SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6397000 | snp | A/G | 0.5 | 0 | intron-variant | Uchl5 | Mm_Celera | 1:143779701 | gcttcaaaggaaaaa[A/G]tgctttattctantt | 56207 |
rs6397012 | snp | A/G | 0.5 | 0 | intron-variant | Uchl5 | Mm_Celera | 1:143779714 | aantgctttattcta[A/G]ttattttcatttttt | 56207 |
rs6397477 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Uchl5 | GRCm38.p3 | 1:143779772 | GGGTTTGGAAGTTTA[C/T]TTGTCTGAAAGTGAA | 56207 |
rs6397992 | snp | A/T | 0.5 | 0 | intron-variant | Uchl5 | Mm_Celera | 1:143779845 | TGAACTCACTGTCTA[A/T]CGTAGCCTTCACTGT | 56207 |
rs6406494 | snp | A/G | 0.5 | 0 | intron-variant | Uchl5 | Mm_Celera | 1:143792290 | TTCTCAGTTTTTATT[A/G]TTTAGTTTCTCTATG | 56207 |
rs6407042 | snp | A/C/G | 0.5 | 0 | intron-variant | Uchl5 | Mm_Celera | 1:143792360 | AAATTAGTAAATGAC[A/C/G]CCTATGGCTGCANCC | 56207 |
rs6407057 | snp | A/T | 0.5 | 0 | intron-variant | Uchl5 | Mm_Celera | 1:143792373 | ACNCCTATGGCTGCA[A/T]CCACATTAATACAAC | 56207 |
rs6408137 | snp | A/G | 0.5 | 0 | intron-variant | Uchl5 | Mm_Celera | 1:143792589 | TTTTATGTCGTTCAT[A/G]TATCTTTGTGATTTC | 56207 |
rs6408799 | snp | C/T | 0.5 | 0 | intron-variant | Uchl5 | Mm_Celera | 1:143792732 | tatgtgtgtatgtta[C/T]atgtatgtaaatctg | 56207 |
rs6409268 | snp | C/T | 0.5 | 0 | intron-variant | Uchl5 | Mm_Celera | 1:143792761 | tgtaggcatgtatcc[C/T]cacatatatacatgc | 56207 |
rs6409787 | snp | C/G | 0.5 | 0 | intron-variant | Uchl5 | Mm_Celera | 1:143792852 | ACAAGGTCTTTGAAT[C/G]TGAAACTCACCTTTT | 56207 |
rs6409826 | snp | A/G | 0.5 | 0 | intron-variant | Uchl5 | Mm_Celera | 1:143792879 | TTTTTAGCCAGGCTA[A/G]ACTTTAGCCAGTGAA | 56207 |
rs13476151 | snp | C/G | 0.458272 | 0.138286 | intron-variant | Uchl5 | GRCm38.p3 | 1:143793027 | ACATAATGAACATCT[C/G]CTCATATCTTTGAAC | 56207 |
rs30471156 | snp | C/T | 0.5 | 0 | intron-variant | Uchl5 | GRCm38.p3 | 1:143795390 | CAGAGACAGAGCATG[C/T]GCACATCTGAGACAG | 56207 |
rs30502300 | snp | C/T | 0.444444 | 0.157135 | upstream-variant-2KB, intron-variant | Uchl5, Trove2 | GRCm38.p3 | 1:143776656 | CAGGAGCTTTGCAAG[C/T]GGGAGAGTTGACCTG | 56207 |
rs30523058 | snp | G/T | 0.375 | 0.216506 | intron-variant | Uchl5 | GRCm38.p3 | 1:143788524 | AGAGTTGGGAATTTT[G/T]CTTTGAAATATAGTA | 56207 |
rs30614796 | snp | C/T | 0.32 | 0.24 | intron-variant | Uchl5 | GRCm38.p3 | 1:143792706 | AAAGCTTAAGGAATC[C/T]TCTCTCTCTGTATGT | 56207 |
rs30889162 | snp | C/T | 0.265928 | 0.249492 | downstream-variant-500B | Uchl5 | Mm_Celera | 1:143807653 | ATTAAAAAAACTAGT[C/T]ATCCAAGCACATGTA | 56207 |
rs30943911 | snp | C/T | 0.375 | 0.216506 | intron-variant | Uchl5 | GRCm38.p3 | 1:143789445 | ACTATTATTATACTA[C/T]TCTTAAGGTGTCAAA | 56207 |
rs30973384 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Uchl5 | Mm_Celera | 1:143804309 | ACACAATAAAAAGCT[A/G]TCAAGGAATTTCTTA | 56207 |
rs30973385 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Uchl5 | Mm_Celera | 1:143804240 | TTTGGAACTCTGTGC[C/T]AATAAACGAAGCAAA | 56207 |
rs30973386 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Uchl5 | Mm_Celera | 1:143804160 | CTAAATAATTTTCTT[A/T]GCAAATGTATTTTTG | 56207 |
rs30973387 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Uchl5 | Mm_Celera | 1:143804058 | TGGCATGGGTTGGCA[A/T]GGAATGAAACAATTA | 56207 |
rs30973388 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Uchl5 | Mm_Celera | 1:143803858 | TAGTTTGTAGCAGGT[G/T]TTATCCTGTAATATT | 56207 |
rs30973389 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Uchl5 | Mm_Celera | 1:143803706 | TGGTTTTGTGAGCTT[A/C]GAGTAAACCTTTGTA | 56207 |
rs30973390 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Uchl5 | Mm_Celera | 1:143803672 | ATTGTCCATGACTGT[A/G]TTCCCCAAATGATGA | 56207 |
rs30973391 | snp | C/T | 0.231111 | 0.249285 | intron-variant, downstream-variant-500B | Uchl5 | Mm_Celera | 1:143803554 | TATCACTTTATTCAA[C/T]GCAAACGGTTCTTTA | 56207 |
rs30973392 | snp | C/T | 0.244898 | 0.249948 | intron-variant, downstream-variant-500B | Uchl5 | Mm_Celera | 1:143803502 | AGAATTCAGAGGCAT[C/T]CGGAATACAGTTTCT | 56207 |
rs30973393 | snp | C/T | 0.124444 | 0.216185 | intron-variant, downstream-variant-500B | Uchl5 | Mm_Celera | 1:143803348 | ACTTGAAGCCTGTGA[C/T]CCTCAAACTGTTATA | 56207 |
rs30974314 | snp | A/G | 0.124444 | 0.216185 | intron-variant, downstream-variant-500B | Uchl5 | Mm_Celera | 1:143803301 | TCGGGGTGCTCTGAG[A/G]TGGGAAACTGAGTTT | 56207 |
rs30974315 | snp | C/G | 0.124444 | 0.216185 | intron-variant, downstream-variant-500B | Uchl5 | Mm_Celera | 1:143803219 | ATTACCTGAGACATA[C/G]GACTCACTTTTTAGC | 56207 |
rs30974316 | snp | A/T | 0.345679 | 0.230967 | intron-variant | Uchl5 | Mm_Celera | 1:143802809 | CACTTAATAAAATAT[A/T]CAAGGAATAAATGAG | 56207 |
rs30974317 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Uchl5 | Mm_Celera | 1:143802682 | GGGGATAAAAGAATA[A/G]TTTGGCTAGCACACA | 56207 |
rs30974318 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Uchl5 | Mm_Celera | 1:143802610 | AGTTTTTTTCCTTAG[C/T]TAATTTTGTAAAATT | 56207 |
rs30974319 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Uchl5 | Mm_Celera | 1:143802478 | ACAAAAACAGGTATC[G/T]CCCCACTACTGTATC | 56207 |
rs30974320 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Uchl5 | Mm_Celera | 1:143802453 | AAGTAATGTAGCCTG[A/G]TACTTTAAAACAAAA | 56207 |
rs30974321 | snp | C/G | 0.32 | 0.24 | intron-variant | Uchl5 | Mm_Celera | 1:143802431 | CTGCTGTTTTGAATT[C/G]TAAGAGAAGTAATGT | 56207 |
rs30974322 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Uchl5 | Mm_Celera | 1:143802380 | GTAGTTATTTTTTTG[C/T]CTAGGGTTTTGTATT | 56207 |
rs30974323 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Uchl5 | Mm_Celera | 1:143802318 | AATGGAGGTAAAATA[C/T]CTGGGGCTTTTGTAG | 56207 |
rs30975214 | snp | C/T | 0.32 | 0.24 | intron-variant | Uchl5 | Mm_Celera | 1:143802256 | GTTTCTTGGTGACTA[C/T]TCAAGCTAGGTTAGG | 56207 |
rs30975215 | snp | A/G | 0.32 | 0.24 | synonymous-codon, nc-transcript-variant | Uchl5 | Mm_Celera | 1:143802182 | GCCTTTCATTATGGA[A/G]TTGTTAAAGACCTTA | 56207 |
rs30975216 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Uchl5 | Mm_Celera | 1:143802059 | TCAAATCTTATTCCT[A/C]ATACTGTTTATGAGA | 56207 |
rs30975217 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Uchl5 | Mm_Celera | 1:143801871 | GTAGACCTTGGTGAG[G/T]TGGTTTTCACAGCTT | 56207 |
rs30975218 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Uchl5 | Mm_Celera | 1:143801758 | CCTCACTGACTAATC[A/T]AAGGCCTCAAGAAAA | 56207 |
rs30975219 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Uchl5 | Mm_Celera | 1:143801647 | GGAGTGCCTTACAAA[C/T]GGGAAAGGAGCAGTG | 56207 |
rs30975220 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Uchl5 | Mm_Celera | 1:143801490 | GCAATGGGGAAGTAT[A/G]AGATGATAGTTTCAA | 56207 |
rs30975221 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Uchl5 | Mm_Celera | 1:143801440 | CTCAACAGGCAACAA[A/G]TCACTGTTAATGATG | 56207 |
rs30975222 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Uchl5 | Mm_Celera | 1:143801362 | CCTTTTCATGTGATG[C/T]TCAAGGCAAGGACTA | 56207 |
rs30975223 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Uchl5 | Mm_Celera | 1:143801335 | GTTATGTACCGAAGT[A/G]GTACAAGATTCCCTT | 56207 |
rs30976215 | snp | C/T | 0.33241 | 0.236027 | downstream-variant-500B | Uchl5 | Mm_Celera | 1:143807935 | ATCTTGTGTTCCCTT[C/T]CTAATTTCATGATTT | 56207 |
rs30976216 | snp | C/G | 0.33241 | 0.236027 | downstream-variant-500B | Uchl5 | GRCm38.p3 | 1:143807907 | ATCACCGAACTAACT[C/G]AAAACCAGTTCTATC | 56207 |
rs30976217 | snp | C/T | 0.124444 | 0.216185 | downstream-variant-500B | Uchl5 | Mm_Celera | 1:143807657 | AAAAAACTAGTCATC[C/T]AAGCACATGTAAAAG | 56207 |
rs30976218 | snp | C/T | 0.124444 | 0.216185 | downstream-variant-500B | Uchl5 | Mm_Celera | 1:143807566 | CACAGTTTCCAGGAT[C/T]TTTGTCTTTCAAGAG | 56207 |
rs30976219 | snp | C/T | 0.32 | 0.24 | utr-variant-3-prime, downstream-variant-500B | Uchl5 | Mm_Celera | 1:143807444 | AGATAACGTTATGTG[C/T]ATTCATTAAAAATTA | 56207 |
rs30976220 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime, downstream-variant-500B | Uchl5 | Mm_Celera | 1:143807415 | TTGAGAGTTTTTTGA[C/T]AACCTGTTTTTCAAG | 56207 |
rs30976221 | snp | G/T | 0.124444 | 0.216185 | utr-variant-3-prime, downstream-variant-500B | Uchl5 | Mm_Celera | 1:143807169 | GTTTTTGTCTTTGGG[G/T]TGTGTTGTGCAGATC | 56207 |
rs30976222 | snp | A/C | 0.231111 | 0.249285 | utr-variant-3-prime, downstream-variant-500B | Uchl5 | Mm_Celera | 1:143807081 | ATTTATTAGCTTAGT[A/C]TATTCAATTTATAAA | 56207 |
rs30976223 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime, downstream-variant-500B | Uchl5 | Mm_Celera | 1:143806981 | TCTGGGAGTTCTTGG[C/T]ACTCTAGAAATACAA | 56207 |
rs30976254 | snp | G/T | 0.32 | 0.24 | intron-variant | Uchl5 | Mm_Celera | 1:143801306 | AGGAGGACTTAGATA[G/T]TGGATGCCTAATGGT | 56207 |
rs30976255 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Uchl5 | Mm_Celera | 1:143801133 | TGTATAACCAAATTG[C/T]TATGCCTTAAAGTTA | 56207 |
rs30976256 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Uchl5 | Mm_Celera | 1:143801016 | CACCACACCCGGCTT[C/T]ATCCTATCTCTATCT | 56207 |
rs30976257 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Uchl5 | Mm_Celera | 1:143800806 | TAATAATACTTAAAT[C/T]TTTTAAATTAATTTC | 56207 |
rs30976258 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Uchl5 | Mm_Celera | 1:143800773 | GTTCCTCTGAACATT[A/T]CTCATTTGGTTCATG | 56207 |
rs30976259 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Uchl5 | Mm_Celera | 1:143800654 | TGTTAGTAGTGCTAG[A/G]TGAATTAATATAATA | 56207 |
rs30976260 | snp | A/T | 0.32 | 0.24 | intron-variant | Uchl5 | Mm_Celera | 1:143800643 | AAGTACATTTTTGTT[A/T]GTAGTGCTAGATGAA | 56207 |
rs30976261 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Uchl5 | Mm_Celera | 1:143800573 | TGAAAATGGTTTAAA[A/G]CGCACTAGGTGATTG | 56207 |
rs30976262 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Uchl5 | Mm_Celera | 1:143800530 | AAACCTCCTGCTGGA[A/G]TACTGATGCATGCTA | 56207 |
rs30976263 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Uchl5 | Mm_Celera | 1:143800511 | ATAGCCTTGAACCAG[C/T]AGTAAACCTCCTGCT | 56207 |
rs30977024 | snp | A/G | 0.124444 | 0.216185 | utr-variant-3-prime, nc-transcript-variant | Uchl5 | Mm_Celera | 1:143806753 | TTGGACGTGTGTACA[A/G]TGTGCTGCACTTAAT | 56207 |
rs30977025 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Uchl5 | Mm_Celera | 1:143806574 | ACAGGCTCTAGTAGC[A/G]TGAACGATGCATAAG | 56207 |
rs30977026 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Uchl5 | Mm_Celera | 1:143806274 | GGACAAATATGTATG[A/G]TTGTTTAGCTTTATA | 56207 |
rs30977027 | snp | A/G | 0.359862 | 0.224567 | intron-variant | Uchl5 | GRCm38.p3 | 1:143806064 | AGGTCTAATAAATTT[A/G]CTAATACTATATACA | 56207 |
rs30977028 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Uchl5 | Mm_Celera | 1:143805902 | TGTCTTTGACATCTA[G/T]TGAAACTTCACTGTA | 56207 |
rs30977029 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Uchl5 | Mm_Celera | 1:143805896 | AACAAGTGTCTTTGA[C/T]ATCTATTGAAACTTC | 56207 |
rs30977030 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Uchl5 | Mm_Celera | 1:143805428 | TTAGATAATACCTGT[A/G]TTTTATGTATACATG | 56207 |
rs30977031 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Uchl5 | GRCm38.p3 | 1:143805288 | CAAAAATAAAGAATC[C/T]AGATGGGAAAAGGAA | 56207 |
rs30977032 | snp | C/T | 0.33241 | 0.236027 | intron-variant | Uchl5 | GRCm38.p3 | 1:143805068 | ATTTTAGTAAACATT[C/T]TGTAAACTATAAAGA | 56207 |
rs30977033 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Uchl5 | Mm_Celera | 1:143805033 | CTTAAAGAAGTAGGA[C/T]GATCACAATAATTTT | 56207 |
rs30977054 | snp | A/G | 0.32 | 0.24 | intron-variant | Uchl5 | Mm_Celera | 1:143800477 | TGCCTGGCCTGTAGT[A/G]AACTGTGTATAAAGG | 56207 |
rs30977055 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Uchl5 | Mm_Celera | 1:143800450 | TCAAATGTAACCCTG[A/G]CTGTGTGGCTGTGCC | 56207 |
rs30977056 | snp | C/T | 0.32 | 0.24 | intron-variant | Uchl5 | Mm_Celera | 1:143800329 | CTGTGCTGTGTAGTG[C/T]CTTGATCAAGACTTG | 56207 |
rs30977057 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Uchl5 | GRCm38.p3 | 1:143800165 | CCCTTGACAGAGTCT[C/T]ACTTTTTAAATGCTC | 56207 |
rs30977058 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Uchl5 | Mm_Celera | 1:143800161 | CAGGCCCTTGACAGA[C/G]TCTCACTTTTTAAAT | 56207 |
rs30977059 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Uchl5 | Mm_Celera | 1:143800045 | ATAAGGTATGTTTTT[A/T]AAAAATAGGCTATAA | 56207 |
rs30977060 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Uchl5 | Mm_Celera | 1:143799830 | CTTGTCTACAAAGTT[A/G]AAATATGAAAATAAT | 56207 |
rs30977061 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Uchl5 | Mm_Celera | 1:143799757 | TTCTAGAACAGAAAT[A/G]TGGAAGGTATATTTA | 56207 |
rs30977062 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Uchl5 | Mm_Celera | 1:143799730 | ATATTGGTAGTAGGT[A/G]AAAGTCAAATATTCT | 56207 |
rs30977063 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Uchl5 | Mm_Celera | 1:143799727 | ACAATATTGGTAGTA[A/G]GTGAAAGTCAAATAT | 56207 |
rs30977724 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Uchl5 | Mm_Celera | 1:143805024 | CTTCTGTCTCTTAAA[A/G]AAGTAGGACGATCAC | 56207 |
rs30977725 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Uchl5 | Mm_Celera | 1:143804957 | TGATAAAGGGATACA[A/G]ATGAATTGAATTTAG | 56207 |
rs30977726 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Uchl5 | Mm_Celera | 1:143804915 | TTTAAACTTCTGGTC[C/T]TTATTATGTAAAACC | 56207 |
rs30977727 | snp | C/T | 0.32 | 0.24 | intron-variant | Uchl5 | Mm_Celera | 1:143804899 | TTGTCTATTTCACCT[C/T]TTTAAACTTCTGGTC | 56207 |
rs30977728 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Uchl5 | Mm_Celera | 1:143804786 | GCTAGATTAAGATTC[C/T]ATTTGTGAGTCCTCT | 56207 |
rs30977729 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Uchl5 | Mm_Celera | 1:143804671 | AAATTTAATGGTTTT[A/G]TTATATGAGAGTTGT | 56207 |
rs30977730 | snp | A/G | 0.18 | 0.24 | intron-variant | Uchl5 | GRCm38.p3 | 1:143804540 | ACTTTGACTGAGACA[A/G]CTGTCTATATAGTCA | 56207 |
rs30977731 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Uchl5 | Mm_Celera | 1:143804380 | CTTGGATTTGGACTT[A/G]GAATATATGGAATTT | 56207 |
rs30977794 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Uchl5 | Mm_Celera | 1:143798329 | TTATATAGTAATCAC[A/G]ATGAATTATCTTAAT | 56207 |
rs30977795 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Uchl5 | Mm_Celera | 1:143797996 | TAAATAAAGTTTAAA[A/T]TCCATTCACCAACAG | 56207 |
rs30977796 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Uchl5 | Mm_Celera | 1:143797763 | TAGAATTTTAAGACA[C/G]TTTTGAAGTATCTTG | 56207 |
rs30977797 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Uchl5 | Mm_Celera | 1:143797545 | CCATGTCACCTTAGG[A/T]TTCTTCAGACCTACA | 56207 |