[C/T]GGTGGAAAATTCTGG | 10475 |
rs774959966 | snp | C/G | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25967735 | AGAGACATGGTCTGC[C/G]TTTCTTGCTTATACT | 10475 |
rs775000919 | snp | C/G | 1.64991e-05 | 0.00287215 | missense, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25966822 | ACACGGAGAGCAGTT[C/G]CACCTGTTCTGCGAA | 10475 |
rs775048235 | snp | G/T | 5.5478e-05 | 0.00526649 | intron-variant | TRIM38 | GRCh38.p7 | 6:25966983 | CAAGTCTTATCCTGC[G/T]CCCCAGGAGCTGAGA | 10475 |
rs775079947 | in-del | -/CT | 1.64811e-05 | 0.00287059 | frameshift-variant, downstream-variant-500B | TRIM38 | GRCh38.p7 | 6:25983291 | ATTTACTGCCTTCCC[-/CT]GTGTCTTGGGTTGTG | 10475 |
rs775423657 | snp | C/G | 3.32132e-05 | 0.00407499 | intron-variant | TRIM38 | GRCh38.p7 | 6:25971865 | CATACTTTCTTGACT[C/G]CAGGAGAAGGTACAG | 10475 |
rs775442895 | snp | A/G | | | missense, downstream-variant-500B | TRIM38 | GRCh38.p7 | 6:25983395 | GTATGGAAAATGTGC[A/G]GAGGGGCACTGGCAT | 10475 |
rs775444865 | snp | C/T | 1.65296e-05 | 0.00287481 | synonymous-codon, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25966741 | GGATAGCCTCCGACC[C/T]AACAAGCAGCTGGGA | 10475 |
rs775480415 | in-del | -/AAG | 1.6817e-05 | 0.0028997 | cds-indel, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25966544 | TCAACCACCAGCACC[-/AAG]AAGATGATGGAGGAA | 10475 |
rs775695242 | snp | A/T | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25964187 | CTCTGCCAATGGGGG[A/T]AGATACTTATATAGC | 10475 |
rs775698960 | snp | A/C | 3.51346e-05 | 0.00419119 | missense, utr-variant-3-prime, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25983179 | TTAGTGTGACTCTGG[A/C]TCCAGATACAGCTCA | 10475 |
rs775709471 | snp | A/G | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25981780 | CCTCTCTGATTCTCA[A/G]TGTTGGTGGTTATTC | 10475 |
rs775836992 | snp | A/G | | | upstream-variant-2KB | TRIM38 | GRCh38.p7 | 6:25960924 | CTGTAAGAGCATGAA[A/G]CATTTTTTCCTGGTA | 10475 |
rs775932780 | snp | A/G | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25963976 | CCAGTGTTGGTTGTT[A/G]TTCTTTGTGGGGGAT | 10475 |
rs775974079 | snp | C/T | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25977563 | CAGTCCTAGCTACTC[C/T]GGAGGCTTAGGCAGA | 10475 |
rs776018434 | snp | C/T | 1.65034e-05 | 0.00287253 | synonymous-codon, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25966630 | TGGACACAGCTACTG[C/T]CACTTGTGTATAACA | 10475 |
rs776022005 | snp | A/G | 3.76967e-05 | 0.00434131 | utr-variant-3-prime, downstream-variant-500B | TRIM38 | GRCh38.p7 | 6:25983729 | AACCAGCACAGAGAA[A/G]ATAATATAAATCCCA | 10475 |
rs776121471 | snp | C/T | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25969475 | TCTAGAGCTTAGGCA[C/T]AGGGGATGATTGAGG | 10475 |
rs776216526 | snp | C/T | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25967917 | AGGGCAGATTTTAAG[C/T]ACGATTCAGGAAGAA | 10475 |
rs776393975 | snp | C/G | 9.30951e-05 | 0.00682194 | intron-variant | TRIM38 | GRCh38.p7 | 6:25983124 | CCTGTGTTCTTCACA[C/G]CAACAAAATTATTTT | 10475 |
rs776404377 | snp | A/C | | | upstream-variant-2KB | TRIM38 | GRCh38.p7 | 6:25961534 | TAGATATCTGCAAGG[A/C]CTCATCGTGGGACCA | 10475 |
rs776667066 | snp | A/G | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25973385 | CTCACAGCCAGAGAG[A/G]TTGTTTAGTTAATTT | 10475 |
rs776774962 | snp | C/G | 9.91359e-05 | 0.00703975 | missense, downstream-variant-500B | TRIM38 | GRCh38.p7 | 6:25983585 | CGGGAATACTGGCTG[C/G]CACATCTTTACTTTC | 10475 |
rs776775338 | snp | A/G | | | utr-variant-3-prime | TRIM38 | GRCh38.p7 | 6:25984651 | TGTGAGGCTGAGGCA[A/G]GTGGATCACTTGAGG | 10475 |
rs776836883 | snp | A/G | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25972130 | TGGAGTAGGGAAAAA[A/G]GGTATGTTATAGTGC | 10475 |
rs776837877 | snp | C/G | 1.83876e-05 | 0.00303207 | intron-variant | TRIM38 | GRCh38.p7 | 6:25966973 | TGGTAAGTACCAAGT[C/G]TTATCCTGCTCCCCA | 10475 |
rs777056666 | snp | A/G | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25980784 | ACTATAACAGTATAT[A/G]ACTATATTATCTATC | 10475 |
rs777118072 | snp | A/C | | | missense, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25966612 | CCCAGTAAGCATCAA[A/C]TGTGGACACAGCTAC | 10475 |
rs777145166 | snp | C/G | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25977811 | TGATGAAGACAATTG[C/G]TAGGTTGGTGAGAGA | 10475 |
rs777263197 | in-del | -/T/TT | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25964812 | TTCTGGTACCAATTA[-/T/TT]TTCTTTTTTTTTTTT | 10475 |
rs777332388 | snp | C/T | 1.6918e-05 | 0.00290839 | synonymous-codon, utr-variant-3-prime, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25983210 | TCACGAACTAATTCT[C/T]TCTGAGGATCGGAGA | 10475 |
rs777343586 | snp | C/T | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25971620 | ACAATAACTGTCCAT[C/T]TTCTGGTCTTGCCAA | 10475 |
rs777377624 | in-del | -/G | 4.95896e-05 | 0.00497919 | intron-variant | TRIM38 | GRCh38.p7 | 6:25973042 | TCACCTTTTCTTTTT[-/G]TTTCTTTATAGAATG | 10475 |
rs777491737 | in-del | -/CTTTAAAACTG | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25966190 | ATTCTTGGCAAACAA[-/CTTTAAAACTG]CTTTAAAACTGCTTT | 10475 |
rs777503139 | snp | C/T | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25965773 | AAATACAAAAATTAG[C/T]TGGGCGTAGTGGTGC | 10475 |
rs777522762 | snp | C/T | | | utr-variant-3-prime | TRIM38 | GRCh38.p7 | 6:25984040 | TTTGTTTGCTGCCAT[C/T]TGAACTCATGTAGGG | 10475 |
rs777560014 | snp | C/G | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25964947 | CTCCTGAGCAGCTGG[C/G]ATTACAGGTGTGCAC | 10475 |
rs777648082 | snp | A/C | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25977319 | GGAGTTCGAGGCTGC[A/C]GTAAGCTATGATCAC | 10475 |
rs777725261 | snp | C/G | 1.78755e-05 | 0.00298955 | missense, downstream-variant-500B | TRIM38 | GRCh38.p7 | 6:25983676 | TTGTTTCTGCCTCCC[C/G]CAGGTGACTAAGGAA | 10475 |
rs777736616 | snp | C/T | 3.29848e-05 | 0.00406095 | intron-variant | TRIM38 | GRCh38.p7 | 6:25973113 | GAGGGGAGGGGTGTG[C/T]GTATATAGAAATGAA | 10475 |
rs777814547 | snp | A/G | 1.77631e-05 | 0.00298014 | intron-variant | TRIM38 | GRCh38.p7 | 6:25969470 | TCCATTCTAGAGCTT[A/G]GGCATAGGGGATGAT | 10475 |
rs777981505 | in-del | -/G | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25967983 | TGAAGCAGAGGGAGA[-/G]GTTTTGTGTACCATC | 10475 |
rs778025222 | snp | A/G/T | 3.34505e-05 | 0.00408954 | missense, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25966550 | ACCAGCACCAAGAAG[A/G/T]TGATGGAGGAAGCCA | 10475 |
rs778093329 | snp | A/G | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25980330 | ATTTTTGCTTTGTAT[A/G]TTAACACAATTCTAA | 10475 |
rs778221800 | snp | A/T | 1.71805e-05 | 0.00293086 | intron-variant | TRIM38 | GRCh38.p7 | 6:25969453 | TTGATCTCAAGCTAT[A/T]TTCCATTCTAGAGCT | 10475 |
rs778390321 | snp | A/C | | | utr-variant-3-prime | TRIM38 | GRCh38.p7 | 6:25984442 | GATTCAGAGAAGAGC[A/C]AATAGACCTTAACTT | 10475 |
rs778398227 | snp | C/G | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25982432 | TAGTGTGGGCTCCCA[C/G]AGCTTAGGGCCTTTG | 10475 |
rs778523462 | snp | G/T | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25973902 | TATACTTTCACAAAT[G/T]TGTATCCGTAAGTAC | 10475 |
rs778551193 | snp | C/G | | | utr-variant-3-prime | TRIM38 | GRCh38.p7 | 6:25985468 | TCTCAGTACTCCCCT[C/G]TGTTTGTACAATGCA | 10475 |
rs778623504 | snp | A/T | | | upstream-variant-2KB | TRIM38 | GRCh38.p7 | 6:25961297 | CTGCAACCTGTTTTA[A/T]CAGCAAGATCTTTAT | 10475 |
rs778845258 | snp | C/T | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25965112 | GCCACCGTGCTGGCC[C/T]GGTAACAATTATTCT | 10475 |
rs778953986 | snp | C/T | 1.74598e-05 | 0.00295459 | missense, downstream-variant-500B | TRIM38 | GRCh38.p7 | 6:25983659 | TTTATCAATATTCTC[C/T]TTTGTTTCTGCCTCC | 10475 |
rs778961381 | snp | A/T | 3.76145e-05 | 0.00433657 | intron-variant | TRIM38 | GRCh38.p7 | 6:25972135 | TAGGGAAAAAAGGTA[A/T]GTTATAGTGCTATTA | 10475 |
rs778969884 | snp | A/G | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25965697 | TTGGGAGGCTGAGGC[A/G]GGTGGATCACAAGGT | 10475 |
rs779155876 | snp | A/G | 1.64895e-05 | 0.00287132 | intron-variant | TRIM38 | GRCh38.p7 | 6:25973100 | TGTTTGAATGCAGGA[A/G]GGGAGGGGTGTGCGT | 10475 |
rs779260358 | snp | A/G | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25970212 | TGAGCCACTGCACCC[A/G]GCCTATACTTGATTT | 10475 |
rs779352106 | snp | G/T | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25982730 | AAAGTTAAATGATTT[G/T]CCTAAGCTCACCCAG | 10475 |
rs779355024 | snp | C/T | 1.65146e-05 | 0.0028735 | missense, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25966797 | CGGATCAAGAAATGT[C/T]ATGTGAGGAACACGG | 10475 |
rs779359695 | snp | C/T | 4.94686e-05 | 0.00497311 | synonymous-codon, downstream-variant-500B | TRIM38 | GRCh38.p7 | 6:25983351 | TGAAGTGGATGTTGG[C/T]GAAGGAACCGGATGG | 10475 |
rs779444009 | snp | A/G | 6.61048e-05 | 0.00574874 | missense, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25966710 | GCTGTCCCCAGTGTC[A/G]GGCTCCATTTCATAT | 10475 |
rs779456926 | snp | A/G | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25979932 | TCTAATGACTTATTA[A/G]TAGTTTACATTTCCT | 10475 |
rs779515169 | snp | A/C | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25981635 | GTGTATTATTATCTC[A/C]TACTAATGCTTATGG | 10475 |
rs779537642 | snp | A/G/T | 0.000168207 | 0.00916936 | missense, downstream-variant-500B | TRIM38 | GRCh38.p7 | 6:25983629 | TCTCTGATACTCTCC[A/G/T]GCCCTATTTCCAGGT | 10475 |
rs779717649 | snp | A/G | | | utr-variant-3-prime | TRIM38 | GRCh38.p7 | 6:25987126 | CTTCACACTCATACT[A/G]TTTAAACTGTCCTAG | 10475 |
rs779734353 | snp | C/T | 1.65457e-05 | 0.00287621 | intron-variant | TRIM38 | GRCh38.p7 | 6:25969318 | ACTTATCAAATTTTT[C/T]CTTCAGGAAAAGCTC | 10475 |
rs779740077 | snp | C/T | 1.74937e-05 | 0.00295745 | intron-variant | TRIM38 | GRCh38.p7 | 6:25972113 | AGGTGAGGCTGTGTA[C/T]TTGGAGTAGGGAAAA | 10475 |
rs779886140 | snp | C/T | | | upstream-variant-2KB | TRIM38 | GRCh38.p7 | 6:25962274 | TTCTATCCTGGCTGA[C/T]CCTCGCTATTGAAGA | 10475 |
rs779932000 | in-del | -/CTTC | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25971368 | GAAACTGGGGACATT[-/CTTC]CAGCTTCAGTGACTC | 10475 |
rs779992750 | snp | C/T | | | utr-variant-3-prime | TRIM38 | GRCh38.p7 | 6:25985622 | TGCACTTGTTCTATA[C/T]ACCCGTAGTCTCGGT | 10475 |
rs780009623 | snp | A/G | | | missense, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25966584 | GCTCCATCTGCCTGA[A/G]CCTGATGACGAACCC | 10475 |
rs780111710 | snp | C/T | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25973129 | GTATATAGAAATGAA[C/T]GGAATGCACCTCTGA | 10475 |
rs780173938 | snp | A/C | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25967304 | GGAAGAAAGACCCAT[A/C]ACCTTTTAGGTATCT | 10475 |
rs780291522 | snp | C/G | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25980005 | TAATCTTATATTGAG[C/G]CTAGAGAAAATGATC | 10475 |
rs780314037 | snp | A/G | 1.65179e-05 | 0.00287379 | missense, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25966785 | CCCTCAAAGAGACGG[A/G]TCAAGAAATGTCATG | 10475 |
rs780325917 | snp | G/T | | | upstream-variant-2KB | TRIM38 | GRCh38.p7 | 6:25961100 | CAAGCGTTCCTCCCC[G/T]TTTTAGACTATATAG | 10475 |
rs780367871 | snp | C/T | 1.64776e-05 | 0.00287028 | stop-gained, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25971977 | CTGGAGAAAGAAGAA[C/T]AACAGACTCTGAGTA | 10475 |
rs780379386 | snp | C/T | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25978557 | CTCTGTTGCCCAAGC[C/T]GAGTGGTACAGTGGT | 10475 |
rs780380560 | in-del | -/T | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25975035 | TTCTTTCTTTCTTTC[-/T]TTTTTTTTTTTTTTT | 10475 |
rs780461812 | snp | C/T | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25971193 | GATAAAGTGTTTGAA[C/T]TTGGCCCTAGTTTCA | 10475 |
rs780565429 | snp | A/T | 5.2248e-05 | 0.0051109 | missense, utr-variant-3-prime, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25983186 | GACTCTGGATCCAGA[A/T]ACAGCTCATCACGAA | 10475 |
rs780581728 | snp | A/G | 6.74002e-05 | 0.00580479 | missense, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25973280 | AAATGTTAAGGAGTC[A/G]TCAAGGTATGTTCAC | 10475 |
rs780599069 | in-del | -/AGG | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25981025 | AATAGAGTTTGAAAA[-/AGG]AGGGTATTTACAAAG | 10475 |
rs780755815 | snp | A/G | 4.95209e-05 | 0.00497574 | missense, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25966811 | TCATGTGAGGAACAC[A/G]GAGAGCAGTTCCACC | 10475 |
rs780788600 | snp | A/G | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25963526 | TCCCTACCTCCTTGG[A/G]TCTGCAAACTCTTTA | 10475 |
rs780867520 | snp | C/T | 1.6477e-05 | 0.00287024 | missense, downstream-variant-500B | TRIM38 | GRCh38.p7 | 6:25983505 | ACTTCCCTTCATCTG[C/T]ATGAGCAGCCCCTGC | 10475 |
rs780973609 | snp | C/T | | | intron-variant, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25975923 | TTTGGGAACATACCC[C/T]AAACTGGGATTGCCG | 10475 |
rs780984450 | in-del | -/TTTGT | 3.69559e-05 | 0.00429844 | intron-variant | TRIM38 | GRCh38.p7 | 6:25983141 | ACAAAATTATTTTTG[-/TTTGT]TTTGTTTTGTTTTGT | 10475 |
rs781065867 | snp | G/T | 1.648e-05 | 0.0028705 | missense, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25971961 | GTCTTATCTCTGGAG[G/T]CTGGAGAAAGAAGAA | 10475 |
rs781155931 | snp | C/G | 1.67992e-05 | 0.00289816 | intron-variant | TRIM38 | GRCh38.p7 | 6:25971849 | ACTTCCACCTTTTGA[C/G]CATACTTTCTTGACT | 10475 |
rs781158747 | snp | A/G | 1.6534e-05 | 0.00287519 | missense, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25966574 | GAAGCCACCTGCTCC[A/G]TCTGCCTGAGCCTGA | 10475 |
rs781270166 | snp | C/G/T | 3.30421e-05 | 0.0040645 | missense, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25966697 | CAGGAGACATTCTGC[C/G/T]GTCCCCAGTGTCGGG | 10475 |
rs781378902 | snp | A/G | | | utr-variant-3-prime | TRIM38 | GRCh38.p7 | 6:25984579 | ATGTTATAATTTAGA[A/G]TTGACATAAAAATTG | 10475 |
rs781437960 | snp | A/G | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25969088 | TTTACCCCTTTCTTA[A/G]TCTCATTTTCTACAG | 10475 |
rs781528129 | snp | A/G | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25967389 | TTTGGTGGTGGGGAG[A/G]GACATTTAGGGTAGA | 10475 |
rs781656771 | in-del | -/A | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25977223 | TGAATTTTATCACCT[-/A]ATTAATTTTATTAGC | 10475 |
rs796723214 | snp | A/G | | | intron-variant, nc-transcript-variant | TRIM38 | GRCh38.p7 | 6:25975662 | TCCCACCCGTCTCCA[A/G]TCTGACTTCTCTAGG | 10475 |
rs796764938 | snp | C/T | | | intron-variant | TRIM38 | GRCh38.p7 | 6:25971641 | GTCTTGCCAACACCT[C/T]GTAACCACTATTTTA | 10475 |
rs796991569 | in-del | -/CC | | | utr-variant-3-prime | TRIM38 | GRCh38.p7 | 6:25987207 | CAAAGGTACTCCCCG[-/CC]CCCCGCCCGCCACAC | 10475 |
rs797001241 | in-del | CG/GCC | | | utr-variant-3-prime | TRIM38 | GRCh38.p7 | 6:25987212 | GTACTCCCCGCCCCC[CG/GCC]CCCGCCACACACCAT | 10475 |