SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3215 | snp | C/T | 0.0777841 | 0.181223 | intron-variant | USP48 | GRCh38.p7 | 1:21738832 | ttagttaattaactg[C/T]tgtatccttcatgcc | 84196 |
rs167988 | snp | C/T | 0.0876345 | 0.190099 | intron-variant | USP48 | GRCh38.p7 | 1:21754740 | GCCTCACTGGAGGCA[C/T]TGTACTGTGAAGCTA | 84196 |
rs333168 | snp | C/T | 0.438666 | 0.164028 | intron-variant | USP48 | GRCh38.p7 | 1:21708509 | ctcaaaaaaCAAaaa[C/T]aaacaaacaaacaaa | 84196 |
rs333169 | snp | A/T | 0.423881 | 0.179625 | intron-variant | USP48 | GRCh38.p7 | 1:21707894 | ATAggccaggcacag[A/T]ggcttgctcctgtaa | 84196 |
rs333170 | snp | C/T | 0.247621 | 0.249989 | intron-variant | USP48 | GRCh38.p7 | 1:21707451 | GCTCAATCTGAAAAC[C/T]ATCTCCAGTCAAGCA | 84196 |
rs333171 | snp | C/T | 0.254664 | 0.249956 | intron-variant | USP48 | GRCh38.p7 | 1:21707212 | GGATTCCAGGAGTCC[C/T]GGGACCTCTGTGCCA | 84196 |
rs333172 | snp | A/C | 0.0759472 | 0.179459 | intron-variant | USP48 | GRCh38.p7 | 1:21706985 | TTTCTTGCTTTGCTA[A/C]AGTTTGGTATTTCTA | 84196 |
rs333173 | snp | G/T | 0.364193 | 0.222396 | intron-variant, downstream-variant-500B | USP48 | GRCh38.p7 | 1:21706077 | TAAAAAATACCAGAG[G/T]CAACCAAATCAGTAA | 84196 |
rs333174 | snp | C/T | 0.39121 | 0.2063 | intron-variant | USP48 | GRCh38.p7 | 1:21740845 | gtgatttccatttct[C/T]ggagtttgatttggt | 84196 |
rs333175 | snp | C/T | 0.0901694 | 0.192235 | intron-variant | USP48 | GRCh38.p7 | 1:21742499 | tggagtgcagtgccg[C/T]gatcttggctcaccg | 84196 |
rs333176 | snp | A/G | 0.0876345 | 0.190099 | intron-variant | USP48 | GRCh38.p7 | 1:21742996 | taaaCCACTTTAAAC[A/G]TTAAAAACACCCAGT | 84196 |
rs333177 | snp | C/G | 0.0883596 | 0.190715 | intron-variant | USP48 | GRCh38.p7 | 1:21743299 | TTGTGTTTCTGAGAA[C/G]TAGGTCCCGCTGAGG | 84196 |
rs333178 | snp | A/G | 0.0879971 | 0.190408 | intron-variant | USP48 | GRCh38.p7 | 1:21743453 | GAAGGTAGTGGGAGA[A/G]GAACCCCACTGGTGA | 84196 |
rs333179 | snp | C/T | 0.0876345 | 0.190099 | intron-variant | USP48 | GRCh38.p7 | 1:21744967 | CTCAAAAGATGGATC[C/T]AAAAGAAGATCTGTT | 84196 |
rs333180 | snp | A/G | 0.0876345 | 0.190099 | intron-variant | USP48 | GRCh38.p7 | 1:21745072 | AGAAATACAAACCAT[A/G]TGTAATTTTGTCATC | 84196 |
rs333181 | snp | C/G | 0.391163 | 0.209671 | intron-variant, upstream-variant-2KB | USP48 | GRCh38.p7 | 1:21734211 | CAAAAGCAACCTGGG[C/G]AACCCAGGGAGACTC | 84196 |
rs333182 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant, upstream-variant-2KB | USP48 | GRCh38.p7 | 1:21733238 | ctggccaacatggtg[A/G]aaccccgtctctact | 84196 |
rs333183 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | USP48 | GRCh38.p7 | 1:21733022 | ATTCTTACAGACAAC[A/G]CCTGAACAAAAAAGG | 84196 |
rs333184 | snp | C/G | 0.0513262 | 0.151752 | intron-variant | USP48 | GRCh38.p7 | 1:21718011 | TATGCATATTAGGGG[C/G]TTCATTTTTGCATGC | 84196 |
rs333185 | snp | A/G | 0.389715 | 0.207315 | intron-variant | USP48 | GRCh38.p7 | 1:21716150 | gaaagaaaaaaaatc[A/G]tatgctgaggttact | 84196 |
rs333186 | snp | C/T | 0.402277 | 0.198272 | intron-variant | USP48 | GRCh38.p7 | 1:21714210 | TAACCCATGTTCATG[C/T]GTTTCTTGTTATGTG | 84196 |
rs333187 | snp | A/G | 0.0490535 | 0.14873 | intron-variant | USP48 | GRCh38.p7 | 1:21713972 | CACTTTAGCTTGCGA[A/G]GTGAGTGGCATTCCC | 84196 |
rs333188 | snp | A/G | 0.417683 | 0.185425 | intron-variant | USP48 | GRCh38.p7 | 1:21713801 | CAGCAGGAGAAGATG[A/G]GTTGACCTCGTGAGT | 84196 |
rs333189 | snp | C/T | 0.0876345 | 0.190099 | intron-variant | USP48 | GRCh38.p7 | 1:21747730 | caaaaattagccggg[C/T]gtggtggcaggcgcc | 84196 |
rs333190 | snp | C/G | 0.0770498 | 0.180522 | intron-variant | USP48 | GRCh38.p7 | 1:21749332 | gaggcctgggacatt[C/G]aaatgttagggatca | 84196 |
rs333191 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | USP48 | GRCh38.p7 | 1:21749430 | gagtttggctttgag[C/T]atgttacgtttgaga | 84196 |
rs333192 | snp | A/G | 0.0777841 | 0.181223 | intron-variant | USP48 | GRCh38.p7 | 1:21750045 | ttttaagggataact[A/G]tgggtgctgagaata | 84196 |
rs333193 | snp | C/T | 0.0876345 | 0.190099 | intron-variant | USP48 | GRCh38.p7 | 1:21751022 | TGAATGTATACATAG[C/T]GTAATAGACAAGCTT | 84196 |
rs333194 | snp | C/T | 0.0876345 | 0.190099 | intron-variant | USP48 | GRCh38.p7 | 1:21751163 | AGAATGTGCTAAATA[C/T]GAAACTTTTTTACAT | 84196 |
rs333195 | snp | G/T | 0.390651 | 0.206682 | intron-variant | USP48 | GRCh38.p7 | 1:21751179 | TTGTCTAATGAAAAC[G/T]AGAATGTGCTAAATA | 84196 |
rs333196 | snp | A/T | 0.0876345 | 0.190099 | intron-variant | USP48 | GRCh38.p7 | 1:21751204 | GTTATCATAAAGGTA[A/T]TTTACCTTGTTGTCT | 84196 |
rs333197 | snp | A/G | 0.0777841 | 0.181223 | intron-variant | USP48 | GRCh38.p7 | 1:21751910 | ctgcctcagcctccc[A/G]agtagctgagattac | 84196 |
rs333198 | snp | C/G | 0.0876345 | 0.190099 | intron-variant | USP48 | GRCh38.p7 | 1:21751917 | gattctcctgcctca[C/G]cctcccgagtagctg | 84196 |
rs333199 | snp | C/T | 0.0876345 | 0.190099 | intron-variant | USP48 | GRCh38.p7 | 1:21752174 | acaacatttgggtga[C/T]ggttacattaaaacc | 84196 |
rs333200 | snp | C/T | 0.0513262 | 0.151752 | intron-variant | USP48 | GRCh38.p7 | 1:21753430 | gtagctgggattaca[C/T]gtgtgcaccaccaca | 84196 |
rs333201 | snp | A/T | 0.0876345 | 0.190099 | intron-variant | USP48 | GRCh38.p7 | 1:21753719 | gaaccccagcctccc[A/T]agtagcagggattac | 84196 |
rs333202 | snp | A/G | 0.0876345 | 0.190099 | intron-variant | USP48 | GRCh38.p7 | 1:21754016 | gtactaccatgcccc[A/G]ctaatttttgtattt | 84196 |
rs333203 | snp | A/G | 0.0876345 | 0.190099 | intron-variant | USP48 | GRCh38.p7 | 1:21754101 | caatcttggctaact[A/G]caacctccgcctgtc | 84196 |
rs333204 | snp | C/T | 0.0777841 | 0.181223 | intron-variant | USP48 | GRCh38.p7 | 1:21754282 | CACTGTAGTCATGAT[C/T]GCTGTTGTTGCTTTA | 84196 |
rs333205 | snp | C/G | 0.0490535 | 0.14873 | intron-variant | USP48 | GRCh38.p7 | 1:21754384 | AACTCTAAAATTCTA[C/G]GGTTTTGTATTCTTC | 84196 |
rs333206 | snp | G/T | 0.0876345 | 0.190099 | intron-variant | USP48 | GRCh38.p7 | 1:21755857 | tttttatagagacag[G/T]gtcttgctctgttgc | 84196 |
rs333207 | snp | C/T | 0.0876345 | 0.190099 | intron-variant | USP48 | GRCh38.p7 | 1:21756247 | gtgatgtggctgcct[C/T]ggccttccaaagtgc | 84196 |
rs333208 | snp | C/G | 0.0883963 | 0.190884 | intron-variant | USP48 | GRCh38.p7 | 1:21757122 | GTTCCCTCTACCACC[C/G]CCAATCTTTAAAATC | 84196 |
rs482599 | snp | A/G | | | intron-variant | USP48 | GRCh38.p7 | 1:21756368 | tcagcctcttgagaa[A/G]ctgggattacaggcg | 84196 |
rs482791 | snp | G/T | 0.0577344 | 0.159793 | intron-variant | USP48 | GRCh38.p7 | 1:21709763 | AAACACTCATCCCAC[G/T]TAAAAGCCAGTCACT | 84196 |
rs487529 | snp | A/G | 0.0872718 | 0.189788 | intron-variant | USP48 | GRCh38.p7 | 1:21729362 | GTTGCTGCCCTGAAG[A/G]CAGTCTGAGTCTGAA | 84196 |
rs499361 | snp | C/T | 0.0879971 | 0.190408 | intron-variant, nc-transcript-variant | USP48 | GRCh38.p7 | 1:21725738 | gagatggaatttcac[C/T]cttgttgcccaggct | 84196 |
rs516056 | snp | A/G | 0 | 0 | intron-variant | USP48 | GRCh38.p7 | 1:21743484 | AATAACCCAGGTGAA[A/G]AAGCAGGGGCAGCAG | 84196 |
rs516058 | snp | C/G | 0 | 0 | intron-variant | USP48 | GRCh38.p7 | 1:21743490 | CCAGGTGAAGAAGCA[C/G]GGGCAGCAGAGTAAG | 84196 |
rs516966 | snp | G/T | 0 | 0 | intron-variant | USP48 | GRCh38.p7 | 1:21743593 | ATGCATGCTTATATA[G/T]TAAAATGCTAAAGAA | 84196 |
rs517285 | snp | G/T | 0 | 0 | intron-variant | USP48 | GRCh38.p7 | 1:21743650 | ATGAAAGTCAGATAA[G/T]TGGTTACACTTAAGG | 84196 |
rs518481 | snp | A/G | 0.0554779 | 0.157039 | intron-variant | USP48 | GRCh38.p7 | 1:21738602 | gggaggccgaggcag[A/G]tggaccacttgaggc | 84196 |
rs518633 | snp | C/G | 0 | 0 | intron-variant | USP48 | GRCh38.p7 | 1:21743728 | GCTTCCGGGGTACCA[C/G]AAATATTTTTCTTTC | 84196 |
rs523504 | snp | A/G | 0.402806 | 0.197864 | intron-variant | USP48 | GRCh38.p7 | 1:21712494 | GTTTCTGTTAAAACC[A/G]CTTTCTGGAGGTGTG | 84196 |
rs527341 | snp | C/G | | | intron-variant | USP48 | GRCh38.p7 | 1:21712332 | tcactgtgtcgccca[C/G]gctggagcgcaatcg | 84196 |
rs529292 | snp | C/T | 0.255503 | 0.249939 | intron-variant | USP48 | GRCh38.p7 | 1:21718715 | CAAAAATTATCCAGG[C/T]GTGGTGGCATGCACC | 84196 |
rs535911 | snp | C/T | 0.38821 | 0.208322 | intron-variant | USP48 | GRCh38.p7 | 1:21722489 | GGCTGTAGTGCACTA[C/T]GATTCCACCACTGTA | 84196 |
rs539791 | snp | G/T | 0 | 0 | intron-variant, nc-transcript-variant | USP48 | GRCh38.p7 | 1:21724769 | GGATAAAGTACACTA[G/T]AACTGAGTCATCAAT | 84196 |
rs540670 | snp | G/T | 0 | 0 | intron-variant, nc-transcript-variant | USP48 | GRCh38.p7 | 1:21724860 | GAAAGGAAGTCCCTA[G/T]AATTCCCTAAAAGCC | 84196 |
rs540842 | snp | G/T | 0 | 0 | intron-variant | USP48 | GRCh38.p7 | 1:21743882 | GAAACTTCAACTATA[G/T]AAGGACAAGGCAAGG | 84196 |
rs540856 | snp | A/G | | | intron-variant | USP48 | GRCh38.p7 | 1:21743885 | ACTTCAACTATAGAA[A/G]GACAAGGCAAGGTAA | 84196 |
rs541552 | snp | A/G | 0.0876345 | 0.190099 | intron-variant | USP48 | GRCh38.p7 | 1:21754518 | CAGGCAAAGAAGGGT[A/G]GATTTGGAGCTGAGA | 84196 |
rs547709 | snp | A/G | 0.0876345 | 0.190099 | intron-variant, upstream-variant-2KB | USP48 | GRCh38.p7 | 1:21737734 | TTTAGAAGAATAATG[A/G]TGTGAAAAGATATTA | 84196 |
rs547940 | snp | C/G | 0 | 0 | intron-variant, nc-transcript-variant | USP48 | GRCh38.p7 | 1:21725195 | TCGAATGTGGCTCCA[C/G]AGGaagagcacagga | 84196 |
rs565029 | snp | A/G | 0.0872718 | 0.189788 | intron-variant | USP48 | GRCh38.p7 | 1:21746166 | ATCTCTTTCCAAAAA[A/G]ATAAAAAATTTCTAG | 84196 |
rs569514 | snp | C/T | 0.0532157 | 0.154195 | intron-variant | USP48 | GRCh38.p7 | 1:21719671 | tcaggagttcaagac[C/T]agcctggccaacatg | 84196 |
rs571721 | snp | C/T | 0 | 0 | intron-variant | USP48 | GRCh38.p7 | 1:21721841 | ATGTTTTCAGCACTT[C/T]ACAAACACAGACACA | 84196 |
rs577753 | snp | C/T | 0.255782 | 0.249933 | intron-variant | USP48 | GRCh38.p7 | 1:21720582 | GCCCAAGCTGCAGTG[C/T]AGTGGCGCAATCTTG | 84196 |
rs692790 | snp | C/T | 0.40263 | 0.198 | intron-variant | USP48 | GRCh38.p7 | 1:21718436 | ATGGGGGAAGGAGAA[C/T]AGAGACATATTACTC | 84196 |
rs829372 | snp | C/T | 0.254664 | 0.249956 | intron-variant | USP48 | GRCh38.p7 | 1:21703696 | AGATCTAAAAACATA[C/T]GTCAAAGTTACTAGT | 84196 |
rs829383 | snp | C/T | 0.0460142 | 0.144533 | intron-variant | USP48 | GRCh38.p7 | 1:21690752 | CAGGCTGGTCTCGAA[C/T]TCTTAGACTCAAGCA | 84196 |
rs829384 | snp | C/G | 0.324619 | 0.238604 | intron-variant | USP48 | GRCh38.p7 | 1:21692442 | CACAGCTGCTGGACT[C/G]TAAAAATGCTTGTTC | 84196 |
rs829385 | snp | A/G | 0.0752113 | 0.178743 | intron-variant | USP48 | GRCh38.p7 | 1:21694074 | CCAGTGGTAAATCTC[A/G]AACCCTAGGCAGAAG | 84196 |
rs829386 | snp | C/T | 0.0456336 | 0.143994 | intron-variant, downstream-variant-500B | USP48 | GRCh38.p7 | 1:21694820 | TAATTTGTCACATGT[C/T]GAGGTTGTGCCAGGA | 84196 |
rs829387 | snp | G/T | 0.134801 | 0.222049 | intron-variant | USP48 | GRCh38.p7 | 1:21696658 | TATTAGGTAGGACAC[G/T]GTCTTTATTTTTAGA | 84196 |
rs829388 | snp | C/T | 0.147991 | 0.228242 | intron-variant | USP48 | GRCh38.p7 | 1:21697490 | AACATGGTGAAACCC[C/T]GTCTCTACTAAAAAT | 84196 |
rs829397 | snp | A/G | 0.093777 | 0.195178 | downstream-variant-500B | USP48 | GRCh38.p7 | 1:21677907 | TGGTCCCTTGGTTCC[A/G]CTCCTAGGATGGTTT | 84196 |
rs829403 | snp | A/C | 0.438666 | 0.164028 | intron-variant | USP48 | GRCh38.p7 | 1:21682672 | atgaggtcacgagtt[A/C]cagagcagcctggac | 84196 |
rs829420 | snp | G/T | 0.440746 | 0.161604 | intron-variant | USP48 | GRCh38.p7 | 1:21687068 | AAGCTTCCACATATT[G/T]TTACAGTAGAATACA | 84196 |
rs853481 | snp | C/T | 0.0494327 | 0.149241 | intron-variant | USP48 | GRCh38.p7 | 1:21686099 | ttttttttagagtct[C/T]tgttgcccagactgg | 84196 |
rs862590 | snp | G/T | 0 | 0 | intron-variant | USP48 | GRCh38.p7 | 1:21702255 | AGGGCATAATTATAA[G/T]TTACCCTTCTAAAAA | 84196 |
rs862591 | snp | C/T | 0 | 0 | intron-variant | USP48 | GRCh38.p7 | 1:21702453 | ttaacacctccactt[C/T]ccaaacatatccaat | 84196 |
rs884726 | snp | A/G | 0.413748 | 0.188909 | upstream-variant-2KB | USP48 | GRCh38.p7 | 1:21783925 | AATTCTCATAAAGCT[A/G]CTCTTTATGTCCTGG | 84196 |
rs900488 | snp | C/G | 0.357877 | 0.225527 | intron-variant | USP48 | GRCh38.p7 | 1:21723771 | TATTCCTTACACTTT[C/G]CACAAAGGATTTGCT | 84196 |
rs900489 | snp | G/T | 0.248188 | 0.249993 | intron-variant | USP48 | GRCh38.p7 | 1:21722158 | ACACTAAAAGGAAAA[G/T]CAAAATGAAGGGCCT | 84196 |
rs1018102 | snp | A/G | 0.499295 | 0.0187567 | intron-variant | USP48 | GRCh38.p7 | 1:21714580 | TAAGTTCCCCTTCCC[A/G]CCTCCAAAGAGTCTG | 84196 |
rs1059218 | snp | C/T | 0.325799 | 0.238232 | utr-variant-3-prime, nc-transcript-variant | USP48 | GRCh38.p7 | 1:21679172 | CGTCTTTACTTGCCC[C/T]CTCCCACCCACCACC | 84196 |
rs1341557 | snp | A/G | 0.498871 | 0.0237351 | intron-variant | USP48 | GRCh38.p7 | 1:21683167 | tactcaggaggctga[A/G]ccaggagaatcactt | 84196 |
rs1384673 | snp | C/T | 0.267364 | 0.249396 | intron-variant | USP48 | GRCh38.p7 | 1:21741766 | CTGGTTTCGGACTTA[C/T]GGCCTTAAGCAGTCC | 84196 |
rs1384674 | snp | C/T | 0.0803491 | 0.183626 | intron-variant | USP48 | GRCh38.p7 | 1:21741709 | gattacaggcgtgaa[C/T]caccacacctggccT | 84196 |
rs1618590 | snp | A/G | 0.0444908 | 0.142359 | intron-variant | USP48 | GRCh38.p7 | 1:21690226 | GTAGGCTGACTGTAA[A/G]CAATAGTGGTTTTGT | 84196 |
rs1630342 | snp | G/T | | | intron-variant | USP48 | GRCh38.p7 | 1:21701663 | AGGCAGTATATGGAG[G/T]ATGTGGGGGCTGGGA | 84196 |
rs1631990 | snp | C/G | | | intron-variant | USP48 | GRCh38.p7 | 1:21701850 | ATACATTTAAGAGGT[C/G]TCTGCAGCAGCAGTT | 84196 |
rs1632697 | snp | A/G | 0.0876345 | 0.190099 | intron-variant | USP48 | GRCh38.p7 | 1:21745831 | CTGCCTCCTTTGTTC[A/G]GGCAATTGAAATTGA | 84196 |
rs1681249 | snp | C/G | | | intron-variant | USP48 | GRCh38.p7 | 1:21702326 | TTGTCTTTAATCCCA[C/G]AAAGCATGGAATTAA | 84196 |
rs1772712 | snp | A/C | 0.00843867 | 0.0644059 | intron-variant | USP48 | GRCh38.p7 | 1:21701655 | CCCTAGGAAGGCAGG[A/C]TATGGAGGATGTGGG | 84196 |
rs1772713 | snp | A/G | 0 | 0 | intron-variant | USP48 | GRCh38.p7 | 1:21702068 | CTCTTATTAAACTGA[A/G]TAATGAAACTACATC | 84196 |
rs1772714 | snp | A/G | 0 | 0 | intron-variant | USP48 | GRCh38.p7 | 1:21702075 | TAAACTGAATAATGA[A/G]ACTACATCTAAATTG | 84196 |
rs1772715 | snp | G/T | 0 | 0 | intron-variant | USP48 | GRCh38.p7 | 1:21702362 | TTAATAAGATATCTA[G/T]AGATATGGGTCAGGA | 84196 |
rs1809474 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | USP48 | GRCh38.p7 | 1:21679855 | CACGCCACCATGCCC[A/G]GCTAATTTTTGTATT | 84196 |