SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs4227859 | snp | G/T | 0.375 | 0.216506 | intron-variant | Copb2 | Mm_Celera | 9:98587712 | TCAGCAAGGGAT[G/T] | 50797 |
rs4227860 | snp | A/T | 0.375 | 0.216506 | intron-variant | Copb2 | Mm_Celera | 9:98587710 | AGCAAGGGAT[A/T] | 50797 |
rs4227861 | snp | A/G | 0.375 | 0.216506 | intron-variant | Copb2 | Mm_Celera | 9:98587709 | GCAAGGGAT[A/G] | 50797 |
rs4227862 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Copb2 | GRCm38.p3 | 9:98587682 | CAGAGGGAGCTCAGG[A/G]TTAGGAAGTGGCTTT | 50797 |
rs4227863 | snp | A/T | 0.21875 | 0.248039 | intron-variant | Copb2 | Mm_Celera | 9:98587450 | TGCAGCACATTTCAA[A/T]CTTGGACTTGTGAAT | 50797 |
rs4227864 | snp | C/T | 0.21875 | 0.248039 | intron-variant | Copb2 | GRCm38.p3 | 9:98587448 | CAGCACATTTCAAAC[C/T]TGGACTTGTGAATGT | 50797 |
rs13466556 | snp | C/T | 0.391111 | 0.206368 | synonymous-codon | Copb2 | Mm_Celera | 9:98588137 | AGATATTCTGGATGA[C/T]TAAAGTTTGCCATTT | 50797 |
rs13480365 | snp | A/G | 0.498047 | 0.0311889 | intron-variant | Copb2 | Mm_Celera | 9:98579312 | ATGACGTGATGCTTG[A/G]GTTTAAGGCAAAGTA | 50797 |
rs30283520 | snp | G/T | 0.401235 | 0.199068 | intron-variant | Copb2 | Mm_Celera | 9:98579781 | GTGTGCTGAGTAGTA[G/T]TCCATTGAATGGATG | 50797 |
rs33164971 | snp | A/G | 0.124444 | 0.216185 | upstream-variant-2KB | Copb2 | Mm_Celera | 9:98561871 | TGGGATGAAGCAGCC[A/G]TCCTAGAGATTGACC | 50797 |
rs33164972 | snp | A/G | 0.132653 | 0.220748 | upstream-variant-2KB, downstream-variant-500B | Copb2, 4930579K19Rik | Mm_Celera | 9:98562014 | TCCACATGCCTCTAA[A/G]CCAGAGTAAACAAGA | 50797 |
rs33164973 | snp | A/G | 0.391111 | 0.206368 | upstream-variant-2KB, downstream-variant-500B | Copb2, 4930579K19Rik | Mm_Celera | 9:98562263 | GTATTGAACTCGCAG[A/G]TCTTCAAGGTTTGTG | 50797 |
rs33165794 | snp | A/T | 0.391111 | 0.206368 | upstream-variant-2KB, nc-transcript-variant | Copb2, 4930579K19Rik | Mm_Celera | 9:98562588 | TATAGTTCACATTTT[A/T]AAAAGTTTCAACTAA | 50797 |
rs33165795 | snp | A/G | 0.391111 | 0.206368 | upstream-variant-2KB, nc-transcript-variant | Copb2, 4930579K19Rik | Mm_Celera | 9:98562621 | CTTGCAATTGGTTGC[A/G]CTACAGTATGCGATT | 50797 |
rs33165796 | snp | C/T | 0.391111 | 0.206368 | upstream-variant-2KB, nc-transcript-variant | Copb2, 4930579K19Rik | Mm_Celera | 9:98562754 | TTTGTATATGAAAAA[C/T]TGAGGCCTATAAATC | 50797 |
rs33165797 | snp | C/T | 0.391111 | 0.206368 | upstream-variant-2KB, nc-transcript-variant | Copb2, 4930579K19Rik | Mm_Celera | 9:98562836 | CTATACAATTCCTTT[C/T]TGGAAACCTAGGCTT | 50797 |
rs33165798 | snp | C/T | 0.391111 | 0.206368 | upstream-variant-2KB, nc-transcript-variant | Copb2, 4930579K19Rik | Mm_Celera | 9:98562909 | TTTGTTTCATAGCAT[C/T]ATCTTTTTAAAAGGT | 50797 |
rs33165799 | snp | A/G | 0.336735 | 0.234472 | upstream-variant-2KB, nc-transcript-variant | Copb2, 4930579K19Rik | Mm_Celera | 9:98562936 | AGGTGTGTGAAATCG[A/G]TACACAATGTATTTG | 50797 |
rs33165800 | snp | C/T | 0.336735 | 0.234472 | upstream-variant-2KB, nc-transcript-variant | Copb2, 4930579K19Rik | GRCm38.p3 | 9:98563227 | ATGCTCTTTGAAGGG[C/T]AATCACCCGACTGCC | 50797 |
rs33165801 | snp | C/G | 0.231111 | 0.249285 | upstream-variant-2KB | Copb2, 4930579K19Rik | Mm_Celera | 9:98563689 | CAGGCGCAGAGCCTG[C/G]CTCCGAGTACCGCGA | 50797 |
rs33165802 | snp | A/G | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Copb2, 4930579K19Rik | Mm_Celera | 9:98564022 | ACAGTAGTGTAACTG[A/G]GTACCCGCGAAGGAG | 50797 |
rs33165803 | snp | G/T | 0.391111 | 0.206368 | intron-variant, upstream-variant-2KB | Copb2, 4930579K19Rik | Mm_Celera | 9:98564126 | AAGTAAATGCTAGAG[G/T]CAGGACTCGGATGCC | 50797 |
rs33166634 | snp | G/T | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Copb2, 4930579K19Rik | Mm_Celera | 9:98564245 | TGTGCAGGCACCACA[G/T]TGCAAACTTAAGCAG | 50797 |
rs33166635 | snp | A/G | 0.391111 | 0.206368 | intron-variant, upstream-variant-2KB | Copb2, 4930579K19Rik | Mm_Celera | 9:98564525 | CTTTCGGTGGAAGAC[A/G]TTTGAGGAAAACTGT | 50797 |
rs33166636 | snp | A/G | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Copb2, 4930579K19Rik | Mm_Celera | 9:98564539 | CATTTGAGGAAAACT[A/G]TTGTGTGAACATGTG | 50797 |
rs33166637 | snp | C/T | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Copb2, 4930579K19Rik | Mm_Celera | 9:98564891 | GTGGTTACTATAAGC[C/T]GTGCTCTGCTCTAAC | 50797 |
rs33166638 | snp | G/T | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Copb2, 4930579K19Rik | Mm_Celera | 9:98565056 | AGACTGTGGACCTCA[G/T]CTATACTACCTGTTC | 50797 |
rs33166639 | snp | A/C/G | 0.152778 | 0.230321 | intron-variant, upstream-variant-2KB | Copb2, 4930579K19Rik | GRCm38.p3 | 9:98565077 | CTACCTGTTCCTCCC[A/C/G]TATTCCCAAATACAT | 50797 |
rs33166640 | snp | C/T | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Copb2, 4930579K19Rik | Mm_Celera | 9:98565205 | ATCCTCTGGCTAGGC[C/T]AATCAGAAAGGGCAT | 50797 |
rs33166641 | snp | C/T | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Copb2, 4930579K19Rik | Mm_Celera | 9:98565218 | GCTAATCAGAAAGGG[C/T]ATAATGGTGGCAGTG | 50797 |
rs33166642 | snp | A/C | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Copb2, 4930579K19Rik | Mm_Celera | 9:98565411 | GGTATGTGCAGCTAT[A/C]TACTAGGTAGTTCAG | 50797 |
rs33166643 | snp | A/G | 0.132653 | 0.220748 | intron-variant, upstream-variant-2KB | Copb2, 4930579K19Rik | Mm_Celera | 9:98565574 | GAAGATCCCACTATG[A/G]CTCCTGGCATAACAT | 50797 |
rs33167414 | snp | A/G | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Copb2, 4930579K19Rik | Mm_Celera | 9:98565590 | CTCCTGGCATAACAT[A/G]CTTCCTGCTTGTTGT | 50797 |
rs33167415 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Copb2 | Mm_Celera | 9:98565748 | GTTAGAGATGGGCAG[C/G]GCTGCATGACAGTGG | 50797 |
rs33167416 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Copb2 | Mm_Celera | 9:98566118 | GAAGAAGAGAGAGTG[C/T]TCCAGGACTTCACTG | 50797 |
rs33167417 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Copb2 | Mm_Celera | 9:98566143 | TCACTGTGGAATGAA[C/T]TAACTTTTCTTCTGG | 50797 |
rs33167418 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Copb2 | Mm_Celera | 9:98566255 | TGGTCTGACTGGAGA[A/G]GGACAGTTTTAAACT | 50797 |
rs33167419 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Copb2 | Mm_Celera | 9:98566324 | TGTTTTTCAGTATGT[A/G]TCTGTAAATTCAAAA | 50797 |
rs33167420 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Copb2 | Mm_Celera | 9:98566542 | GATTTAGCTGATGTT[C/T]TAAATTTATTTACCT | 50797 |
rs33167421 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Copb2 | Mm_Celera | 9:98566857 | ACCACATCCGACCTG[A/G]TAACATGTTCTGATT | 50797 |
rs33167422 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Copb2 | Mm_Celera | 9:98566961 | GCTGTCAATCTCAAC[A/G]CCTCAGGAGGCATCT | 50797 |
rs33167423 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Copb2 | Mm_Celera | 9:98567332 | AATAAAATTTGTTAT[C/T]TGTGTGGATCTGTGT | 50797 |
rs33168164 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Copb2 | Mm_Celera | 9:98567354 | GATCTGTGTAACTCA[A/G]TGAACCATCCTGTCC | 50797 |
rs33168165 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Copb2 | Mm_Celera | 9:98567409 | AAAAACCAAGCAGGA[A/G]CTAAGACTCTGCAGA | 50797 |
rs33168166 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Copb2 | Mm_Celera | 9:98567470 | GCCAAGTGTAAATAG[C/T]TACTTCTAGGCTTCA | 50797 |
rs33168167 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Copb2 | Mm_Celera | 9:98567634 | TTTTGTTATGCCTCA[A/G]CCAGAACCGTATACT | 50797 |
rs33168168 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Copb2 | Mm_Celera | 9:98567878 | CTGTAGAATTGATAC[C/T]ATTCACAATTTAGGA | 50797 |
rs33168169 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Copb2 | Mm_Celera | 9:98568200 | AATAATGAAAGAGCC[A/G]CCAGAGGCCAAGCAG | 50797 |
rs33168170 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Copb2 | Mm_Celera | 9:98568239 | GTGCTGCTGCTCAAA[A/G]TAGGATGGAGTGTTT | 50797 |
rs33168171 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Copb2 | Mm_Celera | 9:98568288 | TGTGTGGGTGTTGCC[C/T]GTGGAAGAAGTTCTG | 50797 |
rs33168172 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Copb2 | Mm_Celera | 9:98568614 | CTAGCCACACTGAGC[C/T]TTGATTTACTACTCT | 50797 |
rs33168173 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Copb2 | Mm_Celera | 9:98568675 | TGAAGAAAGAACGTG[A/G]AATAAAATGTTAGGC | 50797 |
rs33168864 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Copb2 | Mm_Celera | 9:98568721 | ACAAAGAACCATCTT[A/G]GTGTTAGCTGTTGCT | 50797 |
rs33168865 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Copb2 | Mm_Celera | 9:98569087 | TGTTGGTTTTCCAGT[C/G]TACCTTGGTAAATGA | 50797 |
rs33168866 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Copb2 | Mm_Celera | 9:98569451 | CCCCACCTTGAATCC[A/G]TGTAGATGATCCACT | 50797 |
rs33168867 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Copb2 | Mm_Celera | 9:98569603 | TCATTTCTATGGGTT[C/T]CATtttatttattta | 50797 |
rs33168868 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Copb2 | Mm_Celera | 9:98569921 | CTGCCCTTGGAGAGC[A/G]CAGTGGGAAGAGTGA | 50797 |
rs33168869 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Copb2 | Mm_Celera | 9:98569992 | GAGTAAAGCTTCCTC[C/T]CTGGGTAGGTTTCCA | 50797 |
rs33168870 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Copb2 | Mm_Celera | 9:98570086 | CCCGTCTGTCTGTCC[A/G]TCCTATGACCGTCTG | 50797 |
rs33168871 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Copb2 | GRCm38.p3 | 9:98570185 | CTTTAATGCTGAGCT[A/G]TCATACACTTGTTTT | 50797 |
rs33168872 | snp | A/G | 0.132653 | 0.220748 | synonymous-codon | Copb2 | Mm_Celera | 9:98570651 | GTTTGAAGCACACTC[A/G]GATTACATTCGTTGT | 50797 |
rs33168873 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Copb2 | Mm_Celera | 9:98570748 | ATGTGCACTGAGTGA[C/T]GATTTGTTCCCACGA | 50797 |
rs33169664 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Copb2 | Mm_Celera | 9:98571293 | TAGTAGCTGTCCATA[C/T]GCACTTTGTCTGCAC | 50797 |
rs33169665 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Copb2 | Mm_Celera | 9:98571323 | CTGTTCTGTAGTTAG[A/G]AATGCTCTGAGGGCA | 50797 |
rs33169666 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Copb2 | Mm_Celera | 9:98571405 | GGATGTGTGAACTGT[A/G]CTACATTTGTTGCCT | 50797 |
rs33169667 | snp | A/C | 0.260355 | 0.249785 | intron-variant | Copb2 | Mm_Celera | 9:98571430 | TTGCCTTAAAGGACA[A/C]CAAGCCTGTCTTACT | 50797 |
rs33169668 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Copb2 | Mm_Celera | 9:98571661 | AGTGTCCACTGTTGG[A/T]GCTTTACTATGACTG | 50797 |
rs33169669 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Copb2 | Mm_Celera | 9:98571844 | GTCTGTCTGTCCGTC[C/T]GTTAGTCATTCTTGA | 50797 |
rs33169670 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Copb2 | Mm_Celera | 9:98572271 | GAGTGTGTGTCACTC[A/G]CTTTAGATTTTGTTT | 50797 |
rs33169671 | snp | A/C/G | 0.32 | 0.24 | intron-variant | Copb2 | Mm_Celera | 9:98572383 | GGAGCTCTGTCTTCC[A/C/G]TTGCACAGCCCCAGG | 50797 |
rs33169672 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Copb2 | Mm_Celera | 9:98572423 | GAGAGTAGCACAGTG[C/T]GTTGGCTGTACTGGG | 50797 |
rs33169673 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Copb2 | Mm_Celera | 9:98572536 | TTGTTGAATTGCCCT[C/T]GCTTTTGACATAGGT | 50797 |
rs33170224 | snp | A/G | 0.231111 | 0.249285 | synonymous-codon | Copb2 | Mm_Celera | 9:98581182 | TATCGCCACCGAGGA[A/G]TCATTTTTTATTCTT | 50797 |
rs33170225 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Copb2 | Mm_Celera | 9:98581294 | GTGAGTGTCTGAGTC[C/T]AGCTTAGGGCATTGA | 50797 |
rs33170226 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Copb2 | Mm_Celera | 9:98582042 | ACATTCCAGTTTCAT[A/G]TGTTGCAGTTTAGAT | 50797 |
rs33170227 | snp | A/T | 0.260355 | 0.249785 | intron-variant | Copb2 | Mm_Celera | 9:98582131 | TATTCATTGAAAACT[A/T]TTTTTTAAGACAAAA | 50797 |
rs33170228 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Copb2 | Mm_Celera | 9:98582453 | CTAAATTTGAAAGTG[C/T]TTTATGAACCAAATG | 50797 |
rs33170229 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Copb2 | Mm_Celera | 9:98582504 | GTGATGGGTTAATTT[C/T]CCCCCATTAGTTTTA | 50797 |
rs33170230 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Copb2 | Mm_Celera | 9:98583073 | TCTTGCTTCTTTAGG[C/T]GTAGGAACCTCAGTG | 50797 |
rs33170231 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Copb2 | Mm_Celera | 9:98583121 | GCTGATTTTATCACT[C/T]TTCTTACATCCCCTT | 50797 |
rs33170232 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Copb2 | Mm_Celera | 9:98583814 | GAGTTTATGCCCCCC[A/C]AACACAAAAACTACC | 50797 |
rs33170233 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Copb2 | Mm_Celera | 9:98583881 | AAAGCAAGGACATGT[C/T]GCCCTCTTCCTCTGT | 50797 |
rs33170374 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Copb2 | Mm_Celera | 9:98572734 | CCTCTCTCCCTGGCA[A/C]GTGTTCTTTCATTTT | 50797 |
rs33170375 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Copb2 | Mm_Celera | 9:98572830 | GTTAATTGTAGATTC[A/G]TGCACTTCATCTGTA | 50797 |
rs33170376 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Copb2 | Mm_Celera | 9:98572910 | AAAGCAATTTGGCAA[A/G]GAAAGGGTTTATTTC | 50797 |
rs33170377 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Copb2 | Mm_Celera | 9:98573053 | ATTGGCTTGCTCTTC[A/G]TGAGTTGCTCAGCCT | 50797 |
rs33170378 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Copb2 | Mm_Celera | 9:98573285 | GGCACCTTCAGAGAG[C/T]AGTGATTCTGCTTCC | 50797 |
rs33170379 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Copb2 | Mm_Celera | 9:98573335 | AGCAGATATCCTTGA[A/G]CACACTGTGTGTTGG | 50797 |
rs33170380 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Copb2 | Mm_Celera | 9:98573371 | GGTGTTGGATGTCTT[A/G]TGTTAAAAGTGAGTT | 50797 |
rs33170381 | snp | C/T | 0.132653 | 0.220748 | synonymous-codon | Copb2 | Mm_Celera | 9:98573452 | GTGGCAGCTGGGCTC[C/T]TCATCACCAAACTTC | 50797 |
rs33170382 | snp | C/T | 0.231111 | 0.249285 | synonymous-codon | Copb2 | Mm_Celera | 9:98573560 | TGCAGATGACCGGCT[C/T]GTTAAAATATGGGAT | 50797 |
rs33170383 | snp | C/T | 0.260355 | 0.249785 | synonymous-codon | Copb2 | Mm_Celera | 9:98574164 | CACAGGGTCAGAAGA[C/T]GGTAAGTTAGAGGCT | 50797 |
rs33171004 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Copb2 | Mm_Celera | 9:98583928 | CTGACCAGTTCCAAA[C/T]ATCTGCTGTTCACTC | 50797 |
rs33171005 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Copb2 | Mm_Celera | 9:98584092 | CTCTGAATGTTGTCC[A/G]GCTTCTCTGTCCTGA | 50797 |
rs33171006 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Copb2 | Mm_Celera | 9:98584856 | CCATTTGGTCCTCTG[A/G]AATAGATGGCTATGG | 50797 |
rs33171007 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Copb2 | Mm_Celera | 9:98584912 | GAGAAATAATTTGTT[G/T]TGTGCATACTATATG | 50797 |
rs33171008 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Copb2 | Mm_Celera | 9:98585213 | CTGTTGTATCTTTGG[C/T]CTTTTTAAAGGTGCA | 50797 |
rs33171009 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Copb2 | Mm_Celera | 9:98585494 | ATTAGCTGTCAAGAT[C/T]ATTTAAATGTGCATT | 50797 |
rs33171010 | snp | A/C | 0.231111 | 0.249285 | synonymous-codon | Copb2 | Mm_Celera | 9:98585994 | TCAGTTCAGCCTAGC[A/C]CAGGAGTGTCTGCAC | 50797 |
rs33171011 | snp | C/T | 0.231111 | 0.249285 | synonymous-codon | Copb2 | Mm_Celera | 9:98586102 | AGGTGCGGAGAGAGA[C/T]GGCAAAAATAACGTG | 50797 |
rs33171012 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Copb2 | Mm_Celera | 9:98586270 | CAGCTGGTGATGGCC[A/G]ACTGTTGCTGAATGG | 50797 |
rs33171013 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Copb2 | Mm_Celera | 9:98586275 | GGTGATGGCCGACTG[C/T]TGCTGAATGGTGGGG | 50797 |
rs33171134 | snp | A/C | 0.260355 | 0.249785 | intron-variant | Copb2 | Mm_Celera | 9:98574279 | CATATCATGACTAGG[A/C]ATCTAGACTTATACA | 50797 |
rs33171135 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Copb2 | Mm_Celera | 9:98577843 | GAAAATGTTTGGGAT[C/T]GTGACTTTTCTATTT | 50797 |
rs33171136 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Copb2 | Mm_Celera | 9:98577970 | GCTGATGCTCAAGCC[G/T]CTAGAGCAGTGGTTC | 50797 |
rs33171137 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Copb2 | Mm_Celera | 9:98577997 | GTTCTTCCCCTTCCT[A/T]AGTGCTTGGACACCT | 50797 |
rs33171138 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Copb2 | Mm_Celera | 9:98578028 | CAGGCAGTTCCTCAT[C/G]TTACACTGACCTCCA | 50797 |
rs33171139 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Copb2 | Mm_Celera | 9:98578640 | TGTGATGCTGTGAGC[A/G]CGGTATACGCATCTT | 50797 |
rs33171140 | snp | A/G | 0.32 | 0.24 | intron-variant | Copb2 | Mm_Celera | 9:98578678 | AGCAAGCATTGCCGC[A/G]TGGTTGGAGTCGCTG | 50797 |
rs33171141 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Copb2 | Mm_Celera | 9:98578700 | GAGTCGCTGCATCTC[C/T]AGCCGTGCTTGCTCC | 50797 |
rs33171142 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Copb2 | Mm_Celera | 9:98579301 | GGGCCTGTGACATGA[C/T]GTGATGCTTGGGTTT | 50797 |
rs33171143 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Copb2 | Mm_Celera | 9:98579461 | TGCATGTCCCCTACT[A/G]CTCATTCTTAACCTA | 50797 |
rs33171844 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Copb2 | Mm_Celera | 9:98586363 | GGTAACTTTTGATCT[C/T]TATCTTTATGCTTGA | 50797 |
rs33171845 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Copb2 | Mm_Celera | 9:98586577 | TATTTGAGCTCAACT[C/G]TGAAAACATCATGAA | 50797 |
rs33171846 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Copb2 | Mm_Celera | 9:98586729 | CAAACATTTTATTAA[C/G]GTTTGCTAAAGAACC | 50797 |
rs33171847 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Copb2 | Mm_Celera | 9:98586777 | GCACACTAGACAAGT[A/G]TTCATTACTGAGCTG | 50797 |
rs33171848 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Copb2 | Mm_Celera | 9:98586879 | ACACCCACAAAGTTC[A/G]CTGGTTTTGTTCAAC | 50797 |
rs33171849 | snp | C/G | 0.336735 | 0.234472 | intron-variant | Copb2 | Mm_Celera | 9:98587952 | CTGCTCGTGTCAGGA[C/G]GAAGGAGATTTGGTT | 50797 |
rs33171850 | snp | A/C/G | 0.231111 | 0.249285 | utr-variant-3-prime, intron-variant | Copb2, Mrps22 | GRCm38.p3 | 9:98588356 | GTTACTAGATCACCC[A/C/G]TCATAAAATCTTTTG | 50797 |
rs33171851 | snp | A/C | 0.231111 | 0.249285 | downstream-variant-500B | Copb2, Mrps22 | Mm_Celera | 9:98588461 | TCACTCGGGGATCAG[A/C]TTCACCCTTTCCTTG | 50797 |
rs33171852 | snp | C/T | 0.444444 | 0.157135 | downstream-variant-500B, utr-variant-3-prime | Copb2, Mrps22 | GRCm38.p3 | 9:98588826 | AAATGTGTTTTTAAC[C/T]GTTCTCAGGATGCTG | 50797 |
rs33172044 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Copb2 | Mm_Celera | 9:98579533 | AAAGCACAAGTCACA[C/T]TAATTCTTTACATGT | 50797 |
rs33172045 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Copb2 | Mm_Celera | 9:98579585 | ACAGTCAGATTATCC[C/T]TACCCCAATCAGCTC | 50797 |
rs33172046 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Copb2 | Mm_Celera | 9:98579699 | ATAGAGCACTATAGG[C/T]ATGCATTCTTGGATA | 50797 |
rs33172047 | snp | A/G | 0.231111 | 0.249285 | synonymous-codon | Copb2 | Mm_Celera | 9:98580289 | CTTGCTGGGAGTCAG[A/G]TCTGTAAATGGCTTA | 50797 |
rs33172048 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon | Copb2 | Mm_Celera | 9:98580334 | GGAGAATACTGAACT[C/T]ATCCGCAGAATTGAA | 50797 |
rs33172049 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Copb2 | Mm_Celera | 9:98580664 | GTGGAAAAGCCTTTT[C/G]ATACTTCATGTGAAG | 50797 |
rs33172050 | snp | C/T | 0.32 | 0.24 | intron-variant | Copb2 | Mm_Celera | 9:98580745 | GAAAGCATCTCACCT[C/T]GTTATGGTCCTGAGT | 50797 |
rs33172051 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Copb2 | Mm_Celera | 9:98580969 | GTGCTGTGCTGTCCA[C/T]CTTCCCAAGTGCATA | 50797 |
rs33642170 | snp | A/G | 0.375 | 0.216506 | intron-variant | Copb2 | Mm_Celera | 9:98570067 | CAGAGGGTCTGGAGT[A/G]CCGCCCGTCTGTCTG | 50797 |
rs47154675 | snp | C/T | | | intron-variant | Copb2 | Mm_Celera | 9:98566474 | CAGCTTCATAAATGA[C/T]ATACCTTCACAACAT | 50797 |
rs48737862 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98566468 | TTACTACAGCTTCAT[A/G]AATGATATACCTTCA | 50797 |
rs108383348 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98579386 | AACTAGTTGGGAGGT[A/G]CTGCTTATGCCAGGT | 50797 |
rs211871423 | snp | G/T | | | intron-variant | Copb2 | Mm_Celera | 9:98578102 | GACTGTTAGGAATCA[G/T]AATATAAATATCTGA | 50797 |
rs212141182 | snp | C/T | | | intron-variant | Copb2 | Mm_Celera | 9:98566574 | TCTATAAACTGGGGG[C/T]TTCAGAAGTGTCTTC | 50797 |
rs212156001 | snp | G/T | | | intron-variant, upstream-variant-2KB | Copb2, 4930579K19Rik | Mm_Celera | 9:98563900 | TCTTGGCTAGGAGCA[G/T]TAGCTAGAAGCGGTC | 50797 |
rs212175180 | snp | C/T | | | intron-variant | Copb2 | Mm_Celera | 9:98579349 | CCCAGACATGGCCTC[C/T]GAGGGCCGGTTGCGC | 50797 |
rs212320575 | in-del | -/CCCC | | | intron-variant | Copb2 | Mm_Celera | 9:98569321 | GAAACCCTGTCTTGA[-/CCCC]CCCCCCCCCCAAAAA | 50797 |
rs212916066 | snp | A/G | | | synonymous-codon | Copb2 | Mm_Celera | 9:98582837 | TAGCATGGCGGATAA[A/G]GTCCTCCCTACCATC | 50797 |
rs213214979 | snp | C/T | | | intron-variant | Copb2 | Mm_Celera | 9:98571180 | AGGCAAATGCTGCCT[C/T]TTTCCACAGTCAGCA | 50797 |
rs213266274 | snp | A/C | | | upstream-variant-2KB | Copb2 | Mm_Celera | 9:98561863 | TGCCCACTTGGGATG[A/C]AGCAGCCGTCCTAGA | 50797 |
rs213305851 | in-del | -/A | | | intron-variant | Copb2 | Mm_Celera | 9:98584796 | TGCATTGTTGGTAGC[-/A]TGTTCATGGATGCTA | 50797 |
rs213359602 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98586996 | TCAGCTTTATCTGCT[A/G]TTACCATTTGTTTGT | 50797 |
rs213375544 | in-del | -/CCC | | | intron-variant | Copb2 | Mm_Celera | 9:98584541 | TACCTGTGCCATATG[-/CCC]CCCCCCCATGCAATA | 50797 |
rs213544248 | snp | A/G | | | intron-variant, upstream-variant-2KB | Copb2, 4930579K19Rik | Mm_Celera | 9:98564629 | TCTAGAGATGACCAG[A/G]AGTGATGGGTAAATT | 50797 |
rs213646417 | snp | C/T | | | synonymous-codon | Copb2 | Mm_Celera | 9:98577454 | AAAGATGGAGAAAGA[C/T]TGCCACTGGCAGTAA | 50797 |
rs213736246 | snp | C/T | | | intron-variant | Copb2 | Mm_Celera | 9:98572518 | ACCTGATTTTGATAT[C/T]TTTTGTTGAATTGCC | 50797 |
rs213810778 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98584367 | CCCCTCAGTGCCTGA[A/G]CCGGAGTTACAGGCT | 50797 |
rs213960108 | snp | A/G | | | upstream-variant-2KB, nc-transcript-variant | Copb2, 4930579K19Rik | Mm_Celera | 9:98563167 | CCTACGTGATGTGGC[A/G]GTACCACCAACTGAA | 50797 |
rs214139666 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98569972 | TTGGCAGTGGTGCAG[A/G]AAGGGAGTAAAGCTT | 50797 |
rs214157698 | snp | C/T | | | intron-variant | Copb2 | Mm_Celera | 9:98587940 | AGTAGGATGCTGCTG[C/T]TCGTGTCAGGAGGAA | 50797 |
rs214266851 | in-del | -/G | | | intron-variant | Copb2 | Mm_Celera | 9:98586250 | TGGTACACAAATCCT[-/G]GGGACAGCTGGTGAT | 50797 |
rs214692778 | snp | C/G | | | intron-variant | Copb2 | Mm_Celera | 9:98568993 | CTCAGTCGCCTGGTA[C/G]CAGCTGTGTATCTGT | 50797 |
rs214807084 | snp | C/T | | | intron-variant | Copb2 | Mm_Celera | 9:98581529 | CATGACCAAGGGCAC[C/T]CTTATAAAGAACATT | 50797 |
rs214937671 | snp | A/G | | | upstream-variant-2KB | Copb2 | Mm_Celera | 9:98561834 | CGGTACTGCTAAATC[A/G]ATGCTGGAAGGGATG | 50797 |
rs215467706 | in-del | -/TTG | | | intron-variant | Copb2 | Mm_Celera | 9:98582215 | CTCATCATATCTAGC[-/TTG]TTGTTCAGATTTCTG | 50797 |
rs215552219 | snp | C/T | | | intron-variant | Copb2 | Mm_Celera | 9:98585851 | TCTCCTAATTGTTAT[C/T]ACAGTGATATTCAAA | 50797 |
rs215577060 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98570044 | TGGGAAGGAGAGGCA[A/G]GCCAGGACAGAGGGT | 50797 |
rs215618362 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98567603 | TGTTATGTGTTTGAG[A/G]CCAGATGGTGGTTGC | 50797 |
rs215721794 | snp | C/T | | | intron-variant | Copb2 | Mm_Celera | 9:98566777 | TTGCCTTGGAGCTCA[C/T]GCTGACTTTGAACTC | 50797 |
rs215906309 | in-del | -/TCTG | | | intron-variant | Copb2 | Mm_Celera | 9:98581100 | AAAGGTGGTCAGTCA[-/TCTG]TCTGTCTGTCTGTCT | 50797 |
rs215982612 | snp | C/T | | | intron-variant | Copb2 | Mm_Celera | 9:98584382 | ACCGGAGTTACAGGC[C/T]AGATGATCTACAGAT | 50797 |
rs216167621 | snp | A/T | | | intron-variant | Copb2 | Mm_Celera | 9:98582518 | TCCCCCCATTAGTTT[A/T]AGTAGATTTTCTGAT | 50797 |
rs216446973 | snp | C/T | | | synonymous-codon | Copb2 | Mm_Celera | 9:98580154 | AAAATCATTTAAACC[C/T]GATTTTGGAGCTGAA | 50797 |
rs216540615 | snp | C/T | | | intron-variant | Copb2 | Mm_Celera | 9:98570920 | TCCTGCCAGAAAATT[C/T]GAAGGTCTAGATGCA | 50797 |
rs216636546 | snp | C/T | | | intron-variant | Copb2 | Mm_Celera | 9:98571840 | GTCTGTCTGTCTGTC[C/T]GTCTGTTAGTCATTC | 50797 |
rs216950795 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98582158 | AAAAATTCTTAGGAA[A/G]AATGTTCTTGAAATT | 50797 |
rs217071326 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98587998 | GGACTGGGTAACCCC[A/G]TAAGTACTGTGTAAC | 50797 |
rs217232555 | in-del | -/AGAG | | | upstream-variant-2KB, downstream-variant-500B | Copb2, 4930579K19Rik | Mm_Celera | 9:98562219 | TTTTAAAAGATTAAA[-/AGAG]AGAGAGAGAGAGAGT | 50797 |
rs217341258 | snp | C/T | | | intron-variant | Copb2 | Mm_Celera | 9:98573872 | ACTTCTGTAGCTGAG[C/T]GAAACAGGCACGACA | 50797 |
rs217370102 | snp | C/T | | | intron-variant | Copb2 | Mm_Celera | 9:98581990 | GAAAATCAAACCATC[C/T]ACTGTTTAGATGTCC | 50797 |
rs217508324 | snp | C/T | | | intron-variant, upstream-variant-2KB | Copb2, 4930579K19Rik | Mm_Celera | 9:98563887 | GGTTCCCGGGGCTTC[C/T]TGGCTAGGAGCAGTA | 50797 |
rs217728667 | in-del | -/AA | | | intron-variant | Copb2 | Mm_Celera | 9:98585582 | TTTTCTACTCTTCCT[-/AA]AAAGTGTTACTAATT | 50797 |
rs217729998 | snp | C/G | | | intron-variant | Copb2 | Mm_Celera | 9:98568849 | ATCTCATGTGGTACT[C/G]AGTCATGGAGGCTCT | 50797 |
rs217821196 | snp | A/T | | | intron-variant | Copb2 | Mm_Celera | 9:98567875 | GTGCTGTAGAATTGA[A/T]ACCATTCACAATTTA | 50797 |
rs217946322 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98577574 | TGTGTGTGGTGGAGC[A/G]ACTGTGCATATGGAC | 50797 |
rs218174366 | snp | A/C | | | intron-variant | Copb2 | Mm_Celera | 9:98565662 | AATTAGTGGGGCAAA[A/C]ATTTAGAAATCATCG | 50797 |
rs218214339 | snp | C/T | | | intron-variant | Copb2 | Mm_Celera | 9:98570161 | TTGATTGGTCCTCCC[C/T]GCCCCCCACTTTAAT | 50797 |
rs218349908 | snp | C/T | | | intron-variant | Copb2 | Mm_Celera | 9:98583697 | GGCATCAGGCACATA[C/T]ATACATGTATGGCAA | 50797 |
rs218369686 | snp | A/G | | | synonymous-codon | Copb2 | Mm_Celera | 9:98587279 | CCAGAAAGCAGCAGA[A/G]TCCCTTGCTGATCCT | 50797 |
rs218382151 | snp | C/T | | | intron-variant | Copb2 | Mm_Celera | 9:98584824 | CTAGTGGGTATCTGG[C/T]TACTTGGGGTTAGAT | 50797 |
rs218399777 | in-del | -/G | | | intron-variant | Copb2 | Mm_Celera | 9:98574636 | GTTTTCTAGTTGCAA[-/G]GTTTTTTAAAAATTT | 50797 |
rs218401662 | snp | C/T | | | upstream-variant-2KB, nc-transcript-variant | Copb2, 4930579K19Rik | Mm_Celera | 9:98562946 | AATCGATACACAATG[C/T]ATTTGCACTTTTCCT | 50797 |
rs218402280 | snp | A/C | | | intron-variant | Copb2 | Mm_Celera | 9:98574552 | CACAGCAAACATGTA[A/C]TACATGGTGAGCACT | 50797 |
rs218430496 | in-del | -/T | | | intron-variant, upstream-variant-2KB | Copb2, 4930579K19Rik | Mm_Celera | 9:98565472 | AAAACCTTGTTAGGA[-/T]TTATCCTAACAATCC | 50797 |
rs218457133 | snp | G/T | | | intron-variant | Copb2 | Mm_Celera | 9:98580404 | TTTGGGAGGTTCATC[G/T]TTGAAATGTCTGAGT | 50797 |
rs218735853 | snp | C/T | | | synonymous-codon | Copb2 | Mm_Celera | 9:98577495 | CAGTTGTGAAATATA[C/T]CCACAGACCATTCAG | 50797 |
rs218859658 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98569233 | ACGCAGGAGGCAGAG[A/G]CAGGCAGATTTCTGA | 50797 |
rs218927236 | in-del | -/TTAGA | | | intron-variant | Copb2 | Mm_Celera | 9:98583985 | AAGAAAATCAGTAAC[-/TTAGA]TTATTTAGAACCAGT | 50797 |
rs219015065 | snp | C/G | | | intron-variant | Copb2 | Mm_Celera | 9:98581935 | GGTGTTTGGTTCTAA[C/G]ACTGTTGAGCTAGAA | 50797 |
rs219037079 | snp | A/C | | | intron-variant | Copb2 | Mm_Celera | 9:98566502 | CATTGTCTGCTACAA[A/C]ACTAATGCATGGACA | 50797 |
rs219074106 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98571845 | TCTGTCTGTCCGTCT[A/G]TTAGTCATTCTTGAA | 50797 |
rs219226967 | snp | C/T | | | upstream-variant-2KB, nc-transcript-variant | Copb2, 4930579K19Rik | Mm_Celera | 9:98563532 | CCGAAGGTGAGCAGC[C/T]CAGACCGCCGCTAGT | 50797 |
rs219301021 | snp | A/T | | | intron-variant | Copb2 | Mm_Celera | 9:98586732 | ACATTTTATTAAGGT[A/T]TGCTAAAGAACCGAA | 50797 |
rs219415788 | in-del | -/TGAATCCCCACCT | | | intron-variant | Copb2 | Mm_Celera | 9:98569431 | TTTTCCTAGGTCTCC[-/TGAATCCCCACCT]TGAATCCGTGTAGAT | 50797 |
rs219465212 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98572717 | GGGAACATAGTCTTG[A/G]TCCTCTCTCCCTGGC | 50797 |
rs219690721 | in-del | -/AT | | | intron-variant, upstream-variant-2KB | Copb2, 4930579K19Rik | Mm_Celera | 9:98564942 | AGAATGCTAAGAGAG[-/AT]ATATTATTATTATCC | 50797 |
rs219705077 | snp | A/T | | | intron-variant | Copb2 | Mm_Celera | 9:98570189 | AATGCTGAGCTATCA[A/T]ACACTTGTTTTACAT | 50797 |
rs219856056 | snp | C/T | | | intron-variant, upstream-variant-2KB | Copb2, 4930579K19Rik | Mm_Celera | 9:98564970 | TCCCTGTTATACAAG[C/T]CAAACCTTGGGTGTT | 50797 |
rs220058582 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98578891 | TATAATAACCGACTA[A/G]CATAGCATCTGTTAG | 50797 |
rs220093406 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98579686 | TAGTTTTATATGAAT[A/G]GAGCACTATAGGCAT | 50797 |
rs220126856 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98582017 | GTCCTTAAGGACTTG[A/G]AGATACTTAACATTC | 50797 |
rs220189518 | in-del | -/GCCCAGCGGTG | | | intron-variant | Copb2 | Mm_Celera | 9:98573096 | CACCCGGGTTTACCT[-/GCCCAGCGGTG]GCCCATCATGGTTCC | 50797 |
rs220222558 | in-del | -/AC | | | intron-variant | Copb2 | Mm_Celera | 9:98578553 | AACTAACAGTTGAAT[-/AC]AGTCTTTTGTTCATT | 50797 |
rs220313869 | in-del | -/A | | | intron-variant | Copb2 | Mm_Celera | 9:98586968 | TTTTGCCTCTGCAAC[-/A]AGGTTCACACTTTCA | 50797 |
rs220354185 | snp | A/T | | | intron-variant | Copb2 | Mm_Celera | 9:98567005 | TATTAGTATTACAAA[A/T]GAGGATGTGTAAAAT | 50797 |
rs220425498 | in-del | -/TG/TGTG | | | intron-variant | Copb2 | GRCm38.p3 | 9:98571771 | AAGAAGCGGTCACTT[-/TG/TGTG]TGTGTGTGTGTGTGT | 50797 |
rs220834821 | snp | A/T | | | intron-variant | Copb2 | Mm_Celera | 9:98568333 | TAAATACAGCAACAT[A/T]GATGTAGGTCATATT | 50797 |
rs220933743 | snp | A/C | | | upstream-variant-2KB, nc-transcript-variant | Copb2, 4930579K19Rik | Mm_Celera | 9:98563512 | TCTTGCCTTTCTGAA[A/C]CTGACCGAAGGTGAG | 50797 |
rs221084161 | snp | G/T | | | intron-variant | Copb2 | Mm_Celera | 9:98572788 | TCTCCCATCAAATCA[G/T]TACTTCCTTTAGAGG | 50797 |
rs221282550 | snp | C/G | | | intron-variant | Copb2 | Mm_Celera | 9:98568415 | AATTTAGCTGCCATT[C/G]ATGTGCATTGAGAGT | 50797 |
rs221463301 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98571688 | ACTGGCCAGAAAGCT[A/G]CTCCTGTGCTCCTGT | 50797 |
rs221579659 | snp | C/G | | | intron-variant | Copb2 | Mm_Celera | 9:98565857 | CAGTTAGAAGTACAT[C/G]TGTCAAACAGACACA | 50797 |
rs221624965 | in-del | -/TT | | | intron-variant | Copb2 | Mm_Celera | 9:98569606 | TTTCTATGGGTTCCA[-/TT]TTATTTATTTATTTA | 50797 |
rs221648997 | snp | A/C | | | intron-variant | Copb2 | Mm_Celera | 9:98586193 | TAAGGAGTTGTAAGC[A/C]GTGTTTCTCCACTGA | 50797 |
rs221867960 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98569297 | TCCAGAACAGCCAGG[A/G]CTATACAGAGAAACC | 50797 |
rs221983916 | snp | A/G | | | downstream-variant-500B | Copb2, Mrps22 | Mm_Celera | 9:98588638 | CTGCACTCACATATA[A/G]ATGCCAGCCGTCCCC | 50797 |
rs222112337 | snp | C/T | | | intron-variant | Copb2 | Mm_Celera | 9:98577622 | CCTCCCGGAACTGTG[C/T]CCTGGCCCACAGGCC | 50797 |
rs222148388 | snp | C/T | | | intron-variant, upstream-variant-2KB | Copb2, 4930579K19Rik | Mm_Celera | 9:98565094 | ATTCCCAAATACATA[C/T]GGTGTGGAGAGAAGG | 50797 |
rs222157347 | snp | C/T | | | intron-variant | Copb2 | Mm_Celera | 9:98569824 | AAGCTAAGAGATAAT[C/T]CACTCAACAGATGGT | 50797 |
rs222332084 | snp | C/T | | | intron-variant | Copb2 | Mm_Celera | 9:98584877 | ATGGCTATGGGGTCT[C/T]CTTGTCTGTAAGGTC | 50797 |
rs222350509 | snp | A/G | | | upstream-variant-2KB, nc-transcript-variant | Copb2, 4930579K19Rik | Mm_Celera | 9:98563584 | GCAATACACTCCATC[A/G]GCCAGCTCAGCAGCG | 50797 |
rs222543521 | snp | C/G | | | intron-variant | Copb2 | Mm_Celera | 9:98580746 | AAAGCATCTCACCTT[C/G]TTATGGTCCTGAGTC | 50797 |
rs222855476 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98569955 | TGGAGTCTGCTTAGC[A/G]CTTGGCAGTGGTGCA | 50797 |
rs223051364 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98579773 | ATTGTTTTGTGTGCT[A/G]AGTAGTAGTCCATTG | 50797 |
rs223110283 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98576777 | TTATCATAGTTGCAA[A/G]TTTTTTGTTGTTTCA | 50797 |
rs223249599 | snp | C/G | | | intron-variant | Copb2 | Mm_Celera | 9:98587010 | TGTTACCATTTGTTT[C/G]TCTAACAGCATCTCC | 50797 |
rs223337623 | snp | C/G | | | intron-variant | Copb2 | Mm_Celera | 9:98587918 | TAGTTCAGAGAGAAG[C/G]CTTCAAAGTAGGATG | 50797 |
rs223426407 | snp | C/T | | | downstream-variant-500B | Copb2, Mrps22 | Mm_Celera | 9:98588655 | TGCCAGCCGTCCCCA[C/T]GCCACCTAGAAATTG | 50797 |
rs223427949 | snp | C/T | | | intron-variant | Copb2 | Mm_Celera | 9:98576863 | ATTGCTAGAAAATAC[C/T]TGTATTGAAATAGAA | 50797 |
rs223823145 | snp | C/T | | | intron-variant | Copb2 | Mm_Celera | 9:98568861 | ACTGAGTCATGGAGG[C/T]TCTGCAGCCGCCTCT | 50797 |
rs223840891 | snp | C/G | | | intron-variant | Copb2 | Mm_Celera | 9:98582096 | GTTAATGACTCAACA[C/G]TGAGATTTCATACTG | 50797 |
rs223913222 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98587002 | TTATCTGCTGTTACC[A/G]TTTGTTTGTCTAACA | 50797 |
rs224047701 | snp | C/T | | | intron-variant | Copb2 | Mm_Celera | 9:98570257 | CGGAATAAGACTTTT[C/T]GGTTACTTCCTTGTA | 50797 |
rs224060680 | snp | C/T | | | intron-variant | Copb2 | Mm_Celera | 9:98571466 | GATGAAAGCAGACCA[C/T]GACTGACTTGGCTTT | 50797 |
rs224173538 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98583576 | CACAGGAAGGGTACA[A/G]CTTTTACAGAGGGCT | 50797 |
rs224258053 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98580691 | GAAGATGGTCAGGAG[A/G]ACTCTAGTAGCAAAC | 50797 |
rs224300274 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98581103 | GGTGGTCAGTCAtct[A/G]tctgtctgtctgtct | 50797 |
rs224329660 | snp | C/T | | | intron-variant | Copb2 | Mm_Celera | 9:98585274 | AAATTCAGGGTACTC[C/T]TAAGTTCTATACTCT | 50797 |
rs224388693 | snp | C/T | | | intron-variant | Copb2 | Mm_Celera | 9:98578885 | TTAAATTATAATAAC[C/T]GACTAACATAGCATC | 50797 |
rs224550678 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98572424 | AGAGTAGCACAGTGC[A/G]TTGGCTGTACTGGGT | 50797 |
rs224552778 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98586291 | TGCTGAATGGTGGGG[A/G]CAGCCAGAGAACAGT | 50797 |
rs224641511 | in-del | -/T | | | intron-variant | Copb2 | Mm_Celera | 9:98574638 | TTTTCTAGTTGCAAG[-/T]TTTTTAAAAATTTTT | 50797 |
rs224749050 | snp | C/T | | | intron-variant | Copb2 | Mm_Celera | 9:98581380 | TATTCTTTAAACAGA[C/T]TAAATTGATTCTAAT | 50797 |
rs224898842 | snp | A/G | | | upstream-variant-2KB | Copb2 | Mm_Celera | 9:98561801 | AGAACAGATGGGGGT[A/G]GGGCTGGGGTGTACA | 50797 |
rs225061808 | snp | C/G | | | intron-variant, upstream-variant-2KB | Copb2, 4930579K19Rik | Mm_Celera | 9:98564097 | CTTGCAGTCTGCACC[C/G]GGTCCGGTAGTGCAA | 50797 |
rs225112776 | in-del | -/AAAAG | | | intron-variant | Copb2 | Mm_Celera | 9:98569339 | CCCCCCCCAAAAAAA[-/AAAAG]AAATCATAGCTTAAT | 50797 |
rs225128574 | in-del | -/GTGTGTGTGTGTGTGTGTGTGTGT | | | intron-variant | Copb2 | Mm_Celera | 9:98582582 | ATTTGAGCAAGAAGG[-/GTGTGTGTGTGTGTGTGTGTGTGT]GTGTGTGTGTGTGTG | 50797 |
rs225247806 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98578649 | GTGAGCGCGGTATAC[A/G]CATCTTGGTGCTCAG | 50797 |
rs225542973 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98574763 | cttcttggctctggt[A/G]ttcccctgtactggg | 50797 |
rs225880367 | snp | C/T | | | intron-variant | Copb2 | Mm_Celera | 9:98577725 | TGTTCTTAAGATACC[C/T]TGGATTAGTGCCCTT | 50797 |
rs226081843 | snp | G/T | | | intron-variant | Copb2 | Mm_Celera | 9:98566886 | TTGTCAGACACTTAT[G/T]TGTAAGAAGCAAGGT | 50797 |
rs226250351 | in-del | -/A | | | intron-variant | Copb2 | Mm_Celera | 9:98573734 | GATTTTCCCCTTTAT[-/A]AAAAAAGAATGCAAA | 50797 |
rs226301911 | in-del | -/GCACTACCT | | | intron-variant | Copb2 | Mm_Celera | 9:98587669 | CATTGTTGATTTAAA[-/GCACTACCT]GCCACTTCCTAACCC | 50797 |
rs226358320 | in-del | -/TATT | | | intron-variant | Copb2 | Mm_Celera | 9:98587707 | CCTCTGCATGGGGAA[-/TATT]TACATCTCTGGGCCA | 50797 |
rs226387256 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98573349 | AGCACACTGTGTGTT[A/G]GGCTGTGGTGTTGGA | 50797 |
rs226406936 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98568594 | AGCTAATTTACTGGC[A/G]AGTCCTAGCCACACT | 50797 |
rs226412707 | snp | A/C | | | intron-variant | Copb2 | Mm_Celera | 9:98573172 | TTCTCTCAATTGAAT[A/C]CCCTCTTCCCAGATA | 50797 |
rs226486737 | snp | C/G | | | intron-variant | Copb2 | Mm_Celera | 9:98566032 | TAACTCATCCTGGCA[C/G]TAAGGTCCAGGTTGT | 50797 |
rs226513172 | snp | C/T | | | intron-variant | Copb2 | Mm_Celera | 9:98580926 | ACCTGAATGATAGAA[C/T]CCTGTTTCCCATTGG | 50797 |
rs226520449 | snp | C/T | | | intron-variant | Copb2 | Mm_Celera | 9:98567482 | TAGCTACTTCTAGGC[C/T]TCACATCCCACAGTA | 50797 |
rs226532169 | in-del | -/T | | | intron-variant | Copb2 | Mm_Celera | 9:98581389 | AACAGACTAAATTGA[-/T]TCTAATAGTTCTGTG | 50797 |
rs226585936 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98565618 | TGTTGACTCAAAGAT[A/G]AGAGGGAGAAGTTAA | 50797 |
rs226621976 | snp | A/C | | | intron-variant | Copb2 | Mm_Celera | 9:98578720 | GTGCTTGCTCCTCAT[A/C]TCCAGGCTCTGAGAC | 50797 |
rs226670168 | snp | G/T | | | intron-variant, upstream-variant-2KB | Copb2, 4930579K19Rik | Mm_Celera | 9:98564892 | TGGTTACTATAAGCC[G/T]TGCTCTGCTCTAACT | 50797 |
rs226796444 | in-del | -/A | | | intron-variant | Copb2 | Mm_Celera | 9:98567701 | TAAAAAATGAAATTG[-/A]AAAAAATTGACATAA | 50797 |
rs226971232 | snp | A/C | | | intron-variant | Copb2 | Mm_Celera | 9:98566469 | TACTACAGCTTCATA[A/C]ATGATATACCTTCAC | 50797 |
rs227085080 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98586217 | CCACTGACTGTGAGG[A/G]TGGTGCTTGAGAGGC | 50797 |
rs227350428 | in-del | -/AG | | | intron-variant | Copb2 | Mm_Celera | 9:98567543 | AGGCAGCATCAAAGC[-/AG]AACGTCCAAAAATGG | 50797 |
rs228237132 | snp | C/T | | | intron-variant, upstream-variant-2KB | Copb2, 4930579K19Rik | Mm_Celera | 9:98564350 | CTCGTCGTTTTCTAG[C/T]TGATGTTGATTGGGC | 50797 |
rs228303847 | snp | C/T | | | intron-variant, upstream-variant-2KB | Copb2, 4930579K19Rik | Mm_Celera | 9:98563851 | TCAGGGGACAGAGAG[C/T]GGAGCCCACCGGCTG | 50797 |
rs228303941 | snp | A/T | | | intron-variant | Copb2 | Mm_Celera | 9:98574648 | GCAAGTTTTTTAAAA[A/T]TTTTTTTTATTTATT | 50797 |
rs228456444 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98579788 | GAGTAGTAGTCCATT[A/G]AATGGATGTACCACC | 50797 |
rs228619331 | snp | G/T | | | upstream-variant-2KB | Copb2, 4930579K19Rik | Mm_Celera | 9:98563684 | GTGCGCAGGCGCAGA[G/T]CCTGGCTCCGAGTAC | 50797 |
rs228621932 | in-del | -/CCCC | | | intron-variant | Copb2 | Mm_Celera | 9:98584540 | TACCTGTGCCATATG[-/CCCC]CCCCCCCCCCATGCA | 50797 |
rs228741813 | in-del | -/TGAGAGACACTGA | | | intron-variant | Copb2 | Mm_Celera | 9:98585358 | AATTTGCCATATTGG[-/TGAGAGACACTGA]TTTTAAACAAGAGAT | 50797 |
rs228854069 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98570495 | AGTTAATTCAATGTA[A/G]TGTTCTAAAGGGTGG | 50797 |
rs229516333 | snp | A/C | | | upstream-variant-2KB | Copb2 | Mm_Celera | 9:98561835 | GGTACTGCTAAATCG[A/C]TGCTGGAAGGGATGC | 50797 |
rs229549300 | in-del | -/AT | | | upstream-variant-2KB, downstream-variant-500B | Copb2, 4930579K19Rik | Mm_Celera | 9:98562372 | GCAAAAGATGGAGAC[-/AT]ACAAAATGAGCACGG | 50797 |
rs229686053 | snp | C/T | | | synonymous-codon | Copb2 | Mm_Celera | 9:98586015 | GTGTCTGCACCATGC[C/T]CAGGATTATGGTGGT | 50797 |
rs229902265 | snp | G/T | | | intron-variant | Copb2 | Mm_Celera | 9:98584286 | GGCTTTATGCCCTAA[G/T]AGAGCACAAGGGAGG | 50797 |
rs229992118 | snp | A/C | | | intron-variant | Copb2 | Mm_Celera | 9:98586920 | AGGGCTGAGCAACAG[A/C]AGTGAATGTGCAAGG | 50797 |
rs230253542 | snp | A/T | | | intron-variant, upstream-variant-2KB | Copb2, 4930579K19Rik | Mm_Celera | 9:98564284 | CAGAACTAAACAAAG[A/T]TAAATGTATATGGAG | 50797 |
rs230277129 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98582473 | TGAACCAAATGTCAT[A/G]CTGACTTGTGTAACA | 50797 |
rs230507675 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98581959 | GCTAGAATGATTCAA[A/G]TGAGCTCTGAAATGG | 50797 |
rs230601206 | snp | C/T | | | intron-variant | Copb2 | Mm_Celera | 9:98583883 | AGCAAGGACATGTCG[C/T]CCTCTTCCTCTGTCC | 50797 |
rs230863599 | in-del | -/A | | | upstream-variant-2KB, nc-transcript-variant | Copb2, 4930579K19Rik | Mm_Celera | 9:98562509 | GATACTGTGTCAAAT[-/A]TAAAAATGCAAAGAG | 50797 |
rs230920883 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98580407 | GGGAGGTTCATCTTT[A/G]AAATGTCTGAGTCCC | 50797 |
rs231316530 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98581071 | AGTGAATACATTTTG[A/G]GGTGGCTGCTCAGAA | 50797 |
rs231775345 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98581570 | GGCTTACAGTTTCAG[A/G]GGTTCAGTCCATTAT | 50797 |
rs231993120 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98578101 | TGACTGTTAGGAATC[A/G]TAATATAAATATCTG | 50797 |
rs232092958 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98569153 | ATTATTGCTTTCTTG[A/G]TACAAAAAGAGACAT | 50797 |
rs232215198 | in-del | -/A | | | intron-variant | Copb2 | Mm_Celera | 9:98579431 | TTTAATGTATCTTTT[-/A]AAAAGTTCAATTTCT | 50797 |
rs232299450 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98579148 | TTTTCCCTGGTAAAA[A/G]ACAGTCCCAGCACAG | 50797 |
rs232461225 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98566673 | TGTGTTGCCCTTCCC[A/G]CTAGGTTTATATTTG | 50797 |
rs232536449 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98578262 | AAATGACAAAGTATG[A/G]TATTAAGACTCAGTC | 50797 |
rs232569226 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98585639 | TGACATTTTAATTCC[A/G]TTTACATGGTTTTAG | 50797 |
rs232744619 | in-del | -/T | | | downstream-variant-500B | Copb2, Mrps22 | Mm_Celera | 9:98588678 | AGAAATTGAGTGGAG[-/T]TAATAATACTTTGAG | 50797 |
rs233007349 | snp | A/C | | | intron-variant | Copb2 | Mm_Celera | 9:98567439 | AGTGTAGGATAGACT[A/C]GTGGATTTTAATTTA | 50797 |
rs233406118 | snp | C/T | | | intron-variant | Copb2 | Mm_Celera | 9:98567627 | TGGTTGCTTTTGTTA[C/T]GCCTCAACCAGAACC | 50797 |
rs233427638 | snp | C/T | | | intron-variant, upstream-variant-2KB | Copb2, 4930579K19Rik | Mm_Celera | 9:98564801 | CATAGGAGCATTTCA[C/T]TGTCCTGCATTTTGC | 50797 |
rs233571379 | snp | C/T | | | intron-variant, upstream-variant-2KB | Copb2, 4930579K19Rik | Mm_Celera | 9:98564068 | TCAGGGCGGTCAGGG[C/T]GCCTGTCAGTGCCCT | 50797 |
rs233640920 | snp | C/T | | | intron-variant | Copb2 | Mm_Celera | 9:98566807 | CACAGTCCTCTTTTT[C/T]AGAGGCCACAGTGCT | 50797 |
rs233888437 | snp | A/G | | | upstream-variant-2KB | Copb2 | Mm_Celera | 9:98561820 | CTGGGGTGTACACAC[A/G]GTACTGCTAAATCGA | 50797 |
rs234023885 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98579190 | AAGCACTTGGAGAGT[A/G]TAAAGCGCCCTTGTC | 50797 |
rs234127593 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98576362 | TCTTTTCTACTGGAT[A/G]GTTTTATATTATTTG | 50797 |
rs234168571 | snp | A/G | | | intron-variant, upstream-variant-2KB | Copb2, 4930579K19Rik | Mm_Celera | 9:98564477 | CTTTCCTTCTTCAAT[A/G]TTTGTGAGTTCCATA | 50797 |
rs234248570 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98583940 | AAATATCTGCTGTTC[A/G]CTCTGGGGTTTTCTG | 50797 |
rs234293942 | in-del | -/C | | | intron-variant | Copb2 | Mm_Celera | 9:98581899 | GGCTTGCTTTGCTAT[-/C]CTTCACTAAGGAAAT | 50797 |
rs234361743 | in-del | -/CTCT | | | intron-variant | Copb2 | Mm_Celera | 9:98582933 | CTTTCCTTCCCTCCC[-/CTCT]CTCTCTTTCTTTTTA | 50797 |
rs234428866 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98573884 | GAGCGAAACAGGCAC[A/G]ACAGTGAATGTTGTG | 50797 |
rs234462949 | in-del | -/TTTATTTA | | | intron-variant | Copb2 | Mm_Celera | 9:98569607 | TTCTATGGGTTCCAT[-/TTTATTTA]TTTATTTATTTATTT | 50797 |
rs234497111 | snp | G/T | | | intron-variant | Copb2 | Mm_Celera | 9:98572471 | ATTTAACTCATAGAA[G/T]CTATTTGTATTTAAA | 50797 |
rs234809676 | snp | C/T | | | upstream-variant-2KB, downstream-variant-500B | Copb2, 4930579K19Rik | Mm_Celera | 9:98562016 | CACATGCCTCTAAGC[C/T]AGAGTAAACAAGAGA | 50797 |
rs234904974 | snp | A/G | | | upstream-variant-2KB, nc-transcript-variant | Copb2, 4930579K19Rik | Mm_Celera | 9:98563177 | GTGGCAGTACCACCA[A/G]CTGAAGGTACATAGC | 50797 |
rs234911270 | snp | C/T | | | intron-variant | Copb2 | Mm_Celera | 9:98587025 | GTCTAACAGCATCTC[C/T]GCTTTACTCTGTAGG | 50797 |
rs235015312 | snp | C/T | | | intron-variant | Copb2 | Mm_Celera | 9:98585894 | TGTTGAAAGTTGAAA[C/T]GCTATTTCCAAAAAT | 50797 |
rs235242006 | snp | C/G | | | intron-variant | Copb2 | Mm_Celera | 9:98585161 | TTGGGTGTTGCTATT[C/G]CTGTAACATTATTAC | 50797 |
rs235357229 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98588014 | TAAGTACTGTGTAAC[A/G]TTTACCCTCTGCCTC | 50797 |
rs235373966 | snp | C/G | | | intron-variant | Copb2 | GRCm38.p3 | 9:98569331 | tcttgaCCCCCCCCC[C/G]AAAAAAAAAAAGAAA | 50797 |
rs235594200 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98570506 | TGTAGTGTTCTAAAG[A/G]GTGGAGGTTGTAATA | 50797 |
rs235594327 | snp | G/T | | | intron-variant | Copb2 | Mm_Celera | 9:98584839 | CTACTTGGGGTTAGA[G/T]TCCATTTGGTCCTCT | 50797 |
rs235670512 | snp | C/G | | | upstream-variant-2KB, nc-transcript-variant | Copb2, 4930579K19Rik | Mm_Celera | 9:98563322 | ACATCTTTTCCGCCT[C/G]GGTCGGTTTCACCCA | 50797 |
rs235698375 | snp | C/T | | | intron-variant | Copb2 | Mm_Celera | 9:98583853 | CATCTTAGTGTAGAT[C/T]GGAAATACAGCAAAA | 50797 |
rs235752989 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98587855 | CATCCTCTGCCCCAC[A/G]TCCCATGTCAGGAAC | 50797 |
rs235790153 | snp | C/T | | | intron-variant | Copb2 | Mm_Celera | 9:98584772 | GTTTGCTAAAAATGG[C/T]TCCCATTTTGCATTG | 50797 |
rs236088208 | snp | C/T | | | intron-variant | Copb2 | Mm_Celera | 9:98583128 | TTATCACTTTTCTTA[C/T]ATCCCCTTTAAGGTT | 50797 |
rs236117924 | snp | A/C | | | intron-variant, upstream-variant-2KB | Copb2, 4930579K19Rik | Mm_Celera | 9:98563906 | CTAGGAGCAGTAGCT[A/C]GAAGCGGTCTGCGCT | 50797 |
rs236495187 | in-del | -/T | | | intron-variant | Copb2 | Mm_Celera | 9:98571259 | TAAAAAGTTTCCCCA[-/T]TTTTTTTTTTTATGT | 50797 |
rs236797011 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98578731 | TCATATCCAGGCTCT[A/G]AGACTGAGTGAGGAG | 50797 |
rs236871346 | snp | C/T | | | downstream-variant-500B | Copb2, Mrps22 | Mm_Celera | 9:98588642 | ACTCACATATAGATG[C/T]CAGCCGTCCCCACGC | 50797 |
rs236890573 | in-del | -/G | | | intron-variant | Copb2 | Mm_Celera | 9:98565826 | TTTTGGAAGTGAAGA[-/G]GCAAACAATGAAGAA | 50797 |
rs237137704 | snp | C/G | | | intron-variant | Copb2 | Mm_Celera | 9:98579355 | CATGGCCTCTGAGGG[C/G]CGGTTGCGCTTTATA | 50797 |
rs237152593 | snp | A/T | | | intron-variant, upstream-variant-2KB | Copb2, 4930579K19Rik | Mm_Celera | 9:98564622 | TAACTAATCTAGAGA[A/T]GACCAGGAGTGATGG | 50797 |
rs237257435 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98565670 | GGGCAAACATTTAGA[A/G]ATCATCGAAAAGGTT | 50797 |
rs237440625 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98566892 | GACACTTATTTGTAA[A/G]AAGCAAGGTTTTCAG | 50797 |
rs237648737 | snp | C/T | | | intron-variant | Copb2 | Mm_Celera | 9:98583331 | AACATGTGGTAAAGC[C/T]CCCTTAATAAAACTT | 50797 |
rs237687756 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98567044 | AGTAACATGTGGCTG[A/G]TGGAAAAGGCACTTT | 50797 |
rs237725110 | snp | C/T | | | intron-variant | Copb2 | Mm_Celera | 9:98577736 | TACCTTGGATTAGTG[C/T]CCTTGGGGGTCTAGA | 50797 |
rs237764382 | snp | C/T | | | intron-variant | Copb2 | Mm_Celera | 9:98578948 | TAGTTTCCTGACACC[C/T]ATGTCATTGTCCCTG | 50797 |
rs237878004 | in-del | -/T | | | intron-variant | Copb2 | Mm_Celera | 9:98579427 | GAATTTTAATGTATC[-/T]TTTTAAAAGTTCAAT | 50797 |
rs237938000 | snp | C/G | | | intron-variant | Copb2 | Mm_Celera | 9:98580802 | CCACCAAAGGTGCTC[C/G]CTTGTGGTATTATTG | 50797 |
rs237947067 | snp | C/G | | | intron-variant | Copb2 | Mm_Celera | 9:98584370 | CTCAGTGCCTGAACC[C/G]GAGTTACAGGCTAGA | 50797 |
rs238047734 | snp | C/T | | | intron-variant | Copb2 | Mm_Celera | 9:98579867 | ATGGCTTCTAAGCTT[C/T]CATAATTTGCATAAC | 50797 |
rs238087703 | snp | A/C | | | intron-variant | Copb2 | Mm_Celera | 9:98582114 | AGATTTCATACTGTA[A/C]ATATTCATTGAAAAC | 50797 |
rs238103073 | in-del | -/T | | | intron-variant, upstream-variant-2KB | Copb2, 4930579K19Rik | Mm_Celera | 9:98565276 | ATGCAGTGTGAGTAG[-/T]TTAATCGTCTAAGAC | 50797 |
rs238187958 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98579357 | TGGCCTCTGAGGGCC[A/G]GTTGCGCTTTATAAA | 50797 |
rs238620843 | in-del | -/A | | | intron-variant | Copb2 | Mm_Celera | 9:98586168 | ATTATCTCAAGGTCT[-/A]AAACACTTTTAAGGA | 50797 |
rs238676855 | snp | A/G | | | synonymous-codon | Copb2 | Mm_Celera | 9:98577468 | ATTGCCACTGGCAGT[A/G]AAGGACATGGGCAGT | 50797 |
rs238760523 | snp | A/T | | | intron-variant | Copb2 | Mm_Celera | 9:98570200 | ATCATACACTTGTTT[A/T]ACATTTTTAGTGAAA | 50797 |
rs238816524 | in-del | -/A | | | intron-variant | Copb2 | Mm_Celera | 9:98583247 | GTGTGTCTCTAAAAC[-/A]AAAAAACAAACAAAA | 50797 |
rs239205196 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98578074 | CATTGCTATTTCACA[A/G]CTGTCATTTTGTGAC | 50797 |
rs239223903 | snp | C/G | | | intron-variant | Copb2 | Mm_Celera | 9:98574388 | AGATATTCTAGAGAA[C/G]AACTTGAAAAAGCCT | 50797 |
rs239305290 | snp | A/G | | | utr-variant-3-prime, intron-variant | Copb2, Mrps22 | Mm_Celera | 9:98588283 | GAGTTGATGGGCAGC[A/G]TTTAAGTTACTATGT | 50797 |
rs239531549 | snp | G/T | | | intron-variant, upstream-variant-2KB | Copb2, 4930579K19Rik | Mm_Celera | 9:98563888 | GTTCCCGGGGCTTCT[G/T]GGCTAGGAGCAGTAG | 50797 |
rs239581824 | in-del | -/CCC | | | intron-variant | Copb2 | Mm_Celera | 9:98569331 | CTTGACCCCCCCCCC[-/CCC]AAAAAAAAAAAGAAA | 50797 |
rs239731026 | snp | A/C | | | upstream-variant-2KB, nc-transcript-variant | Copb2, 4930579K19Rik | Mm_Celera | 9:98563533 | CGAAGGTGAGCAGCC[A/C]AGACCGCCGCTAGTC | 50797 |
rs239803971 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98572065 | CACCAGTATAAATTT[A/G]ACCTACTTGCTGTCC | 50797 |
rs239994795 | snp | C/T | | | intron-variant | Copb2 | Mm_Celera | 9:98574553 | ACAGCAAACATGTAC[C/T]ACATGGTGAGCACTC | 50797 |
rs240032541 | snp | C/T | | | intron-variant | Copb2 | Mm_Celera | 9:98577612 | CCCCAGTCTGCCTCC[C/T]GGAACTGTGCCCTGG | 50797 |
rs240112991 | in-del | -/AAG | | | intron-variant | Copb2 | Mm_Celera | 9:98580493 | CTGTGCTGTTTACCT[-/AAG]AAGTGCTCAGGATAT | 50797 |
rs240305084 | snp | C/G | | | intron-variant | Copb2 | Mm_Celera | 9:98584701 | GGATGATCTTAAAGA[C/G]CTAAGTATAAAATTG | 50797 |
rs240341806 | snp | C/T | | | intron-variant | Copb2 | Mm_Celera | 9:98581766 | CTTCCTCTAACAAGG[C/T]CATACCTAATAATGC | 50797 |
rs240405945 | in-del | -/GTGTGTGTGTGTGTGTGT | | | intron-variant | Copb2 | Mm_Celera | 9:98582583 | ATTTGAGCAAGAAGG[-/GTGTGTGTGTGTGTGTGT]GTGTGTGTGTGTGTG | 50797 |
rs240624357 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98574210 | CTCATGACTCACTGG[A/G]TATTTAAACCAAGTG | 50797 |
rs240743508 | snp | A/G | | | intron-variant, upstream-variant-2KB | Copb2, 4930579K19Rik | Mm_Celera | 9:98565119 | AGAAGGAGCTGGATA[A/G]GCACTGAGCCTGCCC | 50797 |
rs240827065 | snp | A/C | | | intron-variant | Copb2 | Mm_Celera | 9:98565921 | CTGTTTCAGGGCATT[A/C]CCTCTGCCGGGTCCT | 50797 |
rs240967061 | snp | C/G | | | upstream-variant-2KB, nc-transcript-variant | Copb2, 4930579K19Rik | Mm_Celera | 9:98563513 | CTTGCCTTTCTGAAA[C/G]TGACCGAAGGTGAGC | 50797 |
rs241361079 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98583936 | TTCCAAATATCTGCT[A/G]TTCACTCTGGGGTTT | 50797 |
rs241428763 | snp | C/T | | | intron-variant | Copb2 | Mm_Celera | 9:98580909 | AGAGAGCAGCCCACC[C/T]CACCTGAATGATAGA | 50797 |
rs241636309 | snp | C/G | | | intron-variant | Copb2 | Mm_Celera | 9:98577567 | CTGAGCTTGTGTGTG[C/G]TGGAGCAACTGTGCA | 50797 |
rs241750657 | snp | A/C | | | intron-variant, upstream-variant-2KB | Copb2, 4930579K19Rik | Mm_Celera | 9:98564895 | TTACTATAAGCCGTG[A/C]TCTGCTCTAACTGAA | 50797 |
rs242080628 | snp | C/T | | | intron-variant | Copb2 | Mm_Celera | 9:98582196 | ACTTTGCATTCCTTA[C/T]CACTCTCATCATATC | 50797 |
rs242084371 | snp | C/T | | | intron-variant | Copb2 | Mm_Celera | 9:98568421 | GCTGCCATTCATGTG[C/T]ATTGAGAGTGGTAAG | 50797 |
rs242299727 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98581107 | GTCAGTCAtctgtct[A/G]tctgtctgtctgtct | 50797 |
rs242562655 | snp | G/T | | | intron-variant | Copb2 | Mm_Celera | 9:98581473 | GCAAAAACAGAATTT[G/T]AAAGTATGTGTCTTA | 50797 |
rs242681870 | snp | A/T | | | upstream-variant-2KB, downstream-variant-500B | Copb2, 4930579K19Rik | Mm_Celera | 9:98562328 | GATCATAGTCACTAT[A/T]GCAGAACTTGATGTT | 50797 |
rs242811549 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98580636 | TGAAGACAGAAATTG[A/G]GGAATGATTGATGTG | 50797 |
rs243076974 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98580964 | CAACAGTGCTGTGCT[A/G]TCCACCTTCCCAAGT | 50797 |
rs243192303 | snp | C/T | | | synonymous-codon | Copb2 | Mm_Celera | 9:98582822 | CATGCGGAGGGATTT[C/T]AGCATGGCGGATAAA | 50797 |
rs243481816 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98570053 | GAGGCAAGCCAGGAC[A/G]GAGGGTCTGGAGTAC | 50797 |
rs243967970 | snp | C/T | | | intron-variant | Copb2 | Mm_Celera | 9:98577889 | AATTGTCAACTCTGT[C/T]TTCCCTGAAGATTTA | 50797 |
rs243970019 | snp | A/G | | | intron-variant, upstream-variant-2KB | Copb2, 4930579K19Rik | Mm_Celera | 9:98564628 | ATCTAGAGATGACCA[A/G]GAGTGATGGGTAAAT | 50797 |
rs244002231 | snp | C/T | | | intron-variant, upstream-variant-2KB | Copb2, 4930579K19Rik | Mm_Celera | 9:98565552 | ATGTGGGGGCTTATG[C/T]TATGTTGAAGATCCC | 50797 |
rs244229927 | snp | C/T | | | intron-variant | Copb2 | Mm_Celera | 9:98579254 | TGTGATAAATCCATT[C/T]GACTGGGGATTCAAG | 50797 |
rs244257444 | snp | C/T | | | intron-variant | Copb2 | Mm_Celera | 9:98569301 | GAACAGCCAGGACTA[C/T]ACAGAGAAACCCTGT | 50797 |
rs244441044 | snp | A/G | | | synonymous-codon | Copb2 | Mm_Celera | 9:98577396 | GGCCAAGCATTCAGA[A/G]GTCCAGCAGGCCAAC | 50797 |
rs244687417 | snp | A/G | | | missense | Copb2 | Mm_Celera | 9:98580107 | AGAGAAAGCAACAGT[A/G]TTGTAAAGATATTTA | 50797 |
rs244909136 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98568867 | TCATGGAGGCTCTGC[A/G]GCCGCCTCTCTTACT | 50797 |
rs244930171 | in-del | -/T | | | intron-variant | Copb2 | Mm_Celera | 9:98569168 | ATACAAAAAGAGACA[-/T]TAAAATGATAGCTTA | 50797 |
rs244953953 | snp | C/G | | | intron-variant | Copb2 | Mm_Celera | 9:98567559 | GAACGTCCAAAAATG[C/G]CTTATATATTCCTCT | 50797 |
rs245001777 | in-del | -/T | | | intron-variant, upstream-variant-2KB | Copb2, 4930579K19Rik | Mm_Celera | 9:98565550 | GGATGTGGGGGCTTA[-/T]GTTATGTTGAAGATC | 50797 |
rs245105874 | snp | C/T | | | intron-variant | Copb2 | Mm_Celera | 9:98579779 | TTGTGTGCTGAGTAG[C/T]AGTCCATTGAATGGA | 50797 |
rs245108694 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98577733 | AGATACCTTGGATTA[A/G]TGCCCTTGGGGGTCT | 50797 |
rs245146184 | snp | A/G | | | intron-variant, upstream-variant-2KB | Copb2, 4930579K19Rik | Mm_Celera | 9:98565324 | AAACACTCATGACTG[A/G]GATGGTAAGTATGAC | 50797 |
rs245393475 | snp | G/T | | | downstream-variant-500B | Copb2, Mrps22 | Mm_Celera | 9:98588486 | TCCTTGAATAGCTAA[G/T]GGCGTCTTTCAAAAC | 50797 |
rs245738573 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98575129 | atgggatggatcccc[A/G]ggtgcagcagtctct | 50797 |
rs245782858 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98571294 | AGTAGCTGTCCATAC[A/G]CACTTTGTCTGCACT | 50797 |
rs245784283 | snp | C/T | | | intron-variant | Copb2 | Mm_Celera | 9:98585275 | AATTCAGGGTACTCT[C/T]AAGTTCTATACTCTG | 50797 |
rs245827414 | snp | C/T | | | intron-variant | Copb2 | Mm_Celera | 9:98577625 | CCCGGAACTGTGCCC[C/T]GGCCCACAGGCCGCA | 50797 |
rs245924560 | snp | C/T | | | intron-variant | Copb2 | Mm_Celera | 9:98584304 | AGCACAAGGGAGGGA[C/T]ATTGATAGGCTGAAT | 50797 |
rs246103674 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98586194 | AAGGAGTTGTAAGCA[A/G]TGTTTCTCCACTGAC | 50797 |
rs246220798 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98569996 | AAAGCTTCCTCCCTG[A/G]GTAGGTTTCCAGACA | 50797 |
rs246252546 | snp | C/T | | | intron-variant | Copb2 | Mm_Celera | 9:98570901 | ATATTGCAATTGCTC[C/T]GATTCCTGCCAGAAA | 50797 |
rs246314729 | in-del | -/C | | | intron-variant | Copb2 | Mm_Celera | 9:98577533 | CTAATGGGAGGTAAG[-/C]TGTCAGTGACATCCC | 50797 |
rs246503613 | snp | C/G | | | intron-variant | Copb2 | Mm_Celera | 9:98569829 | AAGAGATAATTCACT[C/G]AACAGATGGTGGGGT | 50797 |
rs246573767 | snp | C/T | | | intron-variant | Copb2 | Mm_Celera | 9:98586855 | CAGTCATGAACACTG[C/T]TGTGCCTCACACCCA | 50797 |
rs246596296 | snp | C/T | | | intron-variant, upstream-variant-2KB | Copb2, 4930579K19Rik | Mm_Celera | 9:98563878 | GCTGCGGCGGGTTCC[C/T]GGGGCTTCTTGGCTA | 50797 |
rs246876944 | snp | A/C | | | intron-variant, upstream-variant-2KB | Copb2, 4930579K19Rik | Mm_Celera | 9:98564389 | CACACAGAGGATGAC[A/C]TTTTTGGGGAAGGCC | 50797 |
rs246935534 | snp | C/T | | | intron-variant, upstream-variant-2KB | Copb2, 4930579K19Rik | Mm_Celera | 9:98564167 | TTGACCAAGTCACTT[C/T]ATTCTGTCATTGAGG | 50797 |
rs247153696 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98574458 | TCTGTCACTTTGCAG[A/G]TGTATGGTTTGGGTA | 50797 |
rs247365981 | snp | C/T | | | intron-variant | Copb2 | Mm_Celera | 9:98578677 | CAGCAAGCATTGCCG[C/T]ATGGTTGGAGTCGCT | 50797 |
rs247450875 | snp | A/C | | | intron-variant, upstream-variant-2KB | Copb2, 4930579K19Rik | Mm_Celera | 9:98563899 | TTCTTGGCTAGGAGC[A/C]GTAGCTAGAAGCGGT | 50797 |
rs248430794 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98573069 | TGAGTTGCTCAGCCT[A/G]CTTTCTTACACCACC | 50797 |
rs248483918 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98579640 | GATTTTTCTGTTACT[A/G]TATAGGTCAGACTTT | 50797 |
rs248573968 | snp | C/T | | | intron-variant | Copb2 | Mm_Celera | 9:98580479 | CACTGTGCTGAACAC[C/T]GTGCTGTTTACCTAA | 50797 |
rs248783326 | snp | A/C | | | upstream-variant-2KB, nc-transcript-variant | Copb2, 4930579K19Rik | Mm_Celera | 9:98563534 | GAAGGTGAGCAGCCC[A/C]GACCGCCGCTAGTCA | 50797 |
rs248885955 | in-del | -/A | | | intron-variant | Copb2 | Mm_Celera | 9:98566628 | CTGTTTGAGGAAGTC[-/A]ACAGATGAGAAGTTT | 50797 |
rs249014174 | in-del | -/A | | | intron-variant | Copb2 | Mm_Celera | 9:98583814 | GAGTTTATGCCCCCC[-/A]AACACAAAAACTACC | 50797 |
rs249078522 | snp | C/T | | | intron-variant | Copb2 | Mm_Celera | 9:98572726 | GTCTTGGTCCTCTCT[C/T]CCTGGCAAGTGTTCT | 50797 |
rs249258430 | snp | C/T | | | intron-variant | Copb2 | Mm_Celera | 9:98580065 | GTGTTTAATATGCTG[C/T]TTCCCCTGTCCCTCA | 50797 |
rs249285338 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98568394 | CCTCTGTCACCAGTG[A/G]CAAAGAATTTAGCTG | 50797 |
rs249878537 | snp | G/T | | | upstream-variant-2KB | Copb2, 4930579K19Rik | Mm_Celera | 9:98563613 | CGGGAGACGCGGAAG[G/T]CCGCGTTACCTAGGA | 50797 |
rs249881897 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98566558 | TAAATTTATTTACCT[A/G]TCTATAAACTGGGGG | 50797 |
rs250060952 | snp | C/T | | | intron-variant | Copb2 | Mm_Celera | 9:98565631 | ATGAGAGGGAGAAGT[C/T]AAATTTTGTGACAGT | 50797 |
rs250082526 | snp | C/G | | | intron-variant | Copb2 | Mm_Celera | 9:98576733 | AACATTTACTTTGAT[C/G]TTGGCTACTGGTTTG | 50797 |
rs250161556 | snp | A/T | | | synonymous-codon | Copb2 | Mm_Celera | 9:98588110 | TGACACAACAGACAT[A/T]AATCTGGATGAAGAT | 50797 |
rs250253694 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98577571 | GCTTGTGTGTGGTGG[A/G]GCAACTGTGCATATG | 50797 |
rs250270778 | snp | C/T | | | upstream-variant-2KB, nc-transcript-variant | Copb2, 4930579K19Rik | Mm_Celera | 9:98563531 | ACCGAAGGTGAGCAG[C/T]CCAGACCGCCGCTAG | 50797 |
rs250283903 | snp | A/C | | | intron-variant | Copb2 | Mm_Celera | 9:98569332 | CTTGACCCCCCCCCC[A/C]AAAAAAAAAAGAAAT | 50797 |
rs250306526 | in-del | -/A | | | intron-variant | Copb2 | Mm_Celera | 9:98586388 | CTTGAGTTGTTAATT[-/A]AATGTGTGGTTCAGA | 50797 |
rs250350451 | snp | C/T | | | intron-variant, upstream-variant-2KB | Copb2, 4930579K19Rik | Mm_Celera | 9:98563940 | ACTGCTGCGGCCTGA[C/T]GGGGTCCTCCTGTCC | 50797 |
rs250501474 | snp | A/G | | | synonymous-codon | Copb2 | Mm_Celera | 9:98574119 | GAATGTGTCGTGTGC[A/G]AGCTTCCATCCTGAG | 50797 |
rs250745493 | snp | G/T | | | intron-variant | Copb2 | Mm_Celera | 9:98587138 | AGGTCTCAAGGTATG[G/T]ATTTAGTTTAGAGAG | 50797 |
rs250800845 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98583606 | TTAAGTTTGGTTCCA[A/G]TGAACTACTTACCTG | 50797 |
rs250827982 | snp | A/C | | | intron-variant | Copb2 | Mm_Celera | 9:98581733 | ATATTACCTCAAAGC[A/C]CCACCTCCAGTGACA | 50797 |
rs250912208 | snp | C/T | | | intron-variant | Copb2 | Mm_Celera | 9:98566710 | TGAAAGGTGACCATG[C/T]TGGTGCACTAATGGC | 50797 |
rs251018525 | snp | G/T | | | intron-variant | Copb2 | Mm_Celera | 9:98565789 | ACGAGAACTGACTAG[G/T]TAGAGCACGGGCCTA | 50797 |
rs251174943 | snp | A/C | | | intron-variant, upstream-variant-2KB | Copb2, 4930579K19Rik | Mm_Celera | 9:98564111 | CGGGTCCGGTAGTGC[A/C]AGTAAATGCTAGAGT | 50797 |
rs251289245 | snp | A/T | | | intron-variant | Copb2 | Mm_Celera | 9:98570428 | GACCCTACCTTCTGA[A/T]TGGTCAGTGGTTATA | 50797 |
rs251452262 | snp | G/T | | | intron-variant | Copb2 | Mm_Celera | 9:98577620 | TGCCTCCCGGAACTG[G/T]GCCCTGGCCCACAGG | 50797 |
rs251534552 | snp | G/T | | | intron-variant | Copb2 | Mm_Celera | 9:98587939 | AAGTAGGATGCTGCT[G/T]CTCGTGTCAGGAGGA | 50797 |
rs251645477 | snp | G/T | | | intron-variant | Copb2 | Mm_Celera | 9:98580716 | GCAAACTTAAGAGCT[G/T]CTGGTTGCCATTAGA | 50797 |
rs251943443 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98570941 | TCTAGATGCATCAAC[A/G]TCTGGGGAGCAGAAA | 50797 |
rs252176442 | snp | C/T | | | intron-variant | Copb2 | Mm_Celera | 9:98583116 | TTGGAGCTGATTTTA[C/T]CACTTTTCTTACATC | 50797 |
rs252248691 | snp | G/T | | | intron-variant | Copb2 | Mm_Celera | 9:98578016 | GCTTGGACACCTCAG[G/T]CAGTTCCTCATGTTA | 50797 |
rs252456616 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98586730 | AAACATTTTATTAAG[A/G]TTTGCTAAAGAACCG | 50797 |
rs252459052 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98587681 | TAAAGCCACTTCCTA[A/G]CCCTGAGCTCCCTCT | 50797 |
rs252646376 | snp | C/T | | | synonymous-codon | Copb2 | Mm_Celera | 9:98585964 | ACAACTTGCTGAACT[C/T]GCCATTAGTAAATGT | 50797 |
rs252651771 | in-del | -/TTTTA | | | intron-variant | Copb2 | Mm_Celera | 9:98583152 | TAAGGTTCTTGGCAT[-/TTTTA]TTTCTAGCACACCTT | 50797 |
rs252908670 | snp | C/G | | | upstream-variant-2KB, nc-transcript-variant | Copb2, 4930579K19Rik | Mm_Celera | 9:98563206 | GCCAAACAAACGACC[C/G]GGTGGATGCTCTTTG | 50797 |
rs252929312 | in-del | -/T | | | intron-variant | Copb2 | Mm_Celera | 9:98581284 | CGCCTTTGAGGTGAG[-/T]GTCTGAGTCCAGCTT | 50797 |
rs253031805 | snp | A/G | | | upstream-variant-2KB, downstream-variant-500B | Copb2, 4930579K19Rik | Mm_Celera | 9:98562026 | TAAGCCAGAGTAAAC[A/G]AGAGATTTTGTTTTA | 50797 |
rs253471646 | snp | C/T | | | intron-variant | Copb2 | Mm_Celera | 9:98570211 | GTTTTACATTTTTAG[C/T]GAAAAATACAGTTTG | 50797 |
rs253546891 | in-del | -/TGT | | | intron-variant | Copb2 | Mm_Celera | 9:98571258 | TAAAAAGTTTCCCCA[-/TGT]TTTTTTTTTTTTATG | 50797 |
rs253974182 | snp | C/T | | | synonymous-codon | Copb2 | Mm_Celera | 9:98582834 | TTTTAGCATGGCGGA[C/T]AAAGTCCTCCCTACC | 50797 |
rs254017684 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98567458 | GATTTTAATTTAGCC[A/G]AGTGTAAATAGCTAC | 50797 |
rs254051133 | snp | A/G | | | downstream-variant-500B | Copb2, Mrps22 | Mm_Celera | 9:98588648 | ATATAGATGCCAGCC[A/G]TCCCCACGCCACCTA | 50797 |
rs254342567 | in-del | -/TA | | | intron-variant | Copb2 | Mm_Celera | 9:98585407 | TTTTGTAGTTCTTTG[-/TA]TATATATATGTACTG | 50797 |
rs254375120 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98573831 | GTCATATTAAACCAC[A/G]CATCTCTGAGTGTCC | 50797 |
rs254519472 | snp | C/T | | | intron-variant | Copb2 | Mm_Celera | 9:98587891 | TCTGAGGTTGAGATG[C/T]CTTTGGCATCCTAGT | 50797 |
rs254617953 | in-del | -/T | | | intron-variant | Copb2 | Mm_Celera | 9:98573817 | AGGGTTTTTACACTG[-/T]CATATTAAACCACAC | 50797 |
rs254879158 | in-del | -/A | | | downstream-variant-500B | Copb2, Mrps22 | Mm_Celera | 9:98588406 | GTTTCCTTCCTAGTG[-/A]AAATGGCCATTGAGT | 50797 |
rs255163766 | snp | G/T | | | intron-variant | Copb2 | GRCm38.p3 | 9:98571775 | AAGCGGTCACTTtgt[G/T]tgtgtgtgtgtgtgt | 50797 |
rs255623442 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98575220 | aagaagaggtgaagt[A/G]tccacactttggtct | 50797 |
rs255681291 | in-del | -/TTTTCTTGCCAT | | | intron-variant | Copb2 | Mm_Celera | 9:98568819 | GGAGTGTGAGTTGAC[-/TTTTCTTGCCAT]TTGTCCCGCCAGGCA | 50797 |
rs255819300 | snp | C/T | | | intron-variant | Copb2 | Mm_Celera | 9:98573348 | GAGCACACTGTGTGT[C/T]GGGCTGTGGTGTTGG | 50797 |
rs255932593 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98568551 | GCAAGTCAATGTTGT[A/G]AAACATCAACAGTGT | 50797 |
rs255941536 | snp | A/G | | | intron-variant, upstream-variant-2KB | Copb2, 4930579K19Rik | Mm_Celera | 9:98564928 | CTGATTTTAATTCTC[A/G]GAATGCTAAGAGAGA | 50797 |
rs255960798 | snp | C/T | | | intron-variant | Copb2 | Mm_Celera | 9:98580062 | TTAGTGTTTAATATG[C/T]TGCTTCCCCTGTCCC | 50797 |
rs256109848 | snp | C/T | | | downstream-variant-500B, utr-variant-3-prime | Copb2, Mrps22 | Mm_Celera | 9:98588756 | AAGTACCTTTTAATC[C/T]CAAGATTTTTAAATG | 50797 |
rs256195940 | snp | A/C | | | intron-variant | Copb2 | Mm_Celera | 9:98586945 | GCAAGGGGCAGAGGC[A/C]CTGGAGGATTTTGCC | 50797 |
rs256429201 | snp | G/T | | | upstream-variant-2KB, nc-transcript-variant | Copb2, 4930579K19Rik | Mm_Celera | 9:98563477 | GACGTTCAGCAGGAA[G/T]CCAGCACTGCGCTCC | 50797 |
rs256730251 | snp | C/T | | | upstream-variant-2KB, nc-transcript-variant | Copb2, 4930579K19Rik | Mm_Celera | 9:98563105 | CTTGGCCAGTAAACC[C/T]GAGTTCTTTGAGTCT | 50797 |
rs256758496 | snp | A/T | | | intron-variant | Copb2 | Mm_Celera | 9:98565635 | GAGGGAGAAGTTAAA[A/T]TTTGTGACAGTAATT | 50797 |
rs256809384 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98587985 | GGCCTTGGACTGTGG[A/G]CTGGGTAACCCCGTA | 50797 |
rs256907565 | snp | C/T | | | intron-variant | Copb2 | Mm_Celera | 9:98569214 | GCACACCTTTAATCC[C/T]AGCACGCAGGAGGCA | 50797 |
rs257018031 | snp | C/T | | | upstream-variant-2KB, nc-transcript-variant | Copb2, 4930579K19Rik | Mm_Celera | 9:98562894 | TAAGGGCAACTTCCA[C/T]TTGTTTCATAGCATT | 50797 |
rs257067502 | snp | C/T | | | intron-variant | Copb2 | Mm_Celera | 9:98569754 | TGCTGGAATTAAAGG[C/T]ATATGTCAGCCACTA | 50797 |
rs257089291 | snp | C/T | | | intron-variant | Copb2 | Mm_Celera | 9:98579170 | CCAGCACAGCTGCTT[C/T]ATTGAAGCACTTGGA | 50797 |
rs257133641 | snp | A/C | | | intron-variant | Copb2 | Mm_Celera | 9:98585273 | TAAATTCAGGGTACT[A/C]TTAAGTTCTATACTC | 50797 |
rs257322025 | snp | C/T | | | intron-variant | Copb2 | Mm_Celera | 9:98574674 | TTATTATTTTCTTTA[C/T]ATACATTTCAAATGC | 50797 |
rs257429772 | snp | A/T | | | intron-variant | Copb2 | Mm_Celera | 9:98585646 | TTAATTCCGTTTACA[A/T]GGTTTTAGATTCAGT | 50797 |
rs257482842 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98572627 | GGGTCTATAGTGTGT[A/G]CTAAGGTGGCCTAGA | 50797 |
rs257602982 | in-del | -/GA | | | upstream-variant-2KB, nc-transcript-variant | Copb2, 4930579K19Rik | Mm_Celera | 9:98562697 | AAATTTGTTTTTACT[-/GA]GACAGAATAGTAAAA | 50797 |
rs257791957 | snp | C/T | | | intron-variant, upstream-variant-2KB | Copb2, 4930579K19Rik | Mm_Celera | 9:98564340 | GGCAGCCCAGCTCGT[C/T]GTTTTCTAGTTGATG | 50797 |
rs257967121 | snp | G/T | | | utr-variant-5-prime, upstream-variant-2KB | Copb2, 4930579K19Rik | Mm_Celera | 9:98563779 | CTGAGTGTGTCGCCT[G/T]GAGCCTGTGACGGGC | 50797 |
rs257967247 | snp | A/C | | | intron-variant | Copb2 | Mm_Celera | 9:98574582 | TCTACCCAGGAAACC[A/C]TGCTGTGATTTTATA | 50797 |
rs258239022 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98579122 | GGTGTTGATGCCAAT[A/G]TGGTTGATGCTTTTC | 50797 |
rs258304062 | in-del | -/TAT | | | intron-variant, upstream-variant-2KB | Copb2, 4930579K19Rik | Mm_Celera | 9:98564943 | GAATGCTAAGAGAGA[-/TAT]TATTATTATTATCCC | 50797 |
rs258467543 | in-del | -/AG | | | upstream-variant-2KB, downstream-variant-500B | Copb2, 4930579K19Rik | Mm_Celera | 9:98562220 | TTTTAAAAGATTAAA[-/AG]AGAGAGAGAGAGTCT | 50797 |
rs258498291 | in-del | -/C | | | intron-variant | Copb2 | Mm_Celera | 9:98584352 | CCTAACTGATGACAG[-/C]CCCTCAGTGCCTGAA | 50797 |
rs258536536 | in-del | -/TG | | | upstream-variant-2KB, downstream-variant-500B | Copb2, 4930579K19Rik | Mm_Celera | 9:98562069 | AACACTTAAGAGTTA[-/TG]TGTGTGTGTGTTTAT | 50797 |
rs258609822 | in-del | -/A | | | intron-variant | Copb2 | Mm_Celera | 9:98583724 | CAAACATTCATACAC[-/A]AAAAATCTTAAAGCA | 50797 |
rs258636096 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98583679 | CCTCTTCTGGCTTCT[A/G]TAGGCATCAGGCACA | 50797 |
rs258803054 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98584037 | GATGGGGGAAGCAGA[A/G]TGGCACATTTCCAGC | 50797 |
rs259298567 | snp | C/G | | | intron-variant | Copb2 | Mm_Celera | 9:98584371 | TCAGTGCCTGAACCG[C/G]AGTTACAGGCTAGAT | 50797 |
rs259477503 | snp | A/T | | | upstream-variant-2KB | Copb2 | Mm_Celera | 9:98561847 | TCGATGCTGGAAGGG[A/T]TGCCCACTTGGGATG | 50797 |
rs259567971 | in-del | -/AT | | | intron-variant | Copb2 | Mm_Celera | 9:98583016 | GTCTTACCACTGACC[-/AT]ATCAGGTTGGCAGCA | 50797 |
rs259665363 | snp | C/T | | | intron-variant | Copb2 | Mm_Celera | 9:98571085 | TCACCTGCAGGAAGG[C/T]GATTACCTGGGTATC | 50797 |
rs259675600 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98579710 | TAGGCATGCATTCTT[A/G]GATATGGCTTTTGAG | 50797 |
rs259762426 | snp | A/T | | | intron-variant | Copb2 | Mm_Celera | 9:98568726 | GAACCATCTTGGTGT[A/T]AGCTGTTGCTTCCTT | 50797 |
rs259804872 | snp | C/T | | | intron-variant | Copb2 | Mm_Celera | 9:98581603 | TGATGGGAAGCATGG[C/T]ATCCTACAGGCAGAC | 50797 |
rs259870166 | in-del | -/GTGTGC | | | upstream-variant-2KB, nc-transcript-variant | Copb2, 4930579K19Rik | Mm_Celera | 9:98562924 | ATCTTTTTAAAAGGT[-/GTGTGC]GTGTGAAATCGATAC | 50797 |
rs259937521 | snp | C/T | | | intron-variant | Copb2 | Mm_Celera | 9:98569772 | ATGTCAGCCACTATG[C/T]CTGGTTTATGGGCTC | 50797 |
rs260176494 | snp | C/T | | | intron-variant | Copb2 | Mm_Celera | 9:98573746 | TTATAAAAAAGAATG[C/T]AAATGCATTTTAAGA | 50797 |
rs260280311 | snp | A/G | | | upstream-variant-2KB, downstream-variant-500B | Copb2, 4930579K19Rik | Mm_Celera | 9:98562004 | TTCCCAACCTTCCAC[A/G]TGCCTCTAAGCCAGA | 50797 |
rs260562136 | in-del | -/AA | | | downstream-variant-500B | Copb2, Mrps22 | Mm_Celera | 9:98588604 | TATCTGCATTAATAT[-/AA]AAAGAGAGATTCATA | 50797 |
rs260738793 | in-del | -/GGAGGGAG | | | intron-variant | Copb2 | Mm_Celera | 9:98577221 | TCAATGTGGAAGGAA[-/GGAGGGAG]GGAGGGAAAGGAAGG | 50797 |
rs260988870 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98573238 | CACCAGCTGAACTAT[A/G]TATATAGTCTCCATG | 50797 |
rs261082996 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98565964 | GAGAAGCAAACCTTC[A/G]CTTTCTGTTGAATTC | 50797 |
rs261098770 | snp | A/T | | | intron-variant | Copb2 | Mm_Celera | 9:98567898 | ACAATTTAGGAAAGT[A/T]AAAACAATGTTTATA | 50797 |
rs261333314 | snp | G/T | | | intron-variant | Copb2 | Mm_Celera | 9:98574463 | CACTTTGCAGGTGTA[G/T]GGTTTGGGTAGACTA | 50797 |
rs261483675 | in-del | -/TCAGGGCGG | | | intron-variant, upstream-variant-2KB | Copb2, 4930579K19Rik | Mm_Celera | 9:98564053 | CGGCGCCCCCGACTC[-/TCAGGGCGG]TCAGGGCGCCTGTCA | 50797 |
rs261532286 | snp | A/G | | | intron-variant, upstream-variant-2KB | Copb2, 4930579K19Rik | Mm_Celera | 9:98564398 | GATGACCTTTTTGGG[A/G]AAGGCCCTGAGATCT | 50797 |
rs261576859 | snp | C/G | | | intron-variant, upstream-variant-2KB | Copb2, 4930579K19Rik | Mm_Celera | 9:98565380 | GCACATTTTAAAATG[C/G]GTGTCTTTACTTTGG | 50797 |
rs261807315 | snp | C/T | | | upstream-variant-2KB | Copb2, 4930579K19Rik | Mm_Celera | 9:98563642 | GAAACTGGGGCGGGA[C/T]CATGCACGGACCGCC | 50797 |
rs262094986 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98573284 | TGGCACCTTCAGAGA[A/G]TAGTGATTCTGCTTC | 50797 |
rs262368714 | snp | A/G | | | downstream-variant-500B, utr-variant-3-prime | Copb2, Mrps22 | Mm_Celera | 9:98588810 | GAAGGGCATTACTAT[A/G]AAATGTGTTTTTAAC | 50797 |
rs262732297 | snp | C/T | | | intron-variant | Copb2 | Mm_Celera | 9:98587856 | ATCCTCTGCCCCACG[C/T]CCCATGTCAGGAACA | 50797 |
rs262746556 | snp | C/T | | | intron-variant | Copb2 | Mm_Celera | 9:98586199 | GTTGTAAGCAGTGTT[C/T]CTCCACTGACTGTGA | 50797 |
rs262748346 | snp | A/G | | | upstream-variant-2KB, nc-transcript-variant | Copb2, 4930579K19Rik | Mm_Celera | 9:98562641 | AGTATGCGATTATGT[A/G]ATTATTCATGTCAAT | 50797 |
rs262819985 | in-del | -/AA | | | intron-variant | Copb2 | Mm_Celera | 9:98569332 | CTTGACCCCCCCCCC[-/AA]AAAAAAAAAGAAATC | 50797 |
rs262867805 | snp | C/T | | | synonymous-codon | Copb2 | Mm_Celera | 9:98577483 | AAAGGACATGGGCAG[C/T]TGTGAAATATATCCA | 50797 |
rs263040425 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98572212 | GGGTTAGCACAGATA[A/G]TCCTTCTGGGAAACT | 50797 |
rs263133717 | snp | C/T | | | upstream-variant-2KB | Copb2, 4930579K19Rik | Mm_Celera | 9:98563661 | GCACGGACCGCCTTA[C/T]GGAGGGTGTGCGCAG | 50797 |
rs263149984 | snp | C/T | | | intron-variant | Copb2 | Mm_Celera | 9:98587001 | TTTATCTGCTGTTAC[C/T]ATTTGTTTGTCTAAC | 50797 |
rs263186875 | in-del | -/A | | | intron-variant | Copb2 | Mm_Celera | 9:98567818 | TGTAAATACAAACTT[-/A]AAAAATACCCCATTT | 50797 |
rs263271363 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98568401 | CACCAGTGACAAAGA[A/G]TTTAGCTGCCATTCA | 50797 |
rs263318688 | snp | A/T | | | intron-variant | Copb2 | Mm_Celera | 9:98585120 | TCCAAGACTTTTCCA[A/T]AACCCAGGGAAGGGT | 50797 |
rs263534501 | snp | A/T | | | intron-variant | Copb2 | Mm_Celera | 9:98582060 | TTGCAGTTTAGATTG[A/T]TATTTTTTAGTTATG | 50797 |
rs263539617 | in-del | -/T | | | intron-variant | Copb2 | Mm_Celera | 9:98582421 | TGAGTGTCATTTTGC[-/T]TTTTGTCTAAAGCAG | 50797 |
rs263613691 | snp | A/G | | | upstream-variant-2KB, nc-transcript-variant | Copb2, 4930579K19Rik | Mm_Celera | 9:98562943 | TGAAATCGATACACA[A/G]TGTATTTGCACTTTT | 50797 |
rs263685091 | snp | C/G | | | upstream-variant-2KB, downstream-variant-500B | Copb2, 4930579K19Rik | Mm_Celera | 9:98562345 | CAGAACTTGATGTTG[C/G]TGACCTGCAGCAGCA | 50797 |
rs263761033 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98571680 | TTACTATGACTGGCC[A/G]GAAAGCTACTCCTGT | 50797 |
rs263782038 | snp | C/T | | | intron-variant | Copb2 | Mm_Celera | 9:98569242 | GCAGAGACAGGCAGA[C/T]TTCTGAGTTCGTAGA | 50797 |
rs263891314 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98581802 | CCCATGGGCCAACAC[A/G]TGAGTTTATGGGGTC | 50797 |
rs263916392 | in-del | -/CT | | | intron-variant | Copb2 | Mm_Celera | 9:98582934 | CTTTCCTTCCCTCCC[-/CT]CTCTTTCTTTTTAAA | 50797 |
rs263987167 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98570444 | TGGTCAGTGGTTATA[A/G]ATACCAGTTGCAGAG | 50797 |
rs264434207 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98579171 | CAGCACAGCTGCTTC[A/G]TTGAAGCACTTGGAG | 50797 |
rs264473309 | snp | C/T | | | intron-variant | Copb2 | Mm_Celera | 9:98575214 | AATTCTAAGAAGAGG[C/T]GAAGTGTCCACACTT | 50797 |
rs264486955 | in-del | -/GCTAGCTCCCTG | | | intron-variant | Copb2 | Mm_Celera | 9:98571041 | CAGACAAGCTAGCTA[-/GCTAGCTCCCTG]GTATTAATGTAAAGC | 50797 |
rs264527644 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98587697 | CCCTGAGCTCCCTCT[A/G]CATGGGGAATATTTA | 50797 |
rs264814455 | snp | C/T | | | intron-variant, upstream-variant-2KB | Copb2, 4930579K19Rik | Mm_Celera | 9:98564178 | ACTTTATTCTGTCAT[C/T]GAGGGTGGTGCTTGC | 50797 |
rs264948215 | in-del | -/ACC | | | intron-variant, upstream-variant-2KB | Copb2, 4930579K19Rik | Mm_Celera | 9:98565146 | GCCCTTCAGAAATAA[-/ACC]ACTCCACAAGCAAGA | 50797 |
rs265153844 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98572978 | CAAGGAAGTTGGGGA[A/G]GAACTCAAGGGAGGA | 50797 |
rs265192394 | snp | G/T | | | upstream-variant-2KB | Copb2 | Mm_Celera | 9:98561798 | ACTAGAACAGATGGG[G/T]GTGGGGCTGGGGTGT | 50797 |
rs265454529 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98573086 | TTTCTTACACCACCC[A/G]GGTTTACCTGCCCAG | 50797 |
rs265656563 | snp | G/T | | | intron-variant | Copb2 | Mm_Celera | 9:98580642 | CAGAAATTGGGGAAT[G/T]ATTGATGTGGAAAAG | 50797 |
rs265843429 | snp | A/G | | | intron-variant | Copb2 | Mm_Celera | 9:98569837 | ATTCACTCAACAGAT[A/G]GTGGGGTGAAGTGCA | 50797 |
rs265960786 | snp | A/C | | | intron-variant | Copb2 | Mm_Celera | 9:98567416 | AAGCAGGAGCTAAGA[A/C]TCTGCAGAGTGTAGG | 50797 |
rs266161793 | in-del | -/TA | | | intron-variant | Copb2 | Mm_Celera | 9:98584268 | TTTAAAAGCCTGTCC[-/TA]TGGCTTTATGCCCTA | 50797 |
rs266166206 | snp | A/T | | | downstream-variant-500B | Copb2, Mrps22 | Mm_Celera | 9:98588551 | CATTACCTGTCGGAC[A/T]CTTTGGTATTGTGGC | 50797 |
rs266210079 | in-del | -/A | | | intron-variant | Copb2 | Mm_Celera | 9:98573207 | TTGTGTCAAGTTGAG[-/A]AAAGTATAACCAGTT | 50797 |
rs266232388 | snp | A/C | | | intron-variant | Copb2 | Mm_Celera | 9:98577718 | GTTTCCTTGTTCTTA[A/C]GATACCTTGGATTAG | 50797 |
rs387647324 | in-del | -/GT | | | intron-variant | Copb2 | Mm_Celera | 9:98571826 | TGTGTGTGTGTGTGT[-/GT]CTGTCTGTCTGTCCG | 50797 |
rs578366098 | snp | C/T | | | intron-variant | Copb2 | GRCm38.p3 | 9:98576548 | GGTCAGTTATATATA[C/T]TATCATATCATCTGC | 50797 |
rs578446187 | snp | A/G | | | intron-variant | Copb2 | GRCm38.p3 | 9:98576489 | TCCAGCTACTTCACT[A/G]AAGCTGTTTATCAGG | 50797 |
rs578571771 | snp | C/T | | | intron-variant | Copb2 | GRCm38.p3 | 9:98574974 | TTGGGGGCCGTGTGA[C/T]CCATCCAATAGCTGA | 50797 |
rs578762283 | snp | C/G | | | intron-variant | Copb2 | GRCm38.p3 | 9:98574968 | CCTCCATTGGGGGCC[C/G]TGTGACCCATCCAAT | 50797 |
rs578937323 | snp | A/G | | | intron-variant | Copb2 | GRCm38.p3 | 9:98574873 | AGAGACACGAGCCCC[A/G]GGGCTACTGGTTAGT | 50797 |
rs579130810 | snp | C/T | | | intron-variant | Copb2 | GRCm38.p3 | 9:98566616 | GGAGGTCTCTTACTG[C/T]TTGAGGAAGTCAACA | 50797 |
rs579137321 | snp | A/G | | | intron-variant | Copb2 | GRCm38.p3 | 9:98576449 | GTGTAGAGAAAGGCC[A/G]TTGACTTGTTGAGTT | 50797 |
rs579429818 | snp | C/T | | | intron-variant | Copb2 | GRCm38.p3 | 9:98581906 | CTTTGCTATCTTCAC[C/T]AAGGAAATGTGAAGG | 50797 |
rs579833004 | snp | A/G | | | intron-variant | Copb2 | GRCm38.p3 | 9:98575376 | CTCACTTAGGATGAT[A/G]CCCTCCAGGTCCATC | 50797 |
rs580129054 | snp | C/T | | | intron-variant | Copb2 | GRCm38.p3 | 9:98575161 | GATGGTCCATCCTTT[C/T]GTTTCAGCTCTAAAC | 50797 |
rs580267597 | snp | C/T | | | intron-variant | Copb2 | GRCm38.p3 | 9:98578541 | GTTCATTTTAGTAAC[C/T]AACAGTTGAATACAG | 50797 |
rs580318301 | snp | C/G | | | intron-variant | Copb2 | GRCm38.p3 | 9:98571815 | TGTGTGTGTGTGTGT[C/G]TGTGTGTGTGTCTGT | 50797 |
rs580494002 | snp | A/G | | | intron-variant | Copb2 | GRCm38.p3 | 9:98584348 | AAAGCCTAACTGATG[A/G]CAGCCCCTCAGTGCC | 50797 |
rs580637109 | snp | A/T | | | intron-variant | Copb2 | GRCm38.p3 | 9:98574643 | TAGTTGCAAGTTTTT[A/T]AAAAATTTTTTTTAT | 50797 |
rs580683469 | snp | C/T | | | intron-variant | Copb2 | GRCm38.p3 | 9:98586265 | TGGGACAGCTGGTGA[C/T]GGCCGACTGTTGCTG | 50797 |
rs580800503 | snp | A/G | | | intron-variant | Copb2 | GRCm38.p3 | 9:98575646 | TATGTCCAACTTTCT[A/G]AGGAACCACCAGACT | 50797 |
rs580923122 | snp | A/G | | | upstream-variant-2KB, downstream-variant-500B | Copb2, 4930579K19Rik | GRCm38.p3 | 9:98562214 | CATAAGTTTTAAAAG[A/G]TTAAAAGAGAGAGAG | 50797 |
rs580944307 | snp | C/T | | | intron-variant | Copb2 | GRCm38.p3 | 9:98576488 | ATCCAGCTACTTCAC[C/T]GAAGCTGTTTATCAG | 50797 |
rs581275746 | snp | A/G | | | intron-variant | Copb2 | GRCm38.p3 | 9:98575925 | GCCCCATTTTTTAAT[A/G]GGGTTATTTGATTTT | 50797 |
rs581411070 | snp | C/G | | | intron-variant | Copb2 | GRCm38.p3 | 9:98586174 | TCAAGGTCTAAAACA[C/G]TTTTAAGGAGTTGTA | 50797 |
rs581453081 | snp | C/G | | | intron-variant | Copb2 | GRCm38.p3 | 9:98574877 | ACACGAGCCCCAGGG[C/G]TACTGGTTAGTTCAT | 50797 |
rs581476405 | snp | C/T | | | intron-variant | Copb2 | GRCm38.p3 | 9:98574865 | ATGTAGCTAGAGACA[C/T]GAGCCCCAGGGCTAC | 50797 |
rs581750070 | snp | G/T | | | intron-variant | Copb2 | GRCm38.p3 | 9:98574970 | TCCATTGGGGGCCGT[G/T]TGACCCATCCAATAG | 50797 |
rs581816422 | snp | A/G | | | intron-variant | Copb2 | GRCm38.p3 | 9:98569162 | TTCTTGATACAAAAA[A/G]AGACATTAAAATGAT | 50797 |
rs581943243 | snp | C/T | | | intron-variant | Copb2 | GRCm38.p3 | 9:98576610 | TTTGTATCCCCTTGA[C/T]TTCCTTTTGTTGTCG | 50797 |
rs582007892 | snp | A/G | | | intron-variant | Copb2 | GRCm38.p3 | 9:98578684 | CATTGCCGCATGGTT[A/G]GAGTCGCTGCATCTC | 50797 |
rs582246627 | snp | A/G | | | intron-variant | Copb2 | GRCm38.p3 | 9:98566640 | GTCAACAGATGAGAA[A/G]TTTTACCAACAGTAA | 50797 |
rs582347835 | snp | C/T | | | intron-variant | Copb2 | GRCm38.p3 | 9:98569639 | TTATTTATTTATTTA[C/T]TTATTTTTGAGACAG | 50797 |
rs582354418 | snp | A/G | | | intron-variant, upstream-variant-2KB | Copb2, 4930579K19Rik | GRCm38.p3 | 9:98565484 | AGGATTATCCTAACA[A/G]TCCTATTTTACACAC | 50797 |
rs582455107 | snp | C/T | | | synonymous-codon | Copb2 | GRCm38.p3 | 9:98577516 | GACCATTCAGCACAA[C/T]CCTAATGGGAGGTAA | 50797 |
rs582582538 | snp | A/G | | | intron-variant | Copb2 | GRCm38.p3 | 9:98574995 | CAATAGCTGACTGTG[A/G]TCATCCACTTCTGTG | 50797 |
rs582925940 | snp | A/T | | | intron-variant | Copb2 | GRCm38.p3 | 9:98574644 | AGTTGCAAGTTTTTT[A/T]AAAATTTTTTTTATT | 50797 |
rs583216101 | snp | A/G | | | intron-variant | Copb2 | GRCm38.p3 | 9:98583148 | CCTTTAAGGTTCTTG[A/G]CATTTTTATTTCTAG | 50797 |
rs583495202 | snp | C/T | | | intron-variant | Copb2 | GRCm38.p3 | 9:98575425 | ATAAATTCATTCTTT[C/T]TAATAGCTGAGTAGT | 50797 |
rs583799906 | snp | C/T | | | intron-variant | Copb2 | GRCm38.p3 | 9:98575262 | GAGTTTCATGTGTTT[C/T]GCAAATTGTATCTTG | 50797 |
rs584003765 | snp | A/G | | | intron-variant | Copb2 | GRCm38.p3 | 9:98575654 | ACTTTCTGAGGAACC[A/G]CCAGACTGATTTCCA | 50797 |
rs584201237 | snp | C/T | | | intron-variant | Copb2 | GRCm38.p3 | 9:98585401 | CTAACATTTTTGTAG[C/T]TCTTTGTATATATAT | 50797 |
rs584228247 | snp | A/G | | | intron-variant | Copb2 | GRCm38.p3 | 9:98586235 | GTGCTTGAGAGGCAT[A/G]TGGTACACAAATCCT | 50797 |
rs584537866 | snp | A/G | | | intron-variant | Copb2 | GRCm38.p3 | 9:98574912 | TTGTTCCACCTATAG[A/G]GTTGCAGGTCCCTTT | 50797 |
rs584624788 | snp | A/G | | | intron-variant | Copb2 | GRCm38.p3 | 9:98565834 | AGTGAAGAGCAAACA[A/G]TGAAGAACAGTTAGA | 50797 |
rs584779239 | snp | A/C | | | upstream-variant-2KB, downstream-variant-500B | Copb2, 4930579K19Rik | GRCm38.p3 | 9:98562203 | GAAATTCAGTACATA[A/C]GTTTTAAAAGATTAA | 50797 |
rs584951983 | snp | A/C | | | intron-variant | Copb2 | GRCm38.p3 | 9:98576180 | CCCATATTTTCGAGG[A/C]TTTTCCCCACTTTCT | 50797 |
rs585125511 | snp | C/T | | | intron-variant | Copb2 | GRCm38.p3 | 9:98576611 | TTGTATCCCCTTGAC[C/T]TCCTTTTGTTGTCGA | 50797 |
rs585130732 | snp | A/T | | | intron-variant | Copb2 | GRCm38.p3 | 9:98574973 | ATTGGGGGCCGTGTG[A/T]CCCATCCAATAGCTG | 50797 |
rs585219493 | snp | A/G | | | downstream-variant-500B | Copb2, Mrps22 | GRCm38.p3 | 9:98588613 | TAATATAAAAAGAGA[A/G]ATTCATAACCTGCAC | 50797 |
rs585371707 | snp | C/G | | | intron-variant | Copb2 | GRCm38.p3 | 9:98571819 | TGTGTGTGTGTGTGT[C/G]TGTGTGTCTGTCTGT | 50797 |
rs585397803 | snp | C/T | | | intron-variant | Copb2 | GRCm38.p3 | 9:98574870 | GCTAGAGACACGAGC[C/T]CCAGGGCTACTGGTT | 50797 |
rs585651038 | snp | A/G | | | intron-variant | Copb2 | GRCm38.p3 | 9:98575263 | AGTTTCATGTGTTTT[A/G]CAAATTGTATCTTGT | 50797 |
rs585839781 | snp | C/T | | | intron-variant | Copb2 | GRCm38.p3 | 9:98581298 | GTGTCTGAGTCCAGC[C/T]TAGGGCATTGAAGAC | 50797 |
rs585937774 | snp | C/T | | | intron-variant | Copb2 | GRCm38.p3 | 9:98567803 | TTGGAAAACCACCTC[C/T]GTAAATACAAACTTA | 50797 |
rs586053334 | snp | A/C | | | intron-variant | Copb2 | GRCm38.p3 | 9:98577530 | ATCCTAATGGGAGGT[A/C]AGCTGTCAGTGACAT | 50797 |
rs586083151 | snp | C/G | | | intron-variant | Copb2 | GRCm38.p3 | 9:98571811 | TGTGTGTGTGTGTGT[C/G]TGTGTGTGTGTGTGT | 50797 |
rs586240534 | snp | A/G | | | intron-variant | Copb2 | GRCm38.p3 | 9:98569638 | TTTATTTATTTATTT[A/G]TTTATTTTTGAGACA | 50797 |
rs586243499 | snp | C/T | | | intron-variant | Copb2 | GRCm38.p3 | 9:98575640 | TAGTACTATGTCCAA[C/T]TTTCTGAGGAACCAC | 50797 |
rs586469911 | snp | G/T | | | intron-variant | Copb2 | GRCm38.p3 | 9:98574996 | AATAGCTGACTGTGA[G/T]CATCCACTTCTGTGT | 50797 |
rs586590669 | snp | A/G | | | upstream-variant-2KB, downstream-variant-500B | Copb2, 4930579K19Rik | GRCm38.p3 | 9:98562213 | ACATAAGTTTTAAAA[A/G]ATTAAAAGAGAGAGA | 50797 |
rs586767296 | snp | C/G | | | intron-variant | Copb2 | GRCm38.p3 | 9:98586158 | GCAAGTAAGTATTAT[C/G]TCAAGGTCTAAAACA | 50797 |
rs586982756 | snp | C/G | | | intron-variant | Copb2 | GRCm38.p3 | 9:98571823 | TGTGTGTGTGTGTGT[C/G]TGTCTGTCTGTCTGT | 50797 |
rs587005450 | snp | C/T | | | intron-variant | Copb2 | GRCm38.p3 | 9:98586239 | TTGAGAGGCATATGG[C/T]ACACAAATCCTGGGA | 50797 |
rs587375585 | snp | G/T | | | intron-variant | Copb2 | GRCm38.p3 | 9:98574853 | CTTCTGCTACATATG[G/T]AGCTAGAGACACGAG | 50797 |
rs587451798 | snp | A/G | | | intron-variant | Copb2 | GRCm38.p3 | 9:98584257 | ACAGTAGTAGATTTA[A/G]AAGCCTGTCCTATGG | 50797 |
rs587566277 | snp | A/G | | | intron-variant | Copb2 | GRCm38.p3 | 9:98575910 | TTTGTTTAGCTCTGA[A/G]CCCCATTTTTTAATA | 50797 |
rs864279931 | snp | A/G | | | utr-variant-3-prime, intron-variant | Copb2, Mrps22 | GRCm38.p3 | 9:98588359 | ACTAGATCACCCGTC[A/G]TAAAATCTTTTGAAT | 50797 |