SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs456899 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | USP25 | GRCh38.p7 | 21:15751536 | TGCATAAAGATTTAA[C/T]TGGACAAGAGAGCTA | 29761 |
rs459438 | snp | A/C | 0.00119737 | 0.0244387 | upstream-variant-2KB | USP25 | GRCh38.p7 | 21:15728866 | GACAACAGGTGGTAC[A/C]AGACATCTGAGCTGC | 29761 |
rs459495 | snp | A/G | 0.122758 | 0.215196 | intron-variant, upstream-variant-2KB | USP25 | GRCh38.p7 | 21:15761690 | agccatcctgtagga[A/G]gaatcaggggagaag | 29761 |
rs459605 | snp | A/G | 0.0718919 | 0.175435 | intron-variant | USP25 | GRCh38.p7 | 21:15763445 | CTAAGTTAAACATTC[A/G]ATTTCAAACTCTTCA | 29761 |
rs459684 | snp | C/T | 0.182933 | 0.240836 | upstream-variant-2KB | USP25 | GRCh38.p7 | 21:15727956 | CAACATAGAGTAATG[C/T]AGCAGTTTAGAAGTT | 29761 |
rs461182 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP25 | GRCh38.p7 | 21:15765473 | TCTGTCTAGAGTTCT[A/G]TGTGTCTTTCCATAA | 29761 |
rs463977 | snp | A/C | 0.067446 | 0.170804 | intron-variant | USP25 | GRCh38.p7 | 21:15758314 | ttgtgtccccaacca[A/C]atctcatcttgaatt | 29761 |
rs465864 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | USP25 | GRCh38.p7 | 21:15773265 | CACAAGCAGCTTTAT[C/T]CTTTTACACCCATGT | 29761 |
rs465954 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | USP25 | GRCh38.p7 | 21:15753066 | TGGAGTATTCTTTAG[A/G]GCATTGTTGCCTCTA | 29761 |
rs722887 | snp | C/T | 0.398174 | 0.201356 | intron-variant | USP25 | GRCh38.p7 | 21:15738436 | AAGAGATATTAAACA[C/T]GACCTAATAAAAATA | 29761 |
rs725799 | snp | C/T | 0.0505692 | 0.150756 | intron-variant | USP25 | GRCh38.p7 | 21:15737571 | AAAAAATACCTTCAG[C/T]CATTGATATAGATGC | 29761 |
rs926612 | snp | A/G | 0.272511 | 0.248984 | intron-variant | USP25 | GRCh38.p7 | 21:15733991 | TCATTAAGTGCTTCT[A/G]AAGGTTCTTTCAAAG | 29761 |
rs995121 | snp | A/G | 0.0562307 | 0.157967 | intron-variant | USP25 | GRCh38.p7 | 21:15735453 | tgctggaggatgtgt[A/G]gatgtgtaagttaca | 29761 |
rs1022457 | snp | A/G | 0.39709 | 0.20215 | intron-variant | USP25 | GRCh38.p7 | 21:15867412 | CTTAGCTAGTTTGGC[A/G]TATAAGGTAACTACC | 29761 |
rs1046764 | snp | C/T | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | USP25 | GRCh38.p7 | 21:15879397 | TTTGCAATATATAAA[C/T]CATTCTATTTTTGTA | 29761 |
rs1986788 | snp | C/T | 0.325799 | 0.238232 | intron-variant | USP25 | GRCh38.p7 | 21:15745728 | agcactttgggagac[C/T]gaggcgggcggatca | 29761 |
rs1989381 | snp | C/T | 0.398354 | 0.201224 | intron-variant | USP25 | GRCh38.p7 | 21:15738782 | cccagggtgtggccc[C/T]gggctgtctgcttgt | 29761 |
rs2026853 | snp | A/G | 0.229747 | 0.249178 | intron-variant | USP25 | GRCh38.p7 | 21:15826970 | AATACTCTATGCTTT[A/G]ATACAGCACAACAGA | 29761 |
rs2183553 | snp | A/C | 0.0685596 | 0.171987 | intron-variant, upstream-variant-2KB | USP25 | GRCh38.p7 | 21:15803318 | AAGCAAACCACACAC[A/C]AATATTTCTCATGAA | 29761 |
rs2205585 | snp | C/T | 0.365439 | 0.221752 | intron-variant | USP25 | GRCh38.p7 | 21:15794352 | TAAATAATCTTTTGG[C/T]TGCTGGCAACATTAG | 29761 |
rs2205588 | snp | A/G | 0.125874 | 0.217008 | intron-variant | USP25 | GRCh38.p7 | 21:15823369 | TAGGGGCTGGGGGTA[A/G]GGGAAGGAAATTACG | 29761 |
rs2205589 | snp | A/G | 0.367503 | 0.220665 | intron-variant | USP25 | GRCh38.p7 | 21:15823384 | GGGGAAGGAAATTAC[A/G]GCTATACTCATTATC | 29761 |
rs2223176 | snp | A/T | 0.365853 | 0.221536 | intron-variant | USP25 | GRCh38.p7 | 21:15794115 | GACTAATTTGAAACA[A/T]CTGGGAATTCTTTTT | 29761 |
rs2242676 | snp | C/T | 0.119978 | 0.213528 | intron-variant | USP25 | GRCh38.p7 | 21:15746932 | ATGGAAAGCAGTCTT[C/T]TACTACTAAGTATGG | 29761 |
rs2242677 | snp | A/C | 0.244205 | 0.249933 | intron-variant | USP25 | GRCh38.p7 | 21:15774009 | AAAATCTGGCTTTAC[A/C]CAGATAATAATTTAG | 29761 |
rs2242678 | snp | A/C | | | intron-variant | USP25 | GRCh38.p7 | 21:15794309 | GAAAGGGAATATAAA[A/C]AAAGAGAAGATTGTA | 29761 |
rs2242679 | snp | A/G | 0.0520825 | 0.152737 | intron-variant | USP25 | GRCh38.p7 | 21:15815835 | ATTTTCTCCCTTCTT[A/G]tagggagtaactagc | 29761 |
rs2242680 | snp | C/T | 0.123798 | 0.215808 | intron-variant | USP25 | GRCh38.p7 | 21:15830197 | CTTTGTTCTTAAGTT[C/T]ACTTGTGTTATAGCA | 29761 |
rs2242681 | snp | A/C | 0.128288 | 0.218372 | intron-variant | USP25 | GRCh38.p7 | 21:15840075 | TGCCTTCCAGTGTAG[A/C]GTCTCATATATAGCA | 29761 |
rs2245574 | snp | A/C | 0.361474 | 0.223771 | intron-variant | USP25 | GRCh38.p7 | 21:15805485 | TGAAAACGATGGATA[A/C]AATTAAGATTATTTA | 29761 |
rs2248859 | snp | A/G | 0.239902 | 0.249796 | intron-variant | USP25 | GRCh38.p7 | 21:15869915 | TGTGTGCCAGAAAGT[A/G]AAGTCTTGTTTTAGT | 29761 |
rs2252133 | snp | G/T | 0.225597 | 0.248806 | intron-variant | USP25 | GRCh38.p7 | 21:15874699 | CTCAGTACTTTATTC[G/T]TTTCTCTTTATGAAT | 29761 |
rs2274797 | snp | C/T | 6.60447e-05 | 0.00574613 | missense, nc-transcript-variant, intron-variant | USP25 | GRCh38.p7 | 21:15842521 | ATGAAGATAAAAGTC[C/T]TGAAACAGTTTTGCA | 29761 |
rs2297247 | snp | G/T | 0.393434 | 0.20476 | intron-variant | USP25 | GRCh38.p7 | 21:15763053 | GTTGATTTTTTTTTT[G/T]GGGTATACCATGTGG | 29761 |
rs2297248 | snp | A/T | 0.174781 | 0.238416 | synonymous-codon, nc-transcript-variant | USP25 | GRCh38.p7 | 21:15831466 | TGGGCACTACTGGGC[A/T]TATATTTTTGATCAT | 29761 |
rs2297249 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | USP25 | GRCh38.p7 | 21:15874655 | GATGTCTATAAACTG[A/G]TTCTAGTCCCTTCAG | 29761 |
rs2404000 | snp | A/G | 0.136506 | 0.222754 | intron-variant | USP25 | GRCh38.p7 | 21:15813111 | CTGAAGATTGCTGGC[A/G]AAAAGTCACAGAAAT | 29761 |
rs2404001 | snp | C/T | 0.486133 | 0.082104 | intron-variant | USP25 | GRCh38.p7 | 21:15838519 | CCCACACCCCTCAGA[C/T]TTTCTTCGGAATGGG | 29761 |
rs2823464 | snp | A/G | 0.130351 | 0.219509 | intron-variant | USP25 | GRCh38.p7 | 21:15734568 | TTCACATCATTTCTA[A/G]TAAATATTCTGTTGA | 29761 |
rs2823465 | snp | C/T | 0 | 0 | intron-variant | USP25 | GRCh38.p7 | 21:15735826 | AGAGCAAATTTTAGG[C/T]AAAGTTTCCAAATTT | 29761 |
rs2823466 | snp | C/G | 0.0850919 | 0.187897 | intron-variant | USP25 | GRCh38.p7 | 21:15738521 | GATAATTTCTGATAA[C/G]TGTTATATGGCAGTG | 29761 |
rs2823467 | snp | G/T | 0.327914 | 0.237549 | intron-variant | USP25 | GRCh38.p7 | 21:15740095 | GTTTAGATCAGTTTC[G/T]TATAATATGGTTTTT | 29761 |
rs2823468 | snp | A/G | 0.151668 | 0.229849 | intron-variant | USP25 | GRCh38.p7 | 21:15740829 | ATATCTTATTGTCCT[A/G]GAAATTTCCTTTGTT | 29761 |
rs2823469 | snp | C/T | 0.394354 | 0.204112 | intron-variant | USP25 | GRCh38.p7 | 21:15743206 | CCCCCAGAGGGGTCG[C/T]GGCTCATCACTCCCA | 29761 |
rs2823470 | snp | A/G | 0.395087 | 0.203592 | intron-variant | USP25 | GRCh38.p7 | 21:15744997 | GCAAGAGGGCTGACT[A/G]ACCACTTTAGGGCCA | 29761 |
rs2823471 | snp | C/T | 0.288646 | 0.246995 | intron-variant | USP25 | GRCh38.p7 | 21:15748271 | CAGGTGTCAGGAACT[C/T]TCGCCCTTGAATTAA | 29761 |
rs2823472 | snp | A/G | 0.398534 | 0.201091 | intron-variant | USP25 | GRCh38.p7 | 21:15748880 | ATGTTAAGCTTTTGG[A/G]AGTAAATTTTATTTC | 29761 |
rs2823473 | snp | C/G | 0.327445 | 0.237702 | intron-variant | USP25 | GRCh38.p7 | 21:15751087 | ACAGATGATTGGCTG[C/G]TAGAGGGTAAAGAGA | 29761 |
rs2823474 | snp | C/T | 0 | 0 | intron-variant | USP25 | GRCh38.p7 | 21:15755265 | GAAACCTTTGACTTT[C/T]TTTTCCTGAACCAAG | 29761 |
rs2823475 | snp | A/G/T | 0.0829062 | 0.185956 | intron-variant | USP25 | GRCh38.p7 | 21:15765395 | CTATACTTTTGATGA[A/G/T]AACTATGCAAAATGT | 29761 |
rs2823476 | snp | A/G | 0.394354 | 0.204112 | intron-variant | USP25 | GRCh38.p7 | 21:15767850 | GAAAATTAGGATTAT[A/G]TGTGTCCTGCACAAA | 29761 |
rs2823477 | snp | C/T | 0.330016 | 0.236849 | intron-variant | USP25 | GRCh38.p7 | 21:15769265 | TGCCTTTTTGGTGTA[C/T]TTTTTACCTTTCACT | 29761 |
rs2823478 | snp | C/T | 0.196771 | 0.244268 | intron-variant | USP25 | GRCh38.p7 | 21:15769668 | CAAGTTTTTGTGTCA[C/T]GGCAAACTCTGTCAT | 29761 |
rs2823479 | snp | A/T | 0.271162 | 0.249103 | intron-variant | USP25 | GRCh38.p7 | 21:15769862 | TTTGGGTAGGTAATT[A/T]TAACACAGAAAGTAA | 29761 |
rs2823480 | snp | A/G | 0.269538 | 0.249235 | intron-variant | USP25 | GRCh38.p7 | 21:15771125 | GTACTTTTATAGACC[A/G]TTAAGAAAGCATGCA | 29761 |
rs2823481 | snp | A/G | 0.248755 | 0.249997 | intron-variant | USP25 | GRCh38.p7 | 21:15772253 | GTATAAGTTTTACTC[A/G]TGGTATTCCTTTGTA | 29761 |
rs2823482 | snp | A/G | 0.426354 | 0.177198 | intron-variant | USP25 | GRCh38.p7 | 21:15772692 | ATAAATTGATAATTC[A/G]TTACATGTTTTACAC | 29761 |
rs2823483 | snp | C/G | 0.248755 | 0.249997 | intron-variant | USP25 | GRCh38.p7 | 21:15772881 | TTGTATGTGTGGACC[C/G]TATGTGAGGGATCTT | 29761 |
rs2823484 | snp | A/G | 0.251296 | 0.249997 | intron-variant | USP25 | GRCh38.p7 | 21:15773154 | GGGATTGGAGGCTCA[A/G]ATTCCCAGCTGGGGT | 29761 |
rs2823485 | snp | A/G/T | 0.0836354 | 0.186609 | intron-variant | USP25 | GRCh38.p7 | 21:15773242 | CCATTTAATATGGTC[A/G/T]TTCTAGCCACAAGCA | 29761 |
rs2823487 | snp | A/T | 0.328148 | 0.237472 | intron-variant | USP25 | GRCh38.p7 | 21:15775920 | ACTTAAGAGAACGAG[A/T]TAATGGAATCTGACC | 29761 |
rs2823488 | snp | A/G | 0.330249 | 0.23677 | intron-variant, upstream-variant-2KB | USP25 | GRCh38.p7 | 21:15777276 | CTGCATATTTATTAA[A/G]CAATTCAGATTGTAT | 29761 |
rs2823489 | snp | A/G | 0.39709 | 0.20215 | intron-variant | USP25 | GRCh38.p7 | 21:15778326 | TGCACTGTCCAATTT[A/G]CAACAATTTATAGCA | 29761 |
rs2823490 | snp | G/T | 0.0829062 | 0.185956 | intron-variant | USP25 | GRCh38.p7 | 21:15779546 | GTATCAGTCGTTCTA[G/T]TATGTGTTTTCTAAT | 29761 |
rs2823491 | snp | C/T | 0.153 | 0.230415 | intron-variant | USP25 | GRCh38.p7 | 21:15782437 | CAGCCTCCAGACCTG[C/T]GTGCATCCACCCCTG | 29761 |
rs2823492 | snp | C/T | 0.0596104 | 0.162024 | intron-variant | USP25 | GRCh38.p7 | 21:15788764 | GTGTATTGTGATAAA[C/T]CCATTTCTTTAAAAC | 29761 |
rs2823493 | snp | A/G | 0.361684 | 0.223667 | intron-variant | USP25 | GRCh38.p7 | 21:15789385 | AAGTTTTCTGTAGCT[A/G]ATGTATGTATGAACC | 29761 |
rs2823494 | snp | A/T | 0 | 0 | intron-variant | USP25 | GRCh38.p7 | 21:15791292 | CATTTTATGTTTGAA[A/T]TTTCATTTTTCTTAG | 29761 |
rs2823495 | snp | A/G | 0.365024 | 0.221967 | intron-variant | USP25 | GRCh38.p7 | 21:15792082 | AATTATAGACACTTA[A/G]TATTTTTAATAAGCA | 29761 |
rs2823496 | snp | A/T | 0.365853 | 0.221536 | intron-variant | USP25 | GRCh38.p7 | 21:15792981 | ATTGATACCTTAGAG[A/T]TTCTTAGATCATCTT | 29761 |
rs2823497 | snp | A/C | 0.364817 | 0.222075 | intron-variant | USP25 | GRCh38.p7 | 21:15810352 | TTTTAAACAATACTT[A/C]ACAAATCAATTAATA | 29761 |
rs2823498 | snp | A/G | 0.171057 | 0.237209 | intron-variant | USP25 | GRCh38.p7 | 21:15810564 | CTTGGAAAATTTGTA[A/G]ATGACTAATTCTACC | 29761 |
rs2823499 | snp | A/G | 0.359787 | 0.224604 | intron-variant | USP25 | GRCh38.p7 | 21:15820203 | TGTTTGCTGTTAAAT[A/G]AAAGGATGATTGGGG | 29761 |
rs2823500 | snp | A/G | 0.367297 | 0.220775 | intron-variant | USP25 | GRCh38.p7 | 21:15823022 | TCCTCCTCAGATTCA[A/G]TTTGCCAGATGTGTG | 29761 |
rs2823501 | snp | A/G | 0.145642 | 0.227177 | intron-variant | USP25 | GRCh38.p7 | 21:15828108 | GGATATTATATGACC[A/G]ACTTAACTCTTTATA | 29761 |
rs2823502 | snp | A/C | 0.412416 | 0.190055 | intron-variant | USP25 | GRCh38.p7 | 21:15830461 | ATGTTTGTAGGAAAA[A/C]CATTAGTCCTTATCT | 29761 |
rs2823503 | snp | C/T | 0.301872 | 0.244559 | intron-variant | USP25 | GRCh38.p7 | 21:15830493 | ATAAGTAGAAACACA[C/T]TTGCTGTTAATCATT | 29761 |
rs2823504 | snp | A/T | 0.453818 | 0.144769 | intron-variant | USP25 | GRCh38.p7 | 21:15835329 | CATCTCTCCAAATTT[A/T]CAGAGTTAACATATT | 29761 |
rs2823505 | snp | A/G | 0.372391 | 0.217992 | intron-variant | USP25 | GRCh38.p7 | 21:15849667 | AATTTGGTATTAAAA[A/G]TGCAACATTTGATTT | 29761 |
rs2823506 | snp | A/G | 0.447938 | 0.152711 | intron-variant | USP25 | GRCh38.p7 | 21:15852976 | CTTAAAAATTTTTTC[A/G]TATAAAAAATGAAAG | 29761 |
rs2823507 | snp | C/T | 0.460813 | 0.134379 | intron-variant | USP25 | GRCh38.p7 | 21:15853709 | TGTATTAAATGAATT[C/T]GGTGTTTTTCTATTT | 29761 |
rs2823508 | snp | A/G | 0.32153 | 0.239548 | intron-variant | USP25 | GRCh38.p7 | 21:15854072 | TTTCCCCTCAATTAG[A/G]TATAGTATTTTTAAA | 29761 |
rs2823509 | snp | C/G | 0.225893 | 0.248835 | intron-variant | USP25 | GRCh38.p7 | 21:15857085 | GTCCTAGGTTTAAAT[C/G]CTAACATTATCATTT | 29761 |
rs2823510 | snp | A/G | 0.405082 | 0.196086 | intron-variant | USP25 | GRCh38.p7 | 21:15857642 | ACAATTGATTCATCT[A/G]TAATTTGCAAATTAT | 29761 |
rs2823511 | snp | A/G | 0.404907 | 0.196224 | intron-variant | USP25 | GRCh38.p7 | 21:15858361 | GTTGTGTTCTTTAGT[A/G]AGGTTTTATAATTTT | 29761 |
rs2823512 | snp | A/C | 0.0941369 | 0.195465 | intron-variant | USP25 | GRCh38.p7 | 21:15858670 | ATTGCGGTGATCAGA[A/C]ATTTTTATTACATAT | 29761 |
rs2823513 | snp | A/G | 0.260227 | 0.249791 | intron-variant | USP25 | GRCh38.p7 | 21:15862465 | CCTGTGACAATCATT[A/G]TCGAAGGTTCATATC | 29761 |
rs3215890 | in-del | -/T | | | intron-variant | USP25 | GRCh38.p7 | 21:15811448 | ATCCTCATGTTTTTT[-/T]CCAGTGAGAGGGCTT | 29761 |
rs3787577 | snp | C/T | 0.11963 | 0.213316 | intron-variant | USP25 | GRCh38.p7 | 21:15796060 | ACCAAACTTCATTTT[C/T]GTAAGTGCTTTTCAA | 29761 |
rs4143347 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | USP25 | GRCh38.p7 | 21:15839947 | ATCCCAGAGTCTTTG[A/T]gagtttctctgagag | 29761 |
rs4143348 | snp | G/T | | | intron-variant | USP25 | GRCh38.p7 | 21:15731063 | ATTCCAGGAATCTTT[G/T]gtcccctaagtttga | 29761 |
rs4580465 | snp | A/T | 0.325327 | 0.238382 | intron-variant | USP25 | GRCh38.p7 | 21:15749023 | GTGTGTTTTTTTTTT[A/T]AATTTTTTTTTCTTA | 29761 |
rs5842545 | in-del | -/C/CC | | | intron-variant | USP25 | GRCh38.p7 | 21:15787912 | CCTCACCCCCCCCCC[-/C/CC]AAGTAAAACCACCGT | 29761 |
rs5842546 | in-del | -/T | 0.0648419 | 0.167978 | intron-variant | USP25 | GRCh38.p7 | 21:15792603 | TATGACAGCTTAAAC[-/T]TTCATATGATATTAA | 29761 |
rs6517609 | snp | A/C | 0.394171 | 0.204242 | intron-variant | USP25 | GRCh38.p7 | 21:15742177 | ATCTGAATTGGAAAA[A/C]CCCCACTATATCTGT | 29761 |
rs6517611 | snp | A/G | 0.39527 | 0.203462 | intron-variant | USP25 | GRCh38.p7 | 21:15745130 | CTTTTATGGTCGGGG[A/G]GAGGGAGGTGTGGGA | 29761 |
rs6517612 | snp | C/T | 0.32955 | 0.237006 | intron-variant | USP25 | GRCh38.p7 | 21:15745976 | ctgtcctttcatcat[C/T]gaattatattggtac | 29761 |
rs6517613 | snp | A/G | 0.395635 | 0.2032 | intron-variant | USP25 | GRCh38.p7 | 21:15746069 | tccttatgtggtgcc[A/G]ttctttcttgattac | 29761 |
rs6517648 | snp | C/T | 0.397633 | 0.201754 | intron-variant, upstream-variant-2KB | USP25 | GRCh38.p7 | 21:15775950 | CGCTAATTAATCACA[C/T]ACCTAAACCCTGTTT | 29761 |
rs6517652 | snp | C/T | 0.397452 | 0.201886 | intron-variant | USP25 | GRCh38.p7 | 21:15782283 | TGCTCCCAGCTTGAA[C/T]AGCTGGCCCAGAGGT | 29761 |