SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs2220 | snp | A/C/T | 0.4998 | 0.00999798 | intron-variant | USP13 | GRCh38.p7 | 3:179709983 | TATCAAATGAAAAAC[A/C/T]ACACCGGTTCAATGA | 8975 |
rs15241 | snp | A/G | 0 | 0 | utr-variant-3-prime | USP13 | GRCh38.p7 | 3:179789216 | GGACAGGTGGGCACA[A/G]GAACAGACTCAGCCT | 8975 |
rs721384 | snp | G/T | 0.307671 | 0.243257 | intron-variant, upstream-variant-2KB | USP13, LOC107986158 | GRCh38.p7 | 3:179670094 | agccttttctggagt[G/T]gggacctttgcacat | 8975 |
rs734368 | snp | C/T | 0.159622 | 0.233092 | intron-variant | USP13 | GRCh38.p7 | 3:179704552 | GTAGCCCAGTGTCAT[C/T]GGTCAGTAGCGTTGA | 8975 |
rs734778 | snp | G/T | 0.420096 | 0.183214 | intron-variant | USP13 | GRCh38.p7 | 3:179737337 | CATATATATTTTTCT[G/T]AACTCACCCAACCCC | 8975 |
rs735360 | snp | C/T | 0.498568 | 0.0267188 | intron-variant | USP13 | GRCh38.p7 | 3:179738744 | AGACTAAAACTGGCT[C/T]TTTAATACGGGTAAC | 8975 |
rs741430 | snp | G/T | 0.321292 | 0.23962 | intron-variant | USP13 | GRCh38.p7 | 3:179738798 | CTAATGCTTCAGCAC[G/T]GCTGTTTTCTGAAAC | 8975 |
rs759596 | snp | G/T | 0.322721 | 0.23919 | intron-variant | USP13 | GRCh38.p7 | 3:179781177 | CATGATTATAACGTA[G/T]GTGGGACCAAACTTC | 8975 |
rs759597 | snp | A/G | 0.259397 | 0.249823 | intron-variant | USP13 | GRCh38.p7 | 3:179780897 | GTAAAATGTATGTCT[A/G]TTGAATTTAATAAGG | 8975 |
rs800364 | snp | C/T | 0.283684 | 0.24772 | intron-variant | USP13 | GRCh38.p7 | 3:179728859 | gactgcctgcgattg[C/T]aggcgcgcgccgcca | 8975 |
rs800365 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | USP13 | GRCh38.p7 | 3:179726427 | GTGTTGTTCTTTCCC[C/T]GTTGTCTTTGACTCT | 8975 |
rs800366 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | USP13 | GRCh38.p7 | 3:179722795 | TTCAACTCAGACAGA[C/T]GATGCTTTTTAAAAA | 8975 |
rs800367 | snp | C/T | 0.117188 | 0.211804 | intron-variant | USP13 | GRCh38.p7 | 3:179720559 | AGGGCTAAAACGAAA[C/T]GCACATTGAAATAGT | 8975 |
rs800368 | snp | C/T | 0.243633 | 0.249919 | intron-variant | USP13 | GRCh38.p7 | 3:179713153 | TTTCTATGATTGAAA[C/T]AGATGCATTCAAATA | 8975 |
rs800369 | snp | A/T | 0.290718 | 0.246662 | intron-variant | USP13 | GRCh38.p7 | 3:179711218 | aaacaaaacaaaaca[A/T]aaaaaagtgtacagc | 8975 |
rs1024852 | snp | A/G | 0.476052 | 0.106772 | intron-variant | USP13 | GRCh38.p7 | 3:179764694 | ACCCTGTAGTTTCAG[A/G]GTCCCTTGTTTCTTG | 8975 |
rs1025864 | snp | C/T | 0.307176 | 0.243374 | intron-variant | USP13 | GRCh38.p7 | 3:179735100 | CATCCAACTAAGGAA[C/T]CTGTCATATTAATAA | 8975 |
rs1036826 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | USP13 | GRCh38.p7 | 3:179735284 | GAGTGTCCCCTATGG[G/T]CCCAACACCTCACAA | 8975 |
rs1045545 | snp | A/C | | | utr-variant-3-prime | USP13 | GRCh38.p7 | 3:179789290 | TATTTTGCACTAGTC[A/C]CAGTTGTTGTTAAAC | 8975 |
rs1180265 | snp | A/C | 0 | 0 | intron-variant | USP13 | GRCh38.p7 | 3:179705531 | cagtcacaaatagca[A/C]catattacatgattc | 8975 |
rs1185668 | snp | A/C | 0 | 0 | intron-variant | USP13 | GRCh38.p7 | 3:179777152 | TACATACTCAGAACC[A/C]CAAAAATAAAATTTA | 8975 |
rs1320222 | snp | G/T | 0.251014 | 0.249998 | intron-variant | USP13, LOC107986158 | GRCh38.p7 | 3:179660667 | CACGTTGCCTTGCAG[G/T]CAATGAGACTTCCCA | 8975 |
rs1442494 | snp | C/G | 0.311859 | 0.242226 | intron-variant | USP13 | GRCh38.p7 | 3:179685971 | CTGTTTGGAGTTCTG[C/G]AGGACAGTTAAGGAG | 8975 |
rs1561842 | snp | C/T | 0.495095 | 0.0492773 | intron-variant | USP13 | GRCh38.p7 | 3:179682593 | GAAACATTTGGATGC[C/T]GAGGGGAAAAACTCT | 8975 |
rs1561843 | snp | A/G | 0.477768 | 0.103061 | intron-variant | USP13 | GRCh38.p7 | 3:179682307 | TTTTTTATGATTTTT[A/G]GATCCATGGGTGTCT | 8975 |
rs1596181 | snp | G/T | 0.489318 | 0.0722982 | intron-variant | USP13 | GRCh38.p7 | 3:179692057 | TCATACATGCATGCA[G/T]ACATACATATACATG | 8975 |
rs1966757 | snp | A/C | 0.44306 | 0.158832 | intron-variant | USP13 | GRCh38.p7 | 3:179724491 | TTCTTTAATTTTCTT[A/C]TTATTATTTCTTTCT | 8975 |
rs1966758 | snp | C/T | 0.427575 | 0.175975 | intron-variant | USP13 | GRCh38.p7 | 3:179724441 | agacagagtctcact[C/T]ggttgcccaggctgg | 8975 |
rs2080579 | snp | C/T | 0.474992 | 0.108989 | intron-variant | USP13 | GRCh38.p7 | 3:179761508 | TCTTCATCTCTTGAC[C/T]TCGTGATCCGCCTGC | 8975 |
rs2080580 | snp | G/T | | | intron-variant | USP13 | GRCh38.p7 | 3:179780466 | CAgtaaatgatattg[G/T]tttcttaatttcatt | 8975 |
rs2098450 | snp | C/T | 0.305186 | 0.243833 | intron-variant | USP13 | GRCh38.p7 | 3:179779458 | ACTGCAACCTCCACC[C/T]CCTGGCTTCAAGTGA | 8975 |
rs2111391 | snp | A/G | 0.29175 | 0.246489 | intron-variant | USP13 | GRCh38.p7 | 3:179725643 | TAACCAAACAGAAAA[A/G]GCATTTTTGCAATGA | 8975 |
rs2111392 | snp | A/G | 0.282369 | 0.247896 | intron-variant | USP13 | GRCh38.p7 | 3:179705847 | tagtcccagctactc[A/G]ggagactgaggcagg | 8975 |
rs2119898 | snp | A/G | 0.442655 | 0.159323 | intron-variant | USP13 | GRCh38.p7 | 3:179721678 | GTCCTGAAGCAATAA[A/G]GATGGGCTTCGCAGC | 8975 |
rs2160666 | snp | A/T | | | intron-variant | USP13 | GRCh38.p7 | 3:179702699 | TATGCCCTACTGAAC[A/T]CTGTGCACTTAGTAC | 8975 |
rs2165679 | snp | C/T | 0.442926 | 0.158996 | intron-variant | USP13 | GRCh38.p7 | 3:179721779 | CGGCCACAAAGCTCT[C/T]CTTATCTCACCTGAT | 8975 |
rs2239637 | snp | C/T | 0.485528 | 0.0838238 | intron-variant | USP13 | GRCh38.p7 | 3:179753071 | ATTCTTCCACACCAC[C/T]GAGGACAACCTAGTA | 8975 |
rs2239638 | snp | A/G | 0.388398 | 0.208197 | intron-variant | USP13 | GRCh38.p7 | 3:179752587 | CACTCTTAGAATTTG[A/G]TCATTCCAGAAACCA | 8975 |
rs2239639 | snp | C/T | 0.387263 | 0.208947 | intron-variant | USP13 | GRCh38.p7 | 3:179752207 | AAAGCATATCAACTT[C/T]GTCTGAGGCACACCT | 8975 |
rs2261441 | snp | C/T | 0.420096 | 0.183214 | intron-variant | USP13 | GRCh38.p7 | 3:179739100 | ATCAGGGAAAGGTCC[C/T]TGTAAGGTCCCTGAG | 8975 |
rs2268926 | snp | A/C | 0.408871 | 0.193029 | intron-variant | USP13 | GRCh38.p7 | 3:179743456 | GACCCACCACCCCCC[A/C]CACACAAGAAAGAGC | 8975 |
rs2268927 | snp | A/C | 0.416545 | 0.186448 | intron-variant | USP13 | GRCh38.p7 | 3:179743389 | TCTTTATTCTCAAAA[A/C]AAAAAACAAAAAACA | 8975 |
rs2268928 | snp | C/T | 0.322483 | 0.239262 | intron-variant | USP13 | GRCh38.p7 | 3:179743346 | GATACATGTGTAGAA[C/T]GTGCAGGTCTGTTAC | 8975 |
rs2268929 | snp | A/G | 0.498871 | 0.0237351 | intron-variant | USP13 | GRCh38.p7 | 3:179743037 | TTTACAAAAATGACT[A/G]GTTCACAGGAGATGC | 8975 |
rs2268930 | snp | C/T | 0.48978 | 0.0707512 | intron-variant | USP13 | GRCh38.p7 | 3:179741694 | AGACCTGGAAAGTGA[C/T]GGGAGGGGCAGATGC | 8975 |
rs2268931 | snp | A/T | 0.212728 | 0.247206 | intron-variant | USP13 | GRCh38.p7 | 3:179739151 | AAGGCTCAGGGCAGG[A/T]GGAGGTGACGGCTGC | 8975 |
rs2268933 | snp | A/G | 0.439363 | 0.163222 | intron-variant | USP13 | GRCh38.p7 | 3:179737823 | CTTCTAGGAGCTTAC[A/G]GACAACAGAGGAGAT | 8975 |
rs2268934 | snp | C/T | 0.216349 | 0.247725 | intron-variant | USP13 | GRCh38.p7 | 3:179737652 | GCTTACACACATACA[C/T]GGCTTCAGTTGTGCT | 8975 |
rs2268935 | snp | C/G | 0.499527 | 0.0153681 | intron-variant | USP13 | GRCh38.p7 | 3:179733482 | CTGCCAGTGAAAATC[C/G]TGATGCCTGAGAAAC | 8975 |
rs2268936 | snp | A/G | 0.4231 | 0.180378 | intron-variant | USP13 | GRCh38.p7 | 3:179731200 | TGGTCTCGAACTCCC[A/G]ACCTCAGGTGATCCA | 8975 |
rs2268937 | snp | C/G | 0.460027 | 0.135605 | intron-variant | USP13 | GRCh38.p7 | 3:179731081 | AGAAACTCTAGCCAA[C/G]AAAGTTGAGGCTTAG | 8975 |
rs2268938 | snp | A/G | 0.423881 | 0.179625 | intron-variant | USP13 | GRCh38.p7 | 3:179720438 | TGGTTTATTCGTTCT[A/G]TCCCCTAGGAGCTTT | 8975 |
rs2268939 | snp | C/T | 0.474992 | 0.108989 | intron-variant | USP13 | GRCh38.p7 | 3:179708171 | AGGCTAGGAGAGGAG[C/T]TCATTTCCTTAAAAC | 8975 |
rs2268940 | snp | A/G | 0.340108 | 0.233197 | intron-variant | USP13 | GRCh38.p7 | 3:179708109 | GTTTAAAATATTAAG[A/G]ATCCTGTGTGTATAA | 8975 |
rs2268941 | snp | C/T | 0.271972 | 0.249033 | intron-variant | USP13 | GRCh38.p7 | 3:179703759 | GAGGTTTTATTTACA[C/T]GCATGTCAGCGGAAT | 8975 |
rs2268942 | snp | A/G | 0.271162 | 0.249103 | intron-variant | USP13 | GRCh38.p7 | 3:179703716 | GTACAATGGTCTGCT[A/G]CTACCAATCTCTTTC | 8975 |
rs2276803 | snp | C/T | 0.387512 | 0.208827 | synonymous-codon, upstream-variant-2KB, intron-variant | USP13, LOC107986158 | GRCh38.p7 | 3:179653366 | CAGGGTCTACAAGAA[C/T]GAGTGCGCCTTCTCC | 8975 |
rs2284884 | snp | A/G | 0.27893 | 0.24832 | intron-variant | USP13 | GRCh38.p7 | 3:179772579 | CAGTCGACCACTGGG[A/G]CTTAGCTTCCCTGGG | 8975 |
rs2284885 | snp | A/G | 0.0752113 | 0.178743 | intron-variant | USP13 | GRCh38.p7 | 3:179772381 | GCCAGAGCAGGCTCT[A/G]AGTAATCACAGCCTA | 8975 |
rs2284886 | snp | A/G | 0.4231 | 0.180378 | intron-variant | USP13 | GRCh38.p7 | 3:179707545 | GGTACAGGATATGTC[A/G]GTGAGCAAATGTACA | 8975 |
rs2284887 | snp | C/T | 0.443732 | 0.158012 | intron-variant | USP13 | GRCh38.p7 | 3:179707359 | GACTGTCCCGTGCAC[C/T]GGCATAACTGGCTTC | 8975 |
rs2287240 | snp | A/G | 0.5 | 0.000184051 | intron-variant | USP13 | GRCh38.p7 | 3:179754886 | GAACAGGGTGGGAGG[A/G]TAGCGCATATTCTCC | 8975 |
rs2300762 | snp | C/T | 0.493013 | 0.058691 | intron-variant | USP13 | GRCh38.p7 | 3:179780515 | ccagactctctttct[C/T]tctctctctggctga | 8975 |
rs2300763 | snp | C/G | 0.48491 | 0.0855403 | intron-variant | USP13 | GRCh38.p7 | 3:179754157 | CAAAGTGGGAACACC[C/G]AAGCAAGACCAAGAT | 8975 |
rs2300764 | snp | C/T | 0.316243 | 0.241064 | intron-variant | USP13 | GRCh38.p7 | 3:179733055 | GAAGGGAGGGCTGCC[C/T]CTTGGCTCCAGCTGT | 8975 |
rs2300765 | snp | C/T | 0.214541 | 0.247473 | intron-variant | USP13 | GRCh38.p7 | 3:179732860 | TGGAGATGTAAGGAG[C/T]TACTACACTACAGCC | 8975 |
rs2300767 | snp | A/G | 0.293037 | 0.246268 | intron-variant | USP13 | GRCh38.p7 | 3:179723290 | ATGAAAAATAGACAT[A/G]GAAAATGCACCATAA | 8975 |
rs2300768 | snp | A/G | 0.435263 | 0.167862 | intron-variant | USP13 | GRCh38.p7 | 3:179722791 | ACTCAGACAGATGAT[A/G]CTTTTTAAAAATACA | 8975 |
rs2300769 | snp | A/C | 0.424348 | 0.179172 | intron-variant | USP13 | GRCh38.p7 | 3:179702878 | TAAGAGTTATATTAA[A/C]CAAGGCAGTAAGAAC | 8975 |
rs2300770 | snp | C/T | 0.444533 | 0.15787 | intron-variant | USP13 | GRCh38.p7 | 3:179702656 | CACAATAAATAAATA[C/T]ACACAAAATTCTGAT | 8975 |
rs2300771 | snp | C/T | 0.423413 | 0.180077 | intron-variant | USP13 | GRCh38.p7 | 3:179702654 | CAATAAATAAATACA[C/T]ACAAAATTCTGATTT | 8975 |
rs2300772 | snp | A/G | 0.444133 | 0.157519 | intron-variant | USP13 | GRCh38.p7 | 3:179702602 | AGATTGGGGCAAAAG[A/G]GAATGAATGGTGGAA | 8975 |
rs2339803 | snp | C/T | 0.293294 | 0.246223 | intron-variant | USP13, LOC107986158 | GRCh38.p7 | 3:179662627 | TTGTGTCATTTGCCA[C/T]GTGTACCCTAAAATC | 8975 |
rs2339847 | snp | A/G | 0.278664 | 0.248351 | intron-variant | USP13 | GRCh38.p7 | 3:179775704 | ttcgagtgcagtgcc[A/G]gcaggctggcactgc | 8975 |
rs2879588 | snp | C/T | 0.465368 | 0.126951 | intron-variant | USP13, LOC107986158 | GRCh38.p7 | 3:179661814 | GGCAAGATTCTGATA[C/T]TGATTTTTCCAGTAA | 8975 |
rs2879608 | snp | A/G | | | intron-variant | USP13 | GRCh38.p7 | 3:179754495 | CAATTTGTAACCTCA[A/G]GCTTAAATGATTTGC | 8975 |
rs3213761 | snp | A/G | 0.409021 | 0.192905 | intron-variant | USP13 | GRCh38.p7 | 3:179730595 | CAGGACAGAGAAACA[A/G]AAACAAAAAGGTCAT | 8975 |
rs3216642 | in-del | -/A | | | intron-variant | USP13 | GRCh38.p7 | 3:179751731 | atctcaaaaaaaaaa[-/A]gaaTGCTTTTGGACC | 8975 |
rs3216643 | in-del | -/A | 0.24019 | 0.249807 | intron-variant | USP13 | GRCh38.p7 | 3:179744344 | AAAACAAAAAAAAAA[-/A]CAGAACCACCACTAA | 8975 |
rs3216644 | in-del | -/T | 0.422315 | 0.181128 | intron-variant | USP13 | GRCh38.p7 | 3:179732745 | AGAACTACTTTTTTT[-/T]AACATAAAAGGACAC | 8975 |
rs3222346 | in-del | -/CACA | | | intron-variant | USP13 | GRCh38.p7 | 3:179764184 | ACACACACACACACA[-/CACA]GTCTCTCATGCTCAC | 8975 |
rs3732992 | snp | A/G | 0.295343 | 0.245854 | intron-variant | USP13 | GRCh38.p7 | 3:179756979 | GAAATGCCCTGGATC[A/G]ATGGGTTTTCTTTTT | 8975 |
rs3732993 | snp | C/G | 0.280256 | 0.248162 | utr-variant-3-prime | USP13 | GRCh38.p7 | 3:179788933 | AATATATATATGTAT[C/G]ATCCCAATTAAAAGA | 8975 |
rs3831867 | in-del | -/AATCCCA | 0.441432 | 0.160792 | intron-variant | USP13 | GRCh38.p7 | 3:179708440 | GCACCTGTAATCCCA[-/AATCCCA]GCTACTCGGGAGGCT | 8975 |
rs4041265 | in-del | -/T/TT/TTT | 0 | 0 | intron-variant | USP13 | GRCh38.p7 | 3:179696347 | TTTTTTTTTTTTTTT[-/T/TT/TTT]GAGATGGAGTCTTGC | 8975 |
rs4346543 | snp | C/T | 0.452719 | 0.146304 | intron-variant | USP13 | GRCh38.p7 | 3:179723633 | TTGTTTCAAGAGTCT[C/T]AGAATTTTATATTAC | 8975 |
rs4447764 | snp | A/G | 0.301932 | 0.244547 | intron-variant | USP13, LOC107986158 | GRCh38.p7 | 3:179669232 | TTGGGAGGCCAAGGC[A/G]AGCAGATCACCTGAG | 8975 |
rs4619783 | snp | A/G | 0.4444 | 0.15719 | intron-variant | USP13 | GRCh38.p7 | 3:179728606 | agaggctgcaatctc[A/G]gcactttgggaggcc | 8975 |
rs4632541 | snp | A/G | 0.431473 | 0.171952 | intron-variant | USP13 | GRCh38.p7 | 3:179728222 | ccccacctccctgcc[A/G]gacgaggtggctgcc | 8975 |
rs4637291 | snp | A/G | 0.285519 | 0.247464 | intron-variant | USP13, LOC107986158 | GRCh38.p7 | 3:179669385 | GAATCTCTTGAACTC[A/G]GGAGGCAGAGGTGCA | 8975 |
rs4854941 | snp | C/T | 0.270621 | 0.249148 | intron-variant | USP13, LOC107986158 | GRCh38.p7 | 3:179659385 | Gagcagttttcaaag[C/T]gtgctccctgaacca | 8975 |
rs4854942 | snp | C/T | 0.283158 | 0.247791 | intron-variant, upstream-variant-2KB | USP13, LOC107986158 | GRCh38.p7 | 3:179670618 | GAATTTCCTCAGCTA[C/T]AAATCTCAAGATATT | 8975 |
rs4854945 | snp | G/T | 0.457037 | 0.140127 | intron-variant | USP13 | GRCh38.p7 | 3:179673532 | AAGGAAGCCTGGGTT[G/T]CTCATAGCGATAGAT | 8975 |
rs4854946 | snp | G/T | 0.181978 | 0.240568 | intron-variant | USP13 | GRCh38.p7 | 3:179675697 | GGACTAGAAGCGTGT[G/T]CCGCCACGCCTGGCT | 8975 |
rs4854947 | snp | A/G | 0.264906 | 0.249555 | intron-variant | USP13 | GRCh38.p7 | 3:179696917 | TACAATAAAGCTACA[A/G]ATATGCATAGATATA | 8975 |
rs4854948 | snp | C/T | 0.259951 | 0.249802 | intron-variant, upstream-variant-2KB | USP13 | GRCh38.p7 | 3:179700188 | CAAAGAGGGGACGAC[C/T]TGATAGGTAACAGGC | 8975 |
rs4854949 | snp | C/T | 0.383053 | 0.211653 | intron-variant | USP13 | GRCh38.p7 | 3:179710642 | TTAAATACAGTCCTG[C/T]GTCACTTAAGGATGG | 8975 |
rs4854950 | snp | C/T | 0.434109 | 0.169127 | intron-variant | USP13 | GRCh38.p7 | 3:179710668 | GATGGTGATATGTTC[C/T]GAGAATGCATCATTA | 8975 |
rs4854951 | snp | C/T | 0.426507 | 0.177046 | intron-variant | USP13 | GRCh38.p7 | 3:179718510 | GGAAGAAGATTGGGC[C/T]AGGAGTTAGACTACC | 8975 |
rs4855102 | snp | A/G | 0.474813 | 0.109357 | intron-variant | USP13, LOC107986158 | GRCh38.p7 | 3:179666120 | CTGGGGAGACTGGAA[A/G]GCAAGGTTGAATCCT | 8975 |