SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs236628 | snp | G/T | 0.384401 | 0.210799 | upstream-variant-2KB, intron-variant | TRIM73, LOC541473 | GRCh38.p7 | 7:75394576 | AAAGGGGACATAGGG[G/T]TCCTTAGCTTTCCTC | 375593 |
rs236634 | snp | C/T | 0 | 0 | intron-variant | TRIM73 | GRCh38.p7 | 7:75400267 | agcactttgggaggc[C/T]gaggtgggtggatca | 375593 |
rs236638 | snp | A/G | 0.277778 | 0.248452 | utr-variant-3-prime | TRIM73 | GRCh38.p7 | 7:75405361 | ATAGAGGAAAGTCAC[A/G]TCCCTGCCTTCAAGG | 375593 |
rs450082 | snp | C/G | 0 | 0 | intron-variant | TRIM73 | GRCh38.p7 | 7:75398251 | GAGGCCCAGCGGATT[C/G]TGAGAAGCCAGGTAT | 375593 |
rs454798 | snp | C/T | | | intron-variant | TRIM73 | GRCh38.p7 | 7:75398228 | ATGCTGGCTTGAGGC[C/T]GTAGTGGGAGGCCCA | 375593 |
rs3095181 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM73 | GRCh38.p7 | 7:75398202 | CCTGCTGGGAAGAAG[A/G]AAAGCCAGTGATGCT | 375593 |
rs3095182 | snp | C/T | | | intron-variant | TRIM73 | GRCh38.p7 | 7:75398315 | GCTTCTTCTGTCTCA[C/T]TGACAAGCTTTCATA | 375593 |
rs73702636 | snp | C/T | 0.45328 | 0.145523 | missense | TRIM73 | GRCh38.p7 | 7:75398956 | GGCAGGTGAGCCTGC[C/T]GGAGCTGGAGGACCG | 375593 |
rs73702637 | snp | A/G | 0.450434 | 0.14942 | synonymous-codon | TRIM73 | GRCh38.p7 | 7:75398957 | GCAGGTGAGCCTGCT[A/G]GAGCTGGAGGACCGG | 375593 |
rs111656303 | snp | G/T | | | intron-variant | TRIM73 | GRCh38.p7 | 7:75402415 | TTTTTTTTTTGAGAC[G/T]GAGTCTCGCTCTGTC | 375593 |
rs111923502 | snp | C/T | | | intron-variant | TRIM73 | GRCh38.p7 | 7:75401667 | TGCATAACTTAGTTC[C/T]TCTCACGGGGAAGGA | 375593 |
rs112340704 | snp | C/T | | | intron-variant | TRIM73 | GRCh38.p7 | 7:75399739 | TGGAGTGCAGTGGTG[C/T]GATCATGGCTCACTG | 375593 |
rs112493146 | snp | C/T | 0 | 0 | intron-variant | TRIM73 | GRCh38.p7 | 7:75398245 | TAGTGGGAGGCCCAG[C/T]GGATTGTGAGAAGCC | 375593 |
rs112728736 | snp | A/G | | | intron-variant, upstream-variant-2KB | TRIM73, LOC541473 | GRCh38.p7 | 7:75396500 | GGGATTATAGGCGTA[A/G]GCTACAGCCAACTTT | 375593 |
rs113249493 | snp | A/C | 0.5 | 0 | intron-variant | TRIM73 | GRCh38.p7 | 7:75397849 | CCCCCACCCCCCCCC[A/C]AAAAAGGATATAAGA | 375593 |
rs113406400 | snp | C/T | | | intron-variant | TRIM73 | GRCh38.p7 | 7:75398282 | TCCAATGTCGGGCTC[C/T]CGCTGGGGGCTTCTG | 375593 |
rs138355430 | snp | A/G | 0.00404504 | 0.0447901 | missense | TRIM73 | GRCh38.p7 | 7:75398971 | TGGAGCTGGAGGACC[A/G]GCTTCAGTGTCCCAT | 375593 |
rs139250213 | snp | A/C/G | 6.59146e-05 | 0.00574052 | synonymous-codon, missense | TRIM73 | GRCh38.p7 | 7:75405036 | GTGTGTGCTGGAACA[A/C/G]TTCGGCAATGAGGAC | 375593 |
rs139338132 | snp | C/T | 0.00560542 | 0.052643 | missense | TRIM73 | GRCh38.p7 | 7:75405067 | CACCATGAGTTCATC[C/T]GGGTGAGTGGACAGG | 375593 |
rs139576761 | snp | C/T | | | missense | TRIM73 | GRCh38.p7 | 7:75398970 | CTGGAGCTGGAGGAC[C/T]GGCTTCAGTGTCCCA | 375593 |
rs141046830 | snp | A/G/T | 0.000282211 | 0.0118757 | missense | TRIM73 | GRCh38.p7 | 7:75404999 | AGGCCCAGGGAACCC[A/G/T]GGAGCGGCTGGCCCA | 375593 |
rs141552293 | snp | A/G | 0.000132028 | 0.00812384 | missense | TRIM73 | GRCh38.p7 | 7:75405019 | CGGCTGGCCCAAGCC[A/G]AGTGTGTGCTGGAAC | 375593 |
rs143496774 | snp | C/T | 0.00404584 | 0.0447945 | synonymous-codon | TRIM73 | GRCh38.p7 | 7:75398991 | CAGTGTCCCATCTGC[C/T]TGGAGGTCTTCAAGG | 375593 |
rs143976895 | snp | A/C/T | 0.000490645 | 0.0156564 | stop-gained, synonymous-codon | TRIM73 | GRCh38.p7 | 7:75399026 | CCTAATGCTACAGTG[A/C/T]GGCCACTCCTACTGC | 375593 |
rs146512104 | snp | C/T | 1.64914e-05 | 0.00287149 | stop-gained | TRIM73 | GRCh38.p7 | 7:75398943 | GTGTGGATGGCTTGG[C/T]AGGTGAGCCTGCTGG | 375593 |
rs146570185 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon | TRIM73 | GRCh38.p7 | 7:75405054 | CGGCAATGAGGACCA[C/T]CATGAGTTCATCTGG | 375593 |
rs147290058 | snp | C/T | 0.017251 | 0.0912573 | missense | TRIM73 | GRCh38.p7 | 7:75404972 | TGGCCTCCCTGGACA[C/T]GCAGCTGGAGCAGGC | 375593 |
rs150021451 | snp | C/T | 3.29576e-05 | 0.00405928 | synonymous-codon | TRIM73 | GRCh38.p7 | 7:75405039 | TGTGCTGGAACAGTT[C/T]GGCAATGAGGACCAC | 375593 |
rs150827650 | snp | A/C/G | 4.94901e-05 | 0.00497424 | synonymous-codon, missense | TRIM73 | GRCh38.p7 | 7:75405021 | GCTGGCCCAAGCCGA[A/C/G]TGTGTGCTGGAACAG | 375593 |
rs182608059 | snp | C/T | | | intron-variant | TRIM73 | GRCh38.p7 | 7:75403477 | CGCCCAGACTATTCT[C/T]GAACAATTTAACCTG | 375593 |
rs185066617 | snp | A/G | | | intron-variant | TRIM73 | GRCh38.p7 | 7:75397889 | TGAGATTCAGAAAGA[A/G]CTGTTTCCCAGCACC | 375593 |
rs191991199 | snp | C/G | | | intron-variant | TRIM73 | GRCh38.p7 | 7:75399483 | CCTTAGTGTTTGAGC[C/G]GCAGCTAAACCCAGG | 375593 |
rs199563025 | snp | A/T | 0.000165782 | 0.00910295 | missense | TRIM73 | GRCh38.p7 | 7:75399150 | AACGTCTCCCTGGCC[A/T]GGGTGATCGAAGCCC | 375593 |
rs199603365 | snp | A/G | 0.0855218 | 0.188274 | missense | TRIM73 | GRCh38.p7 | 7:75399315 | ACGCCCGTCTCCACC[A/G]TCTGCAGCCGCATGA | 375593 |
rs199982097 | snp | C/T | | | stop-gained | TRIM73 | GRCh38.p7 | 7:75403732 | GTGAAAAACCGGACC[C/T]GAATCGTCGTGAGTG | 375593 |
rs200201610 | snp | C/T | 0.00199481 | 0.0315187 | utr-variant-3-prime | TRIM73 | GRCh38.p7 | 7:75405314 | TCCCAAGCAGCTGCC[C/T]ATAGCTGGCTCTATA | 375593 |
rs200694955 | snp | A/C | | | missense | TRIM73 | GRCh38.p7 | 7:75403722 | CGCCAAACTGGTGAA[A/C]AACCGGACCCGAATC | 375593 |
rs201121158 | snp | A/G | 0.000295138 | 0.0121442 | intron-variant | TRIM73 | GRCh38.p7 | 7:75405136 | TCCCAACAGTGCCCT[A/G]GCTTCCCACCTTCTA | 375593 |
rs201374916 | snp | A/G | | | missense | TRIM73 | GRCh38.p7 | 7:75405005 | AGGGAACCCGGGAGC[A/G]GCTGGCCCAAGCCGA | 375593 |
rs201856955 | snp | A/C | 0.00199792 | 0.0315431 | missense | TRIM73 | GRCh38.p7 | 7:75405052 | TTCGGCAATGAGGAC[A/C]ACCATGAGTTCATCT | 375593 |
rs202011164 | snp | C/T | 0.0126765 | 0.0785974 | missense | TRIM73 | GRCh38.p7 | 7:75404917 | GACGAGGAGAAGGCC[C/T]GCTGCCTGGAGGGGA | 375593 |
rs367761658 | snp | A/G | 0.000226244 | 0.0106335 | missense | TRIM73 | GRCh38.p7 | 7:75399319 | CCGTCTCCACCGTCT[A/G]CAGCCGCATGAAGGT | 375593 |
rs368276881 | snp | C/G/T | 4.96918e-05 | 0.00498436 | utr-variant-5-prime | TRIM73 | GRCh38.p7 | 7:75398929 | AGCCCGGGCAGTGAG[C/G/T]GTGGATGGCTTGGCA | 375593 |
rs368452848 | snp | C/T | 3.37223e-05 | 0.00410609 | intron-variant | TRIM73 | GRCh38.p7 | 7:75405087 | GAGTGGACAGGGAGG[C/T]GTCCCATCCCCATAC | 375593 |
rs369213293 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | TRIM73 | GRCh38.p7 | 7:75398758 | TTGTTTTACAGCTGT[A/G]GAAACTGAGGCCCAA | 375593 |
rs370073481 | snp | C/T | 0.00953873 | 0.0683987 | upstream-variant-2KB, intron-variant | TRIM73, LOC541473 | GRCh38.p7 | 7:75394425 | ATAATATCGAGTCTC[C/T]CATGATCACACAGAA | 375593 |
rs370416898 | snp | A/C/T | 0.000586826 | 0.01712 | intron-variant | TRIM73 | GRCh38.p7 | 7:75398898 | GGACAGGACTGAGGT[A/C/T]GGATGCCTGTGTTTC | 375593 |
rs371153005 | snp | A/G | 1.64857e-05 | 0.00287099 | missense | TRIM73 | GRCh38.p7 | 7:75398946 | TGGATGGCTTGGCAG[A/G]TGAGCCTGCTGGAGC | 375593 |
rs371634793 | snp | G/T | 0.000313172 | 0.0125095 | missense | TRIM73 | GRCh38.p7 | 7:75399000 | ATCTGCCTGGAGGTC[G/T]TCAAGGAGTCCCTAA | 375593 |
rs373021259 | snp | G/T | | | intron-variant | TRIM73 | GRCh38.p7 | 7:75398882 | ACAGGGGGAGGGGAG[G/T]GGACAGGACTGAGGT | 375593 |
rs374290043 | snp | A/C/T | 8.53809e-05 | 0.0065333 | intron-variant | TRIM73 | GRCh38.p7 | 7:75398906 | CTGAGGTCGGATGCC[A/C/T]GTGTTTCAGCCCGGG | 375593 |
rs374449175 | snp | C/G | 0.000399281 | 0.0141238 | missense | TRIM73 | GRCh38.p7 | 7:75398994 | TGTCCCATCTGCCTG[C/G]AGGTCTTCAAGGAGT | 375593 |
rs374942352 | snp | C/T | 0.000132107 | 0.00812626 | synonymous-codon | TRIM73 | GRCh38.p7 | 7:75405018 | GCGGCTGGCCCAAGC[C/T]GAGTGTGTGCTGGAA | 375593 |
rs375498048 | snp | A/C | 0.00500922 | 0.0497948 | intron-variant | TRIM73 | GRCh38.p7 | 7:75405133 | CCTTCCCAACAGTGC[A/C]CTGGCTTCCCACCTT | 375593 |
rs376052762 | snp | C/T | | | intron-variant | TRIM73 | GRCh38.p7 | 7:75398757 | TTTGTTTTACAGCTG[C/T]GGAAACTGAGGCCCA | 375593 |
rs377759066 | snp | C/T | | | synonymous-codon | TRIM73 | GRCh38.p7 | 7:75399129 | GACGGCAGCAGCTCC[C/T]TGCCCAACGTCTCCC | 375593 |
rs386714731 | multinucleotide-polymorphism | CA/TG | | | intron-variant | TRIM73 | GRCh38.p7 | 7:75398228 | ATGCTGGCTTGAGGC[CA/TG]TAGTGGGAGGCCCAG | 375593 |
rs386714732 | multinucleotide-polymorphism | CC/TG | | | intron-variant | TRIM73 | GRCh38.p7 | 7:75398250 | GGAGGCCCAGCGGAT[CC/TG]TGAGAAGCCAGGTAT | 375593 |
rs587598892 | snp | G/T | 0.00438332 | 0.0466095 | utr-variant-3-prime | TRIM73 | GRCh38.p7 | 7:75405285 | TGGTTCCTCCATTCA[G/T]CTTAACCAGCGCCTC | 375593 |
rs587605084 | snp | G/T | 0.00279162 | 0.0372561 | utr-variant-3-prime | TRIM73 | GRCh38.p7 | 7:75405513 | AGGCCAAGGCAGGAG[G/T]ATTGCTGGAGGCCGG | 375593 |
rs587610299 | snp | A/G | 0.0444908 | 0.142359 | intron-variant | TRIM73 | GRCh38.p7 | 7:75403107 | AGCCTCGGCCTCCCA[A/G]AGTGCTGGGATTACA | 375593 |
rs587619331 | snp | C/G | 0.00557542 | 0.0525036 | missense | TRIM73 | GRCh38.p7 | 7:75399236 | CAGCCTTTTCTGCGA[C/G]AAGGACCAGGAGCTC | 375593 |
rs587619845 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM73 | GRCh38.p7 | 7:75398609 | CTTGCATTATTAGTG[C/T]CACTGCAAATGACCC | 375593 |
rs587621265 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM73 | GRCh38.p7 | 7:75397995 | CCAAGGCCAGCACTT[G/T]AATGTTATCAGAGCA | 375593 |
rs587626362 | snp | A/C | 0.00119737 | 0.0244387 | missense | TRIM73 | GRCh38.p7 | 7:75404876 | GGGTGATCCGCCGCG[A/C]GTTCCAGGAGCTGCG | 375593 |
rs587628357 | snp | A/G | 4.97566e-05 | 0.00498757 | utr-variant-5-prime | TRIM73 | GRCh38.p7 | 7:75398926 | TTCAGCCCGGGCAGT[A/G]AGTGTGGATGGCTTG | 375593 |
rs587629346 | snp | A/G/T | 8.43311e-05 | 0.00649302 | intron-variant | TRIM73 | GRCh38.p7 | 7:75405088 | AGTGGACAGGGAGGC[A/G/T]TCCCATCCCCATACC | 375593 |
rs587629628 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM73 | GRCh38.p7 | 7:75399534 | CGCACAGGATGGGAG[C/T]TCCCTGGTGTCACGT | 375593 |
rs587635016 | snp | G/T | 1.67192e-05 | 0.00289125 | upstream-variant-2KB, nc-transcript-variant | TRIM73, LOC541473 | GRCh38.p7 | 7:75394300 | GCCGAGGAGTTTTCC[G/T]AAAGTAATTAGAATC | 375593 |
rs587636897 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TRIM73, LOC541473 | GRCh38.p7 | 7:75394479 | GCTGCCCGACACCAC[A/G]AGGTACAGGAATAAA | 375593 |
rs587639389 | snp | C/T | 0.000103654 | 0.00719834 | missense | TRIM73 | GRCh38.p7 | 7:75405004 | CAGGGAACCCGGGAG[C/T]GGCTGGCCCAAGCCG | 375593 |
rs587645740 | snp | C/T | 0.00597247 | 0.0543191 | upstream-variant-2KB, intron-variant | TRIM73, LOC541473 | GRCh38.p7 | 7:75394102 | AAGCCATCTCCCAAA[C/T]GCCTAGGTCTCAAGG | 375593 |
rs587646349 | snp | C/G | 0.000336621 | 0.0129691 | missense | TRIM73 | GRCh38.p7 | 7:75399117 | TGGCAGGTGGTGGAC[C/G]GCAGCAGCTCCTTGC | 375593 |
rs587651991 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | TRIM73 | GRCh38.p7 | 7:75398204 | TGCTGGGAAGAAGAA[A/C]AGCCAGTGATGCTGG | 375593 |
rs587652966 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TRIM73, LOC541473 | GRCh38.p7 | 7:75394413 | ACCCACGCCACCATA[A/G]TATCGAGTCTCTCAT | 375593 |
rs587653866 | snp | C/T | 0.00149445 | 0.0272945 | upstream-variant-2KB, intron-variant | TRIM73, LOC541473 | GRCh38.p7 | 7:75394211 | CAGCCTGAGGCATGG[C/T]GCCTCATCTCGCTCC | 375593 |
rs587659619 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM73 | GRCh38.p7 | 7:75399548 | GCTCCCTGGTGTCAC[A/G]TGCTCACCCCTTCCT | 375593 |
rs587661242 | snp | A/T | 0.00279162 | 0.0372561 | utr-variant-3-prime | TRIM73 | GRCh38.p7 | 7:75405514 | GGCCAAGGCAGGAGT[A/T]TTGCTGGAGGCCGGG | 375593 |
rs587663811 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TRIM73, LOC541473 | GRCh38.p7 | 7:75394784 | GTAAATCTCTTATTT[A/G]GGAGGCTGAGGCTGG | 375593 |
rs587672391 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TRIM73, LOC541473 | GRCh38.p7 | 7:75393757 | TTTATTCAAACTTCC[A/G]GGCTCAGTTCAAATG | 375593 |
rs587674136 | snp | C/T | 0.132066 | 0.220435 | intron-variant | TRIM73 | GRCh38.p7 | 7:75403112 | CGGCCTCCCAAAGTG[C/T]TGGGATTACAGGCGT | 375593 |
rs587681828 | snp | A/G | 0.00202088 | 0.0317231 | missense | TRIM73 | GRCh38.p7 | 7:75404891 | AGTTCCAGGAGCTGC[A/G]CCACCCGGTGGACGA | 375593 |
rs587683103 | snp | A/G/T | 4.29562e-05 | 0.00463425 | upstream-variant-2KB, intron-variant | TRIM73, LOC541473 | GRCh38.p7 | 7:75394222 | ATGGTGCCTCATCTC[A/G/T]CTCCTAAACAATCCC | 375593 |
rs587685228 | snp | C/T | 3.60789e-05 | 0.00424714 | synonymous-codon | TRIM73 | GRCh38.p7 | 7:75404997 | GCAGGCCCAGGGAAC[C/T]CGGGAGCGGCTGGCC | 375593 |
rs587685748 | snp | A/G | 0.000560178 | 0.0167265 | synonymous-codon | TRIM73 | GRCh38.p7 | 7:75398993 | GTGTCCCATCTGCCT[A/G]GAGGTCTTCAAGGAG | 375593 |
rs587698427 | snp | A/G | 1.65277e-05 | 0.00287464 | upstream-variant-2KB, intron-variant | TRIM73, LOC541473 | GRCh38.p7 | 7:75394369 | TCACTAGAATAGAGG[A/G]AAGAATGTAAGGAAA | 375593 |
rs587698983 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM73 | GRCh38.p7 | 7:75398145 | GGCAGTGGTGCAGGC[A/G]TCCAGCTGCACTTCC | 375593 |
rs587700844 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM73 | GRCh38.p7 | 7:75399502 | GCTAAACCCAGGTGC[C/T]GGGGATTGAAGCTAC | 375593 |
rs587713603 | snp | C/T | 0.103438 | 0.202533 | utr-variant-3-prime | TRIM73 | GRCh38.p7 | 7:75405264 | GCACGGGCATCTCAG[C/T]TCCACTGGTTCCTCC | 375593 |
rs587721941 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | TRIM73, LOC541473 | GRCh38.p7 | 7:75394003 | TGGGAAGTAAGCATT[C/T]GTCGATTTTTACTTA | 375593 |
rs587723544 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TRIM73, LOC541473 | GRCh38.p7 | 7:75394161 | CCAGCCTCAGCAAAG[C/T]CAATTCAAAGAACCT | 375593 |
rs587725044 | snp | C/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | TRIM73, LOC541473 | GRCh38.p7 | 7:75395562 | GATGGGACACGTAAC[C/G]GGACCACACAGGGCA | 375593 |
rs587728601 | snp | C/T | 0.00199481 | 0.0315187 | utr-variant-3-prime | TRIM73 | GRCh38.p7 | 7:75405316 | CCAAGCAGCTGCCTA[C/T]AGCTGGCTCTATAAC | 375593 |
rs587731907 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM73 | GRCh38.p7 | 7:75399519 | GGGATTGAAGCTACA[C/T]GCACAGGATGGGAGC | 375593 |
rs587732630 | snp | A/G | 0.000798403 | 0.0199641 | missense | TRIM73 | GRCh38.p7 | 7:75404873 | GCTGGGTGATCCGCC[A/G]CGAGTTCCAGGAGCT | 375593 |
rs587741041 | snp | A/G | 0.00184041 | 0.030279 | missense | TRIM73 | GRCh38.p7 | 7:75404918 | ACGAGGAGAAGGCCC[A/G]CTGCCTGGAGGGGAT | 375593 |
rs587741477 | snp | C/G | 0.108402 | 0.206034 | intron-variant | TRIM73 | GRCh38.p7 | 7:75402448 | CCAGGCTGGAGTGCA[C/G]TGGGCGATCTCGGCT | 375593 |
rs587744714 | snp | A/G | 0.000382044 | 0.0138158 | missense | TRIM73 | GRCh38.p7 | 7:75399096 | AAGGTGCGCTGCCCC[A/G]TGTGCTGGCAGGTGG | 375593 |
rs587748577 | snp | A/T | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | TRIM73, LOC541473 | GRCh38.p7 | 7:75394407 | CAAAACACCCACGCC[A/T]CCATAATATCGAGTC | 375593 |
rs587755849 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | TRIM73 | GRCh38.p7 | 7:75398870 | GGTGAGTGCTGGACA[C/G]GGGGAGGGGAGTGGA | 375593 |