SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3685811 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e1 | GRCm38.p3 | 14:18310615 | ACTTCTTAAGGTTCA[A/G]TGTTATCATCAGCTA | 22194 |
rs3685820 | snp | G/T | 0.5 | 0 | intron-variant | Ube2e1 | GRCm38.p3 | 14:18310616 | CTTCTTAAGGTTCAA[G/T]GTTATCATCAGCTAA | 22194 |
rs3685843 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e1 | GRCm38.p3 | 14:18310633 | TTATCATCAGCTAAG[C/T]TCTATTCTATTTTTT | 22194 |
rs6281119 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Ube2e1 | GRCm38.p3 | 14:18285698 | ACACCGCAATCTTGA[C/G]CTCTTGTTTCACTCT | 22194 |
rs6281227 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e1 | GRCm38.p3 | 14:18285768 | TCCCCATGCCCAATA[A/G]CTTCATTCAGTCTGT | 22194 |
rs6281231 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e1 | GRCm38.p3 | 14:18285771 | CCATGCCCAATAGCT[C/T]CATTCAGTCTGTTAG | 22194 |
rs6281809 | snp | G/T | 0.5 | 0 | intron-variant | Ube2e1 | GRCm38.p3 | 14:18285880 | GTGATCATGTCCTCA[G/T]TTTTCATTCAGTGAC | 22194 |
rs13466512 | snp | A/G | 0.487535 | 0.077957 | utr-variant-3-prime | Nkiras1, Ube2e1 | Mm_Celera | 14:18283317 | TCAGTTCTTACATGA[A/G]TTGTCTGTCACAGAA | 22194 |
rs13466513 | snp | A/C | 0.444444 | 0.157135 | utr-variant-3-prime | Nkiras1, Ube2e1 | GRCm38.p3 | 14:18283021 | TCCTATTTTCTTGTT[A/C]AAAAAAAATGGAATT | 22194 |
rs30101577 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e1 | GRCm38.p3 | 14:18287670 | TCAGCTGCAGATCCC[A/G]GCAGTGCTGAGGCCA | 22194 |
rs30105631 | snp | C/G | 0.498615 | 0.0262793 | intron-variant | Ube2e1 | GRCm38.p3 | 14:18324435 | TCCCAAAACATTTCA[C/G]AGTAGTAAGGTTTAC | 22194 |
rs30109653 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2e1 | GRCm38.p3 | 14:18315969 | CACATTCATAAACGG[C/T]AAGACTACAATAAAG | 22194 |
rs30112840 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ube2e1 | Mm_Celera | 14:18294008 | GTGTGTGCGCGCGCG[C/T]GCGTTTCATTCAGGA | 22194 |
rs30125355 | snp | A/G | 0.444444 | 0.157135 | intron-variant, nc-transcript-variant | Ube2e1, LOC105245681 | GRCm38.p3 | 14:18306862 | ATTCTTAGAACTTCT[A/G]AAAAATCTGGCATCT | 22194 |
rs30168085 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Ube2e1 | GRCm38.p3 | 14:18290433 | GCTGCCAATCTCAGA[A/G]TGCAAGTAGGGGCTG | 22194 |
rs30169354 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ube2e1 | Mm_Celera | 14:18286625 | CTGCTTGACACAGAT[A/G]CTGGAAACTGACTGG | 22194 |
rs30169592 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2e1 | GRCm38.p3 | 14:18314024 | TTATCATTCAATGTC[A/G]TCTCCCTCACAGTGG | 22194 |
rs30193202 | snp | G/T | 0.492188 | 0.0620098 | intron-variant | Ube2e1 | GRCm38.p3 | 14:18315919 | ACCCACAGACATGTT[G/T]TAACTTGCAGATGCC | 22194 |
rs30204113 | snp | C/G/T | 0.444444 | 0.157135 | intron-variant | Ube2e1 | GRCm38.p3 | 14:18315900 | CAGAACACCTCTACT[C/G/T]TTTACCCACAGACAT | 22194 |
rs30209377 | snp | C/T | 0.498615 | 0.0262793 | intron-variant, nc-transcript-variant | Ube2e1, LOC105245681 | GRCm38.p3 | 14:18306515 | GCCTCTACAAGAACA[C/T]AAGCATCATCTCTCC | 22194 |
rs30213127 | snp | G/T | 0.49827 | 0.0293608 | intron-variant, downstream-variant-500B | Ube2e1, LOC105245681 | GRCm38.p3 | 14:18297524 | GCCTGCTGCCAGAAC[G/T]CCAGAAAAGTGACCA | 22194 |
rs30240946 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Ube2e1 | GRCm38.p3 | 14:18285396 | ATGGTAGTGAGCCAC[C/G]ACAGAAGAACACCAG | 22194 |
rs30253917 | snp | A/G | 0.444444 | 0.157135 | intron-variant, nc-transcript-variant | Ube2e1, LOC105245681 | GRCm38.p3 | 14:18298973 | CACAAGACATGGAAG[A/G]CAAGTTGGGTCTGAA | 22194 |
rs30261329 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ube2e1 | Mm_Celera | 14:18288215 | TTGGAACTTGCTAGA[C/T]CAGGATCACTTCAAA | 22194 |
rs30269915 | snp | A/G | 0.49827 | 0.0293608 | intron-variant | Ube2e1 | GRCm38.p3 | 14:18322255 | TCAAAGAATCTTTAA[A/G]AGAAAAAAAACTTTA | 22194 |
rs30272636 | snp | C/G | 0.5 | 0 | intron-variant | Ube2e1 | GRCm38.p3 | 14:18312506 | AAGTTCAAATCCTGA[C/G]ACCCACATGGCAGCT | 22194 |
rs30280134 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Ube2e1 | Mm_Celera | 14:18285322 | TTGCATCAGAAAAGG[A/G]AAAAAAAACCCTCCC | 22194 |
rs30287074 | snp | A/C | 0.444444 | 0.157135 | intron-variant, downstream-variant-500B | Ube2e1, LOC105245681 | GRCm38.p3 | 14:18297259 | TTCAGATGCCCAAAC[A/C]CCAAATGAGCCAAAT | 22194 |
rs30291863 | snp | A/C | 0.444444 | 0.157135 | intron-variant, nc-transcript-variant | Ube2e1, LOC105245681 | GRCm38.p3 | 14:18306765 | TATCTGCTGTGTGCC[A/C]AGAAGAAGCCCTCAC | 22194 |
rs30319331 | snp | A/C | 0.444444 | 0.157135 | utr-variant-3-prime, intron-variant | Nkiras1, Ube2e1 | Mm_Celera | 14:18283909 | AAAGGCCAAAAACCC[A/C]GACTTCCAAATAAAT | 22194 |
rs30321357 | snp | C/T | 0.49827 | 0.0293608 | intron-variant, downstream-variant-500B | Ube2e1, LOC105245681 | GRCm38.p3 | 14:18297395 | GAATTCTTTTGACAT[C/T]TACCACACTCTACAC | 22194 |
rs30353639 | snp | G/T | 0.5 | 0 | intron-variant | Ube2e1 | GRCm38.p3 | 14:18329928 | ACAAACTGACAATCT[G/T]TGAGTTCCAGGCTCA | 22194 |
rs30356773 | snp | C/G | 0.5 | 0 | intron-variant, nc-transcript-variant | Ube2e1, LOC105245681 | Mm_Celera | 14:18298060 | GAACATGAATACACG[C/G]TGTATACGCACCCCC | 22194 |
rs30357812 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e1 | GRCm38.p3 | 14:18328941 | TAAAAATCAGCAGGG[C/T]TCAGTGCATTATAGT | 22194 |
rs30408748 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2e1 | GRCm38.p3 | 14:18329652 | GAGAGCTCAAGGCCG[A/G]GGTTGATCAAGAAAG | 22194 |
rs30438255 | snp | A/G | 0.444444 | 0.157135 | utr-variant-3-prime, downstream-variant-500B | Nkiras1, Ube2e1 | Mm_Celera | 14:18282571 | GAAGACAGCTACAGT[A/G]TCTTTATTTATACAC | 22194 |
rs30453678 | snp | A/C | 0.5 | 0 | intron-variant, nc-transcript-variant | Ube2e1, LOC105245681 | Mm_Celera | 14:18304714 | GACCTTCGGAAGAGC[A/C]GTCAGTGCTCTTAAC | 22194 |
rs30469532 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e1 | Mm_Celera | 14:18286793 | GAACAGAATGGGTTC[C/T]CAATTATCAAAAGTT | 22194 |
rs30489153 | snp | C/T | 0.444444 | 0.157135 | intron-variant, nc-transcript-variant | Ube2e1, LOC105245681 | Mm_Celera | 14:18304862 | TGGCTATCCTGGAAC[C/T]CAGAAATCCGCCTGC | 22194 |
rs30492059 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e1 | GRCm38.p3 | 14:18291658 | ACAGGTTTAATGTCA[A/G]CACTTAGGAGGCAGA | 22194 |
rs30498130 | snp | C/T | 0.444444 | 0.157135 | upstream-variant-2KB | Ube2e1 | Mm_Celera | 14:18333728 | ATAATACCAGCCGGT[C/T]ATGGTGGCTTTGTTT | 22194 |
rs30503555 | snp | G/T | 0.408163 | 0.193609 | intron-variant, nc-transcript-variant | Ube2e1, LOC105245681 | GRCm38.p3 | 14:18307155 | ATCCAGCGGTACACA[G/T]GCAATTTATTTACTG | 22194 |
rs30528090 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Ube2e1 | GRCm38.p3 | 14:18313411 | ACAGGGGGTGGCACT[C/G]TTAGGAGGTATGGCC | 22194 |
rs30540920 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e1 | GRCm38.p3 | 14:18318600 | CAATGCTAAGAACCC[C/T]ACTGAGACTACAACA | 22194 |
rs30549441 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2e1 | GRCm38.p3 | 14:18322660 | CTAGTGGCTCAGAGC[C/T]CATGAGCTTGTAGAC | 22194 |
rs30594335 | snp | A/G | 0.5 | 0 | intron-variant, nc-transcript-variant | Ube2e1, LOC105245681 | GRCm38.p3 | 14:18302151 | TGCAGTAAGCTGTTA[A/G]GTAGCAACAGAAATT | 22194 |
rs30616453 | snp | A/G | 0.48 | 0.0979796 | intron-variant, nc-transcript-variant | Ube2e1, LOC105245681 | GRCm38.p3 | 14:18304439 | TGCACTGTGCATGCA[A/G]ACAGGCACACATGCC | 22194 |
rs30629227 | snp | A/T | 0.444444 | 0.157135 | intron-variant, nc-transcript-variant | Ube2e1, LOC105245681 | Mm_Celera | 14:18304948 | CAATCCTTTTTTTTT[A/T]AATTAATTTATTTAT | 22194 |
rs30644028 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Ube2e1 | Mm_Celera | 14:18328288 | TAGCTCAGCACAGTT[C/T]CCACCAGTGCTCTCC | 22194 |
rs30651410 | snp | A/T | 0.498615 | 0.0262793 | intron-variant, nc-transcript-variant | Ube2e1, LOC105245681 | GRCm38.p3 | 14:18306262 | GGATCCTCTATGGAT[A/T]ACAAAGAGATTGAAG | 22194 |
rs30684801 | snp | C/T | 0.48 | 0.0979796 | intron-variant, nc-transcript-variant | Ube2e1, LOC105245681 | GRCm38.p3 | 14:18306213 | TGCATGCAACCTTCA[C/T]GCCCAGTGCCTGTGG | 22194 |
rs30695193 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e1 | GRCm38.p3 | 14:18318287 | ACAGACTTAGTCCTC[A/G]GAGCAATGGCAGTCT | 22194 |
rs30700893 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Ube2e1 | GRCm38.p3 | 14:18328212 | ACCACCATTTGCAGC[A/C]ATTCCAGACTACTGA | 22194 |
rs30702693 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Ube2e1 | GRCm38.p3 | 14:18312915 | GTTTGTGGGCACACC[A/G]AGACACTGGAGTTAC | 22194 |
rs30746084 | snp | A/T | 0.5 | 0 | intron-variant | Ube2e1 | GRCm38.p3 | 14:18330328 | CAAGTCTTTCTGAAA[A/T]GTGTCAAACTGAAGT | 22194 |
rs30753137 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Ube2e1 | GRCm38.p3 | 14:18288571 | CACGTCACTGGTGTC[C/T]AGGAAATCTAGACAT | 22194 |
rs30766068 | snp | A/G | 0.48 | 0.0979796 | intron-variant, nc-transcript-variant | Ube2e1, LOC105245681 | GRCm38.p3 | 14:18305922 | GCAAGAAGACCAGAT[A/G]TCCTGCCACTGAGCA | 22194 |
rs30769645 | snp | A/T | 0.444444 | 0.157135 | utr-variant-3-prime, downstream-variant-500B | Nkiras1, Ube2e1 | GRCm38.p3 | 14:18282390 | CTGGGATTAAAGGCG[A/T]GCACCACCACTGCCT | 22194 |
rs30772453 | snp | A/G | 0.475309 | 0.108333 | intron-variant, nc-transcript-variant | Ube2e1, LOC105245681 | GRCm38.p3 | 14:18300695 | TGTCTTGGCTTCAAT[A/G]GCCTACAGAGATAGA | 22194 |
rs30774181 | snp | A/G | 0.49827 | 0.0293608 | intron-variant | Ube2e1 | GRCm38.p3 | 14:18321159 | GTGATAGCTCTCTCT[A/G]CCTGCCCTCTACTAT | 22194 |
rs30844809 | snp | A/C | 0.49827 | 0.0293608 | intron-variant | Ube2e1 | Mm_Celera | 14:18286419 | AGCAGTAAAACTTGC[A/C]CCCCGATTCTAAGAC | 22194 |
rs30872142 | snp | C/G | 0.498615 | 0.0262793 | intron-variant | Ube2e1 | GRCm38.p3 | 14:18318746 | TCATCAGTCATGTTA[C/G]CAACTTGTTACATTC | 22194 |
rs30875247 | snp | C/T | 0.5 | 0 | intron-variant, nc-transcript-variant | Ube2e1, LOC105245681 | GRCm38.p3 | 14:18305608 | CTGTGAGCTCAAGGC[C/T]GGATGTGGACATTTC | 22194 |
rs30890263 | snp | A/C/T | 0.5 | 0 | intron-variant | Ube2e1 | GRCm38.p3 | 14:18326972 | GCGCCCCCCGCAGGC[A/C/T]GGGACATCAGCGCCC | 22194 |
rs30895638 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Ube2e1 | GRCm38.p3 | 14:18286093 | TAGAAGATCTTCTGG[C/T]CCTCTGAGACAGAGT | 22194 |
rs30902968 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e1 | GRCm38.p3 | 14:18287266 | GCTGTCCTTGAATCT[A/G]AGATCCATTTACCTC | 22194 |
rs30912649 | snp | C/T | 0.444444 | 0.157135 | intron-variant, nc-transcript-variant | Ube2e1, LOC105245681 | GRCm38.p3 | 14:18299003 | AGACTGGATAGGGTA[C/T]GGGTGGCATGAAGTT | 22194 |
rs30924787 | snp | C/G | 0.444444 | 0.157135 | intron-variant, nc-transcript-variant | Ube2e1, LOC105245681 | Mm_Celera | 14:18298068 | ATACACGCTGTATAC[C/G]CACCCCCCCCCCAAA | 22194 |
rs30927562 | snp | A/G | 0.498615 | 0.0262793 | utr-variant-3-prime, intron-variant | Nkiras1, Ube2e1 | GRCm38.p3 | 14:18283470 | GTATGTTACTTTGGA[A/G]AAAGAAAATCAGATA | 22194 |
rs30934435 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2e1 | Mm_Celera | 14:18323846 | GGGTTTCTCTGTGTA[A/G]CCCTGGCTGTCCTGG | 22194 |
rs30938195 | snp | A/G | 0.5 | 0 | intron-variant, nc-transcript-variant | Ube2e1, LOC105245681 | GRCm38.p3 | 14:18298371 | TATAGGAACACATAG[A/G]CACACACACACACTC | 22194 |
rs30938568 | snp | A/C | 0.493827 | 0.0552116 | intron-variant | Ube2e1 | GRCm38.p3 | 14:18286125 | GCTCAAACTGTCTTC[A/C]AAGTCACTCAGCCCT | 22194 |
rs30943434 | snp | A/G/T | 0.5 | 0 | intron-variant | Ube2e1 | GRCm38.p3 | 14:18327366 | CTTTGTCTTCGCTTC[A/G/T]GTTAACCCAGACGCT | 22194 |
rs30951042 | snp | C/G | 0.487535 | 0.077957 | intron-variant | Ube2e1 | GRCm38.p3 | 14:18287749 | AAGAGTTGTAGTTTT[C/G]TTACAATAATAGCTA | 22194 |
rs30964750 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Ube2e1 | GRCm38.p3 | 14:18288309 | TTCTTATCCTGTCTT[C/T]TTTTGCTATAGGGTA | 22194 |
rs30972258 | snp | A/T | 0.5 | 0 | intron-variant | Ube2e1 | Mm_Celera | 14:18329084 | CTTGATGATGTTTCA[A/T]GCCTGCTAGGCCAGT | 22194 |
rs31019753 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ube2e1 | GRCm38.p3 | 14:18313633 | TACACTTCTGAATCT[A/G]TAAGCCAGCCTAAAC | 22194 |
rs31027110 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Ube2e1 | GRCm38.p3 | 14:18324554 | AAGATAAAAAGTCCT[C/T]CGTGCTTCAGAAACA | 22194 |
rs31040773 | snp | C/T | 0.5 | 0 | intron-variant, nc-transcript-variant | Ube2e1, LOC105245681 | GRCm38.p3 | 14:18304642 | TCCAGAAGAGGGCGC[C/T]AGATCTCGTTACAGA | 22194 |
rs31069089 | snp | A/G | 0.444444 | 0.157135 | intron-variant, nc-transcript-variant | Ube2e1, LOC105245681 | Mm_Celera | 14:18304852 | TGTATAGCCCTGGCT[A/G]TCCTGGAACCCAGAA | 22194 |
rs31078098 | snp | G/T | 0.5 | 0 | intron-variant | Ube2e1 | GRCm38.p3 | 14:18290877 | CCCATAAACTCAAGG[G/T]TTCTCAGGGATGCAA | 22194 |
rs31079638 | snp | C/G | 0.5 | 0 | intron-variant | Ube2e1 | GRCm38.p3 | 14:18290706 | AACCTGCACAGCATC[C/G]TCCTTGGAGGACATG | 22194 |
rs31108864 | snp | A/C | 0.5 | 0 | intron-variant | Ube2e1 | GRCm38.p3 | 14:18311163 | AAACAAACAAACAAA[A/C]CAAAAAAAGGATGCA | 22194 |
rs31111634 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Ube2e1 | Mm_Celera | 14:18294657 | GTATTCTTGGGCCCT[C/T]ATTCCTCTCTCTGCC | 22194 |
rs31117207 | snp | C/T | 0.408163 | 0.193609 | intron-variant, nc-transcript-variant | Ube2e1, LOC105245681 | GRCm38.p3 | 14:18307136 | GACTGCTTAATTGAC[C/T]AAAATCCAGCGGTAC | 22194 |
rs31120506 | snp | A/G | 0.498615 | 0.0262793 | intron-variant, nc-transcript-variant | Ube2e1, LOC105245681 | GRCm38.p3 | 14:18304298 | TATGCTTCACGATGC[A/G]TAACTGAACGTGAGG | 22194 |
rs31135094 | snp | A/G | 0.444444 | 0.157135 | intron-variant, nc-transcript-variant | Ube2e1, LOC105245681 | Mm_Celera | 14:18304965 | ATTAATTTATTTATT[A/G]TATACAGTGTTGCTG | 22194 |
rs31144675 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Ube2e1 | GRCm38.p3 | 14:18322551 | GACTTGGGCAAAATA[C/T]GTCCCTTATGATGAG | 22194 |
rs31145265 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Ube2e1 | GRCm38.p3 | 14:18284844 | TCTAACAAGCTAGAC[A/G]GTAACTAGCACAGTT | 22194 |
rs31151036 | snp | A/T | 0.495 | 0.0497494 | intron-variant | Ube2e1 | GRCm38.p3 | 14:18284892 | GAAATGCCTATTGCC[A/T]ACTGAGGAGCCAACC | 22194 |
rs31152124 | snp | G/T | 0.487535 | 0.077957 | intron-variant | Ube2e1 | Mm_Celera | 14:18318236 | GCAGCAATAAACGCC[G/T]TAACAAAAGACACCT | 22194 |
rs31153901 | snp | C/G | 0.493827 | 0.0552116 | intron-variant, nc-transcript-variant | Ube2e1, LOC105245681 | GRCm38.p3 | 14:18306388 | TGTTTTTCAACCTAA[C/G]TTTCACAGACCAGTT | 22194 |
rs31172657 | snp | C/T | 0.5 | 0 | intron-variant | Ube2e1 | GRCm38.p3 | 14:18294458 | TAATTCCTGGTTCAC[C/T]CTGAATAAAGTATAT | 22194 |
rs31176170 | snp | A/C | 0.49827 | 0.0293608 | intron-variant, downstream-variant-500B | Ube2e1, LOC105245681 | Mm_Celera | 14:18297439 | ACATTACAGTCATAT[A/C]AAAAACAAGGACATC | 22194 |
rs31190484 | snp | A/G | 0.498615 | 0.0262793 | intron-variant, nc-transcript-variant | Ube2e1, LOC105245681 | GRCm38.p3 | 14:18305628 | GTGGACATTTCATAG[A/G]AAGCACTCTTTATAC | 22194 |
rs31219064 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Ube2e1 | GRCm38.p3 | 14:18322173 | TGCTTTTTGGTTTTT[C/T]AAGACAGGGTCTCTC | 22194 |
rs31220603 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e1 | GRCm38.p3 | 14:18293596 | GGGACAAGAGGAAGG[A/G]TGTTGCCCAGGAATG | 22194 |
rs31226864 | snp | A/C | 0.444444 | 0.157135 | intron-variant, nc-transcript-variant | Ube2e1, LOC105245681 | GRCm38.p3 | 14:18306746 | TGTCCTACTCCAATC[A/C]CACTATCTGCTGTGT | 22194 |
rs31233081 | snp | A/G | 0.5 | 0 | intron-variant | Ube2e1 | GRCm38.p3 | 14:18288502 | ACCCTTGGAAAGAAC[A/G]TGTGGACCAAAGACA | 22194 |
rs31234609 | snp | G/T | 0.487535 | 0.077957 | intron-variant, nc-transcript-variant | Ube2e1, LOC105245681 | Mm_Celera | 14:18302513 | TTTCAAAACCTCCAG[G/T]GAAAGTCAGCTGAGA | 22194 |