SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs4228651 | snp | A/C | 0.21875 | 0.248039 | utr-variant-3-prime | Ubtd2 | GRCm38.p3 | 11:32516515 | AATAAAAAGGAGCCA[A/C]GGGATCTTGGAAGAA | 327900 |
rs4228652 | snp | A/C | 0.21875 | 0.248039 | synonymous-codon | Ubtd2 | GRCm38.p3 | 11:32516388 | CAGCTTCATCTTATC[A/C]GTGAGAGGCCTGCCA | 327900 |
rs4228653 | snp | C/G | 0.21875 | 0.248039 | synonymous-codon | Ubtd2 | Mm_Celera | 11:32516361 | GCCAGAGAAGAACCA[C/G]CGCTGGCTGCCTGGC | 327900 |
rs4228654 | snp | A/G | 0.21875 | 0.248039 | synonymous-codon | Ubtd2 | GRCm38.p3 | 11:32516340 | GCTGCCTGGCTCCAC[A/G]CCCTCTGTGGCGTGT | 327900 |
rs4228655 | snp | A/G | 0.21875 | 0.248039 | synonymous-codon | Ubtd2 | GRCm38.p3 | 11:32516328 | CACGCCCTCTGTGGC[A/G]TGTAAGCGCCTCTTC | 327900 |
rs4228656 | snp | A/G | 0.21875 | 0.248039 | synonymous-codon | Ubtd2 | GRCm38.p3 | 11:32516280 | TGTGCTGCGGACCAC[A/G]AGCCTGAGGTCTTTG | 327900 |
rs4228657 | snp | C/T | 0.21875 | 0.248039 | missense | Ubtd2 | GRCm38.p3 | 11:32516276 | CTGCGGACCACGAGC[C/T]TGAGGTCTTTGCCTG | 327900 |
rs4228658 | snp | A/G | 0.21875 | 0.248039 | synonymous-codon | Ubtd2 | GRCm38.p3 | 11:32516247 | TGTGGAGAGCCGCAG[A/G]CGGAGCTGAGATTCG | 327900 |
rs4228659 | snp | A/G | 0.21875 | 0.248039 | synonymous-codon | Ubtd2 | GRCm38.p3 | 11:32516232 | GCGGAGCTGAGATTC[A/G]TGTCCAGAATTGGGA | 327900 |
rs6204093 | snp | C/T | 0.5 | 0 | intron-variant | Ubtd2 | Mm_Celera | 11:32494750 | gccactgctcacaca[C/T]gatgcacatatatgc | 327900 |
rs6205294 | snp | A/T | 0.456747 | 0.140554 | intron-variant | Ubtd2 | Mm_Celera | 11:32494978 | CTTATTCTGATTTAT[A/T]TCTGCAGAGGAAATA | 327900 |
rs6281878 | snp | A/G | 0.5 | 0 | intron-variant | Ubtd2 | Mm_Celera | 11:32459587 | ttggggaattatgac[A/G]attctacttatcttt | 327900 |
rs6293206 | snp | A/G | 0.5 | 0 | intron-variant | Ubtd2 | Mm_Celera | 11:32498749 | tcctcagactcagag[A/G]tccacttgcctgcct | 327900 |
rs6384398 | snp | A/C | 0.5 | 0 | intron-variant | Ubtd2 | Mm_Celera | 11:32471272 | GCTTTTCATTTTAGC[A/C]CAACTTCTTTCATGT | 327900 |
rs6385549 | snp | G/T | 0.456747 | 0.140554 | intron-variant | Ubtd2 | Mm_Celera | 11:32471464 | TGGGGATGTTAAGGC[G/T]GCCTTCTGATTTCAC | 327900 |
rs13463159 | snp | C/T | 0.497778 | 0.0332592 | utr-variant-3-prime | Ubtd2 | Mm_Celera | 11:32517885 | CTGAGAAGGGGACTA[C/T]CATGTGACCACACTG | 327900 |
rs26847391 | snp | A/G | 0.444444 | 0.157135 | utr-variant-3-prime | Ubtd2 | Mm_Celera | 11:32517074 | CTCAGTCCTGTGGCC[A/G]TCATGCTGGCAGCGG | 327900 |
rs26847392 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon | Ubtd2 | Mm_Celera | 11:32516379 | GTTCTTCTCTGGCAG[A/G]CCTCTCACGGATAAG | 327900 |
rs26847393 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Ubtd2 | Mm_Celera | 11:32516055 | GTAGAGAGAAGCACA[C/G]TCACTGAAACTGTCC | 327900 |
rs26847394 | snp | C/G | 0.489796 | 0.070696 | intron-variant | Ubtd2 | Mm_Celera | 11:32515960 | CCTCTTAGAGCTTTT[C/G]TCTTGGCTTTCCTGC | 327900 |
rs26847395 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Ubtd2 | Mm_Celera | 11:32515826 | CTGCACCTGATGCAC[A/C]GTCCCGCATGTGGTT | 327900 |
rs26847396 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ubtd2 | Mm_Celera | 11:32514395 | GTTTGTATCTTCATG[C/T]CCCGCTTTGGGTGTG | 327900 |
rs26847397 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Ubtd2 | Mm_Celera | 11:32511705 | GCAAGCTTCACTCAC[A/G]GCCTTCTCCCTTTGG | 327900 |
rs26847398 | snp | C/G | 0.473373 | 0.11227 | intron-variant | Ubtd2 | Mm_Celera | 11:32511595 | TCTGATGTCTGTATG[C/G]CAATTCTTGAAGTTT | 327900 |
rs26847399 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Ubtd2 | Mm_Celera | 11:32511423 | GAGTTCCCATTGCTG[G/T]TCTCTGCTCAGCCTC | 327900 |
rs26847400 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Ubtd2 | Mm_Celera | 11:32511416 | GCTCCTGGAGTTCCC[A/G]TTGCTGTTCTCTGCT | 327900 |
rs26847401 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ubtd2 | Mm_Celera | 11:32511366 | CAGTTCTCTCGATCC[C/T]ACTCAGCTGTTGTTC | 327900 |
rs26847402 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Ubtd2 | Mm_Celera | 11:32508454 | CAGAAACCCAAGGTC[G/T]GTCTGTGTTGGATGC | 327900 |
rs26847403 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Ubtd2 | Mm_Celera | 11:32508288 | TGAGACCTTCTGTAA[A/G]TTCCTAATGCAGCCA | 327900 |
rs26847404 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Ubtd2 | Mm_Celera | 11:32508287 | TTGAGACCTTCTGTA[A/C]GTTCCTAATGCAGCC | 327900 |
rs26847405 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ubtd2 | Mm_Celera | 11:32508277 | GGGGTAGTGATTGAG[A/G]CCTTCTGTAAGTTCC | 327900 |
rs26847406 | snp | A/G | 0.5 | 0 | intron-variant | Ubtd2 | Mm_Celera | 11:32506345 | TTCCTCTTCTTACTT[A/G]AATTCTCTGGTGGTT | 327900 |
rs26847407 | snp | G/T | 0.459184 | 0.136902 | intron-variant | Ubtd2 | Mm_Celera | 11:32506313 | TTCAGGATCCTCTGT[G/T]ACCTGAGCCTCACTA | 327900 |
rs26847408 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ubtd2 | Mm_Celera | 11:32506115 | TCCAAGGACCTTTAG[A/G]CAATTTCACTATGGT | 327900 |
rs26847409 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ubtd2 | Mm_Celera | 11:32505095 | CCTCCAAGAGACAAA[A/G]GTGGATGTTTGAATG | 327900 |
rs26847410 | snp | A/C | 0.396694 | 0.202437 | intron-variant | Ubtd2 | Mm_Celera | 11:32504214 | CTTTCTTTCCAGTCT[A/C]TCCCTATTACCTCCC | 327900 |
rs26847411 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Ubtd2 | Mm_Celera | 11:32504206 | GCTCCCTCCTTTCTT[C/T]CCAGTCTCTCCCTAT | 327900 |
rs26847412 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ubtd2 | Mm_Celera | 11:32503410 | ATTCACACCCAATAT[A/G]CAATTTCAAATCTGT | 327900 |
rs26847413 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ubtd2 | Mm_Celera | 11:32503092 | GTCTGTAAACAGCTT[C/T]TTCCCATAGCTTTTA | 327900 |
rs26847414 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ubtd2 | Mm_Celera | 11:32503021 | GCTAACAGGTAAGTT[C/T]CCTGCACCACCCTTG | 327900 |
rs26847415 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Ubtd2 | Mm_Celera | 11:32501558 | TCAACCAGATGGCTC[A/C]GCAGTGTTTACCATC | 327900 |
rs26847416 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ubtd2 | Mm_Celera | 11:32501509 | TTATGGTCTCCAAAT[C/T]GTGGCTTAATTTAAA | 327900 |
rs26847417 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ubtd2 | Mm_Celera | 11:32501221 | TTGAATTATTTGAGC[A/G]CCATTTCAGGATGCC | 327900 |
rs26847418 | snp | A/G | 0.32 | 0.24 | intron-variant | Ubtd2 | Mm_Celera | 11:32500969 | CATTGTTTTTCCCAA[A/G]GTCTTTTTTATTTTA | 327900 |
rs26847419 | snp | A/T | 0.473373 | 0.11227 | intron-variant | Ubtd2 | Mm_Celera | 11:32500627 | TAAAGATTGTTTTCC[A/T]TGACTATAGTCTGAG | 327900 |
rs26847420 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Ubtd2 | Mm_Celera | 11:32500085 | TCTCTAGAGACAAGC[C/T]CCCAGTCTGCTTCCC | 327900 |
rs26847421 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Ubtd2 | GRCm38.p3 | 11:32500054 | GGTATTTTCTACTTT[C/G]TATGTGACTTAGTTC | 327900 |
rs26847422 | snp | C/T | 0.444444 | 0.157135 | synonymous-codon, intron-variant | Ubtd2 | Mm_Celera | 11:32499436 | ACAGGCAATCATTGA[C/T]GGTGCAAACATAACA | 327900 |
rs26847423 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Ubtd2 | Mm_Celera | 11:32497461 | TCCTCTAGTAGTTAT[C/T]TTCCTGAATTTGGTG | 327900 |
rs26847424 | snp | A/C | 0.32 | 0.24 | intron-variant | Ubtd2 | Mm_Celera | 11:32496985 | GAAAGTGTCTGGGTA[A/C]AGGGGTTGCCGGAGA | 327900 |
rs26847425 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ubtd2 | Mm_Celera | 11:32496762 | GAGTTTTGATGCATA[C/T]TTCTCTGCTTCCCAC | 327900 |
rs26847426 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Ubtd2 | Mm_Celera | 11:32494405 | CGTGTTTTAATGAGA[C/G]GGTGGTTTGAATTAA | 327900 |
rs26847427 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ubtd2 | Mm_Celera | 11:32493463 | ACTGTTCTTAGCTCC[A/G]AAGTGACAGGTTTTT | 327900 |
rs26847428 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ubtd2 | Mm_Celera | 11:32492418 | AATAACAAGGAGATA[C/T]TAAAGTGATCACCAT | 327900 |
rs26847429 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ubtd2 | Mm_Celera | 11:32491521 | ATTTTCTTAGGCCTT[C/T]TAAAACAGTGGCAGT | 327900 |
rs26847430 | snp | A/G/T | 0.459184 | 0.136902 | intron-variant | Ubtd2 | GRCm38.p3 | 11:32491391 | AAGACTTGATCTCCC[A/G/T]GATGATGTTTGGGGA | 327900 |
rs26847431 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ubtd2 | Mm_Celera | 11:32490182 | TCTCTGCTATAGTCA[A/G]TGAGAAACATGAACT | 327900 |
rs26847432 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Ubtd2 | Mm_Celera | 11:32488908 | TCCAGCTGTTTGTAC[C/T]GTGGAGTATTATCAT | 327900 |
rs26847433 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ubtd2 | Mm_Celera | 11:32488003 | GGGTGCTGTGACCCT[A/G]TGAAATTGTCCATTC | 327900 |
rs26847434 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ubtd2 | Mm_Celera | 11:32487977 | TTAACTTGTCAGGTA[A/G]GAACGGGATAGGGTG | 327900 |
rs26847435 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Ubtd2 | Mm_Celera | 11:32487822 | TTCAGACACTAATCT[C/T]TATGCTACCACAGGT | 327900 |
rs26847436 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Ubtd2 | Mm_Celera | 11:32487818 | GATATTCAGACACTA[A/G]TCTCTATGCTACCAC | 327900 |
rs26847437 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ubtd2 | Mm_Celera | 11:32487125 | GTGTTATGCCAGTCA[A/G]GTCAGCTAAAAGCTT | 327900 |
rs26847438 | snp | A/T | 0.426035 | 0.177515 | intron-variant | Ubtd2 | Mm_Celera | 11:32480458 | ACCATGTAGAGACAT[A/T]TATTCAGGGTTGAAG | 327900 |
rs26847439 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ubtd2 | Mm_Celera | 11:32480432 | TTAAGCAACATAGAA[A/G]TGAAGCCAAAACCAT | 327900 |
rs26847440 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Ubtd2 | Mm_Celera | 11:32480382 | ATAGGAGTGTACATT[G/T]TTGAATGGGCATAGA | 327900 |
rs26847441 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Ubtd2 | Mm_Celera | 11:32480330 | AAGGACTGAGGTGGA[A/C]AGGAAAGGGAAAGGA | 327900 |
rs26847442 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ubtd2 | Mm_Celera | 11:32480304 | TGGCGTGTTACAGTG[A/G]AGGAAATGGGAAGGA | 327900 |
rs26847443 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Ubtd2 | Mm_Celera | 11:32480249 | ATGGAGGGTAGTAGG[A/C]TGTTGTTAGACTCAC | 327900 |
rs26847444 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Ubtd2 | Mm_Celera | 11:32480158 | ACTACTAAAGTTAGG[A/G]ATGGAAGGGGTGAGA | 327900 |
rs26847445 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Ubtd2 | Mm_Celera | 11:32480062 | CCCACTGAGCAAATA[C/T]TGTTACAGTTAAAAA | 327900 |
rs26847446 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ubtd2 | Mm_Celera | 11:32479983 | AGTTTATATACCCAG[A/G]GAACAGGGCATACCT | 327900 |
rs26847447 | snp | A/T | 0.426035 | 0.177515 | intron-variant | Ubtd2 | Mm_Celera | 11:32479931 | CAGTTCTCTGGTGAC[A/T]GTGCTGCCTGGGAAT | 327900 |
rs26847448 | snp | A/T | 0.375 | 0.216506 | intron-variant | Ubtd2 | Mm_Celera | 11:32479791 | TATAGCTTGTCTTCC[A/T]GGCCTACTATTTTGT | 327900 |
rs26847449 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Ubtd2 | Mm_Celera | 11:32479562 | TGCTTGTGGGTCTGT[C/T]TCTGTCAGTGCTGCA | 327900 |
rs26847450 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ubtd2 | Mm_Celera | 11:32479156 | GTTGGATAGCTTTTT[C/T]ACATGGGAGTTAAAG | 327900 |
rs26847451 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Ubtd2 | Mm_Celera | 11:32479053 | TTTTTGATGAACCAA[A/G]AGTATGAACAAAGCA | 327900 |
rs26847452 | snp | A/G | 0.46281 | 0.131194 | intron-variant | Ubtd2 | Mm_Celera | 11:32478347 | ATAACAAACTATGTA[A/G]AAATGACAGGAATAT | 327900 |
rs26847453 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Ubtd2 | Mm_Celera | 11:32478200 | TTTTATTGAGCATAC[C/T]ACTTGTCCTTTAGCT | 327900 |
rs26847454 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ubtd2 | Mm_Celera | 11:32477412 | CTCCAGTAAGCAGGG[A/G]CACTGGCTCACATCT | 327900 |
rs26847455 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ubtd2 | Mm_Celera | 11:32476323 | AGAAAGGGAAGGTTG[A/G]TTTCCCAGAACAATT | 327900 |
rs26847456 | snp | A/C/G | 0.444444 | 0.157135 | intron-variant | Ubtd2 | Mm_Celera | 11:32475816 | TTCCTGAAGAGCTTC[A/C/G]GGTGGGTCAGAGAAG | 327900 |
rs26847457 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ubtd2 | Mm_Celera | 11:32475781 | GTAACAACTAGAGCA[A/G]TAAGGGATAGTTGTG | 327900 |
rs26847458 | snp | C/T | 0.18 | 0.24 | intron-variant | Ubtd2 | Mm_Celera | 11:32475389 | TGAGTACTTTACATC[C/T]ATAAGTTTGTTTCCA | 327900 |
rs26847459 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ubtd2 | Mm_Celera | 11:32475363 | TATTTCTCATGTTCA[C/T]CATCCCTACCTGAGT | 327900 |
rs26847460 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Ubtd2 | Mm_Celera | 11:32475284 | AGAAACTAAACCAAA[A/G]CAAATTTTGTCAGTC | 327900 |
rs26847461 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Ubtd2 | Mm_Celera | 11:32475237 | CTCCCCAGCAGCCAT[A/G]TGTTCCTTTTCATGA | 327900 |
rs26847462 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Ubtd2 | Mm_Celera | 11:32475236 | CCTCCCCAGCAGCCA[C/T]GTGTTCCTTTTCATG | 327900 |
rs26847463 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Ubtd2 | Mm_Celera | 11:32474866 | CAACCAAGATGGTAG[A/T]GTGATTGGATCTGTA | 327900 |
rs26847464 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Ubtd2 | Mm_Celera | 11:32474248 | AAACTTGATGACTCT[C/T]TGAGACCTTGCATAT | 327900 |
rs26847465 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ubtd2 | Mm_Celera | 11:32474144 | CTCAGTACATTTTTA[A/G]TGGAACCTGGGATGA | 327900 |
rs26847466 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Ubtd2 | Mm_Celera | 11:32473937 | ATTCAAGAGTCTTGC[A/G]TGTTGTTTCTGTAGT | 327900 |
rs26847467 | snp | C/G | 0.459184 | 0.136902 | intron-variant | Ubtd2 | Mm_Celera | 11:32473883 | TTCTTTAGGACCCTA[C/G]TAGATACTGGAATTC | 327900 |
rs26862468 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ubtd2 | Mm_Celera | 11:32473554 | ATGTTCACACCGAAC[A/G]ACTTCTAAGGTCACT | 327900 |
rs26862469 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ubtd2 | Mm_Celera | 11:32473275 | GTGTGGTTATAATGT[A/G]GGATGGCATATATGT | 327900 |
rs26862470 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ubtd2 | Mm_Celera | 11:32472034 | TATGTGCCATTGCAT[A/G]TAACAGAATGTCACA | 327900 |
rs26862471 | snp | C/G/T | 0.48 | 0.0979796 | intron-variant | Ubtd2 | GRCm38.p3 | 11:32471894 | CCTGTGCTGTGAATC[C/G/T]GGTTGGGTTTTTTTT | 327900 |
rs26862472 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ubtd2 | Mm_Celera | 11:32470593 | TTGTCAGCTGCCTTT[C/T]AGCTAAATCTGCTTA | 327900 |
rs26862473 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ubtd2 | Mm_Celera | 11:32470503 | ATCCTTAGGAAACCT[C/T]GTGAAGCTGCTTTAG | 327900 |
rs26862474 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ubtd2 | Mm_Celera | 11:32470193 | CGATTTATCATTTCT[C/T]TCAAGTTTGTGTAGG | 327900 |