SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6247550 | snp | A/G | 0.471655 | 0.115624 | utr-variant-3-prime | Ube2z | GRCm38.p3 | 11:96048790 | GGAAATTGGAAGCAG[A/G]GTCCCCTTTCAAACC | 268470 |
rs6249119 | snp | C/T | 0.471655 | 0.115624 | utr-variant-3-prime | Ube2z | GRCm38.p3 | 11:96049059 | ATCACTAACCATCCA[C/T]TGGAAGCCAGAACAG | 268470 |
rs6250644 | snp | A/G | 0.433884 | 0.169371 | utr-variant-3-prime | Ube2z | GRCm38.p3 | 11:96049340 | ACAGGGACTACAGAC[A/G]TAACAGCTAAACAAA | 268470 |
rs6375947 | snp | G/T | 0.5 | 0 | intron-variant | Ube2z | Mm_Celera | 11:96056483 | TTTGAACTCAGGACC[G/T]TCAGAAGAGCAGTCA | 268470 |
rs13465345 | snp | A/G | | | utr-variant-3-prime | Ube2z | Mm_Celera | 11:96049843 | GGTGCTGTCCATGAC[A/G]CTTAAGCAGTCTGGT | 268470 |
rs13465346 | snp | A/G | | | utr-variant-3-prime | Ube2z | Mm_Celera | 11:96049907 | AAATGAGAACCCAAG[A/G]GGGAGCATGCCCAAG | 268470 |
rs27071387 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Ube2z | GRCm38.p3 | 11:96058901 | CTCAGCTTTGTAATA[C/T]GACAAGCAGAGTCAA | 268470 |
rs27071388 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Ube2z | Mm_Celera | 11:96058244 | AAAAGACTTTCTGGG[G/T]TAGCTCAGAGCACCT | 268470 |
rs27071389 | snp | C/T | 0.32 | 0.24 | intron-variant | Ube2z | GRCm38.p3 | 11:96058184 | GTCAGTTTCCTTTCT[C/T]TCTATACCAGTATCA | 268470 |
rs27071390 | snp | A/G | 0.32 | 0.24 | intron-variant | Ube2z | GRCm38.p3 | 11:96056621 | CACTTTGGTCCTAGG[A/G]TTCTATTCCAAATAT | 268470 |
rs27071391 | snp | A/T | 0.475309 | 0.108333 | intron-variant | Ube2z | Mm_Celera | 11:96056162 | AGGTCAAATAACTAA[A/T]CAGCAAACTCGATCC | 268470 |
rs27071392 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Ube2z | Mm_Celera | 11:96056134 | CTATACATAAAAATA[C/T]CCCTTCTATTATAGG | 268470 |
rs27071393 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Ube2z | GRCm38.p3 | 11:96056044 | TACATGACCCAAACA[C/T]ATACAGTGAAAGAAT | 268470 |
rs27071394 | snp | C/G | 0.32 | 0.24 | intron-variant | Ube2z | GRCm38.p3 | 11:96056017 | CAAAGATACCTCAGG[C/G]TTAATTCAGAGTACA | 268470 |
rs27071395 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Ube2z | Mm_Celera | 11:96052837 | TGCTCATTGTTCACT[C/G]TCCTCACAAATTTCA | 268470 |
rs27071396 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2z | Mm_Celera | 11:96052783 | CACTGAACCAGAGCA[C/T]TTCAGACACTACTTG | 268470 |
rs27071397 | snp | A/T | 0.124444 | 0.216185 | synonymous-codon | Ube2z | Mm_Celera | 11:96051740 | CAATATTACCTGCAT[A/T]GTTTGGCCTTGAAGA | 268470 |
rs27071398 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ube2z | Mm_Celera | 11:96051326 | CATCGCACTATGCAC[A/G]ACTGCTACCCTAAGT | 268470 |
rs27071399 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ube2z | Mm_Celera | 11:96051295 | AACTAGTTACTACCT[C/T]TAAAGCAGGAATCAA | 268470 |
rs27071400 | snp | A/G | 0.33241 | 0.236027 | intron-variant | Ube2z | GRCm38.p3 | 11:96050519 | AGAGGAAGTACAGGT[A/G]GTCCAAATGGTTCCA | 268470 |
rs27071401 | snp | A/T | 0.475309 | 0.108333 | intron-variant | Ube2z | GRCm38.p3 | 11:96050487 | TAGCTTTGAAATGCA[A/T]GCTCACCTTCTGGCA | 268470 |
rs27071402 | snp | C/T | 0.244898 | 0.249948 | utr-variant-3-prime | Ube2z | Mm_Celera | 11:96049624 | TCGGAGGAAATGGTG[C/T]GAGGGAGAAGGTGCT | 268470 |
rs27071403 | snp | G/T | 0.124444 | 0.216185 | utr-variant-3-prime | Ube2z | Mm_Celera | 11:96048444 | CAGGTTGGCCCAGGT[G/T]ACTCCGTTTCTTTAC | 268470 |
rs27071404 | snp | A/G | 0.475309 | 0.108333 | utr-variant-3-prime | Ube2z | GRCm38.p3 | 11:96048364 | CTTCCAAATGATAGG[A/G]AACCCACCACAAGTA | 268470 |
rs27071405 | snp | A/G | 0.124444 | 0.216185 | utr-variant-3-prime | Ube2z | Mm_Celera | 11:96048270 | ACAGGACATGCTCAC[A/G]CCCAATCTTGAAAGC | 268470 |
rs27071406 | snp | C/T | 0.244898 | 0.249948 | utr-variant-3-prime | Ube2z | Mm_Celera | 11:96048252 | TGACTCCCATCTGCC[C/T]TCACAGGACATGCTC | 268470 |
rs27071407 | snp | A/T | 0.475309 | 0.108333 | utr-variant-3-prime | Ube2z | GRCm38.p3 | 11:96048139 | TTTTTAGAGTTTATA[A/T]CCCAGTCTTACAAGC | 268470 |
rs27071408 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime | Ube2z | Mm_Celera | 11:96047974 | ACTAGCCCACGTTAC[C/T]CTATCATTGCACTCA | 268470 |
rs27071409 | snp | A/T | 0.444444 | 0.157135 | downstream-variant-500B, utr-variant-3-prime | Snf8, Ube2z | GRCm38.p3 | 11:96047600 | TTGTGGCTAGCCTTA[A/T]TATAGCTGTGAAACA | 268470 |
rs27071410 | snp | G/T | 0.345679 | 0.230967 | downstream-variant-500B, utr-variant-3-prime | Snf8, Ube2z | GRCm38.p3 | 11:96047585 | CCAAGATGTAGCTTC[G/T]TGTGGCTAGCCTTAT | 268470 |
rs27071411 | snp | A/G | 0.124444 | 0.216185 | missense, downstream-variant-500B, utr-variant-3-prime | Snf8, Ube2z | Mm_Celera | 11:96047303 | TCCCAGGAGATATCA[A/G]CTGAGGAGGCCAAAG | 268470 |
rs27071412 | snp | A/C | 0.18 | 0.24 | synonymous-codon, downstream-variant-500B, utr-variant-3-prime | Snf8, Ube2z | Mm_Celera | 11:96047266 | CCACTACTGGCTGCC[A/C]GCTCTTTTCACAGAT | 268470 |
rs27071413 | snp | C/T | 0.132653 | 0.220748 | intron-variant, downstream-variant-500B, utr-variant-3-prime | Snf8, Ube2z | Mm_Celera | 11:96047166 | AACTACTCTCCCTTT[C/T]CTCATATCAGTCCTG | 268470 |
rs27071414 | snp | A/C | 0.475309 | 0.108333 | intron-variant, downstream-variant-500B, utr-variant-3-prime | Snf8, Ube2z | GRCm38.p3 | 11:96046986 | ATACACTGTTGGAGC[A/C]TTGCATTCTTTCACT | 268470 |
rs27071415 | snp | C/T | 0.401235 | 0.199068 | intron-variant, downstream-variant-500B, utr-variant-3-prime | Snf8, Ube2z | GRCm38.p3 | 11:96046974 | CCCTGTGTCAGCATA[C/T]ACTGTTGGAGCATTG | 268470 |
rs29382285 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ube2z | GRCm38.p3 | 11:96050431 | TGTGGAAGAAACAAA[C/T]AAAAAATCCACAAGG | 268470 |
rs29389304 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ube2z | GRCm38.p3 | 11:96058853 | AGGTGACTGAAGCTA[C/T]TGCCTATGAGGATAC | 268470 |
rs29391863 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2z | GRCm38.p3 | 11:96054742 | TAGACTGGGCACAAC[A/G]TTAGAACTACAAAGG | 268470 |
rs29392994 | snp | C/T | 0.375 | 0.216506 | downstream-variant-500B, utr-variant-3-prime | Snf8, Ube2z | GRCm38.p3 | 11:96047524 | TGAGGATAACCTGAG[C/T]AACATGTAAAATGAC | 268470 |
rs29393459 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ube2z | GRCm38.p3 | 11:96058871 | CCTATGAGGATACAC[A/G]CTGAAGTTTATAGAC | 268470 |
rs29405174 | snp | C/T | 0.375 | 0.216506 | upstream-variant-2KB | Ube2z | GRCm38.p3 | 11:96065772 | ATGTCTGGTCTTCTC[C/T]CCCATCGACTACTAT | 268470 |
rs29405623 | snp | C/T | 0.32 | 0.24 | intron-variant | Ube2z | GRCm38.p3 | 11:96059578 | CATTTCAGCAGCTAG[C/T]CACCCTGACAGTTAC | 268470 |
rs29407926 | snp | A/G | 0.32 | 0.24 | upstream-variant-2KB | Ube2z | GRCm38.p3 | 11:96065869 | CATTTGAGTTTATTC[A/G]ATATTTATTTATGAA | 268470 |
rs29408200 | snp | C/G | 0.375 | 0.216506 | intron-variant | Ube2z | GRCm38.p3 | 11:96064689 | TAAGGCATCCGGAAC[C/G]GAGCTGCAGGGCTCA | 268470 |
rs29410716 | snp | C/T | 0.32 | 0.24 | upstream-variant-2KB | Ube2z | GRCm38.p3 | 11:96066444 | TTTTTTTTTTTTTTT[C/T]TTCTTCTTTTCCTCC | 268470 |
rs29412195 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Ube2z | GRCm38.p3 | 11:96050975 | GATGCCAGAAGATAG[A/T]TTCAGATCCCCAGGA | 268470 |
rs29413371 | snp | A/G | 0.444444 | 0.157135 | upstream-variant-2KB | Ube2z | GRCm38.p3 | 11:96066630 | AAACCAACAAGTGAA[A/G]AGCCTGCGTTCTGGA | 268470 |
rs29414090 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ube2z | GRCm38.p3 | 11:96058997 | CAATATCTAAAATAA[C/T]AGATAGAAAACTTAA | 268470 |
rs29415348 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Ube2z | GRCm38.p3 | 11:96055326 | CAAGGAGCAGCAGAT[A/T]AAAAAACAAGAGTTT | 268470 |
rs29416011 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ube2z | GRCm38.p3 | 11:96061304 | ATGTACATAGGTCTT[C/T]AATATAAGGAAATCC | 268470 |
rs29419170 | snp | A/T | 0.444444 | 0.157135 | upstream-variant-2KB | Ube2z | GRCm38.p3 | 11:96067085 | TTAGGTTTGATTTTT[A/T]ATAAAATGAAATAAC | 268470 |
rs29422781 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2z | GRCm38.p3 | 11:96057084 | TGGACCCTAGCCCCA[A/G]TACCTATCAGCTCAC | 268470 |
rs29424918 | snp | A/G | 0.32 | 0.24 | intron-variant | Ube2z | GRCm38.p3 | 11:96064676 | GAGGGGGTAGGGATA[A/G]GGCATCCGGAACGGA | 268470 |
rs29430628 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2z | GRCm38.p3 | 11:96053267 | TGTATTACAACAAAA[A/G]GTGGATATAGAGAAA | 268470 |
rs29431258 | snp | C/T | 0.375 | 0.216506 | upstream-variant-2KB | Ube2z | GRCm38.p3 | 11:96066219 | GCTGGTCTGAGACAA[C/T]ATCCGAAACAAACAC | 268470 |
rs29433783 | snp | G/T | 0.375 | 0.216506 | utr-variant-3-prime | Ube2z | GRCm38.p3 | 11:96048450 | GGCCCAGGTGACTCC[G/T]TTTCTTTACACAAAC | 268470 |
rs29437181 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2z | GRCm38.p3 | 11:96059694 | GACCTGTAAAATTTG[C/T]TTCAGGGTGGATCTC | 268470 |
rs29441021 | snp | A/C | 0.375 | 0.216506 | intron-variant | Ube2z | GRCm38.p3 | 11:96060441 | ATCAACTGTTAAATT[A/C]TCATAATCATTATTA | 268470 |
rs29445358 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ube2z | GRCm38.p3 | 11:96057379 | TGGTATTATGGGGGC[A/G]GGGGCGGGGGGCTAG | 268470 |
rs29447100 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2z | GRCm38.p3 | 11:96062903 | GGTAAAATCAGAGAG[A/G]AGAGCTGAACTAATA | 268470 |
rs29447992 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ube2z | GRCm38.p3 | 11:96062217 | TTTGAATGGAGACAG[C/T]ATGTCACCGGAAAAA | 268470 |
rs29449544 | snp | C/T | 0.375 | 0.216506 | upstream-variant-2KB | Ube2z | GRCm38.p3 | 11:96066780 | TACTTGTTCCTCTCA[C/T]CAGCTCTGTGATAGA | 268470 |
rs29450251 | snp | A/G | 0.32 | 0.24 | utr-variant-3-prime | Ube2z | GRCm38.p3 | 11:96049518 | TCAGTGATTGTGGGG[A/G]CACAGTGAGCAGCTT | 268470 |
rs29455643 | snp | C/T | 0.32 | 0.24 | upstream-variant-2KB | Ube2z | GRCm38.p3 | 11:96066491 | CTGTGGTGGCACAGC[C/T]CGTAAGCTAAGCACT | 268470 |
rs29460650 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ube2z | GRCm38.p3 | 11:96052977 | AGGTGGGTGTGGTGG[C/T]ACATACCTGCAACCT | 268470 |
rs29462672 | snp | G/T | 0.375 | 0.216506 | upstream-variant-2KB | Ube2z | GRCm38.p3 | 11:96065494 | GGCTAGCGGACTAGC[G/T]GGCGCTCCAGGCCAG | 268470 |
rs29462752 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2z | GRCm38.p3 | 11:96053308 | ACATTGATCTCTGGC[C/T]TTCACAAAGCATGCA | 268470 |
rs29462898 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2z | GRCm38.p3 | 11:96051235 | TCTGTCCAGCCCCTA[C/T]TCTTTCTTATATGAA | 268470 |
rs29463531 | snp | C/T | 0.5 | 0 | intron-variant | Ube2z | GRCm38.p3 | 11:96054896 | AGATCCAAGTGAAGA[C/T]TCCCAGCACCCATGT | 268470 |
rs29463553 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Ube2z | GRCm38.p3 | 11:96056954 | AAATAATAGATAGCT[A/C]GAGTGACAGAGGCCT | 268470 |
rs29465050 | snp | A/C | 0.32 | 0.24 | intron-variant | Ube2z | GRCm38.p3 | 11:96060776 | TAATAACGTGATCTT[A/C]TTCCTTTCCATCTAG | 268470 |
rs29467057 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2z | GRCm38.p3 | 11:96061690 | AAAAGGGGAGACCAG[C/T]GCCAACAACAATGCA | 268470 |
rs29469369 | snp | C/T | 0.32 | 0.24 | intron-variant | Ube2z | GRCm38.p3 | 11:96059406 | AACAGAACACAACCT[C/T]AGCCACGACTGGCTT | 268470 |
rs29474595 | snp | C/T | 0.444444 | 0.157135 | utr-variant-3-prime, downstream-variant-500B | Snf8, Ube2z | GRCm38.p3 | 11:96047362 | GTAGACAGCAGCAGG[C/T]CAGAAGATGCCCTGT | 268470 |
rs29474702 | snp | A/G | 0.32 | 0.24 | intron-variant | Ube2z | GRCm38.p3 | 11:96064505 | GCAATGCAGGTAGAG[A/G]ATGTTCCAAGCGGGG | 268470 |
rs29477719 | snp | C/T | 0.375 | 0.216506 | upstream-variant-2KB | Ube2z | GRCm38.p3 | 11:96065593 | TGATGTCGGAGAAGA[C/T]AGTTCAAAGAAGATG | 268470 |
rs29479113 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2z | GRCm38.p3 | 11:96057073 | AGACCCATGTTTGGA[C/T]CCTAGCCCCAATACC | 268470 |
rs29479512 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2z | Mm_Celera | 11:96050851 | GCATCACCACTGCCC[A/G]GCTATTTTATTTAAT | 268470 |
rs29480176 | snp | C/G | 0.5 | 0 | intron-variant | Ube2z | Mm_Celera | 11:96057611 | TCATCTGACTCCCTT[C/G]GCATCAAGTACTCAC | 268470 |
rs29480465 | snp | A/T | 0.444444 | 0.157135 | upstream-variant-2KB | Ube2z | GRCm38.p3 | 11:96067087 | AGGTTTGATTTTTTA[A/T]AAAATGAAATAACAC | 268470 |
rs29486069 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Ube2z | Mm_Celera | 11:96051435 | GGCTAGATATTCTTA[G/T]AAGAGTTTAAAGGAC | 268470 |
rs29486265 | snp | A/C | 0.375 | 0.216506 | intron-variant | Ube2z | Mm_Celera | 11:96054622 | TCCCCACCCCCCCCC[A/C]AAAAAAACCAACAAA | 268470 |
rs33849534 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ube2z | GRCm38.p3 | 11:96060721 | GCAGGCAGCTCAAAG[A/G]CTGCACTGAGTAAAC | 268470 |
rs33850784 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ube2z | GRCm38.p3 | 11:96057618 | ACTCCCTTCGCATCA[A/G]GTACTCACAAGGTAC | 268470 |
rs45673975 | snp | A/G | | | upstream-variant-2KB | Ube2z | GRCm38.p3 | 11:96067192 | CAGATTTCTGAGTTC[A/G]AGGCCAGCCTGGTCT | 268470 |
rs47511690 | snp | A/C | | | intron-variant | Ube2z | GRCm38.p3 | 11:96060743 | TGAGTAAACCATTTC[A/C]TAAGACACTCTTACA | 268470 |
rs48244147 | snp | C/T | | | intron-variant | Ube2z | GRCm38.p3 | 11:96063371 | CTATATACTGTCACT[C/T]CTTCCCACATGAAAA | 268470 |
rs48261173 | snp | C/T | | | intron-variant | Ube2z | GRCm38.p3 | 11:96060482 | CTCCAGAGGCGCCCA[C/T]TAAGAGGCTCCAATC | 268470 |
rs48791875 | snp | C/G | | | intron-variant | Ube2z | GRCm38.p3 | 11:96063365 | CACATCCTATATACT[C/G]TCACTTCTTCCCACA | 268470 |
rs49611484 | snp | C/T | | | intron-variant | Ube2z | GRCm38.p3 | 11:96061803 | ATAAATAAAATTTCA[C/T]GGTCTACTCATGGCC | 268470 |
rs50095646 | snp | A/G | | | intron-variant | Ube2z | GRCm38.p3 | 11:96063650 | TCTCTGAAAGATGAC[A/G]TTTAGTAACTAGGAT | 268470 |
rs50428242 | snp | A/T | | | intron-variant | Ube2z | GRCm38.p3 | 11:96064163 | TCGGTCACCCAAGAC[A/T]CAAGCACAGACAGGC | 268470 |
rs50433607 | snp | A/G | | | intron-variant | Ube2z | GRCm38.p3 | 11:96064240 | AAAAGTAAACCAGAC[A/G]ACCTTGGGGGTAAAT | 268470 |
rs51435919 | snp | C/T | | | intron-variant | Ube2z | GRCm38.p3 | 11:96063630 | CTGAAATAACCAGAA[C/T]CTCATCTCTGAAAGA | 268470 |
rs52385869 | snp | C/G | | | intron-variant | Ube2z | Mm_Celera | 11:96061601 | ATGCAAGTCCATTCT[C/G]TGTGTGTGAGTGTGT | 268470 |
rs52506530 | snp | A/C | | | intron-variant | Ube2z | GRCm38.p3 | 11:96052194 | ACACACACACACACA[A/C]ACACACAAACAAGTG | 268470 |
rs52507914 | snp | A/C | | | intron-variant | Ube2z | GRCm38.p3 | 11:96052202 | ACACACAAACACACA[A/C]ACAAGTGAGCATTCC | 268470 |
rs108092271 | snp | C/T | | | upstream-variant-2KB | Ube2z | GRCm38.p3 | 11:96067230 | GAGTTCCAGGACAGC[C/T]AGGGCTACACAGAGA | 268470 |
rs211774068 | snp | C/T | | | intron-variant | Ube2z | Mm_Celera | 11:96060505 | CTCCAATCAGACACC[C/T]ATTGCATGAATACAG | 268470 |
rs212099068 | snp | G/T | | | intron-variant | Ube2z | Mm_Celera | 11:96061769 | AGGATCAAAACTACC[G/T]TGTCAAAGATACAAA | 268470 |