SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6709 | snp | C/T | 0.302686 | 0.244385 | utr-variant-3-prime | TRIM44 | GRCh38.p7 | 11:35807928 | CAGGAAAAGGGATTT[C/T]CCCCAGTGCAGGCTC | 54765 |
rs12809 | snp | A/G | 0 | 0 | utr-variant-3-prime | TRIM44 | GRCh38.p7 | 11:35807757 | CCCACTTGCAAATAA[A/G]AATTACCTTGCAAGA | 54765 |
rs504423 | snp | G/T | 0.0138799 | 0.0821421 | intron-variant | TRIM44 | GRCh38.p7 | 11:35684686 | CTGTGAGTTTTATGG[G/T]TTTTTTTGGTGTTga | 54765 |
rs511160 | snp | C/T | 0.0456336 | 0.143994 | intron-variant | TRIM44 | GRCh38.p7 | 11:35664420 | GAacagtggacactt[C/T]ggaaatatttgttga | 54765 |
rs531239 | snp | C/T | 0.0505692 | 0.150756 | intron-variant | TRIM44 | GRCh38.p7 | 11:35681743 | GAGGCAGCTGTTCTG[C/T]TCCACTATCTTTTCT | 54765 |
rs545562 | snp | A/G | 0.352287 | 0.228117 | intron-variant | TRIM44 | GRCh38.p7 | 11:35669979 | ggcatgtgccaccac[A/G]cccgcctgatttttt | 54765 |
rs561462 | snp | C/T | 0.0505692 | 0.150756 | intron-variant | TRIM44 | GRCh38.p7 | 11:35682768 | CACACTGAATTTTTA[C/T]GAAAGAAGGCTAAGG | 54765 |
rs589100 | snp | G/T | 0.0505692 | 0.150756 | intron-variant | TRIM44 | GRCh38.p7 | 11:35799853 | TTCTCTCTCTAGTTC[G/T]GGTTCTATTTTATCC | 54765 |
rs591101 | snp | A/G | 0.4941 | 0.0539917 | intron-variant | TRIM44 | GRCh38.p7 | 11:35794222 | GGCCAAGATAGAGGT[A/G]AGGGGATACTTAATT | 54765 |
rs597254 | snp | C/G | 0.355954 | 0.226437 | utr-variant-3-prime | TRIM44 | GRCh38.p7 | 11:35807453 | AGAGTGAGATCCAGG[C/G]TGTGGGAGATGATCT | 54765 |
rs600797 | snp | C/T | 0.357024 | 0.225933 | intron-variant | TRIM44 | GRCh38.p7 | 11:35682229 | GCCTGCAGAGCCTCT[C/T]CTTGAGTCCGTCTGC | 54765 |
rs621682 | snp | C/G | 0.101301 | 0.200969 | upstream-variant-2KB | TRIM44 | GRCh38.p7 | 11:35660910 | ttgggaggcacttgg[C/G]aggactgcttgagcc | 54765 |
rs628673 | snp | C/T | 0.170733 | 0.237101 | intron-variant | TRIM44 | GRCh38.p7 | 11:35667942 | tttgatagcaaaatc[C/T]cataagaacagtaaa | 54765 |
rs634229 | snp | A/G | 0.0528381 | 0.153711 | intron-variant | TRIM44 | GRCh38.p7 | 11:35803241 | TTAGGCAGACAGCAC[A/G]TTCTATAGCAGGTAC | 54765 |
rs635138 | snp | A/G | 0.355954 | 0.226437 | intron-variant | TRIM44 | GRCh38.p7 | 11:35796444 | ATAGAAATCTTAAAC[A/G]TAAGATTTAATAAAA | 54765 |
rs635340 | snp | A/G | 0.0520825 | 0.152737 | intron-variant | TRIM44 | GRCh38.p7 | 11:35791226 | AAATGTGATTACATC[A/G]TCAGCACAGATCTAC | 54765 |
rs635889 | snp | A/G | 0.49089 | 0.0668743 | intron-variant | TRIM44 | GRCh38.p7 | 11:35686926 | cccaaactgaaattc[A/G]gtacccattaaatgc | 54765 |
rs639271 | snp | C/T | 0.491987 | 0.0627894 | intron-variant | TRIM44 | GRCh38.p7 | 11:35798345 | agctgggaaccgcga[C/T]cagcaaacttgtccc | 54765 |
rs640255 | snp | C/G | 0.492137 | 0.0622048 | intron-variant | TRIM44 | GRCh38.p7 | 11:35798101 | agttgtcctgccttt[C/G]tggaccgaaccaatg | 54765 |
rs640977 | snp | G/T | 0.145305 | 0.227022 | intron-variant | TRIM44 | GRCh38.p7 | 11:35686296 | GCTGGCTTTGCCTTA[G/T]AATCAAAGTTTCTCA | 54765 |
rs642340 | snp | C/G | 0.0498117 | 0.149749 | intron-variant | TRIM44 | GRCh38.p7 | 11:35804226 | TAACCTAAAAGAGAC[C/G]TGTTCTTGGGCCTGA | 54765 |
rs643290 | snp | C/T | 0.0501905 | 0.150254 | intron-variant | TRIM44 | GRCh38.p7 | 11:35803974 | TTCTTCCCAGAACAG[C/T]ACCTTCAAAGAAAGC | 54765 |
rs643353 | snp | A/C | 0.0456336 | 0.143994 | intron-variant | TRIM44 | GRCh38.p7 | 11:35666908 | cttcacacataatac[A/C]atcaggtatgtagaa | 54765 |
rs643750 | snp | C/T | 0.25634 | 0.24992 | intron-variant | TRIM44 | GRCh38.p7 | 11:35803871 | AGAGCTTTGCTCAGC[C/T]TGTATGTCGTCTCTC | 54765 |
rs647764 | snp | A/G | 0.0501905 | 0.150254 | intron-variant | TRIM44 | GRCh38.p7 | 11:35795884 | AGTACCTATCACACA[A/G]TAAGTGCTCAAAACA | 54765 |
rs657292 | snp | A/C | 0.357238 | 0.225832 | intron-variant | TRIM44 | GRCh38.p7 | 11:35665912 | ACATAGAAAGAACAA[A/C]AAAAAAAATCAGAAA | 54765 |
rs661044 | snp | C/T | 0.0520825 | 0.152737 | utr-variant-3-prime | TRIM44 | GRCh38.p7 | 11:35810345 | AGAAAATTAACTGCA[C/T]GTTTACTGTGTGCTG | 54765 |
rs662905 | snp | C/T | 0.0520825 | 0.152737 | utr-variant-3-prime | TRIM44 | GRCh38.p7 | 11:35809883 | TTGTGTGTGTGTGTG[C/T]GGACATGTATGTATG | 54765 |
rs668763 | snp | G/T | | | intron-variant | TRIM44 | GRCh38.p7 | 11:35665652 | caggctggagtacag[G/T]ggctagatctcagct | 54765 |
rs671554 | snp | A/G | | | intron-variant | TRIM44 | GRCh38.p7 | 11:35665615 | tttttttttttttga[A/G]atagagtcttgctct | 54765 |
rs671783 | snp | A/G | 0.498206 | 0.0298983 | intron-variant | TRIM44 | GRCh38.p7 | 11:35802268 | GGAAACTCTTGGCAA[A/G]GCTGTGTGTTTTATC | 54765 |
rs745193 | snp | C/T | 0.402277 | 0.198272 | intron-variant | TRIM44 | GRCh38.p7 | 11:35729217 | GTGCCACTTTTTTCA[C/T]GATGTTTGCTTCCAG | 54765 |
rs752034 | snp | A/T | 0.308414 | 0.24308 | intron-variant | TRIM44 | GRCh38.p7 | 11:35789654 | ATTTGGATGACAAGG[A/T]TCCCTGCTGTCAGAA | 54765 |
rs792649 | snp | G/T | 0.0520825 | 0.152737 | intron-variant | TRIM44 | GRCh38.p7 | 11:35793350 | TTTAGTAGCGACGGG[G/T]TTTCACCATGTTGGC | 54765 |
rs880415 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TRIM44 | GRCh38.p7 | 11:35788511 | TATAAAAATTGTCTG[A/G]AGGAAGAGAATAGAA | 54765 |
rs907702 | snp | C/T | 0 | 0 | intron-variant | TRIM44 | GRCh38.p7 | 11:35793182 | CGCACAGCTAGATTT[C/T]TTTTTTTTTTTTTCA | 54765 |
rs963811 | snp | C/T | 0.121717 | 0.214577 | intron-variant | TRIM44 | GRCh38.p7 | 11:35687953 | TGCAATTACGTTCAC[C/T]CTTCTTCAAGCTGGC | 54765 |
rs1001964 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | TRIM44 | GRCh38.p7 | 11:35780569 | aggatcagtgttaca[A/G]ttaaatgagACCGTG | 54765 |
rs1007225 | snp | A/G | 0.399253 | 0.200558 | intron-variant | TRIM44 | GRCh38.p7 | 11:35711871 | TTTCTGGAACTTTGT[A/G]GGGAGGAAGGTGCCC | 54765 |
rs1007591 | snp | G/T | 0.202035 | 0.245356 | intron-variant | TRIM44 | GRCh38.p7 | 11:35710252 | tgctttaTATATATA[G/T]AGAGAGAGAGCTTTG | 54765 |
rs1173957 | snp | C/T | | | intron-variant | TRIM44 | GRCh38.p7 | 11:35698294 | ataatcctttgggta[C/T]atacccagtaatggg | 54765 |
rs1173958 | snp | C/T | | | intron-variant | TRIM44 | GRCh38.p7 | 11:35698376 | actcactgacttcca[C/T]aatggttgaactagt | 54765 |
rs1173959 | snp | C/G | | | intron-variant | TRIM44 | GRCh38.p7 | 11:35698409 | acagtcccaccaaca[C/G]tgtaaaagtgttcct | 54765 |
rs1173960 | snp | A/G | | | intron-variant | TRIM44 | GRCh38.p7 | 11:35698499 | taactggtgtgagat[A/G]gtatctcattgtggt | 54765 |
rs1173961 | snp | A/G | | | intron-variant | TRIM44 | GRCh38.p7 | 11:35698580 | gtcttttggctgcat[A/G]aatgtcttcttttga | 54765 |
rs1173962 | snp | C/T | | | intron-variant | TRIM44 | GRCh38.p7 | 11:35698658 | tttcttgtaaatttg[C/T]ttgagttcattgtag | 54765 |
rs1173963 | snp | A/G | | | intron-variant | TRIM44 | GRCh38.p7 | 11:35698707 | ttgtcagatgagtag[A/G]ttgcaaaaattttct | 54765 |
rs1173964 | snp | C/T | | | intron-variant | TRIM44 | GRCh38.p7 | 11:35698729 | aaattttctcccatt[C/T]tgtaggttgcctgtt | 54765 |
rs1173965 | snp | A/G | | | intron-variant | TRIM44 | GRCh38.p7 | 11:35698848 | tttggtgttttagac[A/G]tgaagtccttgccca | 54765 |
rs1173966 | snp | A/T | | | intron-variant | TRIM44 | GRCh38.p7 | 11:35698884 | gtgtcttgaatggta[A/T]tgcctgggttttcta | 54765 |
rs1173967 | snp | A/G | | | intron-variant | TRIM44 | GRCh38.p7 | 11:35698890 | tgaatggtattgcct[A/G]ggttttctaggattt | 54765 |
rs1174115 | snp | G/T | 0 | 0 | intron-variant | TRIM44 | GRCh38.p7 | 11:35664638 | CTCTCAAGGTATTTG[G/T]TATCCCAATGCCAGC | 54765 |
rs1174116 | snp | A/G | 0 | 0 | intron-variant | TRIM44 | GRCh38.p7 | 11:35664800 | CAGATTAAGAAATAG[A/G]ACATTACTAGCAATA | 54765 |
rs1174117 | snp | A/G | 0.36021 | 0.224397 | intron-variant | TRIM44 | GRCh38.p7 | 11:35664930 | ATGCTTTTACTCCAT[A/G]TGTATGCATTCCTAA | 54765 |
rs1174118 | snp | G/T | 0 | 0 | intron-variant | TRIM44 | GRCh38.p7 | 11:35665927 | gttgttctttctatg[G/T]gggttgcaaatatct | 54765 |
rs1183036 | snp | C/T | 0 | 0 | intron-variant | TRIM44 | GRCh38.p7 | 11:35698476 | gactttttaaatgat[C/T]gccattctaactggt | 54765 |
rs1185374 | snp | A/G | | | intron-variant | TRIM44 | GRCh38.p7 | 11:35698902 | cctgggttttctagg[A/G]tttttatggttttag | 54765 |
rs1185764 | snp | A/G | | | intron-variant | TRIM44 | GRCh38.p7 | 11:35675775 | cccagcactttggga[A/G]gccaaggtgggtaga | 54765 |
rs1186119 | snp | G/T | 0 | 0 | intron-variant | TRIM44 | GRCh38.p7 | 11:35665949 | caaatatcttctatg[G/T]ggtttttctttttaa | 54765 |
rs1186447 | snp | A/G | 0 | 0 | intron-variant | TRIM44 | GRCh38.p7 | 11:35665528 | gaaaaatgggcaaaa[A/G]aactgactaggtact | 54765 |
rs1287289 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | TRIM44 | GRCh38.p7 | 11:35783648 | GCACACACACAAGGC[A/G]TCCCTAATTTCCTCT | 54765 |
rs1306043 | snp | A/G | | | intron-variant | TRIM44 | GRCh38.p7 | 11:35675610 | ggcgtgaacccggga[A/G]gcggaggttgcagtg | 54765 |
rs1306044 | snp | C/G | | | intron-variant | TRIM44 | GRCh38.p7 | 11:35675603 | acccgggaagcggag[C/G]ttgcagtgagccgac | 54765 |
rs1323855 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | TRIM44 | GRCh38.p7 | 11:35746610 | AAATCTGCACTCATC[A/G]ACTCTGAACTTCACA | 54765 |
rs1323856 | snp | C/T | 0.207253 | 0.246318 | intron-variant | TRIM44 | GRCh38.p7 | 11:35738340 | TGCCTTTCCATTATC[C/T]TGTCAAAATGATACA | 54765 |
rs1323857 | snp | C/G | 0.105924 | 0.204309 | intron-variant | TRIM44 | GRCh38.p7 | 11:35769741 | ACTGTATGTCCAGCC[C/G]TAGTaataagagtta | 54765 |
rs1359181 | snp | C/T | 0.139564 | 0.224285 | intron-variant | TRIM44 | GRCh38.p7 | 11:35738401 | GACCTCCATAGCAGC[C/T]TGGCTCAAGGGAGAT | 54765 |
rs1535774 | snp | A/C | 0.277778 | 0.248452 | intron-variant | TRIM44 | GRCh38.p7 | 11:35746470 | CAGTGACATAGAGCT[A/C]Caaaaaaaaaaaaaa | 54765 |
rs1555623 | snp | G/T | 0.0263992 | 0.111815 | intron-variant | TRIM44 | GRCh38.p7 | 11:35785294 | AATGGTCAACAGTGG[G/T]GCCATCTCCTCAGAC | 54765 |
rs1555624 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | TRIM44 | GRCh38.p7 | 11:35784864 | CAAGAGGGAAAAGTA[C/T]TCATTATGAAACAGA | 54765 |
rs1590371 | snp | C/T | 0.0759472 | 0.179459 | intron-variant | TRIM44 | GRCh38.p7 | 11:35719351 | TGGCAAATAAGCACA[C/T]GAAAAGATGCTCAAC | 54765 |
rs1830816 | snp | C/T | 0.352938 | 0.227824 | intron-variant | TRIM44 | GRCh38.p7 | 11:35694357 | attcactcttcttaa[C/T]tcacatcatgaatta | 54765 |
rs1969800 | snp | C/T | 0.35574 | 0.226537 | intron-variant | TRIM44 | GRCh38.p7 | 11:35750408 | AAAATAGTGTTTAGT[C/T]TAATATATCTAGAAA | 54765 |
rs2048572 | snp | A/G | 0.422158 | 0.181278 | intron-variant | TRIM44 | GRCh38.p7 | 11:35805196 | TATTATGTAGGGGCT[A/G]TTATTATCCCCCGTT | 54765 |
rs2057520 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM44 | GRCh38.p7 | 11:35751415 | TCTGGCATCAAGGCC[C/T]GGCCATATTAGAGAA | 54765 |
rs2089957 | snp | A/G | 0.339882 | 0.233284 | intron-variant | TRIM44 | GRCh38.p7 | 11:35800471 | AACACACCAATCAGC[A/G]CTCTGTAAAAATGCA | 54765 |
rs2102609 | snp | A/G | 0.339429 | 0.233457 | intron-variant | TRIM44 | GRCh38.p7 | 11:35800483 | TAAAGGATTGTAAAC[A/G]CACCAATCAGCACTC | 54765 |
rs2147094 | snp | A/G | 0.307919 | 0.243198 | intron-variant | TRIM44 | GRCh38.p7 | 11:35780491 | TAAAAAGCAATGTAG[A/G]ATCCCTAAGAAAGTG | 54765 |
rs2181877 | snp | C/T | 0.352504 | 0.228019 | intron-variant | TRIM44 | GRCh38.p7 | 11:35710525 | GCCTGAACTCAAAGC[C/T]ACCTCTTTGGGATTT | 54765 |
rs2281776 | snp | A/G | 0.0763149 | 0.179815 | utr-variant-3-prime | TRIM44 | GRCh38.p7 | 11:35809731 | ATCCTCACAGAGTAC[A/G]CTGGCGGCTAAGTTT | 54765 |
rs2296177 | snp | C/G | 0.492582 | 0.0604491 | intron-variant | TRIM44 | GRCh38.p7 | 11:35735089 | CCCAAAATAGAGGCA[C/G]GTCTTAGACAAAAGC | 54765 |
rs2580198 | snp | G/T | | | | | GRCh38.p7 | 11:35665916 | TGATTTTTTTTTTTG[G/T]TCTTTCTATGTGGGT | 54765 |
rs2671459 | snp | A/C | 0 | 0 | upstream-variant-2KB | TRIM44 | GRCh38.p7 | 11:35661984 | ttggaagatcctctg[A/C]ccgatggtccccaaa | 54765 |
rs2901620 | snp | C/G | 0.357664 | 0.225629 | intron-variant | TRIM44 | GRCh38.p7 | 11:35703320 | ctgtaggctccacct[C/G]tgggggcggggcaca | 54765 |
rs2938180 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | TRIM44 | GRCh38.p7 | 11:35736356 | CTATTCTTCAAAATA[A/G]ACCCTGAGGAGCTTC | 54765 |
rs2938183 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM44 | GRCh38.p7 | 11:35761260 | ATCTTTGGACTTACC[A/G]CTTCTCTATTTGATA | 54765 |
rs2938184 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | TRIM44 | GRCh38.p7 | 11:35773286 | AGGTGCCTTTTTTTT[A/T]AAGAAGTATCTATTC | 54765 |
rs2938185 | snp | G/T | 0 | 0 | intron-variant | TRIM44 | GRCh38.p7 | 11:35778364 | cattcatctaacctt[G/T]tttcaaggtttttag | 54765 |
rs2938186 | snp | C/T | 0.307919 | 0.243198 | intron-variant | TRIM44 | GRCh38.p7 | 11:35779222 | cagtgagcgaggctc[C/T]gtgggcatgggaccc | 54765 |
rs2938187 | snp | A/C | 0.308908 | 0.242961 | intron-variant | TRIM44 | GRCh38.p7 | 11:35782844 | AGTGAGTTGGGAATG[A/C]CTAAGTCAGCCAATC | 54765 |
rs2938188 | snp | G/T | 0.404209 | 0.196773 | intron-variant | TRIM44 | GRCh38.p7 | 11:35792371 | CTGAGGCCTAGATGT[G/T]AAATAGCTTTGCCAA | 54765 |
rs2938189 | snp | C/G | 0.309401 | 0.24284 | intron-variant | TRIM44 | GRCh38.p7 | 11:35728162 | AAAACCCTGTCTGTA[C/G]TAAAAATAGAAAAAT | 54765 |
rs2942380 | snp | A/G | 0.339656 | 0.233371 | intron-variant | TRIM44 | GRCh38.p7 | 11:35800718 | GCCCCTCTCTATCCC[A/G]TCACCACAATCTGAA | 54765 |
rs2942381 | snp | A/T | 0.401747 | 0.198678 | intron-variant | TRIM44 | GRCh38.p7 | 11:35792111 | AATGATGAGAGAGAG[A/T]GTGTGTGTGTGTGTG | 54765 |
rs2956333 | snp | A/G | 0.311369 | 0.242351 | intron-variant | TRIM44 | GRCh38.p7 | 11:35793847 | TTACTTCCTTTGTCT[A/G]CTCTGTATTTTCTTC | 54765 |
rs2956334 | snp | A/G | 0.381308 | 0.21274 | intron-variant | TRIM44 | GRCh38.p7 | 11:35802610 | ACCACAAGGGTATCC[A/G]TACCCCAGTTTTAAG | 54765 |
rs2956335 | snp | A/G | 0.333722 | 0.235565 | utr-variant-3-prime | TRIM44 | GRCh38.p7 | 11:35808493 | CCTTATATTAGCAAT[A/G]GACAGATCATTGGTT | 54765 |
rs2956337 | snp | A/G | 0.303688 | 0.244167 | intron-variant | TRIM44 | GRCh38.p7 | 11:35785233 | AATGTTTGCTGTATC[A/G]CCTAAAAGAAAACAG | 54765 |
rs2957949 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | TRIM44 | GRCh38.p7 | 11:35797874 | TGATACCTTCATACT[A/G]AAGTTCATATTTTGA | 54765 |
rs2970317 | snp | C/T | 0.422473 | 0.180978 | intron-variant | TRIM44 | GRCh38.p7 | 11:35800114 | TGAGTGTTACAGCTC[C/T]TAAAGGTGGCGTGTC | 54765 |