SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs11221 | snp | A/G | 0.0486741 | 0.148216 | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:211865 | TTTAAAATAAATTGT[A/G]ATCAATAATAGTACC | 9097 |
rs16428 | in-del | -/AGAG | 0.460142 | 0.135426 | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:211910 | AATCCACAGTACATC[-/AGAG]AGAGACACAATAATA | 9097 |
rs471274 | snp | G/T | 0.456717 | 0.140599 | intron-variant | USP14 | GRCh38.p7 | 18:203081 | TGAGGAGACAAAATG[G/T]AAAGAAATCCCATTA | 9097 |
rs477066 | snp | C/T | 0.462253 | 0.132093 | intron-variant | USP14 | GRCh38.p7 | 18:159281 | AATCCAATGCAACGT[C/T]TGATGAAACGAAAAC | 9097 |
rs477718 | snp | A/C | 0.22263 | 0.248497 | intron-variant | USP14 | GRCh38.p7 | 18:186210 | ctcatgcctgtgatc[A/C]cagtgctttgggagg | 9097 |
rs478326 | snp | A/G | 0.5 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:181055 | TACGTGTGCTGTAAC[A/G]TGAATGAACCATGAA | 9097 |
rs479140 | snp | A/C/G | 0.5 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:180991 | TACGTGTGCTGTAAC[A/C/G]TGAATGAACCATGAA | 9097 |
rs479167 | snp | A/T | 0.277778 | 0.248452 | intron-variant | USP14 | GRCh38.p7 | 18:180979 | aacatgaatgaacca[A/T]gaaatactattcagc | 9097 |
rs485211 | snp | C/T | 0.222928 | 0.24853 | intron-variant | USP14 | GRCh38.p7 | 18:166277 | TATTGTGTTACCTTA[C/T]GCAGTTGAAGCAAAT | 9097 |
rs489560 | snp | A/G | 0.462034 | 0.132445 | intron-variant | USP14 | GRCh38.p7 | 18:165098 | GGATAACAGGTCACC[A/G]CCACCATGCGTGACA | 9097 |
rs489577 | snp | A/T | 0.465052 | 0.127485 | intron-variant | USP14 | GRCh38.p7 | 18:177101 | TTAGGTGCTTTTTTT[A/T]AAAATATCCTTAAGT | 9097 |
rs490425 | snp | A/C | 0.462363 | 0.131916 | intron-variant | USP14 | GRCh38.p7 | 18:165022 | GGCGCCATCTCGGCT[A/C]ACTGCAACCACCGCC | 9097 |
rs493422 | snp | C/T | 0.269809 | 0.249214 | intron-variant | USP14 | GRCh38.p7 | 18:202494 | AGCCCAAGAAACTCC[C/T]GTTCTTTACGTTTTA | 9097 |
rs495284 | snp | C/T | 0.0865458 | 0.189163 | intron-variant | USP14 | GRCh38.p7 | 18:177063 | GGAAGACATGACAAG[C/T]TCTGGACTTGAAAAA | 9097 |
rs499571 | snp | A/T | 0.0711525 | 0.174681 | intron-variant | USP14 | GRCh38.p7 | 18:189598 | agtgattctcctacc[A/T]cagcctcctgagtag | 9097 |
rs499634 | snp | A/C | 0 | 0 | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:212564 | agctgagatcacacc[A/C]ctgcactccagcctg | 9097 |
rs503086 | snp | A/C | 0 | 0 | synonymous-codon | USP14 | GRCh38.p7 | 18:197672 | ACAGAAATTGGAAGC[A/C]ATAGAGGATGATTCT | 9097 |
rs505610 | snp | C/T | 0.19334 | 0.243495 | intron-variant | USP14 | GRCh38.p7 | 18:173718 | GTGAGCCACCGCACC[C/T]GGTCTATTATCTGTT | 9097 |
rs507184 | snp | A/G | 0.222333 | 0.248464 | intron-variant | USP14 | GRCh38.p7 | 18:186998 | TAGTTTGACCTTTCA[A/G]ATATTGGCAGTTGTT | 9097 |
rs511573 | snp | C/T | 0.260227 | 0.249791 | intron-variant | USP14 | GRCh38.p7 | 18:175140 | agttaatttttataa[C/T]tgactttgtatcctg | 9097 |
rs511859 | snp | C/T | 0.0603597 | 0.1629 | intron-variant | USP14 | GRCh38.p7 | 18:193365 | TTGGACATTTTAATA[C/T]TGTTAAATCTTTGGG | 9097 |
rs513271 | snp | A/T | | | intron-variant | USP14 | GRCh38.p7 | 18:171604 | gttttgagagacata[A/T]acgagatgaatgttg | 9097 |
rs513402 | snp | C/T | 0.474634 | 0.109726 | intron-variant | USP14 | GRCh38.p7 | 18:184704 | GCCTGGGAGGTCGAG[C/T]CTGCAGTGAGCCATC | 9097 |
rs516905 | snp | A/T | 0 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:164428 | CGTTAATGGGTAGGA[A/T]GCAATAAAGGCCAAA | 9097 |
rs523239 | snp | A/G | 0.462253 | 0.132093 | intron-variant | USP14 | GRCh38.p7 | 18:162039 | GTATCTCATATAACC[A/G]GAATCATCCATGTTG | 9097 |
rs541733 | snp | A/G | 0.261332 | 0.249743 | intron-variant | USP14 | GRCh38.p7 | 18:172410 | gttgttgaaatgaca[A/G]taaaggatttaaaat | 9097 |
rs544730 | snp | G/T | 0 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:164415 | TTCATTTTTTTTTTT[G/T]GGCCTTTATGGCTTC | 9097 |
rs545447 | snp | C/T | 0.496999 | 0.0386216 | intron-variant | USP14 | GRCh38.p7 | 18:208222 | atttacaaaaacaaa[C/T]acaatatgaaataga | 9097 |
rs545684 | snp | A/G | 0.269538 | 0.249235 | intron-variant | USP14 | GRCh38.p7 | 18:159382 | GATTGGCGTTTGACA[A/G]GGGCTTGTATTGTTT | 9097 |
rs551835 | snp | A/G | 0.236434 | 0.249632 | intron-variant | USP14 | GRCh38.p7 | 18:160887 | AGCCTTTCAGGAATT[A/G]CACATTGCCTACAAC | 9097 |
rs553212 | snp | C/T | 0.266546 | 0.249452 | intron-variant | USP14 | GRCh38.p7 | 18:195405 | TGGGTTCAGTCTGTA[C/T]AATGATGATAGGTGA | 9097 |
rs557249 | snp | A/C | 0.4582 | 0.138394 | upstream-variant-2KB, intron-variant | USP14, LOC105371951 | GRCh38.p7 | 18:156739 | atatgcactgggaaa[A/C]caaaaactttgtgtg | 9097 |
rs562117 | snp | G/T | 0.221737 | 0.248397 | upstream-variant-2KB, intron-variant | USP14, LOC105371951 | GRCh38.p7 | 18:157065 | tttgtttgtttgttt[G/T]gagacagggtctcac | 9097 |
rs562748 | snp | A/G | 0.261608 | 0.24973 | intron-variant | USP14 | GRCh38.p7 | 18:167536 | catacgtgagagtga[A/G]accctgtctcaaaaa | 9097 |
rs563155 | snp | C/T | 0.296364 | 0.245663 | synonymous-codon | USP14 | GRCh38.p7 | 18:166819 | CATCAAAATAAAAAA[C/T]GTAAGTATTATCTTA | 9097 |
rs565653 | snp | A/G | 0.22263 | 0.248497 | intron-variant | USP14 | GRCh38.p7 | 18:171973 | tggccaggcatggtg[A/G]ctcactcctataatc | 9097 |
rs566693 | snp | A/C | 0 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:188939 | cggctttggcctccc[A/C]aagtgctgggattac | 9097 |
rs566748 | snp | A/T | 0.219947 | 0.248187 | intron-variant | USP14 | GRCh38.p7 | 18:199557 | caacaaaaagcagaa[A/T]tttttttttaaaaca | 9097 |
rs567685 | snp | A/C | 0 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:189044 | TTTATATTTTCCTAC[A/C]AAATTGTCCTGTCTT | 9097 |
rs569449 | snp | G/T | 0 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:189200 | tagttttcaaagaat[G/T]ggctattagatttgt | 9097 |
rs572981 | snp | A/G | 0.19459 | 0.243782 | intron-variant | USP14 | GRCh38.p7 | 18:206874 | GGGCAATGTTGCCCA[A/G]ACTGGAGGGCAGTGG | 9097 |
rs574176 | snp | A/G | 0.5 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:180923 | TGTGCTGTAACGTGA[A/G]TGAACCATGAAATAC | 9097 |
rs575268 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | USP14 | GRCh38.p7 | 18:185110 | TCTCAATATACACAG[C/T]GTTAACAGTTACTAG | 9097 |
rs575847 | snp | A/C | | | intron-variant | USP14 | GRCh38.p7 | 18:206534 | taaaaattaaaaaaa[A/C]ctttcttctgcaaaa | 9097 |
rs579219 | snp | C/T | 0.455263 | 0.142713 | intron-variant | USP14 | GRCh38.p7 | 18:193162 | TTGATTTGTATAATA[C/T]ATATCTTTGGGGTTG | 9097 |
rs584429 | snp | A/C | | | intron-variant | USP14 | GRCh38.p7 | 18:188955 | aagtgctgggattac[A/C]ggcgtgagccaccgt | 9097 |
rs585578 | snp | C/T | 0.41833 | 0.184838 | intron-variant | USP14 | GRCh38.p7 | 18:204232 | TGTGAAAATAATGGA[C/T]CTCCCAAACTGGAAT | 9097 |
rs585614 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:204209 | ACTGGAATAAACTTA[C/T]GGTTTTTTTTTTTTA | 9097 |
rs585699 | snp | G/T | 0 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:189229 | gttcattcaattttt[G/T]gagttgtctgattca | 9097 |
rs586720 | snp | A/T | 0 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:189497 | tttttctttgttttt[A/T]ttttgagaaggagtc | 9097 |
rs598119 | snp | G/T | 0 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:185354 | agtagagacgggttt[G/T]gctatattgtcaagg | 9097 |
rs605049 | snp | C/T | 0.284995 | 0.247539 | intron-variant | USP14 | GRCh38.p7 | 18:209430 | TTAGGAGGAACTCAC[C/T]GCTTCAACTCATTTT | 9097 |
rs617421 | snp | C/T | 0.27008 | 0.249192 | intron-variant | USP14 | GRCh38.p7 | 18:208998 | TATAGTGGCTTACGC[C/T]GGGGCGAGTGGATCA | 9097 |
rs634810 | snp | G/T | 0 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:185330 | tgcctgactaatttt[G/T]gtatttttagtagag | 9097 |
rs640525 | snp | A/C | 0 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:197911 | TCAAAAAACATTACC[A/C]AAAATCAACAATGAA | 9097 |
rs647843 | snp | A/T | | | intron-variant | USP14 | GRCh38.p7 | 18:189123 | taacaaataagaaat[A/T]aaaataccaaaaaaa | 9097 |
rs652079 | snp | A/G | 0.223819 | 0.248625 | intron-variant | USP14 | GRCh38.p7 | 18:196098 | gaggccgaggctggc[A/G]gatcacaaggtcagg | 9097 |
rs655781 | snp | A/G | 0.430136 | 0.173352 | intron-variant | USP14 | GRCh38.p7 | 18:196829 | TTTCCTACATTTACC[A/G]TACTTACTGGAACAT | 9097 |
rs668734 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:196170 | tgcctggctaatttt[G/T]gcattttttttagta | 9097 |
rs670078 | snp | A/C | 0 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:195876 | TTTGTTTGGGAAGAC[A/C]AAGGCTGGCCAGAAG | 9097 |
rs681760 | snp | G/T | 0.267091 | 0.249415 | intron-variant | USP14 | GRCh38.p7 | 18:195644 | AATTCTTAGTAGTTT[G/T]GGTTCTTAGCTGTCC | 9097 |
rs683635 | snp | A/C | 0 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:195212 | TTTTATACACTACTC[A/C]AAAAAACAGATGATT | 9097 |
rs684076 | snp | G/T | 0 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:195129 | atctatatttcttcT[G/T]GACCTTTTTCTTTCA | 9097 |
rs684100 | snp | A/T | 0 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:195112 | gaagaaatatagatt[A/T]aaagagactaataag | 9097 |
rs684978 | snp | A/C | | | intron-variant | USP14 | GRCh38.p7 | 18:194938 | actgtctcaaaaaac[A/C]aacttttttttagaa | 9097 |
rs688023 | snp | C/T | 0.239614 | 0.249784 | downstream-variant-500B | USP14 | GRCh38.p7 | 18:213827 | TCTTGTGACATTCAA[C/T]TGAGATATATGTGAA | 9097 |
rs692846 | snp | C/T | 0.192401 | 0.243274 | intron-variant | USP14 | GRCh38.p7 | 18:182139 | TTTCCTTTCATACGA[C/T]GGTATAAAAACAAAA | 9097 |
rs948263 | snp | C/T | 0.466515 | 0.124985 | intron-variant | USP14 | GRCh38.p7 | 18:165503 | CAGTTTCATTTAATT[C/T]GCATACTTCTATAAT | 9097 |
rs1061599 | snp | A/C | 0.349233 | 0.229462 | utr-variant-3-prime | USP14 | GRCh38.p7 | 18:212756 | GTTCCAGGACCCTTG[A/C]CTGATGCTAGGGAAA | 9097 |
rs1274275 | snp | C/T | 0.454061 | 0.144427 | intron-variant | USP14 | GRCh38.p7 | 18:188526 | ttttttttttttttt[C/T]ctttGTGAGGGTTTG | 9097 |
rs1274276 | snp | A/G | 0.219648 | 0.248151 | intron-variant | USP14 | GRCh38.p7 | 18:188570 | GCTAGCTCTATGTCT[A/G]TCTTTTCCTGGAACT | 9097 |
rs1299113 | snp | A/G | 0.499673 | 0.0127754 | intron-variant | USP14 | GRCh38.p7 | 18:196465 | GAAGGCGGAGGTTGC[A/G]GTGAGCCGAGATCGC | 9097 |
rs1614227 | snp | C/T | 0.000173052 | 0.00930033 | intron-variant | USP14 | GRCh38.p7 | 18:180227 | TTTTTTTTTTTTTTT[C/T]CCAACTAGATGGAGT | 9097 |
rs1620545 | snp | G/T | 0.00475057 | 0.0485048 | intron-variant | USP14 | GRCh38.p7 | 18:179403 | ATTTAAACTACTCTT[G/T]GACCCTGTTTTCTCA | 9097 |
rs1784371 | snp | A/T | 0 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:177498 | AATGATCTTATAAAA[A/T]GTCTATGTAGAAATA | 9097 |
rs1784372 | snp | A/T | 0 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:177582 | CTAATTTCCTAATTT[A/T]AATCATCATCTGGAT | 9097 |
rs1784375 | snp | A/G | 0.261332 | 0.249743 | intron-variant | USP14 | GRCh38.p7 | 18:162214 | AACATGGGTGTACAA[A/G]TATCTGTTTGAGTCC | 9097 |
rs1784376 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:162855 | caggctggagtgcag[G/T]ggcgtgatcttggct | 9097 |
rs1784380 | snp | C/T | 0.429837 | 0.173662 | intron-variant | USP14 | GRCh38.p7 | 18:168389 | gaaatctgaaagtca[C/T]gaatattgaaaaggg | 9097 |
rs1784381 | snp | C/T | 0 | 0 | missense | USP14 | GRCh38.p7 | 18:196657 | AGAGATTTGTTTGAT[C/T]CCATGGATAAAACTT | 9097 |
rs1784384 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:189501 | tctttgttttttttt[G/T]gagaaggagtctcac | 9097 |
rs1784830 | snp | G/T | 0 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:188457 | TTTAAAAGGATTTTT[G/T]GGGGTCATTTGTTAG | 9097 |
rs1785048 | snp | G/T | | | intron-variant | USP14 | GRCh38.p7 | 18:162866 | gcaggggcgtgatct[G/T]ggctcactgcaacct | 9097 |
rs1785049 | snp | A/C | 0.462144 | 0.132269 | intron-variant | USP14 | GRCh38.p7 | 18:166542 | TTCTTTATATTGGTC[A/C]GGCTGGTTTCGAACT | 9097 |
rs1785050 | snp | A/G | 0.5 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:180927 | TACGTGTGCTGTAAC[A/G]TGAGTGAACCATGAA | 9097 |
rs1785051 | snp | A/T | 0.5 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:180915 | AACGTGAGTGAACCA[A/T]GAAATACTATTCAGC | 9097 |
rs1785052 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:177632 | AAAAAAAAAAAAAAC[A/G]GGGGGGGAAAAATGA | 9097 |
rs1785053 | snp | A/G | | | intron-variant | USP14 | GRCh38.p7 | 18:177628 | AAAAAAAAAACGGGG[A/G]GGGAAAAATGATAGC | 9097 |
rs1785054 | snp | A/T | | | intron-variant | USP14 | GRCh38.p7 | 18:177578 | AGATGATGATTTAAA[A/T]TAGGAAATTTAGTTC | 9097 |
rs2027675 | snp | A/G | 0.344147 | 0.231595 | intron-variant | USP14 | GRCh38.p7 | 18:161922 | TACGTATACAGTTCT[A/G]TAGCATTAAATATAT | 9097 |
rs2155529 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:204792 | ATACAAAGTATAGTT[C/T]TGAAGGAAAAATGAA | 9097 |
rs2276062 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | USP14 | GRCh38.p7 | 18:193108 | GTGAAAAATAATCTT[C/T]GGATTTTTTTGGATT | 9097 |
rs2509312 | snp | A/C | | | intron-variant | USP14 | GRCh38.p7 | 18:196490 | gatcgcgccactgca[A/C]tccagcctgggcaac | 9097 |
rs2509447 | snp | C/T | 0.461923 | 0.132621 | intron-variant | USP14 | GRCh38.p7 | 18:170346 | ttgaacacttagagg[C/T]cactgtagggttatt | 9097 |
rs2846335 | snp | A/G | 0 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:196902 | GCTGTCTCTTGCCTG[A/G]AGCCGCACAGTAGTC | 9097 |
rs2846610 | snp | C/T | | | intron-variant | USP14 | GRCh38.p7 | 18:188507 | CTGTCTCCCTCTGGG[C/T]TTTTTTTTTTTTTTT | 9097 |
rs3016613 | snp | A/C | | | intron-variant | USP14 | GRCh38.p7 | 18:196511 | cctgggcaacggacc[A/C]agactccatctcaaa | 9097 |
rs3016709 | snp | A/T | | | intron-variant | USP14 | GRCh38.p7 | 18:196568 | GCGACTGTAAATTAA[A/T]TTTAATTAATACAAA | 9097 |
rs3132798 | snp | A/T | 0.5 | 0 | intron-variant | USP14 | GRCh38.p7 | 18:180851 | GCTGAATAGTATTTC[A/T]TGGTTCATTCACGTT | 9097 |
rs3211364 | snp | C/T | 0 | 0 | downstream-variant-500B | USP14 | GRCh38.p7 | 18:213785 | TTCTGCTACTACTAC[C/T]TAGTGCTTTGCTGTG | 9097 |